Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 221303 |
| ensemblid | ENSG00000183807.8 |
| hgncid | 21549 |
| symbol | FAM162B |
| name | family with sequence similarity 162 member B |
| refseq_nuc | NM_001085480.3 |
| refseq_prot | NP_001078949.1 |
| ensembl_nuc | ENST00000368557.6 |
| ensembl_prot | ENSP00000357545.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 116752197 |
| end | 116765719 |
| strand | - |
| ver | v1.2 |
| region | chr6:116752197-116765719 |
| region5000 | chr6:116747197-116770719 |
| regionname0 | FAM162B_chr6_116752197_116765719 |
| regionname5000 | FAM162B_chr6_116747197_116770719 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 162 | 416 | 82 | 68 | 212 | 15 | 37 | 171 | FAM162B_chr6_116747197_116770719 | FAM162B | MLRAV others(157): Show |
chr6 | 116747197 | 116770719 |
| a0002 | 0/0 | 162 | 48 | 12 | 12 | 19 | 3 | 2 | 15 | FAM162B_chr6_116747197_116770719 | FAM162B | MLRAV others(157): Show |
chr6 | 116747197 | 116770719 |
| a0003 | 0/0 | 162 | 7 | 1 | 0 | 1 | 0 | 5 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | MLRAV others(157): Show |
chr6 | 116747197 | 116770719 |
| a0004 | 0/0 | 162 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | MLRAV others(157): Show |
chr6 | 116747197 | 116770719 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 486 | 415 | 82 | 68 | 212 | 14 | 37 | FAM162B_chr6_116747197_116770719 | FAM162B | ATGCT others(481): Show |
chr6 | 116747197 | 116770719 | ||
| a0001c0005 | 0/0 | 486 | 1 | 0 | 0 | 0 | 1 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | ATGCT others(481): Show |
chr6 | 116747197 | 116770719 | ||
| a0002c0002 | 0/0 | 486 | 48 | 12 | 12 | 19 | 3 | 2 | FAM162B_chr6_116747197_116770719 | FAM162B | ATGCT others(481): Show |
chr6 | 116747197 | 116770719 | ||
| a0003c0003 | 0/0 | 486 | 7 | 1 | 0 | 1 | 0 | 5 | FAM162B_chr6_116747197_116770719 | FAM162B | ATGCT others(481): Show |
chr6 | 116747197 | 116770719 | ||
| a0004c0004 | 0/0 | 486 | 3 | 3 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | ATGCT others(481): Show |
chr6 | 116747197 | 116770719 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1032 | 396 | 70 | 68 | 206 | 14 | 36 | FAM162B_chr6_116747197_116770719 | FAM162B | GAGTG others(1027): Show |
chr6 | 116747197 | 116770719 |
| a0001c0001t0002 | 0/0 | 1032 | 8 | 8 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | GAGTG others(1027): Show |
chr6 | 116747197 | 116770719 |
| a0001c0001t0003 | 0/0 | 1032 | 3 | 0 | 0 | 3 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | GAGTG others(1027): Show |
chr6 | 116747197 | 116770719 |
| a0001c0001t0004 | 0/0 | 1032 | 2 | 0 | 0 | 2 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | GAGTG others(1027): Show |
chr6 | 116747197 | 116770719 |
| a0001c0001t0005 | 0/0 | 1032 | 2 | 2 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | GAGTG others(1027): Show |
chr6 | 116747197 | 116770719 |
| a0001c0001t0006 | 0/0 | 1032 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | GAGTG others(1027): Show |
chr6 | 116747197 | 116770719 |
| a0001c0001t0007 | 0/0 | 1032 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | GAGTG others(1027): Show |
chr6 | 116747197 | 116770719 |
| a0001c0001t0008 | 0/0 | 1032 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | GAGTG others(1027): Show |
chr6 | 116747197 | 116770719 |
| a0001c0001t0009 | 0/0 | 1032 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | GAGTG others(1027): Show |
chr6 | 116747197 | 116770719 |
| a0001c0005t0001 | 0/0 | 1032 | 1 | 0 | 0 | 0 | 1 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | GAGTG others(1027): Show |
chr6 | 116747197 | 116770719 |
| a0002c0002t0001 | 0/0 | 1032 | 47 | 12 | 12 | 18 | 3 | 2 | FAM162B_chr6_116747197_116770719 | FAM162B | GAGTG others(1027): Show |
chr6 | 116747197 | 116770719 |
| a0002c0002t0010 | 0/0 | 1032 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | GAGTG others(1027): Show |
chr6 | 116747197 | 116770719 |
| a0003c0003t0001 | 0/0 | 1032 | 7 | 1 | 0 | 1 | 0 | 5 | FAM162B_chr6_116747197_116770719 | FAM162B | GAGTG others(1027): Show |
chr6 | 116747197 | 116770719 |
| a0004c0004t0001 | 0/0 | 1032 | 3 | 3 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | GAGTG others(1027): Show |
chr6 | 116747197 | 116770719 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 18 | 1 | 8 | 6 | 1 | 2 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0002 | 0/0 | 15 | 0 | 1 | 13 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0003 | 0/0 | 12 | 0 | 5 | 7 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0004 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 1 | 2 | 1 | 2 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 5 | 1 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0011 | 0/0 | 6 | 0 | 1 | 4 | 1 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0020 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0022 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0023 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0024 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0032 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0033 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0034 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0035 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0036 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0053 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0060 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0061 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0062 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0064 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0065 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0066 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0067 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0068 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0003g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0004g0063 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0006g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0001t0009g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0001c0005t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0005 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0025 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0037 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0038 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0039 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0069 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0070 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0071 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0002c0002t0010g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0003c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0003c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0003c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0003c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0003c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0003c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0003c0003t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0004c0004t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0004c0004t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| a0004c0004t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | GBR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | GBR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | GBR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | GBR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | FIN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00323 | hp1 | a0001 | c0005 | t0001 | g0131 | EUR | FIN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0070 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0253 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0037 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0037 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0255 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0254 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0069 | EUR | IBS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0069 | EUR | IBS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0038 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0276 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0025 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02083 | hp1 | a0003 | c0003 | t0001 | g0244 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | CDX | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CDX | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0260 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02602 | hp1 | a0003 | c0003 | t0001 | g0242 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0157 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0269 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02647 | hp2 | a0003 | c0003 | t0001 | g0247 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02698 | hp1 | a0003 | c0003 | t0001 | g0245 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0257 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02735 | hp2 | a0003 | c0003 | t0001 | g0246 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02809 | hp2 | a0004 | c0004 | t0001 | g0275 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0271 | AFR | ESN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0277 | AFR | ESN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | ESN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03041 | hp1 | a0001 | c0001 | t0009 | g0175 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03041 | hp2 | a0004 | c0004 | t0001 | g0274 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | MSL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0266 | AFR | MSL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0258 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | MSL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0267 | AFR | ESN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03579 | hp2 | a0004 | c0004 | t0001 | g0273 | AFR | MSL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03688 | hp1 | a0003 | c0003 | t0001 | g0243 | SAS | STU | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03927 | hp1 | a0001 | c0001 | t0007 | g0083 | SAS | BEB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | STU | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0241 | SAS | STU | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | STU | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | YRI | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18948 | hp1 | a0001 | c0001 | t0006 | g0213 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0071 | AFR | LWK | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | LWK | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19070 | hp2 | a0002 | c0002 | t0010 | g0263 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | YRI | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ASW | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | TSI | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0259 | EUR | TSI | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | GIH | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | GIH | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0270 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0071 | AFR | ACB | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | MSL | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | USA | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | USA | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | USA | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | USA | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | LWK | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | LWK | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0095 | REF | REF | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0053 | REF | REF | FAM162B_chr6_116747197_116770719 | FAM162B | chr6 | 116747197 | 116770719 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116762009 | C | T | 1 | a0003 | 7 | HG02083.hp1 HG02602.hp1 HG02647.hp2 others(4): Show |
missense_variant | MODERATE | c.358G>A | p.Ala120Thr | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/4 | 501/1032 | 358/489 | 120/162 | chr6 | 116762009 | |||
| chr6:116765215 | C | A | 1 | a0002 | 48 | HG00621.hp1 HG00642.hp1 HG00733.hp2 others(45): Show |
missense_variant | MODERATE | c.213G>T | p.Gln71His | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/4 | 356/1032 | 213/489 | 71/162 | chr6 | 116765215 | |||
| chr6:116765495 | T | C | 1 | a0004 | 3 | HG02809.hp2 HG03041.hp2 HG03579.hp2 |
missense_variant | MODERATE | c.82A>G | p.Thr28Ala | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 1/4 | 225/1032 | 82/489 | 28/162 | chr6 | 116765495 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116762019 | G | A | 1 | a0001c0005 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.348C>T | p.Leu116Leu | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/4 | 491/1032 | 348/489 | 116/162 | chr6 | 116762019 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116752216 | T | C | 1 | a0001c0001t0009 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*381A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 4/4 | 381 | chr6 | 116752216 | ||||||
| chr6:116752254 | T | C | 1 | a0002c0002t0010 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*343A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 4/4 | 343 | chr6 | 116752254 | ||||||
| chr6:116752339 | A | G | 1 | a0001c0001t0008 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*258T>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 4/4 | 258 | chr6 | 116752339 | ||||||
| chr6:116752357 | G | T | 1 | a0001c0001t0007 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*240C>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 4/4 | 240 | chr6 | 116752357 | ||||||
| chr6:116752373 | C | T | 1 | a0001c0001t0006 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*224G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 4/4 | 224 | chr6 | 116752373 | ||||||
| chr6:116752379 | A | C | 1 | a0001c0001t0003 | 3 | NA18955.hp2 NA19056.hp1 NA19076.hp1 |
3_prime_UTR_variant | MODIFIER | c.*218T>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 4/4 | 218 | chr6 | 116752379 | ||||||
| chr6:116752426 | G | A | 1 | a0001c0001t0004 | 2 | NA18988.hp2 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*171C>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 4/4 | 171 | chr6 | 116752426 | ||||||
| chr6:116765580 | G | T | 1 | a0001c0001t0002 | 8 | HG02055.hp1 HG02559.hp1 HG02717.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-4C>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 1/4 | 4 | chr6 | 116765580 | ||||||
| chr6:116765663 | T | C | 1 | a0001c0001t0005 | 2 | HG01891.hp1 HG02970.hp1 |
5_prime_UTR_variant | MODIFIER | c.-87A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 1/4 | 87 | chr6 | 116765663 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116752711 | A | AAT | 5 | a0001c0001t0001g0055 a0001c0001t0001g0100 a0001c0001t0001g0208 others(2): Show |
6 | HG00735.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-18_391-17dupAT | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752711 | |||||||
| chr6:116752711 | A | AATATATA others(5): Show |
1 | a0003c0003t0001g0247 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.391-28_391-17dupAT others(10): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752711 | |||||||
| chr6:116752711 | A | AATATATA others(7): Show |
2 | a0001c0001t0001g0116 a0001c0001t0001g0159 |
2 | HG02109.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.391-30_391-17dupAT others(12): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752711 | |||||||
| chr6:116752711 | A | AATATATA others(11): Show |
1 | a0001c0001t0001g0163 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.391-34_391-17dupAT others(16): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752711 | |||||||
| chr6:116752711 | A | AATATATA others(17): Show |
6 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0133 others(3): Show |
6 | HG02451.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-17_391-16insAT others(22): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752711 | |||||||
| chr6:116752711 | A | AATATATA others(19): Show |
1 | a0001c0001t0001g0150 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.391-17_391-16insAT others(24): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752711 | |||||||
| chr6:116752711 | A | AATATATA others(21): Show |
3 | a0001c0001t0001g0132 a0001c0001t0001g0158 a0002c0002t0001g0265 |
3 | HG01243.hp1 HG02129.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.391-17_391-16insAT others(26): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752711 | |||||||
| chr6:116752711 | A | AATATATA others(23): Show |
1 | a0001c0001t0001g0156 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.391-17_391-16insAT others(28): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752711 | |||||||
| chr6:116752711 | A | AATATATA others(25): Show |
2 | a0001c0001t0001g0084 a0001c0001t0001g0155 |
2 | HG03927.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.391-17_391-16insAT others(30): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752711 | |||||||
| chr6:116752711 | A | AATATATA others(27): Show |
1 | a0001c0001t0001g0144 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.391-17_391-16insAT others(32): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752711 | |||||||
| chr6:116752711 | A | ATATATAT others(28): Show |
1 | a0001c0001t0008g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.391-17_391-16insAT others(33): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752711 | |||||||
| chr6:116752711 | AATAT | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(96): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.391-20_391-17delAT others(2): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752711 | |||||||
| chr6:116752725 | T | G | 5 | a0001c0001t0001g0024 a0001c0001t0001g0204 a0001c0001t0001g0240 others(2): Show |
8 | HG01258.hp1 HG01928.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-30A>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752725 | |||||||
| chr6:116752729 | T | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0204 a0001c0001t0001g0240 others(2): Show |
8 | HG01258.hp1 HG01928.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-34A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752729 | |||||||
| chr6:116752730 | A | AC | 5 | a0001c0001t0001g0024 a0001c0001t0001g0204 a0001c0001t0001g0240 others(2): Show |
8 | HG01258.hp1 HG01928.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-36_391-35insG | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752730 | |||||||
| chr6:116752731 | T | G | 1 | a0001c0001t0001g0105 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.391-36A>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752731 | |||||||
| chr6:116752731 | T | TAG | 46 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(43): Show |
69 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.391-37_391-36insCT | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752731 | |||||||
| chr6:116752731 | T | TATATATA others(13): Show |
1 | a0001c0001t0002g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.391-37_391-36insCT others(18): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752731 | |||||||
| chr6:116752731 | T | TATATATA others(27): Show |
1 | a0001c0001t0001g0238 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.391-37_391-36insCT others(32): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752731 | |||||||
| chr6:116752735 | G | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0204 a0001c0001t0001g0240 others(2): Show |
8 | HG01258.hp1 HG01928.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-40C>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752735 | |||||||
| chr6:116752738 | ACACG | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0204 a0001c0001t0001g0240 others(2): Show |
8 | HG01258.hp1 HG01928.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-47_391-44delCG others(2): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752738 | |||||||
| chr6:116752755 | T | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0204 a0001c0001t0001g0240 others(2): Show |
8 | HG01258.hp1 HG01928.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-60A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752755 | |||||||
| chr6:116752755 | T | TATAC | 3 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0163 |
3 | HG02572.hp1 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.391-64_391-61dupGT others(2): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752755 | |||||||
| chr6:116752755 | T | TATATAC | 20 | a0001c0001t0001g0100 a0001c0001t0001g0132 a0001c0001t0001g0133 others(17): Show |
20 | HG00735.hp2 HG01243.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.391-61_391-60insGT others(4): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752755 | |||||||
| chr6:116752755 | T | TATATATA others(1): Show |
50 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(47): Show |
74 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.391-61_391-60insGT others(6): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752755 | |||||||
| chr6:116752755 | T | TATATATA others(3): Show |
2 | a0001c0001t0001g0115 a0001c0001t0002g0077 |
2 | HG03471.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.391-61_391-60insGT others(8): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752755 | |||||||
| chr6:116752755 | T | TATATATA others(5): Show |
5 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0084 others(2): Show |
5 | HG02129.hp1 HG03017.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.391-61_391-60insGT others(10): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116752755 | |||||||
| chr6:116753033 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.391-338C>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116753033 | |||||||
| chr6:116753084 | C | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0204 a0001c0001t0001g0240 others(2): Show |
8 | HG01258.hp1 HG01928.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-389G>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116753084 | |||||||
| chr6:116753086 | C | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.391-391G>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116753086 | |||||||
| chr6:116753378 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.391-683A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116753378 | |||||||
| chr6:116753465 | G | T | 58 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(55): Show |
81 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.391-770C>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116753465 | |||||||
| chr6:116753620 | A | C | 1 | a0001c0001t0001g0049 | 2 | HG00597.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.391-925T>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116753620 | |||||||
| chr6:116753965 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.391-1270A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116753965 | |||||||
| chr6:116754056 | T | C | 86 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(83): Show |
114 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(111): Show |
intron_variant | MODIFIER | c.391-1361A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116754056 | |||||||
| chr6:116754105 | A | T | 86 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(83): Show |
114 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(111): Show |
intron_variant | MODIFIER | c.391-1410T>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116754105 | |||||||
| chr6:116754205 | G | A | 1 | a0003c0003t0001g0247 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.391-1510C>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116754205 | |||||||
| chr6:116754257 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.391-1562C>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116754257 | |||||||
| chr6:116754287 | C | T | 1 | a0002c0002t0001g0266 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.391-1592G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116754287 | |||||||
| chr6:116754316 | C | T | 1 | a0001c0001t0002g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.391-1621G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116754316 | |||||||
| chr6:116754406 | G | C | 18 | a0001c0001t0001g0024 a0001c0001t0001g0055 a0001c0001t0001g0155 others(15): Show |
22 | HG01243.hp1 HG01258.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.391-1711C>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116754406 | |||||||
| chr6:116754469 | G | A | 57 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(54): Show |
80 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.391-1774C>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116754469 | |||||||
| chr6:116754685 | TTTC | T | 84 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(81): Show |
111 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.391-1993_391-1991d others(5): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116754685 | |||||||
| chr6:116754932 | C | G | 1 | a0003c0003t0001g0246 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.391-2237G>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116754932 | |||||||
| chr6:116755003 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0059 a0001c0001t0001g0185 |
6 | NA18943.hp1 NA18947.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-2308G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116755003 | |||||||
| chr6:116755028 | G | C | 1 | a0002c0002t0001g0260 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.391-2333C>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116755028 | |||||||
| chr6:116755056 | A | G | 5 | a0001c0001t0001g0024 a0001c0001t0001g0204 a0001c0001t0001g0240 others(2): Show |
8 | HG01258.hp1 HG01928.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-2361T>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116755056 | |||||||
| chr6:116755202 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.391-2507G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116755202 | |||||||
| chr6:116755301 | C | G | 1 | a0001c0001t0001g0085 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.391-2606G>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116755301 | |||||||
| chr6:116755317 | AAAG | A | 10 | a0001c0001t0001g0100 a0001c0001t0001g0146 a0001c0001t0001g0148 others(7): Show |
11 | HG00735.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.391-2625_391-2623d others(5): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116755317 | |||||||
| chr6:116755334 | C | T | 15 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0056 others(12): Show |
24 | HG00544.hp2 HG01106.hp2 HG02132.hp2 others(21): Show |
intron_variant | MODIFIER | c.391-2639G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116755334 | |||||||
| chr6:116755403 | TGA | T | 7 | a0001c0001t0001g0051 a0001c0001t0001g0068 a0001c0001t0001g0140 others(4): Show |
9 | HG00639.hp1 HG01074.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-2710_391-2709d others(4): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116755403 | |||||||
| chr6:116755434 | T | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0204 a0001c0001t0001g0240 others(2): Show |
8 | HG01258.hp1 HG01928.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-2739A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116755434 | |||||||
| chr6:116755521 | T | C | 57 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(54): Show |
80 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.391-2826A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116755521 | |||||||
| chr6:116755618 | C | T | 11 | a0001c0001t0001g0100 a0001c0001t0001g0146 a0001c0001t0001g0148 others(8): Show |
12 | HG00735.hp2 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.391-2923G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116755618 | |||||||
| chr6:116755644 | A | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0205 |
2 | NA18966.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.391-2949T>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116755644 | |||||||
| chr6:116755777 | T | C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0015 others(19): Show |
49 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.391-3082A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116755777 | |||||||
| chr6:116755889 | T | C | 1 | a0001c0001t0001g0227 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.391-3194A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116755889 | |||||||
| chr6:116755921 | T | C | 1 | a0001c0001t0002g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.391-3226A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116755921 | |||||||
| chr6:116755988 | A | C | 1 | a0001c0001t0001g0060 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.391-3293T>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116755988 | |||||||
| chr6:116756054 | A | C | 5 | a0001c0001t0001g0034 a0001c0001t0001g0059 a0001c0001t0001g0185 others(2): Show |
8 | NA18943.hp1 NA18947.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-3359T>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116756054 | |||||||
| chr6:116756114 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.391-3419C>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116756114 | |||||||
| chr6:116756216 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(62): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.391-3521C>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116756216 | |||||||
| chr6:116756238 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.391-3543G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116756238 | |||||||
| chr6:116756287 | C | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(64): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.391-3592G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116756287 | |||||||
| chr6:116756456 | A | G | 11 | a0001c0001t0001g0100 a0001c0001t0001g0146 a0001c0001t0001g0148 others(8): Show |
12 | HG00735.hp2 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.391-3761T>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116756456 | |||||||
| chr6:116756459 | C | G | 2 | a0001c0001t0001g0210 a0001c0001t0001g0220 |
2 | HG00099.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.391-3764G>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116756459 | |||||||
| chr6:116756477 | T | C | 7 | a0001c0001t0001g0051 a0001c0001t0001g0068 a0001c0001t0001g0140 others(4): Show |
9 | HG00639.hp1 HG01074.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-3782A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116756477 | |||||||
| chr6:116756554 | G | C | 6 | a0001c0001t0001g0098 a0002c0002t0001g0037 a0002c0002t0001g0253 others(3): Show |
8 | HG00733.hp2 HG01074.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-3859C>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116756554 | |||||||
| chr6:116756610 | C | G | 58 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(55): Show |
81 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.391-3915G>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116756610 | |||||||
| chr6:116756619 | C | A | 86 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(83): Show |
114 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(111): Show |
intron_variant | MODIFIER | c.391-3924G>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116756619 | |||||||
| chr6:116756640 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.391-3945A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116756640 | |||||||
| chr6:116757273 | A | T | 86 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(83): Show |
114 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(111): Show |
intron_variant | MODIFIER | c.391-4578T>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116757273 | |||||||
| chr6:116757316 | G | A | 8 | a0001c0001t0001g0024 a0001c0001t0001g0055 a0001c0001t0001g0204 others(5): Show |
12 | HG01258.hp1 HG01884.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.391-4621C>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116757316 | |||||||
| chr6:116757327 | GATA | G | 9 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(6): Show |
9 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.391-4635_391-4633d others(5): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116757327 | |||||||
| chr6:116757537 | A | C | 1 | a0004c0004t0001g0273 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.390+4440T>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116757537 | |||||||
| chr6:116757564 | T | C | 1 | a0003c0003t0001g0242 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.390+4413A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116757564 | |||||||
| chr6:116757621 | C | T | 86 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(83): Show |
114 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(111): Show |
intron_variant | MODIFIER | c.390+4356G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116757621 | |||||||
| chr6:116757636 | A | C | 86 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(83): Show |
114 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(111): Show |
intron_variant | MODIFIER | c.390+4341T>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116757636 | |||||||
| chr6:116757695 | GC | G | 16 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0032 others(13): Show |
30 | HG00639.hp2 HG00741.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.390+4281delG | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116757695 | |||||||
| chr6:116757754 | C | CA | 10 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0065 others(7): Show |
20 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.390+4222dupT | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116757754 | |||||||
| chr6:116757754 | C | CAA | 75 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(72): Show |
100 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.390+4221_390+4222d others(4): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116757754 | |||||||
| chr6:116757754 | C | CAAA | 11 | a0001c0001t0001g0024 a0001c0001t0001g0082 a0001c0001t0001g0096 others(8): Show |
14 | HG01258.hp1 HG01928.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.390+4220_390+4222d others(5): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116757754 | |||||||
| chr6:116757778 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.390+4199C>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116757778 | |||||||
| chr6:116757837 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(62): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.390+4140A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116757837 | |||||||
| chr6:116757865 | C | T | 9 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(6): Show |
9 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.390+4112G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116757865 | |||||||
| chr6:116758155 | T | C | 2 | a0001c0001t0001g0113 a0002c0002t0001g0270 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.390+3822A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116758155 | |||||||
| chr6:116758156 | G | T | 3 | a0001c0001t0001g0125 a0001c0001t0003g0048 a0001c0001t0003g0138 |
4 | HG00609.hp1 NA18955.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+3821C>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116758156 | |||||||
| chr6:116758189 | A | C | 1 | a0001c0001t0001g0228 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.390+3788T>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116758189 | |||||||
| chr6:116758411 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0002g0072 |
3 | HG02818.hp1 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.390+3566T>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116758411 | |||||||
| chr6:116758483 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0230 |
3 | HG02895.hp2 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.390+3494C>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116758483 | |||||||
| chr6:116758530 | ACTTT | A | 9 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(6): Show |
9 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.390+3443_390+3446d others(6): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116758530 | |||||||
| chr6:116758531 | CTTTA | C | 76 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(73): Show |
104 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.390+3442_390+3445d others(6): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116758531 | |||||||
| chr6:116758554 | A | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0204 a0001c0001t0001g0240 others(1): Show |
7 | HG01258.hp1 HG01928.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.390+3423T>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116758554 | |||||||
| chr6:116758660 | A | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0204 a0001c0001t0001g0240 others(1): Show |
7 | HG01258.hp1 HG01928.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.390+3317T>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116758660 | |||||||
| chr6:116758878 | A | G | 4 | a0001c0001t0001g0113 a0001c0001t0001g0164 a0001c0001t0002g0076 others(1): Show |
4 | HG02109.hp1 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+3099T>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116758878 | |||||||
| chr6:116758883 | CCTGT | C | 7 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0084 others(4): Show |
7 | HG02129.hp1 HG02886.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.390+3090_390+3093d others(6): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116758883 | |||||||
| chr6:116759079 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.390+2898C>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759079 | |||||||
| chr6:116759244 | T | C | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(113): Show |
188 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.390+2733A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759244 | |||||||
| chr6:116759298 | TC | T | 11 | a0001c0001t0001g0055 a0001c0001t0001g0146 a0001c0001t0001g0148 others(8): Show |
12 | HG01884.hp2 HG02280.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.390+2678delG | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759298 | |||||||
| chr6:116759299 | C | CT | 16 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(13): Show |
28 | HG00544.hp2 HG01074.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.390+2677dupA | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759299 | |||||||
| chr6:116759299 | C | T | 26 | a0001c0001t0001g0024 a0001c0001t0001g0081 a0001c0001t0001g0082 others(23): Show |
30 | HG00735.hp2 HG01243.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.390+2678G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759299 | |||||||
| chr6:116759299 | CT | C | 14 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0022 others(11): Show |
14 | HG02809.hp2 HG03041.hp2 HG03579.hp2 others(11): Show |
intron_variant | MODIFIER | c.390+2677delA | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759299 | |||||||
| chr6:116759302 | T | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0204 a0001c0001t0001g0239 others(2): Show |
8 | HG01258.hp1 HG01928.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.390+2675A>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759302 | |||||||
| chr6:116759308 | T | A | 1 | a0001c0001t0001g0200 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.390+2669A>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759308 | |||||||
| chr6:116759317 | A | T | 1 | a0001c0001t0001g0231 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.390+2660T>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759317 | |||||||
| chr6:116759415 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.390+2562G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759415 | |||||||
| chr6:116759417 | T | TC | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(125): Show |
219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.390+2559_390+2560i others(3): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759417 | |||||||
| chr6:116759445 | C | T | 4 | a0001c0001t0001g0224 a0004c0004t0001g0273 a0004c0004t0001g0274 others(1): Show |
4 | HG02809.hp2 HG03041.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+2532G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759445 | |||||||
| chr6:116759461 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.390+2516A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759461 | |||||||
| chr6:116759487 | T | C | 10 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(7): Show |
11 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.390+2490A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759487 | |||||||
| chr6:116759516 | C | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0142 a0001c0001t0001g0215 |
6 | HG01106.hp1 HG01109.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+2461G>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759516 | |||||||
| chr6:116759592 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.390+2385G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759592 | |||||||
| chr6:116759658 | A | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0230 |
3 | HG02895.hp2 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.390+2319T>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759658 | |||||||
| chr6:116759688 | C | T | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(169): Show |
281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.390+2289G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759688 | |||||||
| chr6:116759837 | A | G | 1 | a0002c0002t0001g0264 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.390+2140T>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759837 | |||||||
| chr6:116759894 | T | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(100): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.390+2083A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759894 | |||||||
| chr6:116759909 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.390+2068A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759909 | |||||||
| chr6:116759969 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.390+2008A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116759969 | |||||||
| chr6:116760067 | T | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.390+1910A>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116760067 | |||||||
| chr6:116760160 | A | G | 5 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(2): Show |
5 | NA18954.hp1 NA18971.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+1817T>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116760160 | |||||||
| chr6:116760187 | A | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0165 a0001c0001t0001g0166 others(1): Show |
6 | HG01106.hp2 HG02257.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+1790T>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116760187 | |||||||
| chr6:116760361 | T | C | 3 | a0004c0004t0001g0273 a0004c0004t0001g0274 a0004c0004t0001g0275 |
3 | HG02809.hp2 HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.390+1616A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116760361 | |||||||
| chr6:116760425 | A | G | 45 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0032 others(42): Show |
61 | HG00741.hp1 HG00741.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.390+1552T>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116760425 | |||||||
| chr6:116760594 | A | G | 4 | a0001c0001t0001g0224 a0004c0004t0001g0273 a0004c0004t0001g0274 others(1): Show |
4 | HG02809.hp2 HG03041.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+1383T>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116760594 | |||||||
| chr6:116760687 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.390+1290T>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116760687 | |||||||
| chr6:116760983 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(110): Show |
202 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.390+994A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116760983 | |||||||
| chr6:116761156 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.390+821T>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761156 | |||||||
| chr6:116761228 | T | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0164 |
3 | HG02895.hp2 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.390+749A>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761228 | |||||||
| chr6:116761383 | T | C | 6 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0159 others(3): Show |
6 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+594A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761383 | |||||||
| chr6:116761419 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(181): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.390+558A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761419 | |||||||
| chr6:116761443 | C | A | 1 | a0001c0001t0001g0224 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.390+534G>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761443 | |||||||
| chr6:116761443 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.390+534G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761443 | |||||||
| chr6:116761608 | T | A | 23 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0032 others(20): Show |
35 | HG00099.hp1 HG00741.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.390+369A>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761608 | |||||||
| chr6:116761608 | T | TTA | 1 | a0001c0001t0001g0031 | 3 | HG02080.hp1 NA19081.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.390+367_390+368dup others(2): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761608 | |||||||
| chr6:116761645 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.390+332G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761645 | |||||||
| chr6:116761650 | A | ATATATAT others(11): Show |
171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(168): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.390+326_390+327ins others(18): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761650 | |||||||
| chr6:116761660 | T | TTATATAT others(11): Show |
1 | a0001c0001t0001g0225 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.390+316_390+317ins others(18): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761660 | |||||||
| chr6:116761662 | A | ATATATG | 11 | a0002c0002t0001g0071 a0002c0002t0001g0266 a0002c0002t0001g0267 others(8): Show |
12 | HG02083.hp1 HG02559.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.390+314_390+315ins others(6): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761662 | |||||||
| chr6:116761674 | A | ATATATAT others(3): Show |
4 | a0002c0002t0001g0071 a0002c0002t0001g0266 a0002c0002t0001g0267 others(1): Show |
5 | HG02559.hp2 HG02922.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+302_390+303ins others(10): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761674 | |||||||
| chr6:116761680 | A | ATACT | 7 | a0003c0003t0001g0241 a0003c0003t0001g0242 a0003c0003t0001g0243 others(4): Show |
7 | HG02083.hp1 HG02602.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.390+296_390+297ins others(4): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761680 | |||||||
| chr6:116761681 | C | T | 11 | a0002c0002t0001g0071 a0002c0002t0001g0266 a0002c0002t0001g0267 others(8): Show |
12 | HG02083.hp1 HG02559.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.390+296G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761681 | |||||||
| chr6:116761683 | T | C | 5 | a0001c0001t0001g0129 a0002c0002t0001g0071 a0002c0002t0001g0266 others(2): Show |
6 | HG02559.hp2 HG02922.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+294A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761683 | |||||||
| chr6:116761698 | ATACT | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0130 |
3 | HG02451.hp2 HG03209.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.390+275_390+278del others(4): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761698 | |||||||
| chr6:116761726 | TTA | T | 7 | a0001c0001t0001g0162 a0002c0002t0001g0037 a0002c0002t0001g0253 others(4): Show |
9 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+249_390+250del others(2): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761726 | |||||||
| chr6:116761731 | TATAC | T | 17 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0034 others(14): Show |
29 | NA18943.hp1 NA18947.hp1 NA18949.hp1 others(26): Show |
intron_variant | MODIFIER | c.390+242_390+245del others(4): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761731 | |||||||
| chr6:116761733 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(128): Show |
222 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.390+244A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761733 | |||||||
| chr6:116761753 | CAT | C | 16 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0143 others(13): Show |
20 | HG00140.hp1 HG01168.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.390+222_390+223del others(2): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761753 | |||||||
| chr6:116761755 | T | C | 30 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0032 others(27): Show |
42 | HG00099.hp1 HG00741.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.390+222A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761755 | |||||||
| chr6:116761757 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.390+220A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761757 | |||||||
| chr6:116761792 | T | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0226 a0001c0001t0001g0227 |
3 | NA18972.hp1 NA19078.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.390+185A>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761792 | |||||||
| chr6:116761903 | T | C | 1 | a0001c0001t0001g0052 | 2 | NA18940.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.390+74A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761903 | |||||||
| chr6:116761969 | A | C | 32 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0032 others(29): Show |
46 | HG00099.hp1 HG00741.hp2 HG01074.hp1 others(43): Show |
splice_region_variant&intron_variant | LOW | c.390+8T>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | 116761969 | |||||||
| chr6:116762161 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.282-76T>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116762161 | |||||||
| chr6:116762329 | G | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(158): Show |
265 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(262): Show |
intron_variant | MODIFIER | c.282-244C>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116762329 | |||||||
| chr6:116762419 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0239 a0001c0001t0001g0240 |
6 | HG01258.hp1 HG01928.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.282-334C>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116762419 | |||||||
| chr6:116762499 | TA | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(181): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.282-415delT | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116762499 | |||||||
| chr6:116762500 | A | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0116 |
2 | HG03654.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.282-415T>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116762500 | |||||||
| chr6:116762533 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.282-448G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116762533 | |||||||
| chr6:116762557 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(158): Show |
265 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(262): Show |
intron_variant | MODIFIER | c.282-472T>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116762557 | |||||||
| chr6:116762710 | A | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(182): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.282-625T>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116762710 | |||||||
| chr6:116762764 | A | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0239 a0001c0001t0001g0240 |
6 | HG01258.hp1 HG01928.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.282-679T>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116762764 | |||||||
| chr6:116762802 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.282-717A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116762802 | |||||||
| chr6:116762895 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.282-810A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116762895 | |||||||
| chr6:116762998 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(151): Show |
257 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(254): Show |
intron_variant | MODIFIER | c.282-913T>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116762998 | |||||||
| chr6:116763034 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.282-949G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116763034 | |||||||
| chr6:116763079 | C | T | 7 | a0003c0003t0001g0241 a0003c0003t0001g0242 a0003c0003t0001g0243 others(4): Show |
7 | HG02083.hp1 HG02602.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.282-994G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116763079 | |||||||
| chr6:116763083 | T | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(182): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.282-998A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116763083 | |||||||
| chr6:116763155 | A | G | 7 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.282-1070T>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116763155 | |||||||
| chr6:116763512 | A | C | 1 | a0001c0001t0001g0251 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.282-1427T>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116763512 | |||||||
| chr6:116763598 | C | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(181): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.282-1513G>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116763598 | |||||||
| chr6:116763767 | C | T | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
469 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(466): Show |
intron_variant | MODIFIER | c.281+1380G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116763767 | |||||||
| chr6:116763776 | A | AT | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(140): Show |
248 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(245): Show |
intron_variant | MODIFIER | c.281+1370dupA | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116763776 | |||||||
| chr6:116763776 | AT | A | 21 | a0001c0001t0001g0054 a0001c0001t0001g0134 a0001c0001t0001g0135 others(18): Show |
22 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.281+1370delA | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116763776 | |||||||
| chr6:116763858 | T | G | 10 | a0001c0001t0001g0054 a0001c0001t0001g0145 a0001c0001t0001g0146 others(7): Show |
11 | HG00140.hp1 HG01168.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.281+1289A>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116763858 | |||||||
| chr6:116764075 | T | C | 22 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0143 others(19): Show |
26 | HG00140.hp1 HG01168.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.281+1072A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116764075 | |||||||
| chr6:116764460 | A | C | 1 | a0001c0001t0001g0086 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.281+687T>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116764460 | |||||||
| chr6:116764621 | A | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(183): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.281+526T>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116764621 | |||||||
| chr6:116764637 | C | G | 4 | a0001c0001t0001g0068 a0001c0001t0001g0248 a0001c0001t0001g0249 others(1): Show |
5 | HG01074.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.281+510G>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116764637 | |||||||
| chr6:116764638 | G | C | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.281+509C>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116764638 | |||||||
| chr6:116764665 | A | C | 1 | a0001c0001t0001g0154 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.281+482T>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116764665 | |||||||
| chr6:116764688 | A | AC | 14 | a0001c0001t0001g0054 a0001c0001t0001g0084 a0001c0001t0001g0143 others(11): Show |
15 | HG00140.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.281+458dupG | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116764688 | |||||||
| chr6:116764693 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.281+454G>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116764693 | |||||||
| chr6:116764706 | C | A | 1 | a0001c0001t0001g0251 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.281+441G>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116764706 | |||||||
| chr6:116764821 | G | A | 4 | a0001c0001t0001g0068 a0001c0001t0001g0248 a0001c0001t0001g0249 others(1): Show |
5 | HG01074.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.281+326C>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116764821 | |||||||
| chr6:116764857 | G | T | 1 | a0001c0001t0001g0016 | 4 | NA18965.hp1 NA18972.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.281+290C>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116764857 | |||||||
| chr6:116764889 | C | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG03017.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.281+258G>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116764889 | |||||||
| chr6:116764893 | G | A | 7 | a0001c0001t0002g0040 a0001c0001t0002g0072 a0001c0001t0002g0073 others(4): Show |
8 | HG02055.hp1 HG02559.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.281+254C>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116764893 | |||||||
| chr6:116764902 | G | A | 5 | a0001c0001t0002g0073 a0001c0001t0002g0074 a0001c0001t0002g0075 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.281+245C>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116764902 | |||||||
| chr6:116765026 | T | C | 5 | a0001c0001t0002g0073 a0001c0001t0002g0074 a0001c0001t0002g0075 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.281+121A>G | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116765026 | |||||||
| chr6:116765080 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.281+67C>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116765080 | |||||||
| chr6:116765098 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.281+49G>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116765098 | |||||||
| chr6:116765100 | T | A | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.281+47A>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116765100 | |||||||
| chr6:116765102 | C | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(182): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.281+45G>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116765102 | |||||||
| chr6:116765104 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.281+43C>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116765104 | |||||||
| chr6:116765105 | C | G | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.281+42G>C | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116765105 | |||||||
| chr6:116765106 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.281+41G>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116765106 | |||||||
| chr6:116765107 | G | T | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.281+40C>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116765107 | |||||||
| chr6:116765108 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.281+39C>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116765108 | |||||||
| chr6:116765110 | G | T | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.281+37C>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116765110 | |||||||
| chr6:116765112 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.281+35G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116765112 | |||||||
| chr6:116765113 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.281+34G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116765113 | |||||||
| chr6:116765124 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.281+23G>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2/3 | chr6 | 116765124 | |||||||
| chr6:116765278 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.173-23C>T | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 1/3 | chr6 | 116765278 | |||||||
| chr6:116765299 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.173-44C>A | FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 1/3 | chr6 | 116765299 |