Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 374393 |
| ensemblid | ENSG00000189057.11 |
| hgncid | 24200 |
| symbol | FAM111B |
| name | FAM111 trypsin like peptidase B |
| refseq_nuc | NM_198947.4 |
| refseq_prot | NP_945185.1 |
| ensembl_nuc | ENST00000343597.4 |
| ensembl_prot | ENSP00000341565.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 59107237 |
| end | 59127412 |
| strand | + |
| ver | v1.2 |
| region | chr11:59107237-59127412 |
| region5000 | chr11:59102237-59132412 |
| regionname0 | FAM111B_chr11_59107237_59127412 |
| regionname5000 | FAM111B_chr11_59102237_59132412 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 734 | 385 | 92 | 68 | 172 | 13 | 38 | 141 | FAM111B_chr11_59102237_59132412 | FAM111B | MNSMK others(729): Show |
chr11 | 59102237 | 59132412 |
| a0002 | 0/0 | 734 | 22 | 0 | 1 | 20 | 0 | 1 | 19 | FAM111B_chr11_59102237_59132412 | FAM111B | MNSMK others(729): Show |
chr11 | 59102237 | 59132412 |
| a0003 | 0/0 | 734 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | MNSMK others(729): Show |
chr11 | 59102237 | 59132412 |
| a0004 | 0/0 | 734 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | MNSMK others(729): Show |
chr11 | 59102237 | 59132412 |
| a0005 | 0/0 | 734 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | MNSMK others(729): Show |
chr11 | 59102237 | 59132412 |
| a0006 | 0/0 | 734 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | MNSMK others(729): Show |
chr11 | 59102237 | 59132412 |
| a0007 | 0/0 | 734 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | MNSMK others(729): Show |
chr11 | 59102237 | 59132412 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2202 | 316 | 73 | 61 | 131 | 13 | 36 | FAM111B_chr11_59102237_59132412 | FAM111B | ATGAA others(2197): Show |
chr11 | 59102237 | 59132412 | ||
| a0001c0002 | 0/0 | 2202 | 56 | 15 | 6 | 34 | 0 | 1 | FAM111B_chr11_59102237_59132412 | FAM111B | ATGAA others(2197): Show |
chr11 | 59102237 | 59132412 | ||
| a0001c0004 | 0/0 | 2202 | 4 | 0 | 0 | 4 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | ATGAA others(2197): Show |
chr11 | 59102237 | 59132412 | ||
| a0001c0006 | 0/0 | 2202 | 3 | 0 | 0 | 3 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | ATGAA others(2197): Show |
chr11 | 59102237 | 59132412 | ||
| a0001c0007 | 0/0 | 2202 | 2 | 2 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | ATGAA others(2197): Show |
chr11 | 59102237 | 59132412 | ||
| a0001c0008 | 0/0 | 2202 | 2 | 2 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | ATGAA others(2197): Show |
chr11 | 59102237 | 59132412 | ||
| a0001c0011 | 0/0 | 2202 | 1 | 0 | 0 | 0 | 0 | 1 | FAM111B_chr11_59102237_59132412 | FAM111B | ATGAA others(2197): Show |
chr11 | 59102237 | 59132412 | ||
| a0001c0015 | 0/0 | 2202 | 1 | 0 | 1 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | ATGAA others(2197): Show |
chr11 | 59102237 | 59132412 | ||
| a0002c0003 | 0/0 | 2202 | 21 | 0 | 1 | 19 | 0 | 1 | FAM111B_chr11_59102237_59132412 | FAM111B | ATGAA others(2197): Show |
chr11 | 59102237 | 59132412 | ||
| a0002c0012 | 0/0 | 2202 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | ATGAA others(2197): Show |
chr11 | 59102237 | 59132412 | ||
| a0003c0005 | 0/0 | 2202 | 3 | 2 | 1 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | ATGAA others(2197): Show |
chr11 | 59102237 | 59132412 | ||
| a0004c0009 | 0/0 | 2202 | 1 | 0 | 0 | 0 | 1 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | ATGAA others(2197): Show |
chr11 | 59102237 | 59132412 | ||
| a0005c0013 | 0/0 | 2202 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | ATGAA others(2197): Show |
chr11 | 59102237 | 59132412 | ||
| a0006c0010 | 0/0 | 2202 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | ATGAA others(2197): Show |
chr11 | 59102237 | 59132412 | ||
| a0007c0014 | 0/0 | 2202 | 1 | 0 | 0 | 0 | 0 | 1 | FAM111B_chr11_59102237_59132412 | FAM111B | ATGAA others(2197): Show |
chr11 | 59102237 | 59132412 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3506 | 208 | 43 | 39 | 90 | 10 | 24 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0001c0001t0002 | 0/0 | 3506 | 71 | 7 | 22 | 27 | 3 | 12 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0001c0001t0004 | 0/0 | 3506 | 14 | 0 | 0 | 14 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0001c0001t0005 | 0/0 | 3492 | 8 | 8 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3487): Show |
chr11 | 59102237 | 59132412 |
| a0001c0001t0006 | 0/0 | 3506 | 5 | 5 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0001c0001t0007 | 0/0 | 3506 | 5 | 5 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0001c0001t0008 | 0/0 | 3506 | 3 | 3 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0001c0001t0009 | 0/0 | 3506 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0001c0001t0010 | 0/0 | 3506 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0001c0002t0003 | 0/0 | 3506 | 56 | 15 | 6 | 34 | 0 | 1 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0001c0004t0001 | 0/0 | 3506 | 4 | 0 | 0 | 4 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0001c0006t0002 | 0/0 | 3506 | 3 | 0 | 0 | 3 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0001c0007t0006 | 0/0 | 3506 | 2 | 2 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0001c0008t0001 | 0/0 | 3506 | 2 | 2 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0001c0011t0011 | 0/0 | 3506 | 1 | 0 | 0 | 0 | 0 | 1 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0001c0015t0001 | 0/0 | 3506 | 1 | 0 | 1 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0002c0003t0001 | 0/0 | 3506 | 21 | 0 | 1 | 19 | 0 | 1 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0002c0012t0001 | 0/0 | 3506 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0003c0005t0003 | 0/0 | 3506 | 3 | 2 | 1 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0004c0009t0002 | 0/0 | 3506 | 1 | 0 | 0 | 0 | 1 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0005c0013t0003 | 0/0 | 3506 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0006c0010t0001 | 0/0 | 3506 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| a0007c0014t0001 | 0/0 | 3506 | 1 | 0 | 0 | 0 | 0 | 1 | FAM111B_chr11_59102237_59132412 | FAM111B | AAATC others(3501): Show |
chr11 | 59102237 | 59132412 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 62 | 12 | 16 | 25 | 4 | 5 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0002 | 0/0 | 49 | 5 | 8 | 22 | 3 | 11 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0005 | 0/0 | 15 | 0 | 0 | 15 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0009 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0011 | 0/0 | 6 | 1 | 3 | 0 | 2 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0016 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0033 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0061 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0002g0003 | 0/0 | 33 | 3 | 11 | 11 | 2 | 6 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0002g0007 | 0/0 | 9 | 1 | 1 | 6 | 0 | 1 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0002g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0002g0013 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0002g0014 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0004g0005 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0005g0017 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0006g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0007g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0007g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0008g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0001t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0002t0003g0004 | 0/0 | 30 | 0 | 6 | 24 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0002t0003g0010 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0002t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0002t0003g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0002t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0002t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0002t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0002t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0002t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0002t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0004t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0006t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0007t0006g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0008t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0011t0011g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0001c0015t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0002c0003t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0002c0003t0001g0006 | 0/0 | 18 | 0 | 1 | 16 | 0 | 1 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0002c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0002c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0002c0012t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0003c0005t0003g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0003c0005t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0004c0009t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0005c0013t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0006c0010t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| a0007c0014t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00140 | hp2 | a0004 | c0009 | t0002 | g0014 | EUR | GBR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | CHS | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00544 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | CHS | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00558 | hp1 | a0001 | c0002 | t0003 | g0020 | EAS | CHS | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00597 | hp1 | a0001 | c0002 | t0003 | g0074 | EAS | CHS | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | CHS | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01243 | hp1 | a0003 | c0005 | t0003 | g0028 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0076 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01891 | hp1 | a0001 | c0002 | t0003 | g0067 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01928 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01934 | hp1 | a0002 | c0003 | t0001 | g0006 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01978 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01993 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02015 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | KHV | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02027 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | KHV | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02074 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | KHV | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | KHV | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | KHV | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0071 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02148 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | CDX | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CDX | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0019 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02273 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02280 | hp1 | a0001 | c0007 | t0006 | g0035 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02300 | hp1 | a0001 | c0015 | t0001 | g0002 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0036 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02615 | hp2 | a0001 | c0002 | t0003 | g0095 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02622 | hp1 | a0001 | c0002 | t0003 | g0050 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02886 | hp2 | a0005 | c0013 | t0003 | g0019 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0091 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02895 | hp2 | a0001 | c0002 | t0003 | g0029 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0036 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02897 | hp2 | a0001 | c0002 | t0003 | g0029 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0077 | AFR | ESN | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0021 | AFR | ESN | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0070 | AFR | ESN | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02970 | hp1 | a0001 | c0008 | t0001 | g0030 | AFR | ESN | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | ESN | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03041 | hp1 | a0003 | c0005 | t0003 | g0028 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03041 | hp2 | a0001 | c0002 | t0003 | g0049 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0082 | AFR | MSL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ESN | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03130 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | ESN | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0021 | AFR | ESN | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03195 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | ESN | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03209 | hp1 | a0001 | c0002 | t0003 | g0010 | AFR | MSL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03225 | hp1 | a0001 | c0007 | t0006 | g0035 | AFR | MSL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03225 | hp2 | a0006 | c0010 | t0001 | g0001 | AFR | MSL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03453 | hp2 | a0003 | c0005 | t0003 | g0048 | AFR | MSL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | MSL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | BEB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0006 | SAS | BEB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG04199 | hp2 | a0001 | c0002 | t0003 | g0073 | SAS | STU | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG04204 | hp1 | a0007 | c0014 | t0001 | g0006 | SAS | STU | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG04228 | hp2 | a0001 | c0011 | t0011 | g0068 | SAS | STU | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18522 | hp2 | a0001 | c0002 | t0003 | g0019 | AFR | YRI | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | YRI | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18939 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18945 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18948 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18949 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18951 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18952 | hp2 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18953 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18954 | hp2 | a0001 | c0002 | t0003 | g0052 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18957 | hp1 | a0001 | c0002 | t0003 | g0034 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18959 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18960 | hp2 | a0001 | c0006 | t0002 | g0008 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18961 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18962 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18963 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18964 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18967 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18968 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18969 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18972 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18978 | hp1 | a0001 | c0006 | t0002 | g0008 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18980 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18985 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18990 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18991 | hp2 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18993 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18994 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18999 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19001 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19003 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19004 | hp1 | a0002 | c0003 | t0001 | g0101 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19006 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | LWK | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19030 | hp2 | a0001 | c0008 | t0001 | g0030 | AFR | LWK | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19054 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19055 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19055 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19057 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19058 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19059 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19060 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19062 | hp2 | a0001 | c0002 | t0003 | g0051 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19065 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19066 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19067 | hp2 | a0002 | c0003 | t0001 | g0100 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19068 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19074 | hp1 | a0001 | c0006 | t0002 | g0008 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19074 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19076 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19076 | hp2 | a0001 | c0002 | t0003 | g0075 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19077 | hp1 | a0001 | c0002 | t0003 | g0072 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19079 | hp2 | a0002 | c0012 | t0001 | g0006 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19080 | hp2 | a0001 | c0002 | t0003 | g0034 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19086 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19088 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19088 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19089 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0015 | AFR | YRI | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ASW | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0014 | EUR | TSI | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | GIH | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | GIH | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG03471 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | MSL | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | USA | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| HG06807 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | USA | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0069 | AFR | USA | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0079 | AFR | USA | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | LWK | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0033 | REF | REF | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0061 | REF | REF | FAM111B_chr11_59102237_59132412 | FAM111B | chr11 | 59102237 | 59132412 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:59124750 | G | A | 1 | a0003 | 3 | HG01243.hp1 HG03041.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.653G>A | p.Gly218Asp | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 844/3506 | 653/2205 | 218/734 | chr11 | 59124750 | |||
| chr11:59124792 | G | A | 1 | a0004 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.695G>A | p.Arg232Gln | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 886/3506 | 695/2205 | 232/734 | chr11 | 59124792 | |||
| chr11:59125014 | A | G | 1 | a0007 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.917A>G | p.His306Arg | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 1108/3506 | 917/2205 | 306/734 | chr11 | 59125014 | |||
| chr11:59125785 | G | A | 1 | a0006 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.1688G>A | p.Arg563Gln | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 1879/3506 | 1688/2205 | 563/734 | chr11 | 59125785 | |||
| chr11:59126043 | C | G | 1 | a0005 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.1946C>G | p.Ser649Cys | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 2137/3506 | 1946/2205 | 649/734 | chr11 | 59126043 | |||
| chr11:59126288 | C | G | 1 | a0002 | 22 | HG00544.hp1 HG01934.hp1 HG03831.hp2 others(19): Show |
missense_variant | MODERATE | c.2191C>G | p.Pro731Ala | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 2382/3506 | 2191/2205 | 731/734 | chr11 | 59126288 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:59109664 | C | T | 1 | a0001c0015 | 1 | HG02300.hp1 | synonymous_variant | LOW | c.39C>T | p.Ser13Ser | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/4 | 230/3506 | 39/2205 | 13/734 | chr11 | 59109664 | |||
| chr11:59124511 | T | C | 1 | a0001c0007 | 2 | HG02280.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.414T>C | p.Asp138Asp | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 605/3506 | 414/2205 | 138/734 | chr11 | 59124511 | |||
| chr11:59124700 | C | A | 1 | a0001c0004 | 4 | NA18939.hp2 NA19001.hp2 NA19060.hp2 others(1): Show |
synonymous_variant | LOW | c.603C>A | p.Ile201Ile | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 794/3506 | 603/2205 | 201/734 | chr11 | 59124700 | |||
| chr11:59124922 | A | G | 1 | a0001c0006 | 3 | NA18960.hp2 NA18978.hp1 NA19074.hp1 |
synonymous_variant | LOW | c.825A>G | p.Gln275Gln | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 1016/3506 | 825/2205 | 275/734 | chr11 | 59124922 | |||
| chr11:59125085 | C | T | 3 | a0001c0002 a0003c0005 a0005c0013 |
60 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(57): Show |
synonymous_variant | LOW | c.988C>T | p.Leu330Leu | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 1179/3506 | 988/2205 | 330/734 | chr11 | 59125085 | |||
| chr11:59125120 | A | G | 1 | a0001c0008 | 2 | HG02970.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.1023A>G | p.Thr341Thr | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 1214/3506 | 1023/2205 | 341/734 | chr11 | 59125120 | |||
| chr11:59125387 | A | G | 1 | a0002c0012 | 1 | NA19079.hp2 | synonymous_variant | LOW | c.1290A>G | p.Gln430Gln | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 1481/3506 | 1290/2205 | 430/734 | chr11 | 59125387 | |||
| chr11:59125462 | A | G | 1 | a0001c0011 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.1365A>G | p.Thr455Thr | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 1556/3506 | 1365/2205 | 455/734 | chr11 | 59125462 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:59109551 | G | A | 1 | a0001c0001t0009 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-75G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/4 | 75 | chr11 | 59109551 | ||||||
| chr11:59109620 | C | A | 1 | a0001c0001t0010 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-6C>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/4 | 6 | chr11 | 59109620 | ||||||
| chr11:59126471 | ATGGGAGA others(7): Show |
A | 1 | a0001c0001t0005 | 8 | HG02622.hp2 HG02647.hp1 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*172_*185delGGAGAA others(8): Show |
FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 172 | INFO_REALIGN_3_PRIME | chr11 | 59126471 | |||||
| chr11:59126594 | A | G | 3 | a0001c0001t0002 a0001c0006t0002 a0004c0009t0002 |
75 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*292A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 292 | chr11 | 59126594 | ||||||
| chr11:59126752 | C | T | 4 | a0001c0001t0006 a0001c0001t0010 a0001c0007t0006 others(1): Show |
9 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*450C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 450 | chr11 | 59126752 | ||||||
| chr11:59126780 | T | C | 12 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(9): Show |
150 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*478T>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 478 | chr11 | 59126780 | ||||||
| chr11:59126830 | G | T | 3 | a0001c0002t0003 a0003c0005t0003 a0005c0013t0003 |
60 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*528G>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 528 | chr11 | 59126830 | ||||||
| chr11:59126845 | G | C | 1 | a0001c0011t0011 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*543G>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 543 | chr11 | 59126845 | ||||||
| chr11:59126884 | A | G | 1 | a0001c0001t0008 | 3 | HG02145.hp1 HG02965.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*582A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 582 | chr11 | 59126884 | ||||||
| chr11:59126895 | G | A | 3 | a0001c0002t0003 a0003c0005t0003 a0005c0013t0003 |
60 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*593G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 593 | chr11 | 59126895 | ||||||
| chr11:59127170 | T | C | 1 | a0001c0011t0011 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*868T>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 868 | chr11 | 59127170 | ||||||
| chr11:59127259 | A | T | 1 | a0001c0001t0004 | 14 | HG00438.hp2 HG02132.hp2 HG02155.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*957A>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 4/4 | 957 | chr11 | 59127259 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:59107326 | C | T | 1 | a0001c0001t0002g0102 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-132+30C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 1/3 | chr11 | 59107326 | |||||||
| chr11:59107392 | G | A | 1 | a0001c0001t0002g0025 | 2 | HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-132+96G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 1/3 | chr11 | 59107392 | |||||||
| chr11:59107479 | G | A | 1 | a0001c0001t0001g0009 | 7 | HG01496.hp2 HG02258.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-132+183G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 1/3 | chr11 | 59107479 | |||||||
| chr11:59107522 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0038 |
3 | HG01069.hp2 HG01192.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-132+226G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 1/3 | chr11 | 59107522 | |||||||
| chr11:59107551 | G | A | 19 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(16): Show |
75 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.-132+255G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 1/3 | chr11 | 59107551 | |||||||
| chr11:59107554 | C | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0038 others(5): Show |
28 | HG00544.hp1 HG01069.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.-132+258C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 1/3 | chr11 | 59107554 | |||||||
| chr11:59107571 | A | G | 20 | a0001c0001t0001g0099 a0001c0001t0002g0003 a0001c0001t0002g0007 others(17): Show |
76 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.-132+275A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 1/3 | chr11 | 59107571 | |||||||
| chr11:59107783 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-132+487A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 1/3 | chr11 | 59107783 | |||||||
| chr11:59107872 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-132+576C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 1/3 | chr11 | 59107872 | |||||||
| chr11:59108043 | C | G | 1 | a0001c0002t0003g0095 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-131-625C>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 1/3 | chr11 | 59108043 | |||||||
| chr11:59108252 | A | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(37): Show |
145 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.-131-416A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 1/3 | chr11 | 59108252 | |||||||
| chr11:59108287 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-131-381A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 1/3 | chr11 | 59108287 | |||||||
| chr11:59108336 | C | T | 4 | a0001c0001t0007g0021 a0001c0001t0007g0036 a0001c0001t0007g0077 others(1): Show |
6 | HG02451.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-131-332C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 1/3 | chr11 | 59108336 | |||||||
| chr11:59108372 | C | A | 1 | a0001c0001t0002g0039 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-131-296C>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 1/3 | chr11 | 59108372 | |||||||
| chr11:59108477 | G | A | 2 | a0003c0005t0003g0028 a0003c0005t0003g0048 |
3 | HG01243.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-131-191G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 1/3 | chr11 | 59108477 | |||||||
| chr11:59108553 | G | A | 4 | a0001c0002t0003g0029 a0001c0002t0003g0049 a0001c0002t0003g0050 others(1): Show |
5 | HG02615.hp2 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-115G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 1/3 | chr11 | 59108553 | |||||||
| chr11:59108565 | A | C | 4 | a0001c0001t0007g0021 a0001c0001t0007g0036 a0001c0001t0007g0077 others(1): Show |
6 | HG02451.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-131-103A>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 1/3 | chr11 | 59108565 | |||||||
| chr11:59109017 | CCTA | C | 4 | a0001c0001t0006g0015 a0001c0001t0006g0076 a0001c0001t0010g0015 others(1): Show |
8 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-87+308_-87+310del others(3): Show |
FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 59109017 | ||||||
| chr11:59109025 | G | A | 1 | a0001c0002t0003g0051 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-87+313G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 2/3 | chr11 | 59109025 | |||||||
| chr11:59109086 | G | A | 1 | a0001c0002t0003g0052 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-87+374G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 2/3 | chr11 | 59109086 | |||||||
| chr11:59109246 | T | C | 19 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(16): Show |
75 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.-86-294T>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 2/3 | chr11 | 59109246 | |||||||
| chr11:59109247 | C | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(88): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.-86-293C>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 2/3 | chr11 | 59109247 | |||||||
| chr11:59109381 | T | A | 1 | a0001c0001t0001g0066 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-86-159T>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 2/3 | chr11 | 59109381 | |||||||
| chr11:59109390 | C | A | 1 | a0001c0001t0001g0018 | 4 | NA18965.hp2 NA18975.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.-86-150C>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 2/3 | chr11 | 59109390 | |||||||
| chr11:59109404 | T | A | 1 | a0001c0008t0001g0030 | 2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-86-136T>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 2/3 | chr11 | 59109404 | |||||||
| chr11:59109782 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.81+76G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59109782 | |||||||
| chr11:59109840 | G | T | 1 | a0001c0002t0003g0010 | 7 | HG02451.hp2 HG03130.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+134G>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59109840 | |||||||
| chr11:59109854 | A | T | 1 | a0001c0001t0001g0065 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.81+148A>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59109854 | |||||||
| chr11:59109897 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.81+191C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59109897 | |||||||
| chr11:59109962 | C | G | 9 | a0001c0002t0003g0004 a0001c0002t0003g0020 a0001c0002t0003g0034 others(6): Show |
41 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.81+256C>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59109962 | |||||||
| chr11:59110035 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.81+329A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59110035 | |||||||
| chr11:59110058 | C | T | 19 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(16): Show |
75 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.81+352C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59110058 | |||||||
| chr11:59110268 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.81+562C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59110268 | |||||||
| chr11:59110436 | C | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(41): Show |
149 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.81+730C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59110436 | |||||||
| chr11:59110550 | T | C | 4 | a0001c0001t0006g0015 a0001c0001t0006g0076 a0001c0001t0010g0015 others(1): Show |
8 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+844T>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59110550 | |||||||
| chr11:59110740 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.81+1034G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59110740 | |||||||
| chr11:59110833 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.81+1127G>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59110833 | |||||||
| chr11:59110977 | C | T | 1 | a0001c0011t0011g0068 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.81+1271C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59110977 | |||||||
| chr11:59111188 | A | T | 1 | a0001c0001t0002g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.81+1482A>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59111188 | |||||||
| chr11:59111252 | G | A | 4 | a0001c0001t0006g0015 a0001c0001t0006g0076 a0001c0001t0010g0015 others(1): Show |
8 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+1546G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59111252 | |||||||
| chr11:59111433 | G | A | 1 | a0001c0001t0001g0022 | 3 | NA18947.hp2 NA18961.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.81+1727G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59111433 | |||||||
| chr11:59111532 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.81+1826C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59111532 | |||||||
| chr11:59111675 | C | G | 1 | a0001c0001t0001g0026 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.81+1969C>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59111675 | |||||||
| chr11:59111681 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.81+1975A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59111681 | |||||||
| chr11:59111687 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.81+1981A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59111687 | |||||||
| chr11:59111711 | G | A | 2 | a0003c0005t0003g0028 a0003c0005t0003g0048 |
3 | HG01243.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.81+2005G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59111711 | |||||||
| chr11:59111786 | C | T | 4 | a0001c0002t0003g0029 a0001c0002t0003g0049 a0001c0002t0003g0050 others(1): Show |
5 | HG02615.hp2 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+2080C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59111786 | |||||||
| chr11:59111947 | C | A | 1 | a0001c0001t0002g0007 | 9 | HG00621.hp1 HG01070.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.81+2241C>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59111947 | |||||||
| chr11:59112029 | A | G | 1 | a0001c0001t0008g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.81+2323A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59112029 | |||||||
| chr11:59112160 | C | A | 1 | a0001c0001t0001g0011 | 6 | HG00642.hp2 HG01099.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+2454C>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59112160 | |||||||
| chr11:59112160 | C | T | 1 | a0001c0002t0003g0029 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.81+2454C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59112160 | |||||||
| chr11:59112169 | C | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0022 |
8 | HG02698.hp2 NA18947.hp2 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+2463C>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59112169 | |||||||
| chr11:59112198 | T | A | 19 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(16): Show |
75 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.81+2492T>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59112198 | |||||||
| chr11:59112219 | G | T | 8 | a0001c0002t0003g0019 a0001c0002t0003g0029 a0001c0002t0003g0049 others(5): Show |
11 | HG01243.hp1 HG02257.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+2513G>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59112219 | |||||||
| chr11:59112237 | T | C | 1 | a0001c0001t0002g0027 | 2 | HG02683.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.81+2531T>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59112237 | |||||||
| chr11:59112373 | G | C | 11 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0020 others(8): Show |
49 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.81+2667G>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59112373 | |||||||
| chr11:59112378 | T | C | 8 | a0001c0002t0003g0019 a0001c0002t0003g0029 a0001c0002t0003g0049 others(5): Show |
11 | HG01243.hp1 HG02257.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+2672T>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59112378 | |||||||
| chr11:59112488 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.81+2782T>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59112488 | |||||||
| chr11:59112695 | T | C | 1 | a0001c0001t0007g0077 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.81+2989T>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59112695 | |||||||
| chr11:59112713 | G | A | 1 | a0001c0001t0005g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.81+3007G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59112713 | |||||||
| chr11:59112800 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.81+3094G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59112800 | |||||||
| chr11:59112967 | T | G | 8 | a0001c0002t0003g0019 a0001c0002t0003g0029 a0001c0002t0003g0049 others(5): Show |
11 | HG01243.hp1 HG02257.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+3261T>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59112967 | |||||||
| chr11:59112976 | C | T | 1 | a0001c0001t0005g0091 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.81+3270C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59112976 | |||||||
| chr11:59113019 | A | G | 2 | a0003c0005t0003g0028 a0003c0005t0003g0048 |
3 | HG01243.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.81+3313A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59113019 | |||||||
| chr11:59113067 | C | G | 8 | a0001c0002t0003g0019 a0001c0002t0003g0029 a0001c0002t0003g0049 others(5): Show |
11 | HG01243.hp1 HG02257.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+3361C>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59113067 | |||||||
| chr11:59113188 | T | G | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.81+3482T>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59113188 | |||||||
| chr11:59113201 | A | T | 2 | a0003c0005t0003g0028 a0003c0005t0003g0048 |
3 | HG01243.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.81+3495A>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59113201 | |||||||
| chr11:59113203 | ATTGTGTG | A | 2 | a0003c0005t0003g0028 a0003c0005t0003g0048 |
3 | HG01243.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.81+3504_81+3510del others(7): Show |
FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr11 | 59113203 | ||||||
| chr11:59113210 | G | GTTAA | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(87): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.81+3506_81+3507ins others(4): Show |
FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr11 | 59113210 | ||||||
| chr11:59113434 | A | T | 1 | a0001c0001t0001g0090 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.81+3728A>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59113434 | |||||||
| chr11:59113491 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.81+3785T>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59113491 | |||||||
| chr11:59113646 | C | A | 4 | a0001c0001t0005g0017 a0001c0001t0005g0079 a0001c0001t0005g0082 others(1): Show |
8 | HG02622.hp2 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+3940C>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59113646 | |||||||
| chr11:59113759 | T | C | 1 | a0001c0001t0002g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.81+4053T>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59113759 | |||||||
| chr11:59113765 | C | T | 4 | a0001c0001t0007g0021 a0001c0001t0007g0036 a0001c0001t0007g0077 others(1): Show |
6 | HG02451.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+4059C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59113765 | |||||||
| chr11:59113784 | C | G | 8 | a0001c0002t0003g0019 a0001c0002t0003g0029 a0001c0002t0003g0049 others(5): Show |
11 | HG01243.hp1 HG02257.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+4078C>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59113784 | |||||||
| chr11:59113799 | A | G | 1 | a0001c0001t0002g0046 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.81+4093A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59113799 | |||||||
| chr11:59113825 | G | T | 1 | a0001c0001t0002g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.81+4119G>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59113825 | |||||||
| chr11:59113889 | A | G | 8 | a0001c0002t0003g0019 a0001c0002t0003g0029 a0001c0002t0003g0049 others(5): Show |
11 | HG01243.hp1 HG02257.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+4183A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59113889 | |||||||
| chr11:59113982 | A | C | 1 | a0001c0001t0005g0082 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.81+4276A>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59113982 | |||||||
| chr11:59114022 | T | G | 1 | a0001c0002t0003g0072 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.81+4316T>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59114022 | |||||||
| chr11:59114114 | A | G | 1 | a0001c0002t0003g0050 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81+4408A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59114114 | |||||||
| chr11:59114699 | G | A | 1 | a0001c0011t0011g0068 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.81+4993G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59114699 | |||||||
| chr11:59114716 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.81+5010G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59114716 | |||||||
| chr11:59114871 | C | T | 1 | a0001c0001t0001g0024 | 3 | HG01243.hp2 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.81+5165C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59114871 | |||||||
| chr11:59114918 | A | G | 8 | a0001c0002t0003g0019 a0001c0002t0003g0029 a0001c0002t0003g0049 others(5): Show |
11 | HG01243.hp1 HG02257.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+5212A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59114918 | |||||||
| chr11:59115124 | T | A | 1 | a0001c0001t0001g0065 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.81+5418T>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59115124 | |||||||
| chr11:59115207 | C | T | 1 | a0001c0011t0011g0068 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.81+5501C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59115207 | |||||||
| chr11:59115228 | A | C | 4 | a0001c0002t0003g0029 a0001c0002t0003g0049 a0001c0002t0003g0050 others(1): Show |
5 | HG02615.hp2 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+5522A>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59115228 | |||||||
| chr11:59115493 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0024 |
10 | HG01243.hp2 HG01496.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.81+5787G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59115493 | |||||||
| chr11:59115512 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.81+5806A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59115512 | |||||||
| chr11:59115537 | T | C | 1 | a0001c0001t0001g0037 | 2 | HG03927.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.81+5831T>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59115537 | |||||||
| chr11:59115569 | G | C | 1 | a0001c0001t0002g0041 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.81+5863G>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59115569 | |||||||
| chr11:59115579 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.81+5873T>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59115579 | |||||||
| chr11:59115612 | A | G | 2 | a0003c0005t0003g0028 a0003c0005t0003g0048 |
3 | HG01243.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.81+5906A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59115612 | |||||||
| chr11:59115779 | C | T | 1 | a0001c0011t0011g0068 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.81+6073C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59115779 | |||||||
| chr11:59115944 | T | C | 3 | a0001c0001t0002g0013 a0001c0001t0002g0027 a0001c0001t0002g0041 |
8 | HG00642.hp1 HG00741.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+6238T>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59115944 | |||||||
| chr11:59116007 | C | T | 4 | a0001c0001t0007g0021 a0001c0001t0007g0036 a0001c0001t0007g0077 others(1): Show |
6 | HG02451.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+6301C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59116007 | |||||||
| chr11:59116021 | C | T | 1 | a0001c0001t0008g0070 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.81+6315C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59116021 | |||||||
| chr11:59116212 | T | C | 1 | a0001c0001t0002g0025 | 2 | HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.81+6506T>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59116212 | |||||||
| chr11:59116241 | G | C | 8 | a0001c0002t0003g0019 a0001c0002t0003g0029 a0001c0002t0003g0049 others(5): Show |
11 | HG01243.hp1 HG02257.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+6535G>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59116241 | |||||||
| chr11:59116319 | G | C | 1 | a0001c0002t0003g0034 | 2 | NA18957.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.81+6613G>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59116319 | |||||||
| chr11:59116442 | T | G | 46 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(43): Show |
149 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.81+6736T>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59116442 | |||||||
| chr11:59116569 | C | G | 1 | a0001c0002t0003g0074 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.81+6863C>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59116569 | |||||||
| chr11:59116737 | C | A | 1 | a0001c0001t0001g0081 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.81+7031C>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59116737 | |||||||
| chr11:59116747 | GATAT | G | 18 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0019 others(15): Show |
59 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.81+7044_81+7047del others(4): Show |
FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr11 | 59116747 | ||||||
| chr11:59116761 | G | A | 4 | a0001c0001t0007g0021 a0001c0001t0007g0036 a0001c0001t0007g0077 others(1): Show |
6 | HG02451.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+7055G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59116761 | |||||||
| chr11:59116898 | C | T | 1 | a0001c0001t0002g0045 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.81+7192C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59116898 | |||||||
| chr11:59117004 | A | G | 1 | a0001c0001t0007g0036 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.82-7175A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59117004 | |||||||
| chr11:59117452 | A | G | 4 | a0001c0001t0007g0021 a0001c0001t0007g0036 a0001c0001t0007g0077 others(1): Show |
6 | HG02451.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-6727A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59117452 | |||||||
| chr11:59117525 | A | G | 1 | a0001c0011t0011g0068 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.82-6654A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59117525 | |||||||
| chr11:59117536 | C | T | 4 | a0001c0001t0007g0021 a0001c0001t0007g0036 a0001c0001t0007g0077 others(1): Show |
6 | HG02451.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-6643C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59117536 | |||||||
| chr11:59117668 | C | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0057 |
3 | HG03486.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.82-6511C>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59117668 | |||||||
| chr11:59117956 | G | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0055 others(5): Show |
34 | HG00438.hp2 HG02027.hp1 HG02040.hp2 others(31): Show |
intron_variant | MODIFIER | c.82-6223G>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59117956 | |||||||
| chr11:59117968 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.82-6211A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59117968 | |||||||
| chr11:59118408 | C | T | 19 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0019 others(16): Show |
60 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.82-5771C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59118408 | |||||||
| chr11:59118556 | C | G | 3 | a0001c0001t0005g0017 a0001c0001t0005g0079 a0001c0001t0005g0082 |
7 | HG02622.hp2 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.82-5623C>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59118556 | |||||||
| chr11:59118649 | T | G | 19 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0019 others(16): Show |
60 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.82-5530T>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59118649 | |||||||
| chr11:59118711 | A | G | 19 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0019 others(16): Show |
60 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.82-5468A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59118711 | |||||||
| chr11:59118737 | C | G | 1 | a0001c0001t0001g0062 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.82-5442C>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59118737 | |||||||
| chr11:59118743 | T | G | 1 | a0001c0001t0001g0084 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.82-5436T>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59118743 | |||||||
| chr11:59118785 | TTCTC | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(41): Show |
149 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.82-5392_82-5389del others(4): Show |
FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr11 | 59118785 | ||||||
| chr11:59118917 | T | C | 1 | a0003c0005t0003g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.82-5262T>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59118917 | |||||||
| chr11:59118982 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.82-5197A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59118982 | |||||||
| chr11:59119020 | T | C | 2 | a0001c0001t0002g0014 a0004c0009t0002g0014 |
5 | HG00140.hp2 HG01168.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-5159T>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59119020 | |||||||
| chr11:59119030 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.82-5149G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59119030 | |||||||
| chr11:59119379 | CATT | C | 2 | a0003c0005t0003g0028 a0003c0005t0003g0048 |
3 | HG01243.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.82-4799_82-4797del others(3): Show |
FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59119379 | |||||||
| chr11:59119383 | G | T | 1 | a0001c0001t0001g0060 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.82-4796G>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59119383 | |||||||
| chr11:59119444 | A | G | 1 | a0001c0011t0011g0068 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.82-4735A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59119444 | |||||||
| chr11:59119709 | T | C | 19 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0019 others(16): Show |
60 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.82-4470T>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59119709 | |||||||
| chr11:59120048 | A | C | 1 | a0001c0002t0003g0073 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.82-4131A>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59120048 | |||||||
| chr11:59120204 | A | G | 1 | a0001c0011t0011g0068 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.82-3975A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59120204 | |||||||
| chr11:59120268 | G | C | 4 | a0001c0001t0007g0021 a0001c0001t0007g0036 a0001c0001t0007g0077 others(1): Show |
6 | HG02451.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-3911G>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59120268 | |||||||
| chr11:59120787 | T | A | 4 | a0001c0001t0007g0021 a0001c0001t0007g0036 a0001c0001t0007g0077 others(1): Show |
6 | HG02451.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-3392T>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59120787 | |||||||
| chr11:59120831 | C | A | 5 | a0001c0001t0006g0015 a0001c0001t0006g0076 a0001c0001t0010g0015 others(2): Show |
9 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-3348C>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59120831 | |||||||
| chr11:59120850 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(110): Show |
411 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.82-3329T>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59120850 | |||||||
| chr11:59120949 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG00639.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.82-3230C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59120949 | |||||||
| chr11:59121069 | G | GA | 15 | a0001c0001t0001g0012 a0001c0001t0001g0056 a0001c0001t0001g0058 others(12): Show |
23 | HG00558.hp2 HG01243.hp1 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.82-3094dupA | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr11 | 59121069 | ||||||
| chr11:59121069 | G | GAA | 13 | a0001c0001t0006g0076 a0001c0002t0003g0004 a0001c0002t0003g0010 others(10): Show |
51 | HG00597.hp1 HG00609.hp1 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.82-3095_82-3094dup others(2): Show |
FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr11 | 59121069 | ||||||
| chr11:59121069 | G | GAAA | 8 | a0001c0001t0006g0015 a0001c0001t0010g0015 a0001c0002t0003g0020 others(5): Show |
14 | HG00558.hp1 HG02486.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.82-3096_82-3094dup others(3): Show |
FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr11 | 59121069 | ||||||
| chr11:59121083 | A | C | 1 | a0001c0001t0001g0087 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.82-3096A>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59121083 | |||||||
| chr11:59121242 | A | G | 1 | a0001c0011t0011g0068 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.82-2937A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59121242 | |||||||
| chr11:59121346 | G | C | 4 | a0001c0001t0007g0021 a0001c0001t0007g0036 a0001c0001t0007g0077 others(1): Show |
6 | HG02451.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-2833G>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59121346 | |||||||
| chr11:59121718 | A | C | 19 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(16): Show |
75 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.82-2461A>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59121718 | |||||||
| chr11:59121867 | G | A | 4 | a0001c0001t0007g0021 a0001c0001t0007g0036 a0001c0001t0007g0077 others(1): Show |
6 | HG02451.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-2312G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59121867 | |||||||
| chr11:59121941 | A | C | 1 | a0001c0002t0003g0029 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.82-2238A>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59121941 | |||||||
| chr11:59121958 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(88): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.82-2221A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59121958 | |||||||
| chr11:59121972 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.82-2207G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59121972 | |||||||
| chr11:59121981 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.82-2198A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59121981 | |||||||
| chr11:59122146 | A | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.82-2033A>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59122146 | |||||||
| chr11:59122146 | A | T | 1 | a0001c0001t0004g0059 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.82-2033A>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59122146 | |||||||
| chr11:59122150 | T | A | 1 | a0001c0001t0001g0005 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.82-2029T>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59122150 | |||||||
| chr11:59122342 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.82-1837A>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59122342 | |||||||
| chr11:59122567 | C | T | 2 | a0001c0002t0003g0019 a0005c0013t0003g0019 |
3 | HG02257.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.82-1612C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59122567 | |||||||
| chr11:59122602 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.82-1577G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59122602 | |||||||
| chr11:59122830 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.82-1349T>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59122830 | |||||||
| chr11:59122986 | G | C | 2 | a0003c0005t0003g0028 a0003c0005t0003g0048 |
3 | HG01243.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.82-1193G>C | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59122986 | |||||||
| chr11:59123019 | T | G | 13 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0020 others(10): Show |
52 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.82-1160T>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59123019 | |||||||
| chr11:59123310 | C | T | 1 | a0001c0007t0006g0035 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.82-869C>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59123310 | |||||||
| chr11:59123412 | G | A | 1 | a0001c0001t0002g0043 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.82-767G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59123412 | |||||||
| chr11:59123467 | G | T | 19 | a0001c0002t0003g0004 a0001c0002t0003g0010 a0001c0002t0003g0019 others(16): Show |
60 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.82-712G>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59123467 | |||||||
| chr11:59123671 | G | A | 1 | a0002c0003t0001g0101 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.82-508G>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59123671 | |||||||
| chr11:59123819 | A | T | 47 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(44): Show |
150 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(147): Show |
intron_variant | MODIFIER | c.82-360A>T | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59123819 | |||||||
| chr11:59123976 | C | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0089 |
4 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-203C>G | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59123976 | |||||||
| chr11:59123989 | T | A | 3 | a0001c0001t0002g0008 a0001c0001t0002g0045 a0001c0006t0002g0008 |
10 | HG00438.hp1 HG02071.hp1 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-190T>A | FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | chr11 | 59123989 | |||||||
| chr11:59124017 | GTATC | G | 19 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(16): Show |
75 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.82-159_82-156delTC others(2): Show |
FAM111B | ENSG00000189057.11 | transcript | ENST00000343597.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr11 | 59124017 |