Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79370 |
| ensemblid | ENSG00000121380.12 |
| hgncid | 16657 |
| symbol | BCL2L14 |
| name | BCL2 like 14 |
| refseq_nuc | NM_138723.2 |
| refseq_prot | NP_620049.1 |
| ensembl_nuc | ENST00000308721.9 |
| ensembl_prot | ENSP00000309132.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 12070939 |
| end | 12099695 |
| strand | + |
| ver | v1.2 |
| region | chr12:12070939-12099695 |
| region5000 | chr12:12065939-12104695 |
| regionname0 | BCL2L14_chr12_12070939_12099695 |
| regionname5000 | BCL2L14_chr12_12065939_12104695 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 327 | 410 | 72 | 72 | 199 | 17 | 48 | 153 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | MCSTS others(322): Show |
chr12 | 12065939 | 12104695 |
| a0002 | 0/0 | 327 | 23 | 8 | 5 | 10 | 0 | 0 | 8 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | MCSTS others(322): Show |
chr12 | 12065939 | 12104695 |
| a0003 | 0/0 | 327 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | MCSTS others(322): Show |
chr12 | 12065939 | 12104695 |
| a0004 | 0/0 | 327 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | MCSTS others(322): Show |
chr12 | 12065939 | 12104695 |
| a0005 | 0/0 | 327 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | MCSTS others(322): Show |
chr12 | 12065939 | 12104695 |
| a0006 | 0/0 | 327 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | MCSTS others(322): Show |
chr12 | 12065939 | 12104695 |
| a0007 | 0/0 | 327 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | MCSTS others(322): Show |
chr12 | 12065939 | 12104695 |
| a0008 | 0/0 | 327 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | MCSTS others(322): Show |
chr12 | 12065939 | 12104695 |
| a0009 | 0/0 | 327 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | MCSTS others(322): Show |
chr12 | 12065939 | 12104695 |
| a0010 | 0/0 | 327 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | MCSTS others(322): Show |
chr12 | 12065939 | 12104695 |
| a0011 | 0/0 | 327 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | MCSTS others(322): Show |
chr12 | 12065939 | 12104695 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 981 | 189 | 28 | 28 | 101 | 4 | 27 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0001c0002 | 0/1 | 981 | 164 | 22 | 28 | 93 | 5 | 15 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0001c0003 | 0/0 | 981 | 43 | 9 | 15 | 5 | 8 | 6 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0001c0007 | 0/0 | 981 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0001c0008 | 0/0 | 981 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0001c0011 | 0/0 | 981 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0001c0015 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0001c0021 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0001c0022 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0001c0024 | 0/0 | 981 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0001c0026 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0002c0004 | 0/0 | 981 | 15 | 2 | 5 | 8 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0002c0005 | 0/0 | 981 | 6 | 6 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0002c0014 | 0/0 | 981 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0003c0006 | 0/0 | 981 | 4 | 4 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0003c0012 | 0/0 | 981 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0003c0017 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0004c0010 | 0/0 | 981 | 3 | 1 | 2 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0004c0023 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0005c0009 | 0/0 | 981 | 3 | 0 | 2 | 0 | 1 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0006c0013 | 0/0 | 981 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0007c0018 | 0/0 | 981 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0008c0025 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0009c0019 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0010c0016 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 | ||
| a0011c0020 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | ATGTG others(976): Show |
chr12 | 12065939 | 12104695 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1897 | 182 | 28 | 25 | 98 | 4 | 26 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0001c0001t0002 | 0/0 | 1897 | 5 | 0 | 2 | 3 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0001c0001t0005 | 0/0 | 1897 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0001c0001t0007 | 0/0 | 1897 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0001c0002t0001 | 0/0 | 1897 | 43 | 7 | 8 | 26 | 0 | 2 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0001c0002t0002 | 0/1 | 1897 | 117 | 11 | 20 | 67 | 5 | 13 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0001c0002t0003 | 0/0 | 1897 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0001c0002t0004 | 0/0 | 1897 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0001c0003t0001 | 0/0 | 1897 | 43 | 9 | 15 | 5 | 8 | 6 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0001c0007t0001 | 0/0 | 1897 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0001c0008t0001 | 0/0 | 1897 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0001c0011t0001 | 0/0 | 1897 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0001c0015t0001 | 0/0 | 1897 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0001c0021t0001 | 0/0 | 1897 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0001c0022t0001 | 0/0 | 1897 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0001c0024t0002 | 0/0 | 1897 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0001c0026t0008 | 0/0 | 1897 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0002c0004t0001 | 0/0 | 1897 | 14 | 2 | 5 | 7 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0002c0004t0002 | 0/0 | 1897 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0002c0005t0001 | 0/0 | 1897 | 6 | 6 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0002c0014t0001 | 0/0 | 1897 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0003c0006t0001 | 0/0 | 1897 | 4 | 4 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0003c0012t0001 | 0/0 | 1897 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0003c0017t0006 | 0/0 | 1897 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0004c0010t0001 | 0/0 | 1897 | 3 | 1 | 2 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0004c0023t0001 | 0/0 | 1897 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0005c0009t0001 | 0/0 | 1897 | 3 | 0 | 2 | 0 | 1 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0006c0013t0001 | 0/0 | 1897 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0007c0018t0001 | 0/0 | 1897 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0008c0025t0001 | 0/0 | 1897 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0009c0019t0001 | 0/0 | 1897 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0010c0016t0001 | 0/0 | 1897 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| a0011c0020t0001 | 0/0 | 1897 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | CTCTT others(1892): Show |
chr12 | 12065939 | 12104695 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 18 | 3 | 2 | 12 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0287 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0001t0007g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0275 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0002g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0003g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0002t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0005 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0003t0001g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0007t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0007t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0008t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0008t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0008t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0011t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0011t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0011t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0015t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0021t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0022t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0024t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0001c0026t0008g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0004t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0004t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0004t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0004t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0004t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0004t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0004t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0004t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0004t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0004t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0004t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0005t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0005t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0005t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0005t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0005t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0014t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0002c0014t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0003c0006t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0003c0006t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0003c0006t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0003c0006t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0003c0012t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0003c0017t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0004c0010t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0004c0010t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0004c0023t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0005c0009t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0005c0009t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0005c0009t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0006c0013t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0006c0013t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0007c0018t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0008c0025t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0009c0019t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0010c0016t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| a0011c0020t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0373 | EUR | GBR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0273 | EUR | GBR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00140 | hp2 | a0005 | c0009 | t0001 | g0219 | EUR | GBR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0229 | EUR | FIN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0190 | EUR | FIN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0133 | EUR | FIN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0187 | EUR | FIN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0342 | EAS | CHS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | CHS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | CHS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0331 | EAS | CHS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0139 | EAS | CHS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | CHS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | CHS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0352 | EAS | CHS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0066 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0123 | EAS | CHS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0065 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0045 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0226 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0369 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0188 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0372 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0153 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01081 | hp2 | a0005 | c0009 | t0001 | g0338 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0028 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0210 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0260 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0134 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01167 | hp2 | a0004 | c0010 | t0001 | g0039 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01169 | hp1 | a0004 | c0010 | t0001 | g0039 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0317 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0022 | AMR | PUR | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0158 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0045 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0272 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0374 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0217 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01361 | hp2 | a0002 | c0004 | t0001 | g0361 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0038 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01433 | hp2 | a0001 | c0024 | t0002 | g0299 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0295 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0311 | EUR | IBS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0037 | EUR | IBS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0136 | EUR | IBS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0005 | EUR | IBS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0005 | EUR | IBS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0037 | EUR | IBS | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01884 | hp1 | a0002 | c0005 | t0001 | g0041 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01928 | hp2 | a0002 | c0004 | t0001 | g0220 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0018 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0309 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0362 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01952 | hp1 | a0002 | c0004 | t0001 | g0249 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01952 | hp2 | a0001 | c0003 | t0001 | g0252 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0128 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01993 | hp2 | a0005 | c0009 | t0001 | g0130 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02004 | hp1 | a0007 | c0018 | t0001 | g0277 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0152 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0365 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02040 | hp1 | a0002 | c0004 | t0001 | g0323 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0291 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0370 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02071 | hp2 | a0002 | c0004 | t0001 | g0364 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0371 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0057 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02148 | hp1 | a0002 | c0004 | t0001 | g0280 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0028 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0351 | EAS | CDX | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | CDX | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | CDX | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CDX | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0284 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0297 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02258 | hp1 | a0002 | c0005 | t0001 | g0041 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0278 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02280 | hp1 | a0003 | c0006 | t0001 | g0058 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02293 | hp1 | a0002 | c0004 | t0001 | g0202 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0344 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PEL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02451 | hp1 | a0008 | c0025 | t0001 | g0294 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0348 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02572 | hp1 | a0001 | c0008 | t0001 | g0197 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02572 | hp2 | a0001 | c0002 | t0004 | g0206 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0359 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02622 | hp1 | a0003 | c0006 | t0001 | g0096 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02622 | hp2 | a0003 | c0012 | t0001 | g0012 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0131 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0205 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0306 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0376 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0159 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0282 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0085 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02717 | hp2 | a0001 | c0002 | t0004 | g0302 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02723 | hp1 | a0001 | c0007 | t0001 | g0013 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0375 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0336 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0332 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0117 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02809 | hp1 | a0003 | c0012 | t0001 | g0012 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0288 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02818 | hp2 | a0002 | c0005 | t0001 | g0241 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02886 | hp1 | a0001 | c0021 | t0001 | g0200 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02886 | hp2 | a0003 | c0017 | t0006 | g0059 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02895 | hp1 | a0001 | c0011 | t0001 | g0178 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02895 | hp2 | a0001 | c0015 | t0001 | g0285 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0062 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02896 | hp2 | a0001 | c0011 | t0001 | g0179 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02922 | hp1 | a0006 | c0013 | t0001 | g0086 | AFR | ESN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02965 | hp1 | a0002 | c0005 | t0001 | g0076 | AFR | ESN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0129 | AFR | ESN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02970 | hp1 | a0001 | c0026 | t0008 | g0208 | AFR | ESN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02970 | hp2 | a0009 | c0019 | t0001 | g0063 | AFR | ESN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0018 | AFR | ESN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02976 | hp2 | a0001 | c0008 | t0001 | g0118 | AFR | ESN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0189 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0185 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03098 | hp1 | a0001 | c0022 | t0001 | g0199 | AFR | MSL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03098 | hp2 | a0003 | c0006 | t0001 | g0110 | AFR | MSL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0286 | AFR | ESN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03130 | hp2 | a0002 | c0005 | t0001 | g0196 | AFR | ESN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03139 | hp2 | a0001 | c0007 | t0001 | g0013 | AFR | ESN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03195 | hp2 | a0001 | c0008 | t0001 | g0301 | AFR | ESN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03225 | hp1 | a0002 | c0005 | t0001 | g0233 | AFR | MSL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0276 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0316 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03453 | hp2 | a0002 | c0004 | t0001 | g0198 | AFR | MSL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0162 | AFR | MSL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | ESN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | MSL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03579 | hp2 | a0001 | c0011 | t0001 | g0193 | AFR | MSL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0026 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0201 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | STU | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0184 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0144 | SAS | BEB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | BEB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG04115 | hp1 | a0001 | c0003 | t0001 | g0068 | SAS | STU | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0146 | SAS | STU | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0026 | SAS | BEB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG04199 | hp1 | a0001 | c0001 | t0005 | g0120 | SAS | STU | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0177 | SAS | STU | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | STU | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0038 | SAS | STU | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18522 | hp2 | a0004 | c0010 | t0001 | g0204 | AFR | YRI | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | CHB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | CHB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | CHB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | YRI | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0283 | AFR | YRI | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0363 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0347 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0355 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0353 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18957 | hp1 | a0001 | c0003 | t0001 | g0218 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18959 | hp1 | a0002 | c0004 | t0001 | g0244 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18962 | hp1 | a0002 | c0004 | t0001 | g0264 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18966 | hp2 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0314 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18977 | hp2 | a0002 | c0014 | t0001 | g0071 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18979 | hp1 | a0002 | c0004 | t0001 | g0247 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18989 | hp2 | a0002 | c0004 | t0002 | g0098 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18992 | hp1 | a0001 | c0002 | t0002 | g0368 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0356 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18995 | hp2 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18997 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0308 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19004 | hp2 | a0002 | c0004 | t0001 | g0116 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19012 | hp1 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | LWK | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19030 | hp2 | a0006 | c0013 | t0001 | g0289 | AFR | LWK | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19043 | hp1 | a0001 | c0007 | t0001 | g0194 | AFR | LWK | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19043 | hp2 | a0010 | c0016 | t0001 | g0060 | AFR | LWK | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19055 | hp1 | a0002 | c0004 | t0001 | g0251 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19060 | hp1 | a0011 | c0020 | t0001 | g0014 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19060 | hp2 | a0002 | c0014 | t0001 | g0182 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0367 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0326 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | YRI | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA19240 | hp2 | a0002 | c0004 | t0001 | g0300 | AFR | YRI | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA20129 | hp1 | a0004 | c0023 | t0001 | g0298 | AFR | ASW | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0024 | AFR | ASW | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0191 | EUR | TSI | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | TSI | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0307 | EUR | TSI | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0360 | SAS | GIH | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0216 | SAS | GIH | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0230 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0243 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0084 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0061 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0222 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0053 | AFR | ACB | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03471 | hp1 | a0001 | c0002 | t0003 | g0290 | AFR | MSL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG03471 | hp2 | a0003 | c0006 | t0001 | g0296 | AFR | MSL | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | USA | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | USA | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | USA | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | USA | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0275 | REF | REF | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0287 | REF | REF | BCL2L14_chr12_12065939_12104695 | BCL2L14 | chr12 | 12065939 | 12104695 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:12079370 | T | C | 2 | a0003 a0010 |
8 | HG02280.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
missense_variant | MODERATE | c.65T>C | p.Ile22Thr | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/6 | 271/1897 | 65/984 | 22/327 | chr12 | 12079370 | |||
| chr12:12079655 | A | G | 1 | a0008 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.350A>G | p.Gln117Arg | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/6 | 556/1897 | 350/984 | 117/327 | chr12 | 12079655 | |||
| chr12:12087281 | C | A | 1 | a0007 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.502C>A | p.Gln168Lys | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/6 | 708/1897 | 502/984 | 168/327 | chr12 | 12087281 | |||
| chr12:12087366 | T | A | 2 | a0006 a0010 |
3 | HG02922.hp1 NA19030.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.587T>A | p.Val196Glu | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/6 | 793/1897 | 587/984 | 196/327 | chr12 | 12087366 | |||
| chr12:12094760 | C | A | 1 | a0004 | 4 | HG01167.hp2 HG01169.hp1 NA18522.hp2 others(1): Show |
missense_variant | MODERATE | c.775C>A | p.Pro259Thr | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/6 | 981/1897 | 775/984 | 259/327 | chr12 | 12094760 | |||
| chr12:12094767 | G | A | 1 | a0009 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.782G>A | p.Gly261Glu | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/6 | 988/1897 | 782/984 | 261/327 | chr12 | 12094767 | |||
| chr12:12094817 | G | A | 1 | a0011 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.832G>A | p.Val278Ile | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/6 | 1038/1897 | 832/984 | 278/327 | chr12 | 12094817 | |||
| chr12:12094859 | A | T | 2 | a0002 a0009 |
24 | HG01361.hp2 HG01884.hp1 HG01928.hp2 others(21): Show |
missense_variant | MODERATE | c.874A>T | p.Arg292Trp | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/6 | 1080/1897 | 874/984 | 292/327 | chr12 | 12094859 | |||
| chr12:12094902 | C | T | 1 | a0005 | 3 | HG00140.hp2 HG01081.hp2 HG01993.hp2 |
missense_variant | MODERATE | c.917C>T | p.Ser306Leu | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/6 | 1123/1897 | 917/984 | 306/327 | chr12 | 12094902 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:12079323 | G | C | 1 | a0001c0015 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.18G>C | p.Gly6Gly | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/6 | 224/1897 | 18/984 | 6/327 | chr12 | 12079323 | |||
| chr12:12079386 | C | T | 1 | a0001c0026 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.81C>T | p.Leu27Leu | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/6 | 287/1897 | 81/984 | 27/327 | chr12 | 12079386 | |||
| chr12:12079512 | G | A | 1 | a0001c0007 | 3 | HG02723.hp1 HG03139.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.207G>A | p.Glu69Glu | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/6 | 413/1897 | 207/984 | 69/327 | chr12 | 12079512 | |||
| chr12:12079713 | C | T | 6 | a0001c0011 a0001c0021 a0001c0022 others(3): Show |
13 | HG01433.hp2 HG01884.hp1 HG02258.hp1 others(10): Show |
synonymous_variant | LOW | c.408C>T | p.Asn136Asn | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/6 | 614/1897 | 408/984 | 136/327 | chr12 | 12079713 | |||
| chr12:12087265 | C | T | 12 | a0001c0002 a0001c0003 a0001c0011 others(9): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
synonymous_variant | LOW | c.486C>T | p.Tyr162Tyr | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/6 | 692/1897 | 486/984 | 162/327 | chr12 | 12087265 | |||
| chr12:12094682 | T | C | 8 | a0001c0003 a0001c0008 a0001c0011 others(5): Show |
56 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(53): Show |
synonymous_variant | LOW | c.697T>C | p.Leu233Leu | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/6 | 903/1897 | 697/984 | 233/327 | chr12 | 12094682 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:12071013 | C | G | 1 | a0001c0001t0007 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-132C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/6 | 8293 | chr12 | 12071013 | ||||||
| chr12:12071013 | C | T | 1 | a0001c0026t0008 | 1 | HG02970.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-132C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/6 | chr12 | 12071013 | |||||||
| chr12:12099108 | C | T | 1 | a0001c0002t0004 | 2 | HG02572.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*120C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 6/6 | 120 | chr12 | 12099108 | ||||||
| chr12:12099144 | T | G | 4 | a0001c0001t0002 a0001c0002t0002 a0001c0024t0002 others(1): Show |
123 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*156T>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 6/6 | 156 | chr12 | 12099144 | ||||||
| chr12:12099152 | G | A | 1 | a0001c0001t0005 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*164G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 6/6 | 164 | chr12 | 12099152 | ||||||
| chr12:12099207 | C | T | 1 | a0003c0017t0006 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*219C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 6/6 | 219 | chr12 | 12099207 | ||||||
| chr12:12099343 | A | G | 1 | a0001c0002t0003 | 2 | HG02723.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*355A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 6/6 | 355 | chr12 | 12099343 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:12071196 | C | T | 1 | a0001c0003t0001g0376 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-8+59C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12071196 | |||||||
| chr12:12071272 | A | C | 1 | a0001c0002t0003g0375 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8+135A>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12071272 | |||||||
| chr12:12071550 | G | T | 7 | a0001c0002t0001g0370 a0001c0002t0001g0371 a0001c0003t0001g0005 others(4): Show |
10 | HG00099.hp1 HG00741.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+413G>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12071550 | |||||||
| chr12:12071609 | C | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0043 others(83): Show |
104 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-8+472C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12071609 | |||||||
| chr12:12071737 | A | G | 2 | a0001c0001t0001g0293 a0008c0025t0001g0294 |
2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-8+600A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12071737 | |||||||
| chr12:12071784 | G | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0019 others(277): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-8+647G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12071784 | |||||||
| chr12:12071829 | C | G | 1 | a0001c0003t0001g0283 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-8+692C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12071829 | |||||||
| chr12:12071878 | C | G | 279 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0019 others(276): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-8+741C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12071878 | |||||||
| chr12:12071961 | A | G | 2 | a0001c0001t0001g0281 a0001c0002t0002g0282 |
2 | HG01069.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-8+824A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12071961 | |||||||
| chr12:12072273 | C | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0043 others(103): Show |
127 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.-8+1136C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12072273 | |||||||
| chr12:12072281 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-8+1144G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12072281 | |||||||
| chr12:12072297 | T | C | 1 | a0001c0003t0001g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8+1160T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12072297 | |||||||
| chr12:12072329 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-8+1192G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12072329 | |||||||
| chr12:12072345 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-8+1208C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12072345 | |||||||
| chr12:12072368 | C | T | 56 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(53): Show |
65 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.-8+1231C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12072368 | |||||||
| chr12:12072411 | C | T | 1 | a0001c0002t0002g0253 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-8+1274C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12072411 | |||||||
| chr12:12072479 | G | C | 1 | a0001c0001t0001g0052 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-8+1342G>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12072479 | |||||||
| chr12:12072521 | A | G | 3 | a0001c0001t0001g0279 a0001c0002t0002g0278 a0002c0004t0001g0280 |
3 | HG02148.hp1 HG02273.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-8+1384A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12072521 | |||||||
| chr12:12072522 | T | C | 2 | a0001c0002t0002g0307 a0001c0003t0001g0306 |
2 | HG02683.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-8+1385T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12072522 | |||||||
| chr12:12072631 | A | G | 368 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(365): Show |
442 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(439): Show |
intron_variant | MODIFIER | c.-8+1494A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12072631 | |||||||
| chr12:12072672 | A | T | 1 | a0001c0003t0001g0205 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-8+1535A>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12072672 | |||||||
| chr12:12072679 | A | G | 76 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0043 others(73): Show |
93 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.-8+1542A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12072679 | |||||||
| chr12:12072807 | T | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0043 others(76): Show |
96 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.-8+1670T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12072807 | |||||||
| chr12:12072876 | GT | G | 165 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0029 others(162): Show |
196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-8+1750delT | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12072876 | ||||||
| chr12:12073001 | C | G | 1 | a0004c0010t0001g0204 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-8+1864C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12073001 | |||||||
| chr12:12073002 | T | A | 1 | a0001c0026t0008g0208 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-8+1865T>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12073002 | |||||||
| chr12:12073063 | T | A | 1 | a0001c0003t0001g0369 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-8+1926T>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12073063 | |||||||
| chr12:12073111 | G | T | 107 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0029 others(104): Show |
124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-8+1974G>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12073111 | |||||||
| chr12:12073180 | A | G | 11 | a0001c0001t0001g0195 a0001c0001t0001g0293 a0001c0007t0001g0194 others(8): Show |
11 | HG02451.hp1 HG02572.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8+2043A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12073180 | |||||||
| chr12:12073257 | G | C | 68 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(65): Show |
84 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.-8+2120G>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12073257 | |||||||
| chr12:12073370 | G | A | 53 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(50): Show |
62 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.-8+2233G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12073370 | |||||||
| chr12:12073442 | A | G | 1 | a0001c0002t0002g0368 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-8+2305A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12073442 | |||||||
| chr12:12073555 | G | A | 2 | a0001c0001t0001g0069 a0001c0002t0001g0070 |
2 | HG01496.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-8+2418G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12073555 | |||||||
| chr12:12073577 | C | T | 12 | a0001c0001t0001g0186 a0001c0001t0001g0192 a0001c0002t0002g0026 others(9): Show |
16 | HG00280.hp2 HG00323.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8+2440C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12073577 | |||||||
| chr12:12073598 | A | G | 44 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0180 others(41): Show |
50 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.-8+2461A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12073598 | |||||||
| chr12:12073602 | G | A | 2 | a0001c0001t0001g0293 a0008c0025t0001g0294 |
2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-8+2465G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12073602 | |||||||
| chr12:12073602 | G | GCA | 5 | a0001c0003t0001g0065 a0001c0003t0001g0369 a0001c0003t0001g0372 others(2): Show |
5 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+2478_-8+2479dup others(2): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12073602 | ||||||
| chr12:12073602 | G | GCACA | 13 | a0001c0001t0001g0195 a0001c0001t0001g0303 a0001c0002t0004g0302 others(10): Show |
13 | HG02572.hp1 HG02717.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+2476_-8+2479dup others(4): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12073602 | ||||||
| chr12:12073703 | T | G | 1 | a0001c0003t0001g0306 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-8+2566T>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12073703 | |||||||
| chr12:12073706 | C | T | 1 | a0001c0003t0001g0177 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-8+2569C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12073706 | |||||||
| chr12:12073806 | T | C | 10 | a0001c0001t0001g0049 a0001c0001t0001g0305 a0001c0002t0001g0297 others(7): Show |
11 | HG01433.hp2 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8+2669T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12073806 | |||||||
| chr12:12073913 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0176 |
3 | NA18944.hp2 NA18961.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.-8+2776C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12073913 | |||||||
| chr12:12073981 | C | A | 5 | a0001c0003t0001g0065 a0001c0003t0001g0369 a0001c0003t0001g0372 others(2): Show |
5 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+2844C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12073981 | |||||||
| chr12:12074161 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0019 others(211): Show |
264 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.-8+3024C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12074161 | |||||||
| chr12:12074186 | A | G | 365 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(362): Show |
439 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(436): Show |
intron_variant | MODIFIER | c.-8+3049A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12074186 | |||||||
| chr12:12074216 | C | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0019 others(167): Show |
214 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.-8+3079C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12074216 | |||||||
| chr12:12074295 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8+3158G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12074295 | |||||||
| chr12:12074320 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-8+3183A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12074320 | |||||||
| chr12:12074445 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-8+3308C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12074445 | |||||||
| chr12:12074469 | A | G | 370 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(367): Show |
444 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(441): Show |
intron_variant | MODIFIER | c.-8+3332A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12074469 | |||||||
| chr12:12074540 | G | GTGA | 5 | a0001c0001t0001g0072 a0001c0001t0001g0075 a0001c0002t0002g0073 others(2): Show |
5 | NA18977.hp2 NA18997.hp1 NA19078.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+3405_-8+3407dup others(3): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12074540 | ||||||
| chr12:12074560 | T | TC | 214 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0019 others(211): Show |
264 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.-8+3426dupC | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12074560 | ||||||
| chr12:12074656 | C | A | 1 | a0001c0002t0002g0028 | 2 | HG01099.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-8+3519C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12074656 | |||||||
| chr12:12074691 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0019 others(217): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.-8+3554G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12074691 | |||||||
| chr12:12074718 | C | T | 1 | a0001c0002t0002g0344 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-8+3581C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12074718 | |||||||
| chr12:12074728 | C | T | 13 | a0001c0001t0001g0195 a0001c0001t0001g0303 a0001c0002t0004g0302 others(10): Show |
13 | HG02572.hp1 HG02717.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+3591C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12074728 | |||||||
| chr12:12074730 | C | T | 2 | a0001c0011t0001g0178 a0001c0011t0001g0179 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-8+3593C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12074730 | |||||||
| chr12:12074731 | G | A | 49 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0207 others(46): Show |
57 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.-8+3594G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12074731 | |||||||
| chr12:12074786 | T | C | 1 | a0001c0002t0002g0077 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-8+3649T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12074786 | |||||||
| chr12:12074955 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-8+3818C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12074955 | |||||||
| chr12:12074960 | T | C | 1 | a0001c0002t0002g0359 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-8+3823T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12074960 | |||||||
| chr12:12074980 | CACTGT | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0019 others(287): Show |
351 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.-8+3849_-8+3853del others(5): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12074980 | ||||||
| chr12:12074988 | T | C | 2 | a0001c0001t0001g0293 a0001c0002t0003g0375 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-8+3851T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12074988 | |||||||
| chr12:12075049 | G | T | 13 | a0001c0001t0001g0195 a0001c0001t0001g0303 a0001c0002t0004g0302 others(10): Show |
13 | HG02572.hp1 HG02717.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+3912G>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12075049 | |||||||
| chr12:12075155 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8+4018G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12075155 | |||||||
| chr12:12075205 | C | A | 2 | a0001c0001t0001g0293 a0001c0002t0003g0375 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-8+4068C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12075205 | |||||||
| chr12:12075214 | C | G | 2 | a0001c0011t0001g0178 a0001c0011t0001g0179 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-8+4077C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12075214 | |||||||
| chr12:12075336 | T | G | 13 | a0001c0001t0001g0195 a0001c0001t0001g0303 a0001c0002t0004g0302 others(10): Show |
13 | HG02572.hp1 HG02717.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-3963T>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12075336 | |||||||
| chr12:12075410 | A | ATTCT | 3 | a0001c0001t0001g0254 a0001c0015t0001g0285 a0002c0004t0001g0251 |
3 | HG02895.hp2 NA19030.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.-7-3866_-7-3863dup others(4): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12075410 | ||||||
| chr12:12075410 | A | ATTCTTTC others(1): Show |
70 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0043 others(67): Show |
83 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.-7-3870_-7-3863dup others(8): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12075410 | ||||||
| chr12:12075410 | A | ATTCTTTC others(5): Show |
2 | a0001c0002t0002g0308 a0001c0002t0002g0309 |
2 | HG01934.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-7-3874_-7-3863dup others(12): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12075410 | ||||||
| chr12:12075410 | ATTCT | A | 108 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0029 others(105): Show |
124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-7-3866_-7-3863del others(4): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12075410 | ||||||
| chr12:12075410 | ATTCTTTC others(1): Show |
A | 21 | a0001c0001t0001g0049 a0001c0001t0001g0192 a0001c0001t0001g0305 others(18): Show |
26 | HG00280.hp2 HG00323.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.-7-3870_-7-3863del others(8): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12075410 | ||||||
| chr12:12075429 | C | T | 1 | a0001c0002t0003g0375 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-7-3870C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12075429 | |||||||
| chr12:12075429 | CTTTCTTT others(1): Show |
C | 7 | a0001c0001t0001g0186 a0001c0002t0001g0128 a0001c0002t0002g0026 others(4): Show |
8 | HG01981.hp2 HG01993.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7-3866_-7-3859del others(8): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12075429 | ||||||
| chr12:12075433 | C | T | 2 | a0001c0001t0001g0293 a0001c0002t0003g0375 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-7-3866C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12075433 | |||||||
| chr12:12075433 | CTTTT | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0019 others(132): Show |
172 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.-7-3859_-7-3856del others(4): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12075433 | ||||||
| chr12:12075449 | G | A | 4 | a0001c0001t0001g0303 a0001c0002t0004g0302 a0001c0008t0001g0301 others(1): Show |
4 | HG02717.hp2 HG03195.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-3850G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12075449 | |||||||
| chr12:12075486 | C | T | 4 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(1): Show |
4 | NA18952.hp1 NA18956.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-3813C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12075486 | |||||||
| chr12:12075525 | A | G | 2 | a0001c0001t0001g0293 a0001c0002t0003g0375 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-7-3774A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12075525 | |||||||
| chr12:12075717 | C | G | 2 | a0001c0001t0001g0293 a0001c0002t0003g0375 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-7-3582C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12075717 | |||||||
| chr12:12075733 | T | A | 12 | a0001c0001t0001g0186 a0001c0001t0001g0192 a0001c0002t0002g0026 others(9): Show |
16 | HG00280.hp2 HG00323.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-7-3566T>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12075733 | |||||||
| chr12:12075735 | C | G | 2 | a0001c0001t0001g0293 a0001c0002t0003g0375 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-7-3564C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12075735 | |||||||
| chr12:12075774 | C | T | 1 | a0001c0001t0002g0274 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-7-3525C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12075774 | |||||||
| chr12:12075835 | G | C | 370 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(367): Show |
444 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(441): Show |
intron_variant | MODIFIER | c.-7-3464G>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12075835 | |||||||
| chr12:12075940 | G | A | 2 | a0001c0003t0001g0066 a0001c0003t0001g0210 |
2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.-7-3359G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12075940 | |||||||
| chr12:12075953 | T | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0019 others(269): Show |
331 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.-7-3346T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12075953 | |||||||
| chr12:12076059 | G | A | 13 | a0001c0001t0001g0195 a0001c0001t0001g0303 a0001c0002t0004g0302 others(10): Show |
13 | HG02572.hp1 HG02717.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-3240G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12076059 | |||||||
| chr12:12076099 | A | AGGGAGGG others(51): Show |
1 | a0001c0002t0001g0079 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-7-3197_-7-3196ins others(58): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12076099 | ||||||
| chr12:12076099 | A | AGGGGAGG others(23): Show |
11 | a0001c0001t0001g0027 a0001c0001t0001g0203 a0001c0001t0001g0279 others(8): Show |
12 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7-3095_-7-3066dup others(30): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12076099 | ||||||
| chr12:12076099 | A | AGGGGAGG others(53): Show |
2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | NA18985.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-7-3125_-7-3066dup others(60): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12076099 | ||||||
| chr12:12076099 | AGGGGAGG others(23): Show |
A | 63 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0049 others(60): Show |
72 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.-7-3095_-7-3066del others(30): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12076099 | ||||||
| chr12:12076148 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0293 |
2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-7-3151G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12076148 | |||||||
| chr12:12076292 | C | T | 14 | a0001c0001t0001g0195 a0001c0001t0001g0303 a0001c0002t0001g0162 others(11): Show |
14 | HG02572.hp1 HG02717.hp2 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.-7-3007C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12076292 | |||||||
| chr12:12076302 | C | T | 13 | a0001c0001t0001g0195 a0001c0001t0001g0303 a0001c0002t0004g0302 others(10): Show |
13 | HG02572.hp1 HG02717.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-2997C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12076302 | |||||||
| chr12:12076328 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-7-2971G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12076328 | |||||||
| chr12:12076331 | TTGCATGT others(8): Show |
T | 18 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0186 others(15): Show |
23 | HG00280.hp2 HG00323.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.-7-2953_-7-2939del others(15): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12076331 | ||||||
| chr12:12076453 | C | T | 11 | a0001c0001t0001g0040 a0001c0001t0001g0235 a0001c0001t0001g0239 others(8): Show |
13 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7-2846C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12076453 | |||||||
| chr12:12076502 | C | T | 6 | a0001c0001t0001g0303 a0001c0002t0004g0302 a0001c0008t0001g0301 others(3): Show |
6 | HG02717.hp2 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-2797C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12076502 | |||||||
| chr12:12076504 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-7-2795A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12076504 | |||||||
| chr12:12076525 | G | A | 3 | a0001c0001t0001g0040 a0004c0010t0001g0039 a0006c0013t0001g0289 |
5 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-2774G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12076525 | |||||||
| chr12:12076547 | G | T | 6 | a0001c0001t0001g0303 a0001c0002t0004g0302 a0001c0008t0001g0301 others(3): Show |
6 | HG02717.hp2 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-2752G>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12076547 | |||||||
| chr12:12076548 | T | TATC | 11 | a0001c0001t0001g0040 a0001c0001t0001g0235 a0001c0001t0001g0239 others(8): Show |
13 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7-2750_-7-2748dup others(3): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12076548 | ||||||
| chr12:12076630 | C | G | 2 | a0001c0011t0001g0178 a0001c0011t0001g0179 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-7-2669C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12076630 | |||||||
| chr12:12076684 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-7-2615G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12076684 | |||||||
| chr12:12076852 | C | G | 34 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0075 others(31): Show |
40 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.-7-2447C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12076852 | |||||||
| chr12:12076915 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(118): Show |
150 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.-7-2384C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12076915 | |||||||
| chr12:12076916 | T | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(253): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.-7-2383T>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12076916 | |||||||
| chr12:12076941 | G | A | 1 | a0001c0002t0002g0099 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-7-2358G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12076941 | |||||||
| chr12:12077018 | C | T | 178 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0019 others(175): Show |
213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.-7-2281C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12077018 | |||||||
| chr12:12077187 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-7-2112C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12077187 | |||||||
| chr12:12077284 | G | A | 15 | a0001c0001t0001g0087 a0001c0001t0001g0235 a0001c0001t0001g0312 others(12): Show |
16 | HG00609.hp1 HG02015.hp1 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-7-2015G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12077284 | |||||||
| chr12:12077302 | G | A | 44 | a0001c0001t0001g0027 a0001c0001t0001g0049 a0001c0001t0001g0075 others(41): Show |
52 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.-7-1997G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12077302 | |||||||
| chr12:12077303 | A | G | 44 | a0001c0001t0001g0027 a0001c0001t0001g0049 a0001c0001t0001g0075 others(41): Show |
52 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.-7-1996A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12077303 | |||||||
| chr12:12077314 | G | A | 2 | a0001c0011t0001g0178 a0001c0011t0001g0179 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-7-1985G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12077314 | |||||||
| chr12:12077340 | C | G | 3 | a0001c0011t0001g0178 a0001c0011t0001g0179 a0001c0015t0001g0285 |
3 | HG02895.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-7-1959C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12077340 | |||||||
| chr12:12077344 | C | T | 3 | a0001c0011t0001g0178 a0001c0011t0001g0179 a0001c0015t0001g0285 |
3 | HG02895.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-7-1955C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12077344 | |||||||
| chr12:12077537 | C | CA | 176 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(173): Show |
212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.-7-1745dupA | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12077537 | ||||||
| chr12:12077537 | C | CAA | 9 | a0001c0001t0001g0109 a0001c0001t0001g0171 a0001c0001t0001g0262 others(6): Show |
9 | HG01123.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-1746_-7-1745dup others(2): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12077537 | ||||||
| chr12:12077588 | G | GA | 62 | a0001c0001t0001g0027 a0001c0001t0001g0049 a0001c0001t0001g0105 others(59): Show |
73 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-7-1703dupA | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12077588 | ||||||
| chr12:12077876 | G | A | 1 | a0002c0004t0001g0198 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-1423G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12077876 | |||||||
| chr12:12078004 | C | G | 284 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(281): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.-7-1295C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12078004 | |||||||
| chr12:12078214 | G | C | 1 | a0001c0002t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-7-1085G>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12078214 | |||||||
| chr12:12078261 | G | C | 371 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(368): Show |
445 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(442): Show |
intron_variant | MODIFIER | c.-7-1038G>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12078261 | |||||||
| chr12:12078284 | G | A | 1 | a0001c0002t0002g0367 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-7-1015G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12078284 | |||||||
| chr12:12078335 | G | A | 79 | a0001c0001t0001g0049 a0001c0001t0001g0105 a0001c0001t0001g0167 others(76): Show |
92 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.-7-964G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12078335 | |||||||
| chr12:12078335 | G | T | 3 | a0001c0001t0001g0303 a0001c0008t0001g0301 a0002c0004t0001g0300 |
3 | HG03195.hp2 NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-7-964G>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12078335 | |||||||
| chr12:12078403 | TA | T | 78 | a0001c0001t0001g0049 a0001c0001t0001g0105 a0001c0001t0001g0167 others(75): Show |
91 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.-7-894delA | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12078403 | ||||||
| chr12:12078609 | A | G | 3 | a0001c0001t0001g0072 a0001c0001t0001g0250 a0002c0004t0002g0098 |
3 | NA18989.hp2 NA18990.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-7-690A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12078609 | |||||||
| chr12:12078797 | C | CTTTTGTT | 335 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(332): Show |
405 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(402): Show |
intron_variant | MODIFIER | c.-7-501_-7-500insTT others(5): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12078797 | ||||||
| chr12:12078799 | G | GTTGTTTT | 34 | a0001c0001t0001g0040 a0001c0001t0001g0303 a0001c0002t0001g0297 others(31): Show |
38 | HG00099.hp1 HG01109.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.-7-489_-7-483dupTT others(5): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 12078799 | ||||||
| chr12:12078799 | G | T | 336 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(333): Show |
406 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(403): Show |
intron_variant | MODIFIER | c.-7-500G>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12078799 | |||||||
| chr12:12078821 | G | A | 2 | a0001c0001t0001g0195 a0004c0010t0001g0204 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-7-478G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12078821 | |||||||
| chr12:12078836 | C | T | 3 | a0001c0002t0001g0016 a0001c0002t0001g0079 a0001c0002t0001g0245 |
4 | HG02074.hp1 NA18982.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-463C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12078836 | |||||||
| chr12:12078852 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0019 others(204): Show |
247 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.-7-447A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12078852 | |||||||
| chr12:12078854 | T | C | 2 | a0001c0001t0001g0180 a0001c0001t0001g0324 |
2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-7-445T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12078854 | |||||||
| chr12:12078883 | G | A | 1 | a0001c0008t0001g0301 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-7-416G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12078883 | |||||||
| chr12:12078951 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-7-348C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12078951 | |||||||
| chr12:12078974 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-7-325T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12078974 | |||||||
| chr12:12078989 | C | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0019 others(76): Show |
97 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-7-310C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12078989 | |||||||
| chr12:12078992 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-7-307T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12078992 | |||||||
| chr12:12079085 | G | T | 1 | a0001c0008t0001g0197 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-7-214G>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12079085 | |||||||
| chr12:12079091 | G | A | 1 | a0001c0001t0001g0325 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-7-208G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12079091 | |||||||
| chr12:12079144 | C | T | 2 | a0001c0002t0002g0243 a0001c0002t0003g0375 |
2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-7-155C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 1/5 | chr12 | 12079144 | |||||||
| chr12:12079760 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.433+22C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12079760 | |||||||
| chr12:12079775 | G | A | 2 | a0001c0011t0001g0178 a0001c0011t0001g0179 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.433+37G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12079775 | |||||||
| chr12:12079847 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.433+109G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12079847 | |||||||
| chr12:12079924 | C | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0019 others(191): Show |
232 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.433+186C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12079924 | |||||||
| chr12:12079929 | G | A | 1 | a0001c0002t0002g0187 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.433+191G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12079929 | |||||||
| chr12:12079930 | C | T | 1 | a0001c0015t0001g0285 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.433+192C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12079930 | |||||||
| chr12:12079932 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0343 |
2 | HG03704.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.433+194C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12079932 | |||||||
| chr12:12079971 | A | G | 7 | a0003c0006t0001g0058 a0003c0006t0001g0096 a0003c0006t0001g0110 others(4): Show |
8 | HG02280.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.433+233A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12079971 | |||||||
| chr12:12079975 | C | T | 1 | a0001c0002t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.433+237C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12079975 | |||||||
| chr12:12079979 | T | C | 370 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(367): Show |
444 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(441): Show |
intron_variant | MODIFIER | c.433+241T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12079979 | |||||||
| chr12:12079986 | T | C | 1 | a0001c0003t0001g0068 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.433+248T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12079986 | |||||||
| chr12:12079987 | G | A | 1 | a0001c0003t0001g0068 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.433+249G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12079987 | |||||||
| chr12:12080014 | C | T | 3 | a0001c0003t0001g0066 a0001c0003t0001g0136 a0001c0003t0001g0153 |
3 | HG00639.hp1 HG01081.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.433+276C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080014 | |||||||
| chr12:12080020 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.433+282C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080020 | |||||||
| chr12:12080024 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.433+286A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080024 | |||||||
| chr12:12080028 | C | T | 1 | a0001c0001t0002g0271 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.433+290C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080028 | |||||||
| chr12:12080069 | T | G | 2 | a0001c0001t0001g0089 a0001c0002t0003g0290 |
2 | HG03471.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.433+331T>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080069 | |||||||
| chr12:12080073 | C | T | 71 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0019 others(68): Show |
86 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.433+335C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080073 | |||||||
| chr12:12080137 | G | A | 2 | a0001c0001t0001g0255 a0001c0003t0001g0317 |
2 | HG01243.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.433+399G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080137 | |||||||
| chr12:12080169 | C | G | 61 | a0001c0001t0001g0049 a0001c0001t0001g0105 a0001c0001t0001g0167 others(58): Show |
75 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.433+431C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080169 | |||||||
| chr12:12080199 | C | T | 12 | a0001c0011t0001g0178 a0001c0011t0001g0179 a0001c0011t0001g0193 others(9): Show |
13 | HG01884.hp1 HG02258.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.433+461C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080199 | |||||||
| chr12:12080201 | T | C | 1 | a0001c0003t0001g0066 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.433+463T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080201 | |||||||
| chr12:12080202 | CA | C | 140 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(137): Show |
170 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.433+477delA | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 12080202 | ||||||
| chr12:12080259 | T | A | 1 | a0001c0003t0001g0009 | 3 | HG03516.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.433+521T>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080259 | |||||||
| chr12:12080310 | C | T | 10 | a0001c0003t0001g0159 a0001c0003t0001g0260 a0001c0003t0001g0373 others(7): Show |
11 | HG00099.hp1 HG01109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.433+572C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080310 | |||||||
| chr12:12080329 | A | G | 12 | a0001c0001t0001g0040 a0001c0003t0001g0159 a0001c0003t0001g0260 others(9): Show |
15 | HG00099.hp1 HG01109.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.433+591A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080329 | |||||||
| chr12:12080330 | AAAG | A | 12 | a0001c0001t0001g0040 a0001c0003t0001g0159 a0001c0003t0001g0260 others(9): Show |
15 | HG00099.hp1 HG01109.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.433+596_433+598del others(3): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 12080330 | ||||||
| chr12:12080347 | G | A | 55 | a0001c0001t0001g0049 a0001c0001t0001g0105 a0001c0001t0001g0167 others(52): Show |
68 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.433+609G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080347 | |||||||
| chr12:12080386 | T | C | 59 | a0001c0001t0001g0040 a0001c0001t0001g0087 a0001c0001t0001g0235 others(56): Show |
69 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.433+648T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080386 | |||||||
| chr12:12080489 | G | A | 1 | a0002c0005t0001g0076 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.433+751G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080489 | |||||||
| chr12:12080507 | C | G | 1 | a0001c0002t0002g0355 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.433+769C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080507 | |||||||
| chr12:12080552 | G | A | 3 | a0001c0002t0002g0085 a0001c0002t0002g0243 a0001c0002t0003g0375 |
3 | HG02109.hp1 HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.433+814G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080552 | |||||||
| chr12:12080619 | C | CA | 71 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0056 others(68): Show |
83 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.433+899dupA | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 12080619 | ||||||
| chr12:12080849 | G | A | 2 | a0001c0002t0002g0103 a0001c0002t0002g0168 |
2 | NA18961.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.433+1111G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080849 | |||||||
| chr12:12080896 | C | T | 2 | a0006c0013t0001g0086 a0006c0013t0001g0289 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.433+1158C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080896 | |||||||
| chr12:12080917 | C | T | 15 | a0001c0002t0002g0085 a0001c0002t0002g0243 a0001c0002t0003g0375 others(12): Show |
16 | HG01884.hp1 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.433+1179C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080917 | |||||||
| chr12:12080943 | G | A | 28 | a0001c0001t0001g0087 a0001c0001t0001g0235 a0001c0001t0001g0312 others(25): Show |
34 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.433+1205G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080943 | |||||||
| chr12:12080952 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.433+1214G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12080952 | |||||||
| chr12:12081186 | C | A | 7 | a0003c0006t0001g0058 a0003c0006t0001g0096 a0003c0006t0001g0110 others(4): Show |
8 | HG02280.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.433+1448C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12081186 | |||||||
| chr12:12081320 | T | C | 45 | a0001c0001t0001g0087 a0001c0001t0001g0235 a0001c0001t0001g0312 others(42): Show |
52 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.433+1582T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12081320 | |||||||
| chr12:12081375 | A | G | 4 | a0001c0002t0002g0085 a0001c0002t0002g0243 a0001c0002t0004g0206 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.433+1637A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12081375 | |||||||
| chr12:12081386 | T | C | 62 | a0001c0001t0001g0049 a0001c0001t0001g0105 a0001c0001t0001g0167 others(59): Show |
76 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.433+1648T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12081386 | |||||||
| chr12:12081456 | C | CA | 49 | a0001c0001t0001g0019 a0001c0001t0001g0054 a0001c0001t0001g0072 others(46): Show |
57 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.433+1735dupA | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 12081456 | ||||||
| chr12:12081456 | C | CAA | 13 | a0001c0002t0001g0236 a0001c0002t0002g0154 a0001c0011t0001g0178 others(10): Show |
14 | HG01884.hp1 HG02258.hp1 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.433+1734_433+1735d others(4): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 12081456 | ||||||
| chr12:12081456 | CA | C | 62 | a0001c0001t0001g0049 a0001c0001t0001g0105 a0001c0001t0001g0167 others(59): Show |
76 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.433+1735delA | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 12081456 | ||||||
| chr12:12081526 | A | G | 1 | a0001c0002t0002g0077 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.433+1788A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12081526 | |||||||
| chr12:12081551 | A | AT | 116 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(113): Show |
138 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.433+1829dupT | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 12081551 | ||||||
| chr12:12081551 | AT | A | 11 | a0001c0001t0001g0040 a0001c0001t0001g0115 a0001c0001t0001g0212 others(8): Show |
13 | HG00099.hp1 HG01109.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.433+1829delT | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 12081551 | ||||||
| chr12:12081628 | G | C | 2 | a0001c0001t0001g0319 a0001c0002t0002g0347 |
2 | NA18944.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.433+1890G>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12081628 | |||||||
| chr12:12081645 | G | A | 29 | a0001c0001t0001g0087 a0001c0001t0001g0235 a0001c0001t0001g0312 others(26): Show |
35 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.433+1907G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12081645 | |||||||
| chr12:12081768 | A | C | 4 | a0001c0002t0002g0085 a0001c0002t0002g0243 a0001c0002t0004g0206 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.433+2030A>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12081768 | |||||||
| chr12:12081773 | G | A | 62 | a0001c0001t0001g0049 a0001c0001t0001g0105 a0001c0001t0001g0167 others(59): Show |
76 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.433+2035G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12081773 | |||||||
| chr12:12081775 | C | T | 62 | a0001c0001t0001g0049 a0001c0001t0001g0105 a0001c0001t0001g0167 others(59): Show |
76 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.433+2037C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12081775 | |||||||
| chr12:12081779 | G | A | 1 | a0001c0002t0002g0326 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.433+2041G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12081779 | |||||||
| chr12:12081902 | T | C | 1 | a0004c0010t0001g0039 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.433+2164T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12081902 | |||||||
| chr12:12081961 | A | C | 1 | a0001c0001t0001g0311 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.433+2223A>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12081961 | |||||||
| chr12:12082043 | T | A | 197 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(194): Show |
238 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.433+2305T>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12082043 | |||||||
| chr12:12082103 | G | A | 1 | a0001c0015t0001g0285 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.433+2365G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12082103 | |||||||
| chr12:12082220 | A | C | 1 | a0001c0001t0001g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.433+2482A>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12082220 | |||||||
| chr12:12082272 | G | A | 90 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(87): Show |
110 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.433+2534G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12082272 | |||||||
| chr12:12082284 | G | A | 90 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(87): Show |
110 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.433+2546G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12082284 | |||||||
| chr12:12082485 | A | C | 1 | a0001c0001t0001g0169 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.433+2747A>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12082485 | |||||||
| chr12:12082635 | T | G | 7 | a0003c0006t0001g0058 a0003c0006t0001g0096 a0003c0006t0001g0110 others(4): Show |
8 | HG02280.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.433+2897T>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12082635 | |||||||
| chr12:12082652 | A | G | 1 | a0001c0001t0001g0365 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.433+2914A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12082652 | |||||||
| chr12:12082859 | C | T | 153 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(150): Show |
187 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.433+3121C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12082859 | |||||||
| chr12:12082886 | G | C | 1 | a0001c0002t0002g0359 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.433+3148G>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12082886 | |||||||
| chr12:12082932 | G | A | 153 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(150): Show |
187 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.433+3194G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12082932 | |||||||
| chr12:12082933 | C | A | 153 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(150): Show |
187 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.433+3195C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12082933 | |||||||
| chr12:12083004 | A | C | 2 | a0001c0007t0001g0013 a0001c0007t0001g0194 |
3 | HG02723.hp1 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.433+3266A>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083004 | |||||||
| chr12:12083004 | A | G | 44 | a0001c0001t0001g0087 a0001c0001t0001g0235 a0001c0001t0001g0312 others(41): Show |
51 | HG00609.hp1 HG00642.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.433+3266A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083004 | |||||||
| chr12:12083054 | T | C | 2 | a0001c0002t0002g0326 a0001c0002t0002g0331 |
2 | HG00438.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.433+3316T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083054 | |||||||
| chr12:12083121 | C | A | 2 | a0006c0013t0001g0086 a0006c0013t0001g0289 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.433+3383C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083121 | |||||||
| chr12:12083164 | T | C | 371 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(368): Show |
445 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(442): Show |
intron_variant | MODIFIER | c.433+3426T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083164 | |||||||
| chr12:12083254 | G | A | 2 | a0006c0013t0001g0086 a0006c0013t0001g0289 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.433+3516G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083254 | |||||||
| chr12:12083311 | C | T | 1 | a0001c0002t0001g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.433+3573C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083311 | |||||||
| chr12:12083328 | A | AC | 3 | a0001c0002t0001g0265 a0001c0002t0002g0147 a0001c0003t0001g0222 |
3 | HG02559.hp1 NA18966.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.433+3592dupC | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 12083328 | ||||||
| chr12:12083419 | C | T | 152 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(149): Show |
186 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.433+3681C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083419 | |||||||
| chr12:12083449 | T | C | 44 | a0001c0001t0001g0087 a0001c0001t0001g0235 a0001c0001t0001g0312 others(41): Show |
51 | HG00609.hp1 HG00642.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.433+3711T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083449 | |||||||
| chr12:12083517 | G | A | 1 | a0001c0002t0003g0290 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.434-3696G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083517 | |||||||
| chr12:12083588 | T | C | 27 | a0001c0001t0001g0087 a0001c0001t0001g0235 a0001c0001t0001g0312 others(24): Show |
33 | HG00609.hp1 HG00642.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.434-3625T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083588 | |||||||
| chr12:12083632 | C | A | 28 | a0001c0001t0001g0087 a0001c0001t0001g0235 a0001c0001t0001g0312 others(25): Show |
34 | HG00609.hp1 HG00642.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.434-3581C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083632 | |||||||
| chr12:12083665 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.434-3548C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083665 | |||||||
| chr12:12083774 | G | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0032 others(51): Show |
67 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.434-3439G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083774 | |||||||
| chr12:12083817 | G | A | 1 | a0001c0002t0002g0368 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.434-3396G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083817 | |||||||
| chr12:12083819 | G | A | 263 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(260): Show |
323 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.434-3394G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083819 | |||||||
| chr12:12083838 | C | G | 1 | a0001c0001t0001g0232 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.434-3375C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083838 | |||||||
| chr12:12083881 | C | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(264): Show |
327 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(324): Show |
intron_variant | MODIFIER | c.434-3332C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083881 | |||||||
| chr12:12083882 | A | G | 1 | a0001c0003t0001g0222 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.434-3331A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083882 | |||||||
| chr12:12083929 | C | T | 2 | a0001c0007t0001g0013 a0001c0007t0001g0194 |
3 | HG02723.hp1 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.434-3284C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083929 | |||||||
| chr12:12083974 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.434-3239C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12083974 | |||||||
| chr12:12084176 | C | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(81): Show |
106 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(103): Show |
intron_variant | MODIFIER | c.434-3037C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12084176 | |||||||
| chr12:12084205 | C | T | 162 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(159): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.434-3008C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12084205 | |||||||
| chr12:12084225 | C | T | 2 | a0001c0002t0002g0085 a0001c0002t0002g0243 |
2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.434-2988C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12084225 | |||||||
| chr12:12084295 | C | T | 13 | a0001c0002t0001g0057 a0001c0002t0001g0297 a0001c0002t0002g0085 others(10): Show |
14 | HG00099.hp1 HG01109.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.434-2918C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12084295 | |||||||
| chr12:12084461 | C | A | 1 | a0001c0002t0002g0272 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.434-2752C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12084461 | |||||||
| chr12:12084525 | C | T | 2 | a0002c0005t0001g0196 a0002c0005t0001g0241 |
2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.434-2688C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12084525 | |||||||
| chr12:12084526 | G | A | 1 | a0002c0004t0001g0361 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.434-2687G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12084526 | |||||||
| chr12:12084537 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.434-2676C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12084537 | |||||||
| chr12:12084552 | G | C | 3 | a0001c0002t0003g0375 a0001c0011t0001g0178 a0001c0011t0001g0179 |
3 | HG02723.hp2 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.434-2661G>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12084552 | |||||||
| chr12:12084641 | AG | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0027 others(129): Show |
158 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.434-2570delG | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 12084641 | ||||||
| chr12:12084661 | T | C | 6 | a0001c0001t0001g0090 a0003c0006t0001g0058 a0003c0006t0001g0096 others(3): Show |
7 | HG02280.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.434-2552T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12084661 | |||||||
| chr12:12084689 | A | G | 4 | a0002c0004t0001g0202 a0002c0004t0001g0244 a0002c0004t0001g0264 others(1): Show |
4 | HG02148.hp1 HG02293.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.434-2524A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12084689 | |||||||
| chr12:12084795 | C | T | 233 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(230): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.434-2418C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12084795 | |||||||
| chr12:12084942 | C | T | 1 | a0001c0002t0002g0359 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.434-2271C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12084942 | |||||||
| chr12:12084946 | A | C | 156 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(153): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.434-2267A>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12084946 | |||||||
| chr12:12084947 | G | A | 2 | a0001c0002t0004g0206 a0001c0002t0004g0302 |
2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.434-2266G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12084947 | |||||||
| chr12:12085026 | G | A | 3 | a0001c0002t0001g0057 a0004c0010t0001g0039 a0004c0010t0001g0204 |
4 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-2187G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12085026 | |||||||
| chr12:12085039 | G | A | 39 | a0001c0002t0001g0070 a0001c0002t0001g0117 a0001c0002t0001g0128 others(36): Show |
50 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.434-2174G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12085039 | |||||||
| chr12:12085083 | CA | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(273): Show |
341 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(338): Show |
intron_variant | MODIFIER | c.434-2109delA | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 12085083 | ||||||
| chr12:12085083 | CAA | C | 83 | a0001c0001t0001g0083 a0001c0001t0001g0122 a0001c0001t0001g0132 others(80): Show |
92 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.434-2110_434-2109d others(4): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 12085083 | ||||||
| chr12:12085113 | C | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0032 others(76): Show |
87 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.434-2100C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12085113 | |||||||
| chr12:12085149 | C | T | 41 | a0001c0002t0001g0070 a0001c0002t0001g0117 a0001c0002t0001g0128 others(38): Show |
52 | HG00423.hp2 HG00639.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.434-2064C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12085149 | |||||||
| chr12:12085180 | T | A | 1 | a0001c0001t0001g0255 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.434-2033T>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12085180 | |||||||
| chr12:12085221 | G | C | 76 | a0001c0001t0001g0132 a0001c0001t0001g0160 a0001c0001t0001g0161 others(73): Show |
85 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.434-1992G>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12085221 | |||||||
| chr12:12085280 | T | C | 90 | a0001c0001t0001g0132 a0001c0001t0001g0160 a0001c0001t0001g0161 others(87): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.434-1933T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12085280 | |||||||
| chr12:12085340 | T | G | 1 | a0001c0002t0002g0368 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.434-1873T>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12085340 | |||||||
| chr12:12085383 | T | C | 83 | a0001c0001t0001g0132 a0001c0001t0001g0160 a0001c0001t0001g0161 others(80): Show |
94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.434-1830T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12085383 | |||||||
| chr12:12085421 | G | T | 65 | a0001c0001t0001g0132 a0001c0001t0001g0160 a0001c0001t0001g0161 others(62): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.434-1792G>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12085421 | |||||||
| chr12:12085477 | A | G | 53 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0032 others(50): Show |
60 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.434-1736A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12085477 | |||||||
| chr12:12085568 | A | T | 1 | a0001c0021t0001g0200 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.434-1645A>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12085568 | |||||||
| chr12:12085757 | G | T | 41 | a0001c0002t0001g0070 a0001c0002t0001g0117 a0001c0002t0001g0128 others(38): Show |
52 | HG00423.hp2 HG00639.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.434-1456G>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12085757 | |||||||
| chr12:12085764 | G | C | 83 | a0001c0001t0001g0132 a0001c0001t0001g0160 a0001c0001t0001g0161 others(80): Show |
94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.434-1449G>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12085764 | |||||||
| chr12:12085835 | C | A | 65 | a0001c0001t0001g0132 a0001c0001t0001g0160 a0001c0001t0001g0161 others(62): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.434-1378C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12085835 | |||||||
| chr12:12085856 | A | G | 111 | a0001c0001t0001g0090 a0001c0001t0001g0121 a0001c0001t0001g0132 others(108): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.434-1357A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12085856 | |||||||
| chr12:12085899 | G | A | 1 | a0001c0002t0002g0124 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.434-1314G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12085899 | |||||||
| chr12:12085998 | C | A | 1 | a0001c0002t0002g0131 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.434-1215C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12085998 | |||||||
| chr12:12086099 | C | A | 41 | a0001c0002t0001g0070 a0001c0002t0001g0117 a0001c0002t0001g0128 others(38): Show |
52 | HG00423.hp2 HG00639.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.434-1114C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12086099 | |||||||
| chr12:12086116 | A | C | 65 | a0001c0001t0001g0132 a0001c0001t0001g0160 a0001c0001t0001g0161 others(62): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.434-1097A>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12086116 | |||||||
| chr12:12086179 | G | A | 88 | a0001c0001t0001g0090 a0001c0002t0001g0257 a0001c0002t0001g0270 others(85): Show |
108 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.434-1034G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12086179 | |||||||
| chr12:12086248 | A | G | 65 | a0001c0001t0001g0132 a0001c0001t0001g0160 a0001c0001t0001g0161 others(62): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.434-965A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12086248 | |||||||
| chr12:12086272 | C | T | 1 | a0001c0002t0001g0057 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.434-941C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12086272 | |||||||
| chr12:12086449 | G | A | 7 | a0001c0002t0001g0297 a0001c0002t0003g0375 a0001c0003t0001g0009 others(4): Show |
9 | HG02257.hp1 HG02257.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.434-764G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12086449 | |||||||
| chr12:12086534 | A | G | 9 | a0001c0002t0001g0297 a0001c0002t0003g0375 a0001c0003t0001g0009 others(6): Show |
11 | HG02257.hp1 HG02257.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.434-679A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12086534 | |||||||
| chr12:12086540 | A | G | 6 | a0002c0004t0001g0198 a0002c0005t0001g0041 a0002c0005t0001g0076 others(3): Show |
7 | HG01884.hp1 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.434-673A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12086540 | |||||||
| chr12:12086544 | A | G | 9 | a0001c0002t0001g0297 a0001c0002t0003g0375 a0001c0003t0001g0009 others(6): Show |
11 | HG02257.hp1 HG02257.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.434-669A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12086544 | |||||||
| chr12:12086559 | TC | T | 28 | a0001c0002t0001g0134 a0001c0003t0001g0030 a0001c0003t0001g0031 others(25): Show |
30 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.434-653delC | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12086559 | |||||||
| chr12:12086686 | G | A | 5 | a0001c0003t0001g0009 a0001c0003t0001g0053 a0001c0003t0001g0284 others(2): Show |
7 | HG02257.hp1 HG02559.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.434-527G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12086686 | |||||||
| chr12:12086793 | T | C | 1 | a0001c0002t0002g0189 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.434-420T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12086793 | |||||||
| chr12:12086821 | T | C | 1 | a0001c0001t0001g0332 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.434-392T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12086821 | |||||||
| chr12:12086825 | T | G | 2 | a0001c0002t0004g0206 a0001c0002t0004g0302 |
2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.434-388T>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12086825 | |||||||
| chr12:12086946 | C | A | 10 | a0001c0002t0001g0297 a0001c0002t0003g0375 a0001c0003t0001g0009 others(7): Show |
12 | HG02257.hp1 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.434-267C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12086946 | |||||||
| chr12:12087036 | G | A | 3 | a0001c0002t0001g0057 a0004c0010t0001g0039 a0004c0010t0001g0204 |
4 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-177G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12087036 | |||||||
| chr12:12087052 | C | T | 1 | a0001c0002t0002g0018 | 2 | HG01934.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.434-161C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 2/5 | chr12 | 12087052 | |||||||
| chr12:12087430 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.607+44G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12087430 | |||||||
| chr12:12087670 | T | C | 1 | a0001c0001t0002g0363 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.607+284T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12087670 | |||||||
| chr12:12087731 | T | C | 317 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(314): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(382): Show |
intron_variant | MODIFIER | c.607+345T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12087731 | |||||||
| chr12:12087851 | G | A | 28 | a0001c0002t0001g0006 a0001c0002t0001g0015 a0001c0002t0001g0016 others(25): Show |
34 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.607+465G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12087851 | |||||||
| chr12:12087917 | G | A | 28 | a0001c0002t0001g0006 a0001c0002t0001g0015 a0001c0002t0001g0016 others(25): Show |
34 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.607+531G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12087917 | |||||||
| chr12:12088012 | G | C | 5 | a0001c0002t0001g0297 a0003c0006t0001g0058 a0003c0006t0001g0096 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.607+626G>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12088012 | |||||||
| chr12:12088092 | G | A | 1 | a0001c0002t0002g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.607+706G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12088092 | |||||||
| chr12:12088137 | A | G | 2 | a0001c0002t0001g0238 a0001c0002t0001g0263 |
2 | NA18991.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.607+751A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12088137 | |||||||
| chr12:12088205 | C | A | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.607+819C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12088205 | |||||||
| chr12:12088214 | G | C | 2 | a0001c0002t0002g0045 a0001c0002t0002g0191 |
3 | HG00735.hp2 HG01261.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.607+828G>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12088214 | |||||||
| chr12:12088266 | G | A | 1 | a0001c0002t0002g0187 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.607+880G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12088266 | |||||||
| chr12:12088396 | T | C | 1 | a0001c0001t0001g0324 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.607+1010T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12088396 | |||||||
| chr12:12088404 | C | T | 30 | a0001c0002t0001g0006 a0001c0002t0001g0015 a0001c0002t0001g0016 others(27): Show |
37 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.607+1018C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12088404 | |||||||
| chr12:12088408 | A | C | 30 | a0001c0002t0001g0006 a0001c0002t0001g0015 a0001c0002t0001g0016 others(27): Show |
37 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.607+1022A>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12088408 | |||||||
| chr12:12088463 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.607+1077C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12088463 | |||||||
| chr12:12088494 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.607+1108C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12088494 | |||||||
| chr12:12088513 | C | T | 1 | a0001c0002t0002g0259 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.607+1127C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12088513 | |||||||
| chr12:12088529 | T | G | 1 | a0001c0002t0001g0230 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.607+1143T>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12088529 | |||||||
| chr12:12088545 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0254 a0001c0015t0001g0285 |
3 | HG02895.hp2 HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.607+1159G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12088545 | |||||||
| chr12:12088758 | C | G | 12 | a0001c0002t0001g0070 a0001c0002t0001g0297 a0001c0002t0003g0375 others(9): Show |
14 | HG02257.hp1 HG02257.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.607+1372C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12088758 | |||||||
| chr12:12088766 | T | C | 28 | a0001c0002t0001g0006 a0001c0002t0001g0015 a0001c0002t0001g0016 others(25): Show |
34 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.607+1380T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12088766 | |||||||
| chr12:12088794 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0281 |
2 | HG01069.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.607+1408G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12088794 | |||||||
| chr12:12088883 | T | TA | 35 | a0001c0002t0001g0134 a0001c0002t0001g0162 a0001c0002t0001g0370 others(32): Show |
40 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.607+1506dupA | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 12088883 | ||||||
| chr12:12088883 | T | TAA | 29 | a0001c0001t0001g0121 a0001c0001t0001g0254 a0001c0001t0002g0248 others(26): Show |
30 | HG01361.hp2 HG01884.hp1 HG01928.hp2 others(27): Show |
intron_variant | MODIFIER | c.607+1505_607+1506d others(4): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 12088883 | ||||||
| chr12:12088978 | C | T | 1 | a0002c0004t0002g0098 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.607+1592C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12088978 | |||||||
| chr12:12089023 | C | T | 156 | a0001c0001t0001g0090 a0001c0001t0002g0145 a0001c0001t0002g0271 others(153): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.607+1637C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089023 | |||||||
| chr12:12089049 | C | T | 33 | a0001c0002t0001g0006 a0001c0002t0001g0015 a0001c0002t0001g0016 others(30): Show |
40 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.607+1663C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089049 | |||||||
| chr12:12089052 | G | A | 27 | a0001c0002t0001g0134 a0001c0003t0001g0030 a0001c0003t0001g0031 others(24): Show |
29 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.607+1666G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089052 | |||||||
| chr12:12089061 | T | C | 62 | a0001c0001t0001g0121 a0001c0001t0001g0254 a0001c0001t0002g0248 others(59): Show |
70 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.607+1675T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089061 | |||||||
| chr12:12089089 | G | A | 2 | a0001c0002t0004g0206 a0001c0002t0004g0302 |
2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.608-1690G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089089 | |||||||
| chr12:12089138 | A | T | 1 | a0001c0001t0001g0232 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.608-1641A>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089138 | |||||||
| chr12:12089160 | C | A | 62 | a0001c0001t0001g0121 a0001c0001t0001g0254 a0001c0001t0002g0248 others(59): Show |
70 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.608-1619C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089160 | |||||||
| chr12:12089195 | C | T | 1 | a0007c0018t0001g0277 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.608-1584C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089195 | |||||||
| chr12:12089248 | G | A | 62 | a0001c0001t0001g0121 a0001c0001t0001g0254 a0001c0001t0002g0248 others(59): Show |
70 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.608-1531G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089248 | |||||||
| chr12:12089267 | G | T | 35 | a0001c0002t0001g0134 a0001c0002t0001g0162 a0001c0002t0001g0370 others(32): Show |
40 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.608-1512G>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089267 | |||||||
| chr12:12089326 | G | A | 2 | a0001c0021t0001g0200 a0003c0017t0006g0059 |
2 | HG02886.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.608-1453G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089326 | |||||||
| chr12:12089327 | C | T | 3 | a0001c0008t0001g0197 a0001c0008t0001g0301 a0001c0021t0001g0200 |
3 | HG02572.hp1 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.608-1452C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089327 | |||||||
| chr12:12089350 | C | T | 117 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0027 others(114): Show |
133 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.608-1429C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089350 | |||||||
| chr12:12089372 | TA | T | 118 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0027 others(115): Show |
134 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.608-1393delA | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 12089372 | ||||||
| chr12:12089373 | A | T | 1 | a0001c0001t0001g0303 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.608-1406A>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089373 | |||||||
| chr12:12089388 | T | A | 34 | a0001c0001t0001g0121 a0001c0001t0001g0254 a0001c0001t0002g0248 others(31): Show |
36 | HG01167.hp2 HG01169.hp1 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.608-1391T>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089388 | |||||||
| chr12:12089453 | C | G | 24 | a0001c0002t0001g0117 a0001c0002t0001g0128 a0001c0002t0001g0129 others(21): Show |
31 | HG00423.hp2 HG00639.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.608-1326C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089453 | |||||||
| chr12:12089461 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0345 |
2 | HG00558.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.608-1318C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089461 | |||||||
| chr12:12089521 | C | T | 28 | a0001c0002t0001g0006 a0001c0002t0001g0015 a0001c0002t0001g0016 others(25): Show |
34 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.608-1258C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089521 | |||||||
| chr12:12089556 | G | C | 1 | a0001c0001t0001g0332 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.608-1223G>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089556 | |||||||
| chr12:12089630 | G | A | 1 | a0001c0008t0001g0197 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.608-1149G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089630 | |||||||
| chr12:12089717 | C | G | 1 | a0001c0001t0001g0332 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.608-1062C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089717 | |||||||
| chr12:12089876 | C | T | 161 | a0001c0001t0001g0090 a0001c0001t0001g0132 a0001c0001t0001g0160 others(158): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.608-903C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089876 | |||||||
| chr12:12089984 | T | C | 190 | a0001c0001t0001g0090 a0001c0001t0001g0121 a0001c0001t0001g0132 others(187): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.608-795T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12089984 | |||||||
| chr12:12090046 | A | G | 1 | a0001c0002t0002g0367 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.608-733A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12090046 | |||||||
| chr12:12090163 | G | A | 35 | a0001c0002t0001g0134 a0001c0002t0001g0162 a0001c0002t0001g0370 others(32): Show |
40 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.608-616G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12090163 | |||||||
| chr12:12090311 | G | A | 1 | a0001c0002t0003g0290 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.608-468G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12090311 | |||||||
| chr12:12090386 | T | A | 4 | a0001c0003t0001g0005 a0001c0003t0001g0159 a0001c0003t0001g0260 others(1): Show |
7 | HG00099.hp1 HG01109.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.608-393T>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12090386 | |||||||
| chr12:12090396 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.608-383G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12090396 | |||||||
| chr12:12090457 | TG | T | 54 | a0001c0001t0001g0090 a0001c0002t0001g0070 a0001c0002t0001g0134 others(51): Show |
62 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.608-319delG | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 12090457 | ||||||
| chr12:12090467 | G | C | 54 | a0001c0001t0001g0090 a0001c0002t0001g0070 a0001c0002t0001g0134 others(51): Show |
62 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.608-312G>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12090467 | |||||||
| chr12:12090506 | G | A | 5 | a0001c0003t0001g0009 a0001c0003t0001g0053 a0001c0003t0001g0284 others(2): Show |
7 | HG02257.hp1 HG02559.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.608-273G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12090506 | |||||||
| chr12:12090644 | AAT | A | 53 | a0001c0001t0001g0090 a0001c0001t0001g0121 a0001c0002t0001g0070 others(50): Show |
61 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.608-133_608-132del others(2): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 12090644 | ||||||
| chr12:12090645 | AT | A | 6 | a0001c0001t0001g0254 a0001c0011t0001g0178 a0001c0011t0001g0179 others(3): Show |
6 | HG02895.hp1 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.608-133delT | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12090645 | |||||||
| chr12:12090646 | T | A | 24 | a0001c0001t0002g0248 a0002c0004t0001g0116 a0002c0004t0001g0198 others(21): Show |
25 | HG01361.hp2 HG01884.hp1 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.608-133T>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12090646 | |||||||
| chr12:12090648 | A | T | 2 | a0001c0011t0001g0178 a0001c0011t0001g0179 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.608-131A>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12090648 | |||||||
| chr12:12090649 | A | T | 51 | a0001c0001t0001g0090 a0001c0002t0001g0070 a0001c0002t0001g0134 others(48): Show |
59 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.608-130A>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 3/5 | chr12 | 12090649 | |||||||
| chr12:12090894 | C | A | 26 | a0001c0001t0001g0121 a0001c0001t0001g0254 a0001c0001t0002g0248 others(23): Show |
27 | HG01361.hp2 HG01884.hp1 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.678+45C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12090894 | |||||||
| chr12:12091091 | G | T | 1 | a0001c0002t0002g0163 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.678+242G>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12091091 | |||||||
| chr12:12091288 | T | G | 188 | a0001c0001t0001g0090 a0001c0001t0001g0121 a0001c0001t0001g0254 others(185): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.678+439T>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12091288 | |||||||
| chr12:12091367 | A | G | 58 | a0001c0001t0001g0090 a0001c0002t0001g0070 a0001c0002t0001g0134 others(55): Show |
66 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.678+518A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12091367 | |||||||
| chr12:12091403 | G | A | 1 | a0001c0002t0002g0201 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.678+554G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12091403 | |||||||
| chr12:12091427 | C | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(316): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(384): Show |
intron_variant | MODIFIER | c.678+578C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12091427 | |||||||
| chr12:12091497 | C | T | 3 | a0001c0002t0001g0162 a0001c0002t0001g0370 a0001c0002t0001g0371 |
3 | HG02055.hp2 HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.678+648C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12091497 | |||||||
| chr12:12091560 | T | G | 193 | a0001c0001t0001g0090 a0001c0001t0001g0121 a0001c0001t0001g0132 others(190): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.678+711T>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12091560 | |||||||
| chr12:12091658 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.678+809C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12091658 | |||||||
| chr12:12091683 | G | A | 2 | a0001c0002t0004g0206 a0001c0002t0004g0302 |
2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.678+834G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12091683 | |||||||
| chr12:12091718 | C | A | 1 | a0001c0001t0001g0328 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.678+869C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12091718 | |||||||
| chr12:12091755 | C | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0203 others(4): Show |
10 | HG00558.hp1 HG01346.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.678+906C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12091755 | |||||||
| chr12:12091756 | G | A | 1 | a0001c0001t0001g0357 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.678+907G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12091756 | |||||||
| chr12:12091792 | G | C | 2 | a0001c0002t0004g0206 a0001c0002t0004g0302 |
2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.678+943G>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12091792 | |||||||
| chr12:12091954 | T | C | 143 | a0001c0001t0001g0090 a0001c0001t0001g0121 a0001c0001t0001g0254 others(140): Show |
170 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.678+1105T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12091954 | |||||||
| chr12:12091978 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.678+1129C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12091978 | |||||||
| chr12:12092012 | G | A | 1 | a0001c0002t0002g0352 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.678+1163G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12092012 | |||||||
| chr12:12092181 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.678+1332G>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12092181 | |||||||
| chr12:12092320 | G | T | 103 | a0001c0001t0002g0145 a0001c0001t0002g0271 a0001c0001t0002g0363 others(100): Show |
128 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.678+1471G>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12092320 | |||||||
| chr12:12092369 | T | C | 1 | a0001c0002t0002g0288 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.678+1520T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12092369 | |||||||
| chr12:12092657 | C | G | 161 | a0001c0001t0001g0121 a0001c0001t0001g0167 a0001c0001t0001g0254 others(158): Show |
193 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.678+1808C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12092657 | |||||||
| chr12:12092845 | T | C | 8 | a0001c0001t0001g0078 a0001c0001t0001g0164 a0001c0001t0001g0165 others(5): Show |
8 | HG00597.hp1 HG02027.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.679-1819T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12092845 | |||||||
| chr12:12092897 | G | T | 1 | a0001c0001t0001g0319 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.679-1767G>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12092897 | |||||||
| chr12:12092906 | A | G | 1 | a0001c0002t0002g0246 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.679-1758A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12092906 | |||||||
| chr12:12092991 | C | G | 135 | a0001c0001t0001g0121 a0001c0001t0001g0167 a0001c0001t0001g0254 others(132): Show |
161 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.679-1673C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12092991 | |||||||
| chr12:12093036 | T | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0181 |
2 | HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.679-1628T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12093036 | |||||||
| chr12:12093442 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0292 |
2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.679-1222G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12093442 | |||||||
| chr12:12093505 | G | C | 3 | a0004c0010t0001g0039 a0004c0010t0001g0204 a0004c0023t0001g0298 |
4 | HG01167.hp2 HG01169.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.679-1159G>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12093505 | |||||||
| chr12:12093515 | G | A | 47 | a0001c0003t0001g0005 a0001c0003t0001g0009 a0001c0003t0001g0030 others(44): Show |
55 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.679-1149G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12093515 | |||||||
| chr12:12093706 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0292 |
2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.679-958T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12093706 | |||||||
| chr12:12093794 | G | GAAA | 126 | a0001c0001t0001g0078 a0001c0001t0001g0336 a0001c0001t0002g0145 others(123): Show |
157 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.679-860_679-858dup others(3): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 12093794 | ||||||
| chr12:12093794 | G | GAAAA | 109 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0027 others(106): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.679-861_679-858dup others(4): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 12093794 | ||||||
| chr12:12093794 | GA | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(95): Show |
125 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.679-858delA | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 12093794 | ||||||
| chr12:12093806 | AG | A | 3 | a0001c0001t0001g0167 a0001c0001t0001g0292 a0001c0002t0001g0057 |
3 | HG02145.hp2 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.679-857delG | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12093806 | |||||||
| chr12:12093848 | A | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0310 |
2 | HG03831.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.679-816A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12093848 | |||||||
| chr12:12093854 | G | A | 1 | a0001c0003t0001g0222 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.679-810G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12093854 | |||||||
| chr12:12093897 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.679-767G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12093897 | |||||||
| chr12:12094028 | G | T | 1 | a0001c0001t0001g0305 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.679-636G>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12094028 | |||||||
| chr12:12094077 | A | C | 1 | a0002c0004t0001g0323 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.679-587A>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12094077 | |||||||
| chr12:12094107 | T | TA | 341 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(338): Show |
411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.679-543dupA | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 12094107 | ||||||
| chr12:12094107 | T | TAA | 26 | a0001c0002t0001g0006 a0001c0002t0001g0015 a0001c0002t0001g0016 others(23): Show |
32 | HG00642.hp2 HG01123.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.679-544_679-543dup others(2): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 12094107 | ||||||
| chr12:12094202 | T | C | 45 | a0001c0003t0001g0005 a0001c0003t0001g0009 a0001c0003t0001g0030 others(42): Show |
52 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.679-462T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12094202 | |||||||
| chr12:12094425 | A | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0292 |
2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.679-239A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12094425 | |||||||
| chr12:12094426 | A | G | 100 | a0001c0001t0002g0145 a0001c0001t0002g0248 a0001c0001t0002g0271 others(97): Show |
125 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.679-238A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12094426 | |||||||
| chr12:12094480 | C | T | 3 | a0004c0010t0001g0039 a0004c0010t0001g0204 a0004c0023t0001g0298 |
4 | HG01167.hp2 HG01169.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.679-184C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12094480 | |||||||
| chr12:12094660 | A | G | 51 | a0001c0001t0001g0090 a0001c0003t0001g0005 a0001c0003t0001g0009 others(48): Show |
60 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(57): Show |
splice_region_variant&intron_variant | LOW | c.679-4A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 4/5 | chr12 | 12094660 | |||||||
| chr12:12094937 | G | A | 1 | a0001c0001t0001g0339 | 1 | NA18997.hp2 | splice_region_variant&intron_variant | LOW | c.945+7G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12094937 | |||||||
| chr12:12094987 | AT | A | 51 | a0001c0001t0001g0075 a0001c0001t0001g0080 a0001c0001t0001g0119 others(48): Show |
58 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.945+73delT | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 12094987 | ||||||
| chr12:12094987 | ATT | A | 7 | a0001c0001t0001g0167 a0001c0001t0001g0292 a0001c0002t0001g0057 others(4): Show |
8 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.945+72_945+73delTT | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 12094987 | ||||||
| chr12:12095165 | A | G | 234 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0027 others(231): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.945+235A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12095165 | |||||||
| chr12:12095346 | G | A | 67 | a0001c0002t0001g0006 a0001c0002t0001g0015 a0001c0002t0001g0016 others(64): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.945+416G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12095346 | |||||||
| chr12:12095363 | G | A | 67 | a0001c0002t0001g0006 a0001c0002t0001g0015 a0001c0002t0001g0016 others(64): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.945+433G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12095363 | |||||||
| chr12:12095552 | A | G | 1 | a0001c0001t0001g0021 | 2 | HG00738.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.945+622A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12095552 | |||||||
| chr12:12095596 | C | G | 100 | a0001c0001t0002g0145 a0001c0001t0002g0248 a0001c0001t0002g0271 others(97): Show |
125 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.945+666C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12095596 | |||||||
| chr12:12095708 | T | C | 3 | a0001c0002t0004g0206 a0001c0002t0004g0302 a0009c0019t0001g0063 |
3 | HG02572.hp2 HG02717.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.945+778T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12095708 | |||||||
| chr12:12095738 | C | A | 2 | a0001c0003t0001g0306 a0001c0003t0001g0376 |
2 | HG02683.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.945+808C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12095738 | |||||||
| chr12:12095764 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.945+834C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12095764 | |||||||
| chr12:12095980 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.945+1050A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12095980 | |||||||
| chr12:12096120 | A | G | 29 | a0001c0001t0001g0090 a0001c0001t0001g0121 a0001c0001t0001g0254 others(26): Show |
31 | HG01361.hp2 HG01884.hp1 HG01928.hp2 others(28): Show |
intron_variant | MODIFIER | c.945+1190A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096120 | |||||||
| chr12:12096290 | G | A | 195 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0027 others(192): Show |
236 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.945+1360G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096290 | |||||||
| chr12:12096325 | A | G | 109 | a0001c0001t0001g0090 a0001c0001t0002g0145 a0001c0001t0002g0248 others(106): Show |
136 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.945+1395A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096325 | |||||||
| chr12:12096385 | A | T | 1 | a0002c0004t0001g0249 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.945+1455A>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096385 | |||||||
| chr12:12096386 | C | T | 1 | a0002c0004t0001g0249 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.945+1456C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096386 | |||||||
| chr12:12096433 | G | GA | 55 | a0001c0001t0001g0091 a0001c0001t0001g0268 a0001c0001t0005g0120 others(52): Show |
61 | HG00323.hp1 HG00642.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.945+1518dupA | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 12096433 | ||||||
| chr12:12096433 | G | GAAA | 48 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0027 others(45): Show |
56 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.945+1516_945+1518d others(5): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 12096433 | ||||||
| chr12:12096433 | G | GAAAA | 8 | a0001c0001t0001g0055 a0001c0001t0001g0126 a0001c0001t0001g0137 others(5): Show |
8 | HG00621.hp2 HG01109.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.945+1515_945+1518d others(6): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 12096433 | ||||||
| chr12:12096434 | A | G | 112 | a0001c0001t0001g0090 a0001c0001t0001g0167 a0001c0001t0001g0292 others(109): Show |
139 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.945+1504A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096434 | |||||||
| chr12:12096435 | A | G | 1 | a0001c0002t0002g0191 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.945+1505A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096435 | |||||||
| chr12:12096447 | AAC | A | 94 | a0001c0001t0002g0145 a0001c0001t0002g0248 a0001c0001t0002g0271 others(91): Show |
117 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.945+1519_945+1520d others(4): Show |
BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 12096447 | ||||||
| chr12:12096448 | AC | A | 14 | a0001c0001t0001g0090 a0001c0001t0001g0167 a0001c0001t0001g0292 others(11): Show |
15 | HG01106.hp2 HG02027.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.945+1519delC | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096448 | |||||||
| chr12:12096449 | C | A | 3 | a0001c0002t0002g0125 a0001c0022t0001g0199 a0003c0006t0001g0110 |
3 | HG03098.hp1 HG03098.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.945+1519C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096449 | |||||||
| chr12:12096452 | C | A | 1 | a0001c0001t0002g0145 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.945+1522C>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096452 | |||||||
| chr12:12096542 | A | T | 2 | a0001c0002t0004g0206 a0001c0002t0004g0302 |
2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.945+1612A>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096542 | |||||||
| chr12:12096551 | A | T | 1 | a0001c0002t0002g0125 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.945+1621A>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096551 | |||||||
| chr12:12096637 | T | C | 1 | a0001c0002t0002g0367 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.945+1707T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096637 | |||||||
| chr12:12096703 | A | G | 1 | a0001c0001t0001g0043 | 2 | NA18971.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.945+1773A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096703 | |||||||
| chr12:12096706 | G | A | 99 | a0001c0001t0002g0145 a0001c0001t0002g0248 a0001c0001t0002g0271 others(96): Show |
124 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.945+1776G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096706 | |||||||
| chr12:12096738 | C | T | 112 | a0001c0001t0001g0090 a0001c0001t0001g0167 a0001c0001t0001g0292 others(109): Show |
139 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.945+1808C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096738 | |||||||
| chr12:12096757 | T | C | 3 | a0001c0001t0001g0167 a0001c0001t0001g0292 a0001c0008t0001g0301 |
3 | HG03041.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.945+1827T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096757 | |||||||
| chr12:12096765 | T | G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0027 others(192): Show |
236 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.945+1835T>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096765 | |||||||
| chr12:12096852 | C | G | 1 | a0001c0002t0004g0302 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.945+1922C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096852 | |||||||
| chr12:12096872 | A | G | 114 | a0001c0001t0001g0090 a0001c0001t0001g0167 a0001c0001t0001g0292 others(111): Show |
142 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.945+1942A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12096872 | |||||||
| chr12:12097000 | C | G | 1 | a0001c0002t0001g0230 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.946-1950C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097000 | |||||||
| chr12:12097001 | G | T | 1 | a0001c0002t0002g0246 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.946-1949G>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097001 | |||||||
| chr12:12097005 | A | G | 8 | a0001c0001t0001g0335 a0001c0003t0001g0009 a0001c0003t0001g0053 others(5): Show |
10 | HG02257.hp1 HG02559.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.946-1945A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097005 | |||||||
| chr12:12097006 | T | C | 117 | a0001c0001t0001g0090 a0001c0001t0001g0167 a0001c0001t0001g0292 others(114): Show |
144 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.946-1944T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097006 | |||||||
| chr12:12097013 | A | G | 8 | a0001c0002t0001g0070 a0001c0002t0001g0297 a0001c0003t0001g0009 others(5): Show |
10 | HG02257.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.946-1937A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097013 | |||||||
| chr12:12097016 | T | C | 6 | a0001c0003t0001g0009 a0001c0003t0001g0053 a0001c0003t0001g0284 others(3): Show |
8 | HG02257.hp1 HG02559.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.946-1934T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097016 | |||||||
| chr12:12097016 | T | G | 1 | a0001c0001t0001g0365 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.946-1934T>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097016 | |||||||
| chr12:12097035 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0027 others(54): Show |
65 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.946-1915T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097035 | |||||||
| chr12:12097037 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0027 others(54): Show |
65 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.946-1913A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097037 | |||||||
| chr12:12097042 | G | C | 113 | a0001c0001t0001g0090 a0001c0001t0001g0140 a0001c0001t0001g0167 others(110): Show |
140 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.946-1908G>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097042 | |||||||
| chr12:12097126 | G | C | 110 | a0001c0001t0001g0090 a0001c0001t0002g0145 a0001c0001t0002g0248 others(107): Show |
137 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.946-1824G>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097126 | |||||||
| chr12:12097137 | T | C | 1 | a0001c0003t0001g0306 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.946-1813T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097137 | |||||||
| chr12:12097211 | T | C | 98 | a0001c0001t0002g0145 a0001c0001t0002g0248 a0001c0001t0002g0271 others(95): Show |
123 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.946-1739T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097211 | |||||||
| chr12:12097254 | T | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0027 others(53): Show |
64 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.946-1696T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097254 | |||||||
| chr12:12097352 | G | A | 108 | a0001c0001t0001g0090 a0001c0001t0002g0145 a0001c0001t0002g0248 others(105): Show |
135 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.946-1598G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097352 | |||||||
| chr12:12097436 | A | C | 97 | a0001c0001t0002g0145 a0001c0001t0002g0248 a0001c0001t0002g0271 others(94): Show |
122 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.946-1514A>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097436 | |||||||
| chr12:12097460 | A | G | 112 | a0001c0001t0001g0090 a0001c0001t0001g0167 a0001c0001t0001g0171 others(109): Show |
139 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.946-1490A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097460 | |||||||
| chr12:12097700 | T | C | 110 | a0001c0001t0001g0090 a0001c0001t0001g0167 a0001c0001t0001g0292 others(107): Show |
137 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.946-1250T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097700 | |||||||
| chr12:12097817 | A | G | 2 | a0001c0002t0003g0290 a0001c0002t0003g0375 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.946-1133A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097817 | |||||||
| chr12:12097841 | A | C | 1 | a0001c0001t0001g0212 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.946-1109A>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097841 | |||||||
| chr12:12097915 | A | G | 110 | a0001c0001t0001g0090 a0001c0001t0001g0167 a0001c0001t0001g0292 others(107): Show |
137 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.946-1035A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097915 | |||||||
| chr12:12097998 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0239 |
2 | NA18962.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.946-952A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12097998 | |||||||
| chr12:12098019 | A | G | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | NA18989.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.946-931A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12098019 | |||||||
| chr12:12098054 | G | GA | 110 | a0001c0001t0001g0090 a0001c0001t0001g0167 a0001c0001t0001g0292 others(107): Show |
137 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.946-889dupA | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 12098054 | ||||||
| chr12:12098070 | G | A | 1 | a0001c0003t0001g0188 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.946-880G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12098070 | |||||||
| chr12:12098111 | T | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0292 |
2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.946-839T>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12098111 | |||||||
| chr12:12098134 | C | T | 21 | a0001c0001t0001g0137 a0001c0001t0001g0341 a0001c0002t0001g0129 others(18): Show |
21 | HG01123.hp1 HG01361.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.946-816C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12098134 | |||||||
| chr12:12098218 | G | A | 97 | a0001c0001t0002g0145 a0001c0001t0002g0248 a0001c0001t0002g0271 others(94): Show |
122 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.946-732G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12098218 | |||||||
| chr12:12098230 | T | C | 3 | a0006c0013t0001g0086 a0006c0013t0001g0289 a0010c0016t0001g0060 |
3 | HG02922.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.946-720T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12098230 | |||||||
| chr12:12098251 | G | A | 1 | a0001c0003t0001g0005 | 4 | HG01168.hp1 HG01169.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.946-699G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12098251 | |||||||
| chr12:12098463 | G | A | 1 | a0001c0003t0001g0306 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.946-487G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12098463 | |||||||
| chr12:12098490 | T | C | 1 | a0001c0001t0001g0043 | 2 | NA18971.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.946-460T>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12098490 | |||||||
| chr12:12098493 | C | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0292 |
2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.946-457C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12098493 | |||||||
| chr12:12098642 | T | G | 27 | a0001c0001t0001g0268 a0001c0002t0001g0006 a0001c0002t0001g0015 others(24): Show |
33 | HG00323.hp1 HG00642.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.946-308T>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12098642 | |||||||
| chr12:12098724 | G | A | 110 | a0001c0001t0001g0090 a0001c0001t0001g0167 a0001c0001t0001g0292 others(107): Show |
137 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.946-226G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12098724 | |||||||
| chr12:12098777 | C | T | 110 | a0001c0001t0001g0090 a0001c0001t0001g0167 a0001c0001t0001g0292 others(107): Show |
137 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.946-173C>T | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12098777 | |||||||
| chr12:12098790 | A | G | 1 | a0001c0002t0001g0093 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.946-160A>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12098790 | |||||||
| chr12:12098827 | C | G | 110 | a0001c0001t0001g0090 a0001c0001t0001g0167 a0001c0001t0001g0292 others(107): Show |
137 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.946-123C>G | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12098827 | |||||||
| chr12:12098853 | G | A | 1 | a0001c0002t0002g0282 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.946-97G>A | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12098853 | |||||||
| chr12:12098870 | G | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0027 others(54): Show |
65 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.946-80G>C | BCL2L14 | ENSG00000121380.12 | transcript | ENST00000308721.9 | protein_coding | 5/5 | chr12 | 12098870 |