Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51283 |
| ensemblid | ENSG00000103429.11 |
| hgncid | 17613 |
| symbol | BFAR |
| name | bifunctional apoptosis regulator |
| refseq_nuc | NM_016561.3 |
| refseq_prot | NP_057645.1 |
| ensembl_nuc | ENST00000261658.7 |
| ensembl_prot | ENSP00000261658.2 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 14632951 |
| end | 14669236 |
| strand | + |
| ver | v1.2 |
| region | chr16:14632951-14669236 |
| region5000 | chr16:14627951-14674236 |
| regionname0 | BFAR_chr16_14632951_14669236 |
| regionname5000 | BFAR_chr16_14627951_14674236 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 450 | 227 | 69 | 36 | 88 | 12 | 22 | 63 | BFAR_chr16_14627951_14674236 | BFAR | MEEPQ others(445): Show |
chr16 | 14627951 | 14674236 |
| a0002 | 0/1 | 450 | 81 | 9 | 23 | 32 | 4 | 12 | 23 | BFAR_chr16_14627951_14674236 | BFAR | MEEPQ others(445): Show |
chr16 | 14627951 | 14674236 |
| a0003 | 0/0 | 450 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | MEEPQ others(445): Show |
chr16 | 14627951 | 14674236 |
| a0004 | 0/0 | 450 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | MEEPQ others(445): Show |
chr16 | 14627951 | 14674236 |
| a0005 | 0/0 | 450 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BFAR_chr16_14627951_14674236 | BFAR | MEEPQ others(445): Show |
chr16 | 14627951 | 14674236 |
| a0006 | 0/0 | 450 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | MEEPQ others(445): Show |
chr16 | 14627951 | 14674236 |
| a0007 | 0/0 | 450 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | MEEPQ others(445): Show |
chr16 | 14627951 | 14674236 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1350 | 226 | 69 | 36 | 87 | 12 | 22 | BFAR_chr16_14627951_14674236 | BFAR | ATGGA others(1345): Show |
chr16 | 14627951 | 14674236 | ||
| a0001c0008 | 0/0 | 1350 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | ATGGA others(1345): Show |
chr16 | 14627951 | 14674236 | ||
| a0002c0002 | 0/1 | 1350 | 80 | 9 | 22 | 32 | 4 | 12 | BFAR_chr16_14627951_14674236 | BFAR | ATGGA others(1345): Show |
chr16 | 14627951 | 14674236 | ||
| a0002c0009 | 0/0 | 1350 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | ATGGA others(1345): Show |
chr16 | 14627951 | 14674236 | ||
| a0003c0003 | 0/0 | 1350 | 3 | 3 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | ATGGA others(1345): Show |
chr16 | 14627951 | 14674236 | ||
| a0004c0004 | 0/0 | 1350 | 2 | 0 | 2 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | ATGGA others(1345): Show |
chr16 | 14627951 | 14674236 | ||
| a0005c0005 | 0/0 | 1350 | 2 | 0 | 0 | 2 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | ATGGA others(1345): Show |
chr16 | 14627951 | 14674236 | ||
| a0006c0006 | 0/0 | 1350 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | ATGGA others(1345): Show |
chr16 | 14627951 | 14674236 | ||
| a0007c0007 | 0/0 | 1350 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | ATGGA others(1345): Show |
chr16 | 14627951 | 14674236 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2903 | 189 | 66 | 28 | 63 | 12 | 20 | BFAR_chr16_14627951_14674236 | BFAR | CTCTT others(2898): Show |
chr16 | 14627951 | 14674236 |
| a0001c0001t0002 | 0/0 | 2903 | 20 | 0 | 0 | 19 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | CTCTT others(2898): Show |
chr16 | 14627951 | 14674236 |
| a0001c0001t0003 | 0/0 | 2903 | 10 | 1 | 8 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | CTCTT others(2898): Show |
chr16 | 14627951 | 14674236 |
| a0001c0001t0005 | 0/0 | 2904 | 3 | 1 | 0 | 2 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | CTCTT others(2899): Show |
chr16 | 14627951 | 14674236 |
| a0001c0001t0008 | 0/0 | 2903 | 2 | 0 | 0 | 2 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | CTCTT others(2898): Show |
chr16 | 14627951 | 14674236 |
| a0001c0001t0009 | 0/0 | 2903 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | CTCTT others(2898): Show |
chr16 | 14627951 | 14674236 |
| a0001c0001t0011 | 0/0 | 2903 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | CTCTT others(2898): Show |
chr16 | 14627951 | 14674236 |
| a0001c0008t0001 | 0/0 | 2903 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | CTCTT others(2898): Show |
chr16 | 14627951 | 14674236 |
| a0002c0002t0001 | 0/1 | 2903 | 72 | 5 | 18 | 32 | 4 | 12 | BFAR_chr16_14627951_14674236 | BFAR | CTCTT others(2898): Show |
chr16 | 14627951 | 14674236 |
| a0002c0002t0004 | 0/0 | 2903 | 2 | 0 | 2 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | CTCTT others(2898): Show |
chr16 | 14627951 | 14674236 |
| a0002c0002t0006 | 0/0 | 2904 | 3 | 3 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | CTCTT others(2899): Show |
chr16 | 14627951 | 14674236 |
| a0002c0002t0007 | 0/0 | 2903 | 2 | 0 | 2 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | CTCTT others(2898): Show |
chr16 | 14627951 | 14674236 |
| a0002c0002t0010 | 0/0 | 2904 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | CTCTT others(2899): Show |
chr16 | 14627951 | 14674236 |
| a0002c0009t0001 | 0/0 | 2903 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | CTCTT others(2898): Show |
chr16 | 14627951 | 14674236 |
| a0003c0003t0004 | 0/0 | 2903 | 3 | 3 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | CTCTT others(2898): Show |
chr16 | 14627951 | 14674236 |
| a0004c0004t0001 | 0/0 | 2903 | 2 | 0 | 2 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | CTCTT others(2898): Show |
chr16 | 14627951 | 14674236 |
| a0005c0005t0001 | 0/0 | 2903 | 2 | 0 | 0 | 2 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | CTCTT others(2898): Show |
chr16 | 14627951 | 14674236 |
| a0006c0006t0001 | 0/0 | 2903 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | CTCTT others(2898): Show |
chr16 | 14627951 | 14674236 |
| a0007c0007t0001 | 0/0 | 2903 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | CTCTT others(2898): Show |
chr16 | 14627951 | 14674236 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 5 | 1 | 0 | 3 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0002g0005 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0003g0003 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0008g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0008g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0009g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0001t0011g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0001c0008t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0001 | 0/0 | 9 | 0 | 1 | 6 | 0 | 2 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0006 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0006g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0006g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0007g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0007g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0002t0010g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0002c0009t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0003c0003t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0003c0003t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0003c0003t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0004c0004t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0004c0004t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0005c0005t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0005c0005t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0006c0006t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| a0007c0007t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | GBR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0226 | EUR | GBR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0239 | EUR | GBR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | FIN | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0006 | EUR | FIN | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | CHS | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | CHS | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | CHS | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00642 | hp1 | a0002 | c0009 | t0001 | g0007 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00735 | hp1 | a0004 | c0004 | t0001 | g0201 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0232 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0247 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0078 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01081 | hp1 | a0004 | c0004 | t0001 | g0200 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01081 | hp2 | a0002 | c0002 | t0004 | g0048 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0223 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0245 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01255 | hp1 | a0002 | c0002 | t0004 | g0047 | AMR | CLM | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0218 | AMR | CLM | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0140 | AMR | CLM | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | CLM | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01257 | hp2 | a0002 | c0002 | t0007 | g0007 | AMR | CLM | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01258 | hp1 | a0002 | c0002 | t0007 | g0069 | AMR | CLM | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0138 | AMR | CLM | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0026 | AMR | CLM | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0081 | EUR | IBS | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | IBS | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0026 | EUR | IBS | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | IBS | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01891 | hp2 | a0003 | c0003 | t0004 | g0259 | AFR | ACB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0227 | AMR | PEL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0248 | AMR | PEL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0139 | AMR | PEL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | PEL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0195 | AMR | PEL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01978 | hp2 | a0006 | c0006 | t0001 | g0178 | AMR | PEL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | KHV | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0171 | EAS | KHV | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | KHV | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02074 | hp1 | a0001 | c0001 | t0008 | g0208 | EAS | KHV | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02129 | hp1 | a0001 | c0001 | t0008 | g0192 | EAS | KHV | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | KHV | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0059 | AFR | ACB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02145 | hp2 | a0007 | c0007 | t0001 | g0052 | AFR | ACB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CDX | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | CDX | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | KHV | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02615 | hp1 | a0002 | c0002 | t0006 | g0251 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0198 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0225 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0169 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02886 | hp1 | a0002 | c0002 | t0006 | g0253 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02922 | hp2 | a0003 | c0003 | t0004 | g0260 | AFR | ESN | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0149 | AFR | ESN | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0038 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | MSL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ESN | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0084 | AFR | MSL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | MSL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | ESN | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0079 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0244 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0064 | SAS | BEB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0071 | SAS | BEB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | STU | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | STU | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0006 | SAS | STU | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0224 | SAS | STU | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | STU | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0045 | SAS | STU | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | STU | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | CHB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18999 | hp1 | a0001 | c0001 | t0011 | g0011 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19030 | hp1 | a0002 | c0002 | t0006 | g0254 | AFR | LWK | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19043 | hp2 | a0002 | c0002 | t0010 | g0252 | AFR | LWK | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19057 | hp1 | a0005 | c0005 | t0001 | g0073 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19060 | hp2 | a0001 | c0008 | t0001 | g0002 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19068 | hp1 | a0005 | c0005 | t0001 | g0001 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19072 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ASW | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ASW | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | TSI | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0170 | AMR | CLM | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | USA | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | USA | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA20300 | hp1 | a0003 | c0003 | t0004 | g0258 | AFR | USA | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | USA | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | LWK | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | LWK | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0051 | REF | REF | BFAR_chr16_14627951_14674236 | BFAR | chr16 | 14627951 | 14674236 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:14644459 | A | G | 1 | a0005 | 2 | NA19057.hp1 NA19068.hp1 |
missense_variant | MODERATE | c.113A>G | p.Tyr38Cys | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/8 | 254/2903 | 113/1353 | 38/450 | chr16 | 14644459 | |||
| chr16:14648543 | T | G | 4 | a0002 a0003 a0005 others(1): Show |
86 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(83): Show |
missense_variant | MODERATE | c.419T>G | p.Met140Arg | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 3/8 | 560/2903 | 419/1353 | 140/450 | chr16 | 14648543 | |||
| chr16:14655161 | G | A | 1 | a0003 | 3 | HG01891.hp2 HG02922.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.734G>A | p.Arg245His | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/8 | 875/2903 | 734/1353 | 245/450 | chr16 | 14655161 | |||
| chr16:14655178 | G | A | 1 | a0007 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.751G>A | p.Val251Met | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/8 | 892/2903 | 751/1353 | 251/450 | chr16 | 14655178 | |||
| chr16:14662051 | G | A | 2 | a0004 a0006 |
3 | HG00735.hp1 HG01081.hp1 HG01978.hp2 |
missense_variant | MODERATE | c.943G>A | p.Val315Ile | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 6/8 | 1084/2903 | 943/1353 | 315/450 | chr16 | 14662051 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:14644415 | C | T | 1 | a0002c0009 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.69C>T | p.Thr23Thr | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/8 | 210/2903 | 69/1353 | 23/450 | chr16 | 14644415 | |||
| chr16:14667671 | A | G | 1 | a0001c0008 | 1 | NA19060.hp2 | synonymous_variant | LOW | c.1197A>G | p.Lys399Lys | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 8/8 | 1338/2903 | 1197/1353 | 399/450 | chr16 | 14667671 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:14668001 | C | T | 1 | a0001c0001t0003 | 10 | HG00733.hp1 HG00738.hp1 HG01255.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*174C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 8/8 | 174 | chr16 | 14668001 | ||||||
| chr16:14668112 | G | A | 1 | a0001c0001t0002 | 20 | HG00558.hp1 HG02135.hp2 HG03834.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*285G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 8/8 | 285 | chr16 | 14668112 | ||||||
| chr16:14668347 | A | G | 1 | a0001c0001t0011 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*520A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 8/8 | 520 | chr16 | 14668347 | ||||||
| chr16:14668521 | G | A | 1 | a0002c0002t0007 | 2 | HG01257.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*694G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 8/8 | 694 | chr16 | 14668521 | ||||||
| chr16:14668650 | A | G | 1 | a0002c0002t0010 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*823A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 8/8 | 823 | chr16 | 14668650 | ||||||
| chr16:14668664 | G | A | 1 | a0001c0001t0008 | 2 | HG02074.hp1 HG02129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*837G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 8/8 | 837 | chr16 | 14668664 | ||||||
| chr16:14668835 | T | TA | 3 | a0001c0001t0005 a0002c0002t0006 a0002c0002t0010 |
7 | HG00609.hp2 HG02071.hp1 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1024dupA | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 8/8 | 1025 | INFO_REALIGN_3_PRIME | chr16 | 14668835 | |||||
| chr16:14668877 | A | C | 1 | a0001c0001t0009 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1050A>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 8/8 | 1050 | chr16 | 14668877 | ||||||
| chr16:14669219 | C | T | 4 | a0002c0002t0004 a0002c0002t0006 a0002c0002t0010 others(1): Show |
9 | HG01081.hp2 HG01255.hp1 HG01891.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1392C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 8/8 | 1392 | chr16 | 14669219 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:14633353 | T | A | 1 | a0001c0001t0001g0028 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-74+335T>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14633353 | |||||||
| chr16:14633644 | AAGAGAAT others(18): Show |
A | 1 | a0002c0002t0001g0027 | 2 | HG00558.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.-74+632_-74+656del others(25): Show |
BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr16 | 14633644 | ||||||
| chr16:14633757 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-74+739A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14633757 | |||||||
| chr16:14633807 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-74+789C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14633807 | |||||||
| chr16:14633811 | C | T | 3 | a0003c0003t0004g0258 a0003c0003t0004g0259 a0003c0003t0004g0260 |
3 | HG01891.hp2 HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-74+793C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14633811 | |||||||
| chr16:14633933 | G | T | 1 | a0002c0002t0001g0026 | 2 | HG01496.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-74+915G>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14633933 | |||||||
| chr16:14633984 | G | T | 1 | a0001c0001t0001g0257 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-74+966G>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14633984 | |||||||
| chr16:14634111 | A | C | 1 | a0001c0001t0001g0261 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-74+1093A>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14634111 | |||||||
| chr16:14634224 | C | G | 1 | a0001c0001t0001g0025 | 2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-74+1206C>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14634224 | |||||||
| chr16:14634265 | T | C | 2 | a0002c0002t0001g0029 a0002c0002t0001g0030 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-74+1247T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14634265 | |||||||
| chr16:14634285 | G | C | 1 | a0002c0002t0001g0031 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-74+1267G>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14634285 | |||||||
| chr16:14634493 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-74+1475A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14634493 | |||||||
| chr16:14634725 | A | C | 1 | a0001c0001t0001g0255 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-74+1707A>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14634725 | |||||||
| chr16:14634803 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-74+1785G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14634803 | |||||||
| chr16:14635029 | G | T | 4 | a0002c0002t0006g0251 a0002c0002t0006g0253 a0002c0002t0006g0254 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-74+2011G>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14635029 | |||||||
| chr16:14635106 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0034 others(1): Show |
5 | HG01243.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-74+2088G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14635106 | |||||||
| chr16:14635382 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-74+2364G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14635382 | |||||||
| chr16:14635684 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0037 |
3 | HG02572.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-74+2666T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14635684 | |||||||
| chr16:14635760 | CT | C | 9 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0040 others(6): Show |
9 | HG00738.hp2 HG02523.hp2 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-74+2755delT | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr16 | 14635760 | ||||||
| chr16:14635974 | T | C | 1 | a0002c0002t0001g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-74+2956T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14635974 | |||||||
| chr16:14636010 | G | A | 1 | a0001c0001t0002g0046 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-74+2992G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14636010 | |||||||
| chr16:14636013 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-74+2995C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14636013 | |||||||
| chr16:14636137 | G | T | 1 | a0002c0002t0006g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-74+3119G>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14636137 | |||||||
| chr16:14636165 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-74+3147C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14636165 | |||||||
| chr16:14636199 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-74+3181C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14636199 | |||||||
| chr16:14636229 | G | A | 1 | a0001c0001t0001g0014 | 2 | HG01361.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-74+3211G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14636229 | |||||||
| chr16:14636286 | C | T | 1 | a0001c0001t0003g0248 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-74+3268C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14636286 | |||||||
| chr16:14636337 | C | G | 1 | a0001c0001t0003g0247 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-74+3319C>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14636337 | |||||||
| chr16:14636902 | A | C | 1 | a0001c0001t0001g0246 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-74+3884A>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14636902 | |||||||
| chr16:14636917 | C | G | 3 | a0002c0002t0001g0243 a0002c0002t0001g0244 a0002c0002t0001g0245 |
3 | HG01168.hp2 HG01169.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-74+3899C>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14636917 | |||||||
| chr16:14636976 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-74+3958G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14636976 | |||||||
| chr16:14637361 | A | AT | 13 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0044 others(10): Show |
14 | HG00140.hp2 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-74+4354dupT | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr16 | 14637361 | ||||||
| chr16:14637534 | C | A | 59 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0055 others(56): Show |
73 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.-74+4516C>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14637534 | |||||||
| chr16:14637700 | C | A | 2 | a0002c0002t0004g0047 a0002c0002t0004g0048 |
2 | HG01081.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.-74+4682C>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14637700 | |||||||
| chr16:14637700 | C | G | 172 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(169): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.-74+4682C>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14637700 | |||||||
| chr16:14637832 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-74+4814A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14637832 | |||||||
| chr16:14638164 | C | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0234 |
3 | NA18973.hp1 NA19002.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-74+5146C>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14638164 | |||||||
| chr16:14638180 | C | G | 4 | a0002c0002t0006g0251 a0002c0002t0006g0253 a0002c0002t0006g0254 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-74+5162C>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14638180 | |||||||
| chr16:14638312 | G | C | 1 | a0001c0001t0001g0159 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-74+5294G>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14638312 | |||||||
| chr16:14638321 | C | T | 9 | a0002c0002t0004g0047 a0002c0002t0004g0048 a0002c0002t0006g0251 others(6): Show |
9 | HG01081.hp2 HG01255.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-74+5303C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14638321 | |||||||
| chr16:14638515 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-74+5497C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14638515 | |||||||
| chr16:14638572 | T | C | 1 | a0003c0003t0004g0258 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-74+5554T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14638572 | |||||||
| chr16:14638632 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-74+5614G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14638632 | |||||||
| chr16:14638950 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-73-5324A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14638950 | |||||||
| chr16:14638956 | A | G | 1 | a0002c0002t0001g0232 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-73-5318A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14638956 | |||||||
| chr16:14638963 | G | A | 1 | a0002c0002t0001g0050 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-73-5311G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14638963 | |||||||
| chr16:14638964 | A | G | 1 | a0002c0002t0001g0050 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-73-5310A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14638964 | |||||||
| chr16:14639070 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-73-5204C>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14639070 | |||||||
| chr16:14639097 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-73-5177G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14639097 | |||||||
| chr16:14639193 | G | C | 2 | a0001c0001t0001g0083 a0001c0001t0001g0249 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-73-5081G>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14639193 | |||||||
| chr16:14639396 | G | A | 4 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(1): Show |
4 | HG02257.hp2 HG03516.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-73-4878G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14639396 | |||||||
| chr16:14639415 | A | C | 1 | a0001c0001t0001g0242 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-73-4859A>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14639415 | |||||||
| chr16:14639452 | C | T | 9 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0150 others(6): Show |
10 | HG00738.hp2 HG00741.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.-73-4822C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14639452 | |||||||
| chr16:14639487 | T | C | 2 | a0001c0001t0003g0166 a0001c0001t0003g0167 |
2 | HG00733.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.-73-4787T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14639487 | |||||||
| chr16:14639536 | A | G | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG02257.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-73-4738A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14639536 | |||||||
| chr16:14639804 | A | G | 1 | a0002c0002t0001g0082 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-73-4470A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14639804 | |||||||
| chr16:14639843 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-73-4431G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14639843 | |||||||
| chr16:14640010 | G | A | 5 | a0002c0002t0004g0047 a0002c0002t0004g0048 a0003c0003t0004g0258 others(2): Show |
5 | HG01081.hp2 HG01255.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-73-4264G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14640010 | |||||||
| chr16:14640020 | G | A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.-73-4254G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14640020 | |||||||
| chr16:14640025 | C | G | 6 | a0002c0002t0001g0029 a0002c0002t0001g0030 a0002c0002t0001g0038 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73-4249C>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14640025 | |||||||
| chr16:14640487 | G | GAATCTAG others(4): Show |
1 | a0002c0002t0001g0050 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-73-3786_-73-3776d others(13): Show |
BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr16 | 14640487 | ||||||
| chr16:14640860 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-73-3414C>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14640860 | |||||||
| chr16:14641118 | C | G | 1 | a0001c0001t0009g0149 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-73-3156C>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14641118 | |||||||
| chr16:14641183 | A | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00099.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-73-3091A>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14641183 | |||||||
| chr16:14641321 | A | G | 2 | a0001c0001t0003g0166 a0001c0001t0003g0167 |
2 | HG00733.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.-73-2953A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14641321 | |||||||
| chr16:14641508 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-73-2766G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14641508 | |||||||
| chr16:14641550 | CA | C | 51 | a0001c0001t0001g0229 a0001c0001t0001g0233 a0002c0002t0001g0001 others(48): Show |
67 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-73-2707delA | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr16 | 14641550 | ||||||
| chr16:14642117 | C | T | 1 | a0001c0001t0003g0248 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-73-2157C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14642117 | |||||||
| chr16:14642125 | G | A | 4 | a0002c0002t0006g0251 a0002c0002t0006g0253 a0002c0002t0006g0254 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-73-2149G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14642125 | |||||||
| chr16:14642678 | G | A | 1 | a0007c0007t0001g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-73-1596G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14642678 | |||||||
| chr16:14643074 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-73-1200A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14643074 | |||||||
| chr16:14643141 | C | T | 1 | a0001c0001t0009g0149 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-73-1133C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14643141 | |||||||
| chr16:14643398 | A | G | 1 | a0003c0003t0004g0260 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-73-876A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14643398 | |||||||
| chr16:14643585 | G | A | 52 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(49): Show |
68 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.-73-689G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14643585 | |||||||
| chr16:14643706 | G | A | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-73-568G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14643706 | |||||||
| chr16:14643861 | C | CA | 6 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(3): Show |
6 | HG00741.hp2 HG02071.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-73-398dupA | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr16 | 14643861 | ||||||
| chr16:14643861 | CA | C | 11 | a0001c0001t0001g0032 a0001c0001t0001g0147 a0001c0001t0001g0219 others(8): Show |
12 | HG00741.hp1 HG01071.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-73-398delA | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr16 | 14643861 | ||||||
| chr16:14643931 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-73-343G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14643931 | |||||||
| chr16:14643964 | A | G | 8 | a0001c0001t0001g0144 a0001c0001t0002g0005 a0001c0001t0002g0046 others(5): Show |
11 | HG03834.hp2 NA18939.hp2 NA18941.hp1 others(8): Show |
intron_variant | MODIFIER | c.-73-310A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14643964 | |||||||
| chr16:14643989 | G | A | 1 | a0002c0002t0006g0251 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-73-285G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14643989 | |||||||
| chr16:14643997 | T | TA | 6 | a0001c0001t0001g0032 a0001c0001t0001g0219 a0001c0001t0001g0220 others(3): Show |
6 | HG01071.hp1 HG01071.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73-270dupA | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr16 | 14643997 | ||||||
| chr16:14644099 | G | C | 1 | a0001c0001t0001g0161 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-73-175G>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14644099 | |||||||
| chr16:14644111 | T | C | 69 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0055 others(66): Show |
86 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.-73-163T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14644111 | |||||||
| chr16:14644143 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-73-131A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14644143 | |||||||
| chr16:14644159 | T | G | 1 | a0001c0001t0001g0022 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-73-115T>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14644159 | |||||||
| chr16:14644162 | C | CA | 18 | a0001c0001t0001g0017 a0001c0001t0001g0091 a0001c0001t0001g0092 others(15): Show |
19 | HG01175.hp1 HG02071.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-73-94dupA | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr16 | 14644162 | ||||||
| chr16:14644162 | CA | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0090 a0001c0001t0003g0218 others(4): Show |
8 | HG01255.hp2 HG02615.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-73-94delA | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr16 | 14644162 | ||||||
| chr16:14644209 | T | A | 4 | a0002c0002t0001g0015 a0002c0002t0001g0057 a0002c0002t0001g0058 others(1): Show |
5 | HG02145.hp1 HG03098.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-73-65T>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 1/7 | chr16 | 14644209 | |||||||
| chr16:14644668 | CT | C | 6 | a0001c0001t0001g0100 a0001c0001t0001g0172 a0001c0001t0001g0174 others(3): Show |
6 | HG01167.hp1 NA18946.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+77delT | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr16 | 14644668 | ||||||
| chr16:14644686 | T | A | 1 | a0001c0001t0001g0099 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.263+77T>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14644686 | |||||||
| chr16:14644869 | C | G | 1 | a0001c0001t0001g0217 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.263+260C>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14644869 | |||||||
| chr16:14645019 | T | A | 1 | a0001c0001t0001g0101 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.263+410T>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14645019 | |||||||
| chr16:14645056 | G | A | 4 | a0002c0002t0006g0251 a0002c0002t0006g0253 a0002c0002t0006g0254 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+447G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14645056 | |||||||
| chr16:14645161 | A | T | 3 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 |
3 | HG01256.hp1 HG01258.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.263+552A>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14645161 | |||||||
| chr16:14645509 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.263+900T>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14645509 | |||||||
| chr16:14645840 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.263+1231T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14645840 | |||||||
| chr16:14645866 | C | T | 172 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(169): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.263+1257C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14645866 | |||||||
| chr16:14646047 | T | A | 1 | a0001c0001t0001g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.263+1438T>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14646047 | |||||||
| chr16:14646117 | T | A | 4 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(1): Show |
4 | HG00733.hp2 HG01175.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+1508T>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14646117 | |||||||
| chr16:14646156 | G | C | 1 | a0001c0001t0001g0161 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.263+1547G>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14646156 | |||||||
| chr16:14646242 | G | A | 1 | a0007c0007t0001g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.263+1633G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14646242 | |||||||
| chr16:14646431 | G | A | 4 | a0002c0002t0006g0251 a0002c0002t0006g0253 a0002c0002t0006g0254 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+1822G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14646431 | |||||||
| chr16:14646451 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0091 a0001c0001t0001g0092 others(1): Show |
5 | HG03098.hp1 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.263+1842G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14646451 | |||||||
| chr16:14646601 | T | C | 69 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0055 others(66): Show |
86 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.264-1787T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14646601 | |||||||
| chr16:14646619 | C | T | 8 | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0043 others(5): Show |
9 | HG00099.hp1 HG02523.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.264-1769C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14646619 | |||||||
| chr16:14646725 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.264-1663C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14646725 | |||||||
| chr16:14646926 | G | A | 1 | a0002c0002t0001g0064 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.264-1462G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14646926 | |||||||
| chr16:14647246 | G | A | 1 | a0002c0002t0006g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.264-1142G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14647246 | |||||||
| chr16:14647274 | A | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0222 |
2 | NA18979.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.264-1114A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14647274 | |||||||
| chr16:14647424 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.264-964G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14647424 | |||||||
| chr16:14647617 | C | T | 1 | a0001c0001t0009g0149 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.264-771C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14647617 | |||||||
| chr16:14647677 | C | CA | 13 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(10): Show |
13 | HG00741.hp2 HG01123.hp2 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.264-696dupA | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr16 | 14647677 | ||||||
| chr16:14647685 | A | T | 1 | a0002c0002t0001g0077 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.264-703A>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14647685 | |||||||
| chr16:14648022 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.264-366C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14648022 | |||||||
| chr16:14648032 | G | T | 1 | a0001c0001t0001g0174 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.264-356G>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14648032 | |||||||
| chr16:14648039 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.264-349A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14648039 | |||||||
| chr16:14648327 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.264-61G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 2/7 | chr16 | 14648327 | |||||||
| chr16:14648769 | T | C | 1 | a0002c0002t0001g0077 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.468+177T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 3/7 | chr16 | 14648769 | |||||||
| chr16:14648956 | A | G | 1 | a0002c0002t0001g0077 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.468+364A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 3/7 | chr16 | 14648956 | |||||||
| chr16:14648960 | T | A | 1 | a0002c0002t0001g0077 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.468+368T>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 3/7 | chr16 | 14648960 | |||||||
| chr16:14649070 | C | CT | 14 | a0001c0001t0001g0056 a0001c0001t0001g0103 a0001c0001t0001g0133 others(11): Show |
14 | HG00639.hp2 HG01167.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.468+501dupT | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr16 | 14649070 | ||||||
| chr16:14649070 | CT | C | 34 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0037 others(31): Show |
36 | HG00639.hp1 HG01167.hp2 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.468+501delT | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr16 | 14649070 | ||||||
| chr16:14649093 | T | G | 1 | a0002c0002t0001g0077 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.468+501T>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 3/7 | chr16 | 14649093 | |||||||
| chr16:14649140 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0132 |
2 | NA18948.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.468+548A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 3/7 | chr16 | 14649140 | |||||||
| chr16:14649169 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.468+577G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 3/7 | chr16 | 14649169 | |||||||
| chr16:14649202 | A | C | 1 | a0001c0001t0001g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.469-602A>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 3/7 | chr16 | 14649202 | |||||||
| chr16:14649264 | T | TG | 4 | a0002c0002t0006g0251 a0002c0002t0006g0253 a0002c0002t0006g0254 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-536dupG | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr16 | 14649264 | ||||||
| chr16:14650151 | A | C | 4 | a0002c0002t0006g0251 a0002c0002t0006g0253 a0002c0002t0006g0254 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.638+178A>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14650151 | |||||||
| chr16:14650508 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.638+535C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14650508 | |||||||
| chr16:14650755 | G | A | 1 | a0002c0002t0001g0079 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.638+782G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14650755 | |||||||
| chr16:14651033 | T | C | 1 | a0002c0002t0001g0066 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.638+1060T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14651033 | |||||||
| chr16:14651237 | C | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0172 a0001c0001t0001g0173 others(6): Show |
10 | HG02040.hp2 NA18942.hp1 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.638+1264C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14651237 | |||||||
| chr16:14651377 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.638+1404A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14651377 | |||||||
| chr16:14651438 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.638+1465A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14651438 | |||||||
| chr16:14651592 | A | C | 1 | a0001c0001t0001g0168 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.638+1619A>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14651592 | |||||||
| chr16:14651708 | A | G | 264 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(261): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.638+1735A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14651708 | |||||||
| chr16:14651867 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.638+1894C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14651867 | |||||||
| chr16:14651880 | A | AT | 20 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0040 others(17): Show |
22 | HG00597.hp2 HG00673.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.638+1932dupT | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr16 | 14651880 | ||||||
| chr16:14651880 | AT | A | 82 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0024 others(79): Show |
100 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.638+1932delT | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr16 | 14651880 | ||||||
| chr16:14651905 | T | A | 1 | a0003c0003t0004g0260 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.638+1932T>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14651905 | |||||||
| chr16:14652286 | A | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0107 |
2 | HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.638+2313A>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14652286 | |||||||
| chr16:14652721 | GT | G | 12 | a0001c0001t0001g0011 a0001c0001t0001g0172 a0001c0001t0001g0173 others(9): Show |
13 | HG00621.hp2 HG02040.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.639-2337delT | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr16 | 14652721 | ||||||
| chr16:14652733 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.639-2333T>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14652733 | |||||||
| chr16:14652952 | T | C | 19 | a0002c0002t0001g0007 a0002c0002t0001g0027 a0002c0002t0001g0031 others(16): Show |
20 | HG00558.hp2 HG00642.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.639-2114T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14652952 | |||||||
| chr16:14653031 | A | C | 1 | a0001c0001t0001g0217 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.639-2035A>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14653031 | |||||||
| chr16:14653042 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.639-2024C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14653042 | |||||||
| chr16:14653043 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.639-2023G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14653043 | |||||||
| chr16:14653088 | A | G | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00099.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.639-1978A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14653088 | |||||||
| chr16:14653257 | C | T | 3 | a0003c0003t0004g0258 a0003c0003t0004g0259 a0003c0003t0004g0260 |
3 | HG01891.hp2 HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.639-1809C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14653257 | |||||||
| chr16:14653291 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.639-1775G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14653291 | |||||||
| chr16:14653310 | T | C | 1 | a0002c0002t0001g0057 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.639-1756T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14653310 | |||||||
| chr16:14653541 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.639-1525G>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14653541 | |||||||
| chr16:14653616 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.639-1450C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14653616 | |||||||
| chr16:14653691 | T | C | 3 | a0002c0002t0006g0251 a0002c0002t0006g0253 a0002c0002t0010g0252 |
3 | HG02615.hp1 HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.639-1375T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14653691 | |||||||
| chr16:14653790 | C | T | 2 | a0004c0004t0001g0200 a0004c0004t0001g0201 |
2 | HG00735.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.639-1276C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14653790 | |||||||
| chr16:14654006 | C | CT | 30 | a0001c0001t0001g0020 a0001c0001t0001g0090 a0001c0001t0001g0091 others(27): Show |
31 | HG00735.hp1 HG01081.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.639-1037dupT | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr16 | 14654006 | ||||||
| chr16:14654006 | CT | C | 18 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0101 others(15): Show |
19 | HG01081.hp1 HG01256.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.639-1037delT | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr16 | 14654006 | ||||||
| chr16:14654006 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0095 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.639-1049_639-1037d others(15): Show |
BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr16 | 14654006 | ||||||
| chr16:14654052 | C | T | 32 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0040 others(29): Show |
35 | HG00099.hp2 HG00323.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.639-1014C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14654052 | |||||||
| chr16:14654202 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.639-864G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14654202 | |||||||
| chr16:14654247 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.639-819G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14654247 | |||||||
| chr16:14654406 | C | G | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG01071.hp2 HG01175.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.639-660C>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14654406 | |||||||
| chr16:14654421 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0179 a0001c0001t0001g0188 |
3 | HG02735.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.639-645T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14654421 | |||||||
| chr16:14654493 | C | CT | 22 | a0001c0001t0001g0040 a0001c0001t0001g0049 a0001c0001t0001g0054 others(19): Show |
22 | HG00673.hp2 HG01175.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.639-548dupT | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr16 | 14654493 | ||||||
| chr16:14654493 | CT | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0092 others(6): Show |
9 | HG01071.hp1 HG01106.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.639-548delT | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr16 | 14654493 | ||||||
| chr16:14654493 | CTTTTTT | C | 50 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(47): Show |
66 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.639-553_639-548del others(6): Show |
BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr16 | 14654493 | ||||||
| chr16:14654580 | T | G | 1 | a0001c0001t0001g0182 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.639-486T>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14654580 | |||||||
| chr16:14654593 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.639-473C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14654593 | |||||||
| chr16:14654916 | A | G | 14 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
15 | HG01071.hp2 HG01175.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.639-150A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14654916 | |||||||
| chr16:14655059 | T | A | 1 | a0001c0001t0001g0093 | 1 | HG03098.hp1 | splice_region_variant&intron_variant | LOW | c.639-7T>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 4/7 | chr16 | 14655059 | |||||||
| chr16:14655223 | AT | A | 21 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0041 others(18): Show |
22 | HG00140.hp2 HG01071.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.783+31delT | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr16 | 14655223 | ||||||
| chr16:14655256 | T | A | 1 | a0001c0001t0001g0042 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.783+46T>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14655256 | |||||||
| chr16:14655320 | T | C | 1 | a0002c0002t0006g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.783+110T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14655320 | |||||||
| chr16:14655360 | C | T | 1 | a0002c0002t0001g0224 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.783+150C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14655360 | |||||||
| chr16:14655720 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.783+510G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14655720 | |||||||
| chr16:14655769 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.783+559C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14655769 | |||||||
| chr16:14655844 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.783+634C>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14655844 | |||||||
| chr16:14655845 | G | A | 1 | a0001c0001t0001g0028 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.783+635G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14655845 | |||||||
| chr16:14655981 | G | T | 1 | a0001c0001t0001g0168 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.783+771G>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14655981 | |||||||
| chr16:14656150 | C | T | 3 | a0003c0003t0004g0258 a0003c0003t0004g0259 a0003c0003t0004g0260 |
3 | HG01891.hp2 HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.783+940C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14656150 | |||||||
| chr16:14656231 | A | G | 2 | a0003c0003t0004g0258 a0003c0003t0004g0259 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.783+1021A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14656231 | |||||||
| chr16:14656270 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.783+1060T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14656270 | |||||||
| chr16:14656271 | A | C | 1 | a0001c0001t0001g0168 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.783+1061A>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14656271 | |||||||
| chr16:14656273 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.783+1063T>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14656273 | |||||||
| chr16:14656750 | C | T | 161 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(158): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.783+1540C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14656750 | |||||||
| chr16:14656800 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.783+1590G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14656800 | |||||||
| chr16:14656804 | A | C | 60 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0055 others(57): Show |
77 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.783+1594A>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14656804 | |||||||
| chr16:14656906 | C | G | 1 | a0002c0002t0001g0224 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.783+1696C>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14656906 | |||||||
| chr16:14657511 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.783+2301G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14657511 | |||||||
| chr16:14657638 | G | C | 1 | a0001c0001t0001g0194 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.783+2428G>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14657638 | |||||||
| chr16:14657731 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0207 |
2 | NA19090.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.783+2521G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14657731 | |||||||
| chr16:14658277 | C | A | 1 | a0001c0001t0001g0022 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.783+3067C>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14658277 | |||||||
| chr16:14658278 | A | G | 1 | a0001c0001t0001g0022 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.783+3068A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14658278 | |||||||
| chr16:14658403 | A | AGAT | 4 | a0002c0002t0001g0006 a0002c0002t0001g0170 a0002c0002t0001g0227 others(1): Show |
7 | HG00323.hp1 HG00735.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.783+3195_783+3197d others(5): Show |
BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr16 | 14658403 | ||||||
| chr16:14658594 | G | A | 1 | a0002c0002t0001g0225 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.784-3298G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14658594 | |||||||
| chr16:14658669 | C | T | 1 | a0002c0002t0006g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.784-3223C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14658669 | |||||||
| chr16:14658776 | A | C | 1 | a0005c0005t0001g0073 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.784-3116A>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14658776 | |||||||
| chr16:14658777 | C | A | 1 | a0005c0005t0001g0073 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.784-3115C>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14658777 | |||||||
| chr16:14658847 | T | A | 4 | a0002c0002t0006g0251 a0002c0002t0006g0253 a0002c0002t0006g0254 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-3045T>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14658847 | |||||||
| chr16:14658908 | A | AT | 8 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0035 others(5): Show |
9 | HG01243.hp1 HG02622.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.784-2970dupT | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr16 | 14658908 | ||||||
| chr16:14659146 | T | C | 2 | a0001c0001t0003g0166 a0001c0001t0003g0167 |
2 | HG00733.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.784-2746T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14659146 | |||||||
| chr16:14659155 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.784-2737C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14659155 | |||||||
| chr16:14659224 | G | GT | 4 | a0002c0002t0006g0251 a0002c0002t0006g0253 a0002c0002t0006g0254 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-2668_784-2667i others(3): Show |
BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14659224 | |||||||
| chr16:14659225 | G | T | 4 | a0002c0002t0006g0251 a0002c0002t0006g0253 a0002c0002t0006g0254 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-2667G>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14659225 | |||||||
| chr16:14659234 | G | T | 2 | a0002c0002t0004g0047 a0002c0002t0004g0048 |
2 | HG01081.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.784-2658G>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14659234 | |||||||
| chr16:14659244 | G | T | 9 | a0002c0002t0004g0047 a0002c0002t0004g0048 a0002c0002t0006g0251 others(6): Show |
9 | HG01081.hp2 HG01255.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.784-2648G>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14659244 | |||||||
| chr16:14659249 | T | G | 4 | a0002c0002t0006g0251 a0002c0002t0006g0253 a0002c0002t0006g0254 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-2643T>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14659249 | |||||||
| chr16:14659251 | G | T | 9 | a0002c0002t0004g0047 a0002c0002t0004g0048 a0002c0002t0006g0251 others(6): Show |
9 | HG01081.hp2 HG01255.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.784-2641G>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14659251 | |||||||
| chr16:14659402 | G | T | 12 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0175 others(9): Show |
13 | HG00140.hp2 HG00642.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.784-2490G>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14659402 | |||||||
| chr16:14659590 | G | A | 2 | a0002c0002t0004g0047 a0002c0002t0004g0048 |
2 | HG01081.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.784-2302G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14659590 | |||||||
| chr16:14659636 | C | T | 1 | a0001c0001t0002g0145 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.784-2256C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14659636 | |||||||
| chr16:14659843 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.784-2049G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14659843 | |||||||
| chr16:14659983 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.784-1909A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14659983 | |||||||
| chr16:14660016 | T | G | 1 | a0001c0001t0001g0044 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.784-1876T>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14660016 | |||||||
| chr16:14660331 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.784-1561C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14660331 | |||||||
| chr16:14660369 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.784-1523C>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14660369 | |||||||
| chr16:14660411 | C | T | 1 | a0003c0003t0004g0260 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.784-1481C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14660411 | |||||||
| chr16:14660437 | C | T | 2 | a0002c0002t0004g0047 a0002c0002t0004g0048 |
2 | HG01081.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.784-1455C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14660437 | |||||||
| chr16:14660446 | C | A | 1 | a0002c0002t0004g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.784-1446C>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14660446 | |||||||
| chr16:14660452 | A | G | 1 | a0002c0002t0004g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.784-1440A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14660452 | |||||||
| chr16:14660584 | C | CT | 55 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0055 others(52): Show |
71 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.784-1291dupT | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr16 | 14660584 | ||||||
| chr16:14660584 | CT | C | 6 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0118 others(3): Show |
6 | HG01167.hp1 HG02735.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.784-1291delT | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr16 | 14660584 | ||||||
| chr16:14660619 | C | G | 70 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0055 others(67): Show |
87 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.784-1273C>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14660619 | |||||||
| chr16:14660667 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0241 a0001c0001t0001g0242 |
3 | HG00642.hp2 HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.784-1225G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14660667 | |||||||
| chr16:14660993 | G | A | 2 | a0002c0002t0001g0053 a0002c0002t0001g0067 |
2 | NA18941.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.784-899G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14660993 | |||||||
| chr16:14661032 | A | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0188 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.784-860A>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14661032 | |||||||
| chr16:14661343 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.784-549C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14661343 | |||||||
| chr16:14661392 | C | CT | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(109): Show |
137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.784-473dupT | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr16 | 14661392 | ||||||
| chr16:14661392 | C | CTT | 23 | a0001c0001t0001g0056 a0001c0001t0001g0126 a0001c0001t0001g0162 others(20): Show |
28 | HG00323.hp1 HG00733.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.784-474_784-473dup others(2): Show |
BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr16 | 14661392 | ||||||
| chr16:14661548 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.784-344A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14661548 | |||||||
| chr16:14661646 | G | A | 3 | a0003c0003t0004g0258 a0003c0003t0004g0259 a0003c0003t0004g0260 |
3 | HG01891.hp2 HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.784-246G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14661646 | |||||||
| chr16:14661683 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.784-209C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 5/7 | chr16 | 14661683 | |||||||
| chr16:14662584 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0188 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.957+519A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 6/7 | chr16 | 14662584 | |||||||
| chr16:14662604 | C | T | 52 | a0001c0001t0001g0174 a0002c0002t0001g0001 a0002c0002t0001g0006 others(49): Show |
68 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.957+539C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 6/7 | chr16 | 14662604 | |||||||
| chr16:14662821 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.957+756A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 6/7 | chr16 | 14662821 | |||||||
| chr16:14662840 | T | C | 4 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
4 | HG02055.hp2 HG02280.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.957+775T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 6/7 | chr16 | 14662840 | |||||||
| chr16:14662865 | C | G | 1 | a0001c0001t0001g0022 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.957+800C>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 6/7 | chr16 | 14662865 | |||||||
| chr16:14663687 | G | A | 1 | a0002c0002t0001g0074 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.958-1182G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 6/7 | chr16 | 14663687 | |||||||
| chr16:14663963 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0179 a0001c0001t0001g0188 |
3 | HG02735.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.958-906C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 6/7 | chr16 | 14663963 | |||||||
| chr16:14664032 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG00673.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.958-837A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 6/7 | chr16 | 14664032 | |||||||
| chr16:14664259 | T | C | 4 | a0002c0002t0006g0251 a0002c0002t0006g0253 a0002c0002t0006g0254 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.958-610T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 6/7 | chr16 | 14664259 | |||||||
| chr16:14664323 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.958-546G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 6/7 | chr16 | 14664323 | |||||||
| chr16:14664390 | C | CA | 60 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(57): Show |
64 | HG00099.hp2 HG00323.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.958-459dupA | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr16 | 14664390 | ||||||
| chr16:14664390 | CA | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0086 a0001c0001t0001g0098 others(10): Show |
15 | HG01496.hp2 HG01515.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.958-459delA | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr16 | 14664390 | ||||||
| chr16:14664406 | A | C | 9 | a0002c0002t0004g0047 a0002c0002t0004g0048 a0002c0002t0006g0251 others(6): Show |
9 | HG01081.hp2 HG01255.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.958-463A>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 6/7 | chr16 | 14664406 | |||||||
| chr16:14664524 | C | G | 9 | a0002c0002t0004g0047 a0002c0002t0004g0048 a0002c0002t0006g0251 others(6): Show |
9 | HG01081.hp2 HG01255.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.958-345C>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 6/7 | chr16 | 14664524 | |||||||
| chr16:14664749 | C | T | 1 | a0002c0002t0001g0072 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.958-120C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 6/7 | chr16 | 14664749 | |||||||
| chr16:14665235 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1160+164C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | chr16 | 14665235 | |||||||
| chr16:14665651 | T | A | 6 | a0001c0001t0001g0096 a0002c0002t0004g0047 a0002c0002t0004g0048 others(3): Show |
6 | HG01081.hp2 HG01255.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1160+580T>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | chr16 | 14665651 | |||||||
| chr16:14665659 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1160+588C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | chr16 | 14665659 | |||||||
| chr16:14665677 | A | T | 2 | a0002c0002t0004g0047 a0002c0002t0004g0048 |
2 | HG01081.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1160+606A>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | chr16 | 14665677 | |||||||
| chr16:14665713 | CA | C | 4 | a0002c0002t0006g0251 a0002c0002t0006g0253 a0002c0002t0006g0254 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1160+644delA | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr16 | 14665713 | ||||||
| chr16:14665867 | C | T | 2 | a0002c0002t0004g0047 a0002c0002t0004g0048 |
2 | HG01081.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1160+796C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | chr16 | 14665867 | |||||||
| chr16:14665911 | A | G | 41 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
45 | HG00099.hp2 HG00323.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.1160+840A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | chr16 | 14665911 | |||||||
| chr16:14666258 | G | A | 8 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0151 others(5): Show |
9 | HG00738.hp2 HG00741.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1160+1187G>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | chr16 | 14666258 | |||||||
| chr16:14666387 | A | G | 4 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0230 others(1): Show |
4 | HG00099.hp2 HG01074.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1161-1248A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | chr16 | 14666387 | |||||||
| chr16:14666464 | G | C | 1 | a0002c0002t0001g0076 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1161-1171G>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | chr16 | 14666464 | |||||||
| chr16:14666480 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1161-1155A>G | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | chr16 | 14666480 | |||||||
| chr16:14666635 | C | A | 4 | a0002c0002t0006g0251 a0002c0002t0006g0253 a0002c0002t0006g0254 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1161-1000C>A | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | chr16 | 14666635 | |||||||
| chr16:14666813 | G | T | 1 | a0001c0001t0001g0099 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1161-822G>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | chr16 | 14666813 | |||||||
| chr16:14666877 | T | C | 3 | a0003c0003t0004g0258 a0003c0003t0004g0259 a0003c0003t0004g0260 |
3 | HG01891.hp2 HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1161-758T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | chr16 | 14666877 | |||||||
| chr16:14666901 | A | C | 2 | a0002c0002t0001g0065 a0002c0002t0001g0068 |
2 | HG02135.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1161-734A>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | chr16 | 14666901 | |||||||
| chr16:14667038 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1161-597C>T | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | chr16 | 14667038 | |||||||
| chr16:14667126 | G | C | 1 | a0002c0002t0001g0227 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1161-509G>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | chr16 | 14667126 | |||||||
| chr16:14667177 | A | AAAT | 31 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0032 others(28): Show |
33 | HG00140.hp2 HG00642.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1161-433_1161-431d others(5): Show |
BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr16 | 14667177 | ||||||
| chr16:14667545 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1161-90T>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | chr16 | 14667545 | |||||||
| chr16:14667574 | G | C | 1 | a0001c0001t0001g0033 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1161-61G>C | BFAR | ENSG00000103429.11 | transcript | ENST00000261658.7 | protein_coding | 7/7 | chr16 | 14667574 |