Item | Value |
---|---|
geneid | 51166 |
ensemblid | ENSG00000109576.14 |
hgncid | 17929 |
symbol | AADAT |
name | aminoadipate aminotransferase |
refseq_nuc | NM_016228.4 |
refseq_prot | NP_057312.1 |
ensembl_nuc | ENST00000337664.9 |
ensembl_prot | ENSP00000336808.4 |
mane_status | MANE Select |
chr | chr4 |
start | 170060222 |
end | 170089956 |
strand | - |
ver | v1.2 |
region | chr4:170060222-170089956 |
region5000 | chr4:170055222-170094956 |
regionname0 | AADAT_chr4_170060222_170089956 |
regionname5000 | AADAT_chr4_170055222_170094956 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1275 | 365 | 94 | 62 | 141 | 18 | 48 | AADAT_chr4_170055222_170094956 | AADAT | ATGAA others(1270): Show |
chr4 | 170055222 | 170094956 | ||
a0001c0002 | 0/0 | 1275 | 13 | 0 | 0 | 13 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | ATGAA others(1270): Show |
chr4 | 170055222 | 170094956 |
acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2250 | 337 | 88 | 54 | 137 | 17 | 40 | AADAT_chr4_170055222_170094956 | AADAT | AGGAG others(2245): Show |
chr4 | 170055222 | 170094956 |
a0001c0001t0002 | 0/1 | 2250 | 13 | 3 | 3 | 2 | 1 | 3 | AADAT_chr4_170055222_170094956 | AADAT | AGGAG others(2245): Show |
chr4 | 170055222 | 170094956 |
a0001c0001t0003 | 0/0 | 2249 | 10 | 0 | 4 | 1 | 0 | 5 | AADAT_chr4_170055222_170094956 | AADAT | AGGAG others(2244): Show |
chr4 | 170055222 | 170094956 |
a0001c0001t0004 | 0/0 | 2250 | 2 | 1 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | AGGAG others(2245): Show |
chr4 | 170055222 | 170094956 |
a0001c0001t0005 | 0/0 | 2250 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | AGGAG others(2245): Show |
chr4 | 170055222 | 170094956 |
a0001c0001t0006 | 0/0 | 2250 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | AGGAG others(2245): Show |
chr4 | 170055222 | 170094956 |
a0001c0001t0007 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | AGGAG others(2245): Show |
chr4 | 170055222 | 170094956 |
a0001c0002t0001 | 0/0 | 2250 | 13 | 0 | 0 | 13 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | AGGAG others(2245): Show |
chr4 | 170055222 | 170094956 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 41 | 0 | 5 | 29 | 2 | 5 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0002 | 0/0 | 23 | 3 | 9 | 2 | 3 | 6 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0003 | 0/0 | 21 | 0 | 0 | 16 | 0 | 5 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0004 | 0/0 | 16 | 1 | 0 | 15 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0006 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 5 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0013 | 0/0 | 5 | 0 | 1 | 0 | 4 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0018 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0027 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0015 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0003g0009 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0004g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0001t0007g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0002t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0002t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | GBR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | GBR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0197 | EUR | FIN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0052 | EUR | FIN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0046 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0198 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0081 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0062 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0046 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0080 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0154 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | STU | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | CHB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18948 | hp2 | a0001 | c0001 | t0007 | g0144 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ASW | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ASW | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | TSI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | GIH | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | GIH | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | USA | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | USA | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0057 | REF | REF | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0027 | REF | REF | AADAT_chr4_170055222_170094956 | AADAT | chr4 | 170055222 | 170094956 |
view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:170073199 | A | G | 1 | a0001c0002 | 13 | HG00438.hp2 HG00609.hp1 NA18941.hp1 others(10): Show |
synonymous_variant | LOW | c.591T>C | p.Val197Val | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/13 | 857/2250 | 591/1278 | 197/425 | chr4 | 170073199 |
view | 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:170060238 | A | T | 1 | a0001c0001t0006 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*690T>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 13/13 | 690 | chr4 | 170060238 | ||||||
chr4:170060288 | T | A | 1 | a0001c0001t0007 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*640A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 13/13 | 640 | chr4 | 170060288 | ||||||
chr4:170060293 | A | G | 1 | a0001c0001t0001 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*635T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 13/13 | 635 | chr4 | 170060293 | ||||||
chr4:170060317 | TA | T | 1 | a0001c0001t0003 | 10 | HG01109.hp2 HG01123.hp1 HG01168.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*610delT | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 13/13 | 610 | chr4 | 170060317 | ||||||
chr4:170060442 | T | C | 1 | a0001c0001t0007 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*486A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 13/13 | 486 | chr4 | 170060442 | ||||||
chr4:170060632 | G | T | 1 | a0001c0001t0002 | 12 | HG00323.hp1 HG01255.hp2 HG01346.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*296C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 13/13 | 296 | chr4 | 170060632 | ||||||
chr4:170060796 | C | A | 1 | a0001c0001t0004 | 2 | HG00639.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*132G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 13/13 | 132 | chr4 | 170060796 | ||||||
chr4:170089905 | G | T | 1 | a0001c0001t0005 | 1 | HG02895.hp2 | 5_prime_UTR_variant | MODIFIER | c.-215C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/13 | 215 | chr4 | 170089905 |
view | 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:170060989 | T | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0181 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1237-20A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 12/12 | chr4 | 170060989 | |||||||
chr4:170061166 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1237-197C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 12/12 | chr4 | 170061166 | |||||||
chr4:170061443 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1236+449A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 12/12 | chr4 | 170061443 | |||||||
chr4:170061535 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1236+357G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 12/12 | chr4 | 170061535 | |||||||
chr4:170061639 | C | T | 9 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0075others(6): Show | 12 | HG02451.hp2 HG02559.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1236+253G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 12/12 | chr4 | 170061639 | |||||||
chr4:170062318 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1135-325A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170062318 | |||||||
chr4:170062561 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1135-568G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170062561 | |||||||
chr4:170062676 | C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0200 | 2 | HG02273.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1135-683G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170062676 | |||||||
chr4:170062692 | G | C | 1 | a0001c0001t0001g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1135-699C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170062692 | |||||||
chr4:170062709 | G | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0189others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1135-716C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170062709 | |||||||
chr4:170062736 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1135-743A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170062736 | |||||||
chr4:170062771 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1135-778A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170062771 | |||||||
chr4:170062965 | C | CT | 6 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0189others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1135-973dupA | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170062965 | |||||||
chr4:170063078 | T | C | 1 | a0001c0001t0001g0036 | 2 | HG00735.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1135-1085A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063078 | |||||||
chr4:170063254 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1135-1261G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063254 | |||||||
chr4:170063509 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1134+1210A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063509 | |||||||
chr4:170063598 | T | C | 2 | a0001c0001t0002g0052a0001c0001t0002g0056 | 2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1134+1121A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063598 | |||||||
chr4:170063603 | T | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0088a0001c0001t0001g0122others(4): Show | 10 | HG02559.hp1 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1134+1116A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063603 | |||||||
chr4:170063631 | A | T | 1 | a0001c0001t0001g0153 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1134+1088T>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063631 | |||||||
chr4:170063674 | C | G | 85 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(82): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1134+1045G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063674 | |||||||
chr4:170063707 | C | T | 1 | a0001c0001t0001g0039 | 2 | NA18942.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1134+1012G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063707 | |||||||
chr4:170063803 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1134+916T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063803 | |||||||
chr4:170063871 | G | A | 1 | a0001c0001t0004g0046 | 2 | HG00639.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1134+848C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063871 | |||||||
chr4:170063956 | AG | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0189others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1134+762delC | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063956 | |||||||
chr4:170063958 | GA | G | 13 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0029others(10): Show | 31 | HG00423.hp2 HG00621.hp1 HG02080.hp1 others(28): Show |
intron_variant | MODIFIER | c.1134+760delT | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063958 | |||||||
chr4:170063967 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1134+752T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170063967 | |||||||
chr4:170064036 | A | G | 1 | a0001c0001t0006g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1134+683T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064036 | |||||||
chr4:170064167 | C | G | 1 | a0001c0001t0001g0042 | 2 | HG02258.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1134+552G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064167 | |||||||
chr4:170064193 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1134+526G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064193 | |||||||
chr4:170064196 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1134+523G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064196 | |||||||
chr4:170064247 | T | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(98): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1134+472A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064247 | |||||||
chr4:170064258 | A | T | 1 | a0001c0001t0001g0156 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1134+461T>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064258 | |||||||
chr4:170064361 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1134+358G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064361 | |||||||
chr4:170064436 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1134+283A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064436 | |||||||
chr4:170064479 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1134+240A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064479 | |||||||
chr4:170064688 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1134+31C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064688 | |||||||
chr4:170064689 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1134+30C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064689 | |||||||
chr4:170064704 | A | ACCT | 6 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0189others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1134+12_1134+14dup others(3): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 11/12 | chr4 | 170064704 | |||||||
chr4:170064834 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1028-9T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170064834 | |||||||
chr4:170065060 | G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0158 | 2 | NA18949.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1028-235C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170065060 | |||||||
chr4:170065129 | T | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0189others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1028-304A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170065129 | |||||||
chr4:170065154 | G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0075 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1028-329C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170065154 | |||||||
chr4:170065157 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1028-332T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170065157 | |||||||
chr4:170065222 | C | G | 1 | a0001c0001t0001g0006 | 6 | HG01109.hp1 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1028-397G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170065222 | |||||||
chr4:170065428 | T | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0189others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1028-603A>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170065428 | |||||||
chr4:170065509 | G | T | 1 | a0001c0001t0001g0180 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1028-684C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170065509 | |||||||
chr4:170065646 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1027+768C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170065646 | |||||||
chr4:170065654 | T | G | 1 | a0001c0001t0001g0156 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1027+760A>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170065654 | |||||||
chr4:170066045 | A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0189others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1027+369T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170066045 | |||||||
chr4:170066120 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1027+294A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170066120 | |||||||
chr4:170066203 | C | A | 13 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0002g0015others(10): Show | 16 | HG00323.hp1 HG00639.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.1027+211G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 10/12 | chr4 | 170066203 | |||||||
chr4:170066485 | A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
splice_region_variant&intron_variant | LOW | c.963-7T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170066485 | |||||||
chr4:170066764 | GTTGTCTA others(5): Show |
G | 2 | a0001c0001t0001g0043a0001c0001t0001g0184 | 3 | HG02622.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.963-298_963-287del others(12): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170066764 | |||||||
chr4:170066887 | T | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0189others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.963-409A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170066887 | |||||||
chr4:170066948 | T | A | 1 | a0001c0001t0003g0081 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.962+379A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170066948 | |||||||
chr4:170066952 | C | T | 10 | a0001c0001t0002g0015a0001c0001t0002g0052a0001c0001t0002g0053others(7): Show | 12 | HG00323.hp1 HG01255.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.962+375G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170066952 | |||||||
chr4:170066980 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.962+347G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170066980 | |||||||
chr4:170066981 | G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0096 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.962+346C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170066981 | |||||||
chr4:170067069 | C | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0173a0001c0001t0001g0174 | 3 | HG03130.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.962+258G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170067069 | |||||||
chr4:170067153 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.962+174A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170067153 | |||||||
chr4:170067200 | C | T | 25 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0024others(22): Show | 37 | HG00733.hp2 HG01257.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.962+127G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170067200 | |||||||
chr4:170067319 | T | G | 1 | a0001c0001t0004g0046 | 2 | HG00639.hp2 HG03195.hp2 |
splice_region_variant&intron_variant | LOW | c.962+8A>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 9/12 | chr4 | 170067319 | |||||||
chr4:170067748 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.901-360G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170067748 | |||||||
chr4:170067804 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.901-416A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170067804 | |||||||
chr4:170067908 | A | G | 1 | a0001c0001t0001g0036 | 2 | HG00735.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.901-520T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170067908 | |||||||
chr4:170067995 | C | T | 1 | a0001c0001t0001g0010 | 5 | HG00558.hp1 NA18950.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.900+596G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170067995 | |||||||
chr4:170068064 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.900+527C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170068064 | |||||||
chr4:170068068 | T | C | 1 | a0001c0001t0003g0069 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.900+523A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170068068 | |||||||
chr4:170068138 | C | CA | 20 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0128others(17): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.900+452dupT | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170068138 | |||||||
chr4:170068138 | CA | C | 39 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0016others(36): Show | 74 | HG00408.hp2 HG00609.hp2 HG01168.hp2 others(71): Show |
intron_variant | MODIFIER | c.900+452delT | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170068138 | |||||||
chr4:170068138 | CAA | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0071a0001c0001t0001g0074others(2): Show | 6 | HG02258.hp2 HG02922.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.900+451_900+452del others(2): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170068138 | |||||||
chr4:170068557 | C | CA | 138 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 274 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.900+33dupT | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170068557 | |||||||
chr4:170068557 | C | CAA | 6 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0189others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.900+32_900+33dupTT | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 8/12 | chr4 | 170068557 | |||||||
chr4:170068710 | C | T | 1 | a0001c0001t0004g0046 | 2 | HG00639.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.804-23G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 7/12 | chr4 | 170068710 | |||||||
chr4:170068831 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.804-144A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 7/12 | chr4 | 170068831 | |||||||
chr4:170068878 | T | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0189others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.804-191A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 7/12 | chr4 | 170068878 | |||||||
chr4:170068902 | C | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(62): Show | 150 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.804-215G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 7/12 | chr4 | 170068902 | |||||||
chr4:170069296 | G | T | 1 | a0001c0001t0004g0046 | 2 | HG00639.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721-66C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069296 | |||||||
chr4:170069494 | A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0189others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.721-264T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069494 | |||||||
chr4:170069520 | C | G | 10 | a0001c0001t0002g0015a0001c0001t0002g0052a0001c0001t0002g0053others(7): Show | 12 | HG00323.hp1 HG01255.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.721-290G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069520 | |||||||
chr4:170069564 | T | A | 1 | a0001c0001t0001g0033 | 2 | HG02683.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.721-334A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069564 | |||||||
chr4:170069599 | G | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0189others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.721-369C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069599 | |||||||
chr4:170069625 | C | G | 5 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 8 | HG02109.hp2 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.721-395G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069625 | |||||||
chr4:170069732 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.721-502T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069732 | |||||||
chr4:170069795 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.721-565A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069795 | |||||||
chr4:170069860 | C | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0189others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.721-630G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069860 | |||||||
chr4:170069879 | C | A | 1 | a0001c0001t0001g0197 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.721-649G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069879 | |||||||
chr4:170069905 | T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0181 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.721-675A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170069905 | |||||||
chr4:170070105 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.720+482G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170070105 | |||||||
chr4:170070111 | T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(83): Show | 179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.720+476A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170070111 | |||||||
chr4:170070334 | T | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0088a0001c0001t0001g0122others(4): Show | 10 | HG02559.hp1 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.720+253A>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170070334 | |||||||
chr4:170070367 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.720+220A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170070367 | |||||||
chr4:170070442 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.720+145A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170070442 | |||||||
chr4:170070487 | G | A | 1 | a0001c0001t0002g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.720+100C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170070487 | |||||||
chr4:170070494 | TCTGACTC others(16): Show |
T | 1 | a0001c0001t0002g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.720+70_720+92delTA others(21): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 6/12 | chr4 | 170070494 | |||||||
chr4:170070660 | AGGTT | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(62): Show | 150 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.655-12_655-9delAAC others(1): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170070660 | |||||||
chr4:170070787 | C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0195a0001c0001t0001g0196 | 7 | HG00099.hp2 HG01070.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.655-135G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170070787 | |||||||
chr4:170071215 | A | C | 1 | a0001c0001t0001g0076 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.655-563T>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170071215 | |||||||
chr4:170071396 | T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 322 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.655-744A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170071396 | |||||||
chr4:170071523 | C | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0195others(2): Show | 10 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.655-871G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170071523 | |||||||
chr4:170071553 | G | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0195others(2): Show | 10 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.655-901C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170071553 | |||||||
chr4:170071609 | G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0195others(2): Show | 10 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.655-957C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170071609 | |||||||
chr4:170071615 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.655-963C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170071615 | |||||||
chr4:170071702 | G | A | 9 | a0001c0001t0002g0015a0001c0001t0002g0052a0001c0001t0002g0053others(6): Show | 11 | HG00323.hp1 HG01255.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.655-1050C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170071702 | |||||||
chr4:170071962 | A | G | 2 | a0001c0001t0002g0053a0001c0001t0002g0099 | 2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.654+1174T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170071962 | |||||||
chr4:170072025 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.654+1111C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072025 | |||||||
chr4:170072137 | G | C | 1 | a0001c0001t0001g0160 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.654+999C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072137 | |||||||
chr4:170072211 | CTGTGTGT others(7): Show |
C | 1 | a0001c0001t0001g0161 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.654+911_654+924del others(14): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072211 | |||||||
chr4:170072241 | G | A | 26 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0020others(23): Show | 53 | HG00408.hp2 HG00609.hp2 HG01255.hp2 others(50): Show |
intron_variant | MODIFIER | c.654+895C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072241 | |||||||
chr4:170072253 | AGATAC | A | 27 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0020others(24): Show | 54 | HG00408.hp2 HG00609.hp2 HG01255.hp2 others(51): Show |
intron_variant | MODIFIER | c.654+878_654+882del others(5): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072253 | |||||||
chr4:170072261 | GTA | G | 7 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0189others(4): Show | 12 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.654+873_654+874del others(2): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072261 | |||||||
chr4:170072299 | G | GTA | 60 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0014others(57): Show | 100 | HG00408.hp2 HG00609.hp2 HG00733.hp2 others(97): Show |
intron_variant | MODIFIER | c.654+835_654+836dup others(2): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072299 | |||||||
chr4:170072299 | G | GTATA | 5 | a0001c0001t0001g0005a0001c0001t0001g0082a0001c0001t0001g0087others(2): Show | 10 | HG02257.hp1 HG02280.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.654+833_654+836dup others(4): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072299 | |||||||
chr4:170072299 | GTA | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0077a0001c0001t0001g0110others(2): Show | 7 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+835_654+836del others(2): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072299 | |||||||
chr4:170072301 | A | G | 7 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0189others(4): Show | 12 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.654+835T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072301 | |||||||
chr4:170072312 | T | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0183a0001c0001t0001g0185 | 4 | HG01358.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.654+824A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072312 | |||||||
chr4:170072398 | G | C | 1 | a0001c0001t0006g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.654+738C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072398 | |||||||
chr4:170072429 | C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0075 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.654+707G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072429 | |||||||
chr4:170072525 | T | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0116 | 3 | HG00438.hp1 NA18985.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.654+611A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072525 | |||||||
chr4:170072579 | T | C | 9 | a0001c0001t0002g0015a0001c0001t0002g0052a0001c0001t0002g0053others(6): Show | 11 | HG00323.hp1 HG01255.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.654+557A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072579 | |||||||
chr4:170072620 | A | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 301 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.654+516T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072620 | |||||||
chr4:170072659 | T | C | 5 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 8 | HG02109.hp2 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.654+477A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072659 | |||||||
chr4:170072832 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.654+304A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072832 | |||||||
chr4:170072843 | C | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0036a0001c0001t0001g0040 | 7 | HG00735.hp1 HG00741.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.654+293G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170072843 | |||||||
chr4:170073054 | G | C | 14 | a0001c0001t0001g0024a0001c0001t0001g0042a0001c0001t0001g0043others(11): Show | 17 | HG01358.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.654+82C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 5/12 | chr4 | 170073054 | |||||||
chr4:170073390 | G | A | 1 | a0001c0001t0001g0019 | 3 | HG03041.hp1 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.445-45C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073390 | |||||||
chr4:170073403 | GT | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 300 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.445-59delA | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073403 | |||||||
chr4:170073510 | TA | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0186a0001c0001t0007g0144 | 3 | HG01975.hp2 HG02145.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.445-166delT | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073510 | |||||||
chr4:170073511 | A | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 302 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.445-166T>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073511 | |||||||
chr4:170073515 | T | A | 1 | a0001c0001t0001g0126 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.445-170A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073515 | |||||||
chr4:170073545 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.445-200G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073545 | |||||||
chr4:170073617 | G | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0045a0001c0001t0001g0190 | 6 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-272C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073617 | |||||||
chr4:170073630 | C | T | 1 | a0001c0001t0001g0035 | 2 | NA18986.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.445-285G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073630 | |||||||
chr4:170073663 | G | C | 1 | a0001c0001t0001g0019 | 3 | HG03041.hp1 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.445-318C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073663 | |||||||
chr4:170073687 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.445-342C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073687 | |||||||
chr4:170073701 | A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0071 | 3 | NA19004.hp1 NA19007.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.445-356T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073701 | |||||||
chr4:170073723 | T | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0181 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.445-378A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073723 | |||||||
chr4:170073743 | C | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0194a0001c0001t0001g0195others(2): Show | 9 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.445-398G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073743 | |||||||
chr4:170073767 | A | G | 5 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0125others(2): Show | 5 | HG00140.hp2 HG01243.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-422T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073767 | |||||||
chr4:170073785 | T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0136 | 3 | HG01168.hp1 HG01169.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.445-440A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073785 | |||||||
chr4:170073786 | G | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0136 | 3 | HG01168.hp1 HG01169.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.445-441C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073786 | |||||||
chr4:170073899 | CAGTGGGC others(15): Show |
C | 3 | a0001c0001t0001g0019a0001c0001t0001g0045a0001c0001t0001g0190 | 6 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-576_445-555del others(22): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073899 | |||||||
chr4:170073915 | C | T | 35 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(32): Show | 81 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.445-570G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073915 | |||||||
chr4:170073933 | T | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0137 | 3 | HG02683.hp1 HG03491.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.445-588A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170073933 | |||||||
chr4:170074018 | G | T | 5 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0141others(2): Show | 13 | HG00438.hp2 HG00609.hp1 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-673C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074018 | |||||||
chr4:170074026 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.445-681A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074026 | |||||||
chr4:170074085 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.445-740A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074085 | |||||||
chr4:170074162 | C | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0194a0001c0001t0001g0195others(2): Show | 9 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.445-817G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074162 | |||||||
chr4:170074294 | C | T | 59 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(56): Show | 101 | HG00408.hp2 HG00609.hp2 HG00733.hp2 others(98): Show |
intron_variant | MODIFIER | c.445-949G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074294 | |||||||
chr4:170074328 | T | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(53): Show | 99 | HG00408.hp2 HG00609.hp2 HG00733.hp2 others(96): Show |
intron_variant | MODIFIER | c.445-983A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074328 | |||||||
chr4:170074347 | T | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0183others(2): Show | 7 | HG01358.hp2 HG02258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-1002A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074347 | |||||||
chr4:170074470 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.445-1125G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074470 | |||||||
chr4:170074505 | CAT | C | 5 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-1162_445-1161d others(4): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074505 | |||||||
chr4:170074534 | T | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0066 | 3 | HG00733.hp2 HG02148.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.445-1189A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074534 | |||||||
chr4:170074718 | C | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0194a0001c0001t0001g0195others(1): Show | 8 | HG00099.hp2 HG01070.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.445-1373G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074718 | |||||||
chr4:170074740 | A | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0045a0001c0001t0001g0190 | 6 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-1395T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074740 | |||||||
chr4:170074748 | AG | A | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0095 | 3 | HG02886.hp2 HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.445-1404delC | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074748 | |||||||
chr4:170074800 | T | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0045a0001c0001t0001g0190 | 6 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-1455A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074800 | |||||||
chr4:170074857 | G | T | 7 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0183others(4): Show | 9 | HG01358.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-1512C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074857 | |||||||
chr4:170074957 | A | C | 1 | a0001c0001t0002g0121 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.445-1612T>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170074957 | |||||||
chr4:170075148 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.445-1803A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170075148 | |||||||
chr4:170075165 | G | A | 3 | a0001c0001t0001g0122a0001c0001t0002g0121a0001c0001t0002g0199 | 3 | HG02451.hp1 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.445-1820C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170075165 | |||||||
chr4:170075179 | G | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(50): Show | 95 | HG00408.hp2 HG00609.hp2 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.445-1834C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170075179 | |||||||
chr4:170075264 | C | T | 7 | a0001c0001t0002g0015a0001c0001t0002g0052a0001c0001t0002g0053others(4): Show | 9 | HG00323.hp1 HG01255.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.445-1919G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170075264 | |||||||
chr4:170075407 | T | C | 5 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-2062A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170075407 | |||||||
chr4:170075605 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.445-2260T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170075605 | |||||||
chr4:170075632 | C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0075 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.445-2287G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170075632 | |||||||
chr4:170075923 | T | A | 1 | a0001c0001t0002g0015 | 3 | HG01255.hp2 HG01433.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.445-2578A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170075923 | |||||||
chr4:170075928 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.444+2581G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170075928 | |||||||
chr4:170076063 | G | A | 5 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+2446C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076063 | |||||||
chr4:170076335 | T | A | 1 | a0001c0001t0001g0165 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.444+2174A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076335 | |||||||
chr4:170076362 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.444+2147A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076362 | |||||||
chr4:170076426 | C | A | 7 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0189others(4): Show | 12 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.444+2083G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076426 | |||||||
chr4:170076506 | C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0045others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+2003G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076506 | |||||||
chr4:170076772 | A | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0045others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+1737T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076772 | |||||||
chr4:170076821 | TC | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0045others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+1687delG | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076821 | |||||||
chr4:170076832 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.444+1677A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076832 | |||||||
chr4:170076872 | G | A | 15 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0020others(12): Show | 40 | HG00408.hp2 HG00609.hp2 HG01346.hp2 others(37): Show |
intron_variant | MODIFIER | c.444+1637C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076872 | |||||||
chr4:170076906 | C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0183 | 3 | HG02258.hp1 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.444+1603G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170076906 | |||||||
chr4:170077034 | A | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG02055.hp1 HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.444+1475T>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170077034 | |||||||
chr4:170077411 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.444+1098A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170077411 | |||||||
chr4:170077430 | C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0190others(2): Show | 9 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+1079G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170077430 | |||||||
chr4:170077539 | T | C | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | NA18968.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.444+970A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170077539 | |||||||
chr4:170077577 | G | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0045others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+932C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170077577 | |||||||
chr4:170077748 | A | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0075 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.444+761T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170077748 | |||||||
chr4:170077915 | C | G | 1 | a0001c0001t0001g0030 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.444+594G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170077915 | |||||||
chr4:170078156 | A | G | 4 | a0001c0001t0001g0074a0001c0001t0001g0106a0001c0001t0001g0173others(1): Show | 4 | HG03130.hp1 HG03130.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+353T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170078156 | |||||||
chr4:170078317 | A | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0047others(5): Show | 14 | HG00099.hp2 HG00280.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.444+192T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 4/12 | chr4 | 170078317 | |||||||
chr4:170078686 | A | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0045others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.370-103T>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170078686 | |||||||
chr4:170078709 | G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 304 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.370-126C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170078709 | |||||||
chr4:170078902 | C | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0059a0001c0001t0001g0061 | 4 | HG02109.hp2 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-319G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170078902 | |||||||
chr4:170078937 | C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0045others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.370-354G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170078937 | |||||||
chr4:170079037 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.370-454T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079037 | |||||||
chr4:170079156 | C | A | 1 | a0001c0001t0001g0095 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.370-573G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079156 | |||||||
chr4:170079242 | C | CG | 5 | a0001c0001t0001g0073a0001c0001t0001g0110a0001c0001t0001g0124others(2): Show | 5 | HG01433.hp1 HG01978.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.370-660dupC | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079242 | |||||||
chr4:170079467 | T | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0189 | 3 | HG02698.hp1 HG02735.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.370-884A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079467 | |||||||
chr4:170079570 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.370-987C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079570 | |||||||
chr4:170079704 | A | G | 1 | a0001c0001t0006g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.370-1121T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079704 | |||||||
chr4:170079774 | C | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0045others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.370-1191G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079774 | |||||||
chr4:170079810 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.370-1227G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079810 | |||||||
chr4:170079938 | G | C | 1 | a0001c0001t0001g0043 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.370-1355C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079938 | |||||||
chr4:170079941 | G | C | 15 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0020others(12): Show | 40 | HG00408.hp2 HG00609.hp2 HG01346.hp2 others(37): Show |
intron_variant | MODIFIER | c.370-1358C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170079941 | |||||||
chr4:170080118 | T | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0047others(5): Show | 14 | HG00099.hp2 HG00280.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.370-1535A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080118 | |||||||
chr4:170080245 | A | G | 15 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0020others(12): Show | 40 | HG00408.hp2 HG00609.hp2 HG01346.hp2 others(37): Show |
intron_variant | MODIFIER | c.370-1662T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080245 | |||||||
chr4:170080255 | G | T | 15 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0020others(12): Show | 40 | HG00408.hp2 HG00609.hp2 HG01346.hp2 others(37): Show |
intron_variant | MODIFIER | c.370-1672C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080255 | |||||||
chr4:170080328 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.370-1745C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080328 | |||||||
chr4:170080351 | C | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | NA18941.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.370-1768G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080351 | |||||||
chr4:170080352 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.370-1769C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080352 | |||||||
chr4:170080419 | G | C | 1 | a0001c0001t0006g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.370-1836C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080419 | |||||||
chr4:170080508 | C | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.370-1925G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080508 | |||||||
chr4:170080514 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.370-1931C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080514 | |||||||
chr4:170080515 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.370-1932G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080515 | |||||||
chr4:170080651 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.370-2068G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080651 | |||||||
chr4:170080674 | T | C | 1 | a0001c0001t0001g0034 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.370-2091A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080674 | |||||||
chr4:170080681 | G | T | 1 | a0001c0001t0003g0069 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.370-2098C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080681 | |||||||
chr4:170080739 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.370-2156C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080739 | |||||||
chr4:170080769 | C | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.370-2186G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080769 | |||||||
chr4:170080884 | A | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0045others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.370-2301T>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080884 | |||||||
chr4:170080970 | C | A | 1 | a0001c0001t0001g0019 | 3 | HG03041.hp1 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.370-2387G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080970 | |||||||
chr4:170080992 | A | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0045others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.370-2409T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170080992 | |||||||
chr4:170081124 | A | C | 1 | a0001c0001t0001g0105 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.370-2541T>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081124 | |||||||
chr4:170081125 | C | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0102 | 7 | HG01109.hp1 HG01884.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.370-2542G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081125 | |||||||
chr4:170081185 | T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.370-2602A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081185 | |||||||
chr4:170081237 | T | G | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.370-2654A>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081237 | |||||||
chr4:170081250 | C | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0047a0001c0001t0001g0194others(3): Show | 11 | HG00099.hp2 HG00280.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.370-2667G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081250 | |||||||
chr4:170081251 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.370-2668C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081251 | |||||||
chr4:170081345 | T | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(50): Show | 131 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.370-2762A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081345 | |||||||
chr4:170081550 | G | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 6 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-2967C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081550 | |||||||
chr4:170081820 | G | A | 7 | a0001c0001t0002g0015a0001c0001t0002g0052a0001c0001t0002g0053others(4): Show | 9 | HG00323.hp1 HG01255.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.370-3237C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081820 | |||||||
chr4:170081879 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.370-3296G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081879 | |||||||
chr4:170081880 | G | A | 9 | a0001c0001t0001g0051a0001c0001t0002g0015a0001c0001t0002g0052others(6): Show | 12 | HG00323.hp1 HG00639.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.370-3297C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081880 | |||||||
chr4:170081886 | C | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0059a0001c0001t0001g0067others(1): Show | 5 | HG02109.hp2 HG02129.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.370-3303G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081886 | |||||||
chr4:170081922 | C | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 6 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-3339G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170081922 | |||||||
chr4:170082043 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.370-3460A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170082043 | |||||||
chr4:170082101 | A | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0045others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.370-3518T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170082101 | |||||||
chr4:170082161 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.370-3578G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170082161 | |||||||
chr4:170082163 | T | C | 1 | a0001c0001t0006g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.370-3580A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170082163 | |||||||
chr4:170082176 | C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0116 | 6 | HG00438.hp1 HG00558.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-3593G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170082176 | |||||||
chr4:170082377 | AT | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0045others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.370-3795delA | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170082377 | |||||||
chr4:170083015 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.369+4101C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083015 | |||||||
chr4:170083171 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.369+3945T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083171 | |||||||
chr4:170083200 | C | G | 1 | a0001c0001t0004g0046 | 2 | HG00639.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.369+3916G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083200 | |||||||
chr4:170083216 | A | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0045others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.369+3900T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083216 | |||||||
chr4:170083233 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.369+3883C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083233 | |||||||
chr4:170083260 | G | A | 5 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.369+3856C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083260 | |||||||
chr4:170083315 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.369+3801T>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083315 | |||||||
chr4:170083346 | C | T | 7 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0183others(4): Show | 9 | HG01358.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.369+3770G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083346 | |||||||
chr4:170083347 | G | A | 1 | a0001c0001t0006g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.369+3769C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083347 | |||||||
chr4:170083546 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.369+3570T>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083546 | |||||||
chr4:170083572 | AT | A | 7 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0183others(4): Show | 9 | HG01358.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.369+3543delA | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083572 | |||||||
chr4:170083573 | T | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 302 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.369+3543A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083573 | |||||||
chr4:170083619 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+3497G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083619 | |||||||
chr4:170083937 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.369+3179A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170083937 | |||||||
chr4:170084134 | T | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0045others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.369+2982A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084134 | |||||||
chr4:170084197 | G | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0190others(2): Show | 9 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.369+2919C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084197 | |||||||
chr4:170084331 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.369+2785T>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084331 | |||||||
chr4:170084406 | G | T | 1 | a0001c0001t0001g0029 | 2 | NA18985.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.369+2710C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084406 | |||||||
chr4:170084540 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.369+2576C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084540 | |||||||
chr4:170084724 | C | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 6 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+2392G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084724 | |||||||
chr4:170084796 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.369+2320C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084796 | |||||||
chr4:170084909 | T | G | 1 | a0001c0001t0001g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.369+2207A>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084909 | |||||||
chr4:170084967 | G | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0190others(2): Show | 9 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.369+2149C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084967 | |||||||
chr4:170084990 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.369+2126A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170084990 | |||||||
chr4:170085064 | T | C | 14 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(11): Show | 26 | HG00099.hp2 HG00280.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.369+2052A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170085064 | |||||||
chr4:170085214 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.369+1902C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170085214 | |||||||
chr4:170085289 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.369+1827G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170085289 | |||||||
chr4:170085597 | G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.369+1519C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170085597 | |||||||
chr4:170085773 | G | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0045others(3): Show | 12 | HG02559.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.369+1343C>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170085773 | |||||||
chr4:170085914 | TAAGATA | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 6 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+1196_369+1201d others(8): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170085914 | |||||||
chr4:170086008 | C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0064 | 4 | NA18942.hp1 NA18944.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+1108G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086008 | |||||||
chr4:170086107 | T | C | 8 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0045others(5): Show | 15 | HG00639.hp2 HG02559.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.369+1009A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086107 | |||||||
chr4:170086158 | T | C | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.369+958A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086158 | |||||||
chr4:170086185 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.369+931C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086185 | |||||||
chr4:170086195 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.369+921C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086195 | |||||||
chr4:170086208 | C | T | 4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 4 | HG01891.hp2 HG02818.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+908G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086208 | |||||||
chr4:170086245 | C | CA | 3 | a0001c0001t0001g0014a0001c0001t0001g0192a0001c0001t0001g0193 | 6 | HG02559.hp1 HG02717.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+870dupT | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086245 | |||||||
chr4:170086317 | G | A | 8 | a0001c0001t0001g0021a0001c0001t0001g0059a0001c0001t0001g0060others(5): Show | 9 | HG01891.hp2 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.369+799C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086317 | |||||||
chr4:170086353 | C | T | 16 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(13): Show | 29 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.369+763G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086353 | |||||||
chr4:170086401 | GGA | G | 10 | a0001c0001t0001g0006a0001c0001t0001g0042a0001c0001t0001g0043others(7): Show | 17 | HG01109.hp1 HG01358.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.369+713_369+714del others(2): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086401 | |||||||
chr4:170086624 | C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0107 | 2 | NA18946.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.369+492G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086624 | |||||||
chr4:170086704 | G | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG00639.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.369+412C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086704 | |||||||
chr4:170086907 | C | A | 1 | a0001c0002t0001g0012 | 5 | NA18941.hp1 NA18991.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.369+209G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086907 | |||||||
chr4:170086929 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.369+187G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086929 | |||||||
chr4:170086932 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.369+184G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086932 | |||||||
chr4:170086949 | C | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 8 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.369+167G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086949 | |||||||
chr4:170086953 | T | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0058 | 3 | HG00408.hp2 NA18950.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.369+163A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 3/12 | chr4 | 170086953 | |||||||
chr4:170087373 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.237-125G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087373 | |||||||
chr4:170087538 | C | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0047others(6): Show | 15 | HG00099.hp2 HG00280.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.237-290G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087538 | |||||||
chr4:170087538 | C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0050a0001c0001t0001g0102others(1): Show | 9 | HG01109.hp1 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-290G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087538 | |||||||
chr4:170087545 | G | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.237-297C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087545 | |||||||
chr4:170087643 | G | A | 8 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0045others(5): Show | 15 | HG00639.hp2 HG02559.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-395C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087643 | |||||||
chr4:170087679 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.237-431A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087679 | |||||||
chr4:170087750 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.237-502T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087750 | |||||||
chr4:170087751 | T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0181 | 3 | HG02630.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.237-503A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087751 | |||||||
chr4:170087858 | G | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0047others(6): Show | 15 | HG00099.hp2 HG00280.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.236+538C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087858 | |||||||
chr4:170087876 | G | GCTGCTTG others(45): Show |
1 | a0001c0001t0001g0026 | 2 | NA19054.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.236+468_236+519dup others(52): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087876 | |||||||
chr4:170087974 | C | T | 52 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(49): Show | 96 | HG00408.hp2 HG00609.hp2 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.236+422G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170087974 | |||||||
chr4:170088186 | C | A | 1 | a0001c0001t0001g0182 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.236+210G>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170088186 | |||||||
chr4:170088209 | A | G | 52 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(49): Show | 96 | HG00408.hp2 HG00609.hp2 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.236+187T>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170088209 | |||||||
chr4:170088255 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.236+141A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 2/12 | chr4 | 170088255 | |||||||
chr4:170088637 | T | C | 8 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0045others(5): Show | 15 | HG00639.hp2 HG02559.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.68-73A>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170088637 | |||||||
chr4:170088684 | C | G | 1 | a0001c0001t0006g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-120G>C | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170088684 | |||||||
chr4:170088715 | T | A | 8 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0045others(5): Show | 15 | HG00639.hp2 HG02559.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.68-151A>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170088715 | |||||||
chr4:170088754 | G | A | 7 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0183others(4): Show | 9 | HG01358.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-190C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170088754 | |||||||
chr4:170088835 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.68-271C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170088835 | |||||||
chr4:170088936 | ATGGT | A | 17 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(14): Show | 30 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.68-376_68-373delAC others(2): Show |
AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170088936 | |||||||
chr4:170088950 | G | A | 7 | a0001c0001t0001g0013a0001c0001t0001g0047a0001c0001t0001g0194others(4): Show | 12 | HG00099.hp2 HG00280.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.68-386C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170088950 | |||||||
chr4:170088960 | C | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 5 | HG02109.hp2 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-396G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170088960 | |||||||
chr4:170089010 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.68-446C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170089010 | |||||||
chr4:170089163 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.67+461C>T | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170089163 | |||||||
chr4:170089292 | G | C | 1 | a0001c0001t0001g0048 | 2 | NA18977.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.67+332C>G | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170089292 | |||||||
chr4:170089328 | C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0058 | 3 | HG00408.hp2 NA18950.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.67+296G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170089328 | |||||||
chr4:170089355 | C | T | 7 | a0001c0001t0001g0051a0001c0001t0002g0015a0001c0001t0002g0052others(4): Show | 9 | HG00323.hp1 HG01255.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+269G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170089355 | |||||||
chr4:170089428 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67+196G>A | AADAT | ENSG00000109576.14 | transcript | ENST00000337664.9 | protein_coding | 1/12 | chr4 | 170089428 |