Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 144809 |
| ensemblid | ENSG00000179813.7 |
| hgncid | 26883 |
| symbol | FAM216B |
| name | family with sequence similarity 216 member B |
| refseq_nuc | NM_001318932.2 |
| refseq_prot | NP_001305861.1 |
| ensembl_nuc | ENST00000313851.3 |
| ensembl_prot | ENSP00000319336.1 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 42781584 |
| end | 42791549 |
| strand | + |
| ver | v1.2 |
| region | chr13:42781584-42791549 |
| region5000 | chr13:42776584-42796549 |
| regionname0 | FAM216B_chr13_42781584_42791549 |
| regionname5000 | FAM216B_chr13_42776584_42796549 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 139 | 447 | 83 | 78 | 218 | 18 | 48 | 174 | FAM216B_chr13_42776584_42796549 | FAM216B | MGQNW others(134): Show |
chr13 | 42776584 | 42796549 |
| a0002 | 0/0 | 139 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | MGQNW others(134): Show |
chr13 | 42776584 | 42796549 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 417 | 446 | 83 | 78 | 218 | 18 | 47 | FAM216B_chr13_42776584_42796549 | FAM216B | ATGGG others(412): Show |
chr13 | 42776584 | 42796549 | ||
| a0001c0003 | 0/0 | 417 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | ATGGG others(412): Show |
chr13 | 42776584 | 42796549 | ||
| a0002c0002 | 0/0 | 417 | 5 | 3 | 2 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | ATGGG others(412): Show |
chr13 | 42776584 | 42796549 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3274 | 110 | 4 | 13 | 75 | 4 | 13 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3269): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0002 | 0/0 | 3263 | 95 | 22 | 19 | 45 | 1 | 8 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3258): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0003 | 0/0 | 3265 | 88 | 26 | 21 | 31 | 4 | 6 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3260): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0004 | 0/0 | 3279 | 58 | 4 | 8 | 33 | 3 | 10 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3274): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0005 | 0/0 | 3267 | 10 | 1 | 6 | 0 | 1 | 2 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3262): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0006 | 0/0 | 3263 | 9 | 0 | 0 | 9 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3258): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0007 | 0/0 | 3277 | 8 | 0 | 1 | 6 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3272): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0008 | 0/0 | 3263 | 8 | 0 | 1 | 0 | 4 | 3 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3258): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0009 | 0/0 | 3272 | 7 | 6 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3267): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0010 | 0/0 | 3283 | 5 | 0 | 1 | 3 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3278): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0011 | 0/0 | 3274 | 5 | 4 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3269): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0012 | 0/0 | 3263 | 5 | 5 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3258): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0013 | 0/0 | 3263 | 4 | 2 | 0 | 0 | 0 | 2 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3258): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0015 | 0/0 | 3281 | 3 | 0 | 0 | 3 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3276): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0016 | 0/0 | 3274 | 3 | 3 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3269): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0017 | 0/0 | 3285 | 2 | 0 | 0 | 2 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3280): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0018 | 0/0 | 3278 | 2 | 0 | 0 | 2 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3273): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0019 | 0/1 | 3276 | 2 | 0 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3271): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0020 | 0/0 | 3275 | 2 | 1 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3270): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0021 | 0/0 | 3274 | 2 | 2 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3269): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0022 | 0/0 | 3265 | 2 | 0 | 2 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3260): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0023 | 0/0 | 3263 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3258): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0025 | 0/0 | 3279 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3274): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0026 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3274): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0027 | 0/0 | 3274 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3269): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0028 | 0/0 | 3274 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3269): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0029 | 0/0 | 3273 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3268): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0030 | 0/0 | 3273 | 1 | 0 | 0 | 0 | 1 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3268): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0031 | 0/0 | 3273 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3268): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0032 | 0/0 | 3272 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3267): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0033 | 0/0 | 3267 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3262): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0034 | 0/0 | 3267 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3262): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0035 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3259): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0036 | 0/0 | 3274 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3269): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0037 | 0/0 | 3274 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3269): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0038 | 0/0 | 3265 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3260): Show |
chr13 | 42776584 | 42796549 |
| a0001c0001t0039 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3274): Show |
chr13 | 42776584 | 42796549 |
| a0001c0003t0004 | 0/0 | 3279 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3274): Show |
chr13 | 42776584 | 42796549 |
| a0002c0002t0014 | 0/0 | 3287 | 4 | 3 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3282): Show |
chr13 | 42776584 | 42796549 |
| a0002c0002t0024 | 0/0 | 3283 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | AGCAT others(3278): Show |
chr13 | 42776584 | 42796549 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 74 | 1 | 9 | 52 | 4 | 8 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0007 | 0/0 | 10 | 0 | 3 | 6 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0022 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0003 | 0/0 | 39 | 0 | 5 | 31 | 0 | 3 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0004 | 0/0 | 21 | 4 | 11 | 2 | 1 | 3 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0008 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0005 | 0/0 | 23 | 0 | 8 | 15 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0006 | 0/0 | 17 | 12 | 3 | 0 | 0 | 2 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0010 | 0/0 | 7 | 0 | 3 | 0 | 3 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0013 | 0/0 | 5 | 0 | 1 | 1 | 1 | 2 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0016 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0021 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0040 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0004g0002 | 0/0 | 41 | 1 | 7 | 26 | 3 | 4 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0004g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0004g0017 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0004g0018 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0004g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0005g0013 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0005g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0006g0012 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0006g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0007g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0007g0009 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0008g0003 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0008g0023 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0008g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0009g0011 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0010g0002 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0010g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0010g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0011g0020 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0011g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0012g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0012g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0012g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0013g0019 | 0/0 | 4 | 2 | 0 | 0 | 0 | 2 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0015g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0015g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0016g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0016g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0017g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0018g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0018g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0019g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0019g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0020g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0020g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0021g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0021g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0022g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0023g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0025g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0026g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0027g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0028g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0029g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0030g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0031g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0032g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0033g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0034g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0035g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0036g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0037g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0038g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0001t0039g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0001c0003t0004g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0002c0002t0014g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| a0002c0002t0024g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0013 | EUR | GBR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00099 | hp2 | a0001 | c0001 | t0030 | g0010 | EUR | GBR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | GBR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | GBR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00280 | hp1 | a0001 | c0001 | t0008 | g0003 | EUR | FIN | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0010 | EUR | FIN | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00323 | hp1 | a0001 | c0001 | t0008 | g0023 | EUR | FIN | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0002 | EUR | FIN | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | CHS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | CHS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0012 | EAS | CHS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | CHS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | CHS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00639 | hp1 | a0002 | c0002 | t0024 | g0015 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00642 | hp2 | a0001 | c0001 | t0010 | g0018 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00673 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | CHS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00733 | hp2 | a0001 | c0001 | t0011 | g0020 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0087 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00741 | hp1 | a0001 | c0001 | t0007 | g0002 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0026 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01071 | hp1 | a0001 | c0001 | t0022 | g0004 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01071 | hp2 | a0001 | c0001 | t0022 | g0004 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01099 | hp2 | a0001 | c0001 | t0033 | g0088 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01109 | hp1 | a0001 | c0001 | t0009 | g0011 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0026 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0026 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01175 | hp2 | a0001 | c0001 | t0027 | g0001 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01192 | hp1 | a0001 | c0001 | t0019 | g0001 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01243 | hp1 | a0001 | c0001 | t0025 | g0002 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01243 | hp2 | a0002 | c0002 | t0014 | g0015 | AMR | PUR | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01257 | hp2 | a0001 | c0001 | t0008 | g0003 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0013 | EUR | IBS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01516 | hp1 | a0001 | c0001 | t0008 | g0023 | EUR | IBS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0010 | EUR | IBS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01517 | hp1 | a0001 | c0001 | t0008 | g0023 | EUR | IBS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ACB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | ACB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0096 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02027 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02055 | hp1 | a0001 | c0001 | t0020 | g0049 | AFR | ACB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | ACB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02074 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | ACB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0104 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CDX | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | CDX | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0011 | AFR | ACB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02257 | hp2 | a0001 | c0001 | t0012 | g0109 | AFR | ACB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0105 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02280 | hp1 | a0001 | c0001 | t0013 | g0019 | AFR | ACB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02451 | hp1 | a0002 | c0002 | t0014 | g0015 | AFR | ACB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02572 | hp1 | a0001 | c0001 | t0012 | g0028 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02602 | hp2 | a0001 | c0001 | t0008 | g0003 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02615 | hp2 | a0001 | c0001 | t0011 | g0020 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02630 | hp1 | a0001 | c0001 | t0016 | g0029 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0020 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02683 | hp1 | a0001 | c0001 | t0008 | g0003 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0018 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02717 | hp1 | a0001 | c0001 | t0011 | g0020 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0011 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02809 | hp2 | a0001 | c0001 | t0016 | g0029 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02818 | hp2 | a0001 | c0001 | t0035 | g0045 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02886 | hp2 | a0001 | c0001 | t0021 | g0050 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0011 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02896 | hp2 | a0001 | c0001 | t0012 | g0028 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0011 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02965 | hp1 | a0001 | c0001 | t0013 | g0019 | AFR | ESN | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | ESN | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | ESN | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | ESN | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02976 | hp1 | a0001 | c0001 | t0023 | g0008 | AFR | ESN | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | ESN | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | MSL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03098 | hp2 | a0002 | c0002 | t0014 | g0015 | AFR | MSL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03139 | hp1 | a0001 | c0001 | t0021 | g0047 | AFR | ESN | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | ESN | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | ESN | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | MSL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0053 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | MSL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0032 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03490 | hp2 | a0001 | c0001 | t0013 | g0019 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0032 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03516 | hp1 | a0002 | c0002 | t0014 | g0015 | AFR | ESN | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0011 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03654 | hp2 | a0001 | c0001 | t0037 | g0001 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03688 | hp2 | a0001 | c0003 | t0004 | g0002 | SAS | STU | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0018 | SAS | BEB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03834 | hp1 | a0001 | c0001 | t0008 | g0069 | SAS | BEB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0017 | SAS | BEB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | BEB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG04115 | hp2 | a0001 | c0001 | t0010 | g0002 | SAS | STU | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0040 | SAS | STU | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | STU | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0101 | SAS | STU | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0013 | SAS | STU | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG04228 | hp1 | a0001 | c0001 | t0007 | g0009 | SAS | STU | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0013 | SAS | STU | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18612 | hp1 | a0001 | c0001 | t0038 | g0016 | EAS | CHB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18944 | hp2 | a0001 | c0001 | t0026 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18950 | hp2 | a0001 | c0001 | t0028 | g0014 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18960 | hp2 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18963 | hp1 | a0001 | c0001 | t0018 | g0007 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18964 | hp2 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18971 | hp1 | a0001 | c0001 | t0010 | g0017 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18976 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18976 | hp2 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18978 | hp1 | a0001 | c0001 | t0006 | g0080 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18979 | hp2 | a0001 | c0001 | t0018 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18981 | hp2 | a0001 | c0001 | t0015 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18983 | hp2 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18984 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18986 | hp2 | a0001 | c0001 | t0015 | g0046 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18987 | hp2 | a0001 | c0001 | t0006 | g0079 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18988 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18992 | hp1 | a0001 | c0001 | t0034 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18997 | hp1 | a0001 | c0001 | t0029 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18997 | hp2 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19002 | hp2 | a0001 | c0001 | t0020 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19007 | hp2 | a0001 | c0001 | t0015 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | LWK | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19030 | hp2 | a0001 | c0001 | t0011 | g0077 | AFR | LWK | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | LWK | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | LWK | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19055 | hp1 | a0001 | c0001 | t0017 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19059 | hp1 | a0001 | c0001 | t0036 | g0070 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19062 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19062 | hp2 | a0001 | c0001 | t0017 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19064 | hp2 | a0001 | c0001 | t0031 | g0009 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19068 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19072 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19075 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19076 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19081 | hp2 | a0001 | c0001 | t0039 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19086 | hp2 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19088 | hp2 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19089 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA19240 | hp2 | a0001 | c0001 | t0012 | g0028 | AFR | YRI | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ASW | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0002 | EUR | TSI | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0010 | EUR | TSI | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA20905 | hp1 | a0001 | c0001 | t0013 | g0019 | SAS | GIH | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | ACB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0011 | AFR | ACB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | ACB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0099 | AFR | ACB | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0108 | AFR | MSL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| HG03471 | hp2 | a0001 | c0001 | t0016 | g0048 | AFR | MSL | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | USA | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0086 | AFR | USA | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | LWK | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| NA21309 | hp2 | a0001 | c0001 | t0032 | g0064 | AFR | LWK | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0019 | g0078 | REF | REF | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0022 | REF | REF | FAM216B_chr13_42776584_42796549 | FAM216B | chr13 | 42776584 | 42796549 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:42788770 | C | T | 1 | a0002 | 5 | HG00639.hp1 HG01243.hp2 HG02451.hp1 others(2): Show |
missense_variant | MODERATE | c.400C>T | p.Arg134Cys | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 495/3274 | 400/420 | 134/139 | chr13 | 42788770 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:42788613 | C | T | 1 | a0001c0003 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.243C>T | p.Ala81Ala | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 338/3274 | 243/420 | 81/139 | chr13 | 42788613 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:42781602 | G | A | 1 | a0001c0001t0013 | 4 | HG02280.hp1 HG02965.hp1 HG03490.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-77G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/4 | 2466 | chr13 | 42781602 | ||||||
| chr13:42788852 | C | T | 1 | a0001c0001t0039 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*62C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 62 | chr13 | 42788852 | ||||||
| chr13:42789203 | T | C | 1 | a0001c0001t0023 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*413T>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 413 | chr13 | 42789203 | ||||||
| chr13:42789411 | A | G | 1 | a0001c0001t0038 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*621A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 621 | chr13 | 42789411 | ||||||
| chr13:42789587 | A | T | 1 | a0001c0001t0037 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*797A>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 797 | chr13 | 42789587 | ||||||
| chr13:42789636 | T | TTG | 4 | a0001c0001t0016 a0001c0001t0019 a0001c0001t0020 others(1): Show |
8 | HG01192.hp1 HG02055.hp1 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*878_*879dupGT | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 880 | INFO_REALIGN_3_PRIME | chr13 | 42789636 | |||||
| chr13:42789636 | T | TTGTG | 2 | a0001c0001t0007 a0001c0001t0018 |
10 | HG00741.hp1 HG04228.hp1 NA18960.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*876_*879dupGTGT | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 880 | INFO_REALIGN_3_PRIME | chr13 | 42789636 | |||||
| chr13:42789636 | T | TTGTGTG | 5 | a0001c0001t0004 a0001c0001t0025 a0001c0001t0026 others(2): Show |
62 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*874_*879dupGTGTGT | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 880 | INFO_REALIGN_3_PRIME | chr13 | 42789636 | |||||
| chr13:42789636 | T | TTGTGTGT others(1): Show |
1 | a0001c0001t0015 | 3 | NA18981.hp2 NA18986.hp2 NA19007.hp2 |
3_prime_UTR_variant | MODIFIER | c.*872_*879dupGTGTGT others(2): Show |
FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 880 | INFO_REALIGN_3_PRIME | chr13 | 42789636 | |||||
| chr13:42789636 | T | TTGTGTGT others(3): Show |
2 | a0001c0001t0010 a0002c0002t0024 |
6 | HG00639.hp1 HG00642.hp2 HG04115.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*870_*879dupGTGTGT others(4): Show |
FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 880 | INFO_REALIGN_3_PRIME | chr13 | 42789636 | |||||
| chr13:42789636 | T | TTGTGTGT others(5): Show |
1 | a0001c0001t0017 | 2 | NA19055.hp1 NA19062.hp2 |
3_prime_UTR_variant | MODIFIER | c.*868_*879dupGTGTGT others(6): Show |
FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 880 | INFO_REALIGN_3_PRIME | chr13 | 42789636 | |||||
| chr13:42789636 | T | TTGTGTGT others(7): Show |
1 | a0002c0002t0014 | 4 | HG01243.hp2 HG02451.hp1 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*866_*879dupGTGTGT others(8): Show |
FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 880 | INFO_REALIGN_3_PRIME | chr13 | 42789636 | |||||
| chr13:42789636 | TTG | T | 2 | a0001c0001t0009 a0001c0001t0032 |
8 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*878_*879delGT | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 878 | INFO_REALIGN_3_PRIME | chr13 | 42789636 | |||||
| chr13:42789636 | TTGTGTG | T | 3 | a0001c0001t0005 a0001c0001t0033 a0001c0001t0034 |
12 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*874_*879delGTGTGT | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 874 | INFO_REALIGN_3_PRIME | chr13 | 42789636 | |||||
| chr13:42789636 | TTGTGTGT others(1): Show |
T | 3 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0038 |
91 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*872_*879delGTGTGT others(2): Show |
FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 872 | INFO_REALIGN_3_PRIME | chr13 | 42789636 | |||||
| chr13:42789636 | TTGTGTGT others(3): Show |
T | 8 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(5): Show |
124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*870_*879delGTGTGT others(4): Show |
FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 870 | INFO_REALIGN_3_PRIME | chr13 | 42789636 | |||||
| chr13:42789716 | C | T | 1 | a0001c0001t0011 | 5 | HG00733.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*926C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 926 | chr13 | 42789716 | ||||||
| chr13:42789959 | A | G | 32 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(29): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
3_prime_UTR_variant | MODIFIER | c.*1169A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 1169 | chr13 | 42789959 | ||||||
| chr13:42790203 | G | A | 1 | a0001c0001t0025 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1413G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 1413 | chr13 | 42790203 | ||||||
| chr13:42790328 | CT | C | 29 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(26): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*1548delT | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 1548 | INFO_REALIGN_3_PRIME | chr13 | 42790328 | |||||
| chr13:42790417 | C | T | 2 | a0001c0001t0016 a0001c0001t0021 |
5 | HG02630.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1627C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 1627 | chr13 | 42790417 | ||||||
| chr13:42790443 | C | T | 1 | a0001c0001t0031 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1653C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 1653 | chr13 | 42790443 | ||||||
| chr13:42790473 | C | A | 1 | a0001c0001t0033 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1683C>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 1683 | chr13 | 42790473 | ||||||
| chr13:42790478 | T | G | 2 | a0002c0002t0014 a0002c0002t0024 |
5 | HG00639.hp1 HG01243.hp2 HG02451.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1688T>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 1688 | chr13 | 42790478 | ||||||
| chr13:42790524 | G | A | 1 | a0001c0001t0006 | 9 | HG00597.hp2 HG00673.hp1 HG02027.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1734G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 1734 | chr13 | 42790524 | ||||||
| chr13:42790623 | A | G | 1 | a0001c0001t0032 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1833A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 1833 | chr13 | 42790623 | ||||||
| chr13:42790684 | G | A | 15 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0010 others(12): Show |
90 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1894G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 1894 | chr13 | 42790684 | ||||||
| chr13:42790723 | C | G | 6 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0012 others(3): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*1933C>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 1933 | chr13 | 42790723 | ||||||
| chr13:42790729 | A | ACTTTATA others(3): Show |
1 | a0001c0001t0036 | 1 | NA19059.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1941_*1942insTTAT others(6): Show |
FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 1942 | INFO_REALIGN_3_PRIME | chr13 | 42790729 | |||||
| chr13:42790735 | G | A | 1 | a0001c0001t0011 | 5 | HG00733.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1945G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 1945 | chr13 | 42790735 | ||||||
| chr13:42790795 | G | A | 1 | a0001c0001t0008 | 8 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2005G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 2005 | chr13 | 42790795 | ||||||
| chr13:42790826 | TA | T | 2 | a0001c0001t0016 a0001c0001t0021 |
5 | HG02630.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2037delA | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 2037 | chr13 | 42790826 | ||||||
| chr13:42790874 | T | C | 1 | a0001c0001t0027 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2084T>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 2084 | chr13 | 42790874 | ||||||
| chr13:42791030 | G | A | 1 | a0001c0001t0028 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2240G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 2240 | chr13 | 42791030 | ||||||
| chr13:42791431 | T | C | 1 | a0001c0001t0026 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2641T>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 2641 | chr13 | 42791431 | ||||||
| chr13:42791471 | G | A | 1 | a0001c0001t0016 | 3 | HG02630.hp1 HG02809.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2681G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 4/4 | 2681 | chr13 | 42791471 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:42781713 | T | C | 2 | a0001c0001t0002g0041 a0001c0001t0002g0042 |
2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-15+49T>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42781713 | |||||||
| chr13:42781894 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | NA18953.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-15+230T>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42781894 | |||||||
| chr13:42781981 | G | A | 10 | a0001c0001t0004g0009 a0001c0001t0007g0009 a0001c0001t0015g0046 others(7): Show |
17 | HG02055.hp1 HG02451.hp2 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.-15+317G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42781981 | |||||||
| chr13:42782091 | G | T | 43 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0010 others(40): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-15+427G>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42782091 | |||||||
| chr13:42782168 | G | A | 1 | a0001c0001t0035g0045 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-15+504G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42782168 | |||||||
| chr13:42782177 | G | A | 38 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0010 others(35): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.-15+513G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42782177 | |||||||
| chr13:42782191 | A | G | 2 | a0001c0001t0003g0027 a0001c0001t0003g0106 |
4 | HG00558.hp1 NA18990.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+527A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42782191 | |||||||
| chr13:42782280 | C | T | 1 | a0001c0001t0002g0038 | 2 | NA19060.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-15+616C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42782280 | |||||||
| chr13:42782334 | T | G | 1 | a0001c0001t0002g0030 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-15+670T>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42782334 | |||||||
| chr13:42782339 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-15+675G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42782339 | |||||||
| chr13:42782423 | G | T | 1 | a0001c0001t0021g0050 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-15+759G>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42782423 | |||||||
| chr13:42782432 | G | A | 1 | a0001c0001t0003g0082 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-15+768G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42782432 | |||||||
| chr13:42782492 | A | T | 1 | a0001c0001t0003g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-15+828A>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42782492 | |||||||
| chr13:42782624 | C | G | 2 | a0001c0001t0005g0104 a0001c0001t0005g0105 |
2 | HG02148.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.-15+960C>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42782624 | |||||||
| chr13:42782633 | C | T | 4 | a0001c0001t0002g0081 a0001c0001t0006g0012 a0001c0001t0006g0079 others(1): Show |
10 | HG00597.hp2 HG00609.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.-15+969C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42782633 | |||||||
| chr13:42782758 | T | C | 1 | a0001c0001t0003g0082 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-15+1094T>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42782758 | |||||||
| chr13:42782763 | C | T | 1 | a0001c0001t0035g0045 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-15+1099C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42782763 | |||||||
| chr13:42782854 | G | A | 4 | a0001c0001t0003g0039 a0001c0001t0003g0083 a0001c0001t0003g0084 others(1): Show |
5 | HG01884.hp1 HG01975.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+1190G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42782854 | |||||||
| chr13:42782859 | A | C | 4 | a0001c0001t0003g0016 a0001c0001t0003g0102 a0001c0001t0003g0103 others(1): Show |
7 | HG01070.hp2 NA18612.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15+1195A>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42782859 | |||||||
| chr13:42782906 | AT | A | 23 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0004g0002 others(20): Show |
76 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.-14-1143delT | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 42782906 | ||||||
| chr13:42782995 | G | GA | 8 | a0001c0001t0003g0013 a0001c0001t0003g0089 a0001c0001t0003g0107 others(5): Show |
15 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.-14-1049dupA | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 42782995 | ||||||
| chr13:42782995 | GA | G | 1 | a0001c0001t0009g0011 | 7 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-1049delA | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 42782995 | ||||||
| chr13:42783002 | A | T | 5 | a0001c0001t0003g0085 a0001c0001t0005g0101 a0001c0001t0012g0028 others(2): Show |
7 | HG02257.hp2 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-1052A>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42783002 | |||||||
| chr13:42783036 | A | G | 110 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0002g0003 others(107): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.-14-1018A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42783036 | |||||||
| chr13:42783082 | C | G | 110 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0002g0003 others(107): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.-14-972C>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42783082 | |||||||
| chr13:42783086 | A | G | 1 | a0001c0001t0020g0049 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-14-968A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42783086 | |||||||
| chr13:42783169 | T | C | 74 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(71): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.-14-885T>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42783169 | |||||||
| chr13:42783182 | C | T | 1 | a0001c0001t0003g0084 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-14-872C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42783182 | |||||||
| chr13:42783237 | G | T | 1 | a0001c0001t0001g0066 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-14-817G>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42783237 | |||||||
| chr13:42783283 | G | A | 3 | a0001c0001t0011g0077 a0002c0002t0014g0015 a0002c0002t0024g0015 |
6 | HG00639.hp1 HG01243.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-771G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42783283 | |||||||
| chr13:42783315 | C | T | 12 | a0001c0001t0004g0009 a0001c0001t0007g0009 a0001c0001t0011g0077 others(9): Show |
22 | HG00639.hp1 HG01243.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-14-739C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42783315 | |||||||
| chr13:42783407 | A | G | 24 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0004g0002 others(21): Show |
80 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.-14-647A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42783407 | |||||||
| chr13:42783483 | T | G | 2 | a0002c0002t0014g0015 a0002c0002t0024g0015 |
5 | HG00639.hp1 HG01243.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-571T>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42783483 | |||||||
| chr13:42783514 | C | T | 12 | a0001c0001t0004g0009 a0001c0001t0007g0009 a0001c0001t0011g0077 others(9): Show |
22 | HG00639.hp1 HG01243.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-14-540C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42783514 | |||||||
| chr13:42783537 | C | T | 1 | a0001c0001t0003g0100 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-14-517C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42783537 | |||||||
| chr13:42783599 | T | C | 40 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0010 others(37): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.-14-455T>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42783599 | |||||||
| chr13:42783601 | A | G | 40 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0010 others(37): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.-14-453A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42783601 | |||||||
| chr13:42783682 | T | A | 1 | a0001c0001t0003g0090 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-14-372T>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42783682 | |||||||
| chr13:42783697 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-14-357A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42783697 | |||||||
| chr13:42783772 | C | A | 1 | a0001c0001t0001g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-14-282C>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42783772 | |||||||
| chr13:42784040 | G | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(22): Show |
118 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.-14-14G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 1/3 | chr13 | 42784040 | |||||||
| chr13:42784173 | C | CT | 45 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0054 others(42): Show |
169 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.99+27dupT | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42784173 | ||||||
| chr13:42784173 | C | CTT | 19 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0025 others(16): Show |
47 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.99+26_99+27dupTT | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42784173 | ||||||
| chr13:42784173 | C | CTTT | 3 | a0001c0001t0002g0037 a0002c0002t0014g0015 a0002c0002t0024g0015 |
7 | HG00621.hp2 HG00639.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+25_99+27dupTTT | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42784173 | ||||||
| chr13:42784173 | C | CTTTTT | 8 | a0001c0001t0003g0010 a0001c0001t0003g0085 a0001c0001t0003g0091 others(5): Show |
16 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+23_99+27dupTTTT others(1): Show |
FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42784173 | ||||||
| chr13:42784173 | C | CTTTTTT | 26 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0013 others(23): Show |
75 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.99+22_99+27dupTTTT others(2): Show |
FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42784173 | ||||||
| chr13:42784173 | C | CTTTTTTT | 10 | a0001c0001t0003g0021 a0001c0001t0003g0040 a0001c0001t0003g0082 others(7): Show |
16 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.99+21_99+27dupTTTT others(3): Show |
FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42784173 | ||||||
| chr13:42784301 | C | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(21): Show |
117 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.99+135C>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784301 | |||||||
| chr13:42784365 | C | T | 1 | a0001c0001t0002g0025 | 3 | HG02723.hp1 HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.99+199C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784365 | |||||||
| chr13:42784563 | A | T | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0010 others(28): Show |
91 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.99+397A>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784563 | |||||||
| chr13:42784584 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.99+418G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784584 | |||||||
| chr13:42784640 | A | G | 1 | a0001c0001t0016g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.99+474A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784640 | |||||||
| chr13:42784661 | C | CA | 26 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0035 others(23): Show |
116 | HG00408.hp1 HG00558.hp2 HG01070.hp1 others(113): Show |
intron_variant | MODIFIER | c.99+518dupA | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42784661 | ||||||
| chr13:42784661 | C | CAA | 21 | a0001c0001t0001g0007 a0001c0001t0001g0051 a0001c0001t0001g0063 others(18): Show |
106 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.99+517_99+518dupAA | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42784661 | ||||||
| chr13:42784661 | CA | C | 20 | a0001c0001t0003g0005 a0001c0001t0003g0021 a0001c0001t0003g0027 others(17): Show |
49 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.99+518delA | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42784661 | ||||||
| chr13:42784661 | CAA | C | 20 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0013 others(17): Show |
54 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.99+517_99+518delAA | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42784661 | ||||||
| chr13:42784661 | CAAA | C | 4 | a0001c0001t0004g0017 a0001c0001t0010g0017 a0001c0001t0015g0046 others(1): Show |
6 | HG00738.hp2 HG01099.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+516_99+518delAA others(1): Show |
FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42784661 | ||||||
| chr13:42784661 | CAAAA | C | 25 | a0001c0001t0001g0054 a0001c0001t0002g0072 a0001c0001t0004g0002 others(22): Show |
82 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.99+515_99+518delAA others(2): Show |
FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42784661 | ||||||
| chr13:42784661 | CAAAAAAA others(3): Show |
C | 2 | a0002c0002t0014g0015 a0002c0002t0024g0015 |
5 | HG00639.hp1 HG01243.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+509_99+518delAA others(8): Show |
FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42784661 | ||||||
| chr13:42784711 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.99+545G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784711 | |||||||
| chr13:42784759 | G | A | 31 | a0001c0001t0001g0054 a0001c0001t0004g0002 a0001c0001t0004g0009 others(28): Show |
91 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.99+593G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784759 | |||||||
| chr13:42784836 | A | AAAAT | 40 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0010 others(37): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.99+687_99+690dupAA others(2): Show |
FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42784836 | ||||||
| chr13:42784840 | T | A | 1 | a0001c0001t0002g0067 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.99+674T>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784840 | |||||||
| chr13:42784853 | A | AAATT | 3 | a0001c0001t0012g0028 a0001c0001t0012g0108 a0001c0001t0012g0109 |
5 | HG02257.hp2 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+690_99+693dupTT others(2): Show |
FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42784853 | ||||||
| chr13:42784873 | A | T | 2 | a0002c0002t0014g0015 a0002c0002t0024g0015 |
5 | HG00639.hp1 HG01243.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+707A>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784873 | |||||||
| chr13:42784874 | T | A | 2 | a0001c0001t0011g0020 a0001c0001t0011g0077 |
5 | HG00733.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+708T>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784874 | |||||||
| chr13:42784887 | C | T | 1 | a0001c0001t0001g0034 | 2 | NA18948.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.99+721C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784887 | |||||||
| chr13:42784895 | C | T | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+729C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784895 | |||||||
| chr13:42784901 | G | C | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+735G>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784901 | |||||||
| chr13:42784904 | G | C | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+738G>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784904 | |||||||
| chr13:42784905 | G | A | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+739G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784905 | |||||||
| chr13:42784912 | A | T | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+746A>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784912 | |||||||
| chr13:42784914 | C | T | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+748C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784914 | |||||||
| chr13:42784923 | A | G | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+757A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784923 | |||||||
| chr13:42784924 | A | C | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+758A>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784924 | |||||||
| chr13:42784930 | G | T | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+764G>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784930 | |||||||
| chr13:42784931 | T | C | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+765T>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784931 | |||||||
| chr13:42784935 | G | T | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+769G>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784935 | |||||||
| chr13:42784939 | C | A | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+773C>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784939 | |||||||
| chr13:42784941 | T | A | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+775T>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784941 | |||||||
| chr13:42784943 | T | G | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+777T>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784943 | |||||||
| chr13:42784944 | T | A | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+778T>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784944 | |||||||
| chr13:42784946 | C | A | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+780C>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784946 | |||||||
| chr13:42784947 | T | A | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+781T>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784947 | |||||||
| chr13:42784949 | C | G | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+783C>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784949 | |||||||
| chr13:42784950 | T | A | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+784T>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784950 | |||||||
| chr13:42784952 | A | G | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+786A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784952 | |||||||
| chr13:42784953 | T | C | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+787T>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784953 | |||||||
| chr13:42784954 | T | C | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+788T>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784954 | |||||||
| chr13:42784956 | A | G | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+790A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784956 | |||||||
| chr13:42784962 | T | C | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+796T>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784962 | |||||||
| chr13:42784964 | T | A | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+798T>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784964 | |||||||
| chr13:42784967 | G | T | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+801G>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784967 | |||||||
| chr13:42784968 | G | A | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+802G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784968 | |||||||
| chr13:42784969 | T | A | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+803T>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784969 | |||||||
| chr13:42784970 | T | C | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+804T>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784970 | |||||||
| chr13:42784973 | A | G | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+807A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784973 | |||||||
| chr13:42784976 | A | C | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+810A>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784976 | |||||||
| chr13:42784981 | A | T | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+815A>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784981 | |||||||
| chr13:42784982 | A | C | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+816A>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784982 | |||||||
| chr13:42784985 | A | G | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+819A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784985 | |||||||
| chr13:42784987 | G | A | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+821G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784987 | |||||||
| chr13:42784990 | G | A | 1 | a0001c0001t0003g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+824G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42784990 | |||||||
| chr13:42785338 | C | A | 1 | a0001c0001t0001g0058 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.99+1172C>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42785338 | |||||||
| chr13:42785382 | A | G | 1 | a0001c0001t0003g0091 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.99+1216A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42785382 | |||||||
| chr13:42785447 | G | A | 2 | a0001c0001t0003g0090 a0001c0001t0003g0095 |
2 | HG02080.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.99+1281G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42785447 | |||||||
| chr13:42785522 | C | G | 1 | a0001c0001t0003g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.100-1241C>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42785522 | |||||||
| chr13:42785590 | A | G | 77 | a0001c0001t0001g0054 a0001c0001t0002g0072 a0001c0001t0003g0005 others(74): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.100-1173A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42785590 | |||||||
| chr13:42785647 | T | C | 1 | a0001c0001t0004g0053 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.100-1116T>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42785647 | |||||||
| chr13:42785800 | CAGTTAAG | C | 43 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0010 others(40): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.100-959_100-953del others(7): Show |
FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42785800 | ||||||
| chr13:42785812 | T | A | 43 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0010 others(40): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.100-951T>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42785812 | |||||||
| chr13:42785845 | C | T | 31 | a0001c0001t0001g0054 a0001c0001t0004g0002 a0001c0001t0004g0009 others(28): Show |
91 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.100-918C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42785845 | |||||||
| chr13:42785900 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.100-863C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42785900 | |||||||
| chr13:42785987 | C | A | 1 | a0001c0001t0003g0082 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.100-776C>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42785987 | |||||||
| chr13:42786103 | A | G | 32 | a0001c0001t0001g0054 a0001c0001t0002g0072 a0001c0001t0004g0002 others(29): Show |
92 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.100-660A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42786103 | |||||||
| chr13:42786191 | G | A | 4 | a0001c0001t0016g0029 a0001c0001t0016g0048 a0001c0001t0021g0047 others(1): Show |
5 | HG02630.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-572G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42786191 | |||||||
| chr13:42786256 | T | C | 1 | a0001c0001t0012g0108 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100-507T>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42786256 | |||||||
| chr13:42786282 | G | A | 2 | a0001c0001t0008g0023 a0001c0001t0008g0069 |
4 | HG00323.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-481G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42786282 | |||||||
| chr13:42786323 | T | C | 2 | a0001c0001t0016g0029 a0001c0001t0016g0048 |
3 | HG02630.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.100-440T>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42786323 | |||||||
| chr13:42786349 | CTCA | C | 30 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(27): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.100-411_100-409del others(3): Show |
FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42786349 | ||||||
| chr13:42786351 | C | G | 1 | a0002c0002t0024g0015 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.100-412C>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42786351 | |||||||
| chr13:42786365 | C | G | 1 | a0001c0001t0002g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.100-398C>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42786365 | |||||||
| chr13:42786462 | A | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(22): Show |
118 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.100-301A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42786462 | |||||||
| chr13:42786474 | G | C | 1 | a0001c0001t0006g0080 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.100-289G>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42786474 | |||||||
| chr13:42786636 | T | TA | 26 | a0001c0001t0001g0059 a0001c0001t0002g0003 a0001c0001t0002g0004 others(23): Show |
104 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.100-115dupA | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42786636 | ||||||
| chr13:42786636 | T | TAA | 4 | a0001c0001t0002g0008 a0001c0001t0002g0074 a0001c0001t0004g0055 others(1): Show |
13 | HG02109.hp2 HG02280.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.100-116_100-115dup others(2): Show |
FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42786636 | ||||||
| chr13:42786636 | T | TAAA | 29 | a0001c0001t0001g0054 a0001c0001t0002g0072 a0001c0001t0004g0002 others(26): Show |
88 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.100-117_100-115dup others(3): Show |
FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 42786636 | ||||||
| chr13:42786760 | C | T | 1 | a0001c0001t0002g0073 | 1 | HG03942.hp2 | splice_region_variant&intron_variant | LOW | c.100-3C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 2/3 | chr13 | 42786760 | |||||||
| chr13:42786898 | G | A | 7 | a0001c0001t0003g0039 a0001c0001t0003g0083 a0001c0001t0003g0084 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.220+15G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42786898 | |||||||
| chr13:42786904 | C | G | 2 | a0002c0002t0014g0015 a0002c0002t0024g0015 |
5 | HG00639.hp1 HG01243.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+21C>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42786904 | |||||||
| chr13:42786936 | G | A | 3 | a0001c0001t0004g0009 a0001c0001t0007g0009 a0001c0001t0031g0009 |
9 | HG02451.hp2 HG02717.hp2 HG04228.hp1 others(6): Show |
intron_variant | MODIFIER | c.220+53G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42786936 | |||||||
| chr13:42786990 | G | A | 1 | a0001c0001t0003g0107 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.220+107G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42786990 | |||||||
| chr13:42787012 | G | A | 40 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0010 others(37): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.220+129G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42787012 | |||||||
| chr13:42787094 | G | A | 2 | a0002c0002t0014g0015 a0002c0002t0024g0015 |
5 | HG00639.hp1 HG01243.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+211G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42787094 | |||||||
| chr13:42787133 | G | T | 30 | a0001c0001t0001g0054 a0001c0001t0004g0002 a0001c0001t0004g0009 others(27): Show |
90 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.220+250G>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42787133 | |||||||
| chr13:42787278 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.220+395C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42787278 | |||||||
| chr13:42787361 | C | T | 2 | a0001c0001t0021g0047 a0001c0001t0021g0050 |
2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.220+478C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42787361 | |||||||
| chr13:42787395 | TA | T | 2 | a0002c0002t0014g0015 a0002c0002t0024g0015 |
5 | HG00639.hp1 HG01243.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+514delA | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 42787395 | ||||||
| chr13:42787510 | C | T | 1 | a0001c0001t0002g0036 | 2 | NA18941.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.220+627C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42787510 | |||||||
| chr13:42787639 | G | A | 1 | a0001c0001t0003g0096 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.220+756G>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42787639 | |||||||
| chr13:42787864 | G | C | 70 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(67): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.221-727G>C | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42787864 | |||||||
| chr13:42787962 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.221-629A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42787962 | |||||||
| chr13:42788118 | C | A | 33 | a0001c0001t0002g0072 a0001c0001t0004g0002 a0001c0001t0004g0009 others(30): Show |
96 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.221-473C>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42788118 | |||||||
| chr13:42788160 | T | G | 2 | a0001c0001t0002g0068 a0001c0001t0002g0076 |
2 | HG00438.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.221-431T>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42788160 | |||||||
| chr13:42788243 | A | G | 1 | a0001c0001t0001g0060 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.221-348A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42788243 | |||||||
| chr13:42788340 | A | G | 34 | a0001c0001t0001g0052 a0001c0001t0002g0072 a0001c0001t0004g0002 others(31): Show |
97 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.221-251A>G | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42788340 | |||||||
| chr13:42788371 | C | T | 73 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(70): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.221-220C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42788371 | |||||||
| chr13:42788387 | C | T | 33 | a0001c0001t0001g0052 a0001c0001t0004g0002 a0001c0001t0004g0009 others(30): Show |
96 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.221-204C>T | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42788387 | |||||||
| chr13:42788449 | C | A | 1 | a0001c0001t0004g0032 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.221-142C>A | FAM216B | ENSG00000179813.7 | transcript | ENST00000313851.3 | protein_coding | 3/3 | chr13 | 42788449 |