Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6005 |
| ensemblid | ENSG00000112077.18 |
| hgncid | 10006 |
| symbol | RHAG |
| name | Rh associated glycoprotein |
| refseq_nuc | NM_000324.3 |
| refseq_prot | NP_000315.2 |
| ensembl_nuc | ENST00000371175.10 |
| ensembl_prot | ENSP00000360217.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 49605175 |
| end | 49636839 |
| strand | - |
| ver | v1.2 |
| region | chr6:49605175-49636839 |
| region5000 | chr6:49600175-49641839 |
| regionname0 | RHAG_chr6_49605175_49636839 |
| regionname5000 | RHAG_chr6_49600175_49641839 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 409 | 366 | 81 | 72 | 158 | 18 | 35 | 121 | RHAG_chr6_49600175_49641839 | RHAG | MRFTF others(404): Show |
chr6 | 49600175 | 49641839 |
| a0002 | 0/0 | 409 | 27 | 8 | 1 | 11 | 0 | 7 | 8 | RHAG_chr6_49600175_49641839 | RHAG | MRFTF others(404): Show |
chr6 | 49600175 | 49641839 |
| a0003 | 0/0 | 409 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | MRFTF others(404): Show |
chr6 | 49600175 | 49641839 |
| a0004 | 0/0 | 409 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | MRFTF others(404): Show |
chr6 | 49600175 | 49641839 |
| a0005 | 0/0 | 5 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | MFSWL | chr6 | 49600175 | 49641839 |
| a0006 | 0/0 | 409 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | MRFTF others(404): Show |
chr6 | 49600175 | 49641839 |
| a0007 | 0/0 | 409 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | MRFTF others(404): Show |
chr6 | 49600175 | 49641839 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1227 | 365 | 80 | 72 | 158 | 18 | 35 | RHAG_chr6_49600175_49641839 | RHAG | ATGAG others(1222): Show |
chr6 | 49600175 | 49641839 | ||
| a0001c0004 | 0/0 | 1227 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | ATGAG others(1222): Show |
chr6 | 49600175 | 49641839 | ||
| a0002c0002 | 0/0 | 1227 | 27 | 8 | 1 | 11 | 0 | 7 | RHAG_chr6_49600175_49641839 | RHAG | ATGAG others(1222): Show |
chr6 | 49600175 | 49641839 | ||
| a0003c0003 | 0/0 | 1227 | 3 | 3 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | ATGAG others(1222): Show |
chr6 | 49600175 | 49641839 | ||
| a0004c0005 | 0/0 | 1227 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | ATGAG others(1222): Show |
chr6 | 49600175 | 49641839 | ||
| a0005c0008 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | ATGTT others(1195): Show |
chr6 | 49600175 | 49641839 | ||
| a0006c0007 | 0/0 | 1227 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | ATGAG others(1222): Show |
chr6 | 49600175 | 49641839 | ||
| a0007c0006 | 0/0 | 1227 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | ATGAG others(1222): Show |
chr6 | 49600175 | 49641839 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1895 | 315 | 49 | 65 | 150 | 16 | 33 | RHAG_chr6_49600175_49641839 | RHAG | AGTGT others(1890): Show |
chr6 | 49600175 | 49641839 |
| a0001c0001t0002 | 0/0 | 1895 | 45 | 28 | 5 | 8 | 2 | 2 | RHAG_chr6_49600175_49641839 | RHAG | AGTGT others(1890): Show |
chr6 | 49600175 | 49641839 |
| a0001c0001t0003 | 0/0 | 1895 | 3 | 3 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | AGTGT others(1890): Show |
chr6 | 49600175 | 49641839 |
| a0001c0001t0004 | 0/0 | 1895 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | AGTGT others(1890): Show |
chr6 | 49600175 | 49641839 |
| a0001c0001t0005 | 0/0 | 1895 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | AGTGT others(1890): Show |
chr6 | 49600175 | 49641839 |
| a0001c0004t0001 | 0/0 | 1895 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | AGTGT others(1890): Show |
chr6 | 49600175 | 49641839 |
| a0002c0002t0001 | 0/0 | 1895 | 27 | 8 | 1 | 11 | 0 | 7 | RHAG_chr6_49600175_49641839 | RHAG | AGTGT others(1890): Show |
chr6 | 49600175 | 49641839 |
| a0003c0003t0001 | 0/0 | 1895 | 3 | 3 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | AGTGT others(1890): Show |
chr6 | 49600175 | 49641839 |
| a0004c0005t0001 | 0/0 | 1895 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | AGTGT others(1890): Show |
chr6 | 49600175 | 49641839 |
| a0005c0008t0002 | 0/0 | 1868 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | AGTGT others(1863): Show |
chr6 | 49600175 | 49641839 |
| a0006c0007t0001 | 0/0 | 1895 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | AGTGT others(1890): Show |
chr6 | 49600175 | 49641839 |
| a0007c0006t0001 | 0/0 | 1895 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | AGTGT others(1890): Show |
chr6 | 49600175 | 49641839 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 34 | 0 | 8 | 16 | 4 | 6 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0002 | 0/0 | 30 | 0 | 5 | 23 | 0 | 2 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0003 | 0/0 | 23 | 7 | 7 | 7 | 1 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0004 | 0/0 | 12 | 1 | 4 | 4 | 1 | 2 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0005 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0139 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0008 | 0/0 | 8 | 2 | 1 | 5 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0043 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0001c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0002c0002t0001g0007 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0002c0002t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0002c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0002c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0003c0003t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0003c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0004c0005t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0005c0008t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0006c0007t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| a0007c0006t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | GBR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0073 | EUR | GBR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0204 | EUR | FIN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | FIN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | CHS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0128 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | CLM | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | CLM | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | IBS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | IBS | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01928 | hp2 | a0004 | c0005 | t0001 | g0182 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0088 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0175 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | CDX | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CDX | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CDX | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0121 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0123 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0025 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02897 | hp2 | a0003 | c0003 | t0001 | g0025 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | MSL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03139 | hp2 | a0005 | c0008 | t0002 | g0211 | AFR | ESN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | MSL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | MSL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | MSL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0092 | AFR | MSL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0124 | AFR | ESN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | MSL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | MSL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0095 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0116 | SAS | STU | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | STU | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0118 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | BEB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0094 | SAS | BEB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | BEB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | STU | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | YRI | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | YRI | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18906 | hp2 | a0006 | c0007 | t0001 | g0210 | AFR | YRI | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19043 | hp1 | a0001 | c0004 | t0001 | g0044 | AFR | LWK | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | LWK | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19079 | hp2 | a0007 | c0006 | t0001 | g0140 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | YRI | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | ASW | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | TSI | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | MSL | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | USA | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | USA | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0119 | AFR | USA | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA20300 | hp2 | a0003 | c0003 | t0001 | g0045 | AFR | USA | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | LWK | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0139 | REF | REF | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0085 | REF | REF | RHAG_chr6_49600175_49641839 | RHAG | chr6 | 49600175 | 49641839 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49612534 | C | T | 1 | a0002 | 27 | HG00438.hp2 HG01934.hp2 HG02056.hp1 others(24): Show |
missense_variant&splice_region_variant | MODERATE | c.808G>A | p.Val270Ile | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/10 | 835/1895 | 808/1230 | 270/409 | chr6 | 49612534 | |||
| chr6:49615692 | C | T | 1 | a0004 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.572G>A | p.Arg191Gln | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 4/10 | 599/1895 | 572/1230 | 191/409 | chr6 | 49615692 | |||
| chr6:49618070 | T | G | 1 | a0007 | 1 | NA19079.hp2 | missense_variant&splice_region_variant | MODERATE | c.490A>C | p.Lys164Gln | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/10 | 517/1895 | 490/1230 | 164/409 | chr6 | 49618070 | |||
| chr6:49636697 | G | T | 1 | a0003 | 3 | HG02896.hp2 HG02897.hp2 NA20300.hp2 |
missense_variant | MODERATE | c.116C>A | p.Thr39Asn | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/10 | 143/1895 | 116/1230 | 39/409 | chr6 | 49636697 | |||
| chr6:49636707 | G | T | 1 | a0005 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.106C>A | p.Leu36Ile | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/10 | 133/1895 | 106/1230 | 36/409 | chr6 | 49636707 | |||
| chr6:49636709 | TGCTCGAG others(7): Show |
T | 1 | a0005 | 1 | HG03139.hp2 | frameshift_variant | HIGH | c.90_103delGACTGTTCT others(5): Show |
p.Thr31fs | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/10 | 130/1895 | 90/1230 | 30/409 | chr6 | 49636709 | |||
| chr6:49636726 | G | C | 1 | a0005 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.87C>G | p.Asp29Glu | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/10 | 114/1895 | 87/1230 | 29/409 | chr6 | 49636726 | |||
| chr6:49636728 | C | G | 1 | a0005 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.85G>C | p.Asp29His | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/10 | 112/1895 | 85/1230 | 29/409 | chr6 | 49636728 | |||
| chr6:49636730 | G | A | 1 | a0006 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.83C>T | p.Thr28Met | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/10 | 110/1895 | 83/1230 | 28/409 | chr6 | 49636730 | |||
| chr6:49636731 | T | A | 1 | a0005 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.82A>T | p.Thr28Ser | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/10 | 109/1895 | 82/1230 | 28/409 | chr6 | 49636731 | |||
| chr6:49636734 | C | G | 1 | a0005 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.79G>C | p.Glu27Gln | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/10 | 106/1895 | 79/1230 | 27/409 | chr6 | 49636734 | |||
| chr6:49636736 | T | G | 1 | a0005 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.77A>C | p.Tyr26Ser | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/10 | 104/1895 | 77/1230 | 26/409 | chr6 | 49636736 | |||
| chr6:49636737 | A | C | 1 | a0005 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.76T>G | p.Tyr26Asp | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/10 | 103/1895 | 76/1230 | 26/409 | chr6 | 49636737 | |||
| chr6:49636747 | T | G | 1 | a0005 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.66A>C | p.Leu22Phe | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/10 | 93/1895 | 66/1230 | 22/409 | chr6 | 49636747 | |||
| chr6:49636779 | G | T | 1 | a0005 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.34C>A | p.Leu12Met | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/10 | 61/1895 | 34/1230 | 12/409 | chr6 | 49636779 | |||
| chr6:49636795 | AGGGAATG others(6): Show |
A | 1 | a0005 | 1 | HG03139.hp2 | frameshift_variant | HIGH | c.5_17delGGTTCACATTC others(2): Show |
p.Arg2fs | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/10 | 44/1895 | 5/1230 | 2/409 | chr6 | 49636795 | |||
| chr6:49636809 | T | A | 1 | a0005 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.4A>T | p.Arg2Trp | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/10 | 31/1895 | 4/1230 | 2/409 | chr6 | 49636809 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49612481 | C | T | 1 | a0002c0002 | 27 | HG00438.hp2 HG01934.hp2 HG02056.hp1 others(24): Show |
synonymous_variant | LOW | c.861G>A | p.Ala287Ala | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/10 | 888/1895 | 861/1230 | 287/409 | chr6 | 49612481 | |||
| chr6:49636729 | C | G | 1 | a0005c0008 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.84G>C | p.Thr28Thr | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/10 | 111/1895 | 84/1230 | 28/409 | chr6 | 49636729 | |||
| chr6:49636729 | C | T | 1 | a0001c0004 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.84G>A | p.Thr28Thr | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/10 | 111/1895 | 84/1230 | 28/409 | chr6 | 49636729 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49605376 | T | C | 1 | a0001c0001t0003 | 3 | HG02145.hp1 HG02615.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*437A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 10/10 | 437 | chr6 | 49605376 | ||||||
| chr6:49605416 | C | T | 1 | a0001c0001t0005 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*397G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 10/10 | 397 | chr6 | 49605416 | ||||||
| chr6:49605589 | C | T | 3 | a0001c0001t0002 a0001c0001t0004 a0005c0008t0002 |
47 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*224G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 10/10 | 224 | chr6 | 49605589 | ||||||
| chr6:49605606 | C | T | 1 | a0001c0001t0004 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*207G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 10/10 | 207 | chr6 | 49605606 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49605893 | T | A | 1 | a0001c0001t0001g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1213-63A>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 9/9 | chr6 | 49605893 | |||||||
| chr6:49606088 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1213-258G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 9/9 | chr6 | 49606088 | |||||||
| chr6:49606146 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1213-316T>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 9/9 | chr6 | 49606146 | |||||||
| chr6:49606188 | C | T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(37): Show |
77 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.1213-358G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 9/9 | chr6 | 49606188 | |||||||
| chr6:49606194 | A | T | 1 | a0001c0001t0001g0163 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1213-364T>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 9/9 | chr6 | 49606194 | |||||||
| chr6:49606249 | G | A | 42 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0024 others(39): Show |
83 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1213-419C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 9/9 | chr6 | 49606249 | |||||||
| chr6:49606641 | G | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(55): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1212+207C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 9/9 | chr6 | 49606641 | |||||||
| chr6:49606698 | C | A | 32 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0022 others(29): Show |
47 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.1212+150G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 9/9 | chr6 | 49606698 | |||||||
| chr6:49606804 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1212+44T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 9/9 | chr6 | 49606804 | |||||||
| chr6:49606818 | C | T | 32 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0022 others(29): Show |
47 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.1212+30G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 9/9 | chr6 | 49606818 | |||||||
| chr6:49607246 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1068-26T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49607246 | |||||||
| chr6:49607281 | A | G | 32 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0022 others(29): Show |
47 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.1068-61T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49607281 | |||||||
| chr6:49607320 | A | C | 1 | a0001c0001t0002g0150 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1068-100T>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49607320 | |||||||
| chr6:49607428 | T | C | 32 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0022 others(29): Show |
47 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.1068-208A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49607428 | |||||||
| chr6:49607471 | C | T | 3 | a0001c0001t0002g0051 a0001c0001t0002g0199 a0001c0001t0002g0200 |
3 | HG01258.hp1 HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1068-251G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49607471 | |||||||
| chr6:49607545 | C | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(27): Show |
80 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1068-325G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49607545 | |||||||
| chr6:49607642 | G | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(97): Show |
187 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.1068-422C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49607642 | |||||||
| chr6:49607719 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1068-499T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49607719 | |||||||
| chr6:49607742 | G | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0036 |
6 | HG00642.hp1 HG01074.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1068-522C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49607742 | |||||||
| chr6:49607890 | A | C | 1 | a0001c0001t0001g0015 | 4 | HG01069.hp1 HG01071.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068-670T>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49607890 | |||||||
| chr6:49607912 | T | G | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1068-692A>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49607912 | |||||||
| chr6:49607978 | T | A | 1 | a0001c0001t0001g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1068-758A>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49607978 | |||||||
| chr6:49608295 | A | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0074 others(1): Show |
9 | HG00099.hp1 HG00323.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1068-1075T>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49608295 | |||||||
| chr6:49608380 | A | G | 18 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0076 others(15): Show |
27 | HG00438.hp2 HG01934.hp2 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.1068-1160T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49608380 | |||||||
| chr6:49608470 | C | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(27): Show |
80 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1068-1250G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49608470 | |||||||
| chr6:49608473 | G | A | 3 | a0001c0001t0001g0072 a0001c0001t0001g0164 a0007c0006t0001g0140 |
3 | NA18998.hp1 NA18999.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1068-1253C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49608473 | |||||||
| chr6:49608473 | GTT | G | 29 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0012 others(26): Show |
52 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1068-1255_1068-125 others(6): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49608473 | |||||||
| chr6:49608537 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1068-1317G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49608537 | |||||||
| chr6:49608574 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1068-1354T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49608574 | |||||||
| chr6:49608681 | T | C | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1068-1461A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49608681 | |||||||
| chr6:49608754 | GTAT | G | 4 | a0001c0001t0001g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 others(1): Show |
4 | HG02145.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068-1537_1068-153 others(7): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49608754 | |||||||
| chr6:49608878 | A | C | 1 | a0001c0001t0001g0185 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1068-1658T>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49608878 | |||||||
| chr6:49608923 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1068-1703G>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49608923 | |||||||
| chr6:49609043 | TTTGCAAA others(2): Show |
T | 1 | a0001c0001t0001g0019 | 3 | HG02451.hp2 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1068-1832_1068-182 others(13): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49609043 | |||||||
| chr6:49609053 | C | A | 1 | a0001c0001t0001g0019 | 3 | HG02451.hp2 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1068-1833G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49609053 | |||||||
| chr6:49609404 | T | G | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1067+1620A>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49609404 | |||||||
| chr6:49609502 | C | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(27): Show |
80 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1067+1522G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49609502 | |||||||
| chr6:49609775 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1067+1249G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49609775 | |||||||
| chr6:49609776 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1067+1248A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49609776 | |||||||
| chr6:49609845 | T | C | 1 | a0001c0001t0002g0151 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1067+1179A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49609845 | |||||||
| chr6:49609912 | C | T | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1067+1112G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49609912 | |||||||
| chr6:49609985 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1067+1039G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49609985 | |||||||
| chr6:49609986 | G | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(96): Show |
186 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.1067+1038C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49609986 | |||||||
| chr6:49610047 | C | A | 1 | a0001c0001t0001g0179 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1067+977G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49610047 | |||||||
| chr6:49610087 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1067+937C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49610087 | |||||||
| chr6:49610121 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0084 |
5 | HG00099.hp1 HG00323.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1067+903G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49610121 | |||||||
| chr6:49610247 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1067+777T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49610247 | |||||||
| chr6:49610253 | G | A | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(100): Show |
190 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.1067+771C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49610253 | |||||||
| chr6:49610270 | A | T | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1067+754T>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49610270 | |||||||
| chr6:49610282 | G | A | 1 | a0001c0004t0001g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1067+742C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49610282 | |||||||
| chr6:49610580 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0074 others(1): Show |
9 | HG00099.hp1 HG00323.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1067+444G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49610580 | |||||||
| chr6:49610777 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1067+247C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49610777 | |||||||
| chr6:49610826 | A | T | 1 | a0001c0001t0001g0155 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1067+198T>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49610826 | |||||||
| chr6:49610988 | G | T | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1067+36C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 7/9 | chr6 | 49610988 | |||||||
| chr6:49611163 | A | C | 1 | a0001c0001t0001g0103 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.946-18T>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49611163 | |||||||
| chr6:49611163 | A | G | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.946-18T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49611163 | |||||||
| chr6:49611240 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.946-95C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49611240 | |||||||
| chr6:49611241 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.946-96T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49611241 | |||||||
| chr6:49611242 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.946-97C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49611242 | |||||||
| chr6:49611245 | A | G | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.946-100T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49611245 | |||||||
| chr6:49611316 | G | A | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.946-171C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49611316 | |||||||
| chr6:49611346 | G | T | 1 | a0002c0002t0001g0021 | 3 | HG02109.hp1 HG02257.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.946-201C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49611346 | |||||||
| chr6:49611408 | T | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0078 others(1): Show |
12 | HG01069.hp2 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.946-263A>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49611408 | |||||||
| chr6:49611443 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.946-298T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49611443 | |||||||
| chr6:49611500 | T | C | 37 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(34): Show |
53 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.946-355A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49611500 | |||||||
| chr6:49611635 | T | C | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.946-490A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49611635 | |||||||
| chr6:49611677 | G | T | 37 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(34): Show |
53 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.946-532C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49611677 | |||||||
| chr6:49611740 | C | CT | 33 | a0001c0001t0001g0019 a0001c0001t0001g0069 a0001c0001t0001g0074 others(30): Show |
53 | HG00280.hp1 HG00438.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.946-596dupA | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49611740 | |||||||
| chr6:49611740 | CT | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0064 a0001c0001t0001g0167 others(3): Show |
6 | HG01169.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.946-596delA | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49611740 | |||||||
| chr6:49611840 | C | G | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.945+557G>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49611840 | |||||||
| chr6:49611916 | AT | A | 19 | a0001c0001t0001g0145 a0002c0002t0001g0007 a0002c0002t0001g0021 others(16): Show |
28 | HG00438.hp2 HG01934.hp2 HG02056.hp1 others(25): Show |
intron_variant | MODIFIER | c.945+480delA | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49611916 | |||||||
| chr6:49611940 | G | T | 2 | a0001c0001t0001g0184 a0001c0001t0004g0128 |
2 | HG00741.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.945+457C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49611940 | |||||||
| chr6:49612206 | T | C | 1 | a0001c0001t0004g0128 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.945+191A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49612206 | |||||||
| chr6:49612232 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0078 others(1): Show |
12 | HG01069.hp2 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.945+165G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49612232 | |||||||
| chr6:49612320 | CT | C | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.945+76delA | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49612320 | |||||||
| chr6:49612341 | A | G | 1 | a0002c0002t0001g0120 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.945+56T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 6/9 | chr6 | 49612341 | |||||||
| chr6:49612742 | T | C | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.808-208A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49612742 | |||||||
| chr6:49612770 | T | C | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.808-236A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49612770 | |||||||
| chr6:49612834 | T | C | 18 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0076 others(15): Show |
27 | HG00438.hp2 HG01934.hp2 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.808-300A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49612834 | |||||||
| chr6:49612845 | A | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(82): Show |
163 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.808-311T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49612845 | |||||||
| chr6:49613025 | G | A | 18 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0076 others(15): Show |
27 | HG00438.hp2 HG01934.hp2 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.808-491C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49613025 | |||||||
| chr6:49613055 | G | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(78): Show |
159 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.808-521C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49613055 | |||||||
| chr6:49613069 | A | ATT | 17 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0076 others(14): Show |
26 | HG00438.hp2 HG01934.hp2 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.808-537_808-536dup others(2): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49613069 | |||||||
| chr6:49613194 | C | G | 1 | a0001c0001t0002g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.808-660G>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49613194 | |||||||
| chr6:49613261 | G | T | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.808-727C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49613261 | |||||||
| chr6:49613267 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.808-733C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49613267 | |||||||
| chr6:49613407 | G | A | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.808-873C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49613407 | |||||||
| chr6:49613444 | A | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0033 others(5): Show |
17 | HG00735.hp1 HG01358.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.808-910T>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49613444 | |||||||
| chr6:49613539 | T | C | 18 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0076 others(15): Show |
27 | HG00438.hp2 HG01934.hp2 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.808-1005A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49613539 | |||||||
| chr6:49613553 | A | T | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.808-1019T>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49613553 | |||||||
| chr6:49613606 | G | T | 1 | a0001c0001t0001g0183 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.808-1072C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49613606 | |||||||
| chr6:49613684 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.807+1003T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49613684 | |||||||
| chr6:49613710 | T | C | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.807+977A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49613710 | |||||||
| chr6:49613836 | C | T | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.807+851G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49613836 | |||||||
| chr6:49614020 | T | G | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.807+667A>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49614020 | |||||||
| chr6:49614146 | C | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
393 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(390): Show |
intron_variant | MODIFIER | c.807+541G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49614146 | |||||||
| chr6:49614184 | T | A | 1 | a0002c0002t0001g0095 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.807+503A>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49614184 | |||||||
| chr6:49614193 | T | C | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.807+494A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49614193 | |||||||
| chr6:49614223 | G | A | 3 | a0001c0001t0001g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 |
3 | HG02145.hp1 HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.807+464C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49614223 | |||||||
| chr6:49614254 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0078 others(1): Show |
12 | HG01069.hp2 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.807+433T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49614254 | |||||||
| chr6:49614333 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.807+354G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49614333 | |||||||
| chr6:49614359 | A | AT | 23 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0078 others(20): Show |
40 | HG00438.hp2 HG00741.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.807+327dupA | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49614359 | |||||||
| chr6:49614407 | G | A | 18 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0076 others(15): Show |
27 | HG00438.hp2 HG01934.hp2 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.807+280C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49614407 | |||||||
| chr6:49614494 | G | A | 2 | a0002c0002t0001g0094 a0002c0002t0001g0095 |
2 | HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.807+193C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49614494 | |||||||
| chr6:49614494 | G | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0078 others(1): Show |
12 | HG01069.hp2 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.807+193C>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49614494 | |||||||
| chr6:49614575 | C | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(79): Show |
160 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.807+112G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 5/9 | chr6 | 49614575 | |||||||
| chr6:49614904 | C | T | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.641-51G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 4/9 | chr6 | 49614904 | |||||||
| chr6:49614948 | GTTTA | G | 3 | a0002c0002t0001g0114 a0002c0002t0001g0115 a0002c0002t0001g0119 |
3 | NA19001.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.641-99_641-96delTA others(2): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 4/9 | chr6 | 49614948 | |||||||
| chr6:49615389 | T | C | 1 | a0001c0001t0001g0040 | 2 | HG00639.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.640+235A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 4/9 | chr6 | 49615389 | |||||||
| chr6:49615778 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG06807.hp2 | splice_region_variant&intron_variant | LOW | c.493-7C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49615778 | |||||||
| chr6:49615853 | T | C | 1 | a0001c0001t0004g0128 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.493-82A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49615853 | |||||||
| chr6:49615871 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.493-100T>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49615871 | |||||||
| chr6:49615943 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.493-172A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49615943 | |||||||
| chr6:49616126 | T | C | 1 | a0002c0002t0001g0021 | 3 | HG02109.hp1 HG02257.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.493-355A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616126 | |||||||
| chr6:49616146 | A | T | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.493-375T>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616146 | |||||||
| chr6:49616158 | G | A | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.493-387C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616158 | |||||||
| chr6:49616174 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.493-403C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616174 | |||||||
| chr6:49616212 | G | A | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.493-441C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616212 | |||||||
| chr6:49616321 | G | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(38): Show |
78 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.493-550C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616321 | |||||||
| chr6:49616354 | C | A | 1 | a0002c0002t0001g0117 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.493-583G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616354 | |||||||
| chr6:49616354 | C | CA | 65 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(62): Show |
120 | HG00323.hp1 HG00438.hp2 HG00621.hp2 others(117): Show |
intron_variant | MODIFIER | c.493-584dupT | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616354 | |||||||
| chr6:49616354 | C | CAA | 6 | a0001c0001t0001g0028 a0001c0001t0001g0103 a0001c0001t0001g0133 others(3): Show |
7 | HG00741.hp2 HG01074.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.493-585_493-584dup others(2): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616354 | |||||||
| chr6:49616354 | CAA | C | 27 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0012 others(24): Show |
50 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.493-585_493-584del others(2): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616354 | |||||||
| chr6:49616354 | CAAAAAAA others(2): Show |
C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(27): Show |
80 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.493-592_493-584del others(9): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616354 | |||||||
| chr6:49616380 | C | A | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.493-609G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616380 | |||||||
| chr6:49616496 | T | A | 1 | a0001c0001t0002g0143 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.493-725A>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616496 | |||||||
| chr6:49616536 | C | G | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.493-765G>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616536 | |||||||
| chr6:49616544 | C | T | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.493-773G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616544 | |||||||
| chr6:49616648 | T | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(27): Show |
80 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.493-877A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616648 | |||||||
| chr6:49616652 | C | T | 3 | a0001c0001t0001g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 |
3 | HG02145.hp1 HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.493-881G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616652 | |||||||
| chr6:49616746 | G | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(27): Show |
80 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.493-975C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616746 | |||||||
| chr6:49616967 | C | T | 30 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0012 others(27): Show |
53 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.492+1101G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616967 | |||||||
| chr6:49616989 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.492+1079T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49616989 | |||||||
| chr6:49617117 | T | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
393 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(390): Show |
intron_variant | MODIFIER | c.492+951A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49617117 | |||||||
| chr6:49617186 | G | A | 18 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0076 others(15): Show |
27 | HG00438.hp2 HG01934.hp2 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.492+882C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49617186 | |||||||
| chr6:49617371 | G | C | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.492+697C>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49617371 | |||||||
| chr6:49617448 | C | T | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0154 others(1): Show |
4 | NA18961.hp2 NA18992.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.492+620G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49617448 | |||||||
| chr6:49617490 | TC | T | 28 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0012 others(25): Show |
51 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.492+577delG | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49617490 | |||||||
| chr6:49617609 | TG | T | 6 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
7 | HG01074.hp1 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.492+458delC | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49617609 | |||||||
| chr6:49617611 | G | T | 6 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
7 | HG01074.hp1 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.492+457C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49617611 | |||||||
| chr6:49617791 | G | A | 1 | a0001c0001t0002g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.492+277C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49617791 | |||||||
| chr6:49617855 | G | A | 1 | a0002c0002t0001g0092 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.492+213C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49617855 | |||||||
| chr6:49617904 | C | G | 1 | a0001c0001t0002g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.492+164G>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49617904 | |||||||
| chr6:49617958 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0078 others(1): Show |
12 | HG01069.hp2 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.492+110G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49617958 | |||||||
| chr6:49617985 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.492+83G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49617985 | |||||||
| chr6:49618052 | A | G | 2 | a0001c0001t0002g0051 a0001c0001t0002g0199 |
2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.492+16T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 3/9 | chr6 | 49618052 | |||||||
| chr6:49618438 | C | T | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.342-220G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 2/9 | chr6 | 49618438 | |||||||
| chr6:49618561 | T | G | 35 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(32): Show |
71 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.342-343A>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 2/9 | chr6 | 49618561 | |||||||
| chr6:49618572 | G | A | 32 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(29): Show |
68 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.342-354C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 2/9 | chr6 | 49618572 | |||||||
| chr6:49618703 | G | A | 29 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0012 others(26): Show |
52 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.341+476C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 2/9 | chr6 | 49618703 | |||||||
| chr6:49618837 | C | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0024 others(75): Show |
135 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.341+342G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 2/9 | chr6 | 49618837 | |||||||
| chr6:49618880 | T | C | 1 | a0001c0001t0002g0190 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.341+299A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 2/9 | chr6 | 49618880 | |||||||
| chr6:49618919 | C | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0024 others(69): Show |
128 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.341+260G>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 2/9 | chr6 | 49618919 | |||||||
| chr6:49618940 | G | C | 1 | a0001c0001t0002g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.341+239C>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 2/9 | chr6 | 49618940 | |||||||
| chr6:49619026 | C | A | 3 | a0001c0001t0001g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 |
3 | HG02145.hp1 HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.341+153G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 2/9 | chr6 | 49619026 | |||||||
| chr6:49619514 | T | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0024 others(75): Show |
135 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.158-152A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49619514 | |||||||
| chr6:49619523 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.158-161C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49619523 | |||||||
| chr6:49619601 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.158-239T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49619601 | |||||||
| chr6:49619629 | A | G | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.158-267T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49619629 | |||||||
| chr6:49619638 | A | T | 3 | a0001c0001t0001g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 |
3 | HG02145.hp1 HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.158-276T>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49619638 | |||||||
| chr6:49619660 | A | C | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.158-298T>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49619660 | |||||||
| chr6:49619826 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.158-464C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49619826 | |||||||
| chr6:49620000 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.158-638C>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49620000 | |||||||
| chr6:49620004 | C | A | 1 | a0001c0001t0001g0165 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.158-642G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49620004 | |||||||
| chr6:49620006 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.158-644T>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49620006 | |||||||
| chr6:49620007 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.158-645T>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49620007 | |||||||
| chr6:49620101 | C | G | 1 | a0001c0001t0001g0194 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.158-739G>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49620101 | |||||||
| chr6:49620259 | C | G | 1 | a0001c0001t0001g0181 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.158-897G>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49620259 | |||||||
| chr6:49620298 | A | T | 1 | a0001c0001t0001g0125 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.158-936T>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49620298 | |||||||
| chr6:49620359 | T | C | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.158-997A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49620359 | |||||||
| chr6:49620396 | A | G | 9 | a0001c0001t0002g0017 a0001c0001t0002g0073 a0001c0001t0002g0079 others(6): Show |
12 | HG00140.hp1 HG00642.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-1034T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49620396 | |||||||
| chr6:49620460 | G | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(27): Show |
80 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.158-1098C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49620460 | |||||||
| chr6:49620508 | A | G | 1 | a0001c0001t0001g0039 | 2 | HG02132.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.158-1146T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49620508 | |||||||
| chr6:49620521 | G | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0033 others(1): Show |
13 | HG00735.hp1 HG01358.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.158-1159C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49620521 | |||||||
| chr6:49620542 | TG | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
13 | HG01069.hp2 HG02257.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.158-1181delC | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49620542 | |||||||
| chr6:49620544 | G | T | 4 | a0001c0001t0001g0056 a0001c0001t0001g0058 a0001c0001t0001g0062 others(1): Show |
4 | HG00280.hp1 HG00733.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-1182C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49620544 | |||||||
| chr6:49620545 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.158-1183C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49620545 | |||||||
| chr6:49620626 | A | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(202): Show |
389 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(386): Show |
intron_variant | MODIFIER | c.158-1264T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49620626 | |||||||
| chr6:49620641 | C | T | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.158-1279G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49620641 | |||||||
| chr6:49620751 | A | C | 18 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0076 others(15): Show |
27 | HG00438.hp2 HG01934.hp2 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.158-1389T>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49620751 | |||||||
| chr6:49620797 | C | T | 18 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0076 others(15): Show |
27 | HG00438.hp2 HG01934.hp2 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.158-1435G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49620797 | |||||||
| chr6:49621060 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.158-1698G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49621060 | |||||||
| chr6:49621062 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.158-1700C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49621062 | |||||||
| chr6:49621193 | A | T | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.158-1831T>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49621193 | |||||||
| chr6:49621284 | G | C | 1 | a0001c0001t0001g0157 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.158-1922C>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49621284 | |||||||
| chr6:49621316 | T | G | 1 | a0001c0001t0001g0097 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.158-1954A>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49621316 | |||||||
| chr6:49621341 | C | T | 18 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0076 others(15): Show |
27 | HG00438.hp2 HG01934.hp2 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.158-1979G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49621341 | |||||||
| chr6:49621342 | G | A | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.158-1980C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49621342 | |||||||
| chr6:49621380 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.158-2018G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49621380 | |||||||
| chr6:49621469 | C | T | 1 | a0001c0001t0002g0032 | 2 | NA18962.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.158-2107G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49621469 | |||||||
| chr6:49621480 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.158-2118G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49621480 | |||||||
| chr6:49621651 | C | G | 4 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0179 others(1): Show |
4 | NA18946.hp2 NA19001.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-2289G>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49621651 | |||||||
| chr6:49621830 | C | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0024 others(64): Show |
115 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.158-2468G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49621830 | |||||||
| chr6:49621841 | A | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0166 |
3 | HG00423.hp1 HG00544.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.158-2479T>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49621841 | |||||||
| chr6:49621982 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.158-2620T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49621982 | |||||||
| chr6:49622056 | A | C | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.158-2694T>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49622056 | |||||||
| chr6:49622060 | T | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(38): Show |
100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.158-2698A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49622060 | |||||||
| chr6:49622216 | G | GT | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(91): Show |
200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.158-2855dupA | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49622216 | |||||||
| chr6:49622216 | G | GTT | 6 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0038 others(3): Show |
9 | HG01071.hp2 HG01978.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.158-2856_158-2855d others(4): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49622216 | |||||||
| chr6:49622216 | GT | G | 10 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0058 others(7): Show |
12 | HG01515.hp1 HG01516.hp1 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-2855delA | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49622216 | |||||||
| chr6:49622216 | GTT | G | 18 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(15): Show |
27 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.158-2856_158-2855d others(4): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49622216 | |||||||
| chr6:49622491 | A | G | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.158-3129T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49622491 | |||||||
| chr6:49622653 | A | C | 1 | a0001c0001t0001g0155 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.158-3291T>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49622653 | |||||||
| chr6:49622775 | G | A | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.158-3413C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49622775 | |||||||
| chr6:49622830 | C | CT | 80 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0019 others(77): Show |
139 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.158-3469dupA | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49622830 | |||||||
| chr6:49622830 | C | CTT | 11 | a0001c0001t0001g0037 a0001c0001t0001g0131 a0001c0001t0001g0132 others(8): Show |
13 | HG00438.hp1 HG01074.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.158-3470_158-3469d others(4): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49622830 | |||||||
| chr6:49622844 | G | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
387 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(384): Show |
intron_variant | MODIFIER | c.158-3482C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49622844 | |||||||
| chr6:49622845 | T | G | 1 | a0001c0001t0001g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.158-3483A>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49622845 | |||||||
| chr6:49622849 | G | T | 20 | a0001c0001t0002g0129 a0001c0001t0004g0128 a0002c0002t0001g0007 others(17): Show |
29 | HG00438.hp2 HG00741.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.158-3487C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49622849 | |||||||
| chr6:49622986 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.158-3624G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49622986 | |||||||
| chr6:49623027 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.158-3665G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49623027 | |||||||
| chr6:49623031 | GT | G | 60 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(57): Show |
106 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.158-3670delA | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49623031 | |||||||
| chr6:49623085 | G | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0052 others(16): Show |
33 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.158-3723C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49623085 | |||||||
| chr6:49623154 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.158-3792A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49623154 | |||||||
| chr6:49623243 | G | A | 1 | a0003c0003t0001g0045 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.158-3881C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49623243 | |||||||
| chr6:49623291 | G | C | 1 | a0001c0001t0003g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.158-3929C>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49623291 | |||||||
| chr6:49623301 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.158-3939A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49623301 | |||||||
| chr6:49623353 | A | C | 1 | a0002c0002t0001g0092 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.158-3991T>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49623353 | |||||||
| chr6:49623597 | G | A | 1 | a0001c0001t0002g0032 | 2 | NA18962.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.158-4235C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49623597 | |||||||
| chr6:49623607 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.158-4245C>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49623607 | |||||||
| chr6:49623637 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.158-4275G>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49623637 | |||||||
| chr6:49623673 | G | C | 17 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0052 others(14): Show |
31 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.158-4311C>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49623673 | |||||||
| chr6:49623945 | C | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0192 |
2 | NA18964.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.158-4583G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49623945 | |||||||
| chr6:49623945 | C | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
387 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(384): Show |
intron_variant | MODIFIER | c.158-4583G>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49623945 | |||||||
| chr6:49624022 | C | T | 1 | a0001c0004t0001g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.158-4660G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49624022 | |||||||
| chr6:49624061 | C | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0024 others(37): Show |
81 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.158-4699G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49624061 | |||||||
| chr6:49624063 | G | T | 61 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(58): Show |
107 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.158-4701C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49624063 | |||||||
| chr6:49624092 | A | G | 59 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(56): Show |
105 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.158-4730T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49624092 | |||||||
| chr6:49624129 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.158-4767C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49624129 | |||||||
| chr6:49624139 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.158-4777A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49624139 | |||||||
| chr6:49624326 | C | T | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.158-4964G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49624326 | |||||||
| chr6:49624351 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.158-4989C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49624351 | |||||||
| chr6:49624415 | G | C | 1 | a0001c0001t0001g0170 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.158-5053C>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49624415 | |||||||
| chr6:49624424 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.158-5062G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49624424 | |||||||
| chr6:49624520 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(49): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.158-5158C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49624520 | |||||||
| chr6:49624585 | T | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0024 others(61): Show |
112 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.158-5223A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49624585 | |||||||
| chr6:49624622 | G | A | 3 | a0001c0001t0001g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 |
3 | HG02145.hp1 HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.158-5260C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49624622 | |||||||
| chr6:49624683 | A | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
13 | HG01069.hp2 HG02257.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.158-5321T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49624683 | |||||||
| chr6:49624706 | A | G | 61 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(58): Show |
107 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.158-5344T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49624706 | |||||||
| chr6:49624757 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.158-5395C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49624757 | |||||||
| chr6:49624800 | G | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | NA18952.hp2 NA18954.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.158-5438C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49624800 | |||||||
| chr6:49624837 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.158-5475G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49624837 | |||||||
| chr6:49624941 | T | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(58): Show |
107 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.158-5579A>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49624941 | |||||||
| chr6:49625003 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.158-5641G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49625003 | |||||||
| chr6:49625120 | A | G | 1 | a0001c0001t0001g0036 | 2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.158-5758T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49625120 | |||||||
| chr6:49625158 | G | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
13 | HG01069.hp2 HG02257.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.158-5796C>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49625158 | |||||||
| chr6:49625527 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.158-6165G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49625527 | |||||||
| chr6:49625552 | G | A | 12 | a0002c0002t0001g0007 a0002c0002t0001g0076 a0002c0002t0001g0086 others(9): Show |
19 | HG00438.hp2 HG01934.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.158-6190C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49625552 | |||||||
| chr6:49625612 | A | G | 3 | a0001c0001t0002g0022 a0001c0001t0002g0208 a0005c0008t0002g0211 |
5 | HG02109.hp2 HG02145.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-6250T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49625612 | |||||||
| chr6:49625645 | G | A | 59 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(56): Show |
105 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.158-6283C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49625645 | |||||||
| chr6:49625701 | C | T | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(202): Show |
389 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(386): Show |
intron_variant | MODIFIER | c.158-6339G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49625701 | |||||||
| chr6:49625956 | C | T | 1 | a0002c0002t0001g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.158-6594G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49625956 | |||||||
| chr6:49625999 | G | A | 1 | a0001c0001t0002g0042 | 2 | HG02572.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.158-6637C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49625999 | |||||||
| chr6:49626075 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.158-6713C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49626075 | |||||||
| chr6:49626076 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.158-6714T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49626076 | |||||||
| chr6:49626110 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.158-6748G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49626110 | |||||||
| chr6:49626166 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.158-6804G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49626166 | |||||||
| chr6:49626167 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(107): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.158-6805C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49626167 | |||||||
| chr6:49626363 | A | C | 1 | a0001c0001t0001g0052 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.158-7001T>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49626363 | |||||||
| chr6:49626525 | C | T | 6 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
7 | HG01074.hp1 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.158-7163G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49626525 | |||||||
| chr6:49626565 | T | G | 1 | a0001c0001t0001g0196 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.158-7203A>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49626565 | |||||||
| chr6:49626582 | C | T | 60 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(57): Show |
106 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.158-7220G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49626582 | |||||||
| chr6:49626653 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0005g0175 |
4 | HG01978.hp2 HG02004.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-7291T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49626653 | |||||||
| chr6:49626887 | C | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
13 | HG01069.hp2 HG02257.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.158-7525G>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49626887 | |||||||
| chr6:49626975 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
13 | HG01069.hp2 HG02257.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.158-7613C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49626975 | |||||||
| chr6:49626988 | G | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(59): Show |
108 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.158-7626C>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49626988 | |||||||
| chr6:49627020 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.158-7658G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49627020 | |||||||
| chr6:49627052 | A | T | 1 | a0001c0001t0002g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.158-7690T>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49627052 | |||||||
| chr6:49627128 | T | G | 6 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
7 | HG01074.hp1 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.158-7766A>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49627128 | |||||||
| chr6:49627189 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0077 others(6): Show |
17 | HG01069.hp2 HG02145.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.158-7827C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49627189 | |||||||
| chr6:49627468 | T | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(59): Show |
108 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.158-8106A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49627468 | |||||||
| chr6:49627480 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.158-8118C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49627480 | |||||||
| chr6:49627555 | G | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(37): Show |
98 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.158-8193C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49627555 | |||||||
| chr6:49627621 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.158-8259C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49627621 | |||||||
| chr6:49627646 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.158-8284G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49627646 | |||||||
| chr6:49627805 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.158-8443A>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49627805 | |||||||
| chr6:49628085 | G | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0052 others(16): Show |
33 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.157+8571C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628085 | |||||||
| chr6:49628135 | G | GAC | 3 | a0001c0001t0001g0035 a0001c0001t0002g0129 a0001c0001t0002g0143 |
4 | HG00423.hp1 HG02055.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+8519_157+8520d others(4): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628135 | |||||||
| chr6:49628135 | GAC | G | 20 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0052 others(17): Show |
34 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.157+8519_157+8520d others(4): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628135 | |||||||
| chr6:49628135 | GACACAC | G | 59 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(56): Show |
105 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.157+8515_157+8520d others(8): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628135 | |||||||
| chr6:49628140 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.157+8516T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628140 | |||||||
| chr6:49628149 | CACACACA others(7): Show |
C | 1 | a0001c0001t0002g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.157+8493_157+8506d others(16): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628149 | |||||||
| chr6:49628157 | CACACAG | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0081 |
3 | HG01358.hp1 HG02135.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.157+8493_157+8498d others(8): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628157 | |||||||
| chr6:49628159 | CACAG | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0078 others(6): Show |
10 | HG02280.hp2 HG03098.hp2 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.157+8493_157+8496d others(6): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628159 | |||||||
| chr6:49628161 | C | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(54): Show |
100 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.157+8495G>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628161 | |||||||
| chr6:49628161 | CAG | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(97): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.157+8493_157+8494d others(4): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628161 | |||||||
| chr6:49628163 | G | C | 14 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0035 others(11): Show |
19 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(16): Show |
intron_variant | MODIFIER | c.157+8493C>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628163 | |||||||
| chr6:49628165 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.157+8491C>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628165 | |||||||
| chr6:49628506 | T | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
393 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(390): Show |
intron_variant | MODIFIER | c.157+8150A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628506 | |||||||
| chr6:49628507 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.157+8149C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628507 | |||||||
| chr6:49628540 | C | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0077 others(8): Show |
24 | HG01069.hp2 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.157+8116G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628540 | |||||||
| chr6:49628550 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.157+8106C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628550 | |||||||
| chr6:49628575 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
13 | HG01069.hp2 HG02257.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.157+8081C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628575 | |||||||
| chr6:49628575 | G | GTGGTCTC others(94): Show |
1 | a0001c0001t0003g0083 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.157+8080_157+8081i others(103): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628575 | |||||||
| chr6:49628613 | G | A | 2 | a0001c0001t0003g0082 a0001c0001t0003g0083 |
2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.157+8043C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628613 | |||||||
| chr6:49628615 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
13 | HG01069.hp2 HG02257.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.157+8041C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628615 | |||||||
| chr6:49628658 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0077 others(6): Show |
17 | HG01069.hp2 HG02145.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.157+7998C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628658 | |||||||
| chr6:49628741 | G | C | 1 | a0002c0002t0001g0021 | 3 | HG02109.hp1 HG02257.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.157+7915C>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628741 | |||||||
| chr6:49628744 | G | A | 1 | a0001c0001t0001g0015 | 4 | HG01069.hp1 HG01071.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+7912C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628744 | |||||||
| chr6:49628819 | G | A | 12 | a0002c0002t0001g0007 a0002c0002t0001g0076 a0002c0002t0001g0086 others(9): Show |
19 | HG00438.hp2 HG01934.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.157+7837C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628819 | |||||||
| chr6:49628865 | C | T | 62 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(59): Show |
108 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.157+7791G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628865 | |||||||
| chr6:49628871 | C | A | 62 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(59): Show |
108 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.157+7785G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628871 | |||||||
| chr6:49628908 | A | ACATTGTG others(66): Show |
1 | a0005c0008t0002g0211 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.157+7747_157+7748i others(75): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628908 | |||||||
| chr6:49628946 | G | C | 1 | a0005c0008t0002g0211 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.157+7710C>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49628946 | |||||||
| chr6:49629139 | C | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0074 |
4 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+7517G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49629139 | |||||||
| chr6:49629265 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0077 others(6): Show |
17 | HG01069.hp2 HG02145.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.157+7391G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49629265 | |||||||
| chr6:49629393 | A | G | 1 | a0002c0002t0001g0088 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.157+7263T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49629393 | |||||||
| chr6:49629424 | C | T | 7 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(4): Show |
8 | HG00099.hp2 HG01074.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.157+7232G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49629424 | |||||||
| chr6:49629497 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.157+7159G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49629497 | |||||||
| chr6:49629538 | T | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(59): Show |
108 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.157+7118A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49629538 | |||||||
| chr6:49629693 | A | G | 62 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(59): Show |
108 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.157+6963T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49629693 | |||||||
| chr6:49629700 | G | A | 1 | a0001c0004t0001g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157+6956C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49629700 | |||||||
| chr6:49629806 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.157+6850A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49629806 | |||||||
| chr6:49629812 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.157+6844C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49629812 | |||||||
| chr6:49629827 | A | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
13 | HG01069.hp2 HG02257.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.157+6829T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49629827 | |||||||
| chr6:49629844 | GC | G | 60 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(57): Show |
106 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.157+6811delG | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49629844 | |||||||
| chr6:49629875 | A | G | 1 | a0001c0001t0001g0030 | 2 | HG00558.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.157+6781T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49629875 | |||||||
| chr6:49629901 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.157+6755G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49629901 | |||||||
| chr6:49629910 | G | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(48): Show |
119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.157+6746C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49629910 | |||||||
| chr6:49629920 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.157+6736G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49629920 | |||||||
| chr6:49629948 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.157+6708T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49629948 | |||||||
| chr6:49629973 | C | G | 62 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(59): Show |
108 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.157+6683G>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49629973 | |||||||
| chr6:49630576 | A | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | NA18992.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.157+6080T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49630576 | |||||||
| chr6:49630744 | T | C | 1 | a0001c0004t0001g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157+5912A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49630744 | |||||||
| chr6:49630856 | G | T | 1 | a0002c0002t0001g0123 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.157+5800C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49630856 | |||||||
| chr6:49630858 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.157+5798G>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49630858 | |||||||
| chr6:49630902 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.157+5754G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49630902 | |||||||
| chr6:49631056 | G | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
393 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(390): Show |
intron_variant | MODIFIER | c.157+5600C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49631056 | |||||||
| chr6:49631078 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157+5578A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49631078 | |||||||
| chr6:49631097 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(112): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.157+5559G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49631097 | |||||||
| chr6:49631164 | G | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(106): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.157+5492C>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49631164 | |||||||
| chr6:49631379 | T | C | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG00408.hp1 HG02155.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.157+5277A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49631379 | |||||||
| chr6:49631444 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.157+5212T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49631444 | |||||||
| chr6:49631474 | C | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0052 others(16): Show |
33 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.157+5182G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49631474 | |||||||
| chr6:49631554 | T | G | 3 | a0001c0001t0002g0051 a0001c0001t0002g0199 a0001c0001t0002g0200 |
3 | HG01258.hp1 HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.157+5102A>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49631554 | |||||||
| chr6:49631573 | C | A | 62 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(59): Show |
108 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.157+5083G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49631573 | |||||||
| chr6:49631592 | T | C | 2 | a0002c0002t0001g0123 a0002c0002t0001g0124 |
2 | HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.157+5064A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49631592 | |||||||
| chr6:49631747 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.157+4909G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49631747 | |||||||
| chr6:49631749 | G | T | 60 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(57): Show |
106 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.157+4907C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49631749 | |||||||
| chr6:49631819 | C | A | 62 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(59): Show |
108 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.157+4837G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49631819 | |||||||
| chr6:49632126 | G | A | 1 | a0001c0001t0002g0042 | 2 | HG02572.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.157+4530C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49632126 | |||||||
| chr6:49632137 | C | A | 1 | a0001c0001t0001g0067 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.157+4519G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49632137 | |||||||
| chr6:49632236 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.157+4420A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49632236 | |||||||
| chr6:49632635 | G | A | 60 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(57): Show |
106 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.157+4021C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49632635 | |||||||
| chr6:49632741 | A | G | 1 | a0007c0006t0001g0140 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.157+3915T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49632741 | |||||||
| chr6:49632752 | G | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(202): Show |
389 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(386): Show |
intron_variant | MODIFIER | c.157+3904C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49632752 | |||||||
| chr6:49632753 | G | A | 62 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(59): Show |
108 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.157+3903C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49632753 | |||||||
| chr6:49632760 | T | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
13 | HG01069.hp2 HG02257.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.157+3896A>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49632760 | |||||||
| chr6:49632829 | T | G | 60 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(57): Show |
106 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.157+3827A>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49632829 | |||||||
| chr6:49632840 | G | A | 2 | a0001c0001t0002g0043 a0001c0001t0002g0204 |
3 | HG00280.hp1 HG03704.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.157+3816C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49632840 | |||||||
| chr6:49633217 | A | G | 1 | a0001c0001t0001g0029 | 2 | NA18940.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.157+3439T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49633217 | |||||||
| chr6:49633238 | C | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG00408.hp1 HG02155.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.157+3418G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49633238 | |||||||
| chr6:49633254 | G | A | 60 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(57): Show |
106 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.157+3402C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49633254 | |||||||
| chr6:49633261 | C | T | 1 | a0001c0001t0004g0128 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.157+3395G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49633261 | |||||||
| chr6:49633282 | T | G | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.157+3374A>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49633282 | |||||||
| chr6:49633348 | ATTGTTTT others(18): Show |
A | 1 | a0002c0002t0001g0086 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.157+3283_157+3307d others(27): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49633348 | |||||||
| chr6:49633383 | T | A | 1 | a0002c0002t0001g0086 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.157+3273A>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49633383 | |||||||
| chr6:49633451 | A | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0052 others(16): Show |
33 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.157+3205T>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49633451 | |||||||
| chr6:49633563 | T | A | 1 | a0002c0002t0001g0086 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.157+3093A>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49633563 | |||||||
| chr6:49633684 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.157+2972A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49633684 | |||||||
| chr6:49633699 | C | A | 1 | a0001c0001t0001g0067 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.157+2957G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49633699 | |||||||
| chr6:49633713 | G | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
13 | HG01069.hp2 HG02257.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.157+2943C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49633713 | |||||||
| chr6:49633716 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.157+2940G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49633716 | |||||||
| chr6:49633727 | C | T | 7 | a0001c0001t0002g0022 a0001c0001t0002g0130 a0001c0001t0002g0137 others(4): Show |
9 | HG02109.hp2 HG02145.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.157+2929G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49633727 | |||||||
| chr6:49633993 | T | G | 62 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(59): Show |
108 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.157+2663A>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49633993 | |||||||
| chr6:49634384 | A | T | 1 | a0002c0002t0001g0086 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.157+2272T>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49634384 | |||||||
| chr6:49634426 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.157+2230T>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49634426 | |||||||
| chr6:49634532 | C | T | 1 | a0001c0001t0001g0019 | 3 | HG02451.hp2 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.157+2124G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49634532 | |||||||
| chr6:49634556 | A | T | 1 | a0001c0001t0002g0137 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.157+2100T>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49634556 | |||||||
| chr6:49634693 | A | T | 1 | a0001c0001t0002g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.157+1963T>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49634693 | |||||||
| chr6:49634956 | C | CTG | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(103): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.157+1698_157+1699d others(4): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49634956 | |||||||
| chr6:49634956 | C | CTGTG | 12 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(9): Show |
13 | HG00741.hp2 HG01074.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.157+1696_157+1699d others(6): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49634956 | |||||||
| chr6:49634956 | C | CTGTGTG | 12 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0059 others(9): Show |
23 | HG00733.hp1 HG00735.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.157+1694_157+1699d others(8): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49634956 | |||||||
| chr6:49634956 | C | CTGTGTGT others(1): Show |
4 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(1): Show |
4 | HG01515.hp1 HG01517.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+1692_157+1699d others(10): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49634956 | |||||||
| chr6:49634956 | C | CTGTGTGT others(3): Show |
5 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
13 | HG01069.hp2 HG02257.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.157+1690_157+1699d others(12): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49634956 | |||||||
| chr6:49634956 | C | CTGTGTGT others(5): Show |
3 | a0001c0001t0001g0012 a0001c0001t0001g0054 a0001c0001t0001g0055 |
6 | HG00639.hp1 HG01123.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+1688_157+1699d others(14): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49634956 | |||||||
| chr6:49634956 | C | CTGTGTGT others(9): Show |
1 | a0001c0001t0001g0053 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.157+1684_157+1699d others(18): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49634956 | |||||||
| chr6:49634966 | GTGTGTGT others(7): Show |
G | 60 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(57): Show |
106 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.157+1676_157+1689d others(16): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49634966 | |||||||
| chr6:49634980 | T | G | 2 | a0001c0001t0002g0129 a0001c0001t0004g0128 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.157+1676A>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49634980 | |||||||
| chr6:49634984 | G | T | 1 | a0002c0002t0001g0086 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.157+1672C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49634984 | |||||||
| chr6:49634987 | T | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(59): Show |
108 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.157+1669A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49634987 | |||||||
| chr6:49635013 | C | T | 60 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(57): Show |
106 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.157+1643G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49635013 | |||||||
| chr6:49635047 | A | G | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
158 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.157+1609T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49635047 | |||||||
| chr6:49635227 | T | A | 2 | a0001c0001t0002g0043 a0001c0001t0002g0204 |
3 | HG00280.hp1 HG03704.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.157+1429A>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49635227 | |||||||
| chr6:49635282 | T | C | 61 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(58): Show |
107 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.157+1374A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49635282 | |||||||
| chr6:49635303 | C | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(112): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.157+1353G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49635303 | |||||||
| chr6:49635372 | C | A | 1 | a0001c0001t0001g0205 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.157+1284G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49635372 | |||||||
| chr6:49635408 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.157+1248C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49635408 | |||||||
| chr6:49635461 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.157+1195A>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49635461 | |||||||
| chr6:49635518 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.157+1138T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49635518 | |||||||
| chr6:49635596 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.157+1060G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49635596 | |||||||
| chr6:49635607 | C | T | 1 | a0001c0001t0002g0073 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.157+1049G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49635607 | |||||||
| chr6:49635718 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.157+938T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49635718 | |||||||
| chr6:49635766 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.157+890T>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49635766 | |||||||
| chr6:49635970 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0070 others(1): Show |
6 | HG03492.hp2 HG03669.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.157+686G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49635970 | |||||||
| chr6:49635990 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.157+666C>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49635990 | |||||||
| chr6:49636200 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.157+456G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49636200 | |||||||
| chr6:49636207 | C | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0052 others(16): Show |
33 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.157+449G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49636207 | |||||||
| chr6:49636252 | G | T | 1 | a0001c0001t0002g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.157+404C>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49636252 | |||||||
| chr6:49636302 | C | A | 2 | a0001c0001t0002g0208 a0005c0008t0002g0211 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.157+354G>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49636302 | |||||||
| chr6:49636309 | C | T | 1 | a0001c0001t0001g0011 | 4 | NA18946.hp1 NA18981.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+347G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49636309 | |||||||
| chr6:49636336 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.157+320G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49636336 | |||||||
| chr6:49636398 | T | A | 1 | a0001c0001t0001g0209 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.157+258A>T | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49636398 | |||||||
| chr6:49636406 | ACAAAAGG others(39): Show |
A | 1 | a0005c0008t0002g0211 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.157+204_157+249del others(46): Show |
RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49636406 | |||||||
| chr6:49636473 | C | T | 1 | a0005c0008t0002g0211 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.157+183G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49636473 | |||||||
| chr6:49636475 | A | C | 1 | a0005c0008t0002g0211 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.157+181T>G | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49636475 | |||||||
| chr6:49636479 | A | T | 1 | a0005c0008t0002g0211 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.157+177T>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49636479 | |||||||
| chr6:49636529 | T | G | 1 | a0005c0008t0002g0211 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.157+127A>C | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49636529 | |||||||
| chr6:49636618 | C | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
6 | HG02056.hp2 NA18940.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.157+38G>A | RHAG | ENSG00000112077.18 | transcript | ENST00000371175.10 | protein_coding | 1/9 | chr6 | 49636618 |