| geneid | 3064 |
|---|---|
| ensemblid | ENSG00000197386.14 |
| hgncid | 4851 |
| symbol | HTT |
| name | huntingtin |
| refseq_nuc | NM_001388492.1 |
| refseq_prot | NP_001375421.1 |
| ensembl_nuc | ENST00000355072.11 |
| ensembl_prot | ENSP00000347184.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 3074681 |
| end | 3243957 |
| strand | + |
| ver | v1.2 |
| region | chr4:3074681-3243957 |
| region5000 | chr4:3069681-3248957 |
| regionname0 | HTT_chr4_3074681_3243957 |
| regionname5000 | HTT_chr4_3069681_3248957 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 3140 | 41 | 2 | 6 | 26 | 3 | 4 | 23 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0002 | 0/0 | 3143 | 40 | 0 | 9 | 25 | 1 | 5 | 21 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0003 | 1/0 | 3142 | 16 | 5 | 2 | 7 | 1 | 0 | 4 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0004 | 0/0 | 3139 | 13 | 7 | 1 | 5 | 0 | 0 | 4 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0005 | 0/0 | 3144 | 13 | 0 | 4 | 9 | 0 | 0 | 9 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0006 | 0/0 | 3141 | 10 | 0 | 3 | 6 | 0 | 1 | 5 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0007 | 0/0 | 3141 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0008 | 0/0 | 3143 | 8 | 3 | 2 | 3 | 0 | 0 | 2 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0009 | 0/0 | 3138 | 7 | 1 | 5 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0010 | 0/0 | 3141 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0011 | 0/0 | 3143 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0012 | 0/0 | 3142 | 5 | 1 | 1 | 1 | 0 | 2 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0013 | 0/0 | 3140 | 4 | 0 | 3 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0014 | 0/0 | 3144 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0015 | 0/0 | 3144 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0016 | 0/0 | 3146 | 4 | 1 | 1 | 0 | 0 | 2 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0017 | 0/0 | 3140 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0018 | 0/0 | 3142 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0019 | 0/0 | 3138 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0020 | 0/0 | 3140 | 3 | 0 | 1 | 1 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0021 | 0/0 | 3144 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0022 | 0/0 | 3145 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0023 | 0/0 | 3145 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0024 | 0/0 | 3136 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0025 | 0/0 | 3138 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0026 | 0/0 | 3142 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0027 | 0/0 | 3135 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0028 | 0/0 | 3140 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0029 | 0/0 | 3140 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0030 | 0/0 | 3140 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0031 | 0/0 | 3144 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0032 | 0/0 | 3141 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0033 | 0/0 | 3141 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0034 | 0/0 | 3145 | 2 | 0 | 1 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0035 | 0/0 | 3142 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0036 | 0/0 | 3142 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0037 | 0/0 | 3148 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0038 | 0/0 | 3149 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0039 | 0/0 | 3151 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0040 | 0/0 | 3134 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0041 | 0/0 | 3136 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0042 | 0/0 | 3136 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0043 | 0/0 | 3138 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0044 | 0/0 | 3138 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0045 | 0/0 | 3137 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0046 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0047 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0048 | 0/0 | 3140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0049 | 0/0 | 3142 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0050 | 0/0 | 3142 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0051 | 0/0 | 3142 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0052 | 0/0 | 3142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0053 | 0/0 | 3142 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0054 | 0/0 | 3138 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0055 | 0/0 | 3139 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0056 | 0/0 | 3143 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0057 | 0/0 | 3143 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0058 | 0/0 | 3143 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0059 | 0/0 | 3143 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0060 | 0/0 | 3142 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0061 | 0/0 | 3142 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0062 | 0/0 | 3140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0063 | 0/0 | 3140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0064 | 0/0 | 3140 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0065 | 0/0 | 3140 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0066 | 0/0 | 3140 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0067 | 0/0 | 3140 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0068 | 0/0 | 3139 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0069 | 0/0 | 3144 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0070 | 0/0 | 3144 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0071 | 0/0 | 3144 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0072 | 0/0 | 3142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0073 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0074 | 0/0 | 3141 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0075 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0076 | 0/0 | 84 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0077 | 0/0 | 3145 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0078 | 0/0 | 3142 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0079 | 0/0 | 3142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0080 | 0/0 | 3146 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0081 | 0/0 | 3146 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0082 | 0/0 | 3143 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0083 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0084 | 0/0 | 3147 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0085 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0086 | 0/0 | 3146 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0087 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0088 | 0/0 | 3151 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0089 | 0/0 | 3149 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0090 | 0/0 | 3153 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0091 | 0/1 | 3151 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0092 | 0/0 | 108 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 9432 | 35 | 0 | 8 | 21 | 1 | 5 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0002 | 0/0 | 9423 | 24 | 0 | 1 | 21 | 0 | 2 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0003 | 0/0 | 9423 | 15 | 1 | 5 | 4 | 3 | 2 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0004 | 0/0 | 9435 | 12 | 0 | 4 | 8 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0005 | 0/0 | 9420 | 7 | 7 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0006 | 0/0 | 9429 | 7 | 0 | 1 | 5 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0007 | 0/0 | 9426 | 6 | 5 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0008 | 0/0 | 9417 | 6 | 0 | 5 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0009 | 0/0 | 9426 | 5 | 4 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0010 | 0/0 | 9432 | 5 | 2 | 2 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0011 | 0/0 | 9420 | 4 | 0 | 0 | 4 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0012 | 0/0 | 9429 | 4 | 1 | 1 | 1 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0013 | 0/0 | 9423 | 4 | 0 | 3 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0014 | 0/0 | 9435 | 4 | 3 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0015 | 0/0 | 9426 | 4 | 0 | 1 | 2 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0016 | 0/0 | 9435 | 4 | 2 | 2 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0017 | 0/0 | 9441 | 4 | 1 | 1 | 0 | 0 | 2 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0018 | 0/0 | 9423 | 3 | 2 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0019 | 0/0 | 9429 | 3 | 0 | 3 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0020 | 0/0 | 9417 | 3 | 3 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0021 | 0/0 | 9435 | 3 | 0 | 0 | 3 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0022 | 0/0 | 9426 | 3 | 0 | 2 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0023 | 0/0 | 9438 | 3 | 3 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0024 | 0/0 | 9429 | 3 | 2 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0025 | 0/0 | 9417 | 2 | 0 | 2 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0026 | 0/0 | 9429 | 2 | 2 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0027 | 0/0 | 9408 | 2 | 2 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0028 | 0/0 | 9432 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0029 | 0/0 | 9432 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0030 | 0/0 | 9432 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0031 | 0/0 | 9432 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0032 | 0/0 | 9423 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0033 | 0/0 | 9423 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0034 | 0/0 | 9423 | 2 | 0 | 0 | 1 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0035 | 0/0 | 9435 | 2 | 0 | 0 | 0 | 2 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0036 | 0/0 | 9426 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0037 | 0/0 | 9426 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0038 | 0/0 | 9438 | 2 | 0 | 1 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0039 | 0/0 | 9438 | 2 | 1 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0040 | 1/0 | 9429 | 2 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0041 | 0/0 | 9429 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0042 | 0/0 | 9429 | 2 | 2 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0043 | 0/0 | 9456 | 2 | 0 | 2 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0044 | 0/0 | 9455 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0045 | 0/0 | 9405 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0046 | 0/0 | 9411 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0047 | 0/0 | 9411 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0048 | 0/0 | 9411 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0049 | 0/0 | 9411 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0050 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0051 | 0/0 | 9414 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0052 | 0/0 | 9423 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0053 | 0/0 | 9426 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0054 | 0/0 | 9426 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0055 | 0/0 | 9426 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0056 | 0/0 | 9426 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0057 | 0/0 | 9423 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0058 | 0/0 | 9426 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0059 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0060 | 0/0 | 9417 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0061 | 0/0 | 9429 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0062 | 0/0 | 9429 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0063 | 0/0 | 9429 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0064 | 0/0 | 9429 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0065 | 0/0 | 9429 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0066 | 0/0 | 9420 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0067 | 0/0 | 9420 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0068 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0069 | 0/0 | 9420 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0070 | 0/0 | 9432 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0071 | 0/0 | 9432 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0072 | 0/0 | 9432 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0073 | 0/0 | 9432 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0074 | 0/0 | 9432 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0075 | 0/0 | 9432 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0076 | 0/0 | 9429 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0077 | 0/0 | 9429 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0078 | 0/0 | 9423 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0079 | 0/0 | 9423 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0080 | 0/0 | 9423 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0081 | 0/0 | 9423 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0082 | 0/0 | 9423 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0083 | 0/0 | 9423 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0084 | 0/0 | 9423 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0085 | 0/0 | 9423 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0086 | 0/0 | 9423 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0087 | 0/0 | 9420 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0088 | 0/0 | 9429 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0089 | 0/0 | 9423 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0090 | 0/0 | 9435 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0091 | 0/0 | 9435 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0092 | 0/0 | 9435 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0093 | 0/0 | 9435 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0094 | 0/0 | 9426 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0095 | 0/0 | 9426 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0096 | 0/0 | 9429 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0097 | 0/0 | 9426 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0098 | 0/0 | 9426 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0099 | 0/0 | 9426 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0100 | 0/0 | 9426 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0101 | 0/0 | 9439 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0102 | 0/0 | 9438 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0103 | 0/0 | 9438 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0104 | 0/0 | 9429 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0105 | 0/0 | 9429 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0106 | 0/0 | 9429 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0107 | 0/0 | 9429 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0108 | 0/0 | 9429 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0109 | 0/0 | 9441 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0110 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0111 | 0/0 | 9432 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0112 | 0/0 | 9432 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0113 | 0/0 | 9432 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0114 | 0/0 | 9432 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0115 | 0/0 | 9444 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0116 | 0/0 | 9444 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0117 | 0/0 | 9444 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0118 | 0/0 | 9441 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0119 | 0/0 | 9453 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0120 | 0/0 | 9456 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0121 | 0/0 | 9447 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0122 | 0/0 | 9447 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0123 | 0/0 | 9450 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0124 | 0/0 | 9450 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0125 | 0/0 | 9450 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0126 | 0/0 | 9462 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0127 | 0/1 | 9456 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| c0128 | 0/0 | 9429 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4047 | 124 | 22 | 23 | 67 | 5 | 7 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0002 | 0/0 | 4047 | 66 | 0 | 18 | 38 | 3 | 7 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0003 | 0/0 | 4063 | 43 | 27 | 8 | 2 | 1 | 5 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0004 | 0/1 | 4047 | 7 | 1 | 4 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0005 | 1/0 | 4044 | 4 | 3 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0006 | 0/0 | 4047 | 4 | 4 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0007 | 0/0 | 4063 | 3 | 3 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0008 | 0/0 | 4063 | 3 | 0 | 1 | 0 | 1 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0009 | 0/0 | 4047 | 3 | 1 | 2 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0010 | 0/0 | 4063 | 2 | 2 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0011 | 0/0 | 4063 | 2 | 1 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0012 | 0/0 | 4047 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0013 | 0/0 | 4047 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0014 | 0/0 | 4047 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0015 | 0/0 | 4047 | 2 | 2 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0016 | 0/0 | 4047 | 2 | 1 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0017 | 0/0 | 4047 | 2 | 0 | 1 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0018 | 0/0 | 4063 | 2 | 2 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0019 | 0/0 | 4047 | 2 | 0 | 2 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0020 | 0/0 | 4047 | 2 | 0 | 1 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0021 | 0/0 | 4047 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0022 | 0/0 | 4047 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0023 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0024 | 0/0 | 4047 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0025 | 0/0 | 4047 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0026 | 0/0 | 4047 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0027 | 0/0 | 4047 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0028 | 0/0 | 4047 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0029 | 0/0 | 4047 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0030 | 0/0 | 4047 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0031 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0032 | 0/0 | 4047 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0033 | 0/0 | 4046 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0034 | 0/0 | 4046 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| t0035 | 0/0 | 4046 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0070 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 9423 | 24 | 0 | 1 | 21 | 0 | 2 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0001c0003 | 0/0 | 9423 | 15 | 1 | 5 | 4 | 3 | 2 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0001c0085 | 0/0 | 9423 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0001c0089 | 0/0 | 9423 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0002c0001 | 0/0 | 9432 | 35 | 0 | 8 | 21 | 1 | 5 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0002c0030 | 0/0 | 9432 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0002c0031 | 0/0 | 9432 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0002c0073 | 0/0 | 9432 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0003c0006 | 0/0 | 9429 | 7 | 0 | 1 | 5 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0003c0024 | 0/0 | 9429 | 3 | 2 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0003c0040 | 1/0 | 9429 | 2 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0003c0041 | 0/0 | 9429 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0003c0105 | 0/0 | 9429 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0003c0128 | 0/0 | 9429 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0004c0005 | 0/0 | 9420 | 7 | 7 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0004c0011 | 0/0 | 9420 | 4 | 0 | 0 | 4 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0004c0066 | 0/0 | 9420 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0004c0067 | 0/0 | 9420 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0005c0004 | 0/0 | 9435 | 12 | 0 | 4 | 8 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0005c0090 | 0/0 | 9435 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0006c0015 | 0/0 | 9426 | 4 | 0 | 1 | 2 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0006c0022 | 0/0 | 9426 | 3 | 0 | 2 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0006c0037 | 0/0 | 9426 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0006c0099 | 0/0 | 9426 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0007c0007 | 0/0 | 9426 | 6 | 5 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0007c0053 | 0/0 | 9426 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0007c0058 | 0/0 | 9426 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0008c0010 | 0/0 | 9432 | 5 | 2 | 2 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0008c0111 | 0/0 | 9432 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0008c0113 | 0/0 | 9432 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0008c0114 | 0/0 | 9432 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0009c0008 | 0/0 | 9417 | 6 | 0 | 5 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0009c0059 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0010c0009 | 0/0 | 9426 | 5 | 4 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0010c0056 | 0/0 | 9426 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0011c0028 | 0/0 | 9432 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0011c0029 | 0/0 | 9432 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0011c0072 | 0/0 | 9432 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0012c0012 | 0/0 | 9429 | 4 | 1 | 1 | 1 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0012c0077 | 0/0 | 9429 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0013c0013 | 0/0 | 9423 | 4 | 0 | 3 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0014c0014 | 0/0 | 9435 | 4 | 3 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0015c0016 | 0/0 | 9435 | 4 | 2 | 2 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0016c0017 | 0/0 | 9441 | 4 | 1 | 1 | 0 | 0 | 2 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0017c0018 | 0/0 | 9423 | 3 | 2 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0018c0019 | 0/0 | 9429 | 3 | 0 | 3 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0019c0020 | 0/0 | 9417 | 3 | 3 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0020c0052 | 0/0 | 9423 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0020c0079 | 0/0 | 9423 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0020c0084 | 0/0 | 9423 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0021c0021 | 0/0 | 9435 | 3 | 0 | 0 | 3 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0022c0023 | 0/0 | 9438 | 3 | 3 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0023c0039 | 0/0 | 9438 | 2 | 1 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0023c0103 | 0/0 | 9438 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0024c0046 | 0/0 | 9411 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0024c0047 | 0/0 | 9411 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0025c0025 | 0/0 | 9417 | 2 | 0 | 2 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0026c0026 | 0/0 | 9429 | 2 | 2 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0027c0027 | 0/0 | 9408 | 2 | 2 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0028c0033 | 0/0 | 9423 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0029c0032 | 0/0 | 9423 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0030c0034 | 0/0 | 9423 | 2 | 0 | 0 | 1 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0031c0035 | 0/0 | 9435 | 2 | 0 | 0 | 0 | 2 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0032c0036 | 0/0 | 9426 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0033c0097 | 0/0 | 9426 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0033c0098 | 0/0 | 9426 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0034c0038 | 0/0 | 9438 | 2 | 0 | 1 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0035c0042 | 0/0 | 9429 | 2 | 2 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0036c0107 | 0/0 | 9429 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0036c0108 | 0/0 | 9429 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0037c0121 | 0/0 | 9447 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0037c0122 | 0/0 | 9447 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0038c0123 | 0/0 | 9450 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0038c0124 | 0/0 | 9450 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0039c0043 | 0/0 | 9456 | 2 | 0 | 2 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0040c0045 | 0/0 | 9405 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0041c0049 | 0/0 | 9411 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0042c0048 | 0/0 | 9411 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0043c0050 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0044c0060 | 0/0 | 9417 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0045c0051 | 0/0 | 9414 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0046c0055 | 0/0 | 9426 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0047c0054 | 0/0 | 9426 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0048c0057 | 0/0 | 9423 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0049c0063 | 0/0 | 9429 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0050c0065 | 0/0 | 9429 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0051c0062 | 0/0 | 9429 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0052c0061 | 0/0 | 9429 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0053c0064 | 0/0 | 9429 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0054c0068 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0055c0069 | 0/0 | 9420 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0056c0070 | 0/0 | 9432 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0057c0074 | 0/0 | 9432 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0058c0071 | 0/0 | 9432 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0059c0075 | 0/0 | 9432 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0060c0088 | 0/0 | 9429 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0061c0076 | 0/0 | 9429 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0062c0082 | 0/0 | 9423 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0063c0081 | 0/0 | 9423 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0064c0080 | 0/0 | 9423 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0065c0078 | 0/0 | 9423 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0066c0083 | 0/0 | 9423 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0067c0086 | 0/0 | 9423 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0068c0087 | 0/0 | 9420 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0069c0093 | 0/0 | 9435 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0070c0092 | 0/0 | 9435 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0071c0091 | 0/0 | 9435 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0072c0096 | 0/0 | 9429 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0073c0100 | 0/0 | 9426 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0074c0095 | 0/0 | 9426 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0075c0094 | 0/0 | 9426 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0076c0101 | 0/0 | 9439 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0077c0102 | 0/0 | 9438 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0078c0104 | 0/0 | 9429 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0079c0106 | 0/0 | 9429 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0080c0110 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0081c0109 | 0/0 | 9441 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0082c0112 | 0/0 | 9432 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0083c0116 | 0/0 | 9444 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0084c0115 | 0/0 | 9444 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0085c0117 | 0/0 | 9444 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0086c0118 | 0/0 | 9441 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0087c0119 | 0/0 | 9453 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0088c0120 | 0/0 | 9456 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0089c0125 | 0/0 | 9450 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0090c0126 | 0/0 | 9462 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0091c0127 | 0/1 | 9456 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0092c0044 | 0/0 | 9455 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 13469 | 24 | 0 | 1 | 21 | 0 | 2 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0001c0003t0001 | 0/0 | 13469 | 12 | 1 | 4 | 4 | 3 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0001c0003t0003 | 0/0 | 13485 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0001c0003t0004 | 0/0 | 13469 | 2 | 0 | 1 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0001c0085t0001 | 0/0 | 13469 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0001c0089t0001 | 0/0 | 13469 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0002c0001t0002 | 0/0 | 13478 | 31 | 0 | 8 | 18 | 1 | 4 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0002c0001t0013 | 0/0 | 13478 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0002c0001t0014 | 0/0 | 13478 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0002c0001t0024 | 0/0 | 13478 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0002c0030t0002 | 0/0 | 13478 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0002c0031t0002 | 0/0 | 13478 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0002c0073t0002 | 0/0 | 13478 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0003c0006t0001 | 0/0 | 13475 | 6 | 0 | 1 | 4 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0003c0006t0027 | 0/0 | 13475 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0003c0024t0001 | 0/0 | 13475 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0003c0024t0019 | 0/0 | 13475 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0003c0024t0030 | 0/0 | 13475 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0003c0040t0001 | 0/0 | 13475 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0003c0040t0005 | 1/0 | 13472 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0003c0041t0001 | 0/0 | 13475 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0003c0105t0001 | 0/0 | 13475 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0003c0128t0026 | 0/0 | 13475 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0004c0005t0001 | 0/0 | 13466 | 7 | 7 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0004c0011t0001 | 0/0 | 13466 | 4 | 0 | 0 | 4 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0004c0066t0001 | 0/0 | 13466 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0004c0067t0001 | 0/0 | 13466 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0005c0004t0002 | 0/0 | 13481 | 12 | 0 | 4 | 8 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0005c0090t0002 | 0/0 | 13481 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0006c0015t0001 | 0/0 | 13472 | 4 | 0 | 1 | 2 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0006c0022t0001 | 0/0 | 13472 | 3 | 0 | 2 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0006c0037t0001 | 0/0 | 13472 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0006c0037t0021 | 0/0 | 13472 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0006c0099t0001 | 0/0 | 13472 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0007c0007t0003 | 0/0 | 13488 | 6 | 5 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0007c0053t0003 | 0/0 | 13488 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0007c0058t0033 | 0/0 | 13471 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0008c0010t0001 | 0/0 | 13478 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0008c0010t0004 | 0/0 | 13478 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0008c0010t0006 | 0/0 | 13478 | 2 | 2 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0008c0010t0020 | 0/0 | 13478 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0008c0111t0004 | 0/0 | 13478 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0008c0113t0001 | 0/0 | 13478 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0008c0114t0001 | 0/0 | 13478 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0009c0008t0001 | 0/0 | 13463 | 6 | 0 | 5 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0009c0059t0001 | 0/0 | 13463 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0010c0009t0003 | 0/0 | 13488 | 5 | 4 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0010c0056t0007 | 0/0 | 13488 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0011c0028t0001 | 0/0 | 13478 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0011c0029t0001 | 0/0 | 13478 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0011c0072t0001 | 0/0 | 13478 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0012c0012t0003 | 0/0 | 13491 | 4 | 1 | 1 | 1 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0012c0077t0003 | 0/0 | 13491 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0013c0013t0001 | 0/0 | 13469 | 3 | 0 | 2 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0013c0013t0028 | 0/0 | 13469 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0014c0014t0003 | 0/0 | 13497 | 3 | 2 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0014c0014t0010 | 0/0 | 13497 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0015c0016t0006 | 0/0 | 13481 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0015c0016t0009 | 0/0 | 13481 | 3 | 1 | 2 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0016c0017t0001 | 0/0 | 13487 | 2 | 0 | 1 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0016c0017t0006 | 0/0 | 13487 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0016c0017t0020 | 0/0 | 13487 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0017c0018t0003 | 0/0 | 13485 | 3 | 2 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0018c0019t0001 | 0/0 | 13475 | 3 | 0 | 3 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0019c0020t0007 | 0/0 | 13479 | 2 | 2 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0019c0020t0023 | 0/0 | 13479 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0020c0052t0003 | 0/0 | 13485 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0020c0079t0003 | 0/0 | 13485 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0020c0084t0003 | 0/0 | 13485 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0021c0021t0002 | 0/0 | 13481 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0021c0021t0012 | 0/0 | 13481 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0022c0023t0003 | 0/0 | 13500 | 3 | 3 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0023c0039t0015 | 0/0 | 13484 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0023c0039t0016 | 0/0 | 13484 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0023c0103t0003 | 0/0 | 13500 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0024c0046t0008 | 0/0 | 13473 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0024c0047t0008 | 0/0 | 13473 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0025c0025t0002 | 0/0 | 13463 | 2 | 0 | 2 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0026c0026t0003 | 0/0 | 13491 | 2 | 2 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0027c0027t0001 | 0/0 | 13454 | 2 | 2 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0028c0033t0001 | 0/0 | 13469 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0029c0032t0001 | 0/0 | 13469 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0030c0034t0002 | 0/0 | 13469 | 2 | 0 | 0 | 1 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0031c0035t0002 | 0/0 | 13481 | 2 | 0 | 0 | 0 | 2 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0032c0036t0001 | 0/0 | 13472 | 2 | 0 | 0 | 2 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0033c0097t0001 | 0/0 | 13472 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0033c0098t0001 | 0/0 | 13472 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0034c0038t0002 | 0/0 | 13484 | 2 | 0 | 1 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0035c0042t0005 | 0/0 | 13472 | 2 | 2 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0036c0107t0018 | 0/0 | 13491 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0036c0108t0018 | 0/0 | 13491 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0037c0121t0001 | 0/0 | 13493 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0037c0122t0001 | 0/0 | 13493 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0038c0123t0001 | 0/0 | 13496 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0038c0124t0019 | 0/0 | 13496 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0039c0043t0001 | 0/0 | 13502 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0039c0043t0004 | 0/0 | 13502 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0040c0045t0002 | 0/0 | 13451 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0041c0049t0001 | 0/0 | 13457 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0042c0048t0008 | 0/0 | 13473 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0043c0050t0010 | 0/0 | 13479 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0044c0060t0001 | 0/0 | 13463 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0045c0051t0001 | 0/0 | 13460 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0046c0055t0011 | 0/0 | 13488 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0047c0054t0001 | 0/0 | 13472 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0048c0057t0003 | 0/0 | 13485 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0049c0063t0011 | 0/0 | 13491 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0050c0065t0003 | 0/0 | 13491 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0051c0062t0002 | 0/0 | 13475 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0052c0061t0035 | 0/0 | 13474 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0053c0064t0001 | 0/0 | 13475 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0054c0068t0034 | 0/0 | 13462 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0055c0069t0001 | 0/0 | 13466 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0056c0070t0001 | 0/0 | 13478 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0057c0074t0002 | 0/0 | 13478 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0058c0071t0001 | 0/0 | 13478 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0059c0075t0014 | 0/0 | 13478 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0060c0088t0002 | 0/0 | 13475 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0061c0076t0003 | 0/0 | 13491 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0062c0082t0005 | 0/0 | 13466 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0063c0081t0001 | 0/0 | 13469 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0064c0080t0001 | 0/0 | 13469 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0065c0078t0004 | 0/0 | 13469 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0066c0083t0001 | 0/0 | 13469 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0067c0086t0025 | 0/0 | 13469 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0068c0087t0031 | 0/0 | 13482 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0069c0093t0003 | 0/0 | 13497 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0070c0092t0032 | 0/0 | 13481 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0071c0091t0001 | 0/0 | 13481 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0072c0096t0003 | 0/0 | 13491 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0073c0100t0001 | 0/0 | 13472 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0074c0095t0002 | 0/0 | 13472 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0075c0094t0003 | 0/0 | 13488 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0076c0101t0002 | 0/0 | 13485 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0077c0102t0029 | 0/0 | 13484 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0078c0104t0001 | 0/0 | 13475 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0079c0106t0003 | 0/0 | 13491 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0080c0110t0003 | 0/0 | 13503 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0081c0109t0002 | 0/0 | 13487 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0082c0112t0001 | 0/0 | 13478 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0083c0116t0016 | 0/0 | 13490 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0084c0115t0017 | 0/0 | 13490 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0085c0117t0001 | 0/0 | 13490 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0086c0118t0003 | 0/0 | 13503 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0087c0119t0022 | 0/0 | 13499 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0088c0120t0017 | 0/0 | 13502 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0089c0125t0002 | 0/0 | 13496 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0090c0126t0003 | 0/0 | 13524 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0091c0127t0004 | 0/1 | 13502 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| a0092c0044t0015 | 0/0 | 13501 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | copy fasta | chr4 | 3069681 | 3248957 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0003t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0003t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0003t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0085t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0001c0089t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0013g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0013g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0014g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0001t0024g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0030t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0030t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0031t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0031t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0002c0073t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0003c0006t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0003c0006t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0003c0006t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0003c0006t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0003c0006t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0003c0006t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0003c0006t0027g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0003c0024t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0003c0024t0019g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0003c0024t0030g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0003c0040t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0003c0040t0005g0070 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0003c0041t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0003c0041t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0003c0105t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0003c0128t0026g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0004c0005t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0004c0005t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0004c0005t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0004c0005t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0004c0005t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0004c0005t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0004c0011t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0004c0011t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0004c0011t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0004c0011t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0004c0066t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0004c0067t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0005c0004t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0005c0004t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0005c0004t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0005c0004t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0005c0004t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0005c0004t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0005c0004t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0005c0004t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0005c0004t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0005c0004t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0005c0004t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0005c0004t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0005c0090t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0006c0015t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0006c0015t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0006c0015t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0006c0015t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0006c0022t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0006c0022t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0006c0022t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0006c0037t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0006c0037t0021g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0006c0099t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0007c0007t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0007c0007t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0007c0007t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0007c0007t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0007c0007t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0007c0007t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0007c0053t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0007c0058t0033g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0008c0010t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0008c0010t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0008c0010t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0008c0010t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0008c0010t0020g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0008c0111t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0008c0113t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0008c0114t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0009c0008t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0009c0008t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0009c0008t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0009c0008t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0009c0008t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0009c0008t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0009c0059t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0010c0009t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0010c0009t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0010c0009t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0010c0009t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0010c0009t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0010c0056t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0011c0028t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0011c0028t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0011c0029t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0011c0029t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0011c0072t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0012c0012t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0012c0012t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0012c0012t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0012c0012t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0012c0077t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0013c0013t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0013c0013t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0013c0013t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0013c0013t0028g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0014c0014t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0014c0014t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0014c0014t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0014c0014t0010g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0015c0016t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0015c0016t0009g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0015c0016t0009g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0016c0017t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0016c0017t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0016c0017t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0016c0017t0020g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0017c0018t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0017c0018t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0017c0018t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0018c0019t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0018c0019t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0018c0019t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0019c0020t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0019c0020t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0019c0020t0023g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0020c0052t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0020c0079t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0020c0084t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0021c0021t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0021c0021t0012g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0021c0021t0012g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0022c0023t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0022c0023t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0022c0023t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0023c0039t0015g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0023c0039t0016g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0023c0103t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0024c0046t0008g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0024c0047t0008g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0025c0025t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0025c0025t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0026c0026t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0026c0026t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0027c0027t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0027c0027t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0028c0033t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0028c0033t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0029c0032t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0029c0032t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0030c0034t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0030c0034t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0031c0035t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0031c0035t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0032c0036t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0032c0036t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0033c0097t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0033c0098t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0034c0038t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0034c0038t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0035c0042t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0035c0042t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0036c0107t0018g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0036c0108t0018g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0037c0121t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0037c0122t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0038c0123t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0038c0124t0019g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0039c0043t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0039c0043t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0040c0045t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0041c0049t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0042c0048t0008g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0043c0050t0010g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0044c0060t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0045c0051t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0046c0055t0011g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0047c0054t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0048c0057t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0049c0063t0011g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0050c0065t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0051c0062t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0052c0061t0035g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0053c0064t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0054c0068t0034g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0055c0069t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0056c0070t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0057c0074t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0058c0071t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0059c0075t0014g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0060c0088t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0061c0076t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0062c0082t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0063c0081t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0064c0080t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0065c0078t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0066c0083t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0067c0086t0025g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0068c0087t0031g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0069c0093t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0070c0092t0032g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0071c0091t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0072c0096t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0073c0100t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0074c0095t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0075c0094t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0076c0101t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0077c0102t0029g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0078c0104t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0079c0106t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0080c0110t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0081c0109t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0082c0112t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0083c0116t0016g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0084c0115t0017g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0085c0117t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0086c0118t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0087c0119t0022g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0088c0120t0017g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0089c0125t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0090c0126t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0091c0127t0004g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| a0092c0044t0015g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0002 | c0001 | t0002 | g0247 | EUR | FIN | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00323 | hp2 | a0024 | c0046 | t0008 | g0257 | EUR | FIN | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00423 | hp1 | a0064 | c0080 | t0001 | g0183 | EAS | CHS | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00423 | hp2 | a0059 | c0075 | t0014 | g0222 | EAS | CHS | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00438 | hp1 | a0003 | c0006 | t0001 | g0060 | EAS | CHS | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00438 | hp2 | a0037 | c0121 | t0001 | g0189 | EAS | CHS | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00597 | hp1 | a0078 | c0104 | t0001 | g0124 | EAS | CHS | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00597 | hp2 | a0002 | c0001 | t0002 | g0283 | EAS | CHS | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00609 | hp1 | a0002 | c0001 | t0002 | g0263 | EAS | CHS | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00609 | hp2 | a0066 | c0083 | t0001 | g0119 | EAS | CHS | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00639 | hp1 | a0042 | c0048 | t0008 | g0259 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0130 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00642 | hp1 | a0050 | c0065 | t0003 | g0286 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00642 | hp2 | a0005 | c0004 | t0002 | g0194 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00673 | hp1 | a0053 | c0064 | t0001 | g0274 | EAS | CHS | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00673 | hp2 | a0021 | c0021 | t0002 | g0232 | EAS | CHS | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00735 | hp1 | a0005 | c0004 | t0002 | g0195 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00735 | hp2 | a0004 | c0067 | t0001 | g0118 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00738 | hp1 | a0088 | c0120 | t0017 | g0201 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00738 | hp2 | a0006 | c0022 | t0001 | g0039 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00741 | hp1 | a0058 | c0071 | t0001 | g0270 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG00741 | hp2 | a0002 | c0001 | t0002 | g0248 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01070 | hp1 | a0040 | c0045 | t0002 | g0103 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01070 | hp2 | a0018 | c0019 | t0001 | g0233 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01071 | hp1 | a0039 | c0043 | t0001 | g0078 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01071 | hp2 | a0018 | c0019 | t0001 | g0234 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01074 | hp1 | a0009 | c0008 | t0001 | g0167 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01074 | hp2 | a0065 | c0078 | t0004 | g0185 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01081 | hp1 | a0039 | c0043 | t0004 | g0073 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01081 | hp2 | a0012 | c0012 | t0003 | g0095 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01099 | hp1 | a0008 | c0010 | t0020 | g0084 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01099 | hp2 | a0001 | c0003 | t0004 | g0134 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01106 | hp1 | a0016 | c0017 | t0001 | g0190 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01106 | hp2 | a0067 | c0086 | t0025 | g0113 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01109 | hp1 | a0007 | c0007 | t0003 | g0026 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01109 | hp2 | a0018 | c0019 | t0001 | g0235 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01167 | hp1 | a0069 | c0093 | t0003 | g0020 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01167 | hp2 | a0013 | c0013 | t0001 | g0032 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01168 | hp1 | a0002 | c0001 | t0002 | g0196 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01168 | hp2 | a0008 | c0010 | t0004 | g0072 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01169 | hp1 | a0002 | c0001 | t0002 | g0193 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01169 | hp2 | a0013 | c0013 | t0001 | g0033 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0174 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01175 | hp2 | a0006 | c0015 | t0001 | g0139 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01192 | hp1 | a0020 | c0079 | t0003 | g0186 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0127 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01243 | hp1 | a0023 | c0039 | t0016 | g0008 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01243 | hp2 | a0014 | c0014 | t0003 | g0015 | AMR | PUR | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01255 | hp1 | a0002 | c0001 | t0002 | g0244 | AMR | CLM | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01255 | hp2 | a0049 | c0063 | t0011 | g0203 | AMR | CLM | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01256 | hp1 | a0005 | c0004 | t0002 | g0229 | AMR | CLM | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01256 | hp2 | a0015 | c0016 | t0009 | g0002 | AMR | CLM | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01257 | hp1 | a0025 | c0025 | t0002 | g0188 | AMR | CLM | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01257 | hp2 | a0003 | c0006 | t0001 | g0052 | AMR | CLM | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01258 | hp1 | a0025 | c0025 | t0002 | g0187 | AMR | CLM | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01258 | hp2 | a0015 | c0016 | t0009 | g0002 | AMR | CLM | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0164 | AMR | CLM | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01346 | hp2 | a0002 | c0001 | t0002 | g0245 | AMR | CLM | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01433 | hp1 | a0010 | c0009 | t0003 | g0291 | AMR | CLM | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01433 | hp2 | a0034 | c0038 | t0002 | g0192 | AMR | CLM | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0122 | EUR | IBS | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01515 | hp2 | a0086 | c0118 | t0003 | g0067 | EUR | IBS | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0128 | EUR | IBS | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01516 | hp2 | a0031 | c0035 | t0002 | g0267 | EUR | IBS | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01517 | hp1 | a0031 | c0035 | t0002 | g0269 | EUR | IBS | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0123 | EUR | IBS | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01884 | hp1 | a0068 | c0087 | t0031 | g0101 | AFR | ACB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01884 | hp2 | a0023 | c0103 | t0003 | g0029 | AFR | ACB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01891 | hp1 | a0045 | c0051 | t0001 | g0048 | AFR | ACB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01891 | hp2 | a0072 | c0096 | t0003 | g0086 | AFR | ACB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01928 | hp1 | a0003 | c0024 | t0019 | g0109 | AMR | PEL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01928 | hp2 | a0009 | c0008 | t0001 | g0105 | AMR | PEL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01934 | hp1 | a0002 | c0001 | t0002 | g0262 | AMR | PEL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01934 | hp2 | a0013 | c0013 | t0028 | g0198 | AMR | PEL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01943 | hp1 | a0089 | c0125 | t0002 | g0108 | AMR | PEL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01943 | hp2 | a0038 | c0124 | t0019 | g0107 | AMR | PEL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01952 | hp1 | a0002 | c0001 | t0002 | g0284 | AMR | PEL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01952 | hp2 | a0009 | c0008 | t0001 | g0179 | AMR | PEL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01975 | hp1 | a0009 | c0008 | t0001 | g0157 | AMR | PEL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG01975 | hp2 | a0017 | c0018 | t0003 | g0092 | AMR | PEL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02040 | hp1 | a0006 | c0022 | t0001 | g0034 | EAS | KHV | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02040 | hp2 | a0002 | c0001 | t0013 | g0224 | EAS | KHV | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02055 | hp1 | a0048 | c0057 | t0003 | g0098 | AFR | ACB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02055 | hp2 | a0092 | c0044 | t0015 | g0003 | AFR | ACB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | KHV | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02056 | hp2 | a0034 | c0038 | t0002 | g0285 | EAS | KHV | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02071 | hp1 | a0008 | c0010 | t0001 | g0068 | EAS | KHV | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02071 | hp2 | a0004 | c0066 | t0001 | g0159 | EAS | KHV | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02080 | hp1 | a0055 | c0069 | t0001 | g0271 | EAS | KHV | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02080 | hp2 | a0056 | c0070 | t0001 | g0280 | EAS | KHV | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02132 | hp1 | a0020 | c0084 | t0003 | g0093 | EAS | KHV | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02132 | hp2 | a0003 | c0006 | t0001 | g0043 | EAS | KHV | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02135 | hp1 | a0001 | c0003 | t0001 | g0197 | EAS | KHV | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02135 | hp2 | a0003 | c0006 | t0001 | g0038 | EAS | KHV | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02145 | hp1 | a0054 | c0068 | t0034 | g0090 | AFR | ACB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02145 | hp2 | a0022 | c0023 | t0003 | g0019 | AFR | ACB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02148 | hp1 | a0009 | c0008 | t0001 | g0180 | AMR | PEL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02148 | hp2 | a0002 | c0073 | t0002 | g0290 | AMR | PEL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02165 | hp1 | a0051 | c0062 | t0002 | g0243 | EAS | CDX | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02165 | hp2 | a0001 | c0003 | t0001 | g0129 | EAS | CDX | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02257 | hp1 | a0008 | c0010 | t0006 | g0135 | AFR | ACB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02257 | hp2 | a0017 | c0018 | t0003 | g0097 | AFR | ACB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02258 | hp1 | a0070 | c0092 | t0032 | g0030 | AFR | ACB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0077 | AFR | ACB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02273 | hp1 | a0002 | c0001 | t0002 | g0220 | AMR | PEL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02273 | hp2 | a0006 | c0022 | t0001 | g0036 | AMR | PEL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02280 | hp1 | a0041 | c0049 | t0001 | g0010 | AFR | ACB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02280 | hp2 | a0036 | c0108 | t0018 | g0066 | AFR | ACB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02300 | hp1 | a0005 | c0004 | t0002 | g0219 | AMR | PEL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0121 | AMR | PEL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02523 | hp1 | a0012 | c0012 | t0003 | g0089 | EAS | KHV | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02523 | hp2 | a0002 | c0001 | t0002 | g0279 | EAS | KHV | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02615 | hp1 | a0085 | c0117 | t0001 | g0007 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02615 | hp2 | a0090 | c0126 | t0003 | g0018 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02622 | hp1 | a0001 | c0089 | t0001 | g0037 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02622 | hp2 | a0077 | c0102 | t0029 | g0006 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02630 | hp1 | a0014 | c0014 | t0003 | g0021 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02630 | hp2 | a0043 | c0050 | t0010 | g0012 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02647 | hp1 | a0033 | c0097 | t0001 | g0061 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02647 | hp2 | a0003 | c0105 | t0001 | g0071 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02683 | hp1 | a0013 | c0013 | t0001 | g0116 | SAS | PJL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02683 | hp2 | a0020 | c0052 | t0003 | g0292 | SAS | PJL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02717 | hp1 | a0026 | c0026 | t0003 | g0022 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02717 | hp2 | a0017 | c0018 | t0003 | g0091 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02723 | hp1 | a0052 | c0061 | t0035 | g0252 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02723 | hp2 | a0062 | c0082 | t0005 | g0083 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02886 | hp1 | a0014 | c0014 | t0003 | g0014 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02886 | hp2 | a0035 | c0042 | t0005 | g0085 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02895 | hp1 | a0007 | c0007 | t0003 | g0024 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02895 | hp2 | a0047 | c0054 | t0001 | g0287 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02896 | hp1 | a0022 | c0023 | t0003 | g0016 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02896 | hp2 | a0004 | c0005 | t0001 | g0001 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02897 | hp1 | a0004 | c0005 | t0001 | g0001 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02897 | hp2 | a0007 | c0007 | t0003 | g0023 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02922 | hp1 | a0007 | c0007 | t0003 | g0028 | AFR | ESN | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02922 | hp2 | a0012 | c0012 | t0003 | g0087 | AFR | ESN | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02965 | hp1 | a0004 | c0005 | t0001 | g0056 | AFR | ESN | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02965 | hp2 | a0010 | c0009 | t0003 | g0289 | AFR | ESN | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02970 | hp1 | a0080 | c0110 | t0003 | g0031 | AFR | ESN | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02970 | hp2 | a0027 | c0027 | t0001 | g0035 | AFR | ESN | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02976 | hp1 | a0004 | c0005 | t0001 | g0055 | AFR | ESN | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02976 | hp2 | a0010 | c0009 | t0003 | g0276 | AFR | ESN | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03017 | hp1 | a0084 | c0115 | t0017 | g0202 | SAS | PJL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03017 | hp2 | a0002 | c0001 | t0002 | g0191 | SAS | PJL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03041 | hp1 | a0023 | c0039 | t0015 | g0004 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03041 | hp2 | a0003 | c0128 | t0026 | g0053 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03098 | hp1 | a0007 | c0007 | t0003 | g0025 | AFR | MSL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03098 | hp2 | a0008 | c0010 | t0006 | g0136 | AFR | MSL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03139 | hp1 | a0046 | c0055 | t0011 | g0204 | AFR | ESN | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03139 | hp2 | a0019 | c0020 | t0023 | g0100 | AFR | ESN | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03195 | hp1 | a0063 | c0081 | t0001 | g0133 | AFR | ESN | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03195 | hp2 | a0016 | c0017 | t0006 | g0131 | AFR | ESN | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03225 | hp1 | a0035 | c0042 | t0005 | g0076 | AFR | MSL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03225 | hp2 | a0007 | c0058 | t0033 | g0009 | AFR | MSL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03239 | hp1 | a0024 | c0047 | t0008 | g0258 | SAS | PJL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0175 | SAS | PJL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03453 | hp1 | a0027 | c0027 | t0001 | g0058 | AFR | MSL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03453 | hp2 | a0010 | c0009 | t0003 | g0288 | AFR | MSL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03491 | hp1 | a0016 | c0017 | t0001 | g0125 | SAS | PJL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03491 | hp2 | a0002 | c0001 | t0002 | g0223 | SAS | PJL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03540 | hp1 | a0004 | c0005 | t0001 | g0049 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03540 | hp2 | a0003 | c0040 | t0001 | g0069 | AFR | GWD | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03579 | hp1 | a0075 | c0094 | t0003 | g0064 | AFR | MSL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03579 | hp2 | a0083 | c0116 | t0016 | g0005 | AFR | MSL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03654 | hp1 | a0057 | c0074 | t0002 | g0268 | SAS | PJL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03654 | hp2 | a0061 | c0076 | t0003 | g0099 | SAS | PJL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03669 | hp1 | a0002 | c0001 | t0002 | g0212 | SAS | PJL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03669 | hp2 | a0044 | c0060 | t0001 | g0059 | SAS | PJL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03704 | hp1 | a0001 | c0003 | t0003 | g0115 | SAS | PJL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03704 | hp2 | a0002 | c0001 | t0024 | g0238 | SAS | PJL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03834 | hp1 | a0001 | c0003 | t0004 | g0117 | SAS | BEB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03834 | hp2 | a0016 | c0017 | t0020 | g0081 | SAS | BEB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03942 | hp1 | a0002 | c0001 | t0002 | g0251 | SAS | BEB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03942 | hp2 | a0006 | c0015 | t0001 | g0158 | SAS | BEB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG04199 | hp1 | a0082 | c0112 | t0001 | g0126 | SAS | STU | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG04199 | hp2 | a0030 | c0034 | t0002 | g0221 | SAS | STU | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG04228 | hp1 | a0012 | c0077 | t0003 | g0094 | SAS | STU | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG04228 | hp2 | a0074 | c0095 | t0002 | g0106 | SAS | STU | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18522 | hp1 | a0079 | c0106 | t0003 | g0074 | AFR | YRI | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18522 | hp2 | a0003 | c0024 | t0001 | g0079 | AFR | YRI | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18906 | hp1 | a0010 | c0056 | t0007 | g0200 | AFR | YRI | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18906 | hp2 | a0004 | c0005 | t0001 | g0050 | AFR | YRI | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18939 | hp1 | a0001 | c0003 | t0001 | g0156 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18939 | hp2 | a0011 | c0028 | t0001 | g0240 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18942 | hp1 | a0001 | c0003 | t0001 | g0114 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18942 | hp2 | a0002 | c0001 | t0002 | g0208 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18947 | hp1 | a0006 | c0037 | t0001 | g0184 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18947 | hp2 | a0002 | c0001 | t0002 | g0250 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18948 | hp2 | a0005 | c0004 | t0002 | g0242 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18950 | hp1 | a0073 | c0100 | t0001 | g0046 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18950 | hp2 | a0002 | c0001 | t0002 | g0241 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18951 | hp1 | a0081 | c0109 | t0002 | g0264 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18952 | hp1 | a0038 | c0123 | t0001 | g0141 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18952 | hp2 | a0005 | c0090 | t0002 | g0215 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18954 | hp2 | a0002 | c0001 | t0013 | g0225 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18956 | hp1 | a0005 | c0004 | t0002 | g0260 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18960 | hp1 | a0002 | c0001 | t0002 | g0211 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18960 | hp2 | a0003 | c0006 | t0001 | g0041 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18961 | hp2 | a0076 | c0101 | t0002 | g0266 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18962 | hp2 | a0002 | c0001 | t0014 | g0214 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18963 | hp1 | a0002 | c0001 | t0002 | g0282 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18964 | hp1 | a0006 | c0037 | t0021 | g0146 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18964 | hp2 | a0002 | c0030 | t0002 | g0218 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18968 | hp1 | a0003 | c0006 | t0027 | g0042 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18969 | hp1 | a0005 | c0004 | t0002 | g0230 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18969 | hp2 | a0011 | c0072 | t0001 | g0205 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18970 | hp1 | a0002 | c0030 | t0002 | g0213 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18973 | hp1 | a0002 | c0001 | t0002 | g0255 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18973 | hp2 | a0011 | c0029 | t0001 | g0275 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18975 | hp1 | a0005 | c0004 | t0002 | g0209 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18975 | hp2 | a0008 | c0113 | t0001 | g0040 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18979 | hp1 | a0005 | c0004 | t0002 | g0256 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18980 | hp1 | a0021 | c0021 | t0012 | g0265 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18983 | hp1 | a0005 | c0004 | t0002 | g0228 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18983 | hp2 | a0004 | c0011 | t0001 | g0160 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18984 | hp1 | a0087 | c0119 | t0022 | g0207 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18986 | hp1 | a0002 | c0001 | t0002 | g0246 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18986 | hp2 | a0006 | c0099 | t0001 | g0047 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18989 | hp1 | a0001 | c0085 | t0001 | g0152 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18989 | hp2 | a0002 | c0001 | t0002 | g0237 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18990 | hp1 | a0060 | c0088 | t0002 | g0261 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18991 | hp1 | a0004 | c0011 | t0001 | g0153 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18991 | hp2 | a0002 | c0001 | t0002 | g0210 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18999 | hp1 | a0002 | c0031 | t0002 | g0253 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA18999 | hp2 | a0003 | c0041 | t0001 | g0144 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19002 | hp1 | a0071 | c0091 | t0001 | g0272 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19002 | hp2 | a0032 | c0036 | t0001 | g0140 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19005 | hp1 | a0028 | c0033 | t0001 | g0132 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19005 | hp2 | a0008 | c0114 | t0001 | g0044 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19007 | hp1 | a0021 | c0021 | t0012 | g0231 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19009 | hp1 | a0030 | c0034 | t0002 | g0278 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19009 | hp2 | a0032 | c0036 | t0001 | g0112 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19010 | hp2 | a0002 | c0001 | t0002 | g0216 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19030 | hp1 | a0037 | c0122 | t0001 | g0062 | AFR | LWK | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19030 | hp2 | a0026 | c0026 | t0003 | g0017 | AFR | LWK | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19056 | hp1 | a0002 | c0001 | t0002 | g0249 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19056 | hp2 | a0003 | c0041 | t0001 | g0143 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19057 | hp1 | a0011 | c0029 | t0001 | g0273 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19057 | hp2 | a0002 | c0001 | t0002 | g0217 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19058 | hp1 | a0029 | c0032 | t0001 | g0138 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19064 | hp1 | a0004 | c0011 | t0001 | g0161 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19064 | hp2 | a0002 | c0001 | t0002 | g0206 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19067 | hp1 | a0005 | c0004 | t0002 | g0254 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19068 | hp1 | a0028 | c0033 | t0001 | g0120 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19079 | hp1 | a0029 | c0032 | t0001 | g0111 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19079 | hp2 | a0002 | c0001 | t0002 | g0227 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19081 | hp2 | a0011 | c0028 | t0001 | g0236 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19082 | hp1 | a0002 | c0001 | t0002 | g0281 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19084 | hp1 | a0006 | c0015 | t0001 | g0163 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19084 | hp2 | a0002 | c0031 | t0002 | g0226 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19087 | hp1 | a0006 | c0015 | t0001 | g0162 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19087 | hp2 | a0005 | c0004 | t0002 | g0239 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19088 | hp1 | a0033 | c0098 | t0001 | g0051 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19088 | hp2 | a0004 | c0011 | t0001 | g0165 | EAS | JPT | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19240 | hp1 | a0004 | c0005 | t0001 | g0057 | AFR | YRI | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA19240 | hp2 | a0019 | c0020 | t0007 | g0088 | AFR | YRI | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA20129 | hp1 | a0007 | c0007 | t0003 | g0027 | AFR | ASW | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA20129 | hp2 | a0015 | c0016 | t0009 | g0082 | AFR | ASW | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA20805 | hp1 | a0009 | c0008 | t0001 | g0168 | EUR | TSI | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA20805 | hp2 | a0003 | c0006 | t0001 | g0045 | EUR | TSI | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0142 | SAS | GIH | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA20905 | hp2 | a0012 | c0012 | t0003 | g0096 | SAS | GIH | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02109 | hp1 | a0007 | c0053 | t0003 | g0104 | AFR | ACB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02109 | hp2 | a0015 | c0016 | t0006 | g0137 | AFR | ACB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02559 | hp1 | a0014 | c0014 | t0010 | g0011 | AFR | ACB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG02559 | hp2 | a0003 | c0024 | t0030 | g0075 | AFR | ACB | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03471 | hp1 | a0036 | c0107 | t0018 | g0065 | AFR | MSL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG03471 | hp2 | a0022 | c0023 | t0003 | g0013 | AFR | MSL | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG06807 | hp1 | a0008 | c0111 | t0004 | g0080 | AFR | USA | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| HG06807 | hp2 | a0019 | c0020 | t0007 | g0102 | AFR | USA | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA21309 | hp1 | a0009 | c0059 | t0001 | g0054 | AFR | LWK | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| NA21309 | hp2 | a0010 | c0009 | t0003 | g0277 | AFR | LWK | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| homoSapiens_chm13v2 | hp1 | a0091 | c0127 | t0004 | g0063 | REF | REF | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| homoSapiens_grch38 | hp1 | a0003 | c0040 | t0005 | g0070 | REF | REF | HTT_chr4_3069681_3248957 | HTT | chr4 | 3069681 | 3248957 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:3074876
|
C | CAGCAGCA others(10): Show |
1 | a0092 | 1 | HG02055.hp2 | frameshift_variant | HIGH | c.51_52insAGCAGCAGCA others(7): Show |
p.Gln18fs | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 197/13472 | 52/9429 | 18/3142 | chr4 | 3074876 | ||
| chr4:3074876
|
C | CCAG | 4 | a0008a0080a0081others(1): Show | 11 | HG01099.hp1 HG01168.hp2 HG02071.hp1 others(8): Show |
disruptive_inframe_insertion | MODERATE | c.108_110dupGCA | p.Gln37dup | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 256/13472 | 111/9429 | 37/3142 | INFO_REALIGN_3_PRIME | chr4 | 3074876 | |
| chr4:3074876
|
C | CCAGCAG | 4 | a0015a0083a0084others(1): Show | 7 | HG01256.hp2 HG01258.hp2 HG02109.hp2 others(4): Show |
disruptive_inframe_insertion | MODERATE | c.105_110dupGCAGCA | p.Gln36_Gln37dup | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 256/13472 | 111/9429 | 37/3142 | INFO_REALIGN_3_PRIME | chr4 | 3074876 | |
| chr4:3074876
|
C | CCAGCAGC others(5): Show |
2 | a0016a0086 | 5 | HG01106.hp1 HG01515.hp2 HG03195.hp2 others(2): Show |
disruptive_inframe_insertion | MODERATE | c.99_110dupGCAGCAGCA others(3): Show |
p.Gln34_Gln37dup | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 256/13472 | 111/9429 | 37/3142 | INFO_REALIGN_3_PRIME | chr4 | 3074876 | |
| chr4:3074876
|
C | CCAGCAGC others(11): Show |
1 | a0037 | 2 | HG00438.hp2 NA19030.hp1 |
disruptive_inframe_insertion | MODERATE | c.93_110dupGCAGCAGCA others(9): Show |
p.Gln32_Gln37dup | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 256/13472 | 111/9429 | 37/3142 | INFO_REALIGN_3_PRIME | chr4 | 3074876 | |
| chr4:3074876
|
C | CCAGCAGC others(14): Show |
2 | a0038a0089 | 3 | HG01943.hp1 HG01943.hp2 NA18952.hp1 |
disruptive_inframe_insertion | MODERATE | c.90_110dupGCAGCAGCA others(12): Show |
p.Gln31_Gln37dup | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 256/13472 | 111/9429 | 37/3142 | INFO_REALIGN_3_PRIME | chr4 | 3074876 | |
| chr4:3074876
|
C | CCAGCAGC others(20): Show |
2 | a0039a0091 | 3 | HG01071.hp1 HG01081.hp1 homoSapiens_chm13v2.hp1 |
disruptive_inframe_insertion | MODERATE | c.84_110dupGCAGCAGCA others(18): Show |
p.Gln29_Gln37dup | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 256/13472 | 111/9429 | 37/3142 | INFO_REALIGN_3_PRIME | chr4 | 3074876 | |
| chr4:3074876
|
CCAG | C | 10 | a0006a0007a0010others(7): Show | 33 | HG00738.hp2 HG01109.hp1 HG01175.hp2 others(30): Show |
disruptive_inframe_deletion | MODERATE | c.108_110delGCA | p.Gln37del | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 253/13472 | 108/9429 | 36/3142 | INFO_REALIGN_3_PRIME | chr4 | 3074876 | |
| chr4:3074876
|
CCAGCAG | C | 13 | a0001a0013a0020others(10): Show | 61 | HG00423.hp1 HG00609.hp2 HG00639.hp2 others(58): Show |
disruptive_inframe_deletion | MODERATE | c.105_110delGCAGCA | p.Gln36_Gln37del | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 250/13472 | 105/9429 | 35/3142 | INFO_REALIGN_3_PRIME | chr4 | 3074876 | |
| chr4:3074876
|
CCAGCAGC others(2): Show |
C | 4 | a0004a0019a0027others(1): Show | 19 | HG00735.hp2 HG02071.hp2 HG02145.hp1 others(16): Show |
disruptive_inframe_deletion | MODERATE | c.102_110delGCAGCAGC others(1): Show |
p.Gln35_Gln37del | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 247/13472 | 102/9429 | 34/3142 | INFO_REALIGN_3_PRIME | chr4 | 3074876 | |
| chr4:3074876
|
CCAGCAGC others(5): Show |
C | 4 | a0009a0025a0043others(1): Show | 11 | HG01074.hp1 HG01257.hp1 HG01258.hp1 others(8): Show |
disruptive_inframe_deletion | MODERATE | c.99_110delGCAGCAGCA others(3): Show |
p.Gln34_Gln37del | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 244/13472 | 99/9429 | 33/3142 | INFO_REALIGN_3_PRIME | chr4 | 3074876 | |
| chr4:3074876
|
CCAGCAGC others(8): Show |
C | 1 | a0045 | 1 | HG01891.hp1 | disruptive_inframe_deletion | MODERATE | c.96_110delGCAGCAGCA others(6): Show |
p.Gln33_Gln37del | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 241/13472 | 96/9429 | 32/3142 | INFO_REALIGN_3_PRIME | chr4 | 3074876 | |
| chr4:3074876
|
CCAGCAGC others(11): Show |
C | 3 | a0024a0041a0042 | 4 | HG00323.hp2 HG00639.hp1 HG02280.hp1 others(1): Show |
disruptive_inframe_deletion | MODERATE | c.93_110delGCAGCAGCA others(9): Show |
p.Gln32_Gln37del | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 238/13472 | 93/9429 | 31/3142 | INFO_REALIGN_3_PRIME | chr4 | 3074876 | |
| chr4:3074911
|
A | C | 1 | a0040 | 1 | HG01070.hp1 | missense_variant | MODERATE | c.86A>C | p.Gln29Pro | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 231/13472 | 86/9429 | 29/3142 | chr4 | 3074911 | ||
| chr4:3074913
|
CAGCAGCA others(16): Show |
C | 1 | a0040 | 1 | HG01070.hp1 | frameshift_variant | HIGH | c.89_111delAGCAGCAGC others(14): Show |
p.Gln30fs | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 234/13472 | 89/9429 | 30/3142 | chr4 | 3074913 | ||
| chr4:3074927
|
G | GCAA | 7 | a0002a0011a0055others(4): Show | 50 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(47): Show |
disruptive_inframe_insertion | MODERATE | c.104_105insACA | p.Gln35dup | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 250/13472 | 105/9429 | 35/3142 | INFO_REALIGN_3_PRIME | chr4 | 3074927 | |
| chr4:3074929
|
A | C | 2 | a0017a0048 | 4 | HG01975.hp2 HG02055.hp1 HG02257.hp2 others(1): Show |
missense_variant | MODERATE | c.104A>C | p.Gln35Pro | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 249/13472 | 104/9429 | 35/3142 | chr4 | 3074929 | ||
| chr4:3074931
|
CAGCAA | C | 2 | a0017a0048 | 4 | HG01975.hp2 HG02055.hp1 HG02257.hp2 others(1): Show |
frameshift_variant | HIGH | c.107_111delAGCAA | p.Gln36fs | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 252/13472 | 107/9429 | 36/3142 | chr4 | 3074931 | ||
| chr4:3074932
|
A | AACAGCC | 7 | a0005a0014a0021others(4): Show | 25 | HG00642.hp2 HG00673.hp2 HG00735.hp1 others(22): Show |
disruptive_inframe_insertion | MODERATE | c.107_108insACAGCC | p.Gln36_Gln37insGlnP others(2): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 253/13472 | 108/9429 | 36/3142 | chr4 | 3074932 | ||
| chr4:3074932
|
A | C | 22 | a0002a0007a0010others(19): Show | 81 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(78): Show |
missense_variant | MODERATE | c.107A>C | p.Gln36Pro | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 252/13472 | 107/9429 | 36/3142 | chr4 | 3074932 | ||
| chr4:3074935
|
A | AGCAGCAG others(17): Show |
1 | a0087 | 1 | NA18984.hp1 | disruptive_inframe_insertion | MODERATE | c.110_111insGCAGCAGC others(16): Show |
p.Gln37_Gln38insGlnG others(20): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 256/13472 | 111/9429 | 37/3142 | chr4 | 3074935 | ||
| chr4:3074935
|
A | AGCAGCAG others(20): Show |
1 | a0088 | 1 | HG00738.hp1 | disruptive_inframe_insertion | MODERATE | c.110_111insGCAGCAGC others(19): Show |
p.Gln37_Gln38insGlnG others(23): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 256/13472 | 111/9429 | 37/3142 | chr4 | 3074935 | ||
| chr4:3074935
|
A | AGCAGCAG others(26): Show |
1 | a0090 | 1 | HG02615.hp2 | disruptive_inframe_insertion | MODERATE | c.110_111insGCAGCAGC others(25): Show |
p.Gln37_Gln38insGlnG others(29): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 256/13472 | 111/9429 | 37/3142 | chr4 | 3074935 | ||
| chr4:3074935
|
A | C | 32 | a0002a0005a0007others(29): Show | 113 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(110): Show |
missense_variant | MODERATE | c.110A>C | p.Gln37Pro | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 255/13472 | 110/9429 | 37/3142 | chr4 | 3074935 | ||
| chr4:3074938
|
A | C | 37 | a0002a0005a0007others(34): Show | 118 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(115): Show |
missense_variant | MODERATE | c.113A>C | p.Gln38Pro | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 258/13472 | 113/9429 | 38/3142 | chr4 | 3074938 | ||
| chr4:3074938
|
AG | A | 3 | a0017a0040a0048 | 5 | HG01070.hp1 HG01975.hp2 HG02055.hp1 others(2): Show |
frameshift_variant | HIGH | c.114delG | p.Gln38fs | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 259/13472 | 114/9429 | 38/3142 | chr4 | 3074938 | ||
| chr4:3074945
|
A | ACCGCCCG others(3): Show |
1 | a0076 | 1 | NA18961.hp2 | frameshift_variant | HIGH | c.125_126insCGCCGCCG others(2): Show |
p.Pro43fs | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 271/13472 | 126/9429 | 42/3142 | INFO_REALIGN_3_PRIME | chr4 | 3074945 | |
| chr4:3074945
|
A | ACCGCCGC others(2): Show |
3 | a0034a0081a0084 | 4 | HG01433.hp2 HG02056.hp2 HG03017.hp1 others(1): Show |
disruptive_inframe_insertion | MODERATE | c.135_143dupGCCGCCGC others(1): Show |
p.Pro46_Pro48dup | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 289/13472 | 144/9429 | 48/3142 | INFO_REALIGN_3_PRIME | chr4 | 3074945 | |
| chr4:3074945
|
ACCG | A | 3 | a0019a0054a0068 | 5 | HG01884.hp1 HG02145.hp1 HG03139.hp2 others(2): Show |
disruptive_inframe_deletion | MODERATE | c.141_143delGCC | p.Pro48del | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 286/13472 | 141/9429 | 47/3142 | INFO_REALIGN_3_PRIME | chr4 | 3074945 | |
| chr4:3074966
|
G | GCCGCCGC others(2): Show |
7 | a0022a0023a0077others(4): Show | 11 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
disruptive_inframe_insertion | MODERATE | c.143_144insGCCGCCTC others(1): Show |
p.Pro46_Pro48dup | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 289/13472 | 144/9429 | 48/3142 | INFO_REALIGN_3_PRIME | chr4 | 3074966 | |
| chr4:3075022
|
AGCCGCCC others(5): Show |
A | 2 | a0027a0055 | 3 | HG02080.hp1 HG02970.hp2 HG03453.hp1 |
disruptive_inframe_deletion | MODERATE | c.213_224delGCCCCCGC others(4): Show |
p.Pro72_Pro75del | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 358/13472 | 213/9429 | 71/3142 | INFO_REALIGN_3_PRIME | chr4 | 3075022 | |
| chr4:3075049
|
C | T | 1 | a0073 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.224C>T | p.Pro75Leu | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 369/13472 | 224/9429 | 75/3142 | chr4 | 3075049 | ||
| chr4:3075082
|
A | C | 1 | a0067 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.257A>C | p.His86Pro | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 402/13472 | 257/9429 | 86/3142 | chr4 | 3075082 | ||
| chr4:3121375
|
G | T | 1 | a0066 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.1216G>T | p.Ala406Ser | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 9/67 | 1361/13472 | 1216/9429 | 406/3142 | chr4 | 3121375 | ||
| chr4:3121376
|
C | T | 1 | a0059 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.1217C>T | p.Ala406Val | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 9/67 | 1362/13472 | 1217/9429 | 406/3142 | chr4 | 3121376 | ||
| chr4:3121397
|
G | T | 1 | a0053 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.1238G>T | p.Gly413Val | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 9/67 | 1383/13472 | 1238/9429 | 413/3142 | chr4 | 3121397 | ||
| chr4:3121406
|
G | A | 1 | a0056 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.1247G>A | p.Arg416His | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 9/67 | 1392/13472 | 1247/9429 | 416/3142 | chr4 | 3121406 | ||
| chr4:3127513
|
G | A | 4 | a0028a0029a0032others(1): Show | 7 | HG00597.hp1 NA19002.hp2 NA19005.hp1 others(4): Show |
missense_variant | MODERATE | c.1652G>A | p.Gly551Glu | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 12/67 | 1797/13472 | 1652/9429 | 551/3142 | chr4 | 3127513 | ||
| chr4:3129952
|
T | C | 1 | a0043 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1772T>C | p.Leu591Ser | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 13/67 | 1917/13472 | 1772/9429 | 591/3142 | chr4 | 3129952 | ||
| chr4:3130311
|
A | G | 2 | a0024a0042 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
missense_variant | MODERATE | c.1874A>G | p.Gln625Arg | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 14/67 | 2019/13472 | 1874/9429 | 625/3142 | chr4 | 3130311 | ||
| chr4:3134509
|
C | T | 1 | a0074 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.2602C>T | p.Leu868Phe | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 19/67 | 2747/13472 | 2602/9429 | 868/3142 | chr4 | 3134509 | ||
| chr4:3135947
|
G | A | 2 | a0065a0091 | 2 | HG01074.hp2 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.2677G>A | p.Gly893Arg | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 20/67 | 2822/13472 | 2677/9429 | 893/3142 | chr4 | 3135947 | ||
| chr4:3142801
|
C | G | 2 | a0031a0057 | 3 | HG01516.hp2 HG01517.hp1 HG03654.hp1 |
missense_variant | MODERATE | c.2981C>G | p.Thr994Arg | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/67 | 3126/13472 | 2981/9429 | 994/3142 | chr4 | 3142801 | ||
| chr4:3146843
|
G | A | 2 | a0065a0091 | 2 | HG01074.hp2 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.3190G>A | p.Val1064Ile | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 25/67 | 3335/13472 | 3190/9429 | 1064/3142 | chr4 | 3146843 | ||
| chr4:3146926
|
T | G | 1 | a0013 | 4 | HG01167.hp2 HG01169.hp2 HG01934.hp2 others(1): Show |
missense_variant | MODERATE | c.3273T>G | p.Ile1091Met | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 25/67 | 3418/13472 | 3273/9429 | 1091/3142 | chr4 | 3146926 | ||
| chr4:3146939
|
T | G | 1 | a0061 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.3286T>G | p.Leu1096Val | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 25/67 | 3431/13472 | 3286/9429 | 1096/3142 | chr4 | 3146939 | ||
| chr4:3154311
|
A | G | 2 | a0046a0049 | 2 | HG01255.hp2 HG03139.hp1 |
missense_variant | MODERATE | c.3517A>G | p.Thr1173Ala | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/67 | 3662/13472 | 3517/9429 | 1173/3142 | chr4 | 3154311 | ||
| chr4:3160307
|
C | T | 2 | a0035a0062 | 3 | HG02723.hp2 HG02886.hp2 HG03225.hp1 |
missense_variant | MODERATE | c.3779C>T | p.Thr1260Met | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/67 | 3924/13472 | 3779/9429 | 1260/3142 | chr4 | 3160307 | ||
| chr4:3173118
|
A | C | 11 | a0014a0022a0026others(8): Show | 17 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(14): Show |
missense_variant | MODERATE | c.4153A>C | p.Asn1385His | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 31/67 | 4298/13472 | 4153/9429 | 1385/3142 | chr4 | 3173118 | ||
| chr4:3187664
|
C | A | 1 | a0077 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.5003C>A | p.Thr1668Asn | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 39/67 | 5148/13472 | 5003/9429 | 1668/3142 | chr4 | 3187664 | ||
| chr4:3187820
|
C | A | 30 | a0010a0012a0014others(27): Show | 55 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(52): Show |
missense_variant | MODERATE | c.5159C>A | p.Thr1720Asn | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 39/67 | 5304/13472 | 5159/9429 | 1720/3142 | chr4 | 3187820 | ||
| chr4:3206848
|
C | G | 1 | a0054 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.5940C>G | p.Ile1980Met | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 44/67 | 6085/13472 | 5940/9429 | 1980/3142 | chr4 | 3206848 | ||
| chr4:3208808
|
G | A | 1 | a0069 | 1 | HG01167.hp1 | missense_variant | MODERATE | c.6188G>A | p.Arg2063His | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 46/67 | 6333/13472 | 6188/9429 | 2063/3142 | chr4 | 3208808 | ||
| chr4:3214108
|
T | C | 54 | a0002a0005a0007others(51): Show | 144 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(141): Show |
missense_variant | MODERATE | c.6925T>C | p.Tyr2309His | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 50/67 | 7070/13472 | 6925/9429 | 2309/3142 | chr4 | 3214108 | ||
| chr4:3215167
|
A | G | 1 | a0042 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.7010A>G | p.Lys2337Arg | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/67 | 7155/13472 | 7010/9429 | 2337/3142 | chr4 | 3215167 | ||
| chr4:3228701
|
C | A | 1 | a0082 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.7935C>A | p.Asp2645Glu | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 58/67 | 8080/13472 | 7935/9429 | 2645/3142 | chr4 | 3228701 | ||
| chr4:3233253
|
G | A | 18 | a0002a0005a0025others(15): Show | 73 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(70): Show |
missense_variant | MODERATE | c.8356G>A | p.Val2786Ile | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/67 | 8501/13472 | 8356/9429 | 2786/3142 | chr4 | 3233253 | ||
| chr4:3238971
|
G | A | 1 | a0029 | 2 | NA19058.hp1 NA19079.hp1 |
missense_variant | MODERATE | c.9208G>A | p.Ala3070Thr | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 66/67 | 9353/13472 | 9208/9429 | 3070/3142 | chr4 | 3238971 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:3074906
|
G | A | 1 | a0040c0045 | 1 | HG01070.hp1 | synonymous_variant | LOW | c.81G>A | p.Gln27Gln | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 226/13472 | 81/9429 | 27/3142 | chr4 | 3074906 | ||
| chr4:3074924
|
G | A | 2 | a0017c0018a0048c0057 | 4 | HG01975.hp2 HG02055.hp1 HG02257.hp2 others(1): Show |
synonymous_variant | LOW | c.99G>A | p.Gln33Gln | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 244/13472 | 99/9429 | 33/3142 | chr4 | 3074924 | ||
| chr4:3074927
|
G | A | 19 | a0007c0007a0007c0053a0007c0058others(16): Show | 31 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(28): Show |
synonymous_variant | LOW | c.102G>A | p.Gln34Gln | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 247/13472 | 102/9429 | 34/3142 | chr4 | 3074927 | ||
| chr4:3074930
|
G | A | 5 | a0012c0012a0012c0077a0020c0052others(2): Show | 8 | HG01081.hp2 HG02523.hp1 HG02683.hp2 others(5): Show |
synonymous_variant | LOW | c.105G>A | p.Gln35Gln | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 250/13472 | 105/9429 | 35/3142 | chr4 | 3074930 | ||
| chr4:3074933
|
G | A | 1 | a0072c0096 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.108G>A | p.Gln36Gln | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 253/13472 | 108/9429 | 36/3142 | chr4 | 3074933 | ||
| chr4:3074936
|
A | G | 6 | a0003c0128a0012c0012a0012c0077others(3): Show | 9 | HG01081.hp2 HG01891.hp2 HG02523.hp1 others(6): Show |
synonymous_variant | LOW | c.111A>G | p.Gln37Gln | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 256/13472 | 111/9429 | 37/3142 | chr4 | 3074936 | ||
| chr4:3074939
|
G | A | 3 | a0012c0012a0012c0077a0061c0076 | 6 | HG01081.hp2 HG02523.hp1 HG02922.hp2 others(3): Show |
synonymous_variant | LOW | c.114G>A | p.Gln38Gln | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 259/13472 | 114/9429 | 38/3142 | chr4 | 3074939 | ||
| chr4:3074945
|
A | G | 66 | a0001c0089a0002c0001a0002c0030others(63): Show | 153 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(150): Show |
synonymous_variant | LOW | c.120A>G | p.Pro40Pro | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 265/13472 | 120/9429 | 40/3142 | chr4 | 3074945 | ||
| chr4:3074966
|
G | T | 9 | a0007c0007a0007c0058a0014c0014others(6): Show | 18 | HG01109.hp1 HG01167.hp1 HG01243.hp2 others(15): Show |
synonymous_variant | LOW | c.141G>T | p.Pro47Pro | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 286/13472 | 141/9429 | 47/3142 | chr4 | 3074966 | ||
| chr4:3086987
|
G | T | 1 | a0001c0085 | 1 | NA18989.hp1 | synonymous_variant | LOW | c.312G>T | p.Leu104Leu | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/67 | 457/13472 | 312/9429 | 104/3142 | chr4 | 3086987 | ||
| chr4:3086993
|
A | C | 1 | a0036c0108 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.318A>C | p.Ile106Ile | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/67 | 463/13472 | 318/9429 | 106/3142 | chr4 | 3086993 | ||
| chr4:3105416
|
G | C | 1 | a0037c0121 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.588G>C | p.Leu196Leu | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 5/67 | 733/13472 | 588/9429 | 196/3142 | chr4 | 3105416 | ||
| chr4:3115441
|
C | G | 5 | a0003c0128a0010c0009a0036c0107others(2): Show | 9 | HG00642.hp1 HG01433.hp1 HG02280.hp2 others(6): Show |
synonymous_variant | LOW | c.885C>G | p.Leu295Leu | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 7/67 | 1030/13472 | 885/9429 | 295/3142 | chr4 | 3115441 | ||
| chr4:3121242
|
G | C | 4 | a0023c0039a0077c0102a0083c0116others(1): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
synonymous_variant | LOW | c.1083G>C | p.Thr361Thr | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 9/67 | 1228/13472 | 1083/9429 | 361/3142 | chr4 | 3121242 | ||
| chr4:3121347
|
C | T | 13 | a0010c0056a0012c0012a0012c0077others(10): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
synonymous_variant | LOW | c.1188C>T | p.Thr396Thr | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 9/67 | 1333/13472 | 1188/9429 | 396/3142 | chr4 | 3121347 | ||
| chr4:3136309
|
C | T | 1 | a0008c0114 | 1 | NA19005.hp2 | synonymous_variant | LOW | c.2781C>T | p.Ala927Ala | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/67 | 2926/13472 | 2781/9429 | 927/3142 | chr4 | 3136309 | ||
| chr4:3140618
|
G | A | 1 | a0008c0111 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.2907G>A | p.Thr969Thr | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 22/67 | 3052/13472 | 2907/9429 | 969/3142 | chr4 | 3140618 | ||
| chr4:3142805
|
C | T | 1 | a0002c0031 | 2 | NA18999.hp1 NA19084.hp2 |
synonymous_variant | LOW | c.2985C>T | p.Asp995Asp | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/67 | 3130/13472 | 2985/9429 | 995/3142 | chr4 | 3142805 | ||
| chr4:3160329
|
C | T | 20 | a0002c0001a0002c0030a0002c0031others(17): Show | 72 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(69): Show |
synonymous_variant | LOW | c.3801C>T | p.Leu1267Leu | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/67 | 3946/13472 | 3801/9429 | 1267/3142 | chr4 | 3160329 | ||
| chr4:3178346
|
A | G | 1 | a0001c0089 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.4512A>G | p.Leu1504Leu | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 35/67 | 4657/13472 | 4512/9429 | 1504/3142 | chr4 | 3178346 | ||
| chr4:3180540
|
C | G | 1 | a0003c0105 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.4638C>G | p.Val1546Val | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 36/67 | 4783/13472 | 4638/9429 | 1546/3142 | chr4 | 3180540 | ||
| chr4:3188957
|
A | G | 1 | a0054c0068 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.5232A>G | p.Leu1744Leu | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/67 | 5377/13472 | 5232/9429 | 1744/3142 | chr4 | 3188957 | ||
| chr4:3199863
|
C | T | 1 | a0012c0077 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.5500C>T | p.Leu1834Leu | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/67 | 5645/13472 | 5500/9429 | 1834/3142 | chr4 | 3199863 | ||
| chr4:3206845
|
G | A | 1 | a0079c0106 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.5937G>A | p.Gly1979Gly | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 44/67 | 6082/13472 | 5937/9429 | 1979/3142 | chr4 | 3206845 | ||
| chr4:3212105
|
G | A | 27 | a0002c0001a0002c0030a0002c0031others(24): Show | 86 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(83): Show |
synonymous_variant | LOW | c.6591G>A | p.Glu2197Glu | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 48/67 | 6736/13472 | 6591/9429 | 2197/3142 | chr4 | 3212105 | ||
| chr4:3212138
|
G | A | 1 | a0033c0098 | 1 | NA19088.hp1 | synonymous_variant | LOW | c.6624G>A | p.Leu2208Leu | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 48/67 | 6769/13472 | 6624/9429 | 2208/3142 | chr4 | 3212138 | ||
| chr4:3217886
|
A | C | 127 | a0001c0002a0001c0003a0001c0085others(124): Show | 292 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(289): Show |
synonymous_variant | LOW | c.7176A>C | p.Leu2392Leu | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/67 | 7321/13472 | 7176/9429 | 2392/3142 | chr4 | 3217886 | ||
| chr4:3220301
|
C | T | 1 | a0070c0092 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.7362C>T | p.Asn2454Asn | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 53/67 | 7507/13472 | 7362/9429 | 2454/3142 | chr4 | 3220301 | ||
| chr4:3223441
|
C | T | 1 | a0037c0121 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.7506C>T | p.Ala2502Ala | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 55/67 | 7651/13472 | 7506/9429 | 2502/3142 | chr4 | 3223441 | ||
| chr4:3223489
|
G | A | 1 | a0051c0062 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.7554G>A | p.Val2518Val | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 55/67 | 7699/13472 | 7554/9429 | 2518/3142 | chr4 | 3223489 | ||
| chr4:3224046
|
A | G | 1 | a0002c0030 | 2 | NA18964.hp2 NA18970.hp1 |
synonymous_variant | LOW | c.7680A>G | p.Ala2560Ala | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 56/67 | 7825/13472 | 7680/9429 | 2560/3142 | chr4 | 3224046 | ||
| chr4:3225692
|
A | G | 32 | a0002c0001a0002c0030a0002c0031others(29): Show | 88 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(85): Show |
synonymous_variant | LOW | c.7797A>G | p.Leu2599Leu | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/67 | 7942/13472 | 7797/9429 | 2599/3142 | chr4 | 3225692 | ||
| chr4:3225737
|
C | T | 2 | a0084c0115a0088c0120 | 2 | HG00738.hp1 HG03017.hp1 |
synonymous_variant | LOW | c.7842C>T | p.Leu2614Leu | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/67 | 7987/13472 | 7842/9429 | 2614/3142 | chr4 | 3225737 | ||
| chr4:3229895
|
G | C | 1 | a0071c0091 | 1 | NA19002.hp1 | synonymous_variant | LOW | c.8118G>C | p.Val2706Val | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/67 | 8263/13472 | 8118/9429 | 2706/3142 | chr4 | 3229895 | ||
| chr4:3229934
|
G | A | 12 | a0001c0002a0001c0085a0003c0041others(9): Show | 46 | HG00423.hp1 HG00438.hp2 HG01070.hp2 others(43): Show |
synonymous_variant | LOW | c.8157G>A | p.Leu2719Leu | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/67 | 8302/13472 | 8157/9429 | 2719/3142 | chr4 | 3229934 | ||
| chr4:3229952
|
A | C | 1 | a0004c0067 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.8175A>C | p.Thr2725Thr | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/67 | 8320/13472 | 8175/9429 | 2725/3142 | chr4 | 3229952 | ||
| chr4:3235374
|
G | A | 1 | a0020c0084 | 1 | HG02132.hp1 | synonymous_variant | LOW | c.8547G>A | p.Pro2849Pro | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 62/67 | 8692/13472 | 8547/9429 | 2849/3142 | chr4 | 3235374 | ||
| chr4:3235649
|
C | T | 1 | a0024c0047 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.8656C>T | p.Leu2886Leu | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 63/67 | 8801/13472 | 8656/9429 | 2886/3142 | chr4 | 3235649 | ||
| chr4:3238940
|
C | T | 3 | a0024c0046a0024c0047a0042c0048 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
synonymous_variant | LOW | c.9177C>T | p.Phe3059Phe | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 66/67 | 9322/13472 | 9177/9429 | 3059/3142 | chr4 | 3238940 | ||
| chr4:3240014
|
G | A | 1 | a0002c0073 | 1 | HG02148.hp2 | synonymous_variant | LOW | c.9384G>A | p.Arg3128Arg | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 9529/13472 | 9384/9429 | 3128/3142 | chr4 | 3240014 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:3074723
|
C | T | 3 | a0008c0010t0020a0015c0016t0009a0016c0017t0020 | 5 | HG01099.hp1 HG01256.hp2 HG01258.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-103C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 103 | chr4 | 3074723 | |||||
| chr4:3074793
|
T | A | 1 | a0006c0037t0021 | 1 | NA18964.hp1 | 5_prime_UTR_variant | MODIFIER | c.-33T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 33 | chr4 | 3074793 | |||||
| chr4:3074796
|
G | A | 1 | a0087c0119t0022 | 1 | NA18984.hp1 | 5_prime_UTR_variant | MODIFIER | c.-30G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/67 | 30 | chr4 | 3074796 | |||||
| chr4:3240118
|
C | T | 2 | a0003c0024t0019a0038c0124t0019 | 2 | HG01928.hp1 HG01943.hp2 |
3_prime_UTR_variant | MODIFIER | c.*59C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 59 | chr4 | 3240118 | |||||
| chr4:3240195
|
T | A | 3 | a0010c0056t0007a0019c0020t0007a0019c0020t0023 | 4 | HG03139.hp2 HG06807.hp2 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*136T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 136 | chr4 | 3240195 | |||||
| chr4:3240247
|
G | A | 4 | a0014c0014t0010a0043c0050t0010a0046c0055t0011others(1): Show | 4 | HG01255.hp2 HG02559.hp1 HG02630.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*188G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 188 | chr4 | 3240247 | |||||
| chr4:3240295
|
C | A | 4 | a0014c0014t0010a0043c0050t0010a0046c0055t0011others(1): Show | 4 | HG01255.hp2 HG02559.hp1 HG02630.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*236C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 236 | chr4 | 3240295 | |||||
| chr4:3240373
|
G | A | 25 | a0002c0001t0002a0002c0001t0013a0002c0001t0014others(22): Show | 74 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*314G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 314 | chr4 | 3240373 | |||||
| chr4:3240421
|
C | G | 29 | a0002c0001t0002a0002c0001t0013a0002c0001t0014others(26): Show | 78 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*362C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 362 | chr4 | 3240421 | |||||
| chr4:3240433
|
C | G | 29 | a0001c0003t0003a0007c0007t0003a0007c0053t0003others(26): Show | 48 | HG00642.hp1 HG00738.hp1 HG01081.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*374C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 374 | chr4 | 3240433 | |||||
| chr4:3240496
|
G | A | 3 | a0024c0046t0008a0024c0047t0008a0042c0048t0008 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*437G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 437 | chr4 | 3240496 | |||||
| chr4:3240545
|
C | A | 36 | a0001c0003t0003a0007c0007t0003a0007c0053t0003others(33): Show | 55 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*486C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 486 | chr4 | 3240545 | |||||
| chr4:3240580
|
C | T | 27 | a0001c0003t0003a0007c0007t0003a0007c0053t0003others(24): Show | 46 | HG00642.hp1 HG01081.hp2 HG01109.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*521C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 521 | chr4 | 3240580 | |||||
| chr4:3240655
|
C | T | 1 | a0003c0024t0030 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*596C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 596 | chr4 | 3240655 | |||||
| chr4:3240776
|
G | T | 3 | a0023c0039t0016a0077c0102t0029a0083c0116t0016 | 3 | HG01243.hp1 HG02622.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*717G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 717 | chr4 | 3240776 | |||||
| chr4:3240791
|
C | T | 3 | a0007c0058t0033a0052c0061t0035a0054c0068t0034 | 3 | HG02145.hp1 HG02723.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*732C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 732 | chr4 | 3240791 | |||||
| chr4:3240831
|
A | C | 3 | a0024c0046t0008a0024c0047t0008a0042c0048t0008 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*772A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 772 | chr4 | 3240831 | |||||
| chr4:3240931
|
C | T | 4 | a0014c0014t0010a0043c0050t0010a0046c0055t0011others(1): Show | 4 | HG01255.hp2 HG02559.hp1 HG02630.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*872C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 872 | chr4 | 3240931 | |||||
| chr4:3241193
|
C | T | 5 | a0024c0046t0008a0024c0047t0008a0042c0048t0008others(2): Show | 5 | HG00323.hp2 HG00639.hp1 HG01255.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1134C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 1134 | chr4 | 3241193 | |||||
| chr4:3241491
|
C | T | 29 | a0002c0001t0002a0002c0001t0013a0002c0001t0014others(26): Show | 77 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1432C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 1432 | chr4 | 3241491 | |||||
| chr4:3241590
|
G | A | 1 | a0077c0102t0029 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1531G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 1531 | chr4 | 3241590 | |||||
| chr4:3241642
|
T | C | 1 | a0067c0086t0025 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1583T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 1583 | chr4 | 3241642 | |||||
| chr4:3241667
|
A | G | 1 | a0019c0020t0023 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1608A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 1608 | chr4 | 3241667 | |||||
| chr4:3241675
|
C | A | 2 | a0014c0014t0010a0043c0050t0010 | 2 | HG02559.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1616C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 1616 | chr4 | 3241675 | |||||
| chr4:3241754
|
G | GAAAGGGA others(10): Show |
37 | a0001c0003t0003a0007c0007t0003a0007c0053t0003others(34): Show | 57 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1708_*1709insGCTC others(13): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 1709 | INFO_REALIGN_3_PRIME | chr4 | 3241754 | ||||
| chr4:3241948
|
A | ATTC | 147 | a0001c0002t0001a0001c0003t0001a0001c0003t0003others(144): Show | 290 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*1890_*1892dupTTC | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 1893 | INFO_REALIGN_3_PRIME | chr4 | 3241948 | ||||
| chr4:3242017
|
G | C | 1 | a0003c0128t0026 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1958G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 1958 | chr4 | 3242017 | |||||
| chr4:3242045
|
TG | T | 40 | a0001c0003t0003a0007c0007t0003a0007c0053t0003others(37): Show | 60 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1988delG | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 1988 | INFO_REALIGN_3_PRIME | chr4 | 3242045 | ||||
| chr4:3242089
|
A | G | 1 | a0068c0087t0031 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2030A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 2030 | chr4 | 3242089 | |||||
| chr4:3242173
|
A | G | 1 | a0013c0013t0028 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2114A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 2114 | chr4 | 3242173 | |||||
| chr4:3242204
|
G | A | 1 | a0007c0058t0033 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2145G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 2145 | chr4 | 3242204 | |||||
| chr4:3242334
|
C | T | 2 | a0046c0055t0011a0049c0063t0011 | 2 | HG01255.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2275C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 2275 | chr4 | 3242334 | |||||
| chr4:3242523
|
G | A | 2 | a0036c0107t0018a0036c0108t0018 | 2 | HG02280.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2464G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 2464 | chr4 | 3242523 | |||||
| chr4:3242549
|
G | C | 2 | a0007c0058t0033a0054c0068t0034 | 2 | HG02145.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2490G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 2490 | chr4 | 3242549 | |||||
| chr4:3242948
|
G | A | 1 | a0002c0001t0013 | 2 | HG02040.hp2 NA18954.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2889G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 2889 | chr4 | 3242948 | |||||
| chr4:3243143
|
C | T | 1 | a0003c0006t0027 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3084C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 3084 | chr4 | 3243143 | |||||
| chr4:3243169
|
G | T | 3 | a0007c0058t0033a0052c0061t0035a0054c0068t0034 | 3 | HG02145.hp1 HG02723.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3110G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 3110 | chr4 | 3243169 | |||||
| chr4:3243201
|
G | A | 5 | a0007c0058t0033a0046c0055t0011a0049c0063t0011others(2): Show | 5 | HG01255.hp2 HG02145.hp1 HG02723.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3142G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 3142 | chr4 | 3243201 | |||||
| chr4:3243330
|
C | T | 7 | a0001c0003t0004a0008c0010t0004a0008c0111t0004others(4): Show | 10 | HG01074.hp2 HG01081.hp1 HG01099.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3271C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 3271 | chr4 | 3243330 | |||||
| chr4:3243486
|
G | A | 1 | a0002c0001t0024 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3427G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 3427 | chr4 | 3243486 | |||||
| chr4:3243592
|
T | A | 3 | a0008c0010t0006a0015c0016t0006a0016c0017t0006 | 4 | HG02109.hp2 HG02257.hp1 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3533T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 3533 | chr4 | 3243592 | |||||
| chr4:3243646
|
C | T | 3 | a0024c0046t0008a0024c0047t0008a0042c0048t0008 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3587C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 3587 | chr4 | 3243646 | |||||
| chr4:3243694
|
G | A | 2 | a0002c0001t0014a0059c0075t0014 | 2 | HG00423.hp2 NA18962.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3635G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 67/67 | 3635 | chr4 | 3243694 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:3075228
|
A | C | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.263+140A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3075228 | ||||||
| chr4:3075230
|
G | A | 6 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+142G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3075230 | ||||||
| chr4:3075310
|
T | C | 30 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(27): Show | 30 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.263+222T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3075310 | ||||||
| chr4:3075522
|
A | T | 6 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+434A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3075522 | ||||||
| chr4:3075558
|
T | C | 2 | a0013c0013t0001g0032a0013c0013t0001g0033 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.263+470T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3075558 | ||||||
| chr4:3075647
|
C | CG | 17 | a0002c0001t0002g0279a0002c0001t0002g0281a0002c0001t0002g0282others(14): Show | 17 | HG00597.hp2 HG00642.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.263+559_263+560ins others(1): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3075647 | ||||||
| chr4:3075647
|
C | CGG | 4 | a0002c0073t0002g0290a0010c0009t0003g0291a0070c0092t0032g0030others(1): Show | 4 | HG01433.hp1 HG02148.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+559_263+560ins others(2): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3075647 | ||||||
| chr4:3075647
|
CA | C | 89 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(86): Show | 89 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.263+560delA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3075647 | ||||||
| chr4:3075648
|
A | G | 131 | a0001c0002t0001g0199a0001c0003t0001g0197a0002c0001t0002g0191others(128): Show | 131 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.263+560A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3075648 | ||||||
| chr4:3075650
|
G | C | 1 | a0006c0022t0001g0034 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.263+562G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3075650 | ||||||
| chr4:3075655
|
G | C | 14 | a0007c0058t0033g0009a0014c0014t0003g0014a0014c0014t0003g0015others(11): Show | 14 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.263+567G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3075655 | ||||||
| chr4:3075867
|
TA | T | 30 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(27): Show | 30 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.263+782delA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3075867 | |||||
| chr4:3076029
|
A | T | 18 | a0012c0012t0003g0087a0012c0012t0003g0089a0012c0012t0003g0095others(15): Show | 18 | HG01070.hp1 HG01081.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.263+941A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3076029 | ||||||
| chr4:3076049
|
G | A | 6 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(3): Show | 6 | HG00642.hp2 HG00735.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+961G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3076049 | ||||||
| chr4:3076143
|
G | A | 1 | a0007c0053t0003g0104 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.263+1055G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3076143 | ||||||
| chr4:3076258
|
T | C | 60 | a0001c0089t0001g0037a0003c0006t0001g0038a0003c0006t0001g0041others(57): Show | 61 | HG00438.hp1 HG00738.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.263+1170T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3076258 | ||||||
| chr4:3076279
|
G | C | 30 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(27): Show | 30 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.263+1191G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3076279 | ||||||
| chr4:3076280
|
T | C | 30 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(27): Show | 30 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.263+1192T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3076280 | ||||||
| chr4:3076320
|
C | G | 30 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(27): Show | 30 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.263+1232C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3076320 | ||||||
| chr4:3076335
|
C | A | 30 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(27): Show | 30 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.263+1247C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3076335 | ||||||
| chr4:3076356
|
A | G | 6 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+1268A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3076356 | ||||||
| chr4:3076364
|
G | A | 30 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(27): Show | 30 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.263+1276G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3076364 | ||||||
| chr4:3076520
|
A | G | 30 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(27): Show | 30 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.263+1432A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3076520 | ||||||
| chr4:3076767
|
G | A | 1 | a0009c0008t0001g0105 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.263+1679G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3076767 | ||||||
| chr4:3076860
|
G | C | 2 | a0007c0058t0033g0009a0041c0049t0001g0010 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.263+1772G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3076860 | ||||||
| chr4:3077033
|
C | T | 2 | a0007c0007t0003g0027a0007c0007t0003g0028 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.263+1945C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3077033 | ||||||
| chr4:3077102
|
C | T | 1 | a0035c0042t0005g0085 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.263+2014C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3077102 | ||||||
| chr4:3077210
|
A | G | 148 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(145): Show | 148 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.263+2122A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3077210 | ||||||
| chr4:3077248
|
C | T | 1 | a0037c0121t0001g0189 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.263+2160C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3077248 | ||||||
| chr4:3077868
|
TAACA | T | 29 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(26): Show | 29 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.263+2785_263+2788d others(6): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3077868 | |||||
| chr4:3077886
|
A | G | 3 | a0023c0103t0003g0029a0070c0092t0032g0030a0080c0110t0003g0031 | 3 | HG01884.hp2 HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.263+2798A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3077886 | ||||||
| chr4:3078025
|
G | A | 1 | a0091c0127t0004g0063 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.263+2937G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3078025 | ||||||
| chr4:3078058
|
G | T | 5 | a0011c0029t0001g0273a0011c0029t0001g0275a0053c0064t0001g0274others(2): Show | 5 | HG00673.hp1 HG02080.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.263+2970G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3078058 | ||||||
| chr4:3078179
|
G | C | 32 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(29): Show | 32 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.263+3091G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3078179 | ||||||
| chr4:3078229
|
A | G | 2 | a0010c0009t0003g0288a0010c0009t0003g0289 | 2 | HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.263+3141A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3078229 | ||||||
| chr4:3078285
|
C | T | 1 | a0008c0010t0020g0084 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.263+3197C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3078285 | ||||||
| chr4:3078446
|
G | A | 126 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(123): Show | 126 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.263+3358G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3078446 | ||||||
| chr4:3078472
|
A | G | 95 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(92): Show | 95 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.263+3384A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3078472 | ||||||
| chr4:3078511
|
T | C | 3 | a0003c0024t0019g0109a0038c0124t0019g0107a0089c0125t0002g0108 | 3 | HG01928.hp1 HG01943.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.263+3423T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3078511 | ||||||
| chr4:3078688
|
C | T | 2 | a0065c0078t0004g0185a0091c0127t0004g0063 | 2 | HG01074.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.263+3600C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3078688 | ||||||
| chr4:3078727
|
C | T | 1 | a0062c0082t0005g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263+3639C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3078727 | ||||||
| chr4:3078730
|
G | C | 12 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.263+3642G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3078730 | ||||||
| chr4:3078735
|
AT | A | 30 | a0001c0002t0001g0110a0002c0001t0002g0191a0007c0007t0003g0023others(27): Show | 30 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.263+3659delT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3078735 | |||||
| chr4:3078753
|
G | A | 1 | a0012c0012t0003g0089 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.263+3665G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3078753 | ||||||
| chr4:3078821
|
G | A | 1 | a0010c0056t0007g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.263+3733G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3078821 | ||||||
| chr4:3078827
|
C | T | 1 | a0069c0093t0003g0020 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.263+3739C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3078827 | ||||||
| chr4:3078835
|
C | T | 48 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(45): Show | 48 | HG00423.hp1 HG00438.hp2 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.263+3747C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3078835 | ||||||
| chr4:3078883
|
T | C | 1 | a0008c0010t0020g0084 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.263+3795T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3078883 | ||||||
| chr4:3078925
|
C | G | 10 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(7): Show | 10 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.263+3837C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3078925 | ||||||
| chr4:3078978
|
G | C | 28 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(25): Show | 28 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.263+3890G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3078978 | ||||||
| chr4:3079002
|
C | T | 14 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(11): Show | 14 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.263+3914C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3079002 | ||||||
| chr4:3079083
|
A | G | 28 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(25): Show | 28 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.263+3995A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3079083 | ||||||
| chr4:3079088
|
G | A | 1 | a0008c0010t0001g0068 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.263+4000G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3079088 | ||||||
| chr4:3079098
|
G | A | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.263+4010G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3079098 | ||||||
| chr4:3079165
|
G | C | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.263+4077G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3079165 | ||||||
| chr4:3079247
|
C | CT | 41 | a0001c0002t0001g0181a0001c0002t0001g0182a0002c0001t0002g0262others(38): Show | 41 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.263+4178dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3079247 | |||||
| chr4:3079247
|
C | CTT | 6 | a0007c0058t0033g0009a0020c0052t0003g0292a0026c0026t0003g0022others(3): Show | 6 | HG01255.hp2 HG02258.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.263+4177_263+4178d others(4): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3079247 | |||||
| chr4:3079266
|
TG | T | 6 | a0001c0002t0001g0110a0002c0001t0002g0206a0011c0072t0001g0205others(3): Show | 6 | HG01167.hp2 HG01884.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+4182delG | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3079266 | |||||
| chr4:3079267
|
G | T | 284 | a0001c0002t0001g0142a0001c0002t0001g0145a0001c0002t0001g0147others(281): Show | 286 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(283): Show |
intron_variant | MODIFIER | c.263+4179G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3079267 | ||||||
| chr4:3079415
|
C | A | 2 | a0046c0055t0011g0204a0049c0063t0011g0203 | 2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.263+4327C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3079415 | ||||||
| chr4:3079762
|
A | G | 2 | a0010c0009t0003g0291a0050c0065t0003g0286 | 2 | HG00642.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.263+4674A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3079762 | ||||||
| chr4:3079915
|
A | G | 23 | a0007c0058t0033g0009a0014c0014t0003g0014a0014c0014t0003g0015others(20): Show | 23 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.263+4827A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3079915 | ||||||
| chr4:3079958
|
C | G | 2 | a0023c0103t0003g0029a0080c0110t0003g0031 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.263+4870C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3079958 | ||||||
| chr4:3080054
|
G | C | 23 | a0007c0058t0033g0009a0014c0014t0003g0014a0014c0014t0003g0015others(20): Show | 23 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.263+4966G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3080054 | ||||||
| chr4:3080116
|
C | T | 4 | a0004c0005t0001g0055a0004c0005t0001g0056a0004c0005t0001g0057others(1): Show | 4 | HG02965.hp1 HG02976.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+5028C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3080116 | ||||||
| chr4:3080125
|
G | A | 8 | a0023c0039t0015g0004a0023c0039t0016g0008a0070c0092t0032g0030others(5): Show | 8 | HG00738.hp1 HG01243.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.263+5037G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3080125 | ||||||
| chr4:3080230
|
G | C | 16 | a0007c0058t0033g0009a0014c0014t0003g0014a0014c0014t0003g0015others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.263+5142G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3080230 | ||||||
| chr4:3080352
|
G | A | 8 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(5): Show | 8 | HG00642.hp1 HG01433.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.263+5264G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3080352 | ||||||
| chr4:3080375
|
T | G | 23 | a0007c0058t0033g0009a0014c0014t0003g0014a0014c0014t0003g0015others(20): Show | 23 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.263+5287T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3080375 | ||||||
| chr4:3080390
|
C | G | 16 | a0007c0058t0033g0009a0014c0014t0003g0014a0014c0014t0003g0015others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.263+5302C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3080390 | ||||||
| chr4:3080435
|
G | T | 1 | a0005c0004t0002g0260 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.263+5347G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3080435 | ||||||
| chr4:3080438
|
C | G | 11 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(8): Show | 11 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.263+5350C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3080438 | ||||||
| chr4:3080549
|
A | G | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.263+5461A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3080549 | ||||||
| chr4:3080584
|
G | A | 8 | a0004c0005t0001g0055a0004c0005t0001g0056a0004c0005t0001g0057others(5): Show | 8 | HG02280.hp1 HG02895.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.263+5496G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3080584 | ||||||
| chr4:3080659
|
C | T | 1 | a0022c0023t0003g0016 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.263+5571C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3080659 | ||||||
| chr4:3080696
|
T | C | 23 | a0007c0058t0033g0009a0014c0014t0003g0014a0014c0014t0003g0015others(20): Show | 23 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.263+5608T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3080696 | ||||||
| chr4:3080963
|
C | G | 1 | a0015c0016t0006g0137 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.263+5875C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3080963 | ||||||
| chr4:3081059
|
G | A | 2 | a0029c0032t0001g0111a0029c0032t0001g0138 | 2 | NA19058.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.264-5880G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3081059 | ||||||
| chr4:3081134
|
A | G | 15 | a0012c0012t0003g0087a0012c0012t0003g0089a0012c0012t0003g0095others(12): Show | 15 | HG01081.hp2 HG01515.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.264-5805A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3081134 | ||||||
| chr4:3081248
|
A | G | 5 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-5691A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3081248 | ||||||
| chr4:3081550
|
C | CT | 45 | a0001c0002t0001g0178a0002c0001t0002g0255a0002c0031t0002g0253others(42): Show | 46 | HG00323.hp2 HG00639.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.264-5364dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3081550 | |||||
| chr4:3081550
|
CT | C | 6 | a0002c0001t0002g0193a0002c0001t0002g0208a0031c0035t0002g0267others(3): Show | 6 | HG01169.hp1 HG01516.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-5364delT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3081550 | |||||
| chr4:3081550
|
CTTTTTTT others(3): Show |
C | 3 | a0023c0039t0015g0004a0069c0093t0003g0020a0092c0044t0015g0003 | 3 | HG01167.hp1 HG02055.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.264-5373_264-5364d others(12): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3081550 | |||||
| chr4:3081550
|
CTTTTTTT others(4): Show |
C | 16 | a0007c0058t0033g0009a0014c0014t0003g0014a0014c0014t0003g0015others(13): Show | 16 | HG01243.hp2 HG01255.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.264-5374_264-5364d others(13): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3081550 | |||||
| chr4:3081619
|
C | T | 1 | a0052c0061t0035g0252 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.264-5320C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3081619 | ||||||
| chr4:3081704
|
T | C | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.264-5235T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3081704 | ||||||
| chr4:3082035
|
CT | C | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.264-4902delT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3082035 | |||||
| chr4:3082046
|
A | G | 6 | a0023c0039t0015g0004a0023c0039t0016g0008a0070c0092t0032g0030others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-4893A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3082046 | ||||||
| chr4:3082096
|
G | C | 1 | a0040c0045t0002g0103 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.264-4843G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3082096 | ||||||
| chr4:3082156
|
A | T | 17 | a0007c0058t0033g0009a0014c0014t0003g0014a0014c0014t0003g0015others(14): Show | 17 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.264-4783A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3082156 | ||||||
| chr4:3082257
|
G | A | 1 | a0006c0022t0001g0034 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.264-4682G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3082257 | ||||||
| chr4:3082456
|
T | C | 2 | a0010c0009t0003g0288a0010c0009t0003g0289 | 2 | HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.264-4483T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3082456 | ||||||
| chr4:3082472
|
G | T | 1 | a0061c0076t0003g0099 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.264-4467G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3082472 | ||||||
| chr4:3082542
|
C | A | 23 | a0007c0058t0033g0009a0014c0014t0003g0014a0014c0014t0003g0015others(20): Show | 23 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.264-4397C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3082542 | ||||||
| chr4:3082886
|
C | G | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.264-4053C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3082886 | ||||||
| chr4:3083263
|
G | A | 2 | a0005c0004t0002g0209a0005c0004t0002g0260 | 2 | NA18956.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.264-3676G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083263 | ||||||
| chr4:3083488
|
C | T | 1 | a0008c0010t0001g0068 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.264-3451C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083488 | ||||||
| chr4:3083493
|
C | T | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-3446C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083493 | ||||||
| chr4:3083526
|
A | AAT | 22 | a0002c0001t0002g0193a0002c0001t0002g0196a0002c0001t0002g0211others(19): Show | 22 | HG00323.hp1 HG00609.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.264-3409_264-3408d others(4): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083526 | |||||
| chr4:3083526
|
A | AATAT | 15 | a0002c0001t0002g0206a0002c0001t0002g0210a0002c0001t0002g0217others(12): Show | 15 | HG00423.hp2 HG00597.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.264-3411_264-3408d others(6): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083526 | |||||
| chr4:3083526
|
A | AATATAT | 8 | a0002c0001t0002g0191a0002c0001t0002g0216a0002c0001t0014g0214others(5): Show | 8 | HG01070.hp1 HG02165.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.264-3408_264-3407i others(8): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083526 | |||||
| chr4:3083526
|
A | AATATATA others(1): Show |
7 | a0002c0001t0002g0237a0002c0001t0002g0241a0002c0001t0002g0281others(4): Show | 7 | HG03704.hp2 NA18939.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-3408_264-3407i others(10): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083526 | |||||
| chr4:3083528
|
TATACACA others(3): Show |
T | 2 | a0003c0040t0001g0069a0058c0071t0001g0270 | 2 | HG00741.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.264-3409_264-3400d others(12): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083528 | |||||
| chr4:3083530
|
T | TAC | 8 | a0001c0002t0001g0142a0001c0002t0001g0145a0001c0002t0001g0181others(5): Show | 8 | HG01106.hp2 HG01928.hp1 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.264-3353_264-3352d others(4): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083530 | |||||
| chr4:3083530
|
T | TATATATA others(5): Show |
2 | a0005c0004t0002g0256a0011c0028t0001g0236 | 2 | NA18979.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.264-3408_264-3407i others(14): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083530 | |||||
| chr4:3083530
|
TAC | T | 39 | a0001c0002t0001g0147a0001c0002t0001g0178a0001c0003t0001g0121others(36): Show | 39 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.264-3353_264-3352d others(4): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083530 | |||||
| chr4:3083530
|
TACAC | T | 24 | a0001c0002t0001g0110a0001c0002t0001g0148a0001c0002t0001g0149others(21): Show | 24 | HG00423.hp1 HG00597.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.264-3355_264-3352d others(6): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083530 | |||||
| chr4:3083530
|
TACACAC | T | 27 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0003t0001g0127others(24): Show | 27 | HG00438.hp2 HG01074.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.264-3357_264-3352d others(8): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083530 | |||||
| chr4:3083530
|
TACACACA others(1): Show |
T | 21 | a0001c0002t0001g0169a0001c0002t0001g0170a0001c0002t0001g0171others(18): Show | 22 | HG00639.hp2 HG01074.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.264-3359_264-3352d others(10): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083530 | |||||
| chr4:3083530
|
TACACACA others(3): Show |
T | 21 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0003t0004g0134others(18): Show | 22 | HG00738.hp2 HG01099.hp2 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.264-3361_264-3352d others(12): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083530 | |||||
| chr4:3083530
|
TACACACA others(5): Show |
T | 21 | a0001c0003t0001g0077a0003c0006t0001g0041a0003c0006t0001g0043others(18): Show | 21 | HG00438.hp1 HG00673.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.264-3363_264-3352d others(14): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083530 | |||||
| chr4:3083530
|
TACACACA others(7): Show |
T | 9 | a0003c0006t0001g0052a0006c0022t0001g0034a0013c0013t0001g0032others(6): Show | 9 | HG01071.hp1 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.264-3365_264-3352d others(16): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083530 | |||||
| chr4:3083530
|
TACACACA others(9): Show |
T | 9 | a0007c0058t0033g0009a0009c0059t0001g0054a0014c0014t0003g0014others(6): Show | 9 | HG01167.hp1 HG01243.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.264-3367_264-3352d others(18): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083530 | |||||
| chr4:3083530
|
TACACACA others(11): Show |
T | 5 | a0020c0052t0003g0292a0022c0023t0003g0019a0026c0026t0003g0022others(2): Show | 5 | HG01255.hp2 HG02145.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-3369_264-3352d others(20): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083530 | |||||
| chr4:3083530
|
TACACACA others(13): Show |
T | 2 | a0014c0014t0010g0011a0043c0050t0010g0012 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.264-3371_264-3352d others(22): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083530 | |||||
| chr4:3083530
|
TACACACA others(15): Show |
T | 1 | a0003c0024t0001g0079 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264-3373_264-3352d others(24): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083530 | |||||
| chr4:3083530
|
TACACACA others(17): Show |
T | 2 | a0001c0002t0001g0177a0038c0124t0019g0107 | 2 | HG01943.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.264-3375_264-3352d others(26): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083530 | |||||
| chr4:3083532
|
C | T | 69 | a0002c0001t0002g0193a0002c0001t0002g0196a0002c0001t0002g0206others(66): Show | 69 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.264-3407C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083532 | ||||||
| chr4:3083534
|
C | T | 87 | a0002c0001t0002g0193a0002c0001t0002g0196a0002c0001t0002g0206others(84): Show | 87 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.264-3405C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083534 | ||||||
| chr4:3083536
|
C | T | 69 | a0002c0001t0002g0208a0002c0001t0002g0246a0002c0001t0002g0247others(66): Show | 69 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.264-3403C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083536 | ||||||
| chr4:3083538
|
C | T | 49 | a0002c0001t0002g0208a0002c0001t0002g0249a0002c0001t0002g0250others(46): Show | 49 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.264-3401C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083538 | ||||||
| chr4:3083540
|
C | T | 35 | a0003c0128t0026g0053a0007c0007t0003g0023a0007c0007t0003g0024others(32): Show | 35 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.264-3399C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083540 | ||||||
| chr4:3083542
|
C | T | 4 | a0017c0018t0003g0097a0023c0103t0003g0029a0048c0057t0003g0098others(1): Show | 4 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-3397C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083542 | ||||||
| chr4:3083544
|
C | T | 1 | a0092c0044t0015g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.264-3395C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083544 | ||||||
| chr4:3083546
|
C | T | 4 | a0022c0023t0003g0016a0023c0039t0015g0004a0026c0026t0003g0017others(1): Show | 4 | HG02055.hp2 HG02896.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-3393C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083546 | ||||||
| chr4:3083548
|
C | T | 11 | a0007c0058t0033g0009a0014c0014t0003g0014a0014c0014t0003g0015others(8): Show | 11 | HG01167.hp1 HG01243.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.264-3391C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083548 | ||||||
| chr4:3083550
|
C | T | 15 | a0007c0058t0033g0009a0014c0014t0003g0014a0014c0014t0003g0015others(12): Show | 15 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.264-3389C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083550 | ||||||
| chr4:3083552
|
C | T | 17 | a0007c0058t0033g0009a0014c0014t0003g0014a0014c0014t0003g0015others(14): Show | 17 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.264-3387C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083552 | ||||||
| chr4:3083554
|
C | T | 17 | a0007c0058t0033g0009a0014c0014t0003g0014a0014c0014t0003g0015others(14): Show | 17 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.264-3385C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083554 | ||||||
| chr4:3083556
|
C | T | 14 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(11): Show | 14 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.264-3383C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083556 | ||||||
| chr4:3083558
|
C | T | 7 | a0014c0014t0010g0011a0020c0052t0003g0292a0022c0023t0003g0019others(4): Show | 7 | HG02145.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-3381C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083558 | ||||||
| chr4:3083564
|
C | G | 2 | a0014c0014t0010g0011a0043c0050t0010g0012 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.264-3375C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083564 | ||||||
| chr4:3083564
|
C | T | 2 | a0012c0012t0003g0087a0072c0096t0003g0086 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.264-3375C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083564 | ||||||
| chr4:3083566
|
C | T | 39 | a0003c0128t0026g0053a0007c0007t0003g0023a0007c0007t0003g0024others(36): Show | 39 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.264-3373C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083566 | ||||||
| chr4:3083568
|
C | T | 1 | a0033c0097t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.264-3371C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083568 | ||||||
| chr4:3083578
|
CACACACA others(3): Show |
C | 3 | a0001c0003t0001g0174a0025c0025t0002g0187a0025c0025t0002g0188 | 3 | HG01175.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.264-3359_264-3350d others(12): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083578 | |||||
| chr4:3083582
|
CACACAT | C | 5 | a0002c0001t0002g0208a0002c0001t0002g0255a0002c0073t0002g0290others(2): Show | 5 | HG02080.hp2 HG02148.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-3355_264-3350d others(8): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083582 | |||||
| chr4:3083584
|
CACAT | C | 4 | a0002c0001t0002g0284a0005c0004t0002g0209a0005c0004t0002g0254others(1): Show | 4 | HG01952.hp1 NA18956.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-3353_264-3350d others(6): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083584 | |||||
| chr4:3083586
|
CAT | C | 6 | a0002c0001t0002g0251a0018c0019t0001g0233a0018c0019t0001g0234others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-3346_264-3345d others(4): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3083586 | |||||
| chr4:3083588
|
T | C | 65 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(62): Show | 65 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.264-3351T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083588 | ||||||
| chr4:3083590
|
T | C | 1 | a0002c0001t0002g0279 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.264-3349T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083590 | ||||||
| chr4:3083656
|
A | G | 3 | a0014c0014t0010g0011a0020c0052t0003g0292a0043c0050t0010g0012 | 3 | HG02559.hp1 HG02630.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.264-3283A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083656 | ||||||
| chr4:3083700
|
C | T | 42 | a0003c0128t0026g0053a0007c0007t0003g0023a0007c0007t0003g0024others(39): Show | 42 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.264-3239C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083700 | ||||||
| chr4:3083750
|
G | A | 144 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(141): Show | 144 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.264-3189G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083750 | ||||||
| chr4:3083887
|
A | G | 1 | a0001c0002t0001g0173 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.264-3052A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3083887 | ||||||
| chr4:3084042
|
C | T | 6 | a0023c0039t0015g0004a0023c0039t0016g0008a0070c0092t0032g0030others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-2897C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3084042 | ||||||
| chr4:3084198
|
CT | C | 140 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(137): Show | 142 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.264-2718delT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3084198 | |||||
| chr4:3084198
|
CTT | C | 13 | a0001c0003t0001g0114a0002c0001t0002g0227a0002c0001t0002g0250others(10): Show | 13 | HG00597.hp2 HG00735.hp1 HG03491.hp1 others(10): Show |
intron_variant | MODIFIER | c.264-2719_264-2718d others(4): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3084198 | |||||
| chr4:3084198
|
CTTT | C | 111 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(108): Show | 111 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.264-2720_264-2718d others(5): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3084198 | |||||
| chr4:3084198
|
CTTTT | C | 10 | a0012c0012t0003g0087a0017c0018t0003g0091a0017c0018t0003g0092others(7): Show | 10 | HG01070.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.264-2721_264-2718d others(6): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3084198 | |||||
| chr4:3084232
|
T | C | 1 | a0035c0042t0005g0076 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.264-2707T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3084232 | ||||||
| chr4:3084402
|
G | T | 8 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(5): Show | 8 | HG00738.hp1 HG01109.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.264-2537G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3084402 | ||||||
| chr4:3084410
|
C | T | 1 | a0002c0001t0002g0227 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.264-2529C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3084410 | ||||||
| chr4:3084690
|
C | CA | 15 | a0001c0002t0001g0181a0002c0001t0002g0210a0014c0014t0003g0014others(12): Show | 15 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.264-2237dupA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3084690 | |||||
| chr4:3084804
|
G | A | 3 | a0007c0058t0033g0009a0052c0061t0035g0252a0054c0068t0034g0090 | 3 | HG02145.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.264-2135G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3084804 | ||||||
| chr4:3084870
|
C | T | 6 | a0023c0039t0015g0004a0023c0039t0016g0008a0070c0092t0032g0030others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-2069C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3084870 | ||||||
| chr4:3084899
|
A | T | 1 | a0001c0002t0001g0145 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.264-2040A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3084899 | ||||||
| chr4:3085018
|
G | A | 1 | a0005c0004t0002g0242 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.264-1921G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3085018 | ||||||
| chr4:3085018
|
GA | G | 30 | a0004c0005t0001g0001a0004c0005t0001g0049a0004c0005t0001g0050others(27): Show | 31 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.264-1910delA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | INFO_REALIGN_3_PRIME | chr4 | 3085018 | |||||
| chr4:3085026
|
A | T | 106 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(103): Show | 106 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.264-1913A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3085026 | ||||||
| chr4:3085030
|
T | A | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.264-1909T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3085030 | ||||||
| chr4:3085059
|
A | C | 2 | a0001c0002t0001g0145a0001c0002t0001g0199 | 2 | NA18948.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.264-1880A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3085059 | ||||||
| chr4:3085129
|
C | T | 1 | a0033c0097t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.264-1810C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3085129 | ||||||
| chr4:3085212
|
A | G | 4 | a0028c0033t0001g0132a0032c0036t0001g0112a0032c0036t0001g0140others(1): Show | 4 | HG00597.hp1 NA19002.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-1727A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3085212 | ||||||
| chr4:3085305
|
T | C | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.264-1634T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3085305 | ||||||
| chr4:3085400
|
T | C | 1 | a0010c0056t0007g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.264-1539T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3085400 | ||||||
| chr4:3085415
|
C | T | 24 | a0003c0128t0026g0053a0007c0007t0003g0023a0007c0007t0003g0024others(21): Show | 24 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.264-1524C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3085415 | ||||||
| chr4:3085655
|
C | T | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-1284C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3085655 | ||||||
| chr4:3085933
|
A | G | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.264-1006A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3085933 | ||||||
| chr4:3086397
|
A | G | 1 | a0001c0002t0001g0155 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.264-542A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3086397 | ||||||
| chr4:3086484
|
A | G | 107 | a0001c0002t0001g0145a0002c0001t0002g0191a0002c0001t0002g0193others(104): Show | 107 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.264-455A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3086484 | ||||||
| chr4:3086487
|
G | C | 1 | a0005c0004t0002g0254 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.264-452G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3086487 | ||||||
| chr4:3086527
|
C | G | 1 | a0042c0048t0008g0259 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.264-412C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3086527 | ||||||
| chr4:3086658
|
A | G | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.264-281A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 1/66 | chr4 | 3086658 | ||||||
| chr4:3087219
|
G | A | 1 | a0001c0003t0001g0121 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.347+197G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3087219 | ||||||
| chr4:3087241
|
A | C | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.347+219A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3087241 | ||||||
| chr4:3087371
|
C | T | 1 | a0079c0106t0003g0074 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.347+349C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3087371 | ||||||
| chr4:3087397
|
C | T | 15 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(12): Show | 15 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.347+375C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3087397 | ||||||
| chr4:3087416
|
A | G | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.347+394A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3087416 | ||||||
| chr4:3087480
|
C | T | 1 | a0006c0099t0001g0047 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.347+458C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3087480 | ||||||
| chr4:3087483
|
G | A | 1 | a0042c0048t0008g0259 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.347+461G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3087483 | ||||||
| chr4:3087532
|
A | G | 149 | a0001c0002t0001g0145a0002c0001t0002g0191a0002c0001t0002g0193others(146): Show | 149 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.347+510A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3087532 | ||||||
| chr4:3087537
|
C | T | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.347+515C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3087537 | ||||||
| chr4:3087720
|
C | G | 10 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(7): Show | 10 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.347+698C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3087720 | ||||||
| chr4:3087825
|
T | C | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.347+803T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3087825 | ||||||
| chr4:3087837
|
C | T | 126 | a0001c0002t0001g0145a0002c0001t0002g0191a0002c0001t0002g0193others(123): Show | 126 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.347+815C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3087837 | ||||||
| chr4:3087908
|
T | G | 1 | a0020c0079t0003g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.347+886T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3087908 | ||||||
| chr4:3087931
|
A | T | 2 | a0007c0058t0033g0009a0054c0068t0034g0090 | 2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.347+909A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3087931 | ||||||
| chr4:3088013
|
G | C | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.347+991G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3088013 | ||||||
| chr4:3088036
|
G | GATGGGGC others(6): Show |
7 | a0020c0052t0003g0292a0023c0039t0015g0004a0023c0039t0016g0008others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.347+1017_347+1018i others(15): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3088036 | |||||
| chr4:3088083
|
C | T | 1 | a0067c0086t0025g0113 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.347+1061C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3088083 | ||||||
| chr4:3088116
|
C | T | 1 | a0069c0093t0003g0020 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.347+1094C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3088116 | ||||||
| chr4:3088128
|
C | A | 1 | a0020c0084t0003g0093 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.347+1106C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3088128 | ||||||
| chr4:3088188
|
G | GT | 6 | a0001c0002t0001g0154a0002c0001t0002g0251a0004c0011t0001g0153others(3): Show | 6 | HG01515.hp2 HG02258.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.347+1182dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3088188 | |||||
| chr4:3088188
|
G | T | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.347+1166G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3088188 | ||||||
| chr4:3088194
|
T | G | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.347+1172T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3088194 | ||||||
| chr4:3088537
|
G | A | 1 | a0003c0128t0026g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.347+1515G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3088537 | ||||||
| chr4:3088598
|
T | G | 3 | a0014c0014t0010g0011a0020c0052t0003g0292a0043c0050t0010g0012 | 3 | HG02559.hp1 HG02630.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.347+1576T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3088598 | ||||||
| chr4:3088599
|
T | A | 1 | a0062c0082t0005g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.347+1577T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3088599 | ||||||
| chr4:3088780
|
C | T | 9 | a0003c0128t0026g0053a0010c0009t0003g0276a0010c0009t0003g0277others(6): Show | 9 | HG00642.hp1 HG01433.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.347+1758C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3088780 | ||||||
| chr4:3089160
|
A | C | 2 | a0023c0039t0015g0004a0092c0044t0015g0003 | 2 | HG02055.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.347+2138A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3089160 | ||||||
| chr4:3089205
|
C | T | 1 | a0002c0001t0002g0206 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.347+2183C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3089205 | ||||||
| chr4:3089225
|
G | A | 1 | a0003c0006t0027g0042 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.347+2203G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3089225 | ||||||
| chr4:3089284
|
T | C | 1 | a0063c0081t0001g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.347+2262T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3089284 | ||||||
| chr4:3089471
|
T | G | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.347+2449T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3089471 | ||||||
| chr4:3089504
|
C | T | 4 | a0017c0018t0003g0091a0017c0018t0003g0092a0017c0018t0003g0097others(1): Show | 4 | HG01975.hp2 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+2482C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3089504 | ||||||
| chr4:3089726
|
G | A | 15 | a0001c0089t0001g0037a0004c0005t0001g0001a0004c0005t0001g0049others(12): Show | 16 | HG01891.hp1 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.347+2704G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3089726 | ||||||
| chr4:3089767
|
T | G | 1 | a0038c0123t0001g0141 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.347+2745T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3089767 | ||||||
| chr4:3089824
|
A | G | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.347+2802A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3089824 | ||||||
| chr4:3089984
|
A | T | 2 | a0046c0055t0011g0204a0049c0063t0011g0203 | 2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.347+2962A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3089984 | ||||||
| chr4:3089987
|
C | T | 24 | a0003c0128t0026g0053a0007c0007t0003g0023a0007c0007t0003g0024others(21): Show | 24 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.347+2965C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3089987 | ||||||
| chr4:3090034
|
T | A | 28 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(25): Show | 28 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.347+3012T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3090034 | ||||||
| chr4:3090069
|
C | G | 2 | a0046c0055t0011g0204a0049c0063t0011g0203 | 2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.347+3047C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3090069 | ||||||
| chr4:3090101
|
T | A | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.347+3079T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3090101 | ||||||
| chr4:3090264
|
C | T | 1 | a0001c0003t0001g0197 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.347+3242C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3090264 | ||||||
| chr4:3090315
|
T | C | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.347+3293T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3090315 | ||||||
| chr4:3090425
|
G | A | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.347+3403G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3090425 | ||||||
| chr4:3090443
|
A | G | 1 | a0001c0003t0001g0121 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.347+3421A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3090443 | ||||||
| chr4:3090510
|
C | T | 2 | a0084c0115t0017g0202a0088c0120t0017g0201 | 2 | HG00738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.347+3488C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3090510 | ||||||
| chr4:3090617
|
C | T | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.347+3595C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3090617 | ||||||
| chr4:3090670
|
T | C | 1 | a0028c0033t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.347+3648T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3090670 | ||||||
| chr4:3090727
|
A | T | 3 | a0018c0019t0001g0233a0018c0019t0001g0234a0018c0019t0001g0235 | 3 | HG01070.hp2 HG01071.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.347+3705A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3090727 | ||||||
| chr4:3090741
|
T | A | 1 | a0008c0010t0004g0072 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.347+3719T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3090741 | ||||||
| chr4:3090804
|
C | G | 1 | a0038c0124t0019g0107 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.347+3782C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3090804 | ||||||
| chr4:3090821
|
T | A | 2 | a0014c0014t0010g0011a0043c0050t0010g0012 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.347+3799T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3090821 | ||||||
| chr4:3090940
|
T | A | 15 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(12): Show | 15 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.347+3918T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3090940 | ||||||
| chr4:3091108
|
G | A | 2 | a0013c0013t0001g0032a0013c0013t0001g0033 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.347+4086G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3091108 | ||||||
| chr4:3091250
|
A | T | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.347+4228A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3091250 | ||||||
| chr4:3091349
|
CAT | C | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.347+4329_347+4330d others(4): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3091349 | |||||
| chr4:3091585
|
G | A | 288 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(285): Show | 290 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(287): Show |
intron_variant | MODIFIER | c.347+4563G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3091585 | ||||||
| chr4:3091602
|
C | T | 2 | a0003c0024t0001g0079a0003c0024t0030g0075 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.347+4580C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3091602 | ||||||
| chr4:3091858
|
A | T | 10 | a0003c0128t0026g0053a0010c0009t0003g0276a0010c0009t0003g0277others(7): Show | 10 | HG00642.hp1 HG01192.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.347+4836A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3091858 | ||||||
| chr4:3091870
|
T | C | 1 | a0058c0071t0001g0270 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.347+4848T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3091870 | ||||||
| chr4:3092184
|
G | T | 15 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(12): Show | 15 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.347+5162G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3092184 | ||||||
| chr4:3092196
|
G | A | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.347+5174G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3092196 | ||||||
| chr4:3092264
|
C | T | 1 | a0003c0006t0001g0060 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.347+5242C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3092264 | ||||||
| chr4:3092271
|
C | G | 1 | a0028c0033t0001g0120 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.347+5249C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3092271 | ||||||
| chr4:3092326
|
A | G | 1 | a0010c0009t0003g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.347+5304A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3092326 | ||||||
| chr4:3092435
|
A | G | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.347+5413A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3092435 | ||||||
| chr4:3092525
|
T | C | 1 | a0003c0024t0019g0109 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.347+5503T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3092525 | ||||||
| chr4:3092592
|
G | A | 1 | a0005c0004t0002g0242 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.347+5570G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3092592 | ||||||
| chr4:3092615
|
C | T | 24 | a0003c0128t0026g0053a0007c0007t0003g0023a0007c0007t0003g0024others(21): Show | 24 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.347+5593C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3092615 | ||||||
| chr4:3093008
|
G | A | 1 | a0019c0020t0023g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.347+5986G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3093008 | ||||||
| chr4:3093163
|
A | C | 2 | a0002c0031t0002g0226a0002c0031t0002g0253 | 2 | NA18999.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.348-6111A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3093163 | ||||||
| chr4:3093483
|
C | T | 2 | a0012c0012t0003g0087a0072c0096t0003g0086 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.348-5791C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3093483 | ||||||
| chr4:3093555
|
A | G | 30 | a0001c0002t0001g0110a0001c0002t0001g0145a0001c0002t0001g0148others(27): Show | 30 | HG00423.hp1 HG02056.hp1 HG02071.hp2 others(27): Show |
intron_variant | MODIFIER | c.348-5719A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3093555 | ||||||
| chr4:3093859
|
C | T | 1 | a0002c0001t0013g0225 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.348-5415C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3093859 | ||||||
| chr4:3093860
|
C | CT | 30 | a0002c0001t0002g0210a0003c0024t0019g0109a0003c0128t0026g0053others(27): Show | 30 | HG00323.hp2 HG00423.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.348-5396dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3093860 | |||||
| chr4:3093861
|
T | C | 1 | a0002c0001t0013g0225 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.348-5413T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3093861 | ||||||
| chr4:3093905
|
G | GT | 63 | a0001c0003t0001g0077a0001c0003t0001g0114a0001c0003t0001g0121others(60): Show | 64 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.348-5345dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3093905 | |||||
| chr4:3093905
|
G | GTT | 110 | a0001c0002t0001g0110a0001c0002t0001g0145a0001c0002t0001g0147others(107): Show | 111 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.348-5346_348-5345d others(4): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3093905 | |||||
| chr4:3093905
|
G | GTTT | 74 | a0001c0002t0001g0142a0001c0002t0001g0164a0001c0002t0001g0166others(71): Show | 74 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.348-5347_348-5345d others(5): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3093905 | |||||
| chr4:3093905
|
G | GTTTT | 15 | a0002c0001t0002g0193a0002c0001t0002g0216a0002c0001t0002g0241others(12): Show | 15 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.348-5348_348-5345d others(6): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3093905 | |||||
| chr4:3093905
|
G | GTTTTTTT others(4): Show |
1 | a0014c0014t0003g0015 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.348-5355_348-5345d others(13): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3093905 | |||||
| chr4:3093905
|
G | GTTTTTTT others(6): Show |
2 | a0014c0014t0010g0011a0043c0050t0010g0012 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.348-5357_348-5345d others(15): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3093905 | |||||
| chr4:3093905
|
G | GTTTTTTT others(7): Show |
2 | a0026c0026t0003g0017a0026c0026t0003g0022 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.348-5358_348-5345d others(16): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3093905 | |||||
| chr4:3093905
|
G | GTTTTTTT others(10): Show |
1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.348-5361_348-5345d others(19): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3093905 | |||||
| chr4:3093905
|
G | GTTTTTTT others(18): Show |
1 | a0046c0055t0011g0204 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.348-5345_348-5344i others(27): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3093905 | |||||
| chr4:3093905
|
G | GTTTTTTT others(20): Show |
1 | a0049c0063t0011g0203 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.348-5345_348-5344i others(29): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3093905 | |||||
| chr4:3093905
|
GTTTTTTT others(3): Show |
G | 7 | a0014c0014t0003g0014a0014c0014t0003g0021a0022c0023t0003g0013others(4): Show | 7 | HG02145.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.348-5354_348-5345d others(12): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3093905 | |||||
| chr4:3094124
|
C | T | 1 | a0002c0001t0002g0245 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.348-5150C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3094124 | ||||||
| chr4:3094199
|
A | G | 5 | a0016c0017t0001g0190a0024c0046t0008g0257a0024c0047t0008g0258others(2): Show | 5 | HG00323.hp2 HG00639.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.348-5075A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3094199 | ||||||
| chr4:3094279
|
T | C | 1 | a0003c0105t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.348-4995T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3094279 | ||||||
| chr4:3094418
|
T | C | 19 | a0003c0006t0001g0038a0003c0006t0001g0041a0003c0006t0001g0043others(16): Show | 19 | HG00438.hp1 HG00673.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.348-4856T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3094418 | ||||||
| chr4:3094522
|
G | A | 15 | a0001c0089t0001g0037a0004c0005t0001g0001a0004c0005t0001g0049others(12): Show | 16 | HG01891.hp1 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.348-4752G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3094522 | ||||||
| chr4:3094533
|
TGGGCGGG others(77): Show |
T | 3 | a0023c0039t0016g0008a0077c0102t0029g0006a0083c0116t0016g0005 | 3 | HG01243.hp1 HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.348-4683_348-4600d others(86): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3094533 | |||||
| chr4:3094560
|
GACGGGGC others(120): Show |
G | 2 | a0084c0115t0017g0202a0088c0120t0017g0201 | 2 | HG00738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.348-4713_348-4587d others(2): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3094560 | ||||||
| chr4:3094576
|
G | A | 1 | a0010c0009t0003g0276 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.348-4698G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3094576 | ||||||
| chr4:3094612
|
C | CTGGCCGG others(35): Show |
8 | a0004c0005t0001g0055a0004c0005t0001g0056a0004c0005t0001g0057others(5): Show | 8 | HG02280.hp1 HG02895.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.348-4620_348-4579d others(44): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3094612 | |||||
| chr4:3094612
|
C | G | 1 | a0026c0026t0003g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.348-4662C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3094612 | ||||||
| chr4:3094621
|
C | T | 2 | a0016c0017t0001g0190a0024c0047t0008g0258 | 2 | HG01106.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.348-4653C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3094621 | ||||||
| chr4:3094630
|
C | T | 1 | a0014c0014t0003g0015 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.348-4644C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3094630 | ||||||
| chr4:3094644
|
GACGGGGC others(36): Show |
G | 23 | a0003c0128t0026g0053a0007c0007t0003g0023a0007c0007t0003g0024others(20): Show | 23 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.348-4629_348-4587d others(45): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3094644 | ||||||
| chr4:3094649
|
GGCGGGTG others(77): Show |
G | 1 | a0014c0014t0003g0015 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.348-4620_348-4537d others(86): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3094649 | |||||
| chr4:3094654
|
GTGGCCGG others(35): Show |
G | 5 | a0028c0033t0001g0120a0029c0032t0001g0111a0029c0032t0001g0138others(2): Show | 5 | HG01255.hp2 HG03139.hp1 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.348-4583_348-4542d others(44): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3094654 | |||||
| chr4:3094691
|
GGCGGCTG others(35): Show |
G | 11 | a0014c0014t0003g0014a0014c0014t0003g0021a0020c0052t0003g0292others(8): Show | 11 | HG01167.hp1 HG02145.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.348-4575_348-4534d others(44): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3094691 | |||||
| chr4:3094696
|
C | G | 25 | a0003c0128t0026g0053a0007c0007t0003g0023a0007c0007t0003g0024others(22): Show | 25 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.348-4578C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3094696 | ||||||
| chr4:3094733
|
A | G | 2 | a0046c0055t0011g0204a0049c0063t0011g0203 | 2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.348-4541A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3094733 | ||||||
| chr4:3094742
|
C | T | 24 | a0003c0128t0026g0053a0007c0007t0003g0023a0007c0007t0003g0024others(21): Show | 24 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.348-4532C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3094742 | ||||||
| chr4:3094810
|
C | T | 14 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(11): Show | 14 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.348-4464C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3094810 | ||||||
| chr4:3095080
|
C | G | 1 | a0003c0128t0026g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.348-4194C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3095080 | ||||||
| chr4:3095119
|
C | T | 1 | a0074c0095t0002g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.348-4155C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3095119 | ||||||
| chr4:3095198
|
T | C | 68 | a0003c0128t0026g0053a0007c0007t0003g0023a0007c0007t0003g0024others(65): Show | 68 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.348-4076T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3095198 | ||||||
| chr4:3095203
|
C | T | 29 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(26): Show | 29 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.348-4071C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3095203 | ||||||
| chr4:3095350
|
C | A | 2 | a0019c0020t0007g0088a0019c0020t0007g0102 | 2 | HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.348-3924C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3095350 | ||||||
| chr4:3095357
|
T | G | 21 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(18): Show | 21 | HG01070.hp1 HG01081.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.348-3917T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3095357 | ||||||
| chr4:3095439
|
T | C | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.348-3835T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3095439 | ||||||
| chr4:3095457
|
G | C | 1 | a0013c0013t0028g0198 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.348-3817G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3095457 | ||||||
| chr4:3095490
|
T | TGGCTC | 3 | a0019c0020t0007g0088a0019c0020t0007g0102a0068c0087t0031g0101 | 3 | HG01884.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.348-3780_348-3776d others(7): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | INFO_REALIGN_3_PRIME | chr4 | 3095490 | |||||
| chr4:3095588
|
A | G | 2 | a0023c0039t0016g0008a0083c0116t0016g0005 | 2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.348-3686A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3095588 | ||||||
| chr4:3095768
|
G | A | 87 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(84): Show | 87 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.348-3506G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3095768 | ||||||
| chr4:3095801
|
G | C | 1 | a0038c0124t0019g0107 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.348-3473G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3095801 | ||||||
| chr4:3095895
|
A | G | 1 | a0016c0017t0020g0081 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.348-3379A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3095895 | ||||||
| chr4:3095927
|
C | A | 43 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(40): Show | 43 | HG01070.hp1 HG01081.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.348-3347C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3095927 | ||||||
| chr4:3095928
|
G | A | 2 | a0002c0001t0002g0193a0002c0001t0002g0196 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.348-3346G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3095928 | ||||||
| chr4:3095943
|
A | G | 1 | a0004c0011t0001g0161 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.348-3331A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3095943 | ||||||
| chr4:3095955
|
G | C | 1 | a0009c0059t0001g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.348-3319G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3095955 | ||||||
| chr4:3096491
|
A | G | 1 | a0006c0015t0001g0139 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.348-2783A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3096491 | ||||||
| chr4:3096594
|
C | G | 105 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(102): Show | 105 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.348-2680C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3096594 | ||||||
| chr4:3096831
|
C | T | 3 | a0014c0014t0010g0011a0043c0050t0010g0012a0070c0092t0032g0030 | 3 | HG02258.hp1 HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.348-2443C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3096831 | ||||||
| chr4:3096954
|
A | G | 1 | a0066c0083t0001g0119 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.348-2320A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3096954 | ||||||
| chr4:3097067
|
T | C | 1 | a0079c0106t0003g0074 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.348-2207T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3097067 | ||||||
| chr4:3097162
|
G | A | 65 | a0003c0128t0026g0053a0007c0007t0003g0023a0007c0007t0003g0024others(62): Show | 65 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.348-2112G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3097162 | ||||||
| chr4:3097519
|
C | A | 3 | a0014c0014t0010g0011a0043c0050t0010g0012a0070c0092t0032g0030 | 3 | HG02258.hp1 HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.348-1755C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3097519 | ||||||
| chr4:3097540
|
G | A | 1 | a0057c0074t0002g0268 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.348-1734G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3097540 | ||||||
| chr4:3097998
|
A | G | 4 | a0013c0013t0001g0032a0013c0013t0001g0033a0013c0013t0001g0116others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-1276A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3097998 | ||||||
| chr4:3098358
|
A | G | 2 | a0014c0014t0010g0011a0043c0050t0010g0012 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.348-916A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3098358 | ||||||
| chr4:3098395
|
T | G | 2 | a0023c0039t0015g0004a0092c0044t0015g0003 | 2 | HG02055.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.348-879T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3098395 | ||||||
| chr4:3098448
|
C | T | 1 | a0001c0002t0001g0176 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.348-826C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3098448 | ||||||
| chr4:3098449
|
G | T | 4 | a0001c0002t0001g0147a0001c0002t0001g0155a0011c0029t0001g0275others(1): Show | 4 | NA18973.hp2 NA18984.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.348-825G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3098449 | ||||||
| chr4:3098811
|
A | G | 1 | a0026c0026t0003g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.348-463A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 2/66 | chr4 | 3098811 | ||||||
| chr4:3099563
|
G | A | 1 | a0002c0001t0002g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.468+169G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3099563 | ||||||
| chr4:3099583
|
TCTATTGT others(37): Show |
T | 1 | a0002c0001t0002g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.468+192_468+235del others(44): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | INFO_REALIGN_3_PRIME | chr4 | 3099583 | |||||
| chr4:3099584
|
CTA | C | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+192_468+193del others(2): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | INFO_REALIGN_3_PRIME | chr4 | 3099584 | |||||
| chr4:3099607
|
CTG | C | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+215_468+216del others(2): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | INFO_REALIGN_3_PRIME | chr4 | 3099607 | |||||
| chr4:3099609
|
GTTGTATG others(14): Show |
G | 104 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(101): Show | 104 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.468+259_468+279del others(21): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | INFO_REALIGN_3_PRIME | chr4 | 3099609 | |||||
| chr4:3099611
|
T | C | 3 | a0014c0014t0010g0011a0043c0050t0010g0012a0070c0092t0032g0030 | 3 | HG02258.hp1 HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.468+217T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3099611 | ||||||
| chr4:3099630
|
C | CTG | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+237_468+238ins others(2): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | INFO_REALIGN_3_PRIME | chr4 | 3099630 | |||||
| chr4:3099630
|
C | G | 1 | a0002c0001t0002g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.468+236C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3099630 | ||||||
| chr4:3099649
|
C | G | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+255C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3099649 | ||||||
| chr4:3099664
|
G | C | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+270G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3099664 | ||||||
| chr4:3099674
|
G | A | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+280G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3099674 | ||||||
| chr4:3099678
|
T | C | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+284T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3099678 | ||||||
| chr4:3099722
|
C | T | 1 | a0009c0008t0001g0168 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.468+328C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3099722 | ||||||
| chr4:3099871
|
CTTGTATG others(16): Show |
C | 14 | a0002c0001t0002g0263a0014c0014t0003g0014a0014c0014t0003g0015others(11): Show | 14 | HG00609.hp1 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.468+523_468+545del others(23): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | INFO_REALIGN_3_PRIME | chr4 | 3099871 | |||||
| chr4:3099957
|
C | T | 1 | a0021c0021t0012g0231 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.468+563C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3099957 | ||||||
| chr4:3099961
|
A | G | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.468+567A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3099961 | ||||||
| chr4:3100335
|
C | T | 1 | a0065c0078t0004g0185 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.468+941C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3100335 | ||||||
| chr4:3100810
|
C | T | 1 | a0077c0102t0029g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.468+1416C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3100810 | ||||||
| chr4:3100819
|
C | A | 1 | a0001c0002t0001g0176 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.468+1425C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3100819 | ||||||
| chr4:3100882
|
C | T | 1 | a0066c0083t0001g0119 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.468+1488C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3100882 | ||||||
| chr4:3100962
|
C | T | 18 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0095others(15): Show | 18 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.468+1568C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3100962 | ||||||
| chr4:3101175
|
A | G | 1 | a0077c0102t0029g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.468+1781A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3101175 | ||||||
| chr4:3101213
|
T | G | 14 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(11): Show | 14 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.468+1819T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3101213 | ||||||
| chr4:3101255
|
G | A | 13 | a0012c0012t0003g0087a0012c0012t0003g0095a0012c0012t0003g0096others(10): Show | 13 | HG01081.hp2 HG01515.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.468+1861G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3101255 | ||||||
| chr4:3101445
|
C | A | 1 | a0026c0026t0003g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.468+2051C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3101445 | ||||||
| chr4:3101474
|
A | G | 18 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0095others(15): Show | 18 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.468+2080A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3101474 | ||||||
| chr4:3101508
|
C | T | 1 | a0073c0100t0001g0046 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.468+2114C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3101508 | ||||||
| chr4:3101520
|
C | T | 1 | a0062c0082t0005g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.468+2126C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3101520 | ||||||
| chr4:3101719
|
C | T | 10 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(7): Show | 10 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-2105C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3101719 | ||||||
| chr4:3101765
|
A | G | 4 | a0016c0017t0001g0190a0024c0046t0008g0257a0024c0047t0008g0258others(1): Show | 4 | HG00323.hp2 HG00639.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-2059A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3101765 | ||||||
| chr4:3102007
|
G | C | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.469-1817G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3102007 | ||||||
| chr4:3102022
|
T | C | 1 | a0065c0078t0004g0185 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.469-1802T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3102022 | ||||||
| chr4:3102027
|
C | T | 1 | a0009c0008t0001g0167 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.469-1797C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3102027 | ||||||
| chr4:3102071
|
G | T | 1 | a0002c0001t0002g0282 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.469-1753G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3102071 | ||||||
| chr4:3102083
|
G | A | 2 | a0023c0039t0015g0004a0092c0044t0015g0003 | 2 | HG02055.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.469-1741G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3102083 | ||||||
| chr4:3102122
|
A | G | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.469-1702A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3102122 | ||||||
| chr4:3102187
|
G | A | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-1637G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3102187 | ||||||
| chr4:3102239
|
G | A | 1 | a0004c0005t0001g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.469-1585G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3102239 | ||||||
| chr4:3102310
|
G | C | 1 | a0019c0020t0023g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.469-1514G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3102310 | ||||||
| chr4:3102461
|
G | A | 7 | a0002c0001t0002g0216a0002c0001t0002g0217a0002c0001t0002g0263others(4): Show | 7 | HG00609.hp1 HG02523.hp2 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.469-1363G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3102461 | ||||||
| chr4:3102528
|
G | A | 18 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0095others(15): Show | 18 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.469-1296G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3102528 | ||||||
| chr4:3102624
|
C | T | 15 | a0012c0012t0003g0087a0012c0012t0003g0095a0012c0012t0003g0096others(12): Show | 15 | HG01081.hp2 HG01515.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.469-1200C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3102624 | ||||||
| chr4:3102663
|
C | T | 81 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(78): Show | 81 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.469-1161C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3102663 | ||||||
| chr4:3102841
|
A | G | 128 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(125): Show | 128 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.469-983A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3102841 | ||||||
| chr4:3102885
|
C | T | 1 | a0019c0020t0023g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.469-939C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3102885 | ||||||
| chr4:3103029
|
G | A | 8 | a0014c0014t0010g0011a0023c0039t0015g0004a0023c0039t0016g0008others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.469-795G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3103029 | ||||||
| chr4:3103221
|
A | AT | 155 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(152): Show | 157 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.469-583dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | INFO_REALIGN_3_PRIME | chr4 | 3103221 | |||||
| chr4:3103221
|
A | ATT | 32 | a0001c0003t0001g0197a0006c0015t0001g0163a0008c0010t0006g0136others(29): Show | 32 | HG01081.hp2 HG01106.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.469-584_469-583dup others(2): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | INFO_REALIGN_3_PRIME | chr4 | 3103221 | |||||
| chr4:3103473
|
G | A | 105 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(102): Show | 105 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.469-351G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3103473 | ||||||
| chr4:3103722
|
T | C | 1 | a0009c0008t0001g0168 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.469-102T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 3/66 | chr4 | 3103722 | ||||||
| chr4:3103890
|
C | G | 1 | a0033c0097t0001g0061 | 1 | HG02647.hp1 | splice_region_variant&intron_variant | LOW | c.528+7C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 4/66 | chr4 | 3103890 | ||||||
| chr4:3103968
|
T | C | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.528+85T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 4/66 | chr4 | 3103968 | ||||||
| chr4:3104084
|
C | T | 24 | a0003c0128t0026g0053a0007c0007t0003g0023a0007c0007t0003g0024others(21): Show | 24 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.528+201C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 4/66 | chr4 | 3104084 | ||||||
| chr4:3104293
|
C | T | 2 | a0010c0009t0003g0288a0010c0009t0003g0289 | 2 | HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.528+410C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 4/66 | chr4 | 3104293 | ||||||
| chr4:3104346
|
A | G | 1 | a0026c0026t0003g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.528+463A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 4/66 | chr4 | 3104346 | ||||||
| chr4:3104482
|
G | A | 6 | a0009c0008t0001g0105a0009c0008t0001g0157a0009c0008t0001g0167others(3): Show | 6 | HG01074.hp1 HG01928.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.528+599G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 4/66 | chr4 | 3104482 | ||||||
| chr4:3104501
|
C | G | 1 | a0008c0010t0004g0072 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.528+618C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 4/66 | chr4 | 3104501 | ||||||
| chr4:3104682
|
G | T | 1 | a0005c0004t0002g0254 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.529-675G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 4/66 | chr4 | 3104682 | ||||||
| chr4:3104720
|
A | G | 1 | a0076c0101t0002g0266 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.529-637A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 4/66 | chr4 | 3104720 | ||||||
| chr4:3104882
|
C | T | 2 | a0001c0002t0001g0142a0001c0003t0001g0174 | 2 | HG01175.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.529-475C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 4/66 | chr4 | 3104882 | ||||||
| chr4:3105019
|
A | G | 2 | a0002c0031t0002g0226a0002c0031t0002g0253 | 2 | NA18999.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.529-338A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 4/66 | chr4 | 3105019 | ||||||
| chr4:3105245
|
G | A | 1 | a0088c0120t0017g0201 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.529-112G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 4/66 | chr4 | 3105245 | ||||||
| chr4:3105325
|
C | T | 6 | a0023c0039t0015g0004a0023c0039t0016g0008a0070c0092t0032g0030others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.529-32C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 4/66 | chr4 | 3105325 | ||||||
| chr4:3105607
|
C | T | 19 | a0003c0006t0001g0038a0003c0006t0001g0041a0003c0006t0001g0043others(16): Show | 19 | HG00438.hp1 HG00673.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.608+171C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 5/66 | chr4 | 3105607 | ||||||
| chr4:3105719
|
C | T | 1 | a0003c0040t0001g0069 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.608+283C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 5/66 | chr4 | 3105719 | ||||||
| chr4:3105866
|
G | C | 1 | a0010c0009t0003g0276 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.608+430G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 5/66 | chr4 | 3105866 | ||||||
| chr4:3105877
|
G | A | 65 | a0003c0128t0026g0053a0007c0007t0003g0023a0007c0007t0003g0024others(62): Show | 65 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.608+441G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 5/66 | chr4 | 3105877 | ||||||
| chr4:3105937
|
A | G | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.608+501A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 5/66 | chr4 | 3105937 | ||||||
| chr4:3106446
|
A | G | 1 | a0017c0018t0003g0092 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.609-839A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 5/66 | chr4 | 3106446 | ||||||
| chr4:3106466
|
A | G | 1 | a0002c0001t0002g0251 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.609-819A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 5/66 | chr4 | 3106466 | ||||||
| chr4:3106499
|
A | G | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.609-786A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 5/66 | chr4 | 3106499 | ||||||
| chr4:3106560
|
T | G | 1 | a0002c0073t0002g0290 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.609-725T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 5/66 | chr4 | 3106560 | ||||||
| chr4:3106666
|
T | G | 2 | a0023c0103t0003g0029a0080c0110t0003g0031 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.609-619T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 5/66 | chr4 | 3106666 | ||||||
| chr4:3106682
|
GT | G | 6 | a0002c0001t0002g0241a0002c0001t0002g0281a0013c0013t0001g0032others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.609-594delT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 5/66 | INFO_REALIGN_3_PRIME | chr4 | 3106682 | |||||
| chr4:3106757
|
G | A | 5 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0026others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.609-528G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 5/66 | chr4 | 3106757 | ||||||
| chr4:3107157
|
T | C | 1 | a0002c0001t0013g0224 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.609-128T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 5/66 | chr4 | 3107157 | ||||||
| chr4:3107166
|
C | G | 1 | a0037c0121t0001g0189 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.609-119C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 5/66 | chr4 | 3107166 | ||||||
| chr4:3107485
|
T | G | 1 | a0001c0002t0001g0171 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.747+62T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3107485 | ||||||
| chr4:3107541
|
C | T | 6 | a0001c0002t0001g0150a0001c0002t0001g0151a0001c0002t0001g0178others(3): Show | 6 | NA18969.hp2 NA18970.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.747+118C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3107541 | ||||||
| chr4:3107696
|
G | A | 2 | a0023c0039t0016g0008a0083c0116t0016g0005 | 2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.747+273G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3107696 | ||||||
| chr4:3107715
|
A | G | 88 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(85): Show | 88 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.747+292A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3107715 | ||||||
| chr4:3107860
|
T | A | 2 | a0014c0014t0010g0011a0043c0050t0010g0012 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.747+437T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3107860 | ||||||
| chr4:3108143
|
C | T | 24 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0095others(21): Show | 24 | HG01081.hp2 HG01243.hp1 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.747+720C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3108143 | ||||||
| chr4:3108182
|
C | G | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.747+759C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3108182 | ||||||
| chr4:3108230
|
T | C | 2 | a0002c0001t0013g0224a0002c0001t0013g0225 | 2 | HG02040.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.747+807T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3108230 | ||||||
| chr4:3108395
|
C | G | 4 | a0017c0018t0003g0091a0017c0018t0003g0092a0017c0018t0003g0097others(1): Show | 4 | HG01975.hp2 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+972C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3108395 | ||||||
| chr4:3108396
|
T | TAGTA | 4 | a0017c0018t0003g0091a0017c0018t0003g0092a0017c0018t0003g0097others(1): Show | 4 | HG01975.hp2 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+973_747+974ins others(4): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3108396 | ||||||
| chr4:3108397
|
C | T | 4 | a0017c0018t0003g0091a0017c0018t0003g0092a0017c0018t0003g0097others(1): Show | 4 | HG01975.hp2 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+974C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3108397 | ||||||
| chr4:3108398
|
A | G | 4 | a0017c0018t0003g0091a0017c0018t0003g0092a0017c0018t0003g0097others(1): Show | 4 | HG01975.hp2 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+975A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3108398 | ||||||
| chr4:3108460
|
C | T | 4 | a0008c0010t0006g0135a0008c0010t0006g0136a0015c0016t0006g0137others(1): Show | 4 | HG02109.hp2 HG02257.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+1037C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3108460 | ||||||
| chr4:3108499
|
A | G | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.747+1076A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3108499 | ||||||
| chr4:3108651
|
A | G | 6 | a0012c0012t0003g0089a0012c0012t0003g0095a0012c0012t0003g0096others(3): Show | 6 | HG01081.hp2 HG01515.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.747+1228A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3108651 | ||||||
| chr4:3108963
|
G | A | 1 | a0009c0008t0001g0105 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.747+1540G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3108963 | ||||||
| chr4:3108977
|
G | A | 1 | a0024c0046t0008g0257 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.747+1554G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3108977 | ||||||
| chr4:3109055
|
T | TA | 7 | a0014c0014t0010g0011a0020c0052t0003g0292a0023c0039t0016g0008others(4): Show | 7 | HG01243.hp1 HG01943.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.747+1644dupA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | INFO_REALIGN_3_PRIME | chr4 | 3109055 | |||||
| chr4:3109066
|
A | AT | 5 | a0003c0024t0019g0109a0023c0039t0015g0004a0037c0121t0001g0189others(2): Show | 5 | HG00438.hp2 HG01928.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.747+1643_747+1644i others(3): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3109066 | ||||||
| chr4:3109066
|
A | T | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.747+1643A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3109066 | ||||||
| chr4:3109066
|
AAT | A | 97 | a0002c0001t0002g0191a0002c0001t0002g0196a0002c0001t0002g0206others(94): Show | 97 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.747+1658_747+1659d others(4): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | INFO_REALIGN_3_PRIME | chr4 | 3109066 | |||||
| chr4:3109067
|
AT | A | 10 | a0002c0001t0002g0216a0002c0001t0002g0284a0002c0073t0002g0290others(7): Show | 10 | HG00323.hp2 HG00639.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.747+1645delT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3109067 | ||||||
| chr4:3109067
|
ATAT | A | 4 | a0002c0001t0002g0193a0002c0001t0002g0223a0002c0001t0002g0282others(1): Show | 4 | HG01169.hp1 HG03491.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+1645_747+1647d others(5): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3109067 | ||||||
| chr4:3109068
|
T | A | 17 | a0001c0003t0001g0114a0003c0006t0001g0043a0012c0012t0003g0087others(14): Show | 17 | HG00609.hp2 HG01243.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.747+1645T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3109068 | ||||||
| chr4:3109070
|
T | A | 96 | a0002c0001t0002g0191a0002c0001t0002g0196a0002c0001t0002g0208others(93): Show | 96 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.747+1647T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3109070 | ||||||
| chr4:3109072
|
T | A | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.747+1649T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3109072 | ||||||
| chr4:3109210
|
T | C | 1 | a0017c0018t0003g0092 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.747+1787T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3109210 | ||||||
| chr4:3109351
|
T | TA | 146 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(143): Show | 146 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.747+1929dupA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | INFO_REALIGN_3_PRIME | chr4 | 3109351 | |||||
| chr4:3109376
|
T | C | 146 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(143): Show | 146 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.747+1953T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3109376 | ||||||
| chr4:3109505
|
G | A | 22 | a0003c0128t0026g0053a0010c0009t0003g0276a0010c0009t0003g0277others(19): Show | 22 | HG00642.hp1 HG01081.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.747+2082G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3109505 | ||||||
| chr4:3109560
|
A | T | 6 | a0023c0039t0015g0004a0023c0039t0016g0008a0070c0092t0032g0030others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.747+2137A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3109560 | ||||||
| chr4:3109683
|
G | A | 146 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(143): Show | 146 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.747+2260G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3109683 | ||||||
| chr4:3109749
|
G | A | 18 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0095others(15): Show | 18 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.747+2326G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3109749 | ||||||
| chr4:3109855
|
G | A | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.747+2432G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3109855 | ||||||
| chr4:3109928
|
G | T | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.747+2505G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3109928 | ||||||
| chr4:3109964
|
G | C | 2 | a0008c0010t0001g0068a0079c0106t0003g0074 | 2 | HG02071.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.747+2541G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3109964 | ||||||
| chr4:3110107
|
C | T | 1 | a0001c0002t0001g0177 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.747+2684C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3110107 | ||||||
| chr4:3110234
|
A | G | 13 | a0012c0012t0003g0087a0012c0012t0003g0095a0012c0012t0003g0096others(10): Show | 13 | HG01081.hp2 HG01515.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.747+2811A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3110234 | ||||||
| chr4:3110283
|
G | A | 6 | a0023c0039t0015g0004a0023c0039t0016g0008a0070c0092t0032g0030others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.747+2860G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3110283 | ||||||
| chr4:3110382
|
A | C | 107 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(104): Show | 107 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.747+2959A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3110382 | ||||||
| chr4:3110533
|
T | A | 2 | a0002c0030t0002g0213a0002c0030t0002g0218 | 2 | NA18964.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.747+3110T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3110533 | ||||||
| chr4:3110681
|
G | A | 1 | a0003c0105t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.747+3258G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3110681 | ||||||
| chr4:3110928
|
T | C | 1 | a0039c0043t0004g0073 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.747+3505T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3110928 | ||||||
| chr4:3111060
|
C | G | 1 | a0017c0018t0003g0092 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.747+3637C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3111060 | ||||||
| chr4:3111193
|
C | CT | 7 | a0001c0002t0001g0155a0001c0002t0001g0199a0007c0058t0033g0009others(4): Show | 7 | HG00673.hp2 HG02056.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.747+3788dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | INFO_REALIGN_3_PRIME | chr4 | 3111193 | |||||
| chr4:3111193
|
CT | C | 14 | a0002c0001t0002g0246a0003c0128t0026g0053a0005c0004t0002g0242others(11): Show | 14 | HG00642.hp1 HG01258.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.747+3788delT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | INFO_REALIGN_3_PRIME | chr4 | 3111193 | |||||
| chr4:3111210
|
T | C | 2 | a0046c0055t0011g0204a0049c0063t0011g0203 | 2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.747+3787T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3111210 | ||||||
| chr4:3111215
|
A | T | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.747+3792A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3111215 | ||||||
| chr4:3111232
|
C | T | 2 | a0023c0103t0003g0029a0080c0110t0003g0031 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.747+3809C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3111232 | ||||||
| chr4:3111298
|
G | A | 64 | a0003c0128t0026g0053a0007c0007t0003g0023a0007c0007t0003g0024others(61): Show | 64 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.747+3875G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3111298 | ||||||
| chr4:3111354
|
C | T | 3 | a0007c0058t0033g0009a0052c0061t0035g0252a0054c0068t0034g0090 | 3 | HG02145.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.747+3931C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3111354 | ||||||
| chr4:3111417
|
C | T | 1 | a0015c0016t0006g0137 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.748-3887C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3111417 | ||||||
| chr4:3111461
|
C | T | 64 | a0003c0128t0026g0053a0007c0007t0003g0023a0007c0007t0003g0024others(61): Show | 64 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.748-3843C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3111461 | ||||||
| chr4:3111608
|
G | A | 2 | a0002c0031t0002g0226a0002c0031t0002g0253 | 2 | NA18999.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.748-3696G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3111608 | ||||||
| chr4:3111610
|
G | A | 80 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(77): Show | 80 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.748-3694G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3111610 | ||||||
| chr4:3111842
|
A | G | 65 | a0003c0128t0026g0053a0007c0007t0003g0023a0007c0007t0003g0024others(62): Show | 65 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.748-3462A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3111842 | ||||||
| chr4:3111910
|
G | A | 1 | a0002c0001t0024g0238 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.748-3394G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3111910 | ||||||
| chr4:3111921
|
C | G | 66 | a0002c0001t0002g0212a0003c0128t0026g0053a0007c0007t0003g0023others(63): Show | 66 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.748-3383C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3111921 | ||||||
| chr4:3111923
|
A | G | 1 | a0024c0046t0008g0257 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.748-3381A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3111923 | ||||||
| chr4:3111998
|
C | T | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.748-3306C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3111998 | ||||||
| chr4:3112109
|
A | G | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-3195A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3112109 | ||||||
| chr4:3112186
|
G | A | 1 | a0003c0105t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.748-3118G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3112186 | ||||||
| chr4:3112433
|
C | T | 1 | a0015c0016t0006g0137 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.748-2871C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3112433 | ||||||
| chr4:3112491
|
T | C | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-2813T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3112491 | ||||||
| chr4:3112774
|
T | C | 19 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(16): Show | 19 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.748-2530T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3112774 | ||||||
| chr4:3112787
|
G | C | 1 | a0001c0003t0004g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.748-2517G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3112787 | ||||||
| chr4:3112881
|
C | T | 1 | a0016c0017t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.748-2423C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3112881 | ||||||
| chr4:3113091
|
C | G | 1 | a0014c0014t0010g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.748-2213C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3113091 | ||||||
| chr4:3113105
|
G | A | 10 | a0003c0105t0001g0071a0008c0010t0004g0072a0008c0010t0020g0084others(7): Show | 11 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.748-2199G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3113105 | ||||||
| chr4:3113159
|
G | T | 1 | a0002c0001t0002g0206 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.748-2145G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3113159 | ||||||
| chr4:3113287
|
A | T | 1 | a0052c0061t0035g0252 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.748-2017A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3113287 | ||||||
| chr4:3113331
|
A | AT | 8 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(5): Show | 8 | HG01243.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.748-1961dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | INFO_REALIGN_3_PRIME | chr4 | 3113331 | |||||
| chr4:3113487
|
G | C | 1 | a0014c0014t0010g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.748-1817G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3113487 | ||||||
| chr4:3113667
|
G | C | 1 | a0039c0043t0001g0078 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.748-1637G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3113667 | ||||||
| chr4:3113719
|
A | G | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.748-1585A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3113719 | ||||||
| chr4:3113767
|
G | C | 1 | a0069c0093t0003g0020 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.748-1537G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3113767 | ||||||
| chr4:3113850
|
C | T | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.748-1454C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3113850 | ||||||
| chr4:3114079
|
A | G | 5 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-1225A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3114079 | ||||||
| chr4:3114106
|
C | T | 2 | a0084c0115t0017g0202a0088c0120t0017g0201 | 2 | HG00738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.748-1198C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3114106 | ||||||
| chr4:3114141
|
G | A | 1 | a0003c0006t0001g0041 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.748-1163G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3114141 | ||||||
| chr4:3114148
|
T | C | 2 | a0002c0001t0002g0245a0002c0001t0002g0247 | 2 | HG00323.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.748-1156T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3114148 | ||||||
| chr4:3114374
|
A | G | 1 | a0026c0026t0003g0017 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.748-930A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3114374 | ||||||
| chr4:3114556
|
C | T | 15 | a0012c0012t0003g0087a0012c0012t0003g0089a0012c0012t0003g0095others(12): Show | 15 | HG01081.hp2 HG01515.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.748-748C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3114556 | ||||||
| chr4:3114832
|
C | T | 2 | a0024c0046t0008g0257a0042c0048t0008g0259 | 2 | HG00323.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.748-472C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3114832 | ||||||
| chr4:3114989
|
A | AT | 6 | a0023c0039t0015g0004a0023c0039t0016g0008a0070c0092t0032g0030others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-306dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | INFO_REALIGN_3_PRIME | chr4 | 3114989 | |||||
| chr4:3115061
|
G | C | 8 | a0012c0012t0003g0087a0017c0018t0003g0091a0017c0018t0003g0092others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.748-243G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3115061 | ||||||
| chr4:3115120
|
A | G | 22 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(19): Show | 22 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.748-184A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3115120 | ||||||
| chr4:3115271
|
A | G | 11 | a0002c0001t0002g0208a0002c0001t0002g0246a0002c0001t0002g0249others(8): Show | 11 | HG01952.hp1 HG02148.hp2 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.748-33A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 6/66 | chr4 | 3115271 | ||||||
| chr4:3115561
|
G | C | 1 | a0010c0009t0003g0276 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.889+116G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 7/66 | chr4 | 3115561 | ||||||
| chr4:3115597
|
C | T | 1 | a0001c0003t0001g0129 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.889+152C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 7/66 | chr4 | 3115597 | ||||||
| chr4:3115750
|
C | T | 3 | a0019c0020t0007g0088a0019c0020t0007g0102a0068c0087t0031g0101 | 3 | HG01884.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.889+305C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 7/66 | chr4 | 3115750 | ||||||
| chr4:3115852
|
T | C | 147 | a0001c0003t0001g0156a0002c0001t0002g0191a0002c0001t0002g0193others(144): Show | 147 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.890-233T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 7/66 | chr4 | 3115852 | ||||||
| chr4:3116332
|
G | T | 1 | a0012c0077t0003g0094 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1068+69G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3116332 | ||||||
| chr4:3116389
|
T | G | 145 | a0001c0003t0001g0156a0002c0001t0002g0191a0002c0001t0002g0193others(142): Show | 145 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1068+126T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3116389 | ||||||
| chr4:3116420
|
C | T | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1068+157C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3116420 | ||||||
| chr4:3116466
|
C | T | 1 | a0002c0001t0002g0255 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1068+203C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3116466 | ||||||
| chr4:3116614
|
C | T | 1 | a0019c0020t0023g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1068+351C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3116614 | ||||||
| chr4:3116706
|
G | A | 38 | a0001c0089t0001g0037a0003c0006t0001g0038a0003c0006t0001g0041others(35): Show | 39 | HG00438.hp1 HG00673.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1068+443G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3116706 | ||||||
| chr4:3116720
|
C | T | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.1068+457C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3116720 | ||||||
| chr4:3116901
|
T | C | 1 | a0002c0001t0002g0216 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1068+638T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3116901 | ||||||
| chr4:3116966
|
G | C | 1 | a0017c0018t0003g0092 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1068+703G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3116966 | ||||||
| chr4:3117249
|
C | T | 1 | a0010c0009t0003g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1068+986C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3117249 | ||||||
| chr4:3117758
|
G | C | 6 | a0009c0008t0001g0105a0009c0008t0001g0157a0009c0008t0001g0167others(3): Show | 6 | HG01074.hp1 HG01928.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1068+1495G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3117758 | ||||||
| chr4:3117847
|
G | C | 43 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(40): Show | 43 | HG01070.hp1 HG01081.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.1068+1584G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3117847 | ||||||
| chr4:3118007
|
A | T | 1 | a0012c0012t0003g0089 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1068+1744A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3118007 | ||||||
| chr4:3118103
|
G | A | 1 | a0049c0063t0011g0203 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1068+1840G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3118103 | ||||||
| chr4:3118194
|
G | A | 2 | a0017c0018t0003g0097a0048c0057t0003g0098 | 2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1068+1931G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3118194 | ||||||
| chr4:3118279
|
C | G | 1 | a0001c0003t0001g0174 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1068+2016C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3118279 | ||||||
| chr4:3118500
|
A | G | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.1068+2237A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3118500 | ||||||
| chr4:3118513
|
T | C | 6 | a0023c0039t0015g0004a0023c0039t0016g0008a0070c0092t0032g0030others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1068+2250T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3118513 | ||||||
| chr4:3118555
|
C | A | 1 | a0001c0003t0001g0174 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1068+2292C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3118555 | ||||||
| chr4:3118630
|
G | A | 6 | a0009c0008t0001g0105a0009c0008t0001g0157a0009c0008t0001g0167others(3): Show | 6 | HG01074.hp1 HG01928.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1068+2367G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3118630 | ||||||
| chr4:3118666
|
C | T | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1068+2403C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3118666 | ||||||
| chr4:3118710
|
G | A | 1 | a0015c0016t0009g0082 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1068+2447G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3118710 | ||||||
| chr4:3118725
|
G | A | 6 | a0023c0039t0015g0004a0023c0039t0016g0008a0070c0092t0032g0030others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1068+2462G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3118725 | ||||||
| chr4:3118776
|
T | C | 1 | a0006c0037t0021g0146 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1069-2452T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3118776 | ||||||
| chr4:3119014
|
A | G | 1 | a0005c0090t0002g0215 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1069-2214A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3119014 | ||||||
| chr4:3119261
|
G | A | 1 | a0033c0097t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1069-1967G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3119261 | ||||||
| chr4:3119417
|
A | G | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.1069-1811A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3119417 | ||||||
| chr4:3119623
|
G | A | 1 | a0003c0041t0001g0143 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1069-1605G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3119623 | ||||||
| chr4:3119744
|
G | A | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1069-1484G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3119744 | ||||||
| chr4:3119788
|
G | A | 2 | a0002c0001t0002g0191a0034c0038t0002g0192 | 2 | HG01433.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1069-1440G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3119788 | ||||||
| chr4:3119889
|
A | G | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1069-1339A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3119889 | ||||||
| chr4:3119911
|
G | A | 1 | a0026c0026t0003g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1069-1317G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3119911 | ||||||
| chr4:3120168
|
T | C | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1069-1060T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3120168 | ||||||
| chr4:3120177
|
T | TA | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1069-1048dupA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | INFO_REALIGN_3_PRIME | chr4 | 3120177 | |||||
| chr4:3120265
|
A | G | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.1069-963A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3120265 | ||||||
| chr4:3120342
|
C | T | 2 | a0004c0067t0001g0118a0058c0071t0001g0270 | 2 | HG00735.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1069-886C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3120342 | ||||||
| chr4:3120560
|
C | T | 1 | a0010c0009t0003g0291 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1069-668C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3120560 | ||||||
| chr4:3120567
|
C | T | 6 | a0028c0033t0001g0120a0028c0033t0001g0132a0029c0032t0001g0111others(3): Show | 6 | NA19002.hp2 NA19005.hp1 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.1069-661C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3120567 | ||||||
| chr4:3120644
|
G | A | 1 | a0066c0083t0001g0119 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1069-584G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3120644 | ||||||
| chr4:3120657
|
G | A | 1 | a0061c0076t0003g0099 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1069-571G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3120657 | ||||||
| chr4:3120659
|
T | C | 5 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(2): Show | 5 | HG01070.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1069-569T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3120659 | ||||||
| chr4:3120780
|
T | G | 147 | a0001c0003t0001g0156a0002c0001t0002g0191a0002c0001t0002g0193others(144): Show | 147 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.1069-448T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 8/66 | chr4 | 3120780 | ||||||
| chr4:3121694
|
C | CA | 11 | a0001c0002t0001g0171a0001c0002t0001g0173a0001c0002t0001g0199others(8): Show | 11 | HG01167.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1273+284dupA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 9/66 | INFO_REALIGN_3_PRIME | chr4 | 3121694 | |||||
| chr4:3121839
|
G | A | 1 | a0054c0068t0034g0090 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1273+407G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 9/66 | chr4 | 3121839 | ||||||
| chr4:3121953
|
C | A | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273+521C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 9/66 | chr4 | 3121953 | ||||||
| chr4:3122133
|
G | A | 15 | a0012c0012t0003g0087a0012c0012t0003g0089a0012c0012t0003g0095others(12): Show | 15 | HG01081.hp2 HG01515.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1273+701G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 9/66 | chr4 | 3122133 | ||||||
| chr4:3122287
|
T | C | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1274-602T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 9/66 | chr4 | 3122287 | ||||||
| chr4:3122368
|
G | C | 20 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(17): Show | 20 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1274-521G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 9/66 | chr4 | 3122368 | ||||||
| chr4:3122388
|
T | C | 1 | a0008c0010t0004g0072 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1274-501T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 9/66 | chr4 | 3122388 | ||||||
| chr4:3122538
|
C | T | 1 | a0001c0003t0001g0114 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1274-351C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 9/66 | chr4 | 3122538 | ||||||
| chr4:3122848
|
A | G | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1274-41A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 9/66 | chr4 | 3122848 | ||||||
| chr4:3123069
|
A | G | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1321+133A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 10/66 | chr4 | 3123069 | ||||||
| chr4:3123323
|
A | G | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.1321+387A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 10/66 | chr4 | 3123323 | ||||||
| chr4:3123451
|
TAGTC | T | 4 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(1): Show | 4 | HG01168.hp1 HG01169.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1321+518_1321+521d others(6): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 10/66 | INFO_REALIGN_3_PRIME | chr4 | 3123451 | |||||
| chr4:3123507
|
C | T | 3 | a0010c0009t0003g0291a0020c0079t0003g0186a0050c0065t0003g0286 | 3 | HG00642.hp1 HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1321+571C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 10/66 | chr4 | 3123507 | ||||||
| chr4:3123516
|
C | CCAAAA | 3 | a0018c0019t0001g0233a0018c0019t0001g0234a0018c0019t0001g0235 | 3 | HG01070.hp2 HG01071.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1321+596_1321+600d others(7): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 10/66 | INFO_REALIGN_3_PRIME | chr4 | 3123516 | |||||
| chr4:3123583
|
A | C | 1 | a0008c0010t0001g0068 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1321+647A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 10/66 | chr4 | 3123583 | ||||||
| chr4:3123681
|
C | T | 4 | a0019c0020t0007g0088a0019c0020t0007g0102a0019c0020t0023g0100others(1): Show | 4 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1321+745C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 10/66 | chr4 | 3123681 | ||||||
| chr4:3123950
|
G | A | 1 | a0009c0008t0001g0179 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1321+1014G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 10/66 | chr4 | 3123950 | ||||||
| chr4:3123953
|
A | G | 1 | a0043c0050t0010g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1321+1017A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 10/66 | chr4 | 3123953 | ||||||
| chr4:3124211
|
C | T | 1 | a0003c0128t0026g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1321+1275C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 10/66 | chr4 | 3124211 | ||||||
| chr4:3124318
|
C | T | 2 | a0014c0014t0010g0011a0043c0050t0010g0012 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1322-1231C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 10/66 | chr4 | 3124318 | ||||||
| chr4:3124468
|
T | A | 1 | a0010c0009t0003g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1322-1081T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 10/66 | chr4 | 3124468 | ||||||
| chr4:3124675
|
A | G | 15 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(12): Show | 15 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1322-874A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 10/66 | chr4 | 3124675 | ||||||
| chr4:3124748
|
A | G | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1322-801A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 10/66 | chr4 | 3124748 | ||||||
| chr4:3125086
|
T | C | 146 | a0001c0003t0001g0156a0002c0001t0002g0191a0002c0001t0002g0193others(143): Show | 146 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1322-463T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 10/66 | chr4 | 3125086 | ||||||
| chr4:3125150
|
G | T | 1 | a0004c0005t0001g0050 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1322-399G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 10/66 | chr4 | 3125150 | ||||||
| chr4:3125403
|
G | C | 1 | a0006c0037t0021g0146 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1322-146G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 10/66 | chr4 | 3125403 | ||||||
| chr4:3126161
|
T | A | 2 | a0046c0055t0011g0204a0049c0063t0011g0203 | 2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1402+532T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 11/66 | chr4 | 3126161 | ||||||
| chr4:3126389
|
A | G | 2 | a0011c0028t0001g0236a0011c0028t0001g0240 | 2 | NA18939.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1402+760A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 11/66 | chr4 | 3126389 | ||||||
| chr4:3126442
|
G | T | 1 | a0007c0058t0033g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1402+813G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 11/66 | chr4 | 3126442 | ||||||
| chr4:3126570
|
AT | A | 21 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(18): Show | 21 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1403-685delT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 11/66 | INFO_REALIGN_3_PRIME | chr4 | 3126570 | |||||
| chr4:3126830
|
A | G | 15 | a0012c0012t0003g0087a0012c0012t0003g0089a0012c0012t0003g0095others(12): Show | 15 | HG01081.hp2 HG01515.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1403-434A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 11/66 | chr4 | 3126830 | ||||||
| chr4:3126920
|
C | T | 4 | a0001c0003t0001g0077a0035c0042t0005g0076a0035c0042t0005g0085others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1403-344C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 11/66 | chr4 | 3126920 | ||||||
| chr4:3126991
|
G | A | 2 | a0010c0009t0003g0291a0050c0065t0003g0286 | 2 | HG00642.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1403-273G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 11/66 | chr4 | 3126991 | ||||||
| chr4:3127219
|
T | C | 15 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(12): Show | 15 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1403-45T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 11/66 | chr4 | 3127219 | ||||||
| chr4:3127639
|
T | A | 1 | a0010c0056t0007g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1743+35T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 12/66 | chr4 | 3127639 | ||||||
| chr4:3127686
|
G | A | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1743+82G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 12/66 | chr4 | 3127686 | ||||||
| chr4:3127752
|
T | A | 1 | a0034c0038t0002g0285 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1743+148T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 12/66 | chr4 | 3127752 | ||||||
| chr4:3127825
|
G | A | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1743+221G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 12/66 | chr4 | 3127825 | ||||||
| chr4:3127969
|
A | C | 15 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(12): Show | 15 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1743+365A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 12/66 | chr4 | 3127969 | ||||||
| chr4:3127979
|
A | G | 1 | a0039c0043t0004g0073 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1743+375A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 12/66 | chr4 | 3127979 | ||||||
| chr4:3128032
|
G | A | 1 | a0006c0022t0001g0036 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1743+428G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 12/66 | chr4 | 3128032 | ||||||
| chr4:3128085
|
A | C | 1 | a0001c0003t0001g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1743+481A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 12/66 | chr4 | 3128085 | ||||||
| chr4:3128228
|
C | T | 1 | a0012c0077t0003g0094 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1743+624C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 12/66 | chr4 | 3128228 | ||||||
| chr4:3128378
|
G | A | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1743+774G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 12/66 | chr4 | 3128378 | ||||||
| chr4:3128960
|
C | T | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1744-964C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 12/66 | chr4 | 3128960 | ||||||
| chr4:3129089
|
C | T | 1 | a0002c0001t0002g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1744-835C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 12/66 | chr4 | 3129089 | ||||||
| chr4:3129117
|
A | G | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1744-807A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 12/66 | chr4 | 3129117 | ||||||
| chr4:3129122
|
A | G | 21 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(18): Show | 21 | HG01070.hp1 HG01081.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.1744-802A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 12/66 | chr4 | 3129122 | ||||||
| chr4:3129553
|
C | A | 1 | a0008c0113t0001g0040 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1744-371C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 12/66 | chr4 | 3129553 | ||||||
| chr4:3129846
|
A | G | 21 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(18): Show | 21 | HG01070.hp1 HG01081.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.1744-78A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 12/66 | chr4 | 3129846 | ||||||
| chr4:3129908
|
C | G | 3 | a0001c0002t0001g0181a0003c0041t0001g0143a0003c0041t0001g0144 | 3 | NA18961.hp1 NA18999.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1744-16C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 12/66 | chr4 | 3129908 | ||||||
| chr4:3130071
|
C | G | 1 | a0024c0046t0008g0257 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1867+24C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 13/66 | chr4 | 3130071 | ||||||
| chr4:3130086
|
T | C | 3 | a0019c0020t0007g0088a0019c0020t0007g0102a0068c0087t0031g0101 | 3 | HG01884.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1867+39T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 13/66 | chr4 | 3130086 | ||||||
| chr4:3130521
|
T | A | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1986+98T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 14/66 | chr4 | 3130521 | ||||||
| chr4:3130546
|
T | C | 1 | a0017c0018t0003g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1986+123T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 14/66 | chr4 | 3130546 | ||||||
| chr4:3130562
|
G | A | 1 | a0056c0070t0001g0280 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1986+139G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 14/66 | chr4 | 3130562 | ||||||
| chr4:3130597
|
A | G | 9 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(6): Show | 9 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1986+174A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 14/66 | chr4 | 3130597 | ||||||
| chr4:3130709
|
G | A | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1986+286G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 14/66 | chr4 | 3130709 | ||||||
| chr4:3130830
|
A | G | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1986+407A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 14/66 | chr4 | 3130830 | ||||||
| chr4:3130986
|
T | C | 25 | a0008c0010t0006g0135a0008c0010t0006g0136a0010c0056t0007g0200others(22): Show | 25 | HG01070.hp1 HG01081.hp2 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.1987-300T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 14/66 | chr4 | 3130986 | ||||||
| chr4:3131006
|
G | A | 8 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(5): Show | 8 | HG00738.hp1 HG01109.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1987-280G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 14/66 | chr4 | 3131006 | ||||||
| chr4:3131124
|
A | G | 25 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(22): Show | 25 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1987-162A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 14/66 | chr4 | 3131124 | ||||||
| chr4:3131151
|
A | G | 24 | a0002c0001t0002g0220a0002c0001t0002g0262a0005c0004t0002g0219others(21): Show | 24 | HG01081.hp2 HG01256.hp1 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1987-135A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 14/66 | chr4 | 3131151 | ||||||
| chr4:3131187
|
C | A | 1 | a0019c0020t0007g0102 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1987-99C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 14/66 | chr4 | 3131187 | ||||||
| chr4:3131193
|
T | G | 26 | a0002c0001t0002g0220a0002c0001t0002g0262a0005c0004t0002g0219others(23): Show | 26 | HG01081.hp2 HG01256.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.1987-93T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 14/66 | chr4 | 3131193 | ||||||
| chr4:3131448
|
A | T | 1 | a0007c0007t0003g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2098+51A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 15/66 | chr4 | 3131448 | ||||||
| chr4:3131808
|
A | T | 1 | a0002c0001t0002g0262 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2236+33A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 16/66 | chr4 | 3131808 | ||||||
| chr4:3131835
|
C | A | 1 | a0088c0120t0017g0201 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2236+60C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 16/66 | chr4 | 3131835 | ||||||
| chr4:3131867
|
G | A | 13 | a0014c0014t0003g0014a0014c0014t0003g0015a0022c0023t0003g0013others(10): Show | 13 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.2236+92G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 16/66 | chr4 | 3131867 | ||||||
| chr4:3132058
|
G | A | 15 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(12): Show | 15 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.2236+283G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 16/66 | chr4 | 3132058 | ||||||
| chr4:3132184
|
C | T | 9 | a0008c0010t0004g0072a0008c0010t0020g0084a0008c0111t0004g0080others(6): Show | 10 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.2237-378C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 16/66 | chr4 | 3132184 | ||||||
| chr4:3132240
|
G | A | 1 | a0052c0061t0035g0252 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2237-322G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 16/66 | chr4 | 3132240 | ||||||
| chr4:3132298
|
C | T | 2 | a0003c0006t0001g0043a0006c0022t0001g0034 | 2 | HG02040.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.2237-264C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 16/66 | chr4 | 3132298 | ||||||
| chr4:3132307
|
T | C | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2237-255T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 16/66 | chr4 | 3132307 | ||||||
| chr4:3132378
|
C | A | 3 | a0001c0002t0001g0181a0003c0041t0001g0143a0003c0041t0001g0144 | 3 | NA18961.hp1 NA18999.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2237-184C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 16/66 | chr4 | 3132378 | ||||||
| chr4:3132552
|
A | G | 1 | a0001c0003t0004g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2237-10A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 16/66 | chr4 | 3132552 | ||||||
| chr4:3132744
|
G | A | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.2395+24G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 17/66 | chr4 | 3132744 | ||||||
| chr4:3132972
|
A | G | 1 | a0002c0001t0002g0251 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2493+61A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 18/66 | chr4 | 3132972 | ||||||
| chr4:3132999
|
T | C | 21 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(18): Show | 21 | HG01070.hp1 HG01081.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.2493+88T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 18/66 | chr4 | 3132999 | ||||||
| chr4:3133109
|
G | A | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2493+198G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 18/66 | chr4 | 3133109 | ||||||
| chr4:3133324
|
T | TA | 6 | a0011c0029t0001g0273a0023c0039t0015g0004a0023c0039t0016g0008others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2493+432dupA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 18/66 | INFO_REALIGN_3_PRIME | chr4 | 3133324 | |||||
| chr4:3133324
|
TA | T | 13 | a0001c0002t0001g0147a0001c0002t0001g0175a0001c0002t0001g0178others(10): Show | 13 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2493+432delA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 18/66 | INFO_REALIGN_3_PRIME | chr4 | 3133324 | |||||
| chr4:3133418
|
C | T | 21 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(18): Show | 21 | HG01070.hp1 HG01081.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.2493+507C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 18/66 | chr4 | 3133418 | ||||||
| chr4:3133467
|
G | A | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2493+556G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 18/66 | chr4 | 3133467 | ||||||
| chr4:3133468
|
C | A | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2493+557C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 18/66 | chr4 | 3133468 | ||||||
| chr4:3133524
|
TA | T | 44 | a0001c0002t0001g0147a0003c0006t0001g0043a0004c0005t0001g0055others(41): Show | 44 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.2493+632delA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 18/66 | INFO_REALIGN_3_PRIME | chr4 | 3133524 | |||||
| chr4:3133524
|
TAAAA | T | 71 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(68): Show | 71 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2493+629_2493+632d others(6): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 18/66 | INFO_REALIGN_3_PRIME | chr4 | 3133524 | |||||
| chr4:3133882
|
G | A | 1 | a0028c0033t0001g0120 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2494-519G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 18/66 | chr4 | 3133882 | ||||||
| chr4:3134226
|
T | G | 77 | a0001c0003t0001g0156a0002c0001t0002g0191a0002c0001t0002g0193others(74): Show | 77 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.2494-175T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 18/66 | chr4 | 3134226 | ||||||
| chr4:3134262
|
T | C | 2 | a0040c0045t0002g0103a0061c0076t0003g0099 | 2 | HG01070.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.2494-139T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 18/66 | chr4 | 3134262 | ||||||
| chr4:3134390
|
T | A | 1 | a0028c0033t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2494-11T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 18/66 | chr4 | 3134390 | ||||||
| chr4:3134726
|
A | G | 1 | a0088c0120t0017g0201 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2633+186A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 19/66 | chr4 | 3134726 | ||||||
| chr4:3134891
|
G | C | 2 | a0036c0107t0018g0065a0036c0108t0018g0066 | 2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2633+351G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 19/66 | chr4 | 3134891 | ||||||
| chr4:3134925
|
G | T | 2 | a0001c0002t0001g0175a0006c0015t0001g0158 | 2 | HG03239.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2633+385G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 19/66 | chr4 | 3134925 | ||||||
| chr4:3134968
|
C | CA | 143 | a0001c0003t0001g0156a0002c0001t0002g0191a0002c0001t0002g0193others(140): Show | 143 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.2633+429dupA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 19/66 | INFO_REALIGN_3_PRIME | chr4 | 3134968 | |||||
| chr4:3135249
|
G | A | 2 | a0014c0014t0010g0011a0043c0050t0010g0012 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2634-655G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 19/66 | chr4 | 3135249 | ||||||
| chr4:3135322
|
CA | C | 22 | a0002c0001t0002g0249a0002c0001t0002g0250a0010c0056t0007g0200others(19): Show | 22 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.2634-569delA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 19/66 | INFO_REALIGN_3_PRIME | chr4 | 3135322 | |||||
| chr4:3135445
|
TG | T | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2634-458delG | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 19/66 | chr4 | 3135445 | ||||||
| chr4:3135446
|
G | T | 2 | a0046c0055t0011g0204a0049c0063t0011g0203 | 2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2634-458G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 19/66 | chr4 | 3135446 | ||||||
| chr4:3135446
|
GT | G | 41 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(38): Show | 41 | HG00642.hp1 HG00738.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.2634-446delT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 19/66 | INFO_REALIGN_3_PRIME | chr4 | 3135446 | |||||
| chr4:3135569
|
A | G | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2634-335A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 19/66 | chr4 | 3135569 | ||||||
| chr4:3135588
|
G | T | 2 | a0019c0020t0007g0088a0019c0020t0007g0102 | 2 | HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2634-316G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 19/66 | chr4 | 3135588 | ||||||
| chr4:3135846
|
C | T | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2634-58C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 19/66 | chr4 | 3135846 | ||||||
| chr4:3136166
|
T | G | 1 | a0004c0005t0001g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2698-60T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 20/66 | chr4 | 3136166 | ||||||
| chr4:3136473
|
G | GA | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.2798+156dupA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | INFO_REALIGN_3_PRIME | chr4 | 3136473 | |||||
| chr4:3136473
|
G | GAAA | 16 | a0012c0012t0003g0087a0012c0012t0003g0089a0012c0012t0003g0095others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.2798+154_2798+156d others(5): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | INFO_REALIGN_3_PRIME | chr4 | 3136473 | |||||
| chr4:3136487
|
A | G | 1 | a0007c0058t0033g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2798+161A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3136487 | ||||||
| chr4:3136518
|
C | T | 2 | a0024c0046t0008g0257a0042c0048t0008g0259 | 2 | HG00323.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.2798+192C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3136518 | ||||||
| chr4:3136597
|
G | GA | 96 | a0001c0003t0001g0156a0002c0001t0002g0191a0002c0001t0002g0193others(93): Show | 96 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.2798+281dupA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | INFO_REALIGN_3_PRIME | chr4 | 3136597 | |||||
| chr4:3136668
|
A | G | 16 | a0012c0012t0003g0087a0012c0012t0003g0089a0012c0012t0003g0095others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.2798+342A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3136668 | ||||||
| chr4:3136793
|
G | A | 46 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(43): Show | 46 | HG00323.hp2 HG00639.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.2798+467G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3136793 | ||||||
| chr4:3136796
|
A | G | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2798+470A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3136796 | ||||||
| chr4:3136917
|
A | AT | 22 | a0001c0002t0001g0149a0010c0056t0007g0200a0012c0012t0003g0087others(19): Show | 22 | HG01070.hp1 HG01081.hp2 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.2798+602dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | INFO_REALIGN_3_PRIME | chr4 | 3136917 | |||||
| chr4:3137011
|
G | A | 1 | a0005c0004t0002g0242 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2798+685G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3137011 | ||||||
| chr4:3137186
|
G | A | 2 | a0014c0014t0010g0011a0043c0050t0010g0012 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2798+860G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3137186 | ||||||
| chr4:3137281
|
T | C | 22 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(19): Show | 22 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2798+955T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3137281 | ||||||
| chr4:3137387
|
A | G | 21 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(18): Show | 21 | HG01070.hp1 HG01081.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.2798+1061A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3137387 | ||||||
| chr4:3137425
|
C | T | 74 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(71): Show | 74 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.2798+1099C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3137425 | ||||||
| chr4:3137476
|
A | T | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2798+1150A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3137476 | ||||||
| chr4:3137555
|
C | T | 1 | a0004c0011t0001g0161 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2798+1229C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3137555 | ||||||
| chr4:3137571
|
C | T | 2 | a0011c0028t0001g0236a0011c0028t0001g0240 | 2 | NA18939.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2798+1245C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3137571 | ||||||
| chr4:3137690
|
C | T | 1 | a0002c0001t0002g0217 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2798+1364C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3137690 | ||||||
| chr4:3138065
|
G | GTTCC | 46 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0147others(43): Show | 46 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.2798+1771_2798+177 others(8): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | INFO_REALIGN_3_PRIME | chr4 | 3138065 | |||||
| chr4:3138065
|
G | GTTCCTTC others(1): Show |
5 | a0001c0002t0001g0169a0001c0002t0001g0171a0001c0002t0001g0172others(2): Show | 5 | NA18954.hp1 NA18956.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.2798+1767_2798+177 others(12): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | INFO_REALIGN_3_PRIME | chr4 | 3138065 | |||||
| chr4:3138065
|
G | GTTCCTTC others(5): Show |
1 | a0006c0037t0021g0146 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2798+1763_2798+177 others(16): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | INFO_REALIGN_3_PRIME | chr4 | 3138065 | |||||
| chr4:3138065
|
GTTCC | G | 128 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(125): Show | 128 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(125): Show |
intron_variant | MODIFIER | c.2798+1771_2798+177 others(8): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | INFO_REALIGN_3_PRIME | chr4 | 3138065 | |||||
| chr4:3138065
|
GTTCCTTC others(1): Show |
G | 4 | a0001c0002t0001g0175a0014c0014t0010g0011a0043c0050t0010g0012others(1): Show | 4 | HG02559.hp1 HG02630.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2798+1767_2798+177 others(12): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | INFO_REALIGN_3_PRIME | chr4 | 3138065 | |||||
| chr4:3138093
|
C | CTTCT | 5 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2798+1770_2798+177 others(8): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | INFO_REALIGN_3_PRIME | chr4 | 3138093 | |||||
| chr4:3138101
|
T | C | 5 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2798+1775T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3138101 | ||||||
| chr4:3138102
|
T | C | 1 | a0001c0002t0001g0151 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2798+1776T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3138102 | ||||||
| chr4:3138103
|
T | C | 5 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2798+1777T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3138103 | ||||||
| chr4:3138164
|
TTTCCCTT others(10): Show |
T | 22 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(19): Show | 22 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2798+1839_2798+185 others(21): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3138164 | ||||||
| chr4:3138180
|
CGCCT | C | 25 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(22): Show | 25 | HG00323.hp2 HG00639.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.2798+1871_2798+187 others(8): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | INFO_REALIGN_3_PRIME | chr4 | 3138180 | |||||
| chr4:3138184
|
T | C | 22 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(19): Show | 22 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2798+1858T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3138184 | ||||||
| chr4:3138189
|
G | T | 21 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(18): Show | 21 | HG01070.hp1 HG01081.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.2798+1863G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3138189 | ||||||
| chr4:3138193
|
G | T | 21 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(18): Show | 21 | HG01070.hp1 HG01081.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.2798+1867G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3138193 | ||||||
| chr4:3138239
|
A | AT | 44 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(41): Show | 44 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.2798+1920dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | INFO_REALIGN_3_PRIME | chr4 | 3138239 | |||||
| chr4:3138246
|
T | A | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2798+1920T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3138246 | ||||||
| chr4:3138246
|
T | TA | 3 | a0007c0058t0033g0009a0052c0061t0035g0252a0054c0068t0034g0090 | 3 | HG02145.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2798+1923dupA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | INFO_REALIGN_3_PRIME | chr4 | 3138246 | |||||
| chr4:3138347
|
A | C | 1 | a0012c0077t0003g0094 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2798+2021A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3138347 | ||||||
| chr4:3138575
|
T | C | 1 | a0007c0007t0003g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2799-1935T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3138575 | ||||||
| chr4:3138682
|
C | T | 4 | a0002c0001t0002g0244a0002c0001t0002g0245a0002c0001t0002g0247others(1): Show | 4 | HG00323.hp1 HG00741.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.2799-1828C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3138682 | ||||||
| chr4:3138772
|
C | T | 3 | a0002c0001t0002g0241a0002c0001t0002g0281a0051c0062t0002g0243 | 3 | HG02165.hp1 NA18950.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.2799-1738C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3138772 | ||||||
| chr4:3139037
|
G | A | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.2799-1473G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3139037 | ||||||
| chr4:3139232
|
C | G | 16 | a0012c0012t0003g0087a0012c0012t0003g0089a0012c0012t0003g0095others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.2799-1278C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3139232 | ||||||
| chr4:3139312
|
C | T | 2 | a0023c0039t0015g0004a0092c0044t0015g0003 | 2 | HG02055.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2799-1198C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3139312 | ||||||
| chr4:3139403
|
G | A | 75 | a0001c0003t0001g0156a0002c0001t0002g0191a0002c0001t0002g0193others(72): Show | 75 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.2799-1107G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3139403 | ||||||
| chr4:3139411
|
T | A | 1 | a0014c0014t0003g0021 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2799-1099T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3139411 | ||||||
| chr4:3139683
|
C | T | 73 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(70): Show | 73 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.2799-827C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3139683 | ||||||
| chr4:3139761
|
G | A | 139 | a0001c0003t0001g0156a0002c0001t0002g0191a0002c0001t0002g0193others(136): Show | 139 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.2799-749G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3139761 | ||||||
| chr4:3139857
|
T | TTGTTGA | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2799-651_2799-646d others(8): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | INFO_REALIGN_3_PRIME | chr4 | 3139857 | |||||
| chr4:3139924
|
A | G | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2799-586A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3139924 | ||||||
| chr4:3140123
|
C | T | 2 | a0046c0055t0011g0204a0049c0063t0011g0203 | 2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2799-387C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3140123 | ||||||
| chr4:3140138
|
G | A | 15 | a0012c0012t0003g0087a0012c0012t0003g0089a0012c0012t0003g0095others(12): Show | 15 | HG01081.hp2 HG01515.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.2799-372G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3140138 | ||||||
| chr4:3140260
|
CA | C | 17 | a0002c0001t0002g0246a0012c0012t0003g0087a0012c0012t0003g0089others(14): Show | 17 | HG01081.hp2 HG01515.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2799-234delA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | INFO_REALIGN_3_PRIME | chr4 | 3140260 | |||||
| chr4:3140309
|
C | T | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2799-201C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3140309 | ||||||
| chr4:3140455
|
T | A | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2799-55T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 21/66 | chr4 | 3140455 | ||||||
| chr4:3140689
|
G | A | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2945+33G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 22/66 | chr4 | 3140689 | ||||||
| chr4:3140713
|
T | G | 1 | a0001c0085t0001g0152 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2945+57T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 22/66 | chr4 | 3140713 | ||||||
| chr4:3140789
|
T | G | 1 | a0006c0037t0021g0146 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2945+133T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 22/66 | chr4 | 3140789 | ||||||
| chr4:3140801
|
A | T | 61 | a0001c0003t0001g0197a0001c0089t0001g0037a0003c0006t0001g0041others(58): Show | 62 | HG00438.hp1 HG00642.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.2945+145A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 22/66 | chr4 | 3140801 | ||||||
| chr4:3141415
|
A | G | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.2945+759A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 22/66 | chr4 | 3141415 | ||||||
| chr4:3141560
|
C | A | 1 | a0007c0058t0033g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2945+904C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 22/66 | chr4 | 3141560 | ||||||
| chr4:3141623
|
G | A | 2 | a0001c0002t0001g0175a0006c0099t0001g0047 | 2 | HG03239.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.2945+967G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 22/66 | chr4 | 3141623 | ||||||
| chr4:3142040
|
A | G | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2946-726A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 22/66 | chr4 | 3142040 | ||||||
| chr4:3142420
|
A | C | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2946-346A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 22/66 | chr4 | 3142420 | ||||||
| chr4:3142714
|
A | G | 9 | a0008c0010t0004g0072a0008c0010t0020g0084a0008c0111t0004g0080others(6): Show | 10 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.2946-52A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 22/66 | chr4 | 3142714 | ||||||
| chr4:3143011
|
G | A | 14 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(11): Show | 14 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.3066+125G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3143011 | ||||||
| chr4:3143122
|
C | T | 1 | a0026c0026t0003g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3066+236C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3143122 | ||||||
| chr4:3143214
|
C | T | 1 | a0006c0022t0001g0036 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.3066+328C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3143214 | ||||||
| chr4:3143278
|
A | G | 1 | a0002c0001t0002g0227 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3066+392A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3143278 | ||||||
| chr4:3143309
|
C | T | 4 | a0017c0018t0003g0091a0017c0018t0003g0092a0017c0018t0003g0097others(1): Show | 4 | HG01975.hp2 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3066+423C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3143309 | ||||||
| chr4:3143436
|
C | CA | 91 | a0001c0003t0001g0156a0002c0001t0002g0191a0002c0001t0002g0193others(88): Show | 91 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.3066+569dupA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | INFO_REALIGN_3_PRIME | chr4 | 3143436 | |||||
| chr4:3143436
|
CAAAA | C | 9 | a0023c0039t0015g0004a0023c0039t0016g0008a0024c0046t0008g0257others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.3066+566_3066+569d others(6): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | INFO_REALIGN_3_PRIME | chr4 | 3143436 | |||||
| chr4:3143609
|
TA | T | 15 | a0012c0012t0003g0087a0012c0012t0003g0089a0012c0012t0003g0095others(12): Show | 15 | HG01081.hp2 HG01515.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.3066+724delA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3143609 | ||||||
| chr4:3143610
|
A | T | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.3066+724A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3143610 | ||||||
| chr4:3143613
|
T | A | 9 | a0023c0039t0015g0004a0023c0039t0016g0008a0024c0046t0008g0257others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.3066+727T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3143613 | ||||||
| chr4:3143689
|
C | T | 1 | a0012c0012t0003g0096 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3066+803C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3143689 | ||||||
| chr4:3143708
|
A | C | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3066+822A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3143708 | ||||||
| chr4:3143985
|
G | T | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3066+1099G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3143985 | ||||||
| chr4:3144139
|
T | C | 79 | a0001c0003t0001g0156a0001c0003t0004g0117a0002c0001t0002g0191others(76): Show | 79 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.3067-1013T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3144139 | ||||||
| chr4:3144310
|
G | C | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.3067-842G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3144310 | ||||||
| chr4:3144366
|
A | G | 1 | a0030c0034t0002g0278 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3067-786A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3144366 | ||||||
| chr4:3144463
|
G | A | 7 | a0002c0001t0002g0220a0002c0001t0002g0262a0005c0004t0002g0219others(4): Show | 7 | HG01256.hp1 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.3067-689G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3144463 | ||||||
| chr4:3144466
|
T | C | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3067-686T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3144466 | ||||||
| chr4:3144561
|
C | A | 1 | a0003c0128t0026g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3067-591C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3144561 | ||||||
| chr4:3144720
|
A | T | 1 | a0001c0002t0001g0177 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3067-432A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3144720 | ||||||
| chr4:3144859
|
G | A | 2 | a0002c0001t0002g0249a0002c0001t0002g0250 | 2 | NA18947.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.3067-293G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3144859 | ||||||
| chr4:3144904
|
G | A | 1 | a0089c0125t0002g0108 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3067-248G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3144904 | ||||||
| chr4:3145086
|
CA | C | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3067-65delA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 23/66 | chr4 | 3145086 | ||||||
| chr4:3145382
|
C | T | 67 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(64): Show | 67 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.3143+154C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 24/66 | chr4 | 3145382 | ||||||
| chr4:3145421
|
C | G | 1 | a0026c0026t0003g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3143+193C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 24/66 | chr4 | 3145421 | ||||||
| chr4:3145441
|
A | T | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3143+213A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 24/66 | chr4 | 3145441 | ||||||
| chr4:3145531
|
A | G | 45 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(42): Show | 45 | HG00323.hp2 HG00639.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.3143+303A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 24/66 | chr4 | 3145531 | ||||||
| chr4:3145540
|
G | C | 39 | a0001c0003t0001g0197a0001c0089t0001g0037a0003c0006t0001g0041others(36): Show | 40 | HG00438.hp1 HG00673.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.3143+312G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 24/66 | chr4 | 3145540 | ||||||
| chr4:3145541
|
C | T | 39 | a0001c0003t0001g0197a0001c0089t0001g0037a0003c0006t0001g0041others(36): Show | 40 | HG00438.hp1 HG00673.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.3143+313C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 24/66 | chr4 | 3145541 | ||||||
| chr4:3145574
|
T | G | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3143+346T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 24/66 | chr4 | 3145574 | ||||||
| chr4:3145753
|
A | C | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.3143+525A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 24/66 | chr4 | 3145753 | ||||||
| chr4:3146056
|
A | G | 3 | a0001c0002t0001g0181a0003c0041t0001g0143a0003c0041t0001g0144 | 3 | NA18961.hp1 NA18999.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.3144-741A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 24/66 | chr4 | 3146056 | ||||||
| chr4:3146081
|
G | A | 2 | a0084c0115t0017g0202a0088c0120t0017g0201 | 2 | HG00738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.3144-716G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 24/66 | chr4 | 3146081 | ||||||
| chr4:3146160
|
A | G | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3144-637A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 24/66 | chr4 | 3146160 | ||||||
| chr4:3146549
|
G | A | 100 | a0001c0003t0001g0156a0001c0003t0004g0117a0002c0001t0002g0191others(97): Show | 100 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.3144-248G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 24/66 | chr4 | 3146549 | ||||||
| chr4:3146705
|
A | C | 1 | a0002c0073t0002g0290 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3144-92A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 24/66 | chr4 | 3146705 | ||||||
| chr4:3147097
|
A | G | 1 | a0017c0018t0003g0092 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3295+149A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 25/66 | chr4 | 3147097 | ||||||
| chr4:3147219
|
C | T | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.3295+271C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 25/66 | chr4 | 3147219 | ||||||
| chr4:3147238
|
C | T | 1 | a0006c0015t0001g0139 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3295+290C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 25/66 | chr4 | 3147238 | ||||||
| chr4:3147239
|
G | A | 2 | a0046c0055t0011g0204a0049c0063t0011g0203 | 2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3295+291G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 25/66 | chr4 | 3147239 | ||||||
| chr4:3147289
|
A | C | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3295+341A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 25/66 | chr4 | 3147289 | ||||||
| chr4:3147289
|
A | G | 50 | a0003c0105t0001g0071a0008c0010t0004g0072a0008c0010t0020g0084others(47): Show | 51 | HG00323.hp2 HG00639.hp1 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.3295+341A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 25/66 | chr4 | 3147289 | ||||||
| chr4:3147325
|
T | TGC | 3 | a0019c0020t0007g0088a0019c0020t0007g0102a0068c0087t0031g0101 | 3 | HG01884.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3295+378_3295+379d others(4): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 25/66 | INFO_REALIGN_3_PRIME | chr4 | 3147325 | |||||
| chr4:3147338
|
C | G | 1 | a0008c0010t0020g0084 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3295+390C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 25/66 | chr4 | 3147338 | ||||||
| chr4:3147400
|
G | A | 3 | a0010c0009t0003g0276a0036c0107t0018g0065a0036c0108t0018g0066 | 3 | HG02280.hp2 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3295+452G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 25/66 | chr4 | 3147400 | ||||||
| chr4:3147495
|
T | G | 1 | a0001c0002t0001g0166 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.3296-510T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 25/66 | chr4 | 3147495 | ||||||
| chr4:3147530
|
A | G | 7 | a0028c0033t0001g0120a0028c0033t0001g0132a0029c0032t0001g0111others(4): Show | 7 | HG00597.hp1 NA19002.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.3296-475A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 25/66 | chr4 | 3147530 | ||||||
| chr4:3147564
|
A | T | 2 | a0046c0055t0011g0204a0049c0063t0011g0203 | 2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3296-441A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 25/66 | chr4 | 3147564 | ||||||
| chr4:3147586
|
T | G | 1 | a0052c0061t0035g0252 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3296-419T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 25/66 | chr4 | 3147586 | ||||||
| chr4:3148429
|
A | G | 1 | a0002c0001t0002g0244 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3498+222A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3148429 | ||||||
| chr4:3148506
|
A | G | 1 | a0006c0037t0021g0146 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3498+299A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3148506 | ||||||
| chr4:3148568
|
T | C | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3498+361T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3148568 | ||||||
| chr4:3148581
|
A | G | 1 | a0006c0015t0001g0158 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3498+374A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3148581 | ||||||
| chr4:3148666
|
C | T | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3498+459C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3148666 | ||||||
| chr4:3148667
|
G | A | 1 | a0008c0010t0001g0068 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3498+460G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3148667 | ||||||
| chr4:3148691
|
G | A | 1 | a0010c0056t0007g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3498+484G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3148691 | ||||||
| chr4:3148793
|
G | T | 1 | a0002c0001t0002g0246 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.3498+586G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3148793 | ||||||
| chr4:3148801
|
A | G | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3498+594A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3148801 | ||||||
| chr4:3148916
|
C | T | 13 | a0007c0058t0033g0009a0010c0009t0003g0276a0010c0009t0003g0277others(10): Show | 13 | HG00642.hp1 HG01192.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.3498+709C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3148916 | ||||||
| chr4:3148925
|
C | G | 1 | a0010c0009t0003g0288 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3498+718C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3148925 | ||||||
| chr4:3148997
|
T | C | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.3498+790T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3148997 | ||||||
| chr4:3149053
|
T | C | 1 | a0007c0058t0033g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3498+846T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3149053 | ||||||
| chr4:3149284
|
A | G | 1 | a0006c0015t0001g0158 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3498+1077A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3149284 | ||||||
| chr4:3149294
|
C | CT | 16 | a0001c0002t0001g0171a0001c0002t0001g0199a0003c0006t0001g0041others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.3498+1107dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | INFO_REALIGN_3_PRIME | chr4 | 3149294 | |||||
| chr4:3149294
|
CT | C | 26 | a0001c0002t0001g0149a0001c0003t0001g0122a0002c0001t0002g0196others(23): Show | 26 | HG01081.hp2 HG01168.hp1 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.3498+1107delT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | INFO_REALIGN_3_PRIME | chr4 | 3149294 | |||||
| chr4:3149319
|
T | C | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3498+1112T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3149319 | ||||||
| chr4:3149400
|
C | T | 1 | a0024c0046t0008g0257 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3498+1193C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3149400 | ||||||
| chr4:3149408
|
C | G | 1 | a0049c0063t0011g0203 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3498+1201C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3149408 | ||||||
| chr4:3149442
|
A | G | 2 | a0036c0107t0018g0065a0036c0108t0018g0066 | 2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3498+1235A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3149442 | ||||||
| chr4:3149475
|
T | G | 1 | a0005c0090t0002g0215 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3498+1268T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3149475 | ||||||
| chr4:3149578
|
GATTACGG others(2): Show |
G | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3498+1374_3498+138 others(13): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | INFO_REALIGN_3_PRIME | chr4 | 3149578 | |||||
| chr4:3149599
|
C | T | 1 | a0019c0020t0023g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3498+1392C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3149599 | ||||||
| chr4:3149634
|
T | C | 20 | a0010c0056t0007g0200a0012c0012t0003g0087a0012c0012t0003g0089others(17): Show | 20 | HG01081.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.3498+1427T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3149634 | ||||||
| chr4:3149803
|
G | A | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3498+1596G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3149803 | ||||||
| chr4:3149911
|
G | A | 1 | a0017c0018t0003g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3498+1704G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3149911 | ||||||
| chr4:3150086
|
C | T | 83 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(80): Show | 83 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.3498+1879C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3150086 | ||||||
| chr4:3150126
|
C | T | 2 | a0001c0002t0001g0150a0005c0004t0002g0194 | 2 | HG00642.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.3498+1919C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3150126 | ||||||
| chr4:3150270
|
A | G | 51 | a0001c0003t0001g0197a0001c0089t0001g0037a0003c0006t0001g0041others(48): Show | 52 | HG00438.hp1 HG00673.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.3498+2063A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3150270 | ||||||
| chr4:3150361
|
G | T | 1 | a0023c0103t0003g0029 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3498+2154G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3150361 | ||||||
| chr4:3150724
|
G | T | 1 | a0002c0001t0002g0191 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3498+2517G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3150724 | ||||||
| chr4:3150779
|
G | A | 1 | a0002c0001t0002g0217 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3498+2572G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3150779 | ||||||
| chr4:3150788
|
G | A | 1 | a0004c0005t0001g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3498+2581G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3150788 | ||||||
| chr4:3150843
|
C | T | 9 | a0023c0039t0015g0004a0023c0039t0016g0008a0024c0046t0008g0257others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.3498+2636C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3150843 | ||||||
| chr4:3150851
|
A | G | 1 | a0028c0033t0001g0120 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3498+2644A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3150851 | ||||||
| chr4:3150863
|
C | T | 1 | a0038c0123t0001g0141 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3498+2656C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3150863 | ||||||
| chr4:3150971
|
G | A | 1 | a0079c0106t0003g0074 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3498+2764G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3150971 | ||||||
| chr4:3151054
|
CA | C | 16 | a0008c0010t0006g0135a0010c0009t0003g0276a0010c0009t0003g0277others(13): Show | 16 | HG00642.hp1 HG01192.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.3498+2861delA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | INFO_REALIGN_3_PRIME | chr4 | 3151054 | |||||
| chr4:3151058
|
A | AC | 24 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(21): Show | 24 | HG00323.hp2 HG00639.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.3498+2851_3498+285 others(5): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3151058 | ||||||
| chr4:3151059
|
A | C | 91 | a0001c0003t0001g0121a0001c0003t0001g0156a0001c0003t0004g0117others(88): Show | 91 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.3498+2852A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3151059 | ||||||
| chr4:3151246
|
G | A | 39 | a0001c0003t0001g0197a0001c0089t0001g0037a0003c0006t0001g0041others(36): Show | 40 | HG00438.hp1 HG00673.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.3498+3039G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3151246 | ||||||
| chr4:3151287
|
G | C | 1 | a0003c0105t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3499-3006G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3151287 | ||||||
| chr4:3151351
|
G | GGA | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3499-2927_3499-292 others(6): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | INFO_REALIGN_3_PRIME | chr4 | 3151351 | |||||
| chr4:3151382
|
G | A | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.3499-2911G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3151382 | ||||||
| chr4:3151584
|
A | G | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3499-2709A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3151584 | ||||||
| chr4:3151693
|
C | G | 2 | a0046c0055t0011g0204a0049c0063t0011g0203 | 2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3499-2600C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3151693 | ||||||
| chr4:3151697
|
A | T | 1 | a0058c0071t0001g0270 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3499-2596A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3151697 | ||||||
| chr4:3151787
|
T | G | 2 | a0014c0014t0010g0011a0043c0050t0010g0012 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3499-2506T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3151787 | ||||||
| chr4:3151829
|
A | G | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3499-2464A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3151829 | ||||||
| chr4:3151838
|
A | G | 9 | a0023c0039t0015g0004a0023c0039t0016g0008a0024c0046t0008g0257others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.3499-2455A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3151838 | ||||||
| chr4:3152028
|
A | C | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3499-2265A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3152028 | ||||||
| chr4:3152101
|
A | AT | 129 | a0001c0003t0001g0156a0001c0003t0004g0117a0001c0089t0001g0037others(126): Show | 130 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.3499-2177dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | INFO_REALIGN_3_PRIME | chr4 | 3152101 | |||||
| chr4:3152122
|
A | C | 1 | a0001c0002t0001g0142 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3499-2171A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3152122 | ||||||
| chr4:3152141
|
C | T | 7 | a0023c0039t0015g0004a0023c0039t0016g0008a0036c0107t0018g0065others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.3499-2152C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3152141 | ||||||
| chr4:3152384
|
T | C | 79 | a0001c0003t0001g0156a0001c0003t0004g0117a0002c0001t0002g0191others(76): Show | 79 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.3499-1909T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3152384 | ||||||
| chr4:3152387
|
C | A | 1 | a0005c0004t0002g0239 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3499-1906C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3152387 | ||||||
| chr4:3152600
|
A | G | 30 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(27): Show | 30 | HG00642.hp1 HG01081.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.3499-1693A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3152600 | ||||||
| chr4:3152813
|
A | AT | 20 | a0001c0002t0001g0175a0001c0003t0001g0129a0003c0006t0001g0038others(17): Show | 20 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.3499-1460dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | INFO_REALIGN_3_PRIME | chr4 | 3152813 | |||||
| chr4:3152813
|
AT | A | 9 | a0001c0002t0001g0169a0002c0001t0002g0191a0002c0001t0002g0223others(6): Show | 9 | HG01256.hp1 HG01515.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.3499-1460delT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | INFO_REALIGN_3_PRIME | chr4 | 3152813 | |||||
| chr4:3152903
|
G | A | 1 | a0009c0008t0001g0168 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3499-1390G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3152903 | ||||||
| chr4:3153152
|
T | G | 1 | a0033c0098t0001g0051 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.3499-1141T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3153152 | ||||||
| chr4:3153155
|
C | T | 1 | a0013c0013t0028g0198 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3499-1138C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3153155 | ||||||
| chr4:3153156
|
G | A | 6 | a0001c0002t0001g0150a0001c0002t0001g0151a0001c0002t0001g0178others(3): Show | 6 | NA18969.hp2 NA18970.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.3499-1137G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3153156 | ||||||
| chr4:3153426
|
A | T | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.3499-867A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3153426 | ||||||
| chr4:3153506
|
T | C | 1 | a0003c0128t0026g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3499-787T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3153506 | ||||||
| chr4:3153719
|
C | T | 1 | a0001c0002t0001g0170 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3499-574C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3153719 | ||||||
| chr4:3153947
|
C | G | 9 | a0023c0039t0015g0004a0023c0039t0016g0008a0024c0046t0008g0257others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.3499-346C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3153947 | ||||||
| chr4:3154072
|
A | C | 1 | a0079c0106t0003g0074 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3499-221A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3154072 | ||||||
| chr4:3154173
|
G | A | 3 | a0035c0042t0005g0076a0035c0042t0005g0085a0062c0082t0005g0083 | 3 | HG02723.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3499-120G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3154173 | ||||||
| chr4:3154210
|
C | G | 1 | a0001c0002t0001g0155 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3499-83C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3154210 | ||||||
| chr4:3154247
|
A | T | 3 | a0010c0009t0003g0291a0020c0079t0003g0186a0050c0065t0003g0286 | 3 | HG00642.hp1 HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.3499-46A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 26/66 | chr4 | 3154247 | ||||||
| chr4:3154442
|
G | A | 1 | a0001c0002t0001g0142 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3625+23G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3154442 | ||||||
| chr4:3154470
|
T | C | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.3625+51T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3154470 | ||||||
| chr4:3154617
|
T | C | 58 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(55): Show | 58 | HG00642.hp1 HG00738.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.3625+198T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3154617 | ||||||
| chr4:3154630
|
T | C | 12 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(9): Show | 12 | HG00738.hp1 HG01109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.3625+211T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3154630 | ||||||
| chr4:3154808
|
A | G | 1 | a0006c0015t0001g0139 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3625+389A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3154808 | ||||||
| chr4:3155060
|
G | A | 1 | a0007c0053t0003g0104 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3625+641G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3155060 | ||||||
| chr4:3155201
|
C | CTATT | 8 | a0002c0001t0002g0220a0002c0001t0002g0262a0002c0030t0002g0213others(5): Show | 8 | HG01256.hp1 HG01257.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.3625+800_3625+803d others(6): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | INFO_REALIGN_3_PRIME | chr4 | 3155201 | |||||
| chr4:3155266
|
G | C | 12 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(9): Show | 12 | HG00738.hp1 HG01109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.3625+847G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3155266 | ||||||
| chr4:3155296
|
A | G | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3625+877A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3155296 | ||||||
| chr4:3155397
|
A | AT | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.3625+984dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | INFO_REALIGN_3_PRIME | chr4 | 3155397 | |||||
| chr4:3155413
|
G | T | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.3625+994G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3155413 | ||||||
| chr4:3155482
|
C | G | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.3625+1063C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3155482 | ||||||
| chr4:3155515
|
G | A | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.3625+1096G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3155515 | ||||||
| chr4:3155520
|
C | T | 13 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(10): Show | 13 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.3625+1101C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3155520 | ||||||
| chr4:3155617
|
C | T | 6 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(3): Show | 6 | HG01109.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3625+1198C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3155617 | ||||||
| chr4:3155620
|
A | G | 1 | a0016c0017t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3625+1201A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3155620 | ||||||
| chr4:3155647
|
T | C | 55 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(52): Show | 55 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.3625+1228T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3155647 | ||||||
| chr4:3155728
|
C | CA | 43 | a0001c0002t0001g0164a0001c0002t0001g0177a0001c0002t0001g0199others(40): Show | 43 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.3626-1321dupA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | INFO_REALIGN_3_PRIME | chr4 | 3155728 | |||||
| chr4:3155728
|
CA | C | 15 | a0011c0029t0001g0273a0014c0014t0003g0014a0014c0014t0003g0015others(12): Show | 15 | HG01167.hp1 HG01243.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.3626-1321delA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | INFO_REALIGN_3_PRIME | chr4 | 3155728 | |||||
| chr4:3155754
|
C | T | 39 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(36): Show | 39 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.3626-1318C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3155754 | ||||||
| chr4:3155758
|
C | A | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.3626-1314C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3155758 | ||||||
| chr4:3155877
|
G | A | 3 | a0007c0058t0033g0009a0052c0061t0035g0252a0054c0068t0034g0090 | 3 | HG02145.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3626-1195G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3155877 | ||||||
| chr4:3155897
|
C | CA | 15 | a0001c0003t0001g0129a0003c0006t0001g0038a0014c0014t0003g0014others(12): Show | 15 | HG01167.hp1 HG01243.hp2 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.3626-1159dupA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | INFO_REALIGN_3_PRIME | chr4 | 3155897 | |||||
| chr4:3155911
|
A | G | 3 | a0035c0042t0005g0076a0035c0042t0005g0085a0062c0082t0005g0083 | 3 | HG02723.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3626-1161A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3155911 | ||||||
| chr4:3156029
|
G | A | 1 | a0063c0081t0001g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3626-1043G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3156029 | ||||||
| chr4:3156114
|
C | G | 1 | a0016c0017t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3626-958C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3156114 | ||||||
| chr4:3156144
|
G | A | 2 | a0023c0103t0003g0029a0080c0110t0003g0031 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3626-928G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3156144 | ||||||
| chr4:3156305
|
A | AAGTTT | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.3626-764_3626-763i others(7): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | INFO_REALIGN_3_PRIME | chr4 | 3156305 | |||||
| chr4:3156309
|
G | A | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.3626-763G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3156309 | ||||||
| chr4:3156415
|
C | T | 2 | a0021c0021t0012g0231a0021c0021t0012g0265 | 2 | NA18980.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.3626-657C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3156415 | ||||||
| chr4:3156428
|
T | G | 2 | a0001c0003t0001g0174a0074c0095t0002g0106 | 2 | HG01175.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3626-644T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3156428 | ||||||
| chr4:3156767
|
C | T | 1 | a0001c0003t0001g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3626-305C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3156767 | ||||||
| chr4:3156786
|
C | T | 1 | a0057c0074t0002g0268 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3626-286C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3156786 | ||||||
| chr4:3156882
|
A | C | 1 | a0003c0024t0019g0109 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.3626-190A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3156882 | ||||||
| chr4:3156987
|
A | C | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3626-85A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 27/66 | chr4 | 3156987 | ||||||
| chr4:3157360
|
A | C | 1 | a0026c0026t0003g0017 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3753+161A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3157360 | ||||||
| chr4:3157563
|
T | C | 1 | a0084c0115t0017g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3753+364T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3157563 | ||||||
| chr4:3157576
|
A | G | 3 | a0001c0002t0001g0151a0001c0002t0001g0182a0011c0072t0001g0205 | 3 | NA18969.hp2 NA19058.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.3753+377A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3157576 | ||||||
| chr4:3157614
|
C | T | 1 | a0001c0003t0001g0130 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3753+415C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3157614 | ||||||
| chr4:3157615
|
G | A | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3753+416G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3157615 | ||||||
| chr4:3157883
|
C | T | 1 | a0014c0014t0003g0015 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3753+684C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3157883 | ||||||
| chr4:3157989
|
C | CT | 14 | a0002c0001t0002g0220a0005c0004t0002g0209a0014c0014t0003g0014others(11): Show | 14 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.3753+792dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | INFO_REALIGN_3_PRIME | chr4 | 3157989 | |||||
| chr4:3157992
|
G | T | 143 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(140): Show | 143 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.3753+793G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3157992 | ||||||
| chr4:3157997
|
T | C | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3753+798T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3157997 | ||||||
| chr4:3158040
|
G | A | 1 | a0007c0053t0003g0104 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3753+841G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3158040 | ||||||
| chr4:3158075
|
T | TCAACCTC | 144 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(141): Show | 144 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.3753+878_3753+879i others(9): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | INFO_REALIGN_3_PRIME | chr4 | 3158075 | |||||
| chr4:3158126
|
G | A | 1 | a0016c0017t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3753+927G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3158126 | ||||||
| chr4:3158195
|
G | A | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.3753+996G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3158195 | ||||||
| chr4:3158329
|
G | T | 1 | a0014c0014t0003g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3753+1130G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3158329 | ||||||
| chr4:3158366
|
A | G | 2 | a0084c0115t0017g0202a0088c0120t0017g0201 | 2 | HG00738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.3753+1167A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3158366 | ||||||
| chr4:3158423
|
G | A | 144 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(141): Show | 144 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.3753+1224G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3158423 | ||||||
| chr4:3158541
|
T | A | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3753+1342T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3158541 | ||||||
| chr4:3158580
|
A | G | 46 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(43): Show | 46 | HG00642.hp1 HG01081.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.3753+1381A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3158580 | ||||||
| chr4:3158644
|
G | T | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3753+1445G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3158644 | ||||||
| chr4:3158644
|
GT | G | 39 | a0001c0003t0001g0197a0001c0089t0001g0037a0003c0006t0001g0041others(36): Show | 40 | HG00438.hp1 HG00673.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.3753+1453delT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | INFO_REALIGN_3_PRIME | chr4 | 3158644 | |||||
| chr4:3158650
|
T | C | 2 | a0001c0002t0001g0166a0001c0002t0001g0172 | 2 | NA18963.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.3753+1451T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3158650 | ||||||
| chr4:3158750
|
A | G | 287 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(284): Show | 289 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(286): Show |
intron_variant | MODIFIER | c.3754-1532A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3158750 | ||||||
| chr4:3158827
|
A | T | 1 | a0008c0010t0020g0084 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3754-1455A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3158827 | ||||||
| chr4:3158903
|
A | G | 46 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(43): Show | 46 | HG00642.hp1 HG01081.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.3754-1379A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3158903 | ||||||
| chr4:3159012
|
C | T | 3 | a0031c0035t0002g0267a0031c0035t0002g0269a0057c0074t0002g0268 | 3 | HG01516.hp2 HG01517.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.3754-1270C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3159012 | ||||||
| chr4:3159083
|
T | G | 1 | a0065c0078t0004g0185 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3754-1199T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3159083 | ||||||
| chr4:3159212
|
C | T | 1 | a0019c0020t0023g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3754-1070C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3159212 | ||||||
| chr4:3159476
|
C | T | 1 | a0063c0081t0001g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3754-806C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3159476 | ||||||
| chr4:3159531
|
C | G | 1 | a0004c0011t0001g0160 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3754-751C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3159531 | ||||||
| chr4:3159562
|
A | T | 1 | a0008c0111t0004g0080 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3754-720A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3159562 | ||||||
| chr4:3159691
|
T | C | 1 | a0067c0086t0025g0113 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3754-591T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3159691 | ||||||
| chr4:3159697
|
T | C | 1 | a0002c0001t0024g0238 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3754-585T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3159697 | ||||||
| chr4:3159719
|
C | T | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.3754-563C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3159719 | ||||||
| chr4:3160119
|
T | C | 55 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(52): Show | 55 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.3754-163T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 28/66 | chr4 | 3160119 | ||||||
| chr4:3160429
|
G | A | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3864+37G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3160429 | ||||||
| chr4:3160443
|
C | T | 9 | a0023c0039t0015g0004a0023c0039t0016g0008a0024c0046t0008g0257others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.3864+51C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3160443 | ||||||
| chr4:3160479
|
G | A | 1 | a0002c0001t0002g0227 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3864+87G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3160479 | ||||||
| chr4:3160634
|
G | A | 1 | a0006c0037t0021g0146 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3864+242G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3160634 | ||||||
| chr4:3160740
|
G | A | 3 | a0019c0020t0007g0088a0019c0020t0007g0102a0068c0087t0031g0101 | 3 | HG01884.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3864+348G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3160740 | ||||||
| chr4:3160780
|
G | C | 1 | a0010c0009t0003g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3864+388G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3160780 | ||||||
| chr4:3160834
|
C | A | 1 | a0003c0128t0026g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3864+442C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3160834 | ||||||
| chr4:3161029
|
A | G | 1 | a0007c0058t0033g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3864+637A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3161029 | ||||||
| chr4:3161142
|
A | G | 2 | a0014c0014t0010g0011a0043c0050t0010g0012 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3864+750A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3161142 | ||||||
| chr4:3161167
|
C | T | 1 | a0001c0002t0001g0145 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3864+775C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3161167 | ||||||
| chr4:3161374
|
A | G | 14 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(11): Show | 14 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.3864+982A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3161374 | ||||||
| chr4:3161589
|
T | A | 1 | a0052c0061t0035g0252 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3864+1197T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3161589 | ||||||
| chr4:3161782
|
T | C | 2 | a0017c0018t0003g0097a0048c0057t0003g0098 | 2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3864+1390T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3161782 | ||||||
| chr4:3161784
|
G | A | 2 | a0002c0001t0002g0191a0034c0038t0002g0192 | 2 | HG01433.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.3864+1392G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3161784 | ||||||
| chr4:3162004
|
A | G | 1 | a0002c0073t0002g0290 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3864+1612A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3162004 | ||||||
| chr4:3162169
|
T | G | 2 | a0046c0055t0011g0204a0049c0063t0011g0203 | 2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3864+1777T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3162169 | ||||||
| chr4:3162197
|
T | C | 1 | a0003c0128t0026g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3864+1805T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3162197 | ||||||
| chr4:3162505
|
T | A | 2 | a0010c0009t0003g0288a0010c0009t0003g0289 | 2 | HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3864+2113T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3162505 | ||||||
| chr4:3162644
|
C | T | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.3864+2252C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3162644 | ||||||
| chr4:3162818
|
A | G | 1 | a0026c0026t0003g0017 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3864+2426A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3162818 | ||||||
| chr4:3162843
|
T | C | 17 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(14): Show | 17 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.3864+2451T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3162843 | ||||||
| chr4:3162901
|
T | C | 47 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(44): Show | 47 | HG00642.hp1 HG01081.hp2 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.3864+2509T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3162901 | ||||||
| chr4:3163042
|
G | A | 1 | a0004c0011t0001g0161 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3864+2650G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3163042 | ||||||
| chr4:3163097
|
T | C | 1 | a0041c0049t0001g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3864+2705T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3163097 | ||||||
| chr4:3163111
|
G | A | 1 | a0008c0114t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.3864+2719G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3163111 | ||||||
| chr4:3163355
|
G | A | 1 | a0002c0001t0002g0191 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3864+2963G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3163355 | ||||||
| chr4:3163371
|
A | G | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3864+2979A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3163371 | ||||||
| chr4:3163835
|
C | T | 2 | a0005c0004t0002g0194a0005c0004t0002g0195 | 2 | HG00642.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.3864+3443C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3163835 | ||||||
| chr4:3163887
|
A | AT | 30 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(27): Show | 30 | HG00642.hp1 HG01081.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.3864+3503dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | INFO_REALIGN_3_PRIME | chr4 | 3163887 | |||||
| chr4:3163910
|
C | T | 1 | a0054c0068t0034g0090 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3864+3518C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3163910 | ||||||
| chr4:3164220
|
A | C | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.3864+3828A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3164220 | ||||||
| chr4:3164287
|
C | T | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3864+3895C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3164287 | ||||||
| chr4:3164334
|
T | C | 47 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(44): Show | 47 | HG00642.hp1 HG01081.hp2 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.3864+3942T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3164334 | ||||||
| chr4:3164452
|
C | T | 1 | a0092c0044t0015g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3864+4060C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3164452 | ||||||
| chr4:3164469
|
C | G | 47 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(44): Show | 47 | HG00642.hp1 HG01081.hp2 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.3864+4077C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3164469 | ||||||
| chr4:3164523
|
G | A | 90 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(87): Show | 90 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.3864+4131G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3164523 | ||||||
| chr4:3164617
|
G | A | 7 | a0012c0012t0003g0089a0012c0012t0003g0095a0012c0012t0003g0096others(4): Show | 7 | HG01081.hp2 HG01515.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.3864+4225G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3164617 | ||||||
| chr4:3164630
|
A | C | 1 | a0085c0117t0001g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3864+4238A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3164630 | ||||||
| chr4:3164677
|
G | C | 1 | a0026c0026t0003g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3864+4285G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3164677 | ||||||
| chr4:3164797
|
T | G | 1 | a0026c0026t0003g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3864+4405T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3164797 | ||||||
| chr4:3164836
|
C | G | 1 | a0021c0021t0012g0265 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3864+4444C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3164836 | ||||||
| chr4:3165209
|
G | A | 46 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(43): Show | 46 | HG00642.hp1 HG01081.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.3864+4817G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3165209 | ||||||
| chr4:3165235
|
T | G | 30 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(27): Show | 30 | HG00642.hp1 HG01081.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.3864+4843T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3165235 | ||||||
| chr4:3165237
|
G | C | 12 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(9): Show | 12 | HG00642.hp1 HG01192.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.3864+4845G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3165237 | ||||||
| chr4:3165487
|
A | G | 1 | a0086c0118t0003g0067 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.3864+5095A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3165487 | ||||||
| chr4:3165697
|
T | C | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3864+5305T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3165697 | ||||||
| chr4:3166052
|
C | G | 2 | a0036c0107t0018g0065a0036c0108t0018g0066 | 2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3864+5660C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3166052 | ||||||
| chr4:3166089
|
G | C | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3864+5697G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3166089 | ||||||
| chr4:3166111
|
T | G | 1 | a0039c0043t0001g0078 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.3864+5719T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3166111 | ||||||
| chr4:3166319
|
A | G | 1 | a0058c0071t0001g0270 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3864+5927A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3166319 | ||||||
| chr4:3166406
|
A | G | 1 | a0020c0084t0003g0093 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3865-5914A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3166406 | ||||||
| chr4:3166647
|
G | A | 1 | a0001c0002t0001g0164 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3865-5673G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3166647 | ||||||
| chr4:3166696
|
T | G | 3 | a0007c0058t0033g0009a0052c0061t0035g0252a0054c0068t0034g0090 | 3 | HG02145.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3865-5624T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3166696 | ||||||
| chr4:3166860
|
T | G | 4 | a0017c0018t0003g0091a0017c0018t0003g0092a0017c0018t0003g0097others(1): Show | 4 | HG01975.hp2 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3865-5460T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3166860 | ||||||
| chr4:3166913
|
G | A | 12 | a0005c0004t0002g0209a0005c0004t0002g0228a0005c0004t0002g0230others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.3865-5407G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3166913 | ||||||
| chr4:3167190
|
G | A | 1 | a0002c0001t0002g0282 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3865-5130G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3167190 | ||||||
| chr4:3167345
|
A | G | 1 | a0001c0002t0001g0199 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3865-4975A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3167345 | ||||||
| chr4:3167449
|
A | T | 39 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(36): Show | 39 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.3865-4871A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3167449 | ||||||
| chr4:3167503
|
AT | A | 17 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(14): Show | 17 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.3865-4815delT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | INFO_REALIGN_3_PRIME | chr4 | 3167503 | |||||
| chr4:3167537
|
C | G | 1 | a0033c0097t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3865-4783C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3167537 | ||||||
| chr4:3167795
|
G | A | 17 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(14): Show | 17 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.3865-4525G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3167795 | ||||||
| chr4:3168025
|
C | T | 1 | a0019c0020t0023g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3865-4295C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3168025 | ||||||
| chr4:3168213
|
G | C | 1 | a0005c0004t0002g0256 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3865-4107G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3168213 | ||||||
| chr4:3168287
|
A | G | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.3865-4033A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3168287 | ||||||
| chr4:3168368
|
C | T | 1 | a0054c0068t0034g0090 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3865-3952C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3168368 | ||||||
| chr4:3168371
|
C | T | 1 | a0055c0069t0001g0271 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3865-3949C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3168371 | ||||||
| chr4:3168459
|
C | T | 1 | a0010c0009t0003g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3865-3861C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3168459 | ||||||
| chr4:3168513
|
C | T | 17 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(14): Show | 17 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.3865-3807C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3168513 | ||||||
| chr4:3168651
|
T | C | 1 | a0001c0003t0004g0134 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3865-3669T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3168651 | ||||||
| chr4:3168695
|
C | T | 17 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(14): Show | 17 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.3865-3625C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3168695 | ||||||
| chr4:3168738
|
C | T | 18 | a0006c0015t0001g0139a0014c0014t0003g0014a0014c0014t0003g0015others(15): Show | 18 | HG01167.hp1 HG01175.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.3865-3582C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3168738 | ||||||
| chr4:3168748
|
T | C | 4 | a0014c0014t0003g0021a0046c0055t0011g0204a0049c0063t0011g0203others(1): Show | 4 | HG01255.hp2 HG02630.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3865-3572T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3168748 | ||||||
| chr4:3168770
|
C | T | 1 | a0024c0047t0008g0258 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3865-3550C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3168770 | ||||||
| chr4:3168806
|
G | C | 30 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(27): Show | 30 | HG00642.hp1 HG01081.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.3865-3514G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3168806 | ||||||
| chr4:3169003
|
A | ATTCT | 30 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(27): Show | 30 | HG00642.hp1 HG01081.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.3865-3298_3865-329 others(8): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | INFO_REALIGN_3_PRIME | chr4 | 3169003 | |||||
| chr4:3169003
|
A | ATTCTTTC others(13): Show |
2 | a0014c0014t0010g0011a0043c0050t0010g0012 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3865-3314_3865-329 others(24): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | INFO_REALIGN_3_PRIME | chr4 | 3169003 | |||||
| chr4:3169003
|
A | ATTCTTTC others(33): Show |
1 | a0014c0014t0003g0021 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3865-3295_3865-329 others(44): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | INFO_REALIGN_3_PRIME | chr4 | 3169003 | |||||
| chr4:3169003
|
A | ATTCTTTC others(37): Show |
4 | a0014c0014t0003g0014a0014c0014t0003g0015a0022c0023t0003g0016others(1): Show | 4 | HG01243.hp2 HG01255.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3865-3295_3865-329 others(48): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | INFO_REALIGN_3_PRIME | chr4 | 3169003 | |||||
| chr4:3169003
|
A | ATTCTTTC others(41): Show |
3 | a0022c0023t0003g0019a0026c0026t0003g0017a0063c0081t0001g0133 | 3 | HG02145.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3865-3295_3865-329 others(52): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | INFO_REALIGN_3_PRIME | chr4 | 3169003 | |||||
| chr4:3169003
|
A | ATTCTTTC others(45): Show |
2 | a0022c0023t0003g0013a0026c0026t0003g0022 | 2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3865-3295_3865-329 others(56): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | INFO_REALIGN_3_PRIME | chr4 | 3169003 | |||||
| chr4:3169003
|
A | T | 1 | a0069c0093t0003g0020 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3865-3317A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3169003 | ||||||
| chr4:3169006
|
C | A | 7 | a0023c0039t0015g0004a0023c0039t0016g0008a0024c0047t0008g0258others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.3865-3314C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3169006 | ||||||
| chr4:3169022
|
C | CTTTCT | 6 | a0023c0039t0015g0004a0023c0039t0016g0008a0070c0092t0032g0030others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3865-3295_3865-329 others(9): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | INFO_REALIGN_3_PRIME | chr4 | 3169022 | |||||
| chr4:3169022
|
C | CTTTCTTT others(38): Show |
1 | a0075c0094t0003g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3865-3295_3865-329 others(49): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | INFO_REALIGN_3_PRIME | chr4 | 3169022 | |||||
| chr4:3169022
|
C | CTTTCTTT others(42): Show |
2 | a0046c0055t0011g0204a0090c0126t0003g0018 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3865-3295_3865-329 others(53): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | INFO_REALIGN_3_PRIME | chr4 | 3169022 | |||||
| chr4:3169024
|
T | TTCTTTCT others(39): Show |
1 | a0079c0106t0003g0074 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3865-3295_3865-329 others(50): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | INFO_REALIGN_3_PRIME | chr4 | 3169024 | |||||
| chr4:3169024
|
T | TTCTTTCT others(43): Show |
1 | a0069c0093t0003g0020 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3865-3295_3865-329 others(54): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | INFO_REALIGN_3_PRIME | chr4 | 3169024 | |||||
| chr4:3169026
|
T | C | 1 | a0044c0060t0001g0059 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3865-3294T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3169026 | ||||||
| chr4:3169050
|
G | A | 3 | a0019c0020t0007g0088a0019c0020t0007g0102a0068c0087t0031g0101 | 3 | HG01884.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3865-3270G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3169050 | ||||||
| chr4:3169061
|
T | C | 56 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(53): Show | 56 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.3865-3259T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3169061 | ||||||
| chr4:3169264
|
C | T | 1 | a0002c0001t0002g0212 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3865-3056C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3169264 | ||||||
| chr4:3169355
|
C | T | 17 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(14): Show | 17 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.3865-2965C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3169355 | ||||||
| chr4:3169502
|
G | A | 1 | a0002c0001t0002g0244 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3865-2818G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3169502 | ||||||
| chr4:3169588
|
G | T | 1 | a0026c0026t0003g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3865-2732G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3169588 | ||||||
| chr4:3169643
|
A | G | 149 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(146): Show | 149 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.3865-2677A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3169643 | ||||||
| chr4:3169714
|
T | C | 56 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(53): Show | 56 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.3865-2606T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3169714 | ||||||
| chr4:3169774
|
A | G | 1 | a0026c0026t0003g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3865-2546A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3169774 | ||||||
| chr4:3169821
|
G | A | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.3865-2499G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3169821 | ||||||
| chr4:3169861
|
A | G | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.3865-2459A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3169861 | ||||||
| chr4:3169864
|
G | A | 1 | a0023c0039t0016g0008 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3865-2456G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3169864 | ||||||
| chr4:3169916
|
G | A | 3 | a0031c0035t0002g0267a0031c0035t0002g0269a0057c0074t0002g0268 | 3 | HG01516.hp2 HG01517.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.3865-2404G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3169916 | ||||||
| chr4:3170017
|
A | T | 1 | a0003c0006t0001g0041 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.3865-2303A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3170017 | ||||||
| chr4:3170072
|
C | T | 1 | a0059c0075t0014g0222 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3865-2248C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3170072 | ||||||
| chr4:3170253
|
A | G | 1 | a0001c0002t0001g0199 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3865-2067A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3170253 | ||||||
| chr4:3170445
|
G | T | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.3865-1875G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3170445 | ||||||
| chr4:3170450
|
C | G | 1 | a0017c0018t0003g0092 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3865-1870C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3170450 | ||||||
| chr4:3170451
|
T | G | 1 | a0017c0018t0003g0092 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3865-1869T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3170451 | ||||||
| chr4:3170535
|
T | G | 1 | a0010c0056t0007g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3865-1785T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3170535 | ||||||
| chr4:3170600
|
G | A | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.3865-1720G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3170600 | ||||||
| chr4:3170600
|
G | C | 2 | a0002c0030t0002g0213a0002c0030t0002g0218 | 2 | NA18964.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.3865-1720G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3170600 | ||||||
| chr4:3170712
|
C | T | 145 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(142): Show | 145 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.3865-1608C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3170712 | ||||||
| chr4:3171206
|
T | C | 1 | a0001c0002t0001g0164 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3865-1114T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3171206 | ||||||
| chr4:3171216
|
A | C | 1 | a0039c0043t0001g0078 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.3865-1104A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3171216 | ||||||
| chr4:3171277
|
G | T | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3865-1043G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3171277 | ||||||
| chr4:3171438
|
G | A | 1 | a0001c0002t0001g0177 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3865-882G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3171438 | ||||||
| chr4:3171472
|
C | CT | 20 | a0002c0001t0002g0210a0003c0006t0001g0052a0006c0022t0001g0039others(17): Show | 20 | HG00738.hp2 HG01167.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.3865-832dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | INFO_REALIGN_3_PRIME | chr4 | 3171472 | |||||
| chr4:3171546
|
C | T | 75 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(72): Show | 75 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.3865-774C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3171546 | ||||||
| chr4:3171657
|
G | A | 67 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(64): Show | 67 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.3865-663G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3171657 | ||||||
| chr4:3171767
|
A | G | 46 | a0010c0009t0003g0276a0010c0009t0003g0288a0010c0009t0003g0289others(43): Show | 46 | HG00642.hp1 HG01081.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.3865-553A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3171767 | ||||||
| chr4:3172107
|
A | G | 46 | a0010c0009t0003g0276a0010c0009t0003g0288a0010c0009t0003g0289others(43): Show | 46 | HG00642.hp1 HG01081.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.3865-213A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3172107 | ||||||
| chr4:3172193
|
C | T | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.3865-127C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3172193 | ||||||
| chr4:3172273
|
A | G | 2 | a0022c0023t0003g0013a0022c0023t0003g0019 | 2 | HG02145.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3865-47A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 29/66 | chr4 | 3172273 | ||||||
| chr4:3172529
|
T | C | 46 | a0010c0009t0003g0276a0010c0009t0003g0288a0010c0009t0003g0289others(43): Show | 46 | HG00642.hp1 HG01081.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.3942+132T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 30/66 | chr4 | 3172529 | ||||||
| chr4:3172659
|
C | T | 2 | a0084c0115t0017g0202a0088c0120t0017g0201 | 2 | HG00738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.3943-249C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 30/66 | chr4 | 3172659 | ||||||
| chr4:3172769
|
TGATTCAC others(1): Show |
T | 76 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(73): Show | 76 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.3943-137_3943-130d others(10): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 30/66 | INFO_REALIGN_3_PRIME | chr4 | 3172769 | |||||
| chr4:3172883
|
T | C | 3 | a0023c0039t0016g0008a0077c0102t0029g0006a0083c0116t0016g0005 | 3 | HG01243.hp1 HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3943-25T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 30/66 | chr4 | 3172883 | ||||||
| chr4:3173244
|
G | T | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4166+113G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 31/66 | chr4 | 3173244 | ||||||
| chr4:3173333
|
TGA | T | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.4166+204_4166+205d others(4): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 31/66 | INFO_REALIGN_3_PRIME | chr4 | 3173333 | |||||
| chr4:3173603
|
A | G | 1 | a0021c0021t0012g0231 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.4166+472A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 31/66 | chr4 | 3173603 | ||||||
| chr4:3173672
|
GT | G | 46 | a0010c0009t0003g0276a0010c0009t0003g0288a0010c0009t0003g0289others(43): Show | 46 | HG00642.hp1 HG01081.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.4166+555delT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 31/66 | INFO_REALIGN_3_PRIME | chr4 | 3173672 | |||||
| chr4:3173692
|
G | A | 44 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(41): Show | 44 | HG00423.hp1 HG00438.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.4166+561G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 31/66 | chr4 | 3173692 | ||||||
| chr4:3173704
|
T | C | 1 | a0026c0026t0003g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4166+573T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 31/66 | chr4 | 3173704 | ||||||
| chr4:3174076
|
C | T | 1 | a0079c0106t0003g0074 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4167-645C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 31/66 | chr4 | 3174076 | ||||||
| chr4:3174559
|
G | T | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.4167-162G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 31/66 | chr4 | 3174559 | ||||||
| chr4:3174587
|
C | G | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4167-134C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 31/66 | chr4 | 3174587 | ||||||
| chr4:3174884
|
C | G | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.4246-62C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 32/66 | chr4 | 3174884 | ||||||
| chr4:3174896
|
A | C | 2 | a0014c0014t0010g0011a0043c0050t0010g0012 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.4246-50A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 32/66 | chr4 | 3174896 | ||||||
| chr4:3175311
|
T | A | 1 | a0071c0091t0001g0272 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.4407+204T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3175311 | ||||||
| chr4:3175312
|
C | A | 1 | a0071c0091t0001g0272 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.4407+205C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3175312 | ||||||
| chr4:3175532
|
A | G | 55 | a0010c0009t0003g0276a0010c0009t0003g0288a0010c0009t0003g0289others(52): Show | 55 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.4407+425A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3175532 | ||||||
| chr4:3175686
|
G | T | 1 | a0002c0001t0002g0251 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4407+579G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3175686 | ||||||
| chr4:3175753
|
C | G | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4407+646C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3175753 | ||||||
| chr4:3175883
|
G | A | 1 | a0002c0001t0002g0191 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4407+776G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3175883 | ||||||
| chr4:3175897
|
C | A | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.4407+790C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3175897 | ||||||
| chr4:3175904
|
G | A | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.4407+797G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3175904 | ||||||
| chr4:3175957
|
G | T | 8 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(5): Show | 8 | HG01243.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.4407+850G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3175957 | ||||||
| chr4:3176009
|
T | G | 1 | a0014c0014t0003g0021 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4407+902T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3176009 | ||||||
| chr4:3176021
|
GTTTGTTT others(3): Show |
G | 1 | a0062c0082t0005g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4407+928_4407+937d others(12): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | INFO_REALIGN_3_PRIME | chr4 | 3176021 | |||||
| chr4:3176025
|
G | GTTTTT | 22 | a0010c0009t0003g0288a0010c0009t0003g0289a0010c0009t0003g0291others(19): Show | 22 | HG00642.hp1 HG01081.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.4407+923_4407+927d others(7): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | INFO_REALIGN_3_PRIME | chr4 | 3176025 | |||||
| chr4:3176025
|
G | GTTTTTT | 6 | a0010c0009t0003g0276a0012c0012t0003g0087a0012c0012t0003g0089others(3): Show | 6 | HG01192.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.4407+922_4407+927d others(8): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | INFO_REALIGN_3_PRIME | chr4 | 3176025 | |||||
| chr4:3176028
|
T | TGG | 17 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(14): Show | 17 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.4407+921_4407+922i others(4): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3176028 | ||||||
| chr4:3176035
|
G | GT | 21 | a0001c0089t0001g0037a0004c0005t0001g0001a0004c0005t0001g0049others(18): Show | 22 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.4407+938dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | INFO_REALIGN_3_PRIME | chr4 | 3176035 | |||||
| chr4:3176035
|
G | T | 46 | a0010c0009t0003g0276a0010c0009t0003g0288a0010c0009t0003g0289others(43): Show | 46 | HG00642.hp1 HG01081.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.4407+928G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3176035 | ||||||
| chr4:3176065
|
T | A | 2 | a0014c0014t0010g0011a0043c0050t0010g0012 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.4407+958T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3176065 | ||||||
| chr4:3176072
|
G | A | 2 | a0005c0004t0002g0194a0005c0004t0002g0195 | 2 | HG00642.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.4407+965G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3176072 | ||||||
| chr4:3176330
|
G | A | 1 | a0005c0090t0002g0215 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.4408-1002G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3176330 | ||||||
| chr4:3176599
|
A | G | 1 | a0062c0082t0005g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4408-733A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3176599 | ||||||
| chr4:3176897
|
A | G | 1 | a0008c0111t0004g0080 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4408-435A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3176897 | ||||||
| chr4:3177070
|
T | C | 1 | a0086c0118t0003g0067 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.4408-262T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3177070 | ||||||
| chr4:3177171
|
A | G | 1 | a0004c0005t0001g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4408-161A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3177171 | ||||||
| chr4:3177260
|
A | G | 1 | a0004c0005t0001g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4408-72A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 33/66 | chr4 | 3177260 | ||||||
| chr4:3177721
|
T | G | 287 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(284): Show | 289 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(286): Show |
intron_variant | MODIFIER | c.4463+334T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 34/66 | chr4 | 3177721 | ||||||
| chr4:3177771
|
G | C | 2 | a0010c0009t0003g0288a0010c0009t0003g0289 | 2 | HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4463+384G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 34/66 | chr4 | 3177771 | ||||||
| chr4:3177951
|
A | G | 1 | a0007c0053t0003g0104 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4464-347A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 34/66 | chr4 | 3177951 | ||||||
| chr4:3178205
|
G | T | 1 | a0074c0095t0002g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4464-93G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 34/66 | chr4 | 3178205 | ||||||
| chr4:3178294
|
T | C | 155 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(152): Show | 156 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(153): Show |
splice_region_variant&intron_variant | LOW | c.4464-4T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 34/66 | chr4 | 3178294 | ||||||
| chr4:3178483
|
C | T | 2 | a0001c0003t0001g0129a0003c0006t0001g0038 | 2 | HG02135.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.4612+37C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 35/66 | chr4 | 3178483 | ||||||
| chr4:3178556
|
G | A | 53 | a0010c0009t0003g0276a0010c0009t0003g0288a0010c0009t0003g0289others(50): Show | 53 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.4612+110G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 35/66 | chr4 | 3178556 | ||||||
| chr4:3178676
|
A | G | 1 | a0010c0056t0007g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4612+230A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 35/66 | chr4 | 3178676 | ||||||
| chr4:3178948
|
G | A | 1 | a0003c0105t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4612+502G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 35/66 | chr4 | 3178948 | ||||||
| chr4:3178968
|
G | C | 1 | a0058c0071t0001g0270 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4612+522G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 35/66 | chr4 | 3178968 | ||||||
| chr4:3179069
|
A | C | 1 | a0001c0003t0001g0156 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.4612+623A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 35/66 | chr4 | 3179069 | ||||||
| chr4:3179086
|
C | G | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.4612+640C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 35/66 | chr4 | 3179086 | ||||||
| chr4:3179160
|
C | T | 1 | a0001c0002t0001g0145 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.4612+714C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 35/66 | chr4 | 3179160 | ||||||
| chr4:3179169
|
G | A | 1 | a0087c0119t0022g0207 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.4612+723G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 35/66 | chr4 | 3179169 | ||||||
| chr4:3179198
|
T | C | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.4612+752T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 35/66 | chr4 | 3179198 | ||||||
| chr4:3179232
|
G | A | 1 | a0020c0084t0003g0093 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4612+786G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 35/66 | chr4 | 3179232 | ||||||
| chr4:3179763
|
T | C | 1 | a0033c0097t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4613-752T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 35/66 | chr4 | 3179763 | ||||||
| chr4:3179956
|
A | T | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.4613-559A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 35/66 | chr4 | 3179956 | ||||||
| chr4:3180123
|
T | TA | 29 | a0010c0009t0003g0276a0010c0009t0003g0288a0010c0009t0003g0289others(26): Show | 29 | HG00642.hp1 HG01081.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.4613-391dupA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 35/66 | INFO_REALIGN_3_PRIME | chr4 | 3180123 | |||||
| chr4:3180264
|
T | C | 1 | a0001c0002t0001g0147 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.4613-251T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 35/66 | chr4 | 3180264 | ||||||
| chr4:3180274
|
T | G | 1 | a0052c0061t0035g0252 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4613-241T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 35/66 | chr4 | 3180274 | ||||||
| chr4:3180303
|
A | G | 3 | a0046c0055t0011g0204a0049c0063t0011g0203a0063c0081t0001g0133 | 3 | HG01255.hp2 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.4613-212A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 35/66 | chr4 | 3180303 | ||||||
| chr4:3180654
|
A | G | 1 | a0002c0001t0002g0223 | 1 | HG03491.hp2 | splice_region_variant&intron_variant | LOW | c.4749+3A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 36/66 | chr4 | 3180654 | ||||||
| chr4:3180783
|
T | G | 1 | a0067c0086t0025g0113 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4749+132T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 36/66 | chr4 | 3180783 | ||||||
| chr4:3180815
|
C | T | 2 | a0007c0058t0033g0009a0052c0061t0035g0252 | 2 | HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4749+164C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 36/66 | chr4 | 3180815 | ||||||
| chr4:3180835
|
T | G | 1 | a0067c0086t0025g0113 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4749+184T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 36/66 | chr4 | 3180835 | ||||||
| chr4:3180841
|
T | G | 199 | a0001c0002t0001g0142a0001c0003t0001g0077a0001c0003t0001g0122others(196): Show | 200 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.4749+190T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 36/66 | chr4 | 3180841 | ||||||
| chr4:3181001
|
C | A | 3 | a0002c0001t0002g0241a0002c0001t0002g0281a0051c0062t0002g0243 | 3 | HG02165.hp1 NA18950.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.4749+350C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 36/66 | chr4 | 3181001 | ||||||
| chr4:3181011
|
G | T | 2 | a0002c0001t0002g0244a0002c0001t0002g0248 | 2 | HG00741.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.4749+360G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 36/66 | chr4 | 3181011 | ||||||
| chr4:3181122
|
T | G | 75 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(72): Show | 75 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.4749+471T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 36/66 | chr4 | 3181122 | ||||||
| chr4:3181209
|
C | T | 29 | a0010c0009t0003g0276a0010c0009t0003g0288a0010c0009t0003g0289others(26): Show | 29 | HG00642.hp1 HG01081.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.4749+558C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 36/66 | chr4 | 3181209 | ||||||
| chr4:3181229
|
C | A | 4 | a0008c0010t0006g0135a0008c0010t0006g0136a0015c0016t0006g0137others(1): Show | 4 | HG02109.hp2 HG02257.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.4749+578C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 36/66 | chr4 | 3181229 | ||||||
| chr4:3181252
|
G | A | 1 | a0003c0006t0027g0042 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.4749+601G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 36/66 | chr4 | 3181252 | ||||||
| chr4:3181361
|
A | T | 1 | a0001c0003t0001g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.4749+710A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 36/66 | chr4 | 3181361 | ||||||
| chr4:3181433
|
T | C | 9 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(6): Show | 9 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.4749+782T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 36/66 | chr4 | 3181433 | ||||||
| chr4:3181456
|
A | G | 3 | a0017c0018t0003g0091a0017c0018t0003g0097a0048c0057t0003g0098 | 3 | HG02055.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4749+805A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 36/66 | chr4 | 3181456 | ||||||
| chr4:3181580
|
G | C | 1 | a0002c0001t0013g0224 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4750-774G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 36/66 | chr4 | 3181580 | ||||||
| chr4:3181593
|
T | C | 1 | a0001c0002t0001g0164 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.4750-761T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 36/66 | chr4 | 3181593 | ||||||
| chr4:3181845
|
A | T | 1 | a0019c0020t0023g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4750-509A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 36/66 | chr4 | 3181845 | ||||||
| chr4:3182289
|
C | T | 3 | a0019c0020t0007g0088a0019c0020t0007g0102a0068c0087t0031g0101 | 3 | HG01884.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4750-65C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 36/66 | chr4 | 3182289 | ||||||
| chr4:3182481
|
G | A | 1 | a0001c0002t0001g0175 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4866+11G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3182481 | ||||||
| chr4:3182502
|
A | G | 43 | a0010c0009t0003g0276a0010c0009t0003g0288a0010c0009t0003g0289others(40): Show | 43 | HG00642.hp1 HG01081.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.4866+32A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3182502 | ||||||
| chr4:3182604
|
T | C | 1 | a0033c0097t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4866+134T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3182604 | ||||||
| chr4:3182737
|
G | T | 77 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(74): Show | 77 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.4866+267G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3182737 | ||||||
| chr4:3182768
|
C | T | 2 | a0023c0039t0016g0008a0083c0116t0016g0005 | 2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4866+298C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3182768 | ||||||
| chr4:3183037
|
C | T | 1 | a0052c0061t0035g0252 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4866+567C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3183037 | ||||||
| chr4:3183110
|
G | A | 1 | a0003c0105t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4866+640G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3183110 | ||||||
| chr4:3183224
|
T | C | 29 | a0010c0009t0003g0276a0010c0009t0003g0288a0010c0009t0003g0289others(26): Show | 29 | HG00642.hp1 HG01081.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.4866+754T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3183224 | ||||||
| chr4:3183240
|
T | C | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4866+770T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3183240 | ||||||
| chr4:3183471
|
C | T | 4 | a0010c0009t0003g0276a0046c0055t0011g0204a0049c0063t0011g0203others(1): Show | 4 | HG01255.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4866+1001C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3183471 | ||||||
| chr4:3183491
|
T | G | 9 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(6): Show | 9 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.4866+1021T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3183491 | ||||||
| chr4:3183770
|
G | T | 1 | a0080c0110t0003g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4866+1300G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3183770 | ||||||
| chr4:3183790
|
C | T | 8 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(5): Show | 8 | HG00738.hp1 HG01109.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.4866+1320C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3183790 | ||||||
| chr4:3183808
|
G | A | 2 | a0002c0001t0002g0212a0002c0001t0002g0223 | 2 | HG03491.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.4866+1338G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3183808 | ||||||
| chr4:3184020
|
T | C | 78 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(75): Show | 78 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.4866+1550T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3184020 | ||||||
| chr4:3184106
|
G | A | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.4866+1636G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3184106 | ||||||
| chr4:3184267
|
G | A | 2 | a0002c0001t0002g0249a0002c0001t0002g0250 | 2 | NA18947.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.4866+1797G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3184267 | ||||||
| chr4:3184490
|
C | T | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.4866+2020C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3184490 | ||||||
| chr4:3184517
|
A | G | 187 | a0001c0003t0001g0197a0001c0003t0003g0115a0001c0089t0001g0037others(184): Show | 188 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.4866+2047A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3184517 | ||||||
| chr4:3184939
|
T | G | 1 | a0003c0006t0001g0038 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4867-1658T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3184939 | ||||||
| chr4:3185018
|
G | A | 1 | a0020c0079t0003g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4867-1579G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3185018 | ||||||
| chr4:3185116
|
A | G | 1 | a0001c0002t0001g0169 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4867-1481A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3185116 | ||||||
| chr4:3185151
|
A | G | 1 | a0069c0093t0003g0020 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4867-1446A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3185151 | ||||||
| chr4:3185201
|
GT | G | 3 | a0007c0058t0033g0009a0052c0061t0035g0252a0054c0068t0034g0090 | 3 | HG02145.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4867-1393delT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | INFO_REALIGN_3_PRIME | chr4 | 3185201 | |||||
| chr4:3185222
|
G | C | 1 | a0026c0026t0003g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4867-1375G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3185222 | ||||||
| chr4:3185228
|
G | A | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.4867-1369G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3185228 | ||||||
| chr4:3185265
|
C | T | 9 | a0001c0002t0001g0142a0001c0003t0001g0174a0009c0008t0001g0105others(6): Show | 9 | HG01074.hp1 HG01175.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.4867-1332C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3185265 | ||||||
| chr4:3185266
|
G | A | 25 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(22): Show | 25 | HG00642.hp1 HG01081.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.4867-1331G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3185266 | ||||||
| chr4:3185552
|
A | T | 1 | a0002c0001t0024g0238 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.4867-1045A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3185552 | ||||||
| chr4:3185636
|
G | A | 9 | a0023c0039t0015g0004a0023c0039t0016g0008a0024c0046t0008g0257others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.4867-961G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3185636 | ||||||
| chr4:3185847
|
G | A | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4867-750G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3185847 | ||||||
| chr4:3185852
|
T | C | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.4867-745T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3185852 | ||||||
| chr4:3186201
|
GAAAA | G | 9 | a0023c0039t0015g0004a0023c0039t0016g0008a0024c0046t0008g0257others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.4867-389_4867-386d others(6): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | INFO_REALIGN_3_PRIME | chr4 | 3186201 | |||||
| chr4:3186219
|
C | T | 1 | a0001c0003t0001g0114 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4867-378C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3186219 | ||||||
| chr4:3186252
|
G | A | 1 | a0015c0016t0006g0137 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4867-345G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3186252 | ||||||
| chr4:3186298
|
G | A | 1 | a0007c0058t0033g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4867-299G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3186298 | ||||||
| chr4:3186538
|
C | T | 56 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(53): Show | 56 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.4867-59C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 37/66 | chr4 | 3186538 | ||||||
| chr4:3186731
|
G | A | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4989+12G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 38/66 | chr4 | 3186731 | ||||||
| chr4:3186838
|
C | CT | 69 | a0001c0002t0001g0149a0001c0002t0001g0164a0001c0002t0001g0166others(66): Show | 69 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.4989+141dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 38/66 | INFO_REALIGN_3_PRIME | chr4 | 3186838 | |||||
| chr4:3186838
|
C | CTT | 9 | a0017c0018t0003g0091a0017c0018t0003g0097a0020c0079t0003g0186others(6): Show | 9 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.4989+140_4989+141d others(4): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 38/66 | INFO_REALIGN_3_PRIME | chr4 | 3186838 | |||||
| chr4:3186889
|
C | T | 2 | a0003c0024t0019g0109a0038c0124t0019g0107 | 2 | HG01928.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.4989+170C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 38/66 | chr4 | 3186889 | ||||||
| chr4:3186897
|
C | T | 3 | a0010c0009t0003g0291a0020c0079t0003g0186a0050c0065t0003g0286 | 3 | HG00642.hp1 HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.4989+178C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 38/66 | chr4 | 3186897 | ||||||
| chr4:3186976
|
A | T | 2 | a0023c0103t0003g0029a0080c0110t0003g0031 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.4989+257A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 38/66 | chr4 | 3186976 | ||||||
| chr4:3187101
|
C | T | 1 | a0052c0061t0035g0252 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4989+382C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 38/66 | chr4 | 3187101 | ||||||
| chr4:3187155
|
G | A | 1 | a0003c0105t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4989+436G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 38/66 | chr4 | 3187155 | ||||||
| chr4:3187260
|
A | G | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.4990-391A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 38/66 | chr4 | 3187260 | ||||||
| chr4:3187280
|
C | T | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.4990-371C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 38/66 | chr4 | 3187280 | ||||||
| chr4:3187281
|
G | A | 1 | a0040c0045t0002g0103 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.4990-370G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 38/66 | chr4 | 3187281 | ||||||
| chr4:3187310
|
T | C | 1 | a0001c0003t0001g0130 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4990-341T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 38/66 | chr4 | 3187310 | ||||||
| chr4:3187412
|
C | T | 2 | a0002c0001t0002g0244a0002c0001t0002g0248 | 2 | HG00741.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.4990-239C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 38/66 | chr4 | 3187412 | ||||||
| chr4:3187421
|
T | C | 2 | a0002c0001t0002g0244a0002c0001t0002g0248 | 2 | HG00741.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.4990-230T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 38/66 | chr4 | 3187421 | ||||||
| chr4:3187460
|
G | T | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4990-191G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 38/66 | chr4 | 3187460 | ||||||
| chr4:3187588
|
A | T | 1 | a0019c0020t0023g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4990-63A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 38/66 | chr4 | 3187588 | ||||||
| chr4:3188085
|
T | C | 56 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(53): Show | 56 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.5225+199T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 39/66 | chr4 | 3188085 | ||||||
| chr4:3188285
|
T | A | 56 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(53): Show | 56 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.5225+399T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 39/66 | chr4 | 3188285 | ||||||
| chr4:3188583
|
C | T | 1 | a0005c0004t0002g0242 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.5226-368C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 39/66 | chr4 | 3188583 | ||||||
| chr4:3188664
|
C | A | 8 | a0023c0039t0015g0004a0023c0039t0016g0008a0024c0046t0008g0257others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.5226-287C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 39/66 | chr4 | 3188664 | ||||||
| chr4:3188759
|
T | C | 146 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(143): Show | 146 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.5226-192T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 39/66 | chr4 | 3188759 | ||||||
| chr4:3188800
|
C | T | 1 | a0008c0010t0006g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5226-151C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 39/66 | chr4 | 3188800 | ||||||
| chr4:3188806
|
C | T | 31 | a0001c0003t0001g0077a0010c0009t0003g0276a0010c0009t0003g0277others(28): Show | 31 | HG00642.hp1 HG01081.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.5226-145C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 39/66 | chr4 | 3188806 | ||||||
| chr4:3188846
|
C | T | 17 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(14): Show | 17 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.5226-105C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 39/66 | chr4 | 3188846 | ||||||
| chr4:3188905
|
T | C | 1 | a0003c0105t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5226-46T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 39/66 | chr4 | 3188905 | ||||||
| chr4:3189385
|
C | T | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.5368+292C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3189385 | ||||||
| chr4:3189457
|
A | T | 1 | a0003c0105t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5368+364A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3189457 | ||||||
| chr4:3189622
|
G | A | 1 | a0003c0006t0001g0043 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.5368+529G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3189622 | ||||||
| chr4:3189712
|
AC | A | 10 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(7): Show | 10 | HG00642.hp1 HG01192.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.5368+620delC | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3189712 | ||||||
| chr4:3189785
|
G | C | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5368+692G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3189785 | ||||||
| chr4:3190091
|
C | T | 1 | a0055c0069t0001g0271 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.5368+998C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3190091 | ||||||
| chr4:3190113
|
G | A | 1 | a0038c0123t0001g0141 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.5368+1020G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3190113 | ||||||
| chr4:3190123
|
C | T | 1 | a0086c0118t0003g0067 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.5368+1030C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3190123 | ||||||
| chr4:3190279
|
C | T | 1 | a0053c0064t0001g0274 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.5368+1186C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3190279 | ||||||
| chr4:3190355
|
C | CA | 6 | a0007c0053t0003g0104a0007c0058t0033g0009a0010c0056t0007g0200others(3): Show | 6 | HG01884.hp1 HG02109.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.5368+1276dupA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | INFO_REALIGN_3_PRIME | chr4 | 3190355 | |||||
| chr4:3190355
|
C | CAA | 26 | a0010c0009t0003g0277a0010c0009t0003g0288a0010c0009t0003g0289others(23): Show | 26 | HG00642.hp1 HG01081.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.5368+1275_5368+127 others(6): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | INFO_REALIGN_3_PRIME | chr4 | 3190355 | |||||
| chr4:3190473
|
A | G | 77 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(74): Show | 77 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.5368+1380A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3190473 | ||||||
| chr4:3190664
|
C | T | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.5368+1571C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3190664 | ||||||
| chr4:3190680
|
C | T | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5368+1587C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3190680 | ||||||
| chr4:3190735
|
A | C | 1 | a0001c0003t0001g0129 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.5368+1642A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3190735 | ||||||
| chr4:3190813
|
G | A | 33 | a0001c0002t0001g0110a0001c0002t0001g0145a0001c0002t0001g0148others(30): Show | 33 | HG00423.hp1 HG01070.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.5368+1720G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3190813 | ||||||
| chr4:3190829
|
C | T | 2 | a0046c0055t0011g0204a0049c0063t0011g0203 | 2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5368+1736C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3190829 | ||||||
| chr4:3191052
|
G | A | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.5368+1959G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3191052 | ||||||
| chr4:3191154
|
G | GCTTT | 145 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(142): Show | 147 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.5368+2086_5368+208 others(8): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | INFO_REALIGN_3_PRIME | chr4 | 3191154 | |||||
| chr4:3191154
|
GCTTT | G | 75 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(72): Show | 75 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.5368+2086_5368+208 others(8): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | INFO_REALIGN_3_PRIME | chr4 | 3191154 | |||||
| chr4:3191230
|
A | G | 1 | a0001c0003t0004g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5368+2137A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3191230 | ||||||
| chr4:3191472
|
C | T | 25 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(22): Show | 25 | HG00642.hp1 HG01081.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.5368+2379C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3191472 | ||||||
| chr4:3192065
|
A | G | 5 | a0001c0002t0001g0169a0001c0002t0001g0170a0001c0002t0001g0173others(2): Show | 5 | HG02056.hp1 NA18954.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.5368+2972A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3192065 | ||||||
| chr4:3192290
|
C | T | 1 | a0061c0076t0003g0099 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.5368+3197C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3192290 | ||||||
| chr4:3192556
|
G | C | 1 | a0022c0023t0003g0013 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5368+3463G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3192556 | ||||||
| chr4:3192910
|
A | T | 5 | a0024c0046t0008g0257a0024c0047t0008g0258a0036c0107t0018g0065others(2): Show | 5 | HG00323.hp2 HG00639.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.5368+3817A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3192910 | ||||||
| chr4:3193135
|
G | A | 1 | a0008c0114t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.5368+4042G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3193135 | ||||||
| chr4:3193150
|
C | A | 1 | a0036c0107t0018g0065 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5368+4057C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3193150 | ||||||
| chr4:3193310
|
C | T | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.5368+4217C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3193310 | ||||||
| chr4:3193477
|
C | A | 1 | a0077c0102t0029g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5368+4384C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3193477 | ||||||
| chr4:3193523
|
G | A | 28 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(25): Show | 28 | HG00642.hp1 HG01081.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.5368+4430G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3193523 | ||||||
| chr4:3193648
|
G | C | 1 | a0036c0107t0018g0065 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5368+4555G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3193648 | ||||||
| chr4:3193675
|
G | T | 1 | a0005c0004t0002g0256 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.5368+4582G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3193675 | ||||||
| chr4:3194237
|
A | T | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.5368+5144A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3194237 | ||||||
| chr4:3194302
|
A | C | 148 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(145): Show | 150 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.5368+5209A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3194302 | ||||||
| chr4:3194884
|
A | G | 18 | a0001c0002t0001g0110a0001c0002t0001g0148a0001c0002t0001g0149others(15): Show | 18 | HG00423.hp1 NA18939.hp2 NA18951.hp2 others(15): Show |
intron_variant | MODIFIER | c.5369-4848A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3194884 | ||||||
| chr4:3195075
|
G | A | 1 | a0015c0016t0006g0137 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5369-4657G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3195075 | ||||||
| chr4:3195412
|
T | C | 3 | a0023c0039t0016g0008a0077c0102t0029g0006a0083c0116t0016g0005 | 3 | HG01243.hp1 HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.5369-4320T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3195412 | ||||||
| chr4:3195478
|
T | C | 288 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(285): Show | 290 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(287): Show |
intron_variant | MODIFIER | c.5369-4254T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3195478 | ||||||
| chr4:3195484
|
C | A | 2 | a0001c0002t0001g0170a0001c0002t0001g0173 | 2 | HG02056.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.5369-4248C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3195484 | ||||||
| chr4:3195826
|
C | T | 2 | a0010c0009t0003g0288a0010c0009t0003g0289 | 2 | HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.5369-3906C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3195826 | ||||||
| chr4:3195921
|
C | T | 12 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(9): Show | 12 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.5369-3811C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3195921 | ||||||
| chr4:3195926
|
T | G | 1 | a0033c0098t0001g0051 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.5369-3806T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3195926 | ||||||
| chr4:3195971
|
G | A | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.5369-3761G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3195971 | ||||||
| chr4:3196108
|
T | G | 1 | a0021c0021t0012g0265 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.5369-3624T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3196108 | ||||||
| chr4:3196243
|
T | C | 1 | a0003c0105t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5369-3489T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3196243 | ||||||
| chr4:3196319
|
A | G | 11 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(8): Show | 11 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.5369-3413A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3196319 | ||||||
| chr4:3196324
|
G | A | 7 | a0002c0001t0002g0216a0002c0001t0002g0217a0002c0001t0002g0263others(4): Show | 7 | HG00609.hp1 HG02523.hp2 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.5369-3408G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3196324 | ||||||
| chr4:3196574
|
T | C | 2 | a0002c0001t0002g0241a0002c0001t0002g0281 | 2 | NA18950.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.5369-3158T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3196574 | ||||||
| chr4:3196654
|
A | G | 1 | a0007c0007t0003g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5369-3078A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3196654 | ||||||
| chr4:3196663
|
C | T | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.5369-3069C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3196663 | ||||||
| chr4:3196678
|
C | T | 1 | a0002c0001t0002g0251 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5369-3054C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3196678 | ||||||
| chr4:3196732
|
C | T | 17 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(14): Show | 17 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.5369-3000C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3196732 | ||||||
| chr4:3196819
|
T | C | 1 | a0061c0076t0003g0099 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.5369-2913T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3196819 | ||||||
| chr4:3196846
|
C | T | 1 | a0019c0020t0023g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5369-2886C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3196846 | ||||||
| chr4:3196932
|
C | T | 1 | a0002c0001t0002g0212 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5369-2800C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3196932 | ||||||
| chr4:3197125
|
G | C | 1 | a0019c0020t0023g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5369-2607G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3197125 | ||||||
| chr4:3197189
|
C | A | 2 | a0002c0001t0002g0284a0002c0073t0002g0290 | 2 | HG01952.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.5369-2543C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3197189 | ||||||
| chr4:3197193
|
G | A | 7 | a0005c0004t0002g0209a0005c0004t0002g0228a0005c0004t0002g0230others(4): Show | 7 | NA18951.hp1 NA18956.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.5369-2539G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3197193 | ||||||
| chr4:3197682
|
A | T | 2 | a0002c0001t0002g0212a0002c0001t0002g0223 | 2 | HG03491.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.5369-2050A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3197682 | ||||||
| chr4:3197745
|
G | A | 1 | a0079c0106t0003g0074 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5369-1987G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3197745 | ||||||
| chr4:3197826
|
A | G | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.5369-1906A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3197826 | ||||||
| chr4:3197925
|
G | T | 22 | a0001c0003t0001g0197a0003c0006t0001g0041a0003c0006t0001g0043others(19): Show | 22 | HG00438.hp1 HG00673.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.5369-1807G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3197925 | ||||||
| chr4:3197990
|
A | G | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.5369-1742A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3197990 | ||||||
| chr4:3198164
|
T | C | 2 | a0046c0055t0011g0204a0049c0063t0011g0203 | 2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5369-1568T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3198164 | ||||||
| chr4:3198192
|
C | T | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.5369-1540C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3198192 | ||||||
| chr4:3198215
|
A | AT | 29 | a0001c0002t0001g0142a0001c0002t0001g0164a0001c0002t0001g0171others(26): Show | 29 | HG00323.hp2 HG00438.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.5369-1489dupT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | INFO_REALIGN_3_PRIME | chr4 | 3198215 | |||||
| chr4:3198215
|
A | ATTT | 12 | a0012c0012t0003g0087a0012c0012t0003g0095a0012c0012t0003g0096others(9): Show | 12 | HG01081.hp2 HG01243.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.5369-1491_5369-148 others(7): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | INFO_REALIGN_3_PRIME | chr4 | 3198215 | |||||
| chr4:3198215
|
A | ATTTT | 8 | a0012c0012t0003g0089a0012c0077t0003g0094a0017c0018t0003g0097others(5): Show | 8 | HG02055.hp1 HG02055.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.5369-1492_5369-148 others(8): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | INFO_REALIGN_3_PRIME | chr4 | 3198215 | |||||
| chr4:3198215
|
AT | A | 115 | a0001c0003t0001g0077a0001c0003t0004g0117a0001c0003t0004g0134others(112): Show | 116 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.5369-1489delT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | INFO_REALIGN_3_PRIME | chr4 | 3198215 | |||||
| chr4:3198215
|
ATT | A | 18 | a0002c0001t0002g0246a0002c0001t0002g0249a0003c0105t0001g0071others(15): Show | 19 | HG01256.hp2 HG01258.hp2 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.5369-1490_5369-148 others(6): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | INFO_REALIGN_3_PRIME | chr4 | 3198215 | |||||
| chr4:3198215
|
ATTTTTTT others(6): Show |
A | 3 | a0035c0042t0005g0076a0035c0042t0005g0085a0062c0082t0005g0083 | 3 | HG02723.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.5369-1501_5369-148 others(17): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | INFO_REALIGN_3_PRIME | chr4 | 3198215 | |||||
| chr4:3198215
|
ATTTTTTT others(8): Show |
A | 2 | a0003c0024t0019g0109a0038c0124t0019g0107 | 2 | HG01928.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.5369-1503_5369-148 others(19): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | INFO_REALIGN_3_PRIME | chr4 | 3198215 | |||||
| chr4:3198338
|
C | T | 1 | a0007c0053t0003g0104 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5369-1394C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3198338 | ||||||
| chr4:3198352
|
A | G | 141 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(138): Show | 141 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.5369-1380A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3198352 | ||||||
| chr4:3198386
|
G | A | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.5369-1346G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3198386 | ||||||
| chr4:3198505
|
G | A | 43 | a0005c0004t0002g0194a0005c0004t0002g0195a0010c0009t0003g0276others(40): Show | 43 | HG00642.hp1 HG00642.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.5369-1227G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3198505 | ||||||
| chr4:3198586
|
G | A | 1 | a0006c0099t0001g0047 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.5369-1146G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3198586 | ||||||
| chr4:3198817
|
G | A | 3 | a0007c0058t0033g0009a0052c0061t0035g0252a0054c0068t0034g0090 | 3 | HG02145.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5369-915G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3198817 | ||||||
| chr4:3198853
|
T | C | 1 | a0002c0001t0024g0238 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5369-879T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3198853 | ||||||
| chr4:3198866
|
A | C | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5369-866A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3198866 | ||||||
| chr4:3199020
|
A | G | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.5369-712A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3199020 | ||||||
| chr4:3199273
|
C | T | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.5369-459C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3199273 | ||||||
| chr4:3199323
|
C | T | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.5369-409C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3199323 | ||||||
| chr4:3199482
|
G | A | 25 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(22): Show | 25 | HG00642.hp1 HG01081.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.5369-250G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3199482 | ||||||
| chr4:3199677
|
T | C | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5369-55T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3199677 | ||||||
| chr4:3199690
|
C | T | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5369-42C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 40/66 | chr4 | 3199690 | ||||||
| chr4:3199969
|
C | T | 1 | a0019c0020t0023g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5576+30C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3199969 | ||||||
| chr4:3200194
|
C | T | 1 | a0092c0044t0015g0003 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5576+255C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3200194 | ||||||
| chr4:3200319
|
G | A | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.5576+380G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3200319 | ||||||
| chr4:3200411
|
G | A | 65 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(62): Show | 65 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.5576+472G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3200411 | ||||||
| chr4:3200496
|
A | G | 2 | a0012c0012t0003g0089a0020c0084t0003g0093 | 2 | HG02132.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.5576+557A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3200496 | ||||||
| chr4:3200585
|
G | A | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.5576+646G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3200585 | ||||||
| chr4:3200640
|
G | A | 1 | a0032c0036t0001g0140 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.5576+701G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3200640 | ||||||
| chr4:3200661
|
T | A | 50 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(47): Show | 50 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.5576+722T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3200661 | ||||||
| chr4:3200708
|
G | A | 2 | a0046c0055t0011g0204a0049c0063t0011g0203 | 2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5576+769G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3200708 | ||||||
| chr4:3200815
|
T | G | 1 | a0002c0001t0002g0227 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.5576+876T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3200815 | ||||||
| chr4:3200905
|
C | T | 12 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(9): Show | 12 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.5576+966C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3200905 | ||||||
| chr4:3200925
|
G | A | 2 | a0019c0020t0007g0088a0019c0020t0007g0102 | 2 | HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.5576+986G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3200925 | ||||||
| chr4:3201126
|
T | G | 1 | a0009c0008t0001g0168 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5576+1187T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3201126 | ||||||
| chr4:3201204
|
T | G | 5 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(2): Show | 5 | HG01884.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.5576+1265T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3201204 | ||||||
| chr4:3201284
|
C | T | 12 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(9): Show | 12 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.5576+1345C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3201284 | ||||||
| chr4:3201323
|
C | G | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5576+1384C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3201323 | ||||||
| chr4:3201529
|
C | CA | 34 | a0001c0002t0001g0166a0001c0002t0001g0171a0001c0002t0001g0172others(31): Show | 34 | HG00423.hp1 HG00597.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.5576+1614dupA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | INFO_REALIGN_3_PRIME | chr4 | 3201529 | |||||
| chr4:3201529
|
CA | C | 13 | a0001c0002t0001g0110a0001c0002t0001g0147a0001c0002t0001g0151others(10): Show | 13 | HG01168.hp1 HG01168.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.5576+1614delA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | INFO_REALIGN_3_PRIME | chr4 | 3201529 | |||||
| chr4:3201529
|
CAA | C | 28 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(25): Show | 28 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.5576+1613_5576+161 others(6): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | INFO_REALIGN_3_PRIME | chr4 | 3201529 | |||||
| chr4:3201573
|
T | G | 1 | a0007c0053t0003g0104 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5576+1634T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3201573 | ||||||
| chr4:3201851
|
A | G | 15 | a0012c0012t0003g0087a0012c0012t0003g0089a0012c0012t0003g0095others(12): Show | 15 | HG01081.hp2 HG01515.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.5576+1912A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3201851 | ||||||
| chr4:3202145
|
A | G | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.5577-1862A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3202145 | ||||||
| chr4:3202838
|
C | A | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.5577-1169C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3202838 | ||||||
| chr4:3202877
|
G | A | 1 | a0002c0001t0002g0279 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.5577-1130G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3202877 | ||||||
| chr4:3203390
|
G | A | 1 | a0052c0061t0035g0252 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.5577-617G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3203390 | ||||||
| chr4:3203391
|
A | G | 1 | a0052c0061t0035g0252 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.5577-616A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3203391 | ||||||
| chr4:3203452
|
C | T | 6 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(3): Show | 6 | HG01109.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5577-555C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3203452 | ||||||
| chr4:3203530
|
T | C | 1 | a0003c0006t0001g0038 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.5577-477T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3203530 | ||||||
| chr4:3203735
|
G | A | 1 | a0040c0045t0002g0103 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.5577-272G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3203735 | ||||||
| chr4:3203898
|
A | G | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5577-109A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 41/66 | chr4 | 3203898 | ||||||
| chr4:3204401
|
C | T | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.5718+253C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 42/66 | chr4 | 3204401 | ||||||
| chr4:3204500
|
C | T | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.5718+352C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 42/66 | chr4 | 3204500 | ||||||
| chr4:3204854
|
A | G | 1 | a0009c0008t0001g0168 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5718+706A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 42/66 | chr4 | 3204854 | ||||||
| chr4:3205133
|
A | G | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.5718+985A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 42/66 | chr4 | 3205133 | ||||||
| chr4:3205309
|
G | A | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.5718+1161G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 42/66 | chr4 | 3205309 | ||||||
| chr4:3205415
|
A | G | 149 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(146): Show | 149 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.5719-1081A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 42/66 | chr4 | 3205415 | ||||||
| chr4:3205695
|
A | G | 2 | a0013c0013t0001g0032a0013c0013t0001g0033 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.5719-801A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 42/66 | chr4 | 3205695 | ||||||
| chr4:3205757
|
C | T | 1 | a0091c0127t0004g0063 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5719-739C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 42/66 | chr4 | 3205757 | ||||||
| chr4:3206072
|
G | T | 7 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(4): Show | 7 | HG01109.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.5719-424G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 42/66 | chr4 | 3206072 | ||||||
| chr4:3206100
|
G | A | 49 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(46): Show | 49 | HG00423.hp1 HG00438.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.5719-396G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 42/66 | chr4 | 3206100 | ||||||
| chr4:3206774
|
G | A | 1 | a0002c0001t0002g0216 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.5899-33G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 43/66 | chr4 | 3206774 | ||||||
| chr4:3206993
|
A | C | 1 | a0044c0060t0001g0059 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.6075+10A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 44/66 | chr4 | 3206993 | ||||||
| chr4:3207149
|
T | C | 1 | a0056c0070t0001g0280 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.6076-132T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 44/66 | chr4 | 3207149 | ||||||
| chr4:3207204
|
C | T | 1 | a0023c0039t0015g0004 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.6076-77C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 44/66 | chr4 | 3207204 | ||||||
| chr4:3207412
|
A | G | 2 | a0039c0043t0001g0078a0067c0086t0025g0113 | 2 | HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.6152+55A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 45/66 | chr4 | 3207412 | ||||||
| chr4:3207498
|
C | T | 11 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(8): Show | 11 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.6152+141C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 45/66 | chr4 | 3207498 | ||||||
| chr4:3208272
|
C | T | 1 | a0007c0007t0003g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.6153-501C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 45/66 | chr4 | 3208272 | ||||||
| chr4:3208400
|
G | A | 1 | a0010c0009t0003g0276 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6153-373G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 45/66 | chr4 | 3208400 | ||||||
| chr4:3208469
|
C | T | 1 | a0026c0026t0003g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6153-304C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 45/66 | chr4 | 3208469 | ||||||
| chr4:3208603
|
A | T | 75 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(72): Show | 75 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.6153-170A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 45/66 | chr4 | 3208603 | ||||||
| chr4:3208719
|
T | TA | 9 | a0001c0002t0001g0181a0001c0002t0001g0199a0002c0001t0002g0251others(6): Show | 9 | HG03942.hp1 HG04199.hp1 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.6153-39dupA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 45/66 | INFO_REALIGN_3_PRIME | chr4 | 3208719 | |||||
| chr4:3208729
|
A | C | 25 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(22): Show | 25 | HG00642.hp1 HG01081.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.6153-44A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 45/66 | chr4 | 3208729 | ||||||
| chr4:3208732
|
A | C | 2 | a0002c0001t0002g0249a0002c0001t0002g0250 | 2 | NA18947.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.6153-41A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 45/66 | chr4 | 3208732 | ||||||
| chr4:3208735
|
C | A | 14 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(11): Show | 14 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.6153-38C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 45/66 | chr4 | 3208735 | ||||||
| chr4:3209211
|
C | G | 1 | a0016c0017t0006g0131 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.6291+300C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 46/66 | chr4 | 3209211 | ||||||
| chr4:3209240
|
T | A | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6291+329T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 46/66 | chr4 | 3209240 | ||||||
| chr4:3209333
|
GGAGCCTT others(4): Show |
G | 2 | a0001c0003t0001g0122a0001c0003t0001g0123 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.6291+445_6291+455d others(13): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 46/66 | INFO_REALIGN_3_PRIME | chr4 | 3209333 | |||||
| chr4:3209477
|
C | T | 1 | a0068c0087t0031g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6292-350C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 46/66 | chr4 | 3209477 | ||||||
| chr4:3209640
|
A | G | 1 | a0001c0089t0001g0037 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6292-187A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 46/66 | chr4 | 3209640 | ||||||
| chr4:3209796
|
A | T | 3 | a0023c0039t0016g0008a0077c0102t0029g0006a0083c0116t0016g0005 | 3 | HG01243.hp1 HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.6292-31A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 46/66 | chr4 | 3209796 | ||||||
| chr4:3210008
|
G | T | 1 | a0009c0008t0001g0180 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.6414+59G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3210008 | ||||||
| chr4:3210037
|
G | C | 2 | a0014c0014t0010g0011a0043c0050t0010g0012 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.6414+88G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3210037 | ||||||
| chr4:3210077
|
G | A | 1 | a0033c0098t0001g0051 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.6414+128G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3210077 | ||||||
| chr4:3210115
|
A | G | 8 | a0001c0003t0001g0122a0001c0003t0001g0123a0001c0003t0001g0127others(5): Show | 8 | HG00639.hp2 HG01099.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.6414+166A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3210115 | ||||||
| chr4:3210352
|
G | A | 41 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(38): Show | 41 | HG00642.hp1 HG01081.hp2 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.6414+403G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3210352 | ||||||
| chr4:3210521
|
A | T | 1 | a0044c0060t0001g0059 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.6414+572A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3210521 | ||||||
| chr4:3210590
|
G | A | 11 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(8): Show | 11 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.6414+641G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3210590 | ||||||
| chr4:3210609
|
T | TG | 109 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(106): Show | 109 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.6414+667dupG | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | INFO_REALIGN_3_PRIME | chr4 | 3210609 | |||||
| chr4:3210610
|
G | T | 2 | a0003c0006t0001g0045a0070c0092t0032g0030 | 2 | HG02258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.6414+661G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3210610 | ||||||
| chr4:3210613
|
G | T | 2 | a0046c0055t0011g0204a0049c0063t0011g0203 | 2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.6414+664G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3210613 | ||||||
| chr4:3210641
|
A | T | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6414+692A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3210641 | ||||||
| chr4:3210768
|
C | G | 1 | a0002c0001t0002g0244 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.6414+819C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3210768 | ||||||
| chr4:3210836
|
T | C | 290 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(287): Show | 292 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.6414+887T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3210836 | ||||||
| chr4:3210904
|
C | CTTTTTTT others(2): Show |
20 | a0012c0012t0003g0087a0012c0012t0003g0089a0012c0012t0003g0095others(17): Show | 20 | HG01081.hp2 HG01243.hp1 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.6414+962_6414+970d others(11): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | INFO_REALIGN_3_PRIME | chr4 | 3210904 | |||||
| chr4:3210904
|
C | CTTTTTTT others(3): Show |
24 | a0002c0001t0002g0247a0007c0007t0003g0023a0007c0058t0033g0009others(21): Show | 24 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.6414+961_6414+970d others(12): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | INFO_REALIGN_3_PRIME | chr4 | 3210904 | |||||
| chr4:3210904
|
C | CTTTTTTT others(4): Show |
73 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(70): Show | 73 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.6414+960_6414+970d others(13): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | INFO_REALIGN_3_PRIME | chr4 | 3210904 | |||||
| chr4:3210904
|
C | CTTTTTTT others(5): Show |
20 | a0002c0001t0002g0210a0002c0001t0002g0216a0002c0001t0002g0263others(17): Show | 20 | HG00609.hp1 HG01167.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.6414+959_6414+970d others(14): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | INFO_REALIGN_3_PRIME | chr4 | 3210904 | |||||
| chr4:3210904
|
C | CTTTTTTT others(6): Show |
2 | a0005c0004t0002g0242a0075c0094t0003g0064 | 2 | HG03579.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.6414+958_6414+970d others(15): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | INFO_REALIGN_3_PRIME | chr4 | 3210904 | |||||
| chr4:3210925
|
A | G | 53 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(50): Show | 53 | HG00642.hp1 HG00741.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.6414+976A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3210925 | ||||||
| chr4:3210974
|
C | T | 11 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(8): Show | 11 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.6415-955C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3210974 | ||||||
| chr4:3211060
|
C | T | 1 | a0013c0013t0028g0198 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.6415-869C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3211060 | ||||||
| chr4:3211147
|
G | A | 1 | a0065c0078t0004g0185 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.6415-782G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3211147 | ||||||
| chr4:3211195
|
C | T | 1 | a0005c0004t0002g0239 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.6415-734C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3211195 | ||||||
| chr4:3211421
|
A | G | 2 | a0039c0043t0001g0078a0067c0086t0025g0113 | 2 | HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.6415-508A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3211421 | ||||||
| chr4:3211528
|
A | G | 1 | a0005c0004t0002g0229 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.6415-401A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3211528 | ||||||
| chr4:3211537
|
G | T | 1 | a0012c0077t0003g0094 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.6415-392G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3211537 | ||||||
| chr4:3211564
|
G | A | 2 | a0017c0018t0003g0091a0017c0018t0003g0097 | 2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.6415-365G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 47/66 | chr4 | 3211564 | ||||||
| chr4:3212148
|
T | C | 41 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(38): Show | 41 | HG00642.hp1 HG00741.hp1 HG01081.hp2 others(38): Show |
splice_region_variant&intron_variant | LOW | c.6628+6T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 48/66 | chr4 | 3212148 | ||||||
| chr4:3212227
|
G | A | 11 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(8): Show | 11 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.6628+85G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 48/66 | chr4 | 3212227 | ||||||
| chr4:3212282
|
G | T | 1 | a0033c0097t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.6628+140G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 48/66 | chr4 | 3212282 | ||||||
| chr4:3212414
|
G | A | 2 | a0001c0002t0001g0147a0001c0002t0001g0155 | 2 | NA18984.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.6629-150G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 48/66 | chr4 | 3212414 | ||||||
| chr4:3212449
|
T | G | 2 | a0010c0009t0003g0288a0010c0009t0003g0289 | 2 | HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.6629-115T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 48/66 | chr4 | 3212449 | ||||||
| chr4:3212545
|
C | T | 1 | a0066c0083t0001g0119 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.6629-19C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 48/66 | chr4 | 3212545 | ||||||
| chr4:3212714
|
G | A | 1 | a0039c0043t0004g0073 | 1 | HG01081.hp1 | splice_region_variant&intron_variant | LOW | c.6774+5G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 49/66 | chr4 | 3212714 | ||||||
| chr4:3212733
|
G | A | 11 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(8): Show | 11 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.6774+24G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 49/66 | chr4 | 3212733 | ||||||
| chr4:3212805
|
T | G | 1 | a0001c0089t0001g0037 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6774+96T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 49/66 | chr4 | 3212805 | ||||||
| chr4:3212892
|
C | T | 1 | a0033c0097t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.6774+183C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 49/66 | chr4 | 3212892 | ||||||
| chr4:3212951
|
A | G | 1 | a0002c0001t0002g0220 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.6774+242A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 49/66 | chr4 | 3212951 | ||||||
| chr4:3213095
|
G | A | 1 | a0020c0052t0003g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.6774+386G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 49/66 | chr4 | 3213095 | ||||||
| chr4:3213152
|
G | A | 7 | a0028c0033t0001g0120a0028c0033t0001g0132a0029c0032t0001g0111others(4): Show | 7 | HG00597.hp1 NA19002.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.6774+443G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 49/66 | chr4 | 3213152 | ||||||
| chr4:3213369
|
G | T | 11 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(8): Show | 11 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.6775-589G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 49/66 | chr4 | 3213369 | ||||||
| chr4:3213392
|
T | C | 1 | a0014c0014t0010g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.6775-566T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 49/66 | chr4 | 3213392 | ||||||
| chr4:3213429
|
G | A | 1 | a0033c0098t0001g0051 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.6775-529G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 49/66 | chr4 | 3213429 | ||||||
| chr4:3213943
|
G | T | 3 | a0004c0011t0001g0153a0004c0011t0001g0160a0004c0011t0001g0165 | 3 | NA18983.hp2 NA18991.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.6775-15G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 49/66 | chr4 | 3213943 | ||||||
| chr4:3214385
|
A | G | 1 | a0039c0043t0004g0073 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.6952+250A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 50/66 | chr4 | 3214385 | ||||||
| chr4:3214543
|
C | G | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.6952+408C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 50/66 | chr4 | 3214543 | ||||||
| chr4:3214605
|
A | G | 11 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(8): Show | 11 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.6952+470A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 50/66 | chr4 | 3214605 | ||||||
| chr4:3214677
|
A | T | 1 | a0043c0050t0010g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6953-433A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 50/66 | chr4 | 3214677 | ||||||
| chr4:3214705
|
GT | G | 30 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(27): Show | 30 | HG00642.hp1 HG00741.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.6953-402delT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 50/66 | INFO_REALIGN_3_PRIME | chr4 | 3214705 | |||||
| chr4:3214757
|
C | T | 2 | a0020c0052t0003g0292a0058c0071t0001g0270 | 2 | HG00741.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.6953-353C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 50/66 | chr4 | 3214757 | ||||||
| chr4:3214765
|
T | G | 1 | a0007c0058t0033g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6953-345T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 50/66 | chr4 | 3214765 | ||||||
| chr4:3214767
|
C | A | 1 | a0033c0098t0001g0051 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.6953-343C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 50/66 | chr4 | 3214767 | ||||||
| chr4:3214793
|
G | T | 2 | a0012c0012t0003g0087a0072c0096t0003g0086 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.6953-317G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 50/66 | chr4 | 3214793 | ||||||
| chr4:3214815
|
T | TAATGA | 57 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(54): Show | 57 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.6953-294_6953-293i others(7): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 50/66 | INFO_REALIGN_3_PRIME | chr4 | 3214815 | |||||
| chr4:3214821
|
G | A | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.6953-289G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 50/66 | chr4 | 3214821 | ||||||
| chr4:3215088
|
C | G | 143 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(140): Show | 143 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.6953-22C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 50/66 | chr4 | 3215088 | ||||||
| chr4:3215311
|
C | T | 6 | a0023c0039t0015g0004a0023c0039t0016g0008a0032c0036t0001g0140others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.7054+100C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3215311 | ||||||
| chr4:3215325
|
G | T | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.7054+114G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3215325 | ||||||
| chr4:3215424
|
G | T | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7054+213G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3215424 | ||||||
| chr4:3215484
|
G | A | 1 | a0033c0098t0001g0051 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.7054+273G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3215484 | ||||||
| chr4:3215565
|
T | A | 11 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(8): Show | 11 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.7054+354T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3215565 | ||||||
| chr4:3215569
|
C | T | 1 | a0019c0020t0007g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7054+358C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3215569 | ||||||
| chr4:3215639
|
A | G | 2 | a0001c0003t0001g0129a0003c0006t0001g0038 | 2 | HG02135.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.7054+428A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3215639 | ||||||
| chr4:3215677
|
G | A | 1 | a0033c0098t0001g0051 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.7054+466G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3215677 | ||||||
| chr4:3215776
|
G | A | 11 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(8): Show | 11 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.7054+565G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3215776 | ||||||
| chr4:3216165
|
C | T | 1 | a0026c0026t0003g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.7054+954C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3216165 | ||||||
| chr4:3216191
|
G | A | 1 | a0003c0105t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.7054+980G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3216191 | ||||||
| chr4:3216232
|
G | A | 1 | a0008c0010t0001g0068 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.7054+1021G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3216232 | ||||||
| chr4:3216378
|
C | T | 1 | a0016c0017t0006g0131 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.7054+1167C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3216378 | ||||||
| chr4:3216439
|
C | T | 2 | a0014c0014t0003g0014a0090c0126t0003g0018 | 2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.7054+1228C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3216439 | ||||||
| chr4:3216454
|
C | T | 1 | a0002c0001t0002g0247 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.7054+1243C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3216454 | ||||||
| chr4:3216476
|
A | G | 1 | a0033c0098t0001g0051 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.7054+1265A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3216476 | ||||||
| chr4:3216489
|
C | T | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7055-1276C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3216489 | ||||||
| chr4:3216697
|
C | T | 1 | a0008c0113t0001g0040 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.7055-1068C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3216697 | ||||||
| chr4:3216704
|
A | G | 1 | a0019c0020t0023g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.7055-1061A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3216704 | ||||||
| chr4:3216780
|
CT | C | 3 | a0019c0020t0007g0088a0019c0020t0007g0102a0068c0087t0031g0101 | 3 | HG01884.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7055-982delT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | INFO_REALIGN_3_PRIME | chr4 | 3216780 | |||||
| chr4:3216791
|
C | T | 2 | a0028c0033t0001g0120a0045c0051t0001g0048 | 2 | HG01891.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.7055-974C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3216791 | ||||||
| chr4:3216821
|
C | T | 1 | a0069c0093t0003g0020 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.7055-944C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3216821 | ||||||
| chr4:3216832
|
C | T | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.7055-933C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3216832 | ||||||
| chr4:3216833
|
A | G | 5 | a0023c0039t0015g0004a0023c0039t0016g0008a0077c0102t0029g0006others(2): Show | 5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.7055-932A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3216833 | ||||||
| chr4:3216888
|
A | G | 1 | a0033c0097t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7055-877A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3216888 | ||||||
| chr4:3216893
|
C | T | 2 | a0033c0097t0001g0061a0033c0098t0001g0051 | 2 | HG02647.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.7055-872C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3216893 | ||||||
| chr4:3216894
|
G | A | 3 | a0035c0042t0005g0076a0035c0042t0005g0085a0062c0082t0005g0083 | 3 | HG02723.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.7055-871G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3216894 | ||||||
| chr4:3216979
|
C | G | 2 | a0012c0012t0003g0095a0012c0012t0003g0096 | 2 | HG01081.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.7055-786C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3216979 | ||||||
| chr4:3216981
|
C | T | 1 | a0001c0003t0001g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.7055-784C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3216981 | ||||||
| chr4:3217012
|
A | G | 147 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(144): Show | 147 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.7055-753A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3217012 | ||||||
| chr4:3217024
|
C | CA | 15 | a0001c0002t0001g0145a0001c0002t0001g0150a0001c0002t0001g0169others(12): Show | 15 | HG00597.hp2 HG02056.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.7055-726dupA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | INFO_REALIGN_3_PRIME | chr4 | 3217024 | |||||
| chr4:3217040
|
T | A | 6 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(3): Show | 6 | HG01884.hp1 HG02132.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.7055-725T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3217040 | ||||||
| chr4:3217326
|
C | T | 69 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(66): Show | 69 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.7055-439C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3217326 | ||||||
| chr4:3217533
|
C | G | 6 | a0023c0039t0015g0004a0023c0039t0016g0008a0070c0092t0032g0030others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.7055-232C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3217533 | ||||||
| chr4:3217536
|
G | A | 1 | a0001c0002t0001g0155 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.7055-229G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3217536 | ||||||
| chr4:3217599
|
T | C | 35 | a0007c0058t0033g0009a0010c0009t0003g0276a0010c0009t0003g0277others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.7055-166T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3217599 | ||||||
| chr4:3217619
|
G | A | 1 | a0033c0098t0001g0051 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.7055-146G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 51/66 | chr4 | 3217619 | ||||||
| chr4:3218126
|
G | A | 1 | a0033c0097t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7242+174G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3218126 | ||||||
| chr4:3218134
|
C | A | 1 | a0002c0001t0024g0238 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.7242+182C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3218134 | ||||||
| chr4:3218283
|
G | A | 7 | a0002c0001t0002g0216a0002c0001t0002g0217a0002c0001t0002g0263others(4): Show | 7 | HG00609.hp1 HG02523.hp2 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.7242+331G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3218283 | ||||||
| chr4:3218320
|
G | A | 1 | a0002c0030t0002g0213 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.7242+368G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3218320 | ||||||
| chr4:3218360
|
C | T | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7242+408C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3218360 | ||||||
| chr4:3218519
|
G | A | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.7242+567G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3218519 | ||||||
| chr4:3218581
|
C | T | 1 | a0002c0001t0002g0211 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.7242+629C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3218581 | ||||||
| chr4:3218632
|
C | CA | 8 | a0002c0001t0013g0224a0002c0001t0013g0225a0012c0012t0003g0095others(5): Show | 8 | HG00673.hp2 HG01081.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.7242+692dupA | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | INFO_REALIGN_3_PRIME | chr4 | 3218632 | |||||
| chr4:3218768
|
C | T | 1 | a0026c0026t0003g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.7242+816C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3218768 | ||||||
| chr4:3218951
|
G | A | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7242+999G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3218951 | ||||||
| chr4:3219034
|
C | T | 6 | a0009c0008t0001g0105a0009c0008t0001g0157a0009c0008t0001g0167others(3): Show | 6 | HG01074.hp1 HG01928.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.7242+1082C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3219034 | ||||||
| chr4:3219182
|
T | C | 1 | a0010c0056t0007g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7243-1000T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3219182 | ||||||
| chr4:3219190
|
G | A | 1 | a0001c0003t0001g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.7243-992G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3219190 | ||||||
| chr4:3219352
|
A | G | 1 | a0054c0068t0034g0090 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.7243-830A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3219352 | ||||||
| chr4:3219557
|
A | G | 4 | a0024c0046t0008g0257a0024c0047t0008g0258a0033c0098t0001g0051others(1): Show | 4 | HG00323.hp2 HG00639.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.7243-625A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3219557 | ||||||
| chr4:3219599
|
C | T | 31 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(28): Show | 31 | HG00642.hp1 HG00741.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.7243-583C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3219599 | ||||||
| chr4:3219638
|
A | G | 16 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(13): Show | 16 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.7243-544A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3219638 | ||||||
| chr4:3219688
|
A | C | 2 | a0002c0001t0002g0263a0060c0088t0002g0261 | 2 | HG00609.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.7243-494A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3219688 | ||||||
| chr4:3219923
|
C | T | 4 | a0024c0046t0008g0257a0024c0047t0008g0258a0033c0098t0001g0051others(1): Show | 4 | HG00323.hp2 HG00639.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.7243-259C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3219923 | ||||||
| chr4:3219937
|
GC | G | 4 | a0017c0018t0003g0091a0017c0018t0003g0092a0017c0018t0003g0097others(1): Show | 4 | HG01975.hp2 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.7243-243delC | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | INFO_REALIGN_3_PRIME | chr4 | 3219937 | |||||
| chr4:3219940
|
A | G | 4 | a0017c0018t0003g0091a0017c0018t0003g0092a0017c0018t0003g0097others(1): Show | 4 | HG01975.hp2 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.7243-242A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3219940 | ||||||
| chr4:3219956
|
G | C | 3 | a0007c0058t0033g0009a0052c0061t0035g0252a0054c0068t0034g0090 | 3 | HG02145.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.7243-226G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3219956 | ||||||
| chr4:3220145
|
C | G | 34 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(31): Show | 34 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.7243-37C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 52/66 | chr4 | 3220145 | ||||||
| chr4:3220345
|
G | A | 1 | a0011c0028t0001g0236 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.7369+37G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 53/66 | chr4 | 3220345 | ||||||
| chr4:3220737
|
G | A | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.7369+429G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 53/66 | chr4 | 3220737 | ||||||
| chr4:3220842
|
C | T | 2 | a0001c0003t0001g0129a0004c0067t0001g0118 | 2 | HG00735.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.7369+534C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 53/66 | chr4 | 3220842 | ||||||
| chr4:3220856
|
G | T | 34 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(31): Show | 34 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.7369+548G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 53/66 | chr4 | 3220856 | ||||||
| chr4:3220904
|
G | A | 1 | a0079c0106t0003g0074 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.7369+596G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 53/66 | chr4 | 3220904 | ||||||
| chr4:3221338
|
A | G | 3 | a0007c0058t0033g0009a0054c0068t0034g0090a0068c0087t0031g0101 | 3 | HG01884.hp1 HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.7369+1030A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 53/66 | chr4 | 3221338 | ||||||
| chr4:3221523
|
A | G | 96 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(93): Show | 96 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.7370-864A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 53/66 | chr4 | 3221523 | ||||||
| chr4:3221777
|
G | A | 7 | a0023c0039t0015g0004a0023c0039t0016g0008a0033c0098t0001g0051others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.7370-610G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 53/66 | chr4 | 3221777 | ||||||
| chr4:3221802
|
C | T | 4 | a0007c0058t0033g0009a0033c0097t0001g0061a0052c0061t0035g0252others(1): Show | 4 | HG02145.hp1 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.7370-585C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 53/66 | chr4 | 3221802 | ||||||
| chr4:3221822
|
C | G | 1 | a0002c0001t0002g0248 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.7370-565C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 53/66 | chr4 | 3221822 | ||||||
| chr4:3222164
|
T | C | 147 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(144): Show | 147 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.7370-223T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 53/66 | chr4 | 3222164 | ||||||
| chr4:3222198
|
C | T | 1 | a0075c0094t0003g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.7370-189C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 53/66 | chr4 | 3222198 | ||||||
| chr4:3222302
|
C | G | 1 | a0002c0001t0002g0282 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.7370-85C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 53/66 | chr4 | 3222302 | ||||||
| chr4:3222612
|
T | C | 1 | a0010c0009t0003g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.7470+125T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 54/66 | chr4 | 3222612 | ||||||
| chr4:3222708
|
C | T | 1 | a0003c0105t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.7470+221C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 54/66 | chr4 | 3222708 | ||||||
| chr4:3222736
|
G | A | 1 | a0033c0097t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7470+249G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 54/66 | chr4 | 3222736 | ||||||
| chr4:3222861
|
T | C | 1 | a0033c0098t0001g0051 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.7470+374T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 54/66 | chr4 | 3222861 | ||||||
| chr4:3222875
|
C | T | 79 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(76): Show | 79 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.7470+388C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 54/66 | chr4 | 3222875 | ||||||
| chr4:3223039
|
A | G | 14 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(11): Show | 14 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.7471-367A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 54/66 | chr4 | 3223039 | ||||||
| chr4:3223206
|
T | G | 140 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(137): Show | 140 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.7471-200T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 54/66 | chr4 | 3223206 | ||||||
| chr4:3223233
|
C | T | 1 | a0010c0009t0003g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.7471-173C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 54/66 | chr4 | 3223233 | ||||||
| chr4:3223252
|
C | G | 1 | a0003c0128t0026g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.7471-154C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 54/66 | chr4 | 3223252 | ||||||
| chr4:3223355
|
G | C | 14 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(11): Show | 14 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.7471-51G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 54/66 | chr4 | 3223355 | ||||||
| chr4:3223630
|
G | A | 2 | a0002c0031t0002g0226a0002c0031t0002g0253 | 2 | NA18999.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.7625+70G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 55/66 | chr4 | 3223630 | ||||||
| chr4:3223644
|
A | C | 99 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(96): Show | 99 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.7625+84A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 55/66 | chr4 | 3223644 | ||||||
| chr4:3223662
|
A | G | 140 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(137): Show | 140 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.7625+102A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 55/66 | chr4 | 3223662 | ||||||
| chr4:3223700
|
A | C | 14 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(11): Show | 14 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.7625+140A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 55/66 | chr4 | 3223700 | ||||||
| chr4:3223739
|
A | G | 99 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(96): Show | 99 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.7625+179A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 55/66 | chr4 | 3223739 | ||||||
| chr4:3223751
|
T | C | 140 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(137): Show | 140 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.7625+191T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 55/66 | chr4 | 3223751 | ||||||
| chr4:3223764
|
C | T | 1 | a0002c0001t0002g0246 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.7625+204C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 55/66 | chr4 | 3223764 | ||||||
| chr4:3223824
|
G | C | 1 | a0076c0101t0002g0266 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.7626-168G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 55/66 | chr4 | 3223824 | ||||||
| chr4:3224141
|
G | A | 14 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(11): Show | 14 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.7765+10G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 56/66 | chr4 | 3224141 | ||||||
| chr4:3224188
|
A | C | 1 | a0004c0066t0001g0159 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.7765+57A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 56/66 | chr4 | 3224188 | ||||||
| chr4:3224301
|
G | A | 1 | a0033c0098t0001g0051 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.7765+170G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 56/66 | chr4 | 3224301 | ||||||
| chr4:3224377
|
C | T | 1 | a0001c0002t0001g0177 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.7765+246C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 56/66 | chr4 | 3224377 | ||||||
| chr4:3224460
|
A | C | 1 | a0016c0017t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.7765+329A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 56/66 | chr4 | 3224460 | ||||||
| chr4:3224461
|
A | G | 2 | a0010c0056t0007g0200a0046c0055t0011g0204 | 2 | HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.7765+330A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 56/66 | chr4 | 3224461 | ||||||
| chr4:3224514
|
C | A | 3 | a0019c0020t0007g0088a0019c0020t0007g0102a0068c0087t0031g0101 | 3 | HG01884.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7765+383C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 56/66 | chr4 | 3224514 | ||||||
| chr4:3224598
|
C | T | 1 | a0016c0017t0001g0125 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.7765+467C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 56/66 | chr4 | 3224598 | ||||||
| chr4:3224707
|
G | A | 36 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(33): Show | 36 | HG00642.hp1 HG00738.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.7765+576G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 56/66 | chr4 | 3224707 | ||||||
| chr4:3224746
|
C | T | 1 | a0021c0021t0012g0231 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.7765+615C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 56/66 | chr4 | 3224746 | ||||||
| chr4:3224777
|
A | G | 1 | a0006c0015t0001g0139 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.7765+646A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 56/66 | chr4 | 3224777 | ||||||
| chr4:3225065
|
G | A | 1 | a0082c0112t0001g0126 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.7766-596G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 56/66 | chr4 | 3225065 | ||||||
| chr4:3225157
|
G | T | 3 | a0001c0002t0001g0181a0003c0041t0001g0143a0003c0041t0001g0144 | 3 | NA18961.hp1 NA18999.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.7766-504G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 56/66 | chr4 | 3225157 | ||||||
| chr4:3225197
|
G | A | 8 | a0001c0002t0001g0142a0006c0015t0001g0139a0009c0008t0001g0105others(5): Show | 8 | HG01074.hp1 HG01175.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.7766-464G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 56/66 | chr4 | 3225197 | ||||||
| chr4:3225318
|
G | A | 1 | a0033c0098t0001g0051 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.7766-343G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 56/66 | chr4 | 3225318 | ||||||
| chr4:3225756
|
C | A | 8 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(5): Show | 8 | HG00738.hp1 HG01109.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.7848+13C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3225756 | ||||||
| chr4:3225812
|
C | T | 19 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(16): Show | 19 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.7848+69C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3225812 | ||||||
| chr4:3225865
|
T | A | 146 | a0001c0003t0004g0117a0002c0001t0002g0191a0002c0001t0002g0193others(143): Show | 146 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.7848+122T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3225865 | ||||||
| chr4:3225918
|
A | G | 8 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(5): Show | 8 | HG00738.hp1 HG01109.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.7848+175A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3225918 | ||||||
| chr4:3226026
|
C | T | 3 | a0019c0020t0007g0088a0019c0020t0007g0102a0068c0087t0031g0101 | 3 | HG01884.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7848+283C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3226026 | ||||||
| chr4:3226137
|
G | A | 1 | a0082c0112t0001g0126 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.7848+394G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3226137 | ||||||
| chr4:3226137
|
G | T | 1 | a0001c0002t0001g0181 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.7848+394G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3226137 | ||||||
| chr4:3226612
|
G | T | 1 | a0074c0095t0002g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.7848+869G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3226612 | ||||||
| chr4:3226740
|
T | A | 1 | a0001c0085t0001g0152 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.7848+997T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3226740 | ||||||
| chr4:3226765
|
A | G | 117 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(114): Show | 117 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.7848+1022A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3226765 | ||||||
| chr4:3226820
|
C | T | 1 | a0003c0024t0001g0079 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.7848+1077C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3226820 | ||||||
| chr4:3226931
|
C | T | 10 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(7): Show | 10 | HG01167.hp1 HG01243.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.7848+1188C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3226931 | ||||||
| chr4:3227089
|
G | A | 1 | a0039c0043t0004g0073 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.7848+1346G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3227089 | ||||||
| chr4:3227187
|
A | T | 1 | a0004c0067t0001g0118 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.7849-1428A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3227187 | ||||||
| chr4:3227211
|
C | CCCACCCC others(27): Show |
1 | a0004c0005t0001g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.7849-1376_7849-134 others(38): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | INFO_REALIGN_3_PRIME | chr4 | 3227211 | |||||
| chr4:3227211
|
CCCACCCC others(61): Show |
C | 36 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(33): Show | 36 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.7849-1327_7849-126 others(72): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | INFO_REALIGN_3_PRIME | chr4 | 3227211 | |||||
| chr4:3227239
|
T | G | 87 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(84): Show | 87 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.7849-1376T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3227239 | ||||||
| chr4:3227239
|
TACAGTGC others(367): Show |
T | 2 | a0012c0012t0003g0089a0020c0084t0003g0093 | 2 | HG02132.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.7849-1308_7849-935 others(3): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | INFO_REALIGN_3_PRIME | chr4 | 3227239 | |||||
| chr4:3227254
|
GCCCTGTC others(95): Show |
G | 1 | a0001c0003t0001g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.7849-1308_7849-120 others(4): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | INFO_REALIGN_3_PRIME | chr4 | 3227254 | |||||
| chr4:3227273
|
GACAGTGC others(27): Show |
G | 1 | a0058c0071t0001g0270 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7849-1308_7849-127 others(38): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | INFO_REALIGN_3_PRIME | chr4 | 3227273 | |||||
| chr4:3227307
|
T | TACAGTGC others(61): Show |
1 | a0068c0087t0031g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7849-1275_7849-127 others(72): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | INFO_REALIGN_3_PRIME | chr4 | 3227307 | |||||
| chr4:3227307
|
T | TACAGTGC others(95): Show |
3 | a0019c0020t0007g0088a0019c0020t0007g0102a0033c0097t0001g0061 | 3 | HG02647.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7849-1275_7849-127 others(106): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | INFO_REALIGN_3_PRIME | chr4 | 3227307 | |||||
| chr4:3227322
|
G | GCCCTGTC others(27): Show |
1 | a0005c0090t0002g0215 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.7849-1275_7849-127 others(38): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | INFO_REALIGN_3_PRIME | chr4 | 3227322 | |||||
| chr4:3227322
|
G | T | 3 | a0014c0014t0010g0011a0043c0050t0010g0012a0058c0071t0001g0270 | 3 | HG00741.hp1 HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.7849-1293G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3227322 | ||||||
| chr4:3227341
|
G | T | 91 | a0002c0001t0002g0191a0002c0001t0002g0206a0002c0001t0002g0208others(88): Show | 91 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.7849-1274G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3227341 | ||||||
| chr4:3227356
|
T | G | 5 | a0019c0020t0007g0088a0019c0020t0007g0102a0033c0097t0001g0061others(2): Show | 5 | HG00741.hp1 HG01884.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.7849-1259T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3227356 | ||||||
| chr4:3227356
|
T | TCCCTGTC others(27): Show |
1 | a0004c0005t0001g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.7849-805_7849-772d others(36): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | INFO_REALIGN_3_PRIME | chr4 | 3227356 | |||||
| chr4:3227356
|
TCCCTGTC others(27): Show |
T | 162 | a0001c0002t0001g0110a0001c0002t0001g0145a0001c0002t0001g0147others(159): Show | 162 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.7849-805_7849-772d others(36): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | INFO_REALIGN_3_PRIME | chr4 | 3227356 | |||||
| chr4:3227356
|
TCCCTGTC others(61): Show |
T | 18 | a0001c0002t0001g0142a0001c0002t0001g0150a0001c0002t0001g0151others(15): Show | 18 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.7849-839_7849-772d others(70): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | INFO_REALIGN_3_PRIME | chr4 | 3227356 | |||||
| chr4:3227356
|
TCCCTGTC others(95): Show |
T | 4 | a0001c0085t0001g0152a0033c0098t0001g0051a0063c0081t0001g0133others(1): Show | 4 | HG02258.hp1 HG03195.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.7849-873_7849-772d others(2): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | INFO_REALIGN_3_PRIME | chr4 | 3227356 | |||||
| chr4:3227356
|
TCCCTGTC others(129): Show |
T | 34 | a0002c0001t0002g0241a0002c0001t0002g0281a0007c0007t0003g0023others(31): Show | 34 | HG00642.hp1 HG00738.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.7849-907_7849-772d others(2): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | INFO_REALIGN_3_PRIME | chr4 | 3227356 | |||||
| chr4:3227356
|
TCCCTGTC others(163): Show |
T | 20 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(17): Show | 20 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.7849-941_7849-772d others(2): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | INFO_REALIGN_3_PRIME | chr4 | 3227356 | |||||
| chr4:3227356
|
TCCCTGTC others(197): Show |
T | 1 | a0007c0053t0003g0104 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7849-975_7849-772d others(2): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | INFO_REALIGN_3_PRIME | chr4 | 3227356 | |||||
| chr4:3227390
|
G | T | 15 | a0002c0001t0002g0206a0002c0001t0002g0208a0002c0001t0002g0237others(12): Show | 15 | HG00597.hp2 HG01952.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.7849-1225G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3227390 | ||||||
| chr4:3227453
|
CCCCTGCC others(26): Show |
C | 1 | a0001c0002t0001g0171 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.7849-1158_7849-112 others(37): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | INFO_REALIGN_3_PRIME | chr4 | 3227453 | |||||
| chr4:3227458
|
G | T | 1 | a0001c0003t0001g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.7849-1157G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3227458 | ||||||
| chr4:3227492
|
G | T | 1 | a0033c0098t0001g0051 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.7849-1123G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3227492 | ||||||
| chr4:3227549
|
G | A | 1 | a0002c0001t0002g0244 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.7849-1066G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3227549 | ||||||
| chr4:3227594
|
G | T | 1 | a0033c0098t0001g0051 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.7849-1021G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3227594 | ||||||
| chr4:3227628
|
G | T | 1 | a0033c0098t0001g0051 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.7849-987G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3227628 | ||||||
| chr4:3227719
|
G | A | 2 | a0003c0006t0001g0045a0003c0006t0001g0052 | 2 | HG01257.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.7849-896G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3227719 | ||||||
| chr4:3227749
|
G | T | 19 | a0014c0014t0003g0014a0014c0014t0003g0015a0014c0014t0003g0021others(16): Show | 19 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.7849-866G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3227749 | ||||||
| chr4:3227903
|
G | A | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7849-712G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3227903 | ||||||
| chr4:3228166
|
G | A | 3 | a0019c0020t0007g0088a0019c0020t0007g0102a0068c0087t0031g0101 | 3 | HG01884.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7849-449G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3228166 | ||||||
| chr4:3228507
|
G | C | 2 | a0025c0025t0002g0187a0025c0025t0002g0188 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.7849-108G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3228507 | ||||||
| chr4:3228579
|
G | T | 2 | a0019c0020t0007g0088a0019c0020t0007g0102 | 2 | HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7849-36G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 57/66 | chr4 | 3228579 | ||||||
| chr4:3229044
|
C | T | 8 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(5): Show | 8 | HG01109.hp1 HG02109.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.8109+35C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | chr4 | 3229044 | ||||||
| chr4:3229073
|
CCCCACAC others(10): Show |
C | 7 | a0005c0004t0002g0209a0005c0004t0002g0228a0005c0004t0002g0230others(4): Show | 7 | NA18951.hp1 NA18956.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.8109+75_8109+91del others(17): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | INFO_REALIGN_3_PRIME | chr4 | 3229073 | |||||
| chr4:3229077
|
A | C | 137 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(134): Show | 138 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.8109+68A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | chr4 | 3229077 | ||||||
| chr4:3229079
|
A | C | 1 | a0016c0017t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.8109+70A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | chr4 | 3229079 | ||||||
| chr4:3229086
|
C | T | 1 | a0002c0073t0002g0290 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.8109+77C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | chr4 | 3229086 | ||||||
| chr4:3229246
|
G | A | 42 | a0001c0003t0004g0117a0001c0003t0004g0134a0007c0007t0003g0023others(39): Show | 43 | HG00642.hp1 HG01074.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.8109+237G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | chr4 | 3229246 | ||||||
| chr4:3229261
|
CCACACAC others(10): Show |
C | 106 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(103): Show | 106 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.8109+261_8109+277d others(19): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | INFO_REALIGN_3_PRIME | chr4 | 3229261 | |||||
| chr4:3229266
|
C | A | 1 | a0001c0002t0001g0181 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.8109+257C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | chr4 | 3229266 | ||||||
| chr4:3229302
|
CCA | C | 111 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(108): Show | 111 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.8109+311_8109+312d others(4): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | INFO_REALIGN_3_PRIME | chr4 | 3229302 | |||||
| chr4:3229302
|
CCACA | C | 124 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(121): Show | 124 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.8109+309_8109+312d others(6): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | INFO_REALIGN_3_PRIME | chr4 | 3229302 | |||||
| chr4:3229389
|
A | G | 3 | a0007c0058t0033g0009a0052c0061t0035g0252a0054c0068t0034g0090 | 3 | HG02145.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.8109+380A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | chr4 | 3229389 | ||||||
| chr4:3229392
|
C | A | 4 | a0002c0001t0002g0208a0002c0001t0002g0282a0002c0001t0002g0284others(1): Show | 4 | HG01952.hp1 HG02148.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.8109+383C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | chr4 | 3229392 | ||||||
| chr4:3229419
|
CAG | C | 37 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(34): Show | 37 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.8109+411_8109+412d others(4): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | chr4 | 3229419 | ||||||
| chr4:3229421
|
G | C | 105 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(102): Show | 105 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.8109+412G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | chr4 | 3229421 | ||||||
| chr4:3229427
|
AACCACAC others(6): Show |
A | 1 | a0006c0015t0001g0139 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.8109+432_8110-434d others(15): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | INFO_REALIGN_3_PRIME | chr4 | 3229427 | |||||
| chr4:3229437
|
A | G | 1 | a0010c0056t0007g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8109+428A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | chr4 | 3229437 | ||||||
| chr4:3229496
|
G | A | 1 | a0026c0026t0003g0017 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.8110-391G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | chr4 | 3229496 | ||||||
| chr4:3229526
|
G | A | 2 | a0010c0056t0007g0200a0011c0028t0001g0236 | 2 | NA18906.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.8110-361G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | chr4 | 3229526 | ||||||
| chr4:3229637
|
A | T | 1 | a0001c0002t0001g0181 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.8110-250A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | chr4 | 3229637 | ||||||
| chr4:3229645
|
A | G | 1 | a0002c0001t0002g0279 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.8110-242A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | chr4 | 3229645 | ||||||
| chr4:3229696
|
C | T | 2 | a0046c0055t0011g0204a0049c0063t0011g0203 | 2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.8110-191C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | chr4 | 3229696 | ||||||
| chr4:3229711
|
G | A | 1 | a0046c0055t0011g0204 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.8110-176G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | chr4 | 3229711 | ||||||
| chr4:3229777
|
T | C | 1 | a0003c0024t0001g0079 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.8110-110T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 59/66 | chr4 | 3229777 | ||||||
| chr4:3230108
|
G | A | 1 | a0006c0015t0001g0139 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.8265+66G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3230108 | ||||||
| chr4:3230179
|
C | T | 1 | a0015c0016t0006g0137 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.8265+137C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3230179 | ||||||
| chr4:3230353
|
A | T | 1 | a0001c0002t0001g0181 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.8265+311A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3230353 | ||||||
| chr4:3230359
|
C | T | 1 | a0076c0101t0002g0266 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.8265+317C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3230359 | ||||||
| chr4:3230413
|
G | T | 1 | a0001c0002t0001g0181 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.8265+371G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3230413 | ||||||
| chr4:3230530
|
C | T | 75 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(72): Show | 75 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.8265+488C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3230530 | ||||||
| chr4:3230846
|
G | T | 1 | a0001c0002t0001g0181 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.8265+804G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3230846 | ||||||
| chr4:3231047
|
C | T | 2 | a0002c0030t0002g0213a0002c0030t0002g0218 | 2 | NA18964.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.8265+1005C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3231047 | ||||||
| chr4:3231062
|
C | T | 6 | a0001c0002t0001g0154a0001c0002t0001g0166a0001c0002t0001g0171others(3): Show | 6 | HG00423.hp1 NA18956.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.8265+1020C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3231062 | ||||||
| chr4:3231081
|
C | T | 2 | a0046c0055t0011g0204a0049c0063t0011g0203 | 2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.8265+1039C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3231081 | ||||||
| chr4:3231325
|
T | G | 1 | a0008c0114t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.8265+1283T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3231325 | ||||||
| chr4:3231609
|
T | C | 7 | a0002c0001t0002g0208a0002c0001t0002g0237a0002c0001t0002g0282others(4): Show | 7 | HG01952.hp1 HG02148.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.8266-1554T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3231609 | ||||||
| chr4:3231666
|
AT | A | 138 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(135): Show | 138 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.8266-1495delT | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | INFO_REALIGN_3_PRIME | chr4 | 3231666 | |||||
| chr4:3231786
|
G | C | 1 | a0001c0002t0001g0171 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.8266-1377G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3231786 | ||||||
| chr4:3231804
|
A | G | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.8266-1359A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3231804 | ||||||
| chr4:3231887
|
T | C | 36 | a0001c0002t0001g0175a0006c0015t0001g0158a0007c0007t0003g0023others(33): Show | 36 | HG00642.hp1 HG01081.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.8266-1276T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3231887 | ||||||
| chr4:3232117
|
A | G | 288 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(285): Show | 290 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(287): Show |
intron_variant | MODIFIER | c.8266-1046A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3232117 | ||||||
| chr4:3232215
|
C | A | 6 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(3): Show | 6 | HG01109.hp1 HG02109.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.8266-948C>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3232215 | ||||||
| chr4:3232246
|
C | G | 54 | a0001c0003t0003g0115a0004c0067t0001g0118a0007c0058t0033g0009others(51): Show | 54 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.8266-917C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3232246 | ||||||
| chr4:3232272
|
C | T | 9 | a0010c0056t0007g0200a0014c0014t0010g0011a0019c0020t0007g0088others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.8266-891C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3232272 | ||||||
| chr4:3232335
|
G | C | 3 | a0007c0058t0033g0009a0052c0061t0035g0252a0054c0068t0034g0090 | 3 | HG02145.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.8266-828G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3232335 | ||||||
| chr4:3232423
|
A | C | 1 | a0001c0003t0001g0129 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.8266-740A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3232423 | ||||||
| chr4:3232431
|
C | T | 7 | a0007c0007t0003g0023a0007c0007t0003g0024a0007c0007t0003g0025others(4): Show | 7 | HG01109.hp1 HG02109.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.8266-732C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3232431 | ||||||
| chr4:3232497
|
C | G | 1 | a0004c0067t0001g0118 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.8266-666C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3232497 | ||||||
| chr4:3232514
|
C | G | 53 | a0001c0003t0003g0115a0007c0007t0003g0023a0007c0007t0003g0024others(50): Show | 53 | HG00642.hp1 HG01081.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.8266-649C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3232514 | ||||||
| chr4:3232761
|
A | G | 2 | a0036c0107t0018g0065a0036c0108t0018g0066 | 2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.8266-402A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3232761 | ||||||
| chr4:3232770
|
C | T | 1 | a0019c0020t0023g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.8266-393C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3232770 | ||||||
| chr4:3232778
|
C | T | 5 | a0003c0006t0001g0045a0003c0006t0001g0052a0006c0022t0001g0036others(2): Show | 5 | HG00738.hp2 HG01257.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.8266-385C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3232778 | ||||||
| chr4:3232779
|
G | A | 1 | a0033c0097t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.8266-384G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3232779 | ||||||
| chr4:3232795
|
C | T | 1 | a0015c0016t0009g0082 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.8266-368C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3232795 | ||||||
| chr4:3232804
|
A | G | 1 | a0002c0001t0002g0251 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.8266-359A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3232804 | ||||||
| chr4:3232817
|
C | T | 14 | a0004c0005t0001g0001a0004c0005t0001g0049a0004c0005t0001g0050others(11): Show | 15 | HG01891.hp1 HG02280.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.8266-346C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3232817 | ||||||
| chr4:3232986
|
C | T | 1 | a0002c0001t0002g0283 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.8266-177C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3232986 | ||||||
| chr4:3232990
|
AC | A | 3 | a0031c0035t0002g0267a0031c0035t0002g0269a0057c0074t0002g0268 | 3 | HG01516.hp2 HG01517.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.8266-172delC | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3232990 | ||||||
| chr4:3233070
|
C | T | 3 | a0002c0001t0002g0247a0084c0115t0017g0202a0088c0120t0017g0201 | 3 | HG00323.hp1 HG00738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.8266-93C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3233070 | ||||||
| chr4:3233101
|
G | T | 129 | a0001c0003t0003g0115a0002c0001t0002g0191a0002c0001t0002g0193others(126): Show | 129 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.8266-62G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 60/66 | chr4 | 3233101 | ||||||
| chr4:3233457
|
GC | G | 142 | a0001c0003t0001g0122a0001c0003t0001g0123a0001c0003t0001g0127others(139): Show | 142 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.8456+106delC | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | INFO_REALIGN_3_PRIME | chr4 | 3233457 | |||||
| chr4:3233509
|
G | A | 1 | a0010c0056t0007g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8456+156G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3233509 | ||||||
| chr4:3233514
|
A | G | 138 | a0001c0003t0003g0115a0002c0001t0002g0191a0002c0001t0002g0193others(135): Show | 138 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.8456+161A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3233514 | ||||||
| chr4:3233552
|
A | G | 1 | a0001c0002t0001g0154 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.8456+199A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3233552 | ||||||
| chr4:3233723
|
T | C | 136 | a0001c0003t0003g0115a0002c0001t0002g0191a0002c0001t0002g0193others(133): Show | 136 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.8456+370T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3233723 | ||||||
| chr4:3233781
|
G | A | 4 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(1): Show | 4 | HG03139.hp2 HG06807.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.8456+428G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3233781 | ||||||
| chr4:3233791
|
G | A | 80 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(77): Show | 80 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.8456+438G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3233791 | ||||||
| chr4:3233862
|
C | T | 13 | a0001c0003t0004g0117a0001c0003t0004g0134a0003c0024t0001g0079others(10): Show | 14 | HG01074.hp2 HG01081.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.8456+509C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3233862 | ||||||
| chr4:3233879
|
A | G | 2 | a0014c0014t0010g0011a0043c0050t0010g0012 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.8456+526A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3233879 | ||||||
| chr4:3233908
|
G | A | 1 | a0019c0020t0023g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.8456+555G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3233908 | ||||||
| chr4:3234158
|
C | T | 1 | a0039c0043t0004g0073 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.8456+805C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3234158 | ||||||
| chr4:3234224
|
C | T | 1 | a0001c0003t0001g0174 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.8456+871C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3234224 | ||||||
| chr4:3234262
|
C | T | 1 | a0017c0018t0003g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.8456+909C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3234262 | ||||||
| chr4:3234408
|
G | T | 80 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(77): Show | 80 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.8457-876G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3234408 | ||||||
| chr4:3234458
|
A | G | 1 | a0002c0001t0002g0262 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.8457-826A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3234458 | ||||||
| chr4:3234475
|
C | T | 1 | a0003c0006t0027g0042 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.8457-809C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3234475 | ||||||
| chr4:3234502
|
A | G | 1 | a0021c0021t0012g0231 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.8457-782A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3234502 | ||||||
| chr4:3234756
|
G | C | 4 | a0002c0001t0013g0224a0002c0001t0013g0225a0021c0021t0002g0232others(1): Show | 4 | HG00673.hp2 HG02040.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.8457-528G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3234756 | ||||||
| chr4:3234778
|
G | T | 27 | a0001c0003t0003g0115a0007c0007t0003g0023a0007c0007t0003g0024others(24): Show | 27 | HG00642.hp1 HG01109.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.8457-506G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3234778 | ||||||
| chr4:3234780
|
G | A | 1 | a0064c0080t0001g0183 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.8457-504G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3234780 | ||||||
| chr4:3234780
|
G | C | 1 | a0005c0090t0002g0215 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.8457-504G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3234780 | ||||||
| chr4:3234893
|
G | A | 1 | a0033c0097t0001g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.8457-391G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3234893 | ||||||
| chr4:3234905
|
T | C | 98 | a0001c0002t0001g0176a0001c0003t0001g0121a0001c0003t0003g0115others(95): Show | 99 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.8457-379T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3234905 | ||||||
| chr4:3235054
|
A | T | 1 | a0038c0124t0019g0107 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.8457-230A>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3235054 | ||||||
| chr4:3235056
|
G | A | 2 | a0001c0003t0001g0114a0061c0076t0003g0099 | 2 | HG03654.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.8457-228G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3235056 | ||||||
| chr4:3235065
|
T | C | 1 | a0070c0092t0032g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.8457-219T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3235065 | ||||||
| chr4:3235078
|
C | T | 1 | a0017c0018t0003g0092 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.8457-206C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3235078 | ||||||
| chr4:3235149
|
G | A | 1 | a0001c0002t0001g0173 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.8457-135G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3235149 | ||||||
| chr4:3235153
|
C | G | 1 | a0002c0001t0002g0283 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.8457-131C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3235153 | ||||||
| chr4:3235154
|
T | G | 272 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(269): Show | 274 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(271): Show |
intron_variant | MODIFIER | c.8457-130T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3235154 | ||||||
| chr4:3235156
|
A | G | 250 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(247): Show | 252 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.8457-128A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3235156 | ||||||
| chr4:3235179
|
G | A | 1 | a0001c0002t0001g0155 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.8457-105G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3235179 | ||||||
| chr4:3235206
|
G | A | 2 | a0001c0003t0004g0134a0015c0016t0009g0082 | 2 | HG01099.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.8457-78G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3235206 | ||||||
| chr4:3235213
|
C | T | 5 | a0007c0058t0033g0009a0039c0043t0001g0078a0052c0061t0035g0252others(2): Show | 5 | HG01071.hp1 HG02145.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.8457-71C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 61/66 | chr4 | 3235213 | ||||||
| chr4:3235431
|
C | T | 1 | a0001c0003t0001g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.8571+33C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 62/66 | chr4 | 3235431 | ||||||
| chr4:3235496
|
C | T | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.8572-69C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 62/66 | chr4 | 3235496 | ||||||
| chr4:3235793
|
G | A | 1 | a0001c0002t0001g0148 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.8785+15G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 63/66 | chr4 | 3235793 | ||||||
| chr4:3235917
|
T | C | 99 | a0001c0003t0003g0115a0002c0001t0002g0191a0002c0001t0002g0193others(96): Show | 99 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.8785+139T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 63/66 | chr4 | 3235917 | ||||||
| chr4:3235964
|
T | C | 2 | a0014c0014t0010g0011a0043c0050t0010g0012 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.8786-185T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 63/66 | chr4 | 3235964 | ||||||
| chr4:3236114
|
A | G | 2 | a0014c0014t0010g0011a0043c0050t0010g0012 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.8786-35A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 63/66 | chr4 | 3236114 | ||||||
| chr4:3236475
|
G | A | 1 | a0002c0001t0002g0246 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8891+221G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3236475 | ||||||
| chr4:3236522
|
C | T | 1 | a0002c0001t0002g0247 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.8891+268C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3236522 | ||||||
| chr4:3236762
|
C | G | 2 | a0046c0055t0011g0204a0049c0063t0011g0203 | 2 | HG01255.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.8891+508C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3236762 | ||||||
| chr4:3236892
|
C | T | 1 | a0063c0081t0001g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.8891+638C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3236892 | ||||||
| chr4:3237027
|
A | G | 79 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(76): Show | 79 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.8891+773A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3237027 | ||||||
| chr4:3237220
|
C | T | 1 | a0001c0003t0001g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.8891+966C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3237220 | ||||||
| chr4:3237254
|
A | G | 79 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(76): Show | 79 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.8891+1000A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3237254 | ||||||
| chr4:3237274
|
G | A | 1 | a0038c0123t0001g0141 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.8891+1020G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3237274 | ||||||
| chr4:3237471
|
A | G | 4 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(1): Show | 4 | HG03139.hp2 HG06807.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.8892-976A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3237471 | ||||||
| chr4:3237484
|
G | A | 4 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(1): Show | 4 | HG03139.hp2 HG06807.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.8892-963G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3237484 | ||||||
| chr4:3237587
|
G | A | 4 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(1): Show | 4 | HG03139.hp2 HG06807.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.8892-860G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3237587 | ||||||
| chr4:3237641
|
C | T | 1 | a0002c0001t0002g0217 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.8892-806C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3237641 | ||||||
| chr4:3237728
|
G | A | 1 | a0034c0038t0002g0192 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.8892-719G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3237728 | ||||||
| chr4:3237916
|
C | G | 1 | a0021c0021t0012g0265 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.8892-531C>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3237916 | ||||||
| chr4:3237975
|
C | T | 72 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(69): Show | 72 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.8892-472C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3237975 | ||||||
| chr4:3238017
|
T | A | 1 | a0004c0011t0001g0153 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.8892-430T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3238017 | ||||||
| chr4:3238030
|
T | G | 1 | a0004c0011t0001g0153 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.8892-417T>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3238030 | ||||||
| chr4:3238031
|
G | T | 1 | a0004c0011t0001g0153 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.8892-416G>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3238031 | ||||||
| chr4:3238032
|
T | A | 1 | a0004c0011t0001g0153 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.8892-415T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3238032 | ||||||
| chr4:3238049
|
C | T | 46 | a0001c0003t0003g0115a0007c0007t0003g0023a0007c0007t0003g0024others(43): Show | 46 | HG00642.hp1 HG01081.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.8892-398C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3238049 | ||||||
| chr4:3238052
|
C | T | 4 | a0010c0056t0007g0200a0019c0020t0007g0088a0019c0020t0007g0102others(1): Show | 4 | HG03139.hp2 HG06807.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.8892-395C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3238052 | ||||||
| chr4:3238072
|
TGTAGCTT others(55): Show |
T | 3 | a0024c0046t0008g0257a0024c0047t0008g0258a0042c0048t0008g0259 | 3 | HG00323.hp2 HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.8892-332_8892-271d others(64): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | INFO_REALIGN_3_PRIME | chr4 | 3238072 | |||||
| chr4:3238384
|
C | T | 1 | a0024c0047t0008g0258 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.8892-63C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3238384 | ||||||
| chr4:3238432
|
C | T | 133 | a0001c0003t0003g0115a0002c0001t0002g0191a0002c0001t0002g0193others(130): Show | 133 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.8892-15C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 64/66 | chr4 | 3238432 | ||||||
| chr4:3238704
|
T | A | 1 | a0004c0011t0001g0153 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.9054+95T>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 65/66 | chr4 | 3238704 | ||||||
| chr4:3238731
|
C | T | 1 | a0003c0006t0001g0038 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.9055-87C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 65/66 | chr4 | 3238731 | ||||||
| chr4:3238799
|
A | G | 287 | a0001c0002t0001g0110a0001c0002t0001g0142a0001c0002t0001g0145others(284): Show | 289 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(286): Show |
intron_variant | MODIFIER | c.9055-19A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 65/66 | chr4 | 3238799 | ||||||
| chr4:3239013
|
T | C | 11 | a0007c0058t0033g0009a0010c0056t0007g0200a0019c0020t0007g0088others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.9215+35T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 66/66 | chr4 | 3239013 | ||||||
| chr4:3239188
|
G | C | 129 | a0001c0003t0003g0115a0002c0001t0002g0191a0002c0001t0002g0193others(126): Show | 129 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.9215+210G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 66/66 | chr4 | 3239188 | ||||||
| chr4:3239372
|
G | C | 1 | a0091c0127t0004g0063 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.9215+394G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 66/66 | chr4 | 3239372 | ||||||
| chr4:3239382
|
A | G | 48 | a0001c0003t0003g0115a0007c0007t0003g0023a0007c0007t0003g0024others(45): Show | 48 | HG00642.hp1 HG00738.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.9215+404A>G | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 66/66 | chr4 | 3239382 | ||||||
| chr4:3239417
|
GGAGTTTC others(2): Show |
G | 74 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(71): Show | 74 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.9216-428_9216-420d others(11): Show |
HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 66/66 | chr4 | 3239417 | ||||||
| chr4:3239428
|
T | C | 74 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(71): Show | 74 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.9216-418T>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 66/66 | chr4 | 3239428 | ||||||
| chr4:3239512
|
G | A | 2 | a0002c0030t0002g0213a0002c0030t0002g0218 | 2 | NA18964.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.9216-334G>A | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 66/66 | chr4 | 3239512 | ||||||
| chr4:3239579
|
C | T | 10 | a0010c0009t0003g0276a0010c0009t0003g0277a0010c0009t0003g0288others(7): Show | 10 | HG00642.hp1 HG01192.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.9216-267C>T | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 66/66 | chr4 | 3239579 | ||||||
| chr4:3239686
|
A | C | 86 | a0002c0001t0002g0191a0002c0001t0002g0193a0002c0001t0002g0196others(83): Show | 86 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.9216-160A>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 66/66 | chr4 | 3239686 | ||||||
| chr4:3239773
|
G | C | 1 | a0024c0047t0008g0258 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.9216-73G>C | HTT | ENSG00000197386.14 | transcript | ENST00000355072.11 | protein_coding | 66/66 | chr4 | 3239773 |