Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7021 |
| ensemblid | ENSG00000008196.13 |
| hgncid | 11743 |
| symbol | TFAP2B |
| name | transcription factor AP-2 beta |
| refseq_nuc | NM_003221.4 |
| refseq_prot | NP_003212.2 |
| ensembl_nuc | ENST00000393655.4 |
| ensembl_prot | ENSP00000377265.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 50818871 |
| end | 50847619 |
| strand | + |
| ver | v1.2 |
| region | chr6:50818871-50847619 |
| region5000 | chr6:50813871-50852619 |
| regionname0 | TFAP2B_chr6_50818871_50847619 |
| regionname5000 | TFAP2B_chr6_50813871_50852619 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 460 | 377 | 89 | 71 | 157 | 16 | 42 | 125 | TFAP2B_chr6_50813871_50852619 | TFAP2B | MHSPP others(455): Show |
chr6 | 50813871 | 50852619 |
| a0002 | 0/0 | 460 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | MHSPP others(455): Show |
chr6 | 50813871 | 50852619 |
| a0003 | 0/0 | 460 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | MHSPP others(455): Show |
chr6 | 50813871 | 50852619 |
| a0004 | 0/0 | 460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | MHSPP others(455): Show |
chr6 | 50813871 | 50852619 |
| a0005 | 0/0 | 460 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | MHSPP others(455): Show |
chr6 | 50813871 | 50852619 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1380 | 375 | 87 | 71 | 157 | 16 | 42 | TFAP2B_chr6_50813871_50852619 | TFAP2B | ATGCA others(1375): Show |
chr6 | 50813871 | 50852619 | ||
| a0001c0003 | 0/0 | 1380 | 2 | 2 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | ATGCA others(1375): Show |
chr6 | 50813871 | 50852619 | ||
| a0002c0002 | 0/0 | 1380 | 2 | 2 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | ATGCA others(1375): Show |
chr6 | 50813871 | 50852619 | ||
| a0003c0005 | 0/0 | 1380 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | ATGCA others(1375): Show |
chr6 | 50813871 | 50852619 | ||
| a0004c0006 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | ATGCA others(1375): Show |
chr6 | 50813871 | 50852619 | ||
| a0005c0004 | 0/0 | 1380 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | ATGCA others(1375): Show |
chr6 | 50813871 | 50852619 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5629 | 94 | 5 | 16 | 59 | 3 | 10 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5624): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0002 | 0/0 | 5631 | 69 | 18 | 7 | 37 | 1 | 6 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5626): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0003 | 0/0 | 5630 | 71 | 9 | 21 | 27 | 3 | 11 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5625): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0004 | 0/0 | 5632 | 15 | 0 | 4 | 8 | 0 | 3 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5627): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0005 | 0/0 | 5631 | 14 | 14 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5626): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0006 | 1/0 | 5631 | 14 | 0 | 5 | 0 | 5 | 3 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5626): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0007 | 0/0 | 5631 | 14 | 1 | 7 | 1 | 0 | 5 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5626): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0008 | 0/0 | 5631 | 9 | 8 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5626): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0009 | 0/0 | 5632 | 7 | 6 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5627): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0010 | 0/0 | 5633 | 7 | 0 | 0 | 6 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5628): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0011 | 0/0 | 5629 | 5 | 0 | 0 | 5 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5624): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0012 | 0/0 | 5630 | 5 | 0 | 3 | 0 | 1 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5625): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0013 | 0/0 | 5630 | 4 | 0 | 0 | 4 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5625): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0014 | 0/0 | 5629 | 4 | 2 | 0 | 2 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5624): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0015 | 0/0 | 5633 | 4 | 4 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5628): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0016 | 0/0 | 5630 | 3 | 0 | 3 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5625): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0017 | 0/0 | 5633 | 3 | 3 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5628): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0018 | 0/0 | 5627 | 3 | 3 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5622): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0020 | 0/0 | 5631 | 2 | 0 | 0 | 0 | 0 | 2 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5626): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0021 | 0/0 | 5632 | 2 | 2 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5627): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0022 | 0/0 | 5632 | 2 | 0 | 0 | 2 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5627): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0023 | 0/0 | 5629 | 2 | 0 | 0 | 0 | 2 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5624): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0024 | 0/0 | 5630 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5625): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0025 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5624): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0026 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5624): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0027 | 0/0 | 5629 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5624): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0029 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5624): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0030 | 0/0 | 5630 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5625): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0031 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5626): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0032 | 0/0 | 5630 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5625): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0034 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5624): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0035 | 0/0 | 5628 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5623): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0036 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5626): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0037 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5626): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0038 | 0/0 | 5630 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5625): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0039 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5626): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0040 | 0/0 | 5630 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5625): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0041 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5626): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0042 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5624): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0043 | 0/0 | 5628 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5623): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0044 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5626): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0045 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5626): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0046 | 0/0 | 5630 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5625): Show |
chr6 | 50813871 | 50852619 |
| a0001c0001t0047 | 0/0 | 5627 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5622): Show |
chr6 | 50813871 | 50852619 |
| a0001c0003t0019 | 0/0 | 5629 | 2 | 2 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5624): Show |
chr6 | 50813871 | 50852619 |
| a0002c0002t0002 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5626): Show |
chr6 | 50813871 | 50852619 |
| a0002c0002t0028 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5624): Show |
chr6 | 50813871 | 50852619 |
| a0003c0005t0033 | 0/0 | 5631 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5626): Show |
chr6 | 50813871 | 50852619 |
| a0004c0006t0002 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5626): Show |
chr6 | 50813871 | 50852619 |
| a0005c0004t0002 | 0/0 | 5631 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | AGACA others(5626): Show |
chr6 | 50813871 | 50852619 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 21 | 1 | 3 | 13 | 2 | 2 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0004 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0003 | 0/0 | 23 | 8 | 0 | 14 | 1 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0005 | 0/0 | 10 | 0 | 4 | 4 | 0 | 2 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0011 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0002 | 0/0 | 19 | 0 | 5 | 11 | 1 | 2 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0006 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0010 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0004g0007 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0004g0009 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0004g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0005g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0005g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0005g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0005g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0006g0020 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0006g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0006g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0006g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0007g0012 | 0/0 | 4 | 1 | 0 | 1 | 0 | 2 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0007g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0007g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0007g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0007g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0007g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0007g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0007g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0007g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0008g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0008g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0008g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0008g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0009g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0009g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0009g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0009g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0009g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0010g0007 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0010g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0010g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0011g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0011g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0012g0001 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0012g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0013g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0014g0002 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0014g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0015g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0015g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0016g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0016g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0017g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0017g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0017g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0018g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0018g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0020g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0020g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0021g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0021g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0022g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0022g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0023g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0023g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0024g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0025g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0026g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0027g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0029g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0030g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0031g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0032g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0034g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0035g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0036g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0037g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0038g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0039g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0040g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0041g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0042g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0043g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0044g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0045g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0046g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0001t0047g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0003t0019g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0001c0003t0019g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0002c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0002c0002t0028g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0003c0005t0033g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0004c0006t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| a0005c0004t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0046 | EUR | GBR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00099 | hp2 | a0001 | c0001 | t0012 | g0001 | EUR | GBR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0107 | EUR | FIN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00280 | hp2 | a0001 | c0001 | t0046 | g0042 | EUR | FIN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0046 | EUR | FIN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00408 | hp2 | a0001 | c0001 | t0010 | g0007 | EAS | CHS | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00544 | hp1 | a0001 | c0001 | t0011 | g0004 | EAS | CHS | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | CHS | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0164 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00642 | hp1 | a0001 | c0001 | t0016 | g0006 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00733 | hp1 | a0001 | c0001 | t0006 | g0020 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00733 | hp2 | a0001 | c0001 | t0032 | g0001 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00735 | hp1 | a0001 | c0001 | t0012 | g0001 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG00741 | hp2 | a0001 | c0001 | t0009 | g0025 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01081 | hp1 | a0001 | c0001 | t0007 | g0042 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01081 | hp2 | a0001 | c0001 | t0016 | g0006 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01099 | hp2 | a0001 | c0001 | t0016 | g0044 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01106 | hp1 | a0001 | c0001 | t0012 | g0001 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0039 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0039 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01169 | hp2 | a0003 | c0005 | t0033 | g0142 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0153 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0088 | AMR | PUR | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01255 | hp1 | a0001 | c0001 | t0008 | g0099 | AMR | CLM | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0124 | AMR | CLM | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01256 | hp2 | a0001 | c0001 | t0012 | g0001 | AMR | CLM | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0041 | AMR | CLM | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0118 | AMR | CLM | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0093 | AMR | CLM | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0020 | AMR | CLM | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0122 | AMR | CLM | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01361 | hp1 | a0001 | c0001 | t0024 | g0002 | AMR | CLM | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0041 | AMR | CLM | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | CLM | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0120 | EUR | IBS | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | IBS | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | IBS | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01516 | hp2 | a0001 | c0001 | t0023 | g0091 | EUR | IBS | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01517 | hp1 | a0001 | c0001 | t0023 | g0092 | EUR | IBS | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0020 | EUR | IBS | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0043 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0026 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0165 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0018 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02055 | hp2 | a0001 | c0001 | t0017 | g0084 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02080 | hp1 | a0001 | c0001 | t0010 | g0007 | EAS | KHV | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02129 | hp2 | a0001 | c0001 | t0010 | g0089 | EAS | KHV | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02132 | hp1 | a0001 | c0001 | t0029 | g0005 | EAS | KHV | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | KHV | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02135 | hp2 | a0001 | c0001 | t0030 | g0003 | EAS | KHV | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0183 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0161 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0053 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02523 | hp2 | a0001 | c0001 | t0014 | g0002 | EAS | KHV | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02572 | hp1 | a0002 | c0002 | t0028 | g0017 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02572 | hp2 | a0001 | c0001 | t0015 | g0016 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0045 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02615 | hp1 | a0001 | c0001 | t0039 | g0110 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0025 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02622 | hp1 | a0004 | c0006 | t0002 | g0003 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02622 | hp2 | a0001 | c0001 | t0044 | g0062 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02630 | hp1 | a0001 | c0001 | t0045 | g0103 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02647 | hp1 | a0001 | c0001 | t0038 | g0180 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0065 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02698 | hp1 | a0001 | c0001 | t0020 | g0073 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0057 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02735 | hp2 | a0001 | c0001 | t0010 | g0007 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02738 | hp1 | a0001 | c0001 | t0012 | g0151 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0154 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0102 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0059 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02818 | hp2 | a0001 | c0001 | t0018 | g0085 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02896 | hp2 | a0001 | c0001 | t0042 | g0063 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02897 | hp1 | a0001 | c0001 | t0043 | g0061 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | ESN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02922 | hp2 | a0001 | c0003 | t0019 | g0150 | AFR | ESN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | ESN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02965 | hp2 | a0001 | c0001 | t0018 | g0038 | AFR | ESN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0080 | AFR | ESN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ESN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02976 | hp1 | a0001 | c0003 | t0019 | g0149 | AFR | ESN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02976 | hp2 | a0001 | c0001 | t0018 | g0038 | AFR | ESN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0155 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | MSL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03098 | hp2 | a0001 | c0001 | t0021 | g0095 | AFR | MSL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03139 | hp1 | a0001 | c0001 | t0031 | g0184 | AFR | ESN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03139 | hp2 | a0001 | c0001 | t0021 | g0094 | AFR | ESN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03195 | hp1 | a0001 | c0001 | t0015 | g0016 | AFR | ESN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03209 | hp1 | a0001 | c0001 | t0017 | g0064 | AFR | MSL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0057 | AFR | MSL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03239 | hp1 | a0001 | c0001 | t0007 | g0012 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | MSL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03486 | hp1 | a0001 | c0001 | t0041 | g0027 | AFR | MSL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0079 | AFR | MSL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0169 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0043 | AFR | ESN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0081 | AFR | ESN | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0026 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03540 | hp2 | a0001 | c0001 | t0036 | g0008 | AFR | GWD | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | MSL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | MSL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0158 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03669 | hp2 | a0001 | c0001 | t0007 | g0098 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03704 | hp1 | a0001 | c0001 | t0006 | g0123 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0176 | SAS | BEB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | BEB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0045 | SAS | BEB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG04115 | hp1 | a0001 | c0001 | t0007 | g0012 | SAS | STU | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0163 | SAS | STU | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG04184 | hp1 | a0001 | c0001 | t0007 | g0101 | SAS | BEB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG04199 | hp1 | a0001 | c0001 | t0007 | g0087 | SAS | STU | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | STU | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0117 | SAS | STU | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0162 | SAS | STU | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG04228 | hp1 | a0001 | c0001 | t0006 | g0119 | SAS | STU | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | STU | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0182 | AFR | YRI | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | CHB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0066 | AFR | YRI | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18906 | hp2 | a0001 | c0001 | t0014 | g0006 | AFR | YRI | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18939 | hp2 | a0001 | c0001 | t0010 | g0007 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18948 | hp2 | a0001 | c0001 | t0013 | g0002 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18949 | hp1 | a0001 | c0001 | t0022 | g0131 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18963 | hp1 | a0001 | c0001 | t0011 | g0019 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18968 | hp1 | a0001 | c0001 | t0010 | g0007 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18970 | hp2 | a0001 | c0001 | t0011 | g0004 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18982 | hp2 | a0001 | c0001 | t0011 | g0019 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18991 | hp2 | a0001 | c0001 | t0010 | g0100 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19001 | hp1 | a0001 | c0001 | t0022 | g0018 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19001 | hp2 | a0001 | c0001 | t0035 | g0167 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19002 | hp1 | a0001 | c0001 | t0014 | g0002 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19006 | hp1 | a0005 | c0004 | t0002 | g0072 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19011 | hp1 | a0001 | c0001 | t0011 | g0019 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19030 | hp1 | a0001 | c0001 | t0037 | g0008 | AFR | LWK | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19043 | hp1 | a0001 | c0001 | t0017 | g0027 | AFR | LWK | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | LWK | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19054 | hp1 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19058 | hp1 | a0001 | c0001 | t0025 | g0145 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19063 | hp1 | a0001 | c0001 | t0013 | g0002 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19082 | hp2 | a0001 | c0001 | t0013 | g0002 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19083 | hp2 | a0001 | c0001 | t0034 | g0001 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19085 | hp2 | a0001 | c0001 | t0013 | g0002 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19091 | hp1 | a0001 | c0001 | t0026 | g0049 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | ASW | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0121 | EUR | TSI | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0105 | EUR | TSI | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | GIH | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA20905 | hp2 | a0001 | c0001 | t0020 | g0077 | SAS | GIH | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG01123 | hp2 | a0001 | c0001 | t0027 | g0185 | AMR | CLM | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02109 | hp1 | a0001 | c0001 | t0047 | g0086 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG02559 | hp2 | a0001 | c0001 | t0015 | g0060 | AFR | ACB | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0024 | AFR | MSL | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0097 | AFR | USA | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| HG06807 | hp2 | a0001 | c0001 | t0040 | g0083 | AFR | USA | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0096 | AFR | USA | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA20300 | hp2 | a0001 | c0001 | t0014 | g0002 | AFR | USA | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | LWK | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| NA21309 | hp2 | a0001 | c0001 | t0015 | g0016 | AFR | LWK | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0129 | REF | REF | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0136 | REF | REF | TFAP2B_chr6_50813871_50852619 | TFAP2B | chr6 | 50813871 | 50852619 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:50823789 | A | G | 1 | a0004 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.464A>G | p.His155Arg | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/7 | 485/5631 | 464/1383 | 155/460 | chr6 | 50823789 | |||
| chr6:50840185 | G | T | 1 | a0003 | 1 | HG01169.hp2 | missense_variant | MODERATE | c.970G>T | p.Gly324Trp | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/7 | 991/5631 | 970/1383 | 324/460 | chr6 | 50840185 | |||
| chr6:50840212 | G | T | 1 | a0002 | 2 | HG02572.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.997G>T | p.Ala333Ser | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/7 | 1018/5631 | 997/1383 | 333/460 | chr6 | 50840212 | |||
| chr6:50840221 | G | A | 1 | a0005 | 1 | NA19006.hp1 | missense_variant | MODERATE | c.1006G>A | p.Val336Ile | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/7 | 1027/5631 | 1006/1383 | 336/460 | chr6 | 50840221 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:50823577 | C | T | 1 | a0001c0003 | 2 | HG02922.hp2 HG02976.hp1 |
synonymous_variant | LOW | c.252C>T | p.Asp84Asp | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/7 | 273/5631 | 252/1383 | 84/460 | chr6 | 50823577 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:50843402 | A | T | 12 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(9): Show |
58 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*10A>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 10 | chr6 | 50843402 | ||||||
| chr6:50843406 | AAAG | A | 4 | a0001c0001t0018 a0001c0001t0042 a0001c0001t0043 others(1): Show |
6 | HG02109.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*18_*20delAAG | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 18 | INFO_REALIGN_3_PRIME | chr6 | 50843406 | |||||
| chr6:50843524 | AT | A | 6 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0016 others(3): Show |
81 | HG00280.hp1 HG00280.hp2 HG00597.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*136delT | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 136 | INFO_REALIGN_3_PRIME | chr6 | 50843524 | |||||
| chr6:50843524 | ATT | A | 1 | a0001c0001t0014 | 4 | HG02523.hp2 NA18906.hp2 NA19002.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*135_*136delTT | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 135 | INFO_REALIGN_3_PRIME | chr6 | 50843524 | |||||
| chr6:50843527 | T | TA | 2 | a0001c0001t0021 a0001c0001t0044 |
3 | HG02622.hp2 HG03098.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*135_*136insA | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 136 | chr6 | 50843527 | ||||||
| chr6:50843528 | T | A | 33 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(30): Show |
323 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*136T>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 136 | chr6 | 50843528 | ||||||
| chr6:50843528 | T | G | 1 | a0001c0001t0023 | 2 | HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*136T>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 136 | chr6 | 50843528 | ||||||
| chr6:50843528 | T | TA | 2 | a0001c0001t0009 a0001c0001t0042 |
8 | HG00741.hp2 HG01891.hp1 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*146dupA | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 147 | INFO_REALIGN_3_PRIME | chr6 | 50843528 | |||||
| chr6:50843529 | A | T | 2 | a0001c0001t0017 a0001c0001t0041 |
4 | HG02055.hp2 HG03209.hp1 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*137A>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 137 | chr6 | 50843529 | ||||||
| chr6:50843570 | C | T | 2 | a0001c0001t0007 a0001c0001t0046 |
15 | HG00280.hp2 HG01081.hp1 HG01167.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*178C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 178 | chr6 | 50843570 | ||||||
| chr6:50843691 | T | C | 2 | a0001c0001t0017 a0001c0001t0041 |
4 | HG02055.hp2 HG03209.hp1 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*299T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 299 | chr6 | 50843691 | ||||||
| chr6:50843726 | A | G | 6 | a0001c0001t0009 a0001c0001t0015 a0001c0001t0017 others(3): Show |
17 | HG00741.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*334A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 334 | chr6 | 50843726 | ||||||
| chr6:50843859 | C | A | 1 | a0001c0001t0036 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*467C>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 467 | chr6 | 50843859 | ||||||
| chr6:50844052 | A | T | 1 | a0001c0001t0034 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*660A>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 660 | chr6 | 50844052 | ||||||
| chr6:50844067 | G | T | 1 | a0003c0005t0033 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*675G>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 675 | chr6 | 50844067 | ||||||
| chr6:50844290 | TA | T | 4 | a0001c0001t0012 a0001c0001t0023 a0001c0001t0032 others(1): Show |
9 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*911delA | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 911 | INFO_REALIGN_3_PRIME | chr6 | 50844290 | |||||
| chr6:50844300 | A | AAC | 4 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0017 others(1): Show |
24 | HG00597.hp1 HG01978.hp2 HG01981.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*909_*910insCA | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 910 | INFO_REALIGN_3_PRIME | chr6 | 50844300 | |||||
| chr6:50844302 | A | AC | 5 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0021 others(2): Show |
27 | HG00280.hp2 HG01081.hp1 HG01167.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*910_*911insC | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 911 | chr6 | 50844302 | ||||||
| chr6:50844302 | A | ACAC | 1 | a0001c0001t0010 | 7 | HG00408.hp2 HG02080.hp1 HG02129.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*910_*911insCAC | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 911 | chr6 | 50844302 | ||||||
| chr6:50844302 | A | C | 10 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0015 others(7): Show |
38 | HG00597.hp1 HG00741.hp2 HG01891.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*910A>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 910 | chr6 | 50844302 | ||||||
| chr6:50844302 | AAC | A | 10 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0025 others(7): Show |
107 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*924_*925delCA | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 924 | INFO_REALIGN_3_PRIME | chr6 | 50844302 | |||||
| chr6:50844303 | AC | A | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(14): Show |
165 | HG00140.hp1 HG00280.hp1 HG00597.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*912delC | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 912 | chr6 | 50844303 | ||||||
| chr6:50844303 | ACAC | A | 1 | a0001c0001t0003 | 6 | HG02071.hp1 HG02738.hp2 NA18949.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*912_*914delCAC | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 912 | chr6 | 50844303 | ||||||
| chr6:50844304 | C | A | 4 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(1): Show |
5 | HG01123.hp1 HG01934.hp1 HG02258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*912C>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 912 | chr6 | 50844304 | ||||||
| chr6:50844306 | C | A | 1 | a0001c0001t0011 | 5 | HG00544.hp1 NA18963.hp1 NA18970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*914C>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 914 | chr6 | 50844306 | ||||||
| chr6:50845027 | G | A | 1 | a0001c0001t0025 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1635G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 1635 | chr6 | 50845027 | ||||||
| chr6:50845182 | A | G | 6 | a0001c0001t0009 a0001c0001t0015 a0001c0001t0017 others(3): Show |
17 | HG00741.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1790A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 1790 | chr6 | 50845182 | ||||||
| chr6:50845193 | G | A | 38 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(35): Show |
286 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*1801G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 1801 | chr6 | 50845193 | ||||||
| chr6:50845270 | C | T | 1 | a0001c0001t0031 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1878C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 1878 | chr6 | 50845270 | ||||||
| chr6:50845271 | T | C | 13 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(10): Show |
59 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1879T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 1879 | chr6 | 50845271 | ||||||
| chr6:50845317 | G | T | 7 | a0001c0001t0002 a0001c0001t0020 a0001c0001t0029 others(4): Show |
76 | HG00140.hp1 HG00639.hp1 HG01123.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1925G>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 1925 | chr6 | 50845317 | ||||||
| chr6:50845342 | C | G | 13 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(10): Show |
59 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1950C>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 1950 | chr6 | 50845342 | ||||||
| chr6:50845373 | T | A | 1 | a0001c0001t0024 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1981T>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 1981 | chr6 | 50845373 | ||||||
| chr6:50845598 | C | A | 1 | a0001c0001t0026 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2206C>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 2206 | chr6 | 50845598 | ||||||
| chr6:50845610 | T | A | 1 | a0001c0001t0018 | 3 | HG02818.hp2 HG02965.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2218T>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 2218 | chr6 | 50845610 | ||||||
| chr6:50845615 | G | A | 1 | a0001c0001t0023 | 2 | HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2223G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 2223 | chr6 | 50845615 | ||||||
| chr6:50845619 | T | C | 48 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(45): Show |
366 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(363): Show |
3_prime_UTR_variant | MODIFIER | c.*2227T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 2227 | chr6 | 50845619 | ||||||
| chr6:50845898 | C | T | 1 | a0001c0001t0032 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2506C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 2506 | chr6 | 50845898 | ||||||
| chr6:50845970 | G | A | 1 | a0001c0001t0035 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2578G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 2578 | chr6 | 50845970 | ||||||
| chr6:50846016 | T | C | 6 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0014 others(3): Show |
82 | HG00280.hp1 HG00597.hp2 HG00639.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2624T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 2624 | chr6 | 50846016 | ||||||
| chr6:50846187 | AC | A | 14 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(11): Show |
60 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2797delC | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 2797 | INFO_REALIGN_3_PRIME | chr6 | 50846187 | |||||
| chr6:50846448 | C | T | 1 | a0001c0001t0039 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3056C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 3056 | chr6 | 50846448 | ||||||
| chr6:50846466 | C | T | 1 | a0001c0003t0019 | 2 | HG02922.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3074C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 3074 | chr6 | 50846466 | ||||||
| chr6:50846586 | C | G | 1 | a0001c0001t0036 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3194C>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 3194 | chr6 | 50846586 | ||||||
| chr6:50846587 | C | G | 1 | a0001c0001t0036 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3195C>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 3195 | chr6 | 50846587 | ||||||
| chr6:50846589 | C | T | 1 | a0001c0001t0036 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3197C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 3197 | chr6 | 50846589 | ||||||
| chr6:50846789 | C | T | 1 | a0001c0001t0020 | 2 | HG02698.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3397C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 3397 | chr6 | 50846789 | ||||||
| chr6:50846914 | C | A | 9 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(6): Show |
53 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*3522C>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 3522 | chr6 | 50846914 | ||||||
| chr6:50846970 | A | G | 1 | a0001c0001t0037 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3578A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 3578 | chr6 | 50846970 | ||||||
| chr6:50847164 | C | A | 13 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(10): Show |
59 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*3772C>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 3772 | chr6 | 50847164 | ||||||
| chr6:50847202 | C | T | 1 | a0001c0001t0013 | 4 | NA18948.hp2 NA19063.hp1 NA19082.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3810C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 3810 | chr6 | 50847202 | ||||||
| chr6:50847387 | T | C | 1 | a0001c0001t0022 | 2 | NA18949.hp1 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3995T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 3995 | chr6 | 50847387 | ||||||
| chr6:50847516 | T | C | 7 | a0001c0001t0002 a0001c0001t0020 a0001c0003t0019 others(4): Show |
77 | HG00140.hp1 HG00639.hp1 HG01123.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*4124T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 4124 | chr6 | 50847516 | ||||||
| chr6:50847601 | T | A | 6 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0014 others(3): Show |
82 | HG00280.hp1 HG00597.hp2 HG00639.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*4209T>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 7/7 | 4209 | chr6 | 50847601 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:50819076 | T | A | 1 | a0001c0001t0002g0058 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.81+104T>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50819076 | |||||||
| chr6:50819564 | A | T | 2 | a0001c0001t0027g0185 a0001c0001t0031g0184 |
2 | HG01123.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.81+592A>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50819564 | |||||||
| chr6:50819597 | C | T | 9 | a0001c0001t0002g0181 a0001c0001t0005g0008 a0001c0001t0005g0024 others(6): Show |
16 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+625C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50819597 | |||||||
| chr6:50819644 | C | A | 48 | a0001c0001t0001g0076 a0001c0001t0002g0003 a0001c0001t0002g0005 others(45): Show |
96 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.81+672C>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50819644 | |||||||
| chr6:50819746 | G | T | 38 | a0001c0001t0001g0023 a0001c0001t0001g0152 a0001c0001t0001g0156 others(35): Show |
73 | HG00544.hp2 HG00597.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.81+774G>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50819746 | |||||||
| chr6:50819768 | G | A | 1 | a0001c0001t0003g0082 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.81+796G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50819768 | |||||||
| chr6:50819808 | G | GCGAGGCG others(11): Show |
2 | a0001c0001t0027g0185 a0001c0001t0031g0184 |
2 | HG01123.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.81+845_81+862dupAC others(16): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 50819808 | ||||||
| chr6:50819836 | CGAGGCGG others(11): Show |
C | 34 | a0001c0001t0001g0152 a0001c0001t0004g0007 a0001c0001t0004g0009 others(31): Show |
55 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.81+890_81+907delGC others(16): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 50819836 | ||||||
| chr6:50819844 | G | A | 1 | a0001c0001t0005g0053 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.81+872G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50819844 | |||||||
| chr6:50819848 | G | C | 2 | a0001c0001t0015g0016 a0001c0001t0015g0060 |
4 | HG02559.hp2 HG02572.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+876G>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50819848 | |||||||
| chr6:50819850 | T | C | 1 | a0001c0001t0005g0053 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.81+878T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50819850 | |||||||
| chr6:50819853 | G | C | 1 | a0001c0001t0005g0053 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.81+881G>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50819853 | |||||||
| chr6:50819854 | A | C | 1 | a0001c0001t0005g0053 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.81+882A>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50819854 | |||||||
| chr6:50819862 | G | C | 53 | a0001c0001t0001g0023 a0001c0001t0001g0156 a0001c0001t0001g0157 others(50): Show |
96 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.81+890G>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50819862 | |||||||
| chr6:50819863 | CGAGGTGG others(2): Show |
C | 53 | a0001c0001t0001g0023 a0001c0001t0001g0156 a0001c0001t0001g0157 others(50): Show |
96 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.81+896_81+904delTG others(7): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 50819863 | ||||||
| chr6:50819880 | C | G | 53 | a0001c0001t0001g0023 a0001c0001t0001g0156 a0001c0001t0001g0157 others(50): Show |
96 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.81+908C>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50819880 | |||||||
| chr6:50820008 | G | A | 1 | a0001c0001t0039g0110 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.81+1036G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50820008 | |||||||
| chr6:50820089 | G | A | 1 | a0001c0001t0003g0153 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.81+1117G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50820089 | |||||||
| chr6:50820240 | C | G | 1 | a0001c0001t0012g0151 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.81+1268C>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50820240 | |||||||
| chr6:50820288 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0111 others(7): Show |
27 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.81+1316G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50820288 | |||||||
| chr6:50820391 | GC | G | 77 | a0001c0001t0001g0023 a0001c0001t0001g0152 a0001c0001t0001g0168 others(74): Show |
141 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.81+1428delC | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 50820391 | ||||||
| chr6:50820549 | T | C | 11 | a0001c0001t0006g0020 a0001c0001t0006g0046 a0001c0001t0006g0117 others(8): Show |
14 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+1577T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50820549 | |||||||
| chr6:50820577 | C | T | 1 | a0001c0001t0003g0179 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.81+1605C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50820577 | |||||||
| chr6:50820602 | G | T | 1 | a0001c0001t0047g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.81+1630G>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50820602 | |||||||
| chr6:50820669 | C | G | 158 | a0001c0001t0001g0023 a0001c0001t0001g0076 a0001c0001t0001g0152 others(155): Show |
281 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.81+1697C>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50820669 | |||||||
| chr6:50820853 | G | A | 2 | a0001c0001t0006g0046 a0001c0001t0006g0117 |
3 | HG00099.hp1 HG00323.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.81+1881G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50820853 | |||||||
| chr6:50820949 | AAG | A | 13 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0059 others(10): Show |
17 | HG00741.hp2 HG01891.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.81+1981_81+1982del others(2): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 50820949 | ||||||
| chr6:50821065 | A | C | 53 | a0001c0001t0001g0023 a0001c0001t0001g0152 a0001c0001t0001g0156 others(50): Show |
96 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.81+2093A>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50821065 | |||||||
| chr6:50821186 | T | C | 1 | a0001c0001t0005g0053 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.81+2214T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50821186 | |||||||
| chr6:50821319 | G | C | 1 | a0001c0001t0007g0087 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.82-2088G>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50821319 | |||||||
| chr6:50821351 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.82-2056A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50821351 | |||||||
| chr6:50821410 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0014 |
4 | HG02056.hp1 NA18990.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-1997T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50821410 | |||||||
| chr6:50821420 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.82-1987C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50821420 | |||||||
| chr6:50821463 | G | A | 158 | a0001c0001t0001g0023 a0001c0001t0001g0076 a0001c0001t0001g0152 others(155): Show |
281 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.82-1944G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50821463 | |||||||
| chr6:50821484 | G | A | 28 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0018 others(25): Show |
48 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.82-1923G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50821484 | |||||||
| chr6:50821537 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.82-1870C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50821537 | |||||||
| chr6:50821738 | T | C | 149 | a0001c0001t0001g0023 a0001c0001t0001g0076 a0001c0001t0001g0152 others(146): Show |
265 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.82-1669T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50821738 | |||||||
| chr6:50821877 | G | C | 1 | a0001c0001t0002g0067 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82-1530G>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50821877 | |||||||
| chr6:50821882 | G | A | 9 | a0001c0001t0002g0181 a0001c0001t0005g0008 a0001c0001t0005g0024 others(6): Show |
16 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.82-1525G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50821882 | |||||||
| chr6:50821934 | A | C | 1 | a0001c0001t0009g0066 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.82-1473A>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50821934 | |||||||
| chr6:50821976 | T | TC | 27 | a0001c0001t0001g0076 a0001c0001t0002g0003 a0001c0001t0002g0005 others(24): Show |
69 | HG00140.hp1 HG00639.hp1 HG01256.hp1 others(66): Show |
intron_variant | MODIFIER | c.82-1431_82-1430ins others(1): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50821976 | |||||||
| chr6:50821976 | T | TG | 109 | a0001c0001t0001g0023 a0001c0001t0001g0152 a0001c0001t0001g0156 others(106): Show |
183 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.82-1425dupG | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 50821976 | ||||||
| chr6:50821976 | T | TGG | 13 | a0001c0001t0001g0178 a0001c0001t0003g0109 a0001c0001t0003g0153 others(10): Show |
13 | HG01192.hp1 HG02109.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.82-1426_82-1425dup others(2): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 50821976 | ||||||
| chr6:50821991 | A | AT | 78 | a0001c0001t0001g0022 a0001c0001t0001g0152 a0001c0001t0001g0156 others(75): Show |
145 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.82-1398dupT | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 50821991 | ||||||
| chr6:50821991 | A | ATT | 14 | a0001c0001t0001g0023 a0001c0001t0001g0157 a0001c0001t0001g0171 others(11): Show |
19 | HG00544.hp2 HG00673.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.82-1399_82-1398dup others(2): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 50821991 | ||||||
| chr6:50821991 | AT | A | 43 | a0001c0001t0001g0076 a0001c0001t0002g0003 a0001c0001t0002g0005 others(40): Show |
88 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.82-1398delT | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 50821991 | ||||||
| chr6:50821991 | ATT | A | 7 | a0001c0001t0002g0028 a0001c0001t0002g0058 a0001c0001t0002g0068 others(4): Show |
8 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-1399_82-1398del others(2): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 50821991 | ||||||
| chr6:50822079 | AT | A | 33 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0018 others(30): Show |
54 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.82-1318delT | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 50822079 | ||||||
| chr6:50822233 | G | C | 1 | a0001c0001t0002g0029 | 2 | NA18990.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.82-1174G>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50822233 | |||||||
| chr6:50822282 | C | T | 1 | a0001c0001t0002g0035 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.82-1125C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50822282 | |||||||
| chr6:50822531 | C | T | 1 | a0001c0001t0040g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.82-876C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50822531 | |||||||
| chr6:50822694 | C | T | 1 | a0001c0001t0002g0037 | 2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.82-713C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50822694 | |||||||
| chr6:50822730 | G | A | 1 | a0001c0001t0005g0053 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.82-677G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50822730 | |||||||
| chr6:50822735 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.82-672C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50822735 | |||||||
| chr6:50822920 | G | A | 48 | a0001c0001t0001g0076 a0001c0001t0002g0003 a0001c0001t0002g0005 others(45): Show |
96 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.82-487G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50822920 | |||||||
| chr6:50822926 | C | A | 2 | a0001c0001t0027g0185 a0001c0001t0031g0184 |
2 | HG01123.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.82-481C>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50822926 | |||||||
| chr6:50822929 | C | T | 19 | a0001c0001t0007g0012 a0001c0001t0007g0039 a0001c0001t0007g0041 others(16): Show |
25 | HG00280.hp2 HG01081.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.82-478C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50822929 | |||||||
| chr6:50823274 | C | A | 1 | a0001c0001t0011g0019 | 3 | NA18963.hp1 NA18982.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.82-133C>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 1/6 | chr6 | 50823274 | |||||||
| chr6:50823871 | CACAA | C | 103 | a0001c0001t0001g0076 a0001c0001t0002g0003 a0001c0001t0002g0005 others(100): Show |
183 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.540+28_540+31delCA others(2): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 50823871 | ||||||
| chr6:50823879 | A | G | 12 | a0001c0001t0006g0020 a0001c0001t0006g0046 a0001c0001t0006g0117 others(9): Show |
15 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.540+14A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50823879 | |||||||
| chr6:50823907 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.540+42A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50823907 | |||||||
| chr6:50823927 | G | C | 69 | a0001c0001t0001g0023 a0001c0001t0001g0152 a0001c0001t0001g0156 others(66): Show |
117 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.540+62G>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50823927 | |||||||
| chr6:50824094 | A | T | 11 | a0001c0001t0006g0020 a0001c0001t0006g0046 a0001c0001t0006g0117 others(8): Show |
14 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.540+229A>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50824094 | |||||||
| chr6:50824124 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.540+259T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50824124 | |||||||
| chr6:50824179 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.540+314A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50824179 | |||||||
| chr6:50824251 | C | G | 1 | a0003c0005t0033g0142 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.540+386C>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50824251 | |||||||
| chr6:50824272 | G | C | 1 | a0001c0001t0001g0157 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.540+407G>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50824272 | |||||||
| chr6:50824278 | G | A | 1 | a0001c0001t0006g0118 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.540+413G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50824278 | |||||||
| chr6:50824292 | G | T | 1 | a0001c0001t0002g0181 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.540+427G>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50824292 | |||||||
| chr6:50824394 | G | T | 1 | a0001c0001t0017g0084 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.540+529G>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50824394 | |||||||
| chr6:50824608 | C | T | 2 | a0001c0003t0019g0149 a0001c0003t0019g0150 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.540+743C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50824608 | |||||||
| chr6:50824704 | G | A | 4 | a0001c0001t0008g0097 a0001c0001t0008g0102 a0001c0001t0023g0091 others(1): Show |
4 | HG01516.hp2 HG01517.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+839G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50824704 | |||||||
| chr6:50824710 | A | G | 1 | a0001c0001t0003g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.540+845A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50824710 | |||||||
| chr6:50824991 | A | G | 2 | a0001c0001t0001g0141 a0001c0001t0001g0148 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.540+1126A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50824991 | |||||||
| chr6:50825035 | C | T | 1 | a0001c0001t0027g0185 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.540+1170C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50825035 | |||||||
| chr6:50825057 | A | G | 10 | a0001c0001t0006g0020 a0001c0001t0006g0046 a0001c0001t0006g0117 others(7): Show |
13 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.540+1192A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50825057 | |||||||
| chr6:50825058 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.540+1193G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50825058 | |||||||
| chr6:50825147 | A | T | 3 | a0001c0001t0007g0039 a0001c0001t0007g0042 a0001c0001t0046g0042 |
4 | HG00280.hp2 HG01081.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+1282A>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50825147 | |||||||
| chr6:50825155 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.540+1290C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50825155 | |||||||
| chr6:50825232 | A | C | 1 | a0001c0001t0038g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.540+1367A>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50825232 | |||||||
| chr6:50825249 | A | G | 2 | a0001c0003t0019g0149 a0001c0003t0019g0150 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.540+1384A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50825249 | |||||||
| chr6:50825295 | G | GT | 53 | a0001c0001t0001g0023 a0001c0001t0001g0152 a0001c0001t0001g0156 others(50): Show |
96 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.540+1440dupT | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 50825295 | ||||||
| chr6:50825295 | GT | G | 61 | a0001c0001t0001g0076 a0001c0001t0002g0003 a0001c0001t0002g0005 others(58): Show |
112 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.540+1440delT | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 50825295 | ||||||
| chr6:50825330 | C | T | 2 | a0001c0001t0003g0108 a0001c0001t0003g0170 |
2 | HG03453.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.540+1465C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50825330 | |||||||
| chr6:50825338 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.540+1473A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50825338 | |||||||
| chr6:50825364 | T | C | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | HG01070.hp2 HG01361.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.540+1499T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50825364 | |||||||
| chr6:50825483 | A | G | 1 | a0001c0001t0005g0024 | 3 | HG02280.hp1 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.540+1618A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50825483 | |||||||
| chr6:50825641 | C | T | 1 | a0001c0001t0006g0124 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.540+1776C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50825641 | |||||||
| chr6:50825757 | G | C | 1 | a0001c0001t0003g0161 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.540+1892G>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50825757 | |||||||
| chr6:50825757 | G | T | 13 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0059 others(10): Show |
17 | HG00741.hp2 HG01891.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.540+1892G>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50825757 | |||||||
| chr6:50825822 | C | T | 3 | a0001c0001t0017g0027 a0001c0001t0017g0064 a0001c0001t0041g0027 |
3 | HG03209.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.540+1957C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50825822 | |||||||
| chr6:50825837 | G | A | 4 | a0001c0001t0006g0020 a0001c0001t0006g0118 a0001c0001t0006g0119 others(1): Show |
6 | HG00733.hp1 HG01261.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+1972G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50825837 | |||||||
| chr6:50825958 | A | G | 150 | a0001c0001t0001g0023 a0001c0001t0001g0076 a0001c0001t0001g0152 others(147): Show |
266 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.540+2093A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50825958 | |||||||
| chr6:50826031 | C | T | 35 | a0001c0001t0001g0076 a0001c0001t0002g0003 a0001c0001t0002g0005 others(32): Show |
79 | HG00140.hp1 HG00639.hp1 HG01123.hp1 others(76): Show |
intron_variant | MODIFIER | c.540+2166C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50826031 | |||||||
| chr6:50826036 | C | A | 11 | a0001c0001t0006g0020 a0001c0001t0006g0046 a0001c0001t0006g0117 others(8): Show |
14 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.540+2171C>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50826036 | |||||||
| chr6:50826566 | A | AGC | 50 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0047 others(47): Show |
70 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.541-2033_541-2032d others(4): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 50826566 | ||||||
| chr6:50826566 | A | AGCGC | 6 | a0001c0001t0006g0117 a0001c0001t0006g0118 a0001c0001t0006g0119 others(3): Show |
6 | HG01255.hp2 HG01261.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-2035_541-2032d others(6): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 50826566 | ||||||
| chr6:50826566 | A | AGCGCGCG others(3): Show |
1 | a0001c0001t0002g0070 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.541-2041_541-2032d others(12): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 50826566 | ||||||
| chr6:50826566 | A | AGCGCGCG others(5): Show |
1 | a0001c0001t0003g0054 | 2 | HG00741.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.541-2043_541-2032d others(14): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 50826566 | ||||||
| chr6:50826566 | AGCGCGCG others(3): Show |
A | 1 | a0001c0001t0001g0114 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.541-2041_541-2032d others(12): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 50826566 | ||||||
| chr6:50826586 | C | CGT | 61 | a0001c0001t0001g0076 a0001c0001t0002g0003 a0001c0001t0002g0005 others(58): Show |
125 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.541-2020_541-2019d others(4): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 50826586 | ||||||
| chr6:50826586 | CGT | C | 12 | a0001c0001t0001g0048 a0001c0001t0006g0020 a0001c0001t0006g0046 others(9): Show |
16 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.541-2020_541-2019d others(4): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 50826586 | ||||||
| chr6:50826588 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.541-2031T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50826588 | |||||||
| chr6:50826977 | T | C | 1 | a0001c0001t0002g0074 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.541-1642T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50826977 | |||||||
| chr6:50827308 | T | A | 1 | a0001c0001t0002g0071 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.541-1311T>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50827308 | |||||||
| chr6:50827736 | C | A | 4 | a0001c0001t0003g0055 a0001c0001t0003g0162 a0001c0001t0003g0164 others(1): Show |
5 | HG00639.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-883C>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50827736 | |||||||
| chr6:50827839 | A | G | 2 | a0001c0001t0020g0073 a0001c0001t0020g0077 |
2 | HG02698.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.541-780A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50827839 | |||||||
| chr6:50827922 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.541-697G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50827922 | |||||||
| chr6:50827943 | G | C | 1 | a0001c0001t0040g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.541-676G>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50827943 | |||||||
| chr6:50827946 | T | C | 1 | a0001c0001t0038g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.541-673T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50827946 | |||||||
| chr6:50828257 | C | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0178 |
2 | NA18955.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.541-362C>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50828257 | |||||||
| chr6:50828278 | G | T | 1 | a0001c0001t0005g0183 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.541-341G>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50828278 | |||||||
| chr6:50828318 | T | A | 9 | a0001c0001t0002g0181 a0001c0001t0005g0008 a0001c0001t0005g0024 others(6): Show |
16 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.541-301T>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50828318 | |||||||
| chr6:50828480 | G | A | 1 | a0001c0001t0002g0031 | 2 | HG03704.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.541-139G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50828480 | |||||||
| chr6:50828537 | C | T | 2 | a0001c0003t0019g0149 a0001c0003t0019g0150 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.541-82C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 2/6 | chr6 | 50828537 | |||||||
| chr6:50828921 | A | G | 159 | a0001c0001t0001g0023 a0001c0001t0001g0076 a0001c0001t0001g0152 others(156): Show |
282 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.601+242A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50828921 | |||||||
| chr6:50828930 | T | A | 1 | a0001c0001t0043g0061 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.601+251T>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50828930 | |||||||
| chr6:50828942 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.601+263C>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50828942 | |||||||
| chr6:50829192 | T | C | 53 | a0001c0001t0001g0023 a0001c0001t0001g0152 a0001c0001t0001g0156 others(50): Show |
96 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.601+513T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50829192 | |||||||
| chr6:50829504 | A | G | 1 | a0001c0001t0003g0169 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.601+825A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50829504 | |||||||
| chr6:50829567 | G | A | 2 | a0001c0003t0019g0149 a0001c0003t0019g0150 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.601+888G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50829567 | |||||||
| chr6:50829573 | A | G | 32 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0018 others(29): Show |
53 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.601+894A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50829573 | |||||||
| chr6:50829671 | G | T | 1 | a0001c0001t0003g0107 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.601+992G>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50829671 | |||||||
| chr6:50829773 | T | G | 2 | a0001c0003t0019g0149 a0001c0003t0019g0150 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.601+1094T>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50829773 | |||||||
| chr6:50829948 | ATCTC | A | 33 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0018 others(30): Show |
54 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.601+1286_601+1289d others(6): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 50829948 | ||||||
| chr6:50830050 | A | G | 32 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0018 others(29): Show |
53 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.601+1371A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50830050 | |||||||
| chr6:50830133 | G | C | 1 | a0001c0001t0003g0174 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.601+1454G>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50830133 | |||||||
| chr6:50830244 | G | A | 1 | a0001c0001t0002g0032 | 2 | NA18951.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.601+1565G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50830244 | |||||||
| chr6:50830302 | C | A | 2 | a0001c0001t0008g0097 a0001c0001t0008g0102 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.601+1623C>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50830302 | |||||||
| chr6:50830376 | G | A | 7 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0032 others(4): Show |
19 | HG00639.hp1 HG01952.hp1 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.601+1697G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50830376 | |||||||
| chr6:50830393 | T | C | 2 | a0001c0001t0003g0082 a0001c0001t0003g0105 |
2 | HG01934.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.601+1714T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50830393 | |||||||
| chr6:50830667 | G | A | 2 | a0001c0003t0019g0149 a0001c0003t0019g0150 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.601+1988G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50830667 | |||||||
| chr6:50830813 | C | T | 55 | a0001c0001t0001g0023 a0001c0001t0001g0152 a0001c0001t0001g0156 others(52): Show |
99 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.601+2134C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50830813 | |||||||
| chr6:50830955 | G | C | 32 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0018 others(29): Show |
53 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.601+2276G>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50830955 | |||||||
| chr6:50831137 | C | T | 1 | a0001c0001t0017g0084 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.601+2458C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50831137 | |||||||
| chr6:50831189 | T | C | 2 | a0001c0001t0001g0049 a0001c0001t0026g0049 |
2 | NA18965.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.601+2510T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50831189 | |||||||
| chr6:50831197 | C | T | 2 | a0001c0003t0019g0149 a0001c0003t0019g0150 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.601+2518C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50831197 | |||||||
| chr6:50831613 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.601+2934C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50831613 | |||||||
| chr6:50831660 | T | TG | 50 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(47): Show |
109 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.601+2987dupG | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 50831660 | ||||||
| chr6:50831804 | A | C | 1 | a0001c0001t0038g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.601+3125A>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50831804 | |||||||
| chr6:50831960 | T | G | 1 | a0001c0001t0040g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.601+3281T>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50831960 | |||||||
| chr6:50831984 | A | G | 1 | a0001c0001t0017g0084 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.601+3305A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50831984 | |||||||
| chr6:50832396 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.602-3665G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50832396 | |||||||
| chr6:50832427 | G | A | 3 | a0001c0001t0002g0017 a0002c0002t0002g0017 a0002c0002t0028g0017 |
3 | HG02258.hp1 HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.602-3634G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50832427 | |||||||
| chr6:50832575 | T | C | 1 | a0001c0001t0005g0053 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.602-3486T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50832575 | |||||||
| chr6:50832595 | G | A | 37 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0018 others(34): Show |
58 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.602-3466G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50832595 | |||||||
| chr6:50832740 | C | CA | 32 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0018 others(29): Show |
52 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.602-3317dupA | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 50832740 | ||||||
| chr6:50832793 | A | G | 1 | a0001c0001t0001g0052 | 2 | HG02148.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.602-3268A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50832793 | |||||||
| chr6:50832880 | C | G | 1 | a0001c0001t0044g0062 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.602-3181C>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50832880 | |||||||
| chr6:50832982 | A | G | 1 | a0001c0001t0002g0181 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.602-3079A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50832982 | |||||||
| chr6:50833172 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0113 |
2 | NA18961.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.602-2889G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50833172 | |||||||
| chr6:50833523 | A | AAAAAAC | 44 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0010 others(41): Show |
85 | HG00280.hp1 HG00597.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.602-2513_602-2508d others(8): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 50833523 | ||||||
| chr6:50833523 | AAAAAAC | A | 3 | a0001c0001t0008g0043 a0001c0001t0008g0096 a0001c0001t0008g0099 |
4 | HG01255.hp1 HG01884.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-2513_602-2508d others(8): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 50833523 | ||||||
| chr6:50833750 | C | T | 1 | a0001c0001t0003g0163 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.602-2311C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50833750 | |||||||
| chr6:50833777 | GAC | G | 37 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0018 others(34): Show |
58 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.602-2282_602-2281d others(4): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 50833777 | ||||||
| chr6:50833887 | A | T | 2 | a0001c0003t0019g0149 a0001c0003t0019g0150 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.602-2174A>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50833887 | |||||||
| chr6:50833996 | C | A | 2 | a0001c0001t0023g0091 a0001c0001t0023g0092 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.602-2065C>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50833996 | |||||||
| chr6:50834144 | C | T | 1 | a0001c0001t0002g0034 | 2 | NA18962.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.602-1917C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50834144 | |||||||
| chr6:50834155 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0139 |
2 | HG02074.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.602-1906C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50834155 | |||||||
| chr6:50834668 | A | G | 6 | a0001c0001t0004g0009 a0001c0001t0004g0018 a0001c0001t0004g0040 others(3): Show |
13 | HG00597.hp1 HG01978.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.602-1393A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50834668 | |||||||
| chr6:50834765 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0051 |
4 | HG01934.hp2 HG03239.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-1296T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50834765 | |||||||
| chr6:50834808 | A | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(192): Show |
367 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.602-1253A>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50834808 | |||||||
| chr6:50834998 | G | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(191): Show |
366 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.602-1063G>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50834998 | |||||||
| chr6:50835090 | A | G | 1 | a0001c0001t0044g0062 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.602-971A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50835090 | |||||||
| chr6:50835231 | C | T | 1 | a0001c0001t0003g0166 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.602-830C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50835231 | |||||||
| chr6:50835337 | A | G | 42 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0010 others(39): Show |
83 | HG00280.hp1 HG00597.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.602-724A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50835337 | |||||||
| chr6:50835579 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.602-482G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50835579 | |||||||
| chr6:50835785 | G | C | 1 | a0001c0001t0040g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.602-276G>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50835785 | |||||||
| chr6:50835828 | C | T | 1 | a0001c0001t0003g0165 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.602-233C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50835828 | |||||||
| chr6:50835839 | C | T | 1 | a0001c0001t0040g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.602-222C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 3/6 | chr6 | 50835839 | |||||||
| chr6:50836318 | A | C | 1 | a0001c0001t0040g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.821+38A>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 4/6 | chr6 | 50836318 | |||||||
| chr6:50836417 | G | A | 1 | a0001c0001t0027g0185 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.821+137G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 4/6 | chr6 | 50836417 | |||||||
| chr6:50836608 | T | C | 1 | a0001c0001t0003g0056 | 2 | NA18946.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.821+328T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 4/6 | chr6 | 50836608 | |||||||
| chr6:50836667 | C | A | 2 | a0001c0001t0005g0024 a0001c0001t0005g0057 |
5 | HG02280.hp1 HG02717.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.821+387C>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 4/6 | chr6 | 50836667 | |||||||
| chr6:50836676 | C | A | 1 | a0001c0001t0006g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.821+396C>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 4/6 | chr6 | 50836676 | |||||||
| chr6:50836808 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(73): Show |
142 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.821+528A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 4/6 | chr6 | 50836808 | |||||||
| chr6:50837522 | T | C | 7 | a0001c0001t0005g0008 a0001c0001t0005g0024 a0001c0001t0005g0057 others(4): Show |
14 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.822-453T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 4/6 | chr6 | 50837522 | |||||||
| chr6:50837623 | A | C | 1 | a0003c0005t0033g0142 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.822-352A>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 4/6 | chr6 | 50837623 | |||||||
| chr6:50837778 | TA | T | 37 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0018 others(34): Show |
58 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.822-189delA | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 50837778 | ||||||
| chr6:50838108 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.940+15T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 5/6 | chr6 | 50838108 | |||||||
| chr6:50838229 | T | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(191): Show |
366 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.940+136T>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 5/6 | chr6 | 50838229 | |||||||
| chr6:50838356 | G | T | 1 | a0001c0001t0002g0058 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.940+263G>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 5/6 | chr6 | 50838356 | |||||||
| chr6:50838372 | C | A | 2 | a0001c0001t0020g0073 a0001c0001t0020g0077 |
2 | HG02698.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.940+279C>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 5/6 | chr6 | 50838372 | |||||||
| chr6:50838524 | C | T | 9 | a0001c0001t0005g0008 a0001c0001t0005g0024 a0001c0001t0005g0053 others(6): Show |
17 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.940+431C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 5/6 | chr6 | 50838524 | |||||||
| chr6:50838641 | G | C | 3 | a0001c0001t0008g0043 a0001c0001t0008g0096 a0001c0001t0008g0099 |
4 | HG01255.hp1 HG01884.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+548G>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 5/6 | chr6 | 50838641 | |||||||
| chr6:50838667 | G | C | 3 | a0001c0001t0008g0043 a0001c0001t0008g0096 a0001c0001t0008g0099 |
4 | HG01255.hp1 HG01884.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+574G>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 5/6 | chr6 | 50838667 | |||||||
| chr6:50838768 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.940+675A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 5/6 | chr6 | 50838768 | |||||||
| chr6:50839082 | A | G | 1 | a0001c0001t0003g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.940+989A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 5/6 | chr6 | 50839082 | |||||||
| chr6:50839357 | C | G | 2 | a0001c0001t0015g0016 a0001c0001t0015g0060 |
4 | HG02559.hp2 HG02572.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.941-799C>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 5/6 | chr6 | 50839357 | |||||||
| chr6:50839361 | A | G | 1 | a0001c0001t0021g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.941-795A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 5/6 | chr6 | 50839361 | |||||||
| chr6:50839464 | T | G | 1 | a0001c0001t0021g0094 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.941-692T>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 5/6 | chr6 | 50839464 | |||||||
| chr6:50839505 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(191): Show |
366 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.941-651T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 5/6 | chr6 | 50839505 | |||||||
| chr6:50839645 | C | T | 10 | a0001c0001t0007g0012 a0001c0001t0007g0039 a0001c0001t0007g0041 others(7): Show |
15 | HG00280.hp2 HG01081.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.941-511C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 5/6 | chr6 | 50839645 | |||||||
| chr6:50839923 | G | A | 3 | a0001c0001t0008g0079 a0001c0001t0008g0080 a0001c0001t0008g0081 |
3 | HG02970.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.941-233G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 5/6 | chr6 | 50839923 | |||||||
| chr6:50840057 | T | G | 1 | a0001c0001t0001g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.941-99T>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 5/6 | chr6 | 50840057 | |||||||
| chr6:50840436 | G | C | 1 | a0001c0001t0007g0093 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1082+139G>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50840436 | |||||||
| chr6:50840759 | G | A | 2 | a0001c0003t0019g0149 a0001c0003t0019g0150 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1082+462G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50840759 | |||||||
| chr6:50840873 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1082+576C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50840873 | |||||||
| chr6:50840883 | C | T | 1 | a0001c0001t0045g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1082+586C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50840883 | |||||||
| chr6:50840984 | C | T | 1 | a0005c0004t0002g0072 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1082+687C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50840984 | |||||||
| chr6:50841019 | G | T | 1 | a0001c0001t0001g0021 | 3 | HG01069.hp2 HG01071.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1082+722G>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50841019 | |||||||
| chr6:50841029 | CAGCGTAA others(8): Show |
C | 1 | a0001c0001t0003g0107 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1082+734_1082+748d others(17): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 50841029 | ||||||
| chr6:50841032 | C | T | 33 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0011 others(30): Show |
77 | HG00140.hp1 HG00639.hp1 HG01123.hp1 others(74): Show |
intron_variant | MODIFIER | c.1082+735C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50841032 | |||||||
| chr6:50841105 | T | A | 1 | a0001c0001t0035g0167 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1082+808T>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50841105 | |||||||
| chr6:50841218 | A | C | 1 | a0001c0001t0021g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1082+921A>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50841218 | |||||||
| chr6:50841264 | G | T | 1 | a0001c0001t0039g0110 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1082+967G>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50841264 | |||||||
| chr6:50841348 | T | C | 1 | a0001c0001t0007g0087 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1082+1051T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50841348 | |||||||
| chr6:50841349 | G | A | 1 | a0001c0001t0005g0182 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1082+1052G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50841349 | |||||||
| chr6:50841361 | A | G | 1 | a0001c0001t0006g0123 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1082+1064A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50841361 | |||||||
| chr6:50841363 | C | A | 4 | a0001c0001t0018g0038 a0001c0001t0018g0085 a0001c0001t0045g0103 others(1): Show |
5 | HG02109.hp1 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1082+1066C>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50841363 | |||||||
| chr6:50841374 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(192): Show |
367 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.1082+1077G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50841374 | |||||||
| chr6:50841428 | G | A | 37 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0018 others(34): Show |
58 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1082+1131G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50841428 | |||||||
| chr6:50841440 | T | G | 1 | a0001c0001t0001g0138 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1082+1143T>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50841440 | |||||||
| chr6:50841440 | T | TG | 42 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0010 others(39): Show |
83 | HG00280.hp1 HG00597.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.1082+1150dupG | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 50841440 | ||||||
| chr6:50841565 | C | T | 44 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0010 others(41): Show |
85 | HG00280.hp1 HG00597.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1082+1268C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50841565 | |||||||
| chr6:50841651 | T | G | 2 | a0001c0001t0004g0040 a0001c0001t0004g0090 |
3 | HG00597.hp1 HG02132.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1082+1354T>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50841651 | |||||||
| chr6:50841684 | TTGGAATT others(2): Show |
T | 13 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0059 others(10): Show |
17 | HG00741.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1082+1392_1083-139 others(13): Show |
TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 50841684 | ||||||
| chr6:50841849 | G | C | 1 | a0001c0001t0002g0036 | 2 | HG01123.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1083-1243G>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50841849 | |||||||
| chr6:50842007 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(52): Show |
109 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1083-1085T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50842007 | |||||||
| chr6:50842015 | T | C | 13 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0059 others(10): Show |
17 | HG00741.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1083-1077T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50842015 | |||||||
| chr6:50842064 | T | C | 37 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0018 others(34): Show |
58 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1083-1028T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50842064 | |||||||
| chr6:50842074 | A | G | 44 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0010 others(41): Show |
85 | HG00280.hp1 HG00597.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1083-1018A>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50842074 | |||||||
| chr6:50842130 | G | T | 13 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0059 others(10): Show |
17 | HG00741.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1083-962G>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50842130 | |||||||
| chr6:50842200 | T | G | 1 | a0001c0001t0003g0161 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1083-892T>G | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50842200 | |||||||
| chr6:50842422 | T | C | 2 | a0001c0001t0009g0059 a0001c0001t0009g0065 |
2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1083-670T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50842422 | |||||||
| chr6:50842519 | C | T | 3 | a0001c0001t0003g0015 a0001c0001t0003g0170 a0001c0001t0003g0174 |
6 | NA18944.hp2 NA18945.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1083-573C>T | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50842519 | |||||||
| chr6:50842577 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1083-515G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50842577 | |||||||
| chr6:50842784 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(192): Show |
367 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.1083-308T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50842784 | |||||||
| chr6:50842827 | T | C | 37 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0018 others(34): Show |
58 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1083-265T>C | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50842827 | |||||||
| chr6:50842883 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0113 |
2 | NA18961.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1083-209G>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50842883 | |||||||
| chr6:50842904 | C | A | 1 | a0001c0001t0002g0033 | 2 | NA18999.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1083-188C>A | TFAP2B | ENSG00000008196.13 | transcript | ENST00000393655.4 | protein_coding | 6/6 | chr6 | 50842904 |