| geneid | 10267 |
|---|---|
| ensemblid | ENSG00000132329.11 |
| hgncid | 9843 |
| symbol | RAMP1 |
| name | receptor activity modifying protein 1 |
| refseq_nuc | NM_005855.4 |
| refseq_prot | NP_005846.1 |
| ensembl_nuc | ENST00000254661.5 |
| ensembl_prot | ENSP00000254661.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 237859623 |
| end | 237912106 |
| strand | + |
| ver | v1.2 |
| region | chr2:237859623-237912106 |
| region5000 | chr2:237854623-237917106 |
| regionname0 | RAMP1_chr2_237859623_237912106 |
| regionname5000 | RAMP1_chr2_237854623_237917106 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 148 | 403 | 98 | 74 | 168 | 17 | 44 | 122 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| a0002 | 0/0 | 148 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 447 | 339 | 95 | 67 | 118 | 16 | 41 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| c0002 | 0/0 | 447 | 63 | 3 | 7 | 50 | 0 | 3 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| c0003 | 0/0 | 447 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| c0004 | 0/0 | 447 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 377 | 390 | 87 | 74 | 167 | 17 | 43 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| t0002 | 0/0 | 377 | 6 | 5 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| t0003 | 0/0 | 377 | 5 | 5 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| t0004 | 0/0 | 377 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| t0005 | 0/0 | 377 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| t0006 | 0/0 | 377 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0384 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0391 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0392 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 447 | 339 | 95 | 67 | 118 | 16 | 41 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| a0001c0002 | 0/0 | 447 | 63 | 3 | 7 | 50 | 0 | 3 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| a0001c0004 | 0/0 | 447 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| a0002c0003 | 0/0 | 447 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 823 | 326 | 84 | 67 | 117 | 16 | 40 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| a0001c0001t0002 | 0/0 | 823 | 6 | 5 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| a0001c0001t0003 | 0/0 | 823 | 5 | 5 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| a0001c0001t0004 | 0/0 | 823 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| a0001c0001t0006 | 0/0 | 823 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| a0001c0002t0001 | 0/0 | 823 | 63 | 3 | 7 | 50 | 0 | 3 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| a0001c0004t0005 | 0/0 | 823 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| a0002c0003t0001 | 0/0 | 823 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | copy fasta | chr2 | 237854623 | 237917106 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0391 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0392 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0001g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0001t0006g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0384 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0002t0001g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0001c0004t0005g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| a0002c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0001 | g0209 | EUR | GBR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0275 | EUR | GBR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | GBR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0251 | EUR | FIN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0322 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0350 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0343 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0392 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0352 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | IBS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | IBS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | IBS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0176 | EUR | IBS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0351 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0391 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0389 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0362 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0371 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0341 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0373 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0329 | EAS | CDX | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CDX | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0336 | EAS | CDX | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0331 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0387 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0330 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0384 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0139 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0395 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0346 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0394 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0393 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03710 | hp2 | a0001 | c0001 | t0006 | g0314 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | STU | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | STU | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0354 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | STU | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | STU | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | STU | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | STU | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | YRI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CHB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | YRI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | YRI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0364 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0380 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0369 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0383 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0357 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0365 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0333 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0356 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0375 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0349 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0342 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0390 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0361 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0368 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0370 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0366 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0339 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0386 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0372 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0376 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0353 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0337 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0348 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0377 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0381 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0382 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0378 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0359 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0396 | AFR | LWK | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | LWK | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | LWK | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0388 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0338 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0379 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0347 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0335 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0355 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0360 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0340 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0358 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0363 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0374 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0345 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0367 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0344 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | YRI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ASW | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0385 | AFR | ASW | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA20752 | hp1 | a0001 | c0004 | t0005 | g0179 | EUR | TSI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | TSI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0315 | EUR | TSI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | TSI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | GIH | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | GIH | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0334 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0317 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | USA | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | USA | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | USA | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | USA | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | LWK | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0206 | REF | REF | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0104 | REF | REF | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:237877268
|
G | A | 1 | a0002 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.97G>A | p.Gly33Ser | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/3 | 150/823 | 97/447 | 33/148 | chr2 | 237877268 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:237859681
|
C | T | 1 | a0001c0002 | 63 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(60): Show |
synonymous_variant | LOW | c.6C>T | p.Ala2Ala | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/3 | 59/823 | 6/447 | 2/148 | chr2 | 237859681 | ||
| chr2:237859723
|
C | T | 1 | a0001c0002 | 63 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(60): Show |
synonymous_variant | LOW | c.48C>T | p.Leu16Leu | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/3 | 101/823 | 48/447 | 16/148 | chr2 | 237859723 | ||
| chr2:237911708
|
G | A | 1 | a0001c0004 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.372G>A | p.Val124Val | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 3/3 | 425/823 | 372/447 | 124/148 | chr2 | 237911708 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:237911786
|
G | C | 1 | a0001c0001t0004 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 3/3 | 3 | chr2 | 237911786 | |||||
| chr2:237911893
|
C | G | 1 | a0001c0001t0002 | 6 | HG01884.hp2 HG01891.hp2 HG02135.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*110C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 3/3 | 110 | chr2 | 237911893 | |||||
| chr2:237912005
|
C | T | 1 | a0001c0001t0003 | 5 | HG02717.hp1 HG02818.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*222C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 3/3 | 222 | chr2 | 237912005 | |||||
| chr2:237912030
|
G | C | 1 | a0001c0004t0005 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*247G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 3/3 | 247 | chr2 | 237912030 | |||||
| chr2:237912099
|
T | C | 1 | a0001c0001t0006 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*316T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 3/3 | 316 | chr2 | 237912099 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:237859797
|
G | GGGGAGCG others(3): Show |
1 | a0001c0001t0001g0023 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.52+94_52+103dupAGC others(7): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237859797 | |||||
| chr2:237859797
|
GGGGAGCG others(3): Show |
G | 69 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325others(66): Show | 69 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.52+94_52+103delAGC others(7): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237859797 | |||||
| chr2:237859806
|
G | A | 12 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG00544.hp1 HG02056.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.52+79G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237859806 | ||||||
| chr2:237859818
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.52+91G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237859818 | ||||||
| chr2:237859821
|
A | G | 6 | a0001c0001t0001g0391a0001c0001t0001g0392a0001c0001t0001g0393others(3): Show | 6 | HG01109.hp2 HG01993.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+94A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237859821 | ||||||
| chr2:237859856
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.52+129C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237859856 | ||||||
| chr2:237859861
|
C | T | 5 | a0001c0002t0001g0386a0001c0002t0001g0387a0001c0002t0001g0388others(2): Show | 5 | HG02004.hp1 HG02300.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+134C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237859861 | ||||||
| chr2:237859924
|
C | T | 1 | a0001c0001t0001g0320 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.52+197C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237859924 | ||||||
| chr2:237859944
|
C | T | 2 | a0001c0002t0001g0384a0001c0002t0001g0385 | 2 | HG02698.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.52+217C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237859944 | ||||||
| chr2:237860109
|
G | A | 1 | a0001c0002t0001g0322 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.52+382G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860109 | ||||||
| chr2:237860147
|
C | G | 63 | a0001c0002t0001g0322a0001c0002t0001g0329a0001c0002t0001g0330others(60): Show | 63 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.52+420C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860147 | ||||||
| chr2:237860417
|
C | T | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | NA19066.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.52+690C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860417 | ||||||
| chr2:237860456
|
G | A | 63 | a0001c0002t0001g0322a0001c0002t0001g0329a0001c0002t0001g0330others(60): Show | 63 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.52+729G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860456 | ||||||
| chr2:237860471
|
A | G | 2 | a0001c0001t0001g0316a0001c0001t0002g0317 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.52+744A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860471 | ||||||
| chr2:237860616
|
C | T | 1 | a0001c0001t0001g0315 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.52+889C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860616 | ||||||
| chr2:237860685
|
G | GTGT | 90 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0229others(87): Show | 92 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.52+959_52+961dupTG others(1): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237860685 | |||||
| chr2:237860718
|
C | G | 1 | a0001c0001t0006g0314 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.52+991C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860718 | ||||||
| chr2:237860732
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.52+1005G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860732 | ||||||
| chr2:237860734
|
A | C | 1 | a0001c0001t0001g0228 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.52+1007A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860734 | ||||||
| chr2:237860799
|
T | C | 64 | a0001c0001t0001g0024a0001c0002t0001g0322a0001c0002t0001g0329others(61): Show | 64 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(61): Show |
intron_variant | MODIFIER | c.52+1072T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860799 | ||||||
| chr2:237860823
|
G | A | 1 | a0001c0001t0001g0391 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.52+1096G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860823 | ||||||
| chr2:237860862
|
A | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG02559.hp2 HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.52+1135A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860862 | ||||||
| chr2:237860888
|
AGATCTGC others(18): Show |
A | 7 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+1165_52+1189del others(25): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237860888 | |||||
| chr2:237861037
|
A | G | 198 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 201 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(198): Show |
intron_variant | MODIFIER | c.52+1310A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861037 | ||||||
| chr2:237861041
|
A | C | 63 | a0001c0002t0001g0322a0001c0002t0001g0329a0001c0002t0001g0330others(60): Show | 63 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.52+1314A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861041 | ||||||
| chr2:237861047
|
A | T | 1 | a0001c0001t0001g0321 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.52+1320A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861047 | ||||||
| chr2:237861218
|
G | A | 63 | a0001c0002t0001g0322a0001c0002t0001g0329a0001c0002t0001g0330others(60): Show | 63 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.52+1491G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861218 | ||||||
| chr2:237861249
|
A | G | 63 | a0001c0002t0001g0322a0001c0002t0001g0329a0001c0002t0001g0330others(60): Show | 63 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.52+1522A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861249 | ||||||
| chr2:237861347
|
A | C | 8 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(5): Show | 8 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+1620A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861347 | ||||||
| chr2:237861422
|
C | A | 13 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(10): Show | 13 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.52+1695C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861422 | ||||||
| chr2:237861583
|
C | A | 1 | a0001c0001t0001g0140 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.52+1856C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861583 | ||||||
| chr2:237861705
|
G | A | 36 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(33): Show | 36 | HG01099.hp2 HG01175.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.52+1978G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861705 | ||||||
| chr2:237861706
|
G | C | 36 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(33): Show | 36 | HG01099.hp2 HG01175.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.52+1979G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861706 | ||||||
| chr2:237861812
|
C | T | 2 | a0001c0001t0003g0138a0001c0001t0004g0139 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.52+2085C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861812 | ||||||
| chr2:237861835
|
G | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(8): Show | 11 | HG00544.hp1 HG02056.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.52+2108G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861835 | ||||||
| chr2:237861851
|
C | CA | 137 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(134): Show | 140 | HG00099.hp1 HG00558.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.52+2138dupA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237861851 | |||||
| chr2:237861972
|
G | A | 1 | a0001c0001t0001g0391 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.52+2245G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861972 | ||||||
| chr2:237862103
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.52+2376C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862103 | ||||||
| chr2:237862173
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.52+2446T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862173 | ||||||
| chr2:237862185
|
G | A | 1 | a0001c0002t0001g0386 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.52+2458G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862185 | ||||||
| chr2:237862244
|
G | A | 7 | a0001c0001t0001g0141a0001c0001t0001g0324a0001c0001t0001g0325others(4): Show | 7 | HG01993.hp2 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+2517G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862244 | ||||||
| chr2:237862402
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.52+2675C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862402 | ||||||
| chr2:237862504
|
G | C | 13 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(10): Show | 13 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.52+2777G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862504 | ||||||
| chr2:237862541
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.52+2814C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862541 | ||||||
| chr2:237862553
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.52+2826C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862553 | ||||||
| chr2:237862667
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52+2940C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862667 | ||||||
| chr2:237862763
|
C | T | 1 | a0001c0002t0001g0382 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.52+3036C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862763 | ||||||
| chr2:237862774
|
T | C | 162 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(159): Show | 163 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(160): Show |
intron_variant | MODIFIER | c.52+3047T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862774 | ||||||
| chr2:237862822
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.52+3095G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862822 | ||||||
| chr2:237862886
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.52+3159G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862886 | ||||||
| chr2:237862919
|
A | G | 3 | a0001c0001t0001g0313a0001c0001t0001g0318a0001c0001t0001g0319 | 3 | NA19066.hp1 NA19074.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.52+3192A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862919 | ||||||
| chr2:237862932
|
T | C | 84 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(81): Show | 84 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(81): Show |
intron_variant | MODIFIER | c.52+3205T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862932 | ||||||
| chr2:237863000
|
T | C | 68 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(65): Show | 68 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.52+3273T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863000 | ||||||
| chr2:237863008
|
A | G | 2 | a0001c0002t0001g0380a0001c0002t0001g0381 | 2 | NA18946.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.52+3281A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863008 | ||||||
| chr2:237863013
|
A | C | 21 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(18): Show | 21 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.52+3286A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863013 | ||||||
| chr2:237863194
|
AGGGGACA others(9): Show |
A | 36 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(33): Show | 37 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.52+3471_52+3486del others(16): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237863194 | |||||
| chr2:237863226
|
T | C | 8 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(5): Show | 8 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+3499T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863226 | ||||||
| chr2:237863441
|
T | C | 21 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(18): Show | 21 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.52+3714T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863441 | ||||||
| chr2:237863481
|
A | G | 8 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(5): Show | 8 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+3754A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863481 | ||||||
| chr2:237863502
|
C | A | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.52+3775C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863502 | ||||||
| chr2:237863540
|
T | C | 16 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(13): Show | 16 | HG01099.hp2 HG01175.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.52+3813T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863540 | ||||||
| chr2:237863550
|
A | G | 1 | a0001c0002t0001g0389 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.52+3823A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863550 | ||||||
| chr2:237863595
|
A | T | 11 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(8): Show | 11 | HG00544.hp1 HG02056.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.52+3868A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863595 | ||||||
| chr2:237863748
|
G | C | 19 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(16): Show | 19 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.52+4021G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863748 | ||||||
| chr2:237863751
|
C | A | 1 | a0001c0001t0001g0020 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.52+4024C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863751 | ||||||
| chr2:237863752
|
C | T | 19 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(16): Show | 19 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.52+4025C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863752 | ||||||
| chr2:237863758
|
T | C | 19 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(16): Show | 19 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.52+4031T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863758 | ||||||
| chr2:237863761
|
A | G | 137 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(134): Show | 137 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.52+4034A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863761 | ||||||
| chr2:237863814
|
C | T | 2 | a0001c0001t0001g0218a0001c0001t0001g0396 | 2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.52+4087C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863814 | ||||||
| chr2:237863877
|
GC | G | 7 | a0001c0001t0001g0141a0001c0001t0001g0324a0001c0001t0001g0325others(4): Show | 7 | HG01993.hp2 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+4154delC | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237863877 | |||||
| chr2:237863893
|
G | C | 136 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(133): Show | 137 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.52+4166G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863893 | ||||||
| chr2:237863970
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.52+4243C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863970 | ||||||
| chr2:237864086
|
A | G | 153 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(150): Show | 155 | HG00558.hp1 HG00609.hp2 HG00639.hp2 others(152): Show |
intron_variant | MODIFIER | c.52+4359A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864086 | ||||||
| chr2:237864145
|
ACCTGGCC others(5): Show |
A | 3 | a0001c0001t0001g0218a0001c0001t0001g0396a0001c0001t0003g0224 | 3 | HG02717.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.52+4424_52+4435del others(12): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237864145 | |||||
| chr2:237864151
|
CCCGTGGC others(5): Show |
C | 25 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(22): Show | 25 | HG01099.hp2 HG01175.hp2 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.52+4427_52+4438del others(12): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237864151 | |||||
| chr2:237864273
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.52+4546C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864273 | ||||||
| chr2:237864303
|
TGCCCAAC others(7): Show |
T | 21 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(18): Show | 21 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.52+4578_52+4591del others(14): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237864303 | |||||
| chr2:237864316
|
G | A | 6 | a0001c0001t0001g0141a0001c0001t0001g0324a0001c0001t0001g0325others(3): Show | 6 | HG02809.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+4589G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864316 | ||||||
| chr2:237864336
|
CTGCCGCT others(1): Show |
C | 21 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(18): Show | 21 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.52+4611_52+4618del others(8): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237864336 | |||||
| chr2:237864345
|
T | G | 21 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(18): Show | 21 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.52+4618T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864345 | ||||||
| chr2:237864347
|
A | G | 21 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(18): Show | 21 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.52+4620A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864347 | ||||||
| chr2:237864399
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(136): Show | 141 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(138): Show |
intron_variant | MODIFIER | c.52+4672T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864399 | ||||||
| chr2:237864404
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(134): Show | 139 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.52+4677T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864404 | ||||||
| chr2:237864430
|
G | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(135): Show | 140 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.52+4703G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864430 | ||||||
| chr2:237864437
|
T | C | 14 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(11): Show | 14 | HG01099.hp2 HG01175.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.52+4710T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864437 | ||||||
| chr2:237864611
|
G | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(139): Show | 144 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.52+4884G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864611 | ||||||
| chr2:237864631
|
C | A | 1 | a0001c0001t0001g0030 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.52+4904C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864631 | ||||||
| chr2:237864664
|
T | G | 1 | a0001c0001t0001g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.52+4937T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864664 | ||||||
| chr2:237864795
|
G | A | 2 | a0001c0001t0001g0230a0001c0001t0002g0187 | 2 | HG02572.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.52+5068G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864795 | ||||||
| chr2:237864888
|
C | CTT | 140 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(137): Show | 142 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.52+5163_52+5164dup others(2): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237864888 | |||||
| chr2:237864954
|
G | T | 34 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(31): Show | 34 | HG01099.hp2 HG01175.hp2 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.52+5227G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864954 | ||||||
| chr2:237865009
|
G | T | 2 | a0001c0001t0001g0395a0001c0001t0002g0215 | 2 | HG01884.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.52+5282G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865009 | ||||||
| chr2:237865062
|
A | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(56): Show | 61 | HG00438.hp2 HG00741.hp1 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.52+5335A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865062 | ||||||
| chr2:237865301
|
A | G | 11 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0156others(8): Show | 11 | HG01884.hp2 HG01993.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.52+5574A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865301 | ||||||
| chr2:237865487
|
A | G | 40 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0120others(37): Show | 42 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.52+5760A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865487 | ||||||
| chr2:237865549
|
C | T | 2 | a0001c0001t0001g0299a0001c0001t0001g0300 | 2 | HG00423.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.52+5822C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865549 | ||||||
| chr2:237865635
|
A | G | 8 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(5): Show | 8 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+5908A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865635 | ||||||
| chr2:237865685
|
C | T | 82 | a0001c0001t0001g0119a0001c0001t0001g0141a0001c0001t0001g0145others(79): Show | 82 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.52+5958C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865685 | ||||||
| chr2:237865725
|
G | A | 3 | a0001c0001t0001g0391a0001c0001t0001g0395a0001c0001t0002g0215 | 3 | HG01884.hp2 HG01993.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.52+5998G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865725 | ||||||
| chr2:237865732
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.52+6005C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865732 | ||||||
| chr2:237865814
|
C | A | 1 | a0001c0001t0001g0030 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.52+6087C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865814 | ||||||
| chr2:237865871
|
G | C | 1 | a0001c0001t0001g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.52+6144G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865871 | ||||||
| chr2:237865895
|
C | T | 56 | a0001c0001t0001g0124a0001c0002t0001g0322a0001c0002t0001g0329others(53): Show | 56 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.52+6168C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865895 | ||||||
| chr2:237865946
|
G | A | 1 | a0001c0001t0001g0318 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.52+6219G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865946 | ||||||
| chr2:237866116
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.52+6389G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866116 | ||||||
| chr2:237866120
|
C | T | 1 | a0001c0002t0001g0378 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.52+6393C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866120 | ||||||
| chr2:237866132
|
G | A | 1 | a0001c0001t0003g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.52+6405G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866132 | ||||||
| chr2:237866176
|
A | T | 1 | a0001c0002t0001g0388 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.52+6449A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866176 | ||||||
| chr2:237866500
|
G | C | 1 | a0001c0001t0001g0324 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.52+6773G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866500 | ||||||
| chr2:237866545
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.52+6818A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866545 | ||||||
| chr2:237866565
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.52+6838G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866565 | ||||||
| chr2:237866588
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.52+6861C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866588 | ||||||
| chr2:237866589
|
A | C | 1 | a0001c0001t0001g0020 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.52+6862A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866589 | ||||||
| chr2:237866605
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.52+6878G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866605 | ||||||
| chr2:237866636
|
C | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG01168.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.52+6909C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866636 | ||||||
| chr2:237866726
|
CT | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0120others(60): Show | 65 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.52+7011delT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237866726 | |||||
| chr2:237866738
|
T | C | 1 | a0001c0001t0001g0020 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.52+7011T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866738 | ||||||
| chr2:237866739
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.52+7012C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866739 | ||||||
| chr2:237866763
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.52+7036C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866763 | ||||||
| chr2:237866815
|
A | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.52+7088A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866815 | ||||||
| chr2:237866822
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.52+7095G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866822 | ||||||
| chr2:237866890
|
G | A | 1 | a0001c0001t0003g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.52+7163G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866890 | ||||||
| chr2:237866996
|
T | A | 1 | a0001c0001t0001g0020 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.52+7269T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866996 | ||||||
| chr2:237867050
|
A | C | 21 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(18): Show | 23 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.52+7323A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867050 | ||||||
| chr2:237867118
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+7391C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867118 | ||||||
| chr2:237867162
|
G | T | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.52+7435G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867162 | ||||||
| chr2:237867304
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.52+7577G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867304 | ||||||
| chr2:237867413
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.52+7686T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867413 | ||||||
| chr2:237867430
|
C | T | 75 | a0001c0001t0001g0127a0001c0001t0001g0141a0001c0001t0001g0158others(72): Show | 75 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(72): Show |
intron_variant | MODIFIER | c.52+7703C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867430 | ||||||
| chr2:237867477
|
T | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0120others(28): Show | 33 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.52+7750T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867477 | ||||||
| chr2:237867526
|
C | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0297 | 2 | HG03490.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.52+7799C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867526 | ||||||
| chr2:237867629
|
A | T | 1 | a0001c0001t0001g0222 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.52+7902A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867629 | ||||||
| chr2:237867634
|
C | T | 23 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0143others(20): Show | 23 | HG00642.hp2 HG01081.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.52+7907C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867634 | ||||||
| chr2:237867678
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.52+7951C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867678 | ||||||
| chr2:237867752
|
C | T | 10 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(7): Show | 10 | HG01175.hp2 HG02074.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.52+8025C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867752 | ||||||
| chr2:237867788
|
G | C | 70 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(67): Show | 70 | HG00609.hp1 HG00639.hp2 HG01109.hp1 others(67): Show |
intron_variant | MODIFIER | c.52+8061G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867788 | ||||||
| chr2:237867852
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.52+8125A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867852 | ||||||
| chr2:237867888
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.52+8161A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867888 | ||||||
| chr2:237868046
|
C | CT | 10 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0025others(7): Show | 10 | HG01884.hp1 HG01993.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.52+8335dupT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237868046 | |||||
| chr2:237868093
|
G | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(19): Show | 24 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.52+8366G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868093 | ||||||
| chr2:237868278
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG02559.hp2 HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.52+8551C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868278 | ||||||
| chr2:237868477
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.53-8747G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868477 | ||||||
| chr2:237868495
|
G | A | 22 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(19): Show | 24 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.53-8729G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868495 | ||||||
| chr2:237868568
|
T | C | 1 | a0001c0001t0001g0020 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.53-8656T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868568 | ||||||
| chr2:237868569
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.53-8655C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868569 | ||||||
| chr2:237868575
|
A | G | 4 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-8649A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868575 | ||||||
| chr2:237868577
|
C | CA | 6 | a0001c0001t0001g0043a0001c0001t0001g0132a0001c0001t0001g0142others(3): Show | 6 | HG02055.hp2 HG03225.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-8635dupA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237868577 | |||||
| chr2:237868585
|
A | C | 4 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-8639A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868585 | ||||||
| chr2:237868589
|
AC | A | 6 | a0001c0001t0001g0145a0001c0001t0001g0198a0001c0002t0001g0336others(3): Show | 6 | HG01109.hp1 HG02165.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-8634delC | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868589 | ||||||
| chr2:237868590
|
C | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-8634C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868590 | ||||||
| chr2:237868590
|
CAA | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(167): Show | 174 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(171): Show |
intron_variant | MODIFIER | c.53-8622_53-8621del others(2): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237868590 | |||||
| chr2:237868590
|
CAAA | C | 11 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 11 | HG00544.hp1 HG02071.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-8623_53-8621del others(3): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237868590 | |||||
| chr2:237868591
|
A | C | 4 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-8633A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868591 | ||||||
| chr2:237868592
|
A | C | 6 | a0001c0001t0001g0145a0001c0001t0001g0198a0001c0002t0001g0336others(3): Show | 6 | HG01109.hp1 HG02165.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-8632A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868592 | ||||||
| chr2:237868593
|
A | C | 1 | a0001c0001t0001g0020 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.53-8631A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868593 | ||||||
| chr2:237868594
|
A | C | 3 | a0001c0001t0001g0112a0001c0001t0001g0295a0001c0001t0001g0296 | 3 | HG00733.hp2 NA18979.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.53-8630A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868594 | ||||||
| chr2:237868595
|
A | C | 4 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-8629A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868595 | ||||||
| chr2:237868617
|
T | G | 12 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(9): Show | 12 | HG00544.hp1 HG02071.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.53-8607T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868617 | ||||||
| chr2:237868674
|
C | T | 9 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304others(6): Show | 9 | NA18941.hp2 NA18950.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.53-8550C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868674 | ||||||
| chr2:237868701
|
TGCTTGGC others(1): Show |
T | 6 | a0001c0001t0001g0033a0001c0001t0001g0038a0001c0001t0001g0039others(3): Show | 6 | HG00609.hp1 HG02056.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-8515_53-8508del others(8): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237868701 | |||||
| chr2:237868813
|
G | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(19): Show | 24 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.53-8411G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868813 | ||||||
| chr2:237868899
|
G | A | 1 | a0001c0001t0006g0314 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.53-8325G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868899 | ||||||
| chr2:237868901
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-8323C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868901 | ||||||
| chr2:237868989
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.53-8235C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868989 | ||||||
| chr2:237869011
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0199a0001c0001t0001g0200 | 4 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-8213G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869011 | ||||||
| chr2:237869111
|
ACCCTGCA others(140): Show |
A | 1 | a0001c0002t0001g0335 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.53-8112_53-7966del | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869111 | ||||||
| chr2:237869115
|
T | G | 1 | a0001c0002t0001g0334 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.53-8109T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869115 | ||||||
| chr2:237869205
|
C | G | 42 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0120others(39): Show | 44 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.53-8019C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869205 | ||||||
| chr2:237869319
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.53-7905T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869319 | ||||||
| chr2:237869341
|
T | G | 1 | a0001c0001t0001g0133 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.53-7883T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869341 | ||||||
| chr2:237869353
|
C | T | 22 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0143others(19): Show | 22 | HG00642.hp2 HG01081.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.53-7871C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869353 | ||||||
| chr2:237869775
|
C | G | 12 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(9): Show | 12 | HG00544.hp1 HG02071.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.53-7449C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869775 | ||||||
| chr2:237869839
|
G | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0173a0001c0001t0001g0174others(6): Show | 10 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-7385G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869839 | ||||||
| chr2:237869861
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.53-7363C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869861 | ||||||
| chr2:237869889
|
C | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02080.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.53-7335C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869889 | ||||||
| chr2:237869907
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.53-7317G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869907 | ||||||
| chr2:237870101
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-7123G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870101 | ||||||
| chr2:237870297
|
G | A | 46 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(43): Show | 48 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.53-6927G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870297 | ||||||
| chr2:237870407
|
C | T | 1 | a0001c0001t0001g0311 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.53-6817C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870407 | ||||||
| chr2:237870427
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.53-6797G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870427 | ||||||
| chr2:237870442
|
A | G | 23 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0143others(20): Show | 23 | HG00642.hp2 HG01081.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.53-6782A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870442 | ||||||
| chr2:237870512
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.53-6712C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870512 | ||||||
| chr2:237870589
|
C | A | 21 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(18): Show | 23 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.53-6635C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870589 | ||||||
| chr2:237870598
|
T | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(46): Show | 51 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.53-6626T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870598 | ||||||
| chr2:237870660
|
G | A | 1 | a0001c0002t0001g0345 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.53-6564G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870660 | ||||||
| chr2:237870891
|
A | C | 86 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(83): Show | 88 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.53-6333A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870891 | ||||||
| chr2:237870893
|
C | A | 1 | a0001c0001t0001g0396 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.53-6331C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870893 | ||||||
| chr2:237870942
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-6282G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870942 | ||||||
| chr2:237871040
|
C | T | 43 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0109others(40): Show | 45 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.53-6184C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871040 | ||||||
| chr2:237871041
|
G | C | 21 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(18): Show | 23 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.53-6183G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871041 | ||||||
| chr2:237871097
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.53-6127G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871097 | ||||||
| chr2:237871116
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.53-6108G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871116 | ||||||
| chr2:237871302
|
C | G | 1 | a0001c0001t0001g0222 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.53-5922C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871302 | ||||||
| chr2:237871430
|
C | G | 1 | a0001c0001t0003g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.53-5794C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871430 | ||||||
| chr2:237871500
|
T | C | 12 | a0001c0001t0001g0129a0001c0001t0001g0143a0001c0001t0001g0144others(9): Show | 12 | HG01099.hp2 HG01891.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.53-5724T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871500 | ||||||
| chr2:237871570
|
G | A | 2 | a0001c0001t0002g0044a0001c0001t0003g0032 | 2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.53-5654G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871570 | ||||||
| chr2:237871593
|
G | GC | 11 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 11 | HG00544.hp1 HG02071.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-5625dupC | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237871593 | |||||
| chr2:237871648
|
G | A | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 4 | HG03239.hp1 HG03669.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-5576G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871648 | ||||||
| chr2:237871674
|
C | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(194): Show | 201 | HG00438.hp2 HG00544.hp1 HG00639.hp2 others(198): Show |
intron_variant | MODIFIER | c.53-5550C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871674 | ||||||
| chr2:237871697
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.53-5527G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871697 | ||||||
| chr2:237871758
|
G | A | 1 | a0001c0001t0001g0318 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.53-5466G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871758 | ||||||
| chr2:237872031
|
G | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-5193G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872031 | ||||||
| chr2:237872208
|
G | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(105): Show | 110 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.53-5016G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872208 | ||||||
| chr2:237872217
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-5007C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872217 | ||||||
| chr2:237872233
|
T | C | 1 | a0001c0001t0001g0391 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.53-4991T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872233 | ||||||
| chr2:237872256
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-4968G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872256 | ||||||
| chr2:237872267
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.53-4957G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872267 | ||||||
| chr2:237872267
|
G | C | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-4957G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872267 | ||||||
| chr2:237872302
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.53-4922G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872302 | ||||||
| chr2:237872320
|
A | C | 1 | a0001c0001t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.53-4904A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872320 | ||||||
| chr2:237872363
|
G | A | 59 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0298others(56): Show | 59 | HG00639.hp2 HG01109.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.53-4861G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872363 | ||||||
| chr2:237872431
|
C | T | 2 | a0001c0001t0003g0138a0001c0001t0004g0139 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.53-4793C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872431 | ||||||
| chr2:237872602
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-4622G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872602 | ||||||
| chr2:237872611
|
G | C | 42 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0120others(39): Show | 44 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.53-4613G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872611 | ||||||
| chr2:237872710
|
G | A | 146 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(143): Show | 148 | HG00438.hp2 HG00544.hp1 HG00639.hp2 others(145): Show |
intron_variant | MODIFIER | c.53-4514G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872710 | ||||||
| chr2:237872740
|
A | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0108a0001c0001t0001g0239others(8): Show | 12 | HG00597.hp2 HG00673.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.53-4484A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872740 | ||||||
| chr2:237872755
|
T | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG02080.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.53-4469T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872755 | ||||||
| chr2:237872765
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.53-4459G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872765 | ||||||
| chr2:237872781
|
CTGTGGGA others(6): Show |
C | 1 | a0001c0001t0001g0241 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.53-4442_53-4430del others(13): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872781 | ||||||
| chr2:237872803
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.53-4421G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872803 | ||||||
| chr2:237872886
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.53-4338G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872886 | ||||||
| chr2:237872908
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.53-4316T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872908 | ||||||
| chr2:237872910
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-4314C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872910 | ||||||
| chr2:237872914
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.53-4310G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872914 | ||||||
| chr2:237873198
|
C | G | 1 | a0001c0001t0001g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.53-4026C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873198 | ||||||
| chr2:237873308
|
G | C | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.53-3916G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873308 | ||||||
| chr2:237873355
|
T | A | 1 | a0001c0001t0001g0395 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.53-3869T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873355 | ||||||
| chr2:237873419
|
G | T | 1 | a0001c0001t0001g0324 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.53-3805G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873419 | ||||||
| chr2:237873426
|
C | T | 1 | a0001c0001t0004g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.53-3798C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873426 | ||||||
| chr2:237873462
|
G | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0225a0001c0001t0003g0138others(1): Show | 4 | HG02647.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-3762G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873462 | ||||||
| chr2:237873508
|
C | T | 61 | a0001c0001t0001g0025a0001c0001t0001g0048a0001c0001t0001g0103others(58): Show | 61 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.53-3716C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873508 | ||||||
| chr2:237873551
|
T | C | 3 | a0001c0001t0001g0225a0001c0001t0001g0234a0001c0001t0001g0396 | 3 | HG02818.hp2 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.53-3673T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873551 | ||||||
| chr2:237873553
|
A | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0234a0001c0001t0001g0396 | 3 | HG02818.hp2 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.53-3671A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873553 | ||||||
| chr2:237873587
|
G | A | 11 | a0001c0001t0001g0023a0001c0001t0001g0048a0001c0001t0001g0103others(8): Show | 11 | HG02055.hp2 HG02559.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.53-3637G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873587 | ||||||
| chr2:237873595
|
T | C | 6 | a0001c0001t0001g0130a0001c0001t0001g0171a0001c0001t0001g0225others(3): Show | 6 | HG02647.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-3629T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873595 | ||||||
| chr2:237873620
|
T | C | 6 | a0001c0001t0001g0130a0001c0001t0001g0225a0001c0001t0001g0234others(3): Show | 6 | HG02647.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-3604T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873620 | ||||||
| chr2:237873630
|
G | A | 6 | a0001c0001t0001g0130a0001c0001t0001g0225a0001c0001t0001g0234others(3): Show | 6 | HG02647.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-3594G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873630 | ||||||
| chr2:237874067
|
A | G | 1 | a0001c0002t0001g0343 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.53-3157A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874067 | ||||||
| chr2:237874173
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.53-3051T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874173 | ||||||
| chr2:237874320
|
G | A | 5 | a0001c0001t0001g0141a0001c0001t0001g0173a0001c0001t0001g0211others(2): Show | 5 | HG00642.hp2 HG01346.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-2904G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874320 | ||||||
| chr2:237874330
|
C | T | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG02129.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.53-2894C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874330 | ||||||
| chr2:237874338
|
G | C | 38 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(35): Show | 38 | HG00544.hp1 HG01099.hp1 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.53-2886G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874338 | ||||||
| chr2:237874406
|
C | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | NA18950.hp2 NA18954.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-2818C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874406 | ||||||
| chr2:237874469
|
C | G | 8 | a0001c0001t0001g0130a0001c0001t0001g0188a0001c0001t0001g0225others(5): Show | 8 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.53-2755C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874469 | ||||||
| chr2:237874514
|
G | A | 23 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0120others(20): Show | 25 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.53-2710G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874514 | ||||||
| chr2:237874531
|
G | A | 23 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0120others(20): Show | 25 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.53-2693G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874531 | ||||||
| chr2:237874596
|
G | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | HG02280.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.53-2628G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874596 | ||||||
| chr2:237874620
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0225 | 2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.53-2604C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874620 | ||||||
| chr2:237874664
|
G | A | 1 | a0001c0002t0001g0383 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.53-2560G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874664 | ||||||
| chr2:237874677
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0199 | 2 | HG01099.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.53-2547C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874677 | ||||||
| chr2:237874884
|
TA | T | 42 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(39): Show | 42 | HG00544.hp1 HG01099.hp1 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.53-2338delA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237874884 | |||||
| chr2:237874924
|
C | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.53-2300C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874924 | ||||||
| chr2:237874943
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.53-2281C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874943 | ||||||
| chr2:237875116
|
C | T | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0021others(90): Show | 95 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.53-2108C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875116 | ||||||
| chr2:237875227
|
G | T | 89 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0021others(86): Show | 91 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(88): Show |
intron_variant | MODIFIER | c.53-1997G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875227 | ||||||
| chr2:237875228
|
G | T | 5 | a0001c0001t0001g0141a0001c0001t0001g0173a0001c0001t0001g0211others(2): Show | 5 | HG00642.hp2 HG01346.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-1996G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875228 | ||||||
| chr2:237875257
|
A | C | 111 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0021others(108): Show | 113 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(110): Show |
intron_variant | MODIFIER | c.53-1967A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875257 | ||||||
| chr2:237875266
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.53-1958G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875266 | ||||||
| chr2:237875393
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(113): Show | 120 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.53-1831G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875393 | ||||||
| chr2:237875395
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(113): Show | 120 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.53-1829A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875395 | ||||||
| chr2:237875404
|
TTCTGCCC others(30): Show |
T | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027 | 3 | HG02109.hp1 HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.53-1815_53-1779del others(37): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237875404 | |||||
| chr2:237875425
|
A | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 118 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.53-1799A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875425 | ||||||
| chr2:237875486
|
G | A | 4 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(1): Show | 4 | HG02280.hp1 HG03195.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-1738G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875486 | ||||||
| chr2:237875488
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0049 | 3 | HG01256.hp1 HG01975.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.53-1736G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875488 | ||||||
| chr2:237875519
|
G | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0191a0001c0001t0002g0128 | 3 | HG01891.hp2 HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.53-1705G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875519 | ||||||
| chr2:237875526
|
T | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(89): Show | 96 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.53-1698T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875526 | ||||||
| chr2:237875530
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(115): Show | 122 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.53-1694G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875530 | ||||||
| chr2:237875651
|
A | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(114): Show | 121 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.53-1573A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875651 | ||||||
| chr2:237875680
|
T | C | 5 | a0001c0001t0001g0141a0001c0001t0001g0173a0001c0001t0001g0211others(2): Show | 5 | HG00642.hp2 HG01346.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-1544T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875680 | ||||||
| chr2:237875682
|
G | GA | 3 | a0001c0002t0001g0329a0001c0002t0001g0362a0001c0002t0001g0363 | 3 | HG02027.hp1 HG02155.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.53-1542_53-1541ins others(1): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875682 | ||||||
| chr2:237875683
|
C | G | 3 | a0001c0002t0001g0329a0001c0002t0001g0362a0001c0002t0001g0363 | 3 | HG02027.hp1 HG02155.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.53-1541C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875683 | ||||||
| chr2:237875692
|
C | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(113): Show | 120 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.53-1532C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875692 | ||||||
| chr2:237875724
|
A | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(113): Show | 120 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.53-1500A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875724 | ||||||
| chr2:237875821
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.53-1403C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875821 | ||||||
| chr2:237875875
|
C | A | 1 | a0001c0001t0001g0034 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.53-1349C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875875 | ||||||
| chr2:237876030
|
T | G | 24 | a0001c0001t0001g0048a0001c0001t0001g0103a0001c0001t0001g0131others(21): Show | 24 | HG01099.hp1 HG01175.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.53-1194T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876030 | ||||||
| chr2:237876041
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.53-1183G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876041 | ||||||
| chr2:237876105
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0003g0224 | 2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.53-1119C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876105 | ||||||
| chr2:237876108
|
C | T | 15 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.53-1116C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876108 | ||||||
| chr2:237876134
|
G | A | 3 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265 | 3 | NA18961.hp2 NA18962.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.53-1090G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876134 | ||||||
| chr2:237876194
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.53-1030G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876194 | ||||||
| chr2:237876343
|
G | A | 1 | a0001c0002t0001g0346 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.53-881G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876343 | ||||||
| chr2:237876372
|
G | T | 1 | a0001c0002t0001g0375 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.53-852G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876372 | ||||||
| chr2:237876424
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(67): Show | 74 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.53-800G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876424 | ||||||
| chr2:237876590
|
C | G | 1 | a0001c0001t0001g0101 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.53-634C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876590 | ||||||
| chr2:237876607
|
G | A | 18 | a0001c0001t0001g0131a0001c0001t0001g0145a0001c0001t0001g0146others(15): Show | 18 | HG01099.hp1 HG01175.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.53-617G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876607 | ||||||
| chr2:237876608
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.53-616C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876608 | ||||||
| chr2:237876631
|
C | T | 1 | a0001c0002t0001g0388 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.53-593C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876631 | ||||||
| chr2:237876644
|
G | A | 23 | a0001c0001t0001g0048a0001c0001t0001g0103a0001c0001t0001g0131others(20): Show | 23 | HG01099.hp1 HG01175.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.53-580G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876644 | ||||||
| chr2:237876652
|
CG | C | 23 | a0001c0001t0001g0048a0001c0001t0001g0103a0001c0001t0001g0131others(20): Show | 23 | HG01099.hp1 HG01175.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.53-571delG | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876652 | ||||||
| chr2:237876656
|
C | G | 23 | a0001c0001t0001g0048a0001c0001t0001g0103a0001c0001t0001g0131others(20): Show | 23 | HG01099.hp1 HG01175.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.53-568C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876656 | ||||||
| chr2:237876658
|
C | A | 23 | a0001c0001t0001g0048a0001c0001t0001g0103a0001c0001t0001g0131others(20): Show | 23 | HG01099.hp1 HG01175.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.53-566C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876658 | ||||||
| chr2:237876709
|
C | T | 1 | a0001c0002t0001g0374 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.53-515C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876709 | ||||||
| chr2:237876752
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.53-472C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876752 | ||||||
| chr2:237876786
|
G | T | 1 | a0001c0002t0001g0374 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.53-438G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876786 | ||||||
| chr2:237876797
|
C | T | 1 | a0001c0001t0001g0396 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.53-427C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876797 | ||||||
| chr2:237876817
|
G | T | 25 | a0001c0001t0001g0048a0001c0001t0001g0103a0001c0001t0001g0131others(22): Show | 25 | HG01099.hp1 HG01175.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.53-407G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876817 | ||||||
| chr2:237876849
|
C | G | 6 | a0001c0002t0001g0345a0001c0002t0001g0357a0001c0002t0001g0358others(3): Show | 6 | NA18950.hp1 NA18975.hp1 NA19012.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-375C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876849 | ||||||
| chr2:237876861
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.53-363G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876861 | ||||||
| chr2:237876876
|
T | G | 1 | a0001c0001t0001g0052 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.53-348T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876876 | ||||||
| chr2:237876904
|
C | A | 6 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0350others(3): Show | 6 | HG00639.hp2 HG01109.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-320C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876904 | ||||||
| chr2:237876956
|
A | G | 25 | a0001c0001t0001g0048a0001c0001t0001g0103a0001c0001t0001g0131others(22): Show | 25 | HG01099.hp1 HG01175.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.53-268A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876956 | ||||||
| chr2:237876978
|
T | A | 25 | a0001c0001t0001g0048a0001c0001t0001g0103a0001c0001t0001g0131others(22): Show | 25 | HG01099.hp1 HG01175.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.53-246T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876978 | ||||||
| chr2:237877000
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.53-224C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877000 | ||||||
| chr2:237877001
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.53-223G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877001 | ||||||
| chr2:237877018
|
C | A | 45 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0021others(42): Show | 47 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.53-206C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877018 | ||||||
| chr2:237877095
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.53-129G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877095 | ||||||
| chr2:237877130
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.53-94G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877130 | ||||||
| chr2:237877133
|
G | A | 1 | a0001c0004t0005g0179 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.53-91G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877133 | ||||||
| chr2:237877154
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.53-70G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877154 | ||||||
| chr2:237877189
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.53-35C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877189 | ||||||
| chr2:237877190
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.53-34G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877190 | ||||||
| chr2:237877210
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0003g0138a0001c0001t0004g0139 | 3 | HG00280.hp1 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.53-14C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877210 | ||||||
| chr2:237877372
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.191+10A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877372 | ||||||
| chr2:237877395
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.191+33G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877395 | ||||||
| chr2:237877397
|
T | C | 2 | a0001c0002t0001g0380a0001c0002t0001g0381 | 2 | NA18946.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.191+35T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877397 | ||||||
| chr2:237877490
|
G | C | 1 | a0001c0001t0001g0210 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.191+128G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877490 | ||||||
| chr2:237877490
|
G | T | 135 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0019others(132): Show | 135 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.191+128G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877490 | ||||||
| chr2:237877494
|
G | T | 1 | a0001c0001t0001g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.191+132G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877494 | ||||||
| chr2:237877561
|
G | A | 23 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0120others(20): Show | 25 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.191+199G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877561 | ||||||
| chr2:237877631
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.191+269C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877631 | ||||||
| chr2:237877851
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.191+489G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877851 | ||||||
| chr2:237877873
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 219 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.191+511A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877873 | ||||||
| chr2:237877881
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0391 | 2 | HG01993.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.191+519C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877881 | ||||||
| chr2:237878018
|
G | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.191+656G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878018 | ||||||
| chr2:237878082
|
C | T | 21 | a0001c0001t0001g0048a0001c0001t0001g0103a0001c0001t0001g0131others(18): Show | 21 | HG01099.hp1 HG01175.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.191+720C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878082 | ||||||
| chr2:237878230
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.191+868G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878230 | ||||||
| chr2:237878417
|
T | G | 10 | a0001c0001t0001g0125a0001c0002t0001g0342a0001c0002t0001g0364others(7): Show | 10 | HG02004.hp1 HG02300.hp1 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.191+1055T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878417 | ||||||
| chr2:237878518
|
G | A | 2 | a0001c0001t0003g0138a0001c0001t0004g0139 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.191+1156G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878518 | ||||||
| chr2:237878605
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(117): Show | 124 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.191+1243C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878605 | ||||||
| chr2:237878635
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.191+1273T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878635 | ||||||
| chr2:237878793
|
G | A | 15 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.191+1431G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878793 | ||||||
| chr2:237878870
|
G | T | 2 | a0001c0001t0001g0261a0001c0002t0001g0335 | 2 | NA19003.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.191+1508G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878870 | ||||||
| chr2:237878892
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.191+1530C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878892 | ||||||
| chr2:237879049
|
A | G | 1 | a0001c0001t0001g0286 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.191+1687A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879049 | ||||||
| chr2:237879266
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.191+1904G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879266 | ||||||
| chr2:237879415
|
C | T | 10 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0183others(7): Show | 10 | HG00642.hp2 HG01884.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.191+2053C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879415 | ||||||
| chr2:237879449
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.191+2087C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879449 | ||||||
| chr2:237879479
|
C | T | 2 | a0001c0002t0001g0378a0001c0002t0001g0388 | 2 | NA19011.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.191+2117C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879479 | ||||||
| chr2:237879482
|
TTTTTTA | T | 20 | a0001c0001t0001g0048a0001c0001t0001g0103a0001c0001t0001g0131others(17): Show | 20 | HG01099.hp1 HG01175.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.191+2123_191+2128d others(8): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237879482 | |||||
| chr2:237879485
|
T | C | 27 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(24): Show | 27 | HG00544.hp1 HG00642.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.191+2123T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879485 | ||||||
| chr2:237879488
|
A | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0395 | 2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.191+2126A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879488 | ||||||
| chr2:237879491
|
A | C | 20 | a0001c0001t0001g0048a0001c0001t0001g0103a0001c0001t0001g0131others(17): Show | 20 | HG01099.hp1 HG01175.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.191+2129A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879491 | ||||||
| chr2:237879502
|
T | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.191+2140T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879502 | ||||||
| chr2:237879537
|
C | T | 6 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0211others(3): Show | 6 | HG00642.hp2 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.191+2175C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879537 | ||||||
| chr2:237879584
|
C | A | 8 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0183others(5): Show | 8 | HG00642.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+2222C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879584 | ||||||
| chr2:237879594
|
C | A | 8 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0183others(5): Show | 8 | HG00642.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+2232C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879594 | ||||||
| chr2:237879596
|
C | G | 8 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0183others(5): Show | 8 | HG00642.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+2234C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879596 | ||||||
| chr2:237879597
|
G | A | 8 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0183others(5): Show | 8 | HG00642.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+2235G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879597 | ||||||
| chr2:237879598
|
T | C | 8 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0183others(5): Show | 8 | HG00642.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+2236T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879598 | ||||||
| chr2:237879599
|
C | G | 8 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0183others(5): Show | 8 | HG00642.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+2237C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879599 | ||||||
| chr2:237879601
|
T | G | 8 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0183others(5): Show | 8 | HG00642.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+2239T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879601 | ||||||
| chr2:237879611
|
T | G | 8 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0183others(5): Show | 8 | HG00642.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+2249T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879611 | ||||||
| chr2:237879622
|
A | G | 88 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(85): Show | 91 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(88): Show |
intron_variant | MODIFIER | c.191+2260A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879622 | ||||||
| chr2:237879690
|
T | TA | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 216 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.191+2342dupA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237879690 | |||||
| chr2:237879705
|
T | C | 114 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 117 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.191+2343T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879705 | ||||||
| chr2:237879771
|
A | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0395 | 2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.191+2409A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879771 | ||||||
| chr2:237879846
|
C | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0223a0001c0001t0003g0224 | 3 | HG02717.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.191+2484C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879846 | ||||||
| chr2:237879847
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0200a0001c0001t0001g0236 | 4 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+2485G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879847 | ||||||
| chr2:237879883
|
G | A | 88 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(85): Show | 91 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(88): Show |
intron_variant | MODIFIER | c.191+2521G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879883 | ||||||
| chr2:237879934
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.191+2572G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879934 | ||||||
| chr2:237879947
|
G | A | 2 | a0001c0001t0003g0138a0001c0001t0004g0139 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.191+2585G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879947 | ||||||
| chr2:237879989
|
C | CA | 31 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(28): Show | 31 | HG00544.hp1 HG00597.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.191+2649dupA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237879989 | |||||
| chr2:237879989
|
C | CAA | 42 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(39): Show | 44 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.191+2648_191+2649d others(4): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237879989 | |||||
| chr2:237879989
|
C | CAAA | 70 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0022others(67): Show | 71 | HG01074.hp1 HG01099.hp2 HG01109.hp2 others(68): Show |
intron_variant | MODIFIER | c.191+2647_191+2649d others(5): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237879989 | |||||
| chr2:237879989
|
C | CAAAA | 18 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(15): Show | 18 | HG00408.hp1 HG00642.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.191+2646_191+2649d others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237879989 | |||||
| chr2:237879989
|
C | CAAAAA | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(44): Show | 51 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.191+2645_191+2649d others(7): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237879989 | |||||
| chr2:237879989
|
C | CAAAAAA | 12 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0155others(9): Show | 12 | HG00621.hp2 HG01255.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.191+2644_191+2649d others(8): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237879989 | |||||
| chr2:237879989
|
CA | C | 12 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0106others(9): Show | 12 | HG01261.hp2 HG02132.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.191+2649delA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237879989 | |||||
| chr2:237880026
|
G | A | 20 | a0001c0001t0001g0048a0001c0001t0001g0103a0001c0001t0001g0131others(17): Show | 20 | HG01099.hp1 HG01175.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.191+2664G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880026 | ||||||
| chr2:237880079
|
G | A | 3 | a0001c0001t0001g0218a0001c0001t0001g0223a0001c0001t0003g0224 | 3 | HG02717.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.191+2717G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880079 | ||||||
| chr2:237880156
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.191+2794G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880156 | ||||||
| chr2:237880185
|
CACAG | C | 19 | a0001c0001t0001g0103a0001c0001t0001g0131a0001c0001t0001g0146others(16): Show | 19 | HG01099.hp1 HG01175.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.191+2829_191+2832d others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237880185 | |||||
| chr2:237880188
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.191+2826A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880188 | ||||||
| chr2:237880215
|
G | A | 19 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(16): Show | 19 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.191+2853G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880215 | ||||||
| chr2:237880232
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.191+2870T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880232 | ||||||
| chr2:237880250
|
C | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(64): Show | 71 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.191+2888C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880250 | ||||||
| chr2:237880275
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 217 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.191+2913G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880275 | ||||||
| chr2:237880379
|
C | T | 28 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(25): Show | 28 | HG00609.hp1 HG00639.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.191+3017C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880379 | ||||||
| chr2:237880398
|
C | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.191+3036C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880398 | ||||||
| chr2:237880402
|
G | T | 348 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(345): Show | 355 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(352): Show |
intron_variant | MODIFIER | c.191+3040G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880402 | ||||||
| chr2:237880552
|
A | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.191+3190A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880552 | ||||||
| chr2:237880553
|
C | A | 85 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(82): Show | 88 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.191+3191C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880553 | ||||||
| chr2:237880961
|
G | A | 4 | a0001c0001t0001g0141a0001c0001t0001g0165a0001c0002t0001g0330others(1): Show | 4 | HG02258.hp1 HG02630.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+3599G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880961 | ||||||
| chr2:237880970
|
C | A | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0120others(17): Show | 22 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.191+3608C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880970 | ||||||
| chr2:237880993
|
C | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(76): Show | 83 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.191+3631C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880993 | ||||||
| chr2:237881133
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.191+3771C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237881133 | ||||||
| chr2:237881216
|
C | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(115): Show | 122 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.191+3854C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237881216 | ||||||
| chr2:237881250
|
T | C | 15 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(12): Show | 15 | HG00544.hp1 HG02056.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.191+3888T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237881250 | ||||||
| chr2:237881280
|
G | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.191+3918G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237881280 | ||||||
| chr2:237881454
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.191+4092G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237881454 | ||||||
| chr2:237881500
|
G | A | 8 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0160others(5): Show | 8 | HG01496.hp1 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+4138G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237881500 | ||||||
| chr2:237881544
|
G | A | 3 | a0001c0001t0001g0211a0001c0001t0003g0138a0001c0001t0004g0139 | 3 | HG00642.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.191+4182G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237881544 | ||||||
| chr2:237881547
|
T | C | 9 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0160others(6): Show | 9 | HG00741.hp1 HG01496.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.191+4185T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237881547 | ||||||
| chr2:237881603
|
G | C | 3 | a0001c0001t0001g0211a0001c0001t0003g0138a0001c0001t0004g0139 | 3 | HG00642.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.191+4241G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237881603 | ||||||
| chr2:237881993
|
TCCTCTAG | T | 68 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(65): Show | 71 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.191+4635_191+4641d others(9): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237881993 | |||||
| chr2:237882004
|
G | T | 3 | a0001c0001t0001g0211a0001c0001t0003g0138a0001c0001t0004g0139 | 3 | HG00642.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.191+4642G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882004 | ||||||
| chr2:237882132
|
ATGCAAAC others(9): Show |
A | 1 | a0001c0001t0001g0283 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.191+4774_191+4789d others(18): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237882132 | |||||
| chr2:237882142
|
C | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 147 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.191+4780C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882142 | ||||||
| chr2:237882156
|
C | T | 59 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(56): Show | 62 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.191+4794C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882156 | ||||||
| chr2:237882188
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.191+4826A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882188 | ||||||
| chr2:237882255
|
C | A | 1 | a0001c0001t0001g0057 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.191+4893C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882255 | ||||||
| chr2:237882368
|
C | T | 59 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(56): Show | 62 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.191+5006C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882368 | ||||||
| chr2:237882424
|
G | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(79): Show | 85 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.191+5062G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882424 | ||||||
| chr2:237882487
|
G | A | 60 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(57): Show | 63 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.191+5125G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882487 | ||||||
| chr2:237882524
|
C | A | 15 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0162others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.191+5162C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882524 | ||||||
| chr2:237882524
|
C | T | 60 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(57): Show | 63 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.191+5162C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882524 | ||||||
| chr2:237882702
|
C | T | 59 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(56): Show | 62 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.191+5340C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882702 | ||||||
| chr2:237882741
|
T | C | 68 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(65): Show | 71 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.191+5379T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882741 | ||||||
| chr2:237882754
|
G | A | 353 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(350): Show | 361 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(358): Show |
intron_variant | MODIFIER | c.191+5392G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882754 | ||||||
| chr2:237882820
|
A | AGGCCATC others(10): Show |
67 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(64): Show | 70 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.191+5462_191+5478d others(19): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237882820 | |||||
| chr2:237882820
|
A | AGGCCATC others(27): Show |
1 | a0001c0001t0001g0026 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.191+5478_191+5479i others(36): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237882820 | |||||
| chr2:237882844
|
T | C | 68 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(65): Show | 71 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.191+5482T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882844 | ||||||
| chr2:237882867
|
C | G | 68 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(65): Show | 71 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.191+5505C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882867 | ||||||
| chr2:237882913
|
T | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 175 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.191+5551T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882913 | ||||||
| chr2:237882914
|
G | A | 68 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(65): Show | 71 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.191+5552G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882914 | ||||||
| chr2:237882971
|
G | A | 8 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0160others(5): Show | 8 | HG01496.hp1 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+5609G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882971 | ||||||
| chr2:237883015
|
A | G | 1 | a0001c0002t0001g0347 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.191+5653A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883015 | ||||||
| chr2:237883021
|
G | C | 8 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0160others(5): Show | 8 | HG01496.hp1 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+5659G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883021 | ||||||
| chr2:237883184
|
G | A | 7 | a0001c0001t0001g0141a0001c0001t0001g0160a0001c0001t0001g0161others(4): Show | 7 | HG01496.hp1 HG02258.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+5822G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883184 | ||||||
| chr2:237883279
|
G | A | 42 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(39): Show | 42 | HG00544.hp1 HG00741.hp1 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.191+5917G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883279 | ||||||
| chr2:237883310
|
G | A | 7 | a0001c0001t0001g0130a0001c0001t0001g0160a0001c0001t0001g0161others(4): Show | 7 | HG01496.hp1 HG02258.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+5948G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883310 | ||||||
| chr2:237883341
|
AG | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0054others(52): Show | 56 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.191+5981delG | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237883341 | |||||
| chr2:237883361
|
A | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 218 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.191+5999A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883361 | ||||||
| chr2:237883491
|
A | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 223 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.191+6129A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883491 | ||||||
| chr2:237883496
|
G | A | 4 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(1): Show | 4 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+6134G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883496 | ||||||
| chr2:237883558
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0003g0224 | 2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.191+6196G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883558 | ||||||
| chr2:237883564
|
C | T | 1 | a0001c0002t0001g0334 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.191+6202C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883564 | ||||||
| chr2:237883749
|
A | G | 2 | a0001c0001t0001g0297a0001c0002t0001g0354 | 2 | HG03490.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.191+6387A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883749 | ||||||
| chr2:237883776
|
A | G | 1 | a0001c0001t0001g0258 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.191+6414A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883776 | ||||||
| chr2:237883816
|
C | CA | 50 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(47): Show | 53 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.191+6468dupA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237883816 | |||||
| chr2:237883816
|
CA | C | 6 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(3): Show | 6 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.191+6468delA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237883816 | |||||
| chr2:237883818
|
AAAAAAAA others(16): Show |
A | 1 | a0001c0002t0001g0353 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.191+6471_191+6493d others(25): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237883818 | |||||
| chr2:237883827
|
AAAAG | A | 8 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0142others(5): Show | 8 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+6469_191+6472d others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237883827 | |||||
| chr2:237883912
|
C | CT | 99 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0017others(96): Show | 100 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.191+6574dupT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237883912 | |||||
| chr2:237883912
|
C | CTT | 48 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(45): Show | 51 | HG00323.hp2 HG00558.hp1 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.191+6573_191+6574d others(4): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237883912 | |||||
| chr2:237883912
|
C | CTTT | 22 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0150others(19): Show | 22 | HG00408.hp2 HG01346.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.191+6572_191+6574d others(5): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237883912 | |||||
| chr2:237883912
|
CT | C | 16 | a0001c0001t0001g0165a0001c0001t0001g0184a0001c0001t0001g0191others(13): Show | 16 | HG01074.hp1 HG02071.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.191+6574delT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237883912 | |||||
| chr2:237884301
|
T | G | 7 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(4): Show | 7 | HG00735.hp1 HG01358.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+6939T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884301 | ||||||
| chr2:237884308
|
A | G | 1 | a0001c0002t0001g0390 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.191+6946A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884308 | ||||||
| chr2:237884383
|
C | T | 15 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(12): Show | 15 | HG00642.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.191+7021C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884383 | ||||||
| chr2:237884426
|
G | A | 131 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(128): Show | 132 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.191+7064G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884426 | ||||||
| chr2:237884622
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.191+7260G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884622 | ||||||
| chr2:237884624
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.191+7262G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884624 | ||||||
| chr2:237884826
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.191+7464C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884826 | ||||||
| chr2:237884888
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.191+7526G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884888 | ||||||
| chr2:237884889
|
A | T | 1 | a0001c0001t0001g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.191+7527A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884889 | ||||||
| chr2:237884903
|
C | T | 6 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(3): Show | 6 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.191+7541C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884903 | ||||||
| chr2:237884932
|
G | T | 1 | a0001c0001t0001g0218 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.191+7570G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884932 | ||||||
| chr2:237884942
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.191+7580G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884942 | ||||||
| chr2:237885023
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.191+7661C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885023 | ||||||
| chr2:237885120
|
T | C | 1 | a0001c0001t0001g0304 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.191+7758T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885120 | ||||||
| chr2:237885130
|
G | C | 1 | a0001c0001t0001g0231 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.191+7768G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885130 | ||||||
| chr2:237885210
|
G | A | 68 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(65): Show | 71 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.191+7848G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885210 | ||||||
| chr2:237885231
|
CGAG | C | 48 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0055others(45): Show | 49 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.191+7871_191+7873d others(5): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237885231 | |||||
| chr2:237885236
|
G | A | 55 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(52): Show | 58 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.191+7874G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885236 | ||||||
| chr2:237885434
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.191+8072G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885434 | ||||||
| chr2:237885439
|
C | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0182 | 2 | HG01255.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.191+8077C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885439 | ||||||
| chr2:237885487
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.191+8125A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885487 | ||||||
| chr2:237885539
|
C | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(231): Show | 241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.191+8177C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885539 | ||||||
| chr2:237885572
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.191+8210C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885572 | ||||||
| chr2:237885589
|
G | A | 4 | a0001c0001t0001g0132a0001c0001t0001g0192a0001c0001t0001g0195others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+8227G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885589 | ||||||
| chr2:237885604
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(51): Show | 57 | HG00438.hp2 HG00642.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.191+8242G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885604 | ||||||
| chr2:237885667
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.191+8305G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885667 | ||||||
| chr2:237885810
|
C | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0293 | 2 | HG00673.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.191+8448C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885810 | ||||||
| chr2:237885812
|
T | A | 3 | a0001c0001t0001g0048a0001c0001t0001g0103a0001c0001t0001g0324 | 3 | HG03209.hp2 HG03471.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.191+8450T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885812 | ||||||
| chr2:237885860
|
C | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0002g0128 | 3 | HG01891.hp2 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.191+8498C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885860 | ||||||
| chr2:237886062
|
A | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(258): Show | 268 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.191+8700A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886062 | ||||||
| chr2:237886092
|
T | C | 10 | a0001c0001t0001g0022a0001c0001t0001g0048a0001c0001t0001g0097others(7): Show | 10 | HG01496.hp1 HG02486.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.191+8730T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886092 | ||||||
| chr2:237886100
|
G | A | 8 | a0001c0001t0001g0022a0001c0001t0001g0048a0001c0001t0001g0097others(5): Show | 8 | HG02486.hp2 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.191+8738G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886100 | ||||||
| chr2:237886218
|
G | A | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG00609.hp1 HG01123.hp1 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.191+8856G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886218 | ||||||
| chr2:237886310
|
A | G | 1 | a0001c0002t0001g0349 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.191+8948A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886310 | ||||||
| chr2:237886321
|
C | G | 33 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(30): Show | 36 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.191+8959C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886321 | ||||||
| chr2:237886342
|
C | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0160a0001c0001t0001g0161others(3): Show | 6 | HG01496.hp1 HG02071.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.191+8980C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886342 | ||||||
| chr2:237886369
|
G | A | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(266): Show | 276 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.191+9007G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886369 | ||||||
| chr2:237886384
|
C | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0103a0001c0001t0001g0223others(3): Show | 6 | HG02071.hp2 HG03098.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.191+9022C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886384 | ||||||
| chr2:237886451
|
G | A | 3 | a0001c0001t0001g0103a0001c0001t0001g0141a0001c0001t0001g0154 | 3 | HG02886.hp1 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.191+9089G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886451 | ||||||
| chr2:237886569
|
G | C | 1 | a0001c0001t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.191+9207G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886569 | ||||||
| chr2:237886616
|
G | A | 3 | a0001c0001t0001g0132a0001c0001t0001g0192a0001c0001t0003g0224 | 3 | HG02717.hp1 HG02895.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.191+9254G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886616 | ||||||
| chr2:237886652
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.191+9290C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886652 | ||||||
| chr2:237886656
|
G | A | 30 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0048others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.191+9294G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886656 | ||||||
| chr2:237886708
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.191+9346C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886708 | ||||||
| chr2:237886735
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.191+9373C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886735 | ||||||
| chr2:237886807
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.191+9445C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886807 | ||||||
| chr2:237886814
|
G | A | 2 | a0001c0001t0001g0316a0001c0001t0002g0317 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.191+9452G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886814 | ||||||
| chr2:237886831
|
C | G | 36 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(33): Show | 36 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.191+9469C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886831 | ||||||
| chr2:237886839
|
C | G | 33 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(30): Show | 33 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.191+9477C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886839 | ||||||
| chr2:237886876
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0002g0187 | 3 | HG02109.hp2 HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.191+9514G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886876 | ||||||
| chr2:237886911
|
T | G | 33 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(30): Show | 33 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.191+9549T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886911 | ||||||
| chr2:237886945
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0154 | 2 | HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.191+9583G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886945 | ||||||
| chr2:237886960
|
A | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(173): Show | 182 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.191+9598A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886960 | ||||||
| chr2:237886991
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0074 | 3 | HG03490.hp1 HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.191+9629G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886991 | ||||||
| chr2:237886998
|
C | T | 1 | a0001c0002t0001g0383 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.191+9636C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886998 | ||||||
| chr2:237887000
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.191+9638G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887000 | ||||||
| chr2:237887010
|
G | A | 4 | a0001c0001t0001g0087a0001c0001t0001g0190a0001c0001t0001g0315others(1): Show | 4 | HG00735.hp1 HG01978.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+9648G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887010 | ||||||
| chr2:237887091
|
G | T | 1 | a0001c0001t0001g0292 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.191+9729G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887091 | ||||||
| chr2:237887144
|
C | T | 48 | a0001c0001t0001g0008a0001c0001t0001g0073a0001c0001t0001g0129others(45): Show | 49 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.191+9782C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887144 | ||||||
| chr2:237887177
|
G | T | 7 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(4): Show | 7 | HG00735.hp1 HG01358.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+9815G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887177 | ||||||
| chr2:237887411
|
T | A | 1 | a0001c0001t0001g0292 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.191+10049T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887411 | ||||||
| chr2:237887413
|
A | AGTATCAA others(3): Show |
46 | a0001c0001t0001g0008a0001c0001t0001g0073a0001c0001t0001g0129others(43): Show | 47 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.191+10052_191+1005 others(14): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237887413 | |||||
| chr2:237887436
|
C | A | 3 | a0001c0001t0001g0113a0001c0001t0001g0295a0001c0001t0001g0296 | 3 | HG00733.hp2 HG03927.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.191+10074C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887436 | ||||||
| chr2:237887478
|
G | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.191+10116G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887478 | ||||||
| chr2:237887737
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.191+10375G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887737 | ||||||
| chr2:237887845
|
C | T | 1 | a0001c0001t0001g0005 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.191+10483C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887845 | ||||||
| chr2:237887898
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(207): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.191+10536A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887898 | ||||||
| chr2:237887908
|
T | C | 37 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(34): Show | 37 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.191+10546T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887908 | ||||||
| chr2:237887962
|
T | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(134): Show | 140 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.191+10600T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887962 | ||||||
| chr2:237888011
|
G | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(168): Show | 176 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.191+10649G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888011 | ||||||
| chr2:237888012
|
CA | C | 34 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(31): Show | 34 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.191+10652delA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237888012 | |||||
| chr2:237888056
|
T | A | 1 | a0001c0001t0001g0292 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.191+10694T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888056 | ||||||
| chr2:237888056
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.191+10694T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888056 | ||||||
| chr2:237888057
|
G | C | 134 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(131): Show | 137 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.191+10695G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888057 | ||||||
| chr2:237888062
|
G | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0061 | 2 | HG02056.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.191+10700G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888062 | ||||||
| chr2:237888093
|
G | A | 34 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(31): Show | 34 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.191+10731G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888093 | ||||||
| chr2:237888106
|
T | G | 34 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(31): Show | 34 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.191+10744T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888106 | ||||||
| chr2:237888193
|
A | G | 2 | a0001c0001t0001g0232a0001c0001t0003g0233 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.191+10831A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888193 | ||||||
| chr2:237888243
|
CAG | C | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0002g0187 | 3 | HG02109.hp2 HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.191+10882_191+1088 others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888243 | ||||||
| chr2:237888260
|
G | A | 4 | a0001c0001t0001g0155a0001c0001t0001g0191a0001c0001t0001g0213others(1): Show | 4 | HG01081.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+10898G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888260 | ||||||
| chr2:237888457
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.191+11095G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888457 | ||||||
| chr2:237888495
|
C | CA | 37 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(34): Show | 37 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.191+11136dupA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237888495 | |||||
| chr2:237888581
|
G | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.191+11219G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888581 | ||||||
| chr2:237888716
|
A | G | 48 | a0001c0001t0001g0008a0001c0001t0001g0073a0001c0001t0001g0129others(45): Show | 49 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.191+11354A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888716 | ||||||
| chr2:237888794
|
C | T | 37 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(34): Show | 40 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.191+11432C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888794 | ||||||
| chr2:237888804
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.191+11442C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888804 | ||||||
| chr2:237888817
|
G | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(32): Show | 38 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.191+11455G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888817 | ||||||
| chr2:237888818
|
C | T | 35 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(32): Show | 38 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.191+11456C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888818 | ||||||
| chr2:237888891
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.191+11529C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888891 | ||||||
| chr2:237888928
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.191+11566C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888928 | ||||||
| chr2:237889061
|
G | A | 22 | a0001c0001t0001g0022a0001c0001t0001g0048a0001c0001t0001g0097others(19): Show | 22 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.191+11699G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889061 | ||||||
| chr2:237889110
|
C | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0200a0001c0001t0001g0236 | 4 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+11748C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889110 | ||||||
| chr2:237889146
|
T | A | 37 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(34): Show | 37 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.191+11784T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889146 | ||||||
| chr2:237889167
|
T | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(69): Show | 75 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.191+11805T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889167 | ||||||
| chr2:237889190
|
A | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0157a0001c0001t0003g0032 | 3 | HG02818.hp1 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.191+11828A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889190 | ||||||
| chr2:237889227
|
G | A | 46 | a0001c0001t0001g0008a0001c0001t0001g0073a0001c0001t0001g0129others(43): Show | 47 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.191+11865G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889227 | ||||||
| chr2:237889518
|
C | G | 1 | a0001c0001t0001g0238 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.191+12156C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889518 | ||||||
| chr2:237889532
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0324 | 2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.191+12170C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889532 | ||||||
| chr2:237889938
|
G | A | 1 | a0001c0001t0001g0319 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.191+12576G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889938 | ||||||
| chr2:237889998
|
G | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0097a0001c0001t0001g0321others(1): Show | 4 | HG02486.hp2 HG02717.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+12636G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889998 | ||||||
| chr2:237890016
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.191+12654G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890016 | ||||||
| chr2:237890022
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.191+12660G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890022 | ||||||
| chr2:237890026
|
C | T | 1 | a0001c0001t0002g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.191+12664C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890026 | ||||||
| chr2:237890035
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.191+12673C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890035 | ||||||
| chr2:237890106
|
C | T | 12 | a0001c0001t0001g0023a0001c0001t0001g0096a0001c0001t0001g0157others(9): Show | 12 | HG02559.hp1 HG02647.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.191+12744C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890106 | ||||||
| chr2:237890207
|
T | A | 16 | a0001c0001t0001g0097a0001c0001t0001g0145a0001c0001t0001g0156others(13): Show | 16 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.191+12845T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890207 | ||||||
| chr2:237890263
|
G | A | 2 | a0001c0001t0001g0316a0001c0001t0002g0317 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.191+12901G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890263 | ||||||
| chr2:237890275
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.191+12913C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890275 | ||||||
| chr2:237890287
|
C | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(115): Show | 120 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.191+12925C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890287 | ||||||
| chr2:237890360
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.191+12998C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890360 | ||||||
| chr2:237890454
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(36): Show | 42 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.191+13092G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890454 | ||||||
| chr2:237890494
|
A | G | 4 | a0001c0001t0001g0096a0001c0001t0001g0157a0001c0001t0001g0171others(1): Show | 4 | HG02818.hp1 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+13132A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890494 | ||||||
| chr2:237890497
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.191+13135G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890497 | ||||||
| chr2:237890564
|
C | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(257): Show | 267 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.191+13202C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890564 | ||||||
| chr2:237890685
|
T | C | 7 | a0001c0001t0001g0062a0001c0001t0001g0247a0001c0001t0001g0248others(4): Show | 7 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+13323T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890685 | ||||||
| chr2:237890729
|
TCCTTTAC others(12): Show |
T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.191+13372_191+1339 others(23): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237890729 | |||||
| chr2:237890736
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.191+13374C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890736 | ||||||
| chr2:237890853
|
G | T | 1 | a0001c0001t0001g0223 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.191+13491G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890853 | ||||||
| chr2:237890872
|
G | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(126): Show | 132 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.191+13510G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890872 | ||||||
| chr2:237890907
|
C | A | 1 | a0001c0002t0001g0372 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.191+13545C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890907 | ||||||
| chr2:237890923
|
C | T | 32 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0027others(29): Show | 32 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.191+13561C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890923 | ||||||
| chr2:237891145
|
T | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.191+13783T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891145 | ||||||
| chr2:237891150
|
TTC | T | 7 | a0001c0001t0001g0025a0001c0001t0001g0103a0001c0001t0001g0135others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+13792_191+1379 others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237891150 | |||||
| chr2:237891154
|
C | CT | 9 | a0001c0001t0001g0023a0001c0001t0001g0096a0001c0001t0001g0112others(6): Show | 9 | HG02559.hp1 HG02818.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.191+13805dupT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237891154 | |||||
| chr2:237891154
|
CT | C | 7 | a0001c0001t0001g0035a0001c0001t0001g0119a0001c0001t0001g0141others(4): Show | 7 | HG01496.hp1 HG02148.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.191+13805delT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237891154 | |||||
| chr2:237891195
|
A | G | 254 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(251): Show | 259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.191+13833A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891195 | ||||||
| chr2:237891196
|
G | C | 254 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(251): Show | 259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.191+13834G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891196 | ||||||
| chr2:237891198
|
GA | G | 254 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(251): Show | 259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.191+13837delA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891198 | ||||||
| chr2:237891201
|
G | A | 254 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(251): Show | 259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.191+13839G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891201 | ||||||
| chr2:237891215
|
G | A | 257 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(254): Show | 262 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.191+13853G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891215 | ||||||
| chr2:237891244
|
G | A | 7 | a0001c0001t0001g0025a0001c0001t0001g0103a0001c0001t0001g0135others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+13882G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891244 | ||||||
| chr2:237891385
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.191+14023C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891385 | ||||||
| chr2:237891442
|
G | T | 1 | a0001c0001t0001g0014 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.191+14080G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891442 | ||||||
| chr2:237891578
|
G | A | 2 | a0001c0001t0001g0217a0001c0001t0001g0392 | 2 | HG00741.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.191+14216G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891578 | ||||||
| chr2:237891740
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.191+14378G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891740 | ||||||
| chr2:237891829
|
T | G | 1 | a0001c0001t0001g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.191+14467T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891829 | ||||||
| chr2:237891957
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.191+14595C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891957 | ||||||
| chr2:237892181
|
C | T | 1 | a0001c0001t0001g0294 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.191+14819C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237892181 | ||||||
| chr2:237892232
|
T | C | 84 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(81): Show | 86 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.191+14870T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237892232 | ||||||
| chr2:237892276
|
CT | C | 74 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0022others(71): Show | 75 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.191+14934delT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237892276 | |||||
| chr2:237892279
|
T | TC | 7 | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0001g0164others(4): Show | 7 | HG01106.hp1 HG01346.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+14917_191+1491 others(5): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237892279 | ||||||
| chr2:237892280
|
T | C | 187 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(184): Show | 192 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.191+14918T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237892280 | ||||||
| chr2:237892281
|
T | C | 8 | a0001c0001t0001g0065a0001c0001t0001g0077a0001c0001t0001g0110others(5): Show | 8 | HG01496.hp1 HG01515.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+14919T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237892281 | ||||||
| chr2:237892320
|
G | A | 20 | a0001c0001t0001g0097a0001c0001t0001g0145a0001c0001t0001g0156others(17): Show | 20 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.191+14958G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237892320 | ||||||
| chr2:237892457
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.191+15095A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237892457 | ||||||
| chr2:237892655
|
C | T | 253 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(250): Show | 259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.191+15293C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237892655 | ||||||
| chr2:237892735
|
T | TTC | 140 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(137): Show | 143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.191+15395_191+1539 others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237892735 | |||||
| chr2:237892735
|
T | TTCTC | 30 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0043others(27): Show | 31 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.191+15393_191+1539 others(8): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237892735 | |||||
| chr2:237892735
|
T | TTCTCTCT others(3): Show |
2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.191+15387_191+1539 others(14): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237892735 | |||||
| chr2:237892735
|
TTC | T | 3 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0002t0001g0353 | 3 | HG01261.hp2 HG03239.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.191+15395_191+1539 others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237892735 | |||||
| chr2:237892735
|
TTCTC | T | 47 | a0001c0001t0001g0008a0001c0001t0001g0048a0001c0001t0001g0052others(44): Show | 48 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.191+15393_191+1539 others(8): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237892735 | |||||
| chr2:237892735
|
TTCTCTCT others(3): Show |
T | 1 | a0001c0001t0002g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.191+15387_191+1539 others(14): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237892735 | |||||
| chr2:237893144
|
A | G | 87 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(84): Show | 90 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.191+15782A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237893144 | ||||||
| chr2:237893240
|
A | C | 1 | a0001c0001t0001g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.191+15878A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237893240 | ||||||
| chr2:237893657
|
G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0241a0001c0002t0001g0340others(1): Show | 4 | HG01074.hp2 HG02071.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+16295G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237893657 | ||||||
| chr2:237893770
|
C | G | 6 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0103others(3): Show | 6 | HG02486.hp2 HG02559.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.191+16408C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237893770 | ||||||
| chr2:237893809
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0396 | 3 | HG02109.hp2 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.191+16447C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237893809 | ||||||
| chr2:237893969
|
TC | T | 23 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0142others(20): Show | 24 | HG01255.hp1 HG01346.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.191+16608delC | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237893969 | ||||||
| chr2:237893970
|
C | CT | 16 | a0001c0001t0001g0022a0001c0001t0001g0048a0001c0001t0001g0065others(13): Show | 16 | HG01167.hp1 HG01496.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.191+16627dupT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237893970 | |||||
| chr2:237893970
|
C | CTT | 44 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0028others(41): Show | 45 | HG00099.hp2 HG01169.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.191+16626_191+1662 others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237893970 | |||||
| chr2:237893970
|
C | CTTT | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 176 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.191+16625_191+1662 others(7): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237893970 | |||||
| chr2:237893970
|
C | CTTTT | 15 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0049others(12): Show | 15 | HG01175.hp2 HG01891.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.191+16624_191+1662 others(8): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237893970 | |||||
| chr2:237893970
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0001g0291a0001c0001t0001g0292 | 3 | HG02647.hp1 NA18975.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.191+16608C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237893970 | ||||||
| chr2:237894197
|
C | T | 1 | a0001c0001t0001g0396 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.191+16835C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894197 | ||||||
| chr2:237894268
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.191+16906G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894268 | ||||||
| chr2:237894288
|
A | G | 7 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0103others(4): Show | 7 | HG02486.hp2 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.191+16926A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894288 | ||||||
| chr2:237894470
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.192-17058G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894470 | ||||||
| chr2:237894476
|
G | A | 1 | a0001c0002t0001g0347 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.192-17052G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894476 | ||||||
| chr2:237894551
|
C | T | 11 | a0001c0001t0001g0131a0001c0001t0001g0141a0001c0001t0001g0143others(8): Show | 11 | HG00642.hp2 HG01099.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.192-16977C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894551 | ||||||
| chr2:237894652
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192-16876A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894652 | ||||||
| chr2:237894654
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.192-16874G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894654 | ||||||
| chr2:237894744
|
C | G | 339 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(336): Show | 346 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(343): Show |
intron_variant | MODIFIER | c.192-16784C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894744 | ||||||
| chr2:237894773
|
C | T | 1 | a0001c0001t0001g0324 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.192-16755C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894773 | ||||||
| chr2:237894776
|
C | T | 5 | a0001c0001t0001g0171a0001c0001t0001g0192a0001c0001t0001g0223others(2): Show | 5 | HG02717.hp1 HG02895.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.192-16752C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894776 | ||||||
| chr2:237894836
|
A | G | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(342): Show | 352 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.192-16692A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894836 | ||||||
| chr2:237894900
|
G | C | 1 | a0001c0001t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.192-16628G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894900 | ||||||
| chr2:237894932
|
C | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0132 | 3 | HG02145.hp2 HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.192-16596C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894932 | ||||||
| chr2:237894938
|
G | C | 4 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265others(1): Show | 4 | NA18961.hp2 NA18962.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-16590G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894938 | ||||||
| chr2:237895280
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.192-16248G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895280 | ||||||
| chr2:237895284
|
G | A | 2 | a0001c0001t0001g0306a0001c0001t0001g0308 | 2 | NA18950.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.192-16244G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895284 | ||||||
| chr2:237895346
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0309 | 2 | HG02132.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.192-16182C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895346 | ||||||
| chr2:237895427
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(105): Show | 110 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.192-16101A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895427 | ||||||
| chr2:237895453
|
G | C | 1 | a0001c0001t0001g0210 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.192-16075G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895453 | ||||||
| chr2:237895520
|
T | G | 346 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(343): Show | 353 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.192-16008T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895520 | ||||||
| chr2:237895547
|
G | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(105): Show | 110 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.192-15981G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895547 | ||||||
| chr2:237895583
|
C | T | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.192-15945C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895583 | ||||||
| chr2:237895645
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.192-15883C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895645 | ||||||
| chr2:237895655
|
G | A | 1 | a0001c0002t0001g0352 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.192-15873G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895655 | ||||||
| chr2:237895703
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(104): Show | 109 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.192-15825A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895703 | ||||||
| chr2:237895713
|
T | C | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(330): Show | 340 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.192-15815T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895713 | ||||||
| chr2:237895729
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.192-15799C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895729 | ||||||
| chr2:237895735
|
G | GC | 395 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(392): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.192-15792dupC | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237895735 | |||||
| chr2:237895775
|
G | A | 1 | a0001c0001t0001g0003 | 2 | NA18942.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.192-15753G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895775 | ||||||
| chr2:237895803
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(91): Show | 95 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.192-15725C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895803 | ||||||
| chr2:237895843
|
T | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(103): Show | 108 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.192-15685T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895843 | ||||||
| chr2:237895901
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.192-15627G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895901 | ||||||
| chr2:237896098
|
G | T | 1 | a0001c0001t0001g0282 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.192-15430G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237896098 | ||||||
| chr2:237896256
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192-15272C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237896256 | ||||||
| chr2:237896264
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(106): Show | 111 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.192-15264T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237896264 | ||||||
| chr2:237896372
|
T | C | 2 | a0001c0001t0001g0393a0001c0001t0001g0394 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.192-15156T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237896372 | ||||||
| chr2:237896373
|
C | G | 3 | a0001c0001t0001g0192a0001c0001t0002g0187a0001c0001t0003g0224 | 3 | HG02717.hp1 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.192-15155C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237896373 | ||||||
| chr2:237896477
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.192-15051C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237896477 | ||||||
| chr2:237896535
|
C | T | 1 | a0001c0002t0001g0371 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.192-14993C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237896535 | ||||||
| chr2:237896685
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.192-14843G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237896685 | ||||||
| chr2:237896832
|
G | A | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 158 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.192-14696G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237896832 | ||||||
| chr2:237897028
|
G | C | 1 | a0001c0001t0001g0030 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.192-14500G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897028 | ||||||
| chr2:237897123
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0171 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.192-14405G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897123 | ||||||
| chr2:237897421
|
T | C | 1 | a0001c0001t0004g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.192-14107T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897421 | ||||||
| chr2:237897432
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.192-14096T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897432 | ||||||
| chr2:237897442
|
C | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(87): Show | 91 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.192-14086C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897442 | ||||||
| chr2:237897541
|
C | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.192-13987C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897541 | ||||||
| chr2:237897728
|
T | C | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.192-13800T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897728 | ||||||
| chr2:237897771
|
G | GT | 9 | a0001c0001t0001g0006a0001c0001t0001g0103a0001c0001t0001g0165others(6): Show | 10 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.192-13751dupT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237897771 | |||||
| chr2:237897771
|
GT | G | 8 | a0001c0001t0001g0118a0001c0001t0001g0206a0001c0001t0001g0222others(5): Show | 8 | HG01168.hp1 HG02071.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.192-13751delT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237897771 | |||||
| chr2:237897777
|
T | G | 3 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221 | 3 | HG02647.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.192-13751T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897777 | ||||||
| chr2:237897777
|
T | TG | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.192-13742dupG | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237897777 | |||||
| chr2:237897777
|
TG | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(99): Show | 104 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.192-13742delG | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237897777 | |||||
| chr2:237897787
|
T | G | 36 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0068others(33): Show | 38 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.192-13741T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897787 | ||||||
| chr2:237897794
|
T | TTTTG | 7 | a0001c0001t0001g0118a0001c0001t0001g0206a0001c0001t0001g0242others(4): Show | 7 | HG01168.hp1 HG02071.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.192-13718_192-1371 others(8): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237897794 | |||||
| chr2:237897910
|
T | C | 2 | a0001c0001t0001g0192a0001c0001t0003g0224 | 2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.192-13618T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897910 | ||||||
| chr2:237897915
|
C | T | 1 | a0001c0001t0001g0295 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.192-13613C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897915 | ||||||
| chr2:237897955
|
C | T | 1 | a0001c0001t0001g0392 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.192-13573C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897955 | ||||||
| chr2:237897965
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.192-13563A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897965 | ||||||
| chr2:237898332
|
G | A | 7 | a0001c0001t0001g0103a0001c0001t0001g0165a0001c0001t0002g0187others(4): Show | 7 | HG02258.hp1 HG02723.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.192-13196G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898332 | ||||||
| chr2:237898415
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.192-13113G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898415 | ||||||
| chr2:237898435
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(87): Show | 91 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.192-13093G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898435 | ||||||
| chr2:237898527
|
G | C | 2 | a0001c0001t0001g0141a0001c0001t0001g0154 | 2 | HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.192-13001G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898527 | ||||||
| chr2:237898542
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.192-12986A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898542 | ||||||
| chr2:237898682
|
C | G | 4 | a0001c0001t0001g0052a0001c0001t0001g0066a0001c0001t0001g0257others(1): Show | 4 | HG01928.hp1 NA18943.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-12846C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898682 | ||||||
| chr2:237898738
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0171 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.192-12790G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898738 | ||||||
| chr2:237898743
|
C | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0056others(4): Show | 7 | HG00558.hp2 NA18951.hp1 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.192-12785C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898743 | ||||||
| chr2:237898807
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(76): Show | 80 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.192-12721C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898807 | ||||||
| chr2:237898808
|
A | G | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(110): Show | 116 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.192-12720A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898808 | ||||||
| chr2:237898819
|
G | A | 1 | a0001c0002t0001g0373 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.192-12709G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898819 | ||||||
| chr2:237898872
|
G | T | 1 | a0001c0001t0001g0263 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.192-12656G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898872 | ||||||
| chr2:237899013
|
C | T | 10 | a0001c0001t0001g0118a0001c0001t0001g0206a0001c0001t0001g0219others(7): Show | 10 | HG01168.hp1 HG02071.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.192-12515C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237899013 | ||||||
| chr2:237899072
|
A | AT | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(317): Show | 327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.192-12444dupT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237899072 | |||||
| chr2:237899140
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.192-12388C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237899140 | ||||||
| chr2:237899310
|
A | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0064 | 2 | HG02523.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.192-12218A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237899310 | ||||||
| chr2:237899496
|
C | T | 9 | a0001c0001t0001g0103a0001c0001t0001g0165a0001c0001t0001g0192others(6): Show | 9 | HG02258.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.192-12032C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237899496 | ||||||
| chr2:237899662
|
G | T | 2 | a0001c0001t0001g0192a0001c0001t0003g0224 | 2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.192-11866G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237899662 | ||||||
| chr2:237899725
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.192-11803G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237899725 | ||||||
| chr2:237899838
|
A | G | 341 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(338): Show | 348 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.192-11690A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237899838 | ||||||
| chr2:237899931
|
G | T | 2 | a0001c0001t0001g0103a0001c0001t0002g0187 | 2 | HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.192-11597G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237899931 | ||||||
| chr2:237899955
|
C | A | 1 | a0001c0001t0001g0207 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.192-11573C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237899955 | ||||||
| chr2:237900124
|
ACTT | A | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-11397_192-1139 others(7): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237900124 | |||||
| chr2:237900282
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0003g0224 | 2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.192-11246C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237900282 | ||||||
| chr2:237900466
|
T | A | 1 | a0001c0001t0001g0236 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.192-11062T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237900466 | ||||||
| chr2:237900466
|
T | TA | 341 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(338): Show | 348 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.192-11062_192-1106 others(5): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237900466 | ||||||
| chr2:237900556
|
TTTTG | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0157a0001c0001t0003g0032 | 3 | HG02818.hp1 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.192-10968_192-1096 others(8): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237900556 | |||||
| chr2:237900595
|
T | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(114): Show | 120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.192-10933T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237900595 | ||||||
| chr2:237900763
|
A | T | 22 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0148others(19): Show | 22 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.192-10765A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237900763 | ||||||
| chr2:237900804
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0002g0187 | 2 | HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.192-10724T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237900804 | ||||||
| chr2:237901062
|
G | C | 1 | a0001c0001t0001g0192 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.192-10466G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901062 | ||||||
| chr2:237901081
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.192-10447C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901081 | ||||||
| chr2:237901083
|
G | A | 344 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(341): Show | 352 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.192-10445G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901083 | ||||||
| chr2:237901145
|
G | T | 2 | a0001c0001t0001g0103a0001c0001t0002g0187 | 2 | HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.192-10383G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901145 | ||||||
| chr2:237901208
|
C | T | 1 | a0001c0001t0003g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.192-10320C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901208 | ||||||
| chr2:237901273
|
G | T | 344 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(341): Show | 352 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.192-10255G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901273 | ||||||
| chr2:237901374
|
A | G | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0141others(2): Show | 5 | HG01496.hp1 HG02109.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.192-10154A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901374 | ||||||
| chr2:237901430
|
T | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0086 | 3 | HG01069.hp2 HG01071.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.192-10098T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901430 | ||||||
| chr2:237901660
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.192-9868G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901660 | ||||||
| chr2:237901699
|
C | T | 14 | a0001c0001t0001g0131a0001c0001t0001g0142a0001c0001t0001g0143others(11): Show | 14 | HG01074.hp1 HG01099.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.192-9829C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901699 | ||||||
| chr2:237901837
|
T | A | 1 | a0001c0001t0001g0072 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.192-9691T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901837 | ||||||
| chr2:237901860
|
T | TACTC | 351 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(348): Show | 359 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(356): Show |
intron_variant | MODIFIER | c.192-9664_192-9661d others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237901860 | |||||
| chr2:237901934
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.192-9594C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901934 | ||||||
| chr2:237902086
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.192-9442G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902086 | ||||||
| chr2:237902102
|
T | A | 10 | a0001c0001t0001g0025a0001c0001t0001g0048a0001c0001t0001g0135others(7): Show | 10 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.192-9426T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902102 | ||||||
| chr2:237902121
|
G | A | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(303): Show | 313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.192-9407G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902121 | ||||||
| chr2:237902177
|
C | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0065others(14): Show | 18 | HG01099.hp2 HG01123.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.192-9351C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902177 | ||||||
| chr2:237902298
|
A | AGGAGGAG others(32): Show |
1 | a0001c0001t0001g0053 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.192-9202_192-9164d others(41): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237902298 | |||||
| chr2:237902298
|
A | AGGAGGAG others(71): Show |
1 | a0001c0004t0005g0179 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.192-9164_192-9163i others(80): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237902298 | |||||
| chr2:237902298
|
AGGAGGAG others(32): Show |
A | 4 | a0001c0001t0001g0025a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | HG02109.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.192-9202_192-9164d others(41): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237902298 | |||||
| chr2:237902300
|
G | GAGGAGGG others(13): Show |
5 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(2): Show | 5 | HG01109.hp2 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.192-9211_192-9210i others(22): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237902300 | |||||
| chr2:237902337
|
T | TGGAGGAG others(32): Show |
1 | a0001c0001t0001g0298 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.192-9164_192-9163i others(41): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237902337 | |||||
| chr2:237902450
|
C | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0026others(38): Show | 42 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.192-9078C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902450 | ||||||
| chr2:237902452
|
C | T | 2 | a0001c0001t0001g0256a0001c0002t0001g0373 | 2 | HG02129.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.192-9076C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902452 | ||||||
| chr2:237902463
|
G | A | 5 | a0001c0001t0001g0087a0001c0001t0001g0099a0001c0001t0001g0181others(2): Show | 5 | HG00735.hp1 HG01261.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.192-9065G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902463 | ||||||
| chr2:237902474
|
G | C | 1 | a0001c0002t0001g0349 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.192-9054G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902474 | ||||||
| chr2:237902581
|
G | A | 1 | a0001c0002t0001g0339 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.192-8947G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902581 | ||||||
| chr2:237902591
|
G | A | 39 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0057others(36): Show | 39 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.192-8937G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902591 | ||||||
| chr2:237902651
|
T | C | 10 | a0001c0001t0001g0103a0001c0001t0001g0135a0001c0001t0001g0136others(7): Show | 10 | HG01070.hp2 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.192-8877T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902651 | ||||||
| chr2:237902659
|
A | G | 8 | a0001c0001t0001g0021a0001c0001t0001g0097a0001c0001t0001g0132others(5): Show | 8 | HG01891.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.192-8869A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902659 | ||||||
| chr2:237902670
|
A | G | 154 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(151): Show | 156 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.192-8858A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902670 | ||||||
| chr2:237902748
|
A | T | 1 | a0001c0002t0001g0382 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.192-8780A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902748 | ||||||
| chr2:237902873
|
A | T | 24 | a0001c0001t0001g0021a0001c0001t0001g0057a0001c0001t0001g0068others(21): Show | 24 | HG00323.hp1 HG00741.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.192-8655A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902873 | ||||||
| chr2:237902974
|
C | G | 7 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0133others(4): Show | 7 | HG01358.hp2 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.192-8554C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902974 | ||||||
| chr2:237903089
|
C | G | 68 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0030others(65): Show | 68 | HG00323.hp1 HG00609.hp2 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.192-8439C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903089 | ||||||
| chr2:237903123
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.192-8405T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903123 | ||||||
| chr2:237903180
|
T | C | 3 | a0001c0001t0001g0126a0001c0001t0001g0182a0001c0001t0001g0205 | 3 | HG01255.hp1 HG03239.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.192-8348T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903180 | ||||||
| chr2:237903187
|
A | G | 12 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0051others(9): Show | 12 | HG01515.hp2 HG02071.hp2 HG04115.hp1 others(9): Show |
intron_variant | MODIFIER | c.192-8341A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903187 | ||||||
| chr2:237903260
|
C | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0048others(12): Show | 16 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.192-8268C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903260 | ||||||
| chr2:237903261
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.192-8267G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903261 | ||||||
| chr2:237903394
|
C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.192-8134C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903394 | ||||||
| chr2:237903474
|
T | C | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG00597.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.192-8054T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903474 | ||||||
| chr2:237903480
|
T | A | 21 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0027others(18): Show | 22 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.192-8048T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903480 | ||||||
| chr2:237903501
|
C | G | 21 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0027others(18): Show | 22 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.192-8027C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903501 | ||||||
| chr2:237903522
|
A | C | 363 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(360): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.192-8006A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903522 | ||||||
| chr2:237903527
|
CT | C | 21 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0027others(18): Show | 22 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.192-7992delT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237903527 | |||||
| chr2:237903551
|
T | C | 351 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(348): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.192-7977T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903551 | ||||||
| chr2:237903604
|
A | C | 1 | a0001c0001t0001g0093 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.192-7924A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903604 | ||||||
| chr2:237903680
|
G | T | 361 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(358): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.192-7848G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903680 | ||||||
| chr2:237903765
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0001g0199 | 2 | HG01099.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.192-7763G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903765 | ||||||
| chr2:237903787
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.192-7741C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903787 | ||||||
| chr2:237903844
|
G | A | 1 | a0001c0002t0001g0382 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.192-7684G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903844 | ||||||
| chr2:237903851
|
C | A | 225 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(222): Show | 231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.192-7677C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903851 | ||||||
| chr2:237903855
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.192-7673C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903855 | ||||||
| chr2:237903918
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.192-7610T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903918 | ||||||
| chr2:237904004
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0327 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.192-7524G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904004 | ||||||
| chr2:237904010
|
T | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0023others(28): Show | 32 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.192-7518T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904010 | ||||||
| chr2:237904031
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0185 | 2 | HG01243.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.192-7497G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904031 | ||||||
| chr2:237904165
|
G | A | 8 | a0001c0001t0001g0097a0001c0001t0001g0132a0001c0001t0001g0158others(5): Show | 8 | HG01891.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.192-7363G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904165 | ||||||
| chr2:237904177
|
T | G | 1 | a0001c0001t0001g0026 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.192-7351T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904177 | ||||||
| chr2:237904195
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192-7333C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904195 | ||||||
| chr2:237904196
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.192-7332G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904196 | ||||||
| chr2:237904257
|
C | CA | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.192-7259dupA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237904257 | |||||
| chr2:237904257
|
CA | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(28): Show | 32 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.192-7259delA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237904257 | |||||
| chr2:237904279
|
C | T | 50 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0030others(47): Show | 51 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.192-7249C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904279 | ||||||
| chr2:237904287
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.192-7241C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904287 | ||||||
| chr2:237904469
|
G | A | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | NA18961.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.192-7059G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904469 | ||||||
| chr2:237904632
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.192-6896C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904632 | ||||||
| chr2:237904642
|
G | A | 8 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0087others(5): Show | 8 | HG00735.hp1 HG01255.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.192-6886G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904642 | ||||||
| chr2:237904807
|
C | T | 1 | a0001c0001t0003g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.192-6721C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904807 | ||||||
| chr2:237904913
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.192-6615C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904913 | ||||||
| chr2:237904941
|
C | G | 1 | a0001c0001t0001g0153 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.192-6587C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904941 | ||||||
| chr2:237905025
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0141 | 2 | HG02559.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.192-6503C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905025 | ||||||
| chr2:237905032
|
T | C | 70 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0030others(67): Show | 71 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.192-6496T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905032 | ||||||
| chr2:237905305
|
A | G | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(223): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.192-6223A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905305 | ||||||
| chr2:237905681
|
G | T | 5 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(2): Show | 5 | HG02280.hp1 HG03195.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.192-5847G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905681 | ||||||
| chr2:237905714
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.192-5814A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905714 | ||||||
| chr2:237905748
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.192-5780C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905748 | ||||||
| chr2:237905858
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0017 | 2 | NA18978.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.192-5670A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905858 | ||||||
| chr2:237905860
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.192-5668A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905860 | ||||||
| chr2:237905909
|
G | A | 16 | a0001c0001t0001g0047a0001c0001t0001g0068a0001c0001t0001g0078others(13): Show | 16 | HG00741.hp2 HG01070.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.192-5619G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905909 | ||||||
| chr2:237905967
|
T | C | 1 | a0001c0001t0001g0254 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.192-5561T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905967 | ||||||
| chr2:237906010
|
C | CA | 20 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0088others(17): Show | 20 | HG00438.hp1 HG01099.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.192-5498dupA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237906010 | |||||
| chr2:237906010
|
C | CAA | 52 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0019others(49): Show | 53 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.192-5499_192-5498d others(4): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237906010 | |||||
| chr2:237906010
|
C | CAAA | 6 | a0001c0001t0001g0120a0001c0001t0001g0145a0001c0001t0001g0164others(3): Show | 6 | HG00642.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.192-5500_192-5498d others(5): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237906010 | |||||
| chr2:237906010
|
CA | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(118): Show | 123 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.192-5498delA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237906010 | |||||
| chr2:237906037
|
A | G | 371 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(368): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.192-5491A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906037 | ||||||
| chr2:237906097
|
C | T | 2 | a0001c0001t0001g0324a0001c0001t0001g0392 | 2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.192-5431C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906097 | ||||||
| chr2:237906181
|
A | C | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.192-5347A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906181 | ||||||
| chr2:237906299
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.192-5229G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906299 | ||||||
| chr2:237906354
|
A | G | 98 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(95): Show | 100 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.192-5174A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906354 | ||||||
| chr2:237906585
|
T | G | 7 | a0001c0001t0001g0131a0001c0001t0001g0143a0001c0001t0001g0191others(4): Show | 7 | HG02257.hp1 HG02572.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.192-4943T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906585 | ||||||
| chr2:237906610
|
C | T | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.192-4918C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906610 | ||||||
| chr2:237906666
|
G | A | 15 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0051others(12): Show | 15 | HG01515.hp2 HG02071.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.192-4862G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906666 | ||||||
| chr2:237906717
|
C | CT | 266 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(263): Show | 273 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.192-4787dupT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237906717 | |||||
| chr2:237906717
|
C | CTT | 70 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(67): Show | 71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.192-4788_192-4787d others(4): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237906717 | |||||
| chr2:237906717
|
C | CTTT | 6 | a0001c0001t0001g0038a0001c0001t0001g0116a0001c0001t0001g0184others(3): Show | 6 | HG01081.hp2 HG02056.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.192-4789_192-4787d others(5): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237906717 | |||||
| chr2:237906717
|
CT | C | 6 | a0001c0001t0001g0058a0001c0001t0001g0065a0001c0001t0001g0161others(3): Show | 6 | HG01167.hp1 NA18522.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.192-4787delT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237906717 | |||||
| chr2:237906823
|
A | G | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.192-4705A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906823 | ||||||
| chr2:237906847
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.192-4681C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906847 | ||||||
| chr2:237906850
|
G | A | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(223): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.192-4678G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906850 | ||||||
| chr2:237906867
|
C | T | 1 | a0001c0001t0001g0003 | 2 | NA18942.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.192-4661C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906867 | ||||||
| chr2:237906942
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0141a0001c0001t0001g0223 | 3 | HG02559.hp1 HG03098.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.192-4586C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906942 | ||||||
| chr2:237906965
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.192-4563C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906965 | ||||||
| chr2:237906966
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.192-4562G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906966 | ||||||
| chr2:237907059
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.192-4469T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907059 | ||||||
| chr2:237907122
|
C | T | 2 | a0001c0001t0001g0184a0001c0001t0001g0231 | 2 | HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.192-4406C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907122 | ||||||
| chr2:237907236
|
T | C | 372 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(369): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.192-4292T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907236 | ||||||
| chr2:237907314
|
G | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0395 | 2 | HG01074.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.192-4214G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907314 | ||||||
| chr2:237907335
|
C | A | 1 | a0001c0001t0001g0223 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192-4193C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907335 | ||||||
| chr2:237907458
|
A | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0260a0001c0002t0001g0347 | 3 | NA18947.hp1 NA19005.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.192-4070A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907458 | ||||||
| chr2:237907490
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.192-4038G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907490 | ||||||
| chr2:237907553
|
C | CAT | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(220): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.192-3974_192-3973d others(4): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237907553 | |||||
| chr2:237907559
|
C | T | 83 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0030others(80): Show | 84 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.192-3969C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907559 | ||||||
| chr2:237907714
|
A | T | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(220): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.192-3814A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907714 | ||||||
| chr2:237907729
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.192-3799G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907729 | ||||||
| chr2:237907946
|
T | G | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(221): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.192-3582T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907946 | ||||||
| chr2:237908002
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.192-3526C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908002 | ||||||
| chr2:237908039
|
A | G | 3 | a0001c0001t0001g0079a0001c0002t0001g0337a0001c0002t0001g0386 | 3 | NA18990.hp2 NA19000.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.192-3489A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908039 | ||||||
| chr2:237908247
|
T | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0027others(24): Show | 28 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.192-3281T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908247 | ||||||
| chr2:237908374
|
T | G | 17 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(14): Show | 17 | HG01515.hp2 HG02071.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.192-3154T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908374 | ||||||
| chr2:237908410
|
C | CTGG | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0172others(5): Show | 8 | HG01081.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.192-3091_192-3089d others(5): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237908410 | |||||
| chr2:237908410
|
C | CTGGTGGT others(5): Show |
1 | a0001c0001t0001g0276 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.192-3108_192-3107i others(14): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237908410 | |||||
| chr2:237908410
|
C | CTGGTGGT others(8): Show |
1 | a0001c0001t0001g0084 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.192-3108_192-3107i others(17): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237908410 | |||||
| chr2:237908410
|
C | CTGGTGGT others(11): Show |
1 | a0001c0001t0001g0142 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.192-3108_192-3107i others(20): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237908410 | |||||
| chr2:237908410
|
C | CTGGTGGT others(11): Show |
212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.192-3108_192-3107i others(20): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237908410 | |||||
| chr2:237908410
|
C | CTGGTGGT others(14): Show |
3 | a0001c0001t0001g0292a0001c0001t0003g0212a0001c0002t0001g0387 | 3 | HG02300.hp1 HG03139.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.192-3108_192-3107i others(23): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237908410 | |||||
| chr2:237908410
|
C | CTGGTGGT others(11): Show |
1 | a0001c0001t0001g0241 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.192-3106_192-3089d others(20): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237908410 | |||||
| chr2:237908410
|
C | CTGGTGGT others(14): Show |
1 | a0001c0001t0001g0031 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.192-3109_192-3089d others(23): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237908410 | |||||
| chr2:237908506
|
C | T | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0152 | 3 | HG02257.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.192-3022C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908506 | ||||||
| chr2:237908551
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0157 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.192-2977C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908551 | ||||||
| chr2:237908564
|
C | A | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.192-2964C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908564 | ||||||
| chr2:237908564
|
C | T | 10 | a0001c0001t0001g0047a0001c0001t0001g0068a0001c0001t0001g0078others(7): Show | 10 | HG00741.hp2 HG02602.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.192-2964C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908564 | ||||||
| chr2:237908584
|
C | A | 1 | a0001c0001t0001g0107 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.192-2944C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908584 | ||||||
| chr2:237908587
|
G | A | 22 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0027others(19): Show | 23 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.192-2941G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908587 | ||||||
| chr2:237908657
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(169): Show | 174 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.192-2871T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908657 | ||||||
| chr2:237908682
|
C | T | 3 | a0001c0001t0001g0057a0001c0001t0003g0138a0001c0001t0003g0212 | 3 | HG03139.hp2 HG03540.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.192-2846C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908682 | ||||||
| chr2:237908688
|
A | G | 374 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(371): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.192-2840A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908688 | ||||||
| chr2:237908715
|
T | C | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.192-2813T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908715 | ||||||
| chr2:237908872
|
T | C | 5 | a0001c0001t0001g0048a0001c0001t0001g0132a0001c0001t0001g0143others(2): Show | 5 | HG02257.hp1 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.192-2656T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908872 | ||||||
| chr2:237908941
|
C | G | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(314): Show | 324 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.192-2587C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908941 | ||||||
| chr2:237909046
|
A | C | 24 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0096others(21): Show | 24 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.192-2482A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909046 | ||||||
| chr2:237909096
|
A | G | 24 | a0001c0001t0001g0025a0001c0001t0001g0097a0001c0001t0001g0130others(21): Show | 24 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.192-2432A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909096 | ||||||
| chr2:237909118
|
C | T | 6 | a0001c0001t0001g0140a0001c0001t0001g0196a0001c0001t0001g0198others(3): Show | 6 | HG01069.hp1 HG01099.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.192-2410C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909118 | ||||||
| chr2:237909132
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.192-2396A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909132 | ||||||
| chr2:237909204
|
G | A | 1 | a0001c0002t0001g0351 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.192-2324G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909204 | ||||||
| chr2:237909269
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.192-2259C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909269 | ||||||
| chr2:237909300
|
C | G | 1 | a0001c0001t0001g0051 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.192-2228C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909300 | ||||||
| chr2:237909325
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.192-2203C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909325 | ||||||
| chr2:237909326
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.192-2202G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909326 | ||||||
| chr2:237909333
|
A | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0066a0001c0001t0001g0262 | 3 | NA18943.hp1 NA18984.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.192-2195A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909333 | ||||||
| chr2:237909343
|
C | G | 1 | a0001c0001t0001g0078 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.192-2185C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909343 | ||||||
| chr2:237909365
|
T | TG | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(116): Show | 122 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.192-2162dupG | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237909365 | |||||
| chr2:237909375
|
G | A | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(128): Show | 134 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.192-2153G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909375 | ||||||
| chr2:237909422
|
T | C | 1 | a0001c0001t0003g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.192-2106T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909422 | ||||||
| chr2:237909470
|
C | T | 5 | a0001c0001t0001g0134a0001c0001t0001g0156a0001c0001t0001g0184others(2): Show | 5 | HG02135.hp1 HG02572.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.192-2058C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909470 | ||||||
| chr2:237909618
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.192-1910G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909618 | ||||||
| chr2:237909646
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.192-1882C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909646 | ||||||
| chr2:237909655
|
C | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.192-1873C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909655 | ||||||
| chr2:237909746
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.192-1782C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909746 | ||||||
| chr2:237909747
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.192-1781A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909747 | ||||||
| chr2:237909899
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0327 | 2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.192-1629G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909899 | ||||||
| chr2:237909915
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.192-1613G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909915 | ||||||
| chr2:237909928
|
C | T | 45 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0016others(42): Show | 46 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.192-1600C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909928 | ||||||
| chr2:237910009
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.192-1519G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237910009 | ||||||
| chr2:237910133
|
T | C | 389 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(386): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.192-1395T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237910133 | ||||||
| chr2:237910167
|
C | T | 1 | a0001c0002t0001g0368 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.192-1361C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237910167 | ||||||
| chr2:237910243
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.192-1285C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237910243 | ||||||
| chr2:237910319
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.192-1209G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237910319 | ||||||
| chr2:237910383
|
TCA | T | 46 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0016others(43): Show | 47 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.192-1132_192-1131d others(4): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237910383 | |||||
| chr2:237910383
|
TCACA | T | 17 | a0001c0001t0001g0023a0001c0001t0001g0097a0001c0001t0001g0129others(14): Show | 17 | HG01496.hp1 HG02055.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.192-1134_192-1131d others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237910383 | |||||
| chr2:237910426
|
TAGAATGT others(9): Show |
T | 1 | a0001c0001t0001g0020 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.192-1098_192-1083d others(18): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237910426 | |||||
| chr2:237910539
|
A | ACACACAG others(37): Show |
1 | a0001c0001t0001g0222 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.192-974_192-931dup others(44): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237910539 | |||||
| chr2:237910583
|
TCACACAG others(21): Show |
T | 3 | a0001c0001t0001g0103a0001c0001t0001g0189a0001c0001t0001g0214 | 3 | HG02965.hp2 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.192-930_192-903del others(28): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237910583 | |||||
| chr2:237910666
|
CAG | C | 25 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0051others(22): Show | 27 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.192-861_192-860del others(2): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237910666 | ||||||
| chr2:237910678
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.192-850G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237910678 | ||||||
| chr2:237910740
|
A | G | 2 | a0001c0001t0001g0154a0001c0001t0004g0139 | 2 | HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.192-788A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237910740 | ||||||
| chr2:237910754
|
TAGTCACA others(5): Show |
T | 19 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0054others(16): Show | 21 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.192-762_192-751del others(12): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237910754 | |||||
| chr2:237910769
|
TCA | T | 6 | a0001c0001t0002g0044a0001c0001t0002g0128a0001c0001t0002g0187others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.192-752_192-751del others(2): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237910769 | |||||
| chr2:237910825
|
TCACA | T | 5 | a0001c0001t0002g0044a0001c0001t0002g0128a0001c0001t0002g0187others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.192-700_192-697del others(4): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237910825 | |||||
| chr2:237910943
|
TCACA | T | 18 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0097others(15): Show | 18 | HG01496.hp1 HG02055.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.192-578_192-575del others(4): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237910943 | |||||
| chr2:237910956
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.192-572G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237910956 | ||||||
| chr2:237911013
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.192-515C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237911013 | ||||||
| chr2:237911033
|
CTG | C | 4 | a0001c0001t0002g0044a0001c0001t0002g0128a0001c0001t0002g0235others(1): Show | 4 | HG01891.hp2 HG02135.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-493_192-492del others(2): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237911033 | |||||
| chr2:237911157
|
C | T | 17 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0097others(14): Show | 17 | HG01496.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.192-371C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237911157 | ||||||
| chr2:237911160
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.192-368G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237911160 | ||||||
| chr2:237911237
|
AT | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(145): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.192-288delT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237911237 | |||||
| chr2:237911240
|
T | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(149): Show | 155 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.192-288T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237911240 | ||||||
| chr2:237911372
|
G | A | 5 | a0001c0001t0001g0105a0001c0001t0001g0195a0001c0001t0001g0201others(2): Show | 5 | HG01074.hp1 HG01192.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.192-156G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237911372 | ||||||
| chr2:237911403
|
G | A | 13 | a0001c0001t0001g0130a0001c0001t0001g0142a0001c0001t0001g0154others(10): Show | 13 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.192-125G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237911403 | ||||||
| chr2:237911406
|
G | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0021others(49): Show | 54 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.192-122G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237911406 | ||||||
| chr2:237911436
|
C | T | 6 | a0001c0001t0002g0044a0001c0001t0002g0128a0001c0001t0002g0187others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.192-92C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237911436 | ||||||
| chr2:237911488
|
C | G | 1 | a0001c0002t0001g0342 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.192-40C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237911488 |