Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 164 |
| ensemblid | ENSG00000166747.13 |
| hgncid | 555 |
| symbol | AP1G1 |
| name | adaptor related protein complex 1 subunit gamma 1 |
| refseq_nuc | NM_001128.6 |
| refseq_prot | NP_001119.3 |
| ensembl_nuc | ENST00000299980.9 |
| ensembl_prot | ENSP00000299980.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 71729000 |
| end | 71808834 |
| strand | - |
| ver | v1.2 |
| region | chr16:71729000-71808834 |
| region5000 | chr16:71724000-71813834 |
| regionname0 | AP1G1_chr16_71729000_71808834 |
| regionname5000 | AP1G1_chr16_71724000_71813834 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 822 | 234 | 79 | 43 | 80 | 13 | 17 | 56 | AP1G1_chr16_71724000_71813834 | AP1G1 | MPAPI others(817): Show |
chr16 | 71724000 | 71813834 |
| a0002 | 0/0 | 822 | 82 | 5 | 19 | 36 | 3 | 19 | 31 | AP1G1_chr16_71724000_71813834 | AP1G1 | MPAPI others(817): Show |
chr16 | 71724000 | 71813834 |
| a0003 | 0/0 | 822 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | MPAPI others(817): Show |
chr16 | 71724000 | 71813834 |
| a0004 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | MPAPI others(817): Show |
chr16 | 71724000 | 71813834 |
| a0005 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | MPAPI others(817): Show |
chr16 | 71724000 | 71813834 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2466 | 217 | 66 | 40 | 80 | 12 | 17 | AP1G1_chr16_71724000_71813834 | AP1G1 | ATGCC others(2461): Show |
chr16 | 71724000 | 71813834 | ||
| a0001c0003 | 0/0 | 2466 | 11 | 11 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | ATGCC others(2461): Show |
chr16 | 71724000 | 71813834 | ||
| a0001c0004 | 0/0 | 2466 | 4 | 0 | 3 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | ATGCC others(2461): Show |
chr16 | 71724000 | 71813834 | ||
| a0001c0008 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | ATGCC others(2461): Show |
chr16 | 71724000 | 71813834 | ||
| a0001c0009 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | ATGCC others(2461): Show |
chr16 | 71724000 | 71813834 | ||
| a0002c0002 | 0/0 | 2466 | 82 | 5 | 19 | 36 | 3 | 19 | AP1G1_chr16_71724000_71813834 | AP1G1 | ATGCC others(2461): Show |
chr16 | 71724000 | 71813834 | ||
| a0003c0005 | 0/0 | 2466 | 2 | 0 | 0 | 0 | 0 | 2 | AP1G1_chr16_71724000_71813834 | AP1G1 | ATGCC others(2461): Show |
chr16 | 71724000 | 71813834 | ||
| a0004c0006 | 0/0 | 2466 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | ATGCC others(2461): Show |
chr16 | 71724000 | 71813834 | ||
| a0005c0007 | 0/0 | 2466 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | ATGCC others(2461): Show |
chr16 | 71724000 | 71813834 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 6602 | 57 | 11 | 12 | 27 | 2 | 5 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6597): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0003 | 0/0 | 6603 | 30 | 3 | 7 | 17 | 0 | 3 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6598): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0004 | 1/0 | 6602 | 27 | 13 | 7 | 3 | 3 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6597): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0005 | 0/0 | 6604 | 24 | 18 | 2 | 0 | 1 | 3 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6599): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0007 | 0/0 | 6604 | 11 | 1 | 5 | 2 | 2 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6599): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0008 | 0/0 | 6601 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6596): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0009 | 0/0 | 6605 | 11 | 0 | 3 | 4 | 2 | 2 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6600): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0010 | 0/0 | 6601 | 8 | 7 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6596): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0011 | 0/0 | 6602 | 8 | 0 | 0 | 8 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6597): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0012 | 0/0 | 6602 | 6 | 0 | 0 | 6 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6597): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0013 | 0/0 | 6602 | 6 | 0 | 0 | 6 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6597): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0014 | 0/0 | 6601 | 5 | 1 | 1 | 0 | 1 | 2 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6596): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0015 | 0/0 | 6602 | 5 | 4 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6597): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0016 | 0/0 | 6601 | 2 | 2 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6596): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0018 | 0/0 | 6603 | 2 | 1 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6598): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0020 | 0/0 | 6602 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6597): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0023 | 0/0 | 6604 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6599): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0024 | 0/0 | 6605 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6600): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0025 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6598): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0026 | 0/0 | 6602 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6597): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0027 | 0/0 | 6602 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6597): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0028 | 0/0 | 6602 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6597): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0029 | 0/0 | 6602 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6597): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0030 | 0/1 | 6604 | 1 | 0 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6599): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0035 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6598): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0036 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6598): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0037 | 0/0 | 6605 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6600): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0038 | 0/0 | 6605 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6600): Show |
chr16 | 71724000 | 71813834 |
| a0001c0001t0040 | 0/0 | 6602 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6597): Show |
chr16 | 71724000 | 71813834 |
| a0001c0003t0008 | 0/0 | 6601 | 11 | 11 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6596): Show |
chr16 | 71724000 | 71813834 |
| a0001c0004t0007 | 0/0 | 6604 | 4 | 0 | 3 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6599): Show |
chr16 | 71724000 | 71813834 |
| a0001c0008t0008 | 0/0 | 6601 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6596): Show |
chr16 | 71724000 | 71813834 |
| a0001c0009t0019 | 0/0 | 6601 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6596): Show |
chr16 | 71724000 | 71813834 |
| a0002c0002t0001 | 0/0 | 6603 | 54 | 5 | 6 | 28 | 2 | 13 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6598): Show |
chr16 | 71724000 | 71813834 |
| a0002c0002t0004 | 0/0 | 6602 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6597): Show |
chr16 | 71724000 | 71813834 |
| a0002c0002t0005 | 0/0 | 6604 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6599): Show |
chr16 | 71724000 | 71813834 |
| a0002c0002t0006 | 0/0 | 6603 | 17 | 0 | 12 | 3 | 0 | 2 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6598): Show |
chr16 | 71724000 | 71813834 |
| a0002c0002t0017 | 0/0 | 6602 | 2 | 0 | 0 | 1 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6597): Show |
chr16 | 71724000 | 71813834 |
| a0002c0002t0021 | 0/0 | 6603 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6598): Show |
chr16 | 71724000 | 71813834 |
| a0002c0002t0022 | 0/0 | 6604 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6599): Show |
chr16 | 71724000 | 71813834 |
| a0002c0002t0031 | 0/0 | 6603 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6598): Show |
chr16 | 71724000 | 71813834 |
| a0002c0002t0032 | 0/0 | 6603 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6598): Show |
chr16 | 71724000 | 71813834 |
| a0002c0002t0033 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6598): Show |
chr16 | 71724000 | 71813834 |
| a0002c0002t0034 | 0/0 | 6604 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6599): Show |
chr16 | 71724000 | 71813834 |
| a0002c0002t0039 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6598): Show |
chr16 | 71724000 | 71813834 |
| a0003c0005t0001 | 0/0 | 6603 | 2 | 0 | 0 | 0 | 0 | 2 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6598): Show |
chr16 | 71724000 | 71813834 |
| a0004c0006t0001 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6598): Show |
chr16 | 71724000 | 71813834 |
| a0005c0007t0001 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | GGATG others(6598): Show |
chr16 | 71724000 | 71813834 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0024 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0008g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0009g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0010g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0010g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0010g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0010g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0010g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0010g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0010g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0010g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0011g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0011g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0011g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0011g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0011g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0011g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0011g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0011g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0012g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0012g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0012g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0012g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0012g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0012g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0013g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0013g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0013g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0013g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0013g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0013g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0014g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0014g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0014g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0014g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0014g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0015g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0015g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0015g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0015g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0015g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0016g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0016g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0018g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0018g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0020g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0023g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0024g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0025g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0026g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0027g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0028g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0029g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0030g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0035g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0036g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0037g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0038g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0001t0040g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0003t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0004t0007g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0004t0007g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0004t0007g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0004t0007g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0008t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0001c0009t0019g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0006g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0017g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0017g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0021g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0022g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0031g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0032g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0033g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0034g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0002c0002t0039g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0003c0005t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0003c0005t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0004c0006t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| a0005c0007t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0028 | EUR | GBR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0020 | EUR | GBR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00140 | hp1 | a0001 | c0001 | t0007 | g0075 | EUR | GBR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00140 | hp2 | a0001 | c0001 | t0014 | g0252 | EUR | GBR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00323 | hp1 | a0002 | c0002 | t0017 | g0129 | EUR | FIN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0131 | EUR | FIN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00408 | hp1 | a0001 | c0001 | t0013 | g0280 | EAS | CHS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | CHS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | CHS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | CHS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00609 | hp1 | a0001 | c0001 | t0011 | g0247 | EAS | CHS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00609 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | CHS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | CHS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00621 | hp2 | a0001 | c0001 | t0013 | g0289 | EAS | CHS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00642 | hp2 | a0002 | c0002 | t0006 | g0173 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00733 | hp1 | a0001 | c0001 | t0005 | g0052 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0081 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00738 | hp1 | a0002 | c0002 | t0006 | g0171 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00738 | hp2 | a0001 | c0001 | t0010 | g0006 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00741 | hp1 | a0002 | c0002 | t0006 | g0101 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01071 | hp1 | a0002 | c0002 | t0006 | g0127 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0284 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0155 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0025 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01106 | hp1 | a0001 | c0004 | t0007 | g0068 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01168 | hp1 | a0001 | c0001 | t0007 | g0078 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0125 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0077 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01175 | hp1 | a0001 | c0001 | t0014 | g0195 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01175 | hp2 | a0001 | c0001 | t0009 | g0062 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01192 | hp2 | a0001 | c0004 | t0007 | g0076 | AMR | PUR | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01255 | hp1 | a0002 | c0002 | t0006 | g0105 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0208 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01256 | hp2 | a0001 | c0001 | t0009 | g0072 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01257 | hp1 | a0002 | c0002 | t0006 | g0179 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01257 | hp2 | a0001 | c0001 | t0007 | g0080 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01258 | hp1 | a0002 | c0002 | t0006 | g0100 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0209 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0071 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0228 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01358 | hp2 | a0001 | c0001 | t0009 | g0085 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0063 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0023 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0217 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0017 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01515 | hp1 | a0001 | c0001 | t0015 | g0037 | EUR | IBS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0294 | EUR | IBS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01516 | hp1 | a0001 | c0004 | t0007 | g0091 | EUR | IBS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01516 | hp2 | a0001 | c0001 | t0009 | g0086 | EUR | IBS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01517 | hp1 | a0001 | c0001 | t0009 | g0065 | EUR | IBS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0239 | EUR | IBS | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0058 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01891 | hp1 | a0001 | c0003 | t0008 | g0183 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0008 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01934 | hp1 | a0001 | c0004 | t0007 | g0074 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0034 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0159 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01981 | hp1 | a0002 | c0002 | t0006 | g0104 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01993 | hp1 | a0002 | c0002 | t0034 | g0098 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02040 | hp1 | a0001 | c0001 | t0011 | g0223 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0108 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02056 | hp1 | a0001 | c0001 | t0011 | g0248 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02071 | hp2 | a0002 | c0002 | t0039 | g0318 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02074 | hp1 | a0001 | c0001 | t0027 | g0265 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02074 | hp2 | a0004 | c0006 | t0001 | g0132 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02083 | hp2 | a0001 | c0001 | t0011 | g0246 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02132 | hp2 | a0001 | c0001 | t0011 | g0256 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0093 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02148 | hp1 | a0002 | c0002 | t0006 | g0103 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | CDX | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | CDX | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02257 | hp1 | a0001 | c0001 | t0016 | g0042 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0084 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02258 | hp2 | a0001 | c0003 | t0008 | g0190 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02293 | hp1 | a0002 | c0002 | t0006 | g0106 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02293 | hp2 | a0001 | c0001 | t0018 | g0226 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02300 | hp1 | a0002 | c0002 | t0006 | g0102 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02300 | hp2 | a0001 | c0001 | t0008 | g0029 | AMR | PEL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0317 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02451 | hp2 | a0001 | c0009 | t0019 | g0010 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02523 | hp1 | a0001 | c0001 | t0040 | g0238 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | KHV | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0004 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0306 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0157 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0050 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0312 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0007 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0311 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0115 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02647 | hp1 | a0001 | c0001 | t0018 | g0314 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0313 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02683 | hp1 | a0002 | c0002 | t0006 | g0099 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0051 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0150 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0110 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0128 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0156 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0277 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02809 | hp2 | a0001 | c0008 | t0008 | g0181 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02818 | hp1 | a0001 | c0001 | t0037 | g0082 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02886 | hp1 | a0001 | c0001 | t0015 | g0038 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0003 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02895 | hp1 | a0001 | c0001 | t0026 | g0304 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02895 | hp2 | a0001 | c0001 | t0015 | g0039 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02897 | hp1 | a0001 | c0001 | t0015 | g0035 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02897 | hp2 | a0001 | c0001 | t0010 | g0005 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0002 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0107 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0060 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02965 | hp2 | a0001 | c0003 | t0008 | g0193 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0113 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02970 | hp2 | a0001 | c0003 | t0008 | g0185 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03017 | hp1 | a0002 | c0002 | t0031 | g0160 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03017 | hp2 | a0002 | c0002 | t0032 | g0140 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03130 | hp1 | a0001 | c0003 | t0008 | g0192 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0122 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0112 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03209 | hp1 | a0001 | c0001 | t0016 | g0041 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0303 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0056 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03225 | hp2 | a0001 | c0001 | t0020 | g0064 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03239 | hp1 | a0002 | c0002 | t0006 | g0168 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0054 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0120 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0059 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03490 | hp1 | a0001 | c0001 | t0014 | g0204 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03490 | hp2 | a0001 | c0001 | t0009 | g0079 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03491 | hp1 | a0003 | c0005 | t0001 | g0166 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03492 | hp1 | a0001 | c0001 | t0009 | g0069 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03492 | hp2 | a0003 | c0005 | t0001 | g0165 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0057 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03516 | hp2 | a0001 | c0001 | t0014 | g0305 | AFR | ESN | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0307 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03540 | hp2 | a0001 | c0003 | t0008 | g0189 | AFR | GWD | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03654 | hp2 | a0002 | c0002 | t0021 | g0097 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0182 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0174 | SAS | STU | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03688 | hp2 | a0001 | c0001 | t0014 | g0268 | SAS | STU | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03710 | hp1 | a0002 | c0002 | t0022 | g0094 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0154 | SAS | PJL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0196 | SAS | BEB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0158 | SAS | BEB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0270 | SAS | BEB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0148 | SAS | BEB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0164 | SAS | BEB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0089 | SAS | BEB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG04204 | hp1 | a0001 | c0001 | t0024 | g0088 | SAS | STU | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0135 | SAS | STU | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0194 | SAS | STU | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG04228 | hp2 | a0001 | c0001 | t0007 | g0073 | SAS | STU | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18612 | hp1 | a0001 | c0001 | t0013 | g0287 | EAS | CHB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | CHB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0114 | AFR | YRI | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18906 | hp2 | a0001 | c0003 | t0008 | g0188 | AFR | YRI | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18941 | hp1 | a0002 | c0002 | t0006 | g0177 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18941 | hp2 | a0002 | c0002 | t0017 | g0047 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18946 | hp1 | a0005 | c0007 | t0001 | g0176 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18950 | hp1 | a0001 | c0001 | t0029 | g0269 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18951 | hp1 | a0001 | c0001 | t0011 | g0199 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18951 | hp2 | a0002 | c0002 | t0033 | g0152 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18952 | hp1 | a0001 | c0001 | t0013 | g0288 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18952 | hp2 | a0001 | c0001 | t0012 | g0202 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18954 | hp1 | a0001 | c0001 | t0012 | g0292 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18957 | hp2 | a0002 | c0002 | t0004 | g0149 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18959 | hp1 | a0001 | c0001 | t0012 | g0200 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18965 | hp1 | a0001 | c0001 | t0035 | g0234 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18966 | hp2 | a0001 | c0001 | t0011 | g0235 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18968 | hp1 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18968 | hp2 | a0001 | c0001 | t0011 | g0260 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18970 | hp1 | a0001 | c0001 | t0012 | g0203 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18971 | hp1 | a0001 | c0001 | t0007 | g0087 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18971 | hp2 | a0001 | c0001 | t0028 | g0251 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18973 | hp1 | a0001 | c0001 | t0009 | g0070 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18973 | hp2 | a0001 | c0001 | t0025 | g0222 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18985 | hp1 | a0001 | c0001 | t0013 | g0282 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18990 | hp1 | a0002 | c0002 | t0006 | g0045 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18993 | hp2 | a0001 | c0001 | t0036 | g0271 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18994 | hp2 | a0001 | c0001 | t0009 | g0067 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18999 | hp2 | a0001 | c0001 | t0013 | g0285 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19011 | hp1 | a0001 | c0001 | t0012 | g0197 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19011 | hp2 | a0002 | c0002 | t0005 | g0142 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0310 | AFR | LWK | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19030 | hp2 | a0001 | c0001 | t0015 | g0036 | AFR | LWK | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19043 | hp1 | a0001 | c0003 | t0008 | g0187 | AFR | LWK | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | LWK | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19054 | hp2 | a0001 | c0001 | t0007 | g0090 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19091 | hp2 | a0002 | c0002 | t0006 | g0046 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19240 | hp1 | a0001 | c0003 | t0008 | g0186 | AFR | YRI | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0300 | AFR | YRI | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | ASW | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA20129 | hp2 | a0001 | c0001 | t0023 | g0121 | AFR | ASW | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0130 | EUR | TSI | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0053 | EUR | TSI | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0027 | EUR | TSI | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA20805 | hp2 | a0001 | c0001 | t0007 | g0066 | EUR | TSI | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01123 | hp1 | a0002 | c0002 | t0006 | g0172 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0026 | AMR | CLM | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0116 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02109 | hp2 | a0001 | c0003 | t0008 | g0184 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0315 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0119 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG02559 | hp2 | a0001 | c0001 | t0038 | g0083 | AFR | ACB | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0117 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0309 | AFR | MSL | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG06807 | hp1 | a0001 | c0003 | t0008 | g0191 | AFR | USA | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | USA | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18955 | hp1 | a0001 | c0001 | t0012 | g0207 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0118 | AFR | USA | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | USA | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0109 | AFR | LWK | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0308 | AFR | LWK | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0030 | g0049 | REF | REF | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0024 | REF | REF | AP1G1_chr16_71724000_71813834 | AP1G1 | chr16 | 71724000 | 71813834 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71739018 | G | A | 1 | a0004 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.2192C>T | p.Thr731Ile | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/23 | 2267/6602 | 2192/2469 | 731/822 | chr16 | 71739018 | |||
| chr16:71739287 | G | T | 4 | a0002 a0003 a0004 others(1): Show |
86 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(83): Show |
missense_variant | MODERATE | c.2054C>A | p.Pro685His | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 20/23 | 2129/6602 | 2054/2469 | 685/822 | chr16 | 71739287 | |||
| chr16:71745206 | G | A | 1 | a0005 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.1937C>T | p.Thr646Ile | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/23 | 2012/6602 | 1937/2469 | 646/822 | chr16 | 71745206 | |||
| chr16:71745593 | C | A | 1 | a0003 | 2 | HG03491.hp1 HG03492.hp2 |
missense_variant | MODERATE | c.1752G>T | p.Met584Ile | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 18/23 | 1827/6602 | 1752/2469 | 584/822 | chr16 | 71745593 | |||
| chr16:71745604 | G | A | 1 | a0003 | 2 | HG03491.hp1 HG03492.hp2 |
missense_variant | MODERATE | c.1741C>T | p.Leu581Phe | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 18/23 | 1816/6602 | 1741/2469 | 581/822 | chr16 | 71745604 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71756129 | T | C | 1 | a0001c0003 | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
synonymous_variant | LOW | c.1119A>G | p.Val373Val | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/23 | 1194/6602 | 1119/2469 | 373/822 | chr16 | 71756129 | |||
| chr16:71769668 | T | C | 1 | a0001c0008 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.597A>G | p.Thr199Thr | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/23 | 672/6602 | 597/2469 | 199/822 | chr16 | 71769668 | |||
| chr16:71769686 | T | C | 1 | a0001c0009 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.579A>G | p.Thr193Thr | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/23 | 654/6602 | 579/2469 | 193/822 | chr16 | 71769686 | |||
| chr16:71773329 | C | A | 1 | a0001c0004 | 4 | HG01106.hp1 HG01192.hp2 HG01516.hp1 others(1): Show |
synonymous_variant | LOW | c.360G>T | p.Gly120Gly | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/23 | 435/6602 | 360/2469 | 120/822 | chr16 | 71773329 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71729016 | A | G | 1 | a0001c0001t0026 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4042T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 4042 | chr16 | 71729016 | ||||||
| chr16:71729159 | A | AT | 23 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0009 others(20): Show |
140 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*3898dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 3898 | chr16 | 71729159 | ||||||
| chr16:71729159 | AT | A | 1 | a0001c0001t0010 | 8 | HG00738.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3898delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 3898 | chr16 | 71729159 | ||||||
| chr16:71729182 | A | G | 1 | a0002c0002t0033 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3876T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 3876 | chr16 | 71729182 | ||||||
| chr16:71729432 | G | GA | 13 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(10): Show |
76 | HG00423.hp1 HG00609.hp2 HG00733.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*3625dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 3625 | chr16 | 71729432 | ||||||
| chr16:71729432 | GA | G | 7 | a0001c0001t0008 a0001c0001t0014 a0001c0001t0016 others(4): Show |
23 | HG00140.hp2 HG00323.hp1 HG01175.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3625delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 3625 | chr16 | 71729432 | ||||||
| chr16:71729451 | A | C | 1 | a0002c0002t0032 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3607T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 3607 | chr16 | 71729451 | ||||||
| chr16:71729452 | C | A | 3 | a0001c0001t0011 a0001c0001t0027 a0001c0001t0035 |
10 | HG00609.hp1 HG02040.hp1 HG02056.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3606G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 3606 | chr16 | 71729452 | ||||||
| chr16:71729876 | C | A | 2 | a0002c0002t0006 a0002c0002t0034 |
18 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3182G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 3182 | chr16 | 71729876 | ||||||
| chr16:71729914 | A | G | 1 | a0002c0002t0031 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3144T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 3144 | chr16 | 71729914 | ||||||
| chr16:71730460 | C | G | 1 | a0001c0009t0019 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2598G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 2598 | chr16 | 71730460 | ||||||
| chr16:71730512 | C | G | 3 | a0001c0001t0016 a0001c0001t0020 a0001c0009t0019 |
4 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2546G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 2546 | chr16 | 71730512 | ||||||
| chr16:71730754 | G | A | 1 | a0001c0001t0010 | 8 | HG00738.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2304C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 2304 | chr16 | 71730754 | ||||||
| chr16:71730923 | G | C | 1 | a0001c0001t0013 | 6 | HG00408.hp1 HG00621.hp2 NA18612.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2135C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 2135 | chr16 | 71730923 | ||||||
| chr16:71730931 | C | T | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0011 others(12): Show |
121 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*2127G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 2127 | chr16 | 71730931 | ||||||
| chr16:71731329 | A | C | 1 | a0001c0001t0035 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1729T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 1729 | chr16 | 71731329 | ||||||
| chr16:71731490 | A | G | 1 | a0001c0001t0024 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1568T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 1568 | chr16 | 71731490 | ||||||
| chr16:71731502 | T | C | 1 | a0001c0001t0028 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1556A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 1556 | chr16 | 71731502 | ||||||
| chr16:71731510 | A | G | 1 | a0001c0001t0015 | 5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1548T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 1548 | chr16 | 71731510 | ||||||
| chr16:71731513 | G | T | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0011 others(10): Show |
119 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*1545C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 1545 | chr16 | 71731513 | ||||||
| chr16:71731534 | C | CT | 6 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0024 others(3): Show |
29 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1523dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 1523 | chr16 | 71731534 | ||||||
| chr16:71731562 | G | C | 3 | a0001c0001t0011 a0001c0001t0035 a0001c0001t0036 |
10 | HG00609.hp1 HG02040.hp1 HG02056.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1496C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 1496 | chr16 | 71731562 | ||||||
| chr16:71731583 | A | G | 1 | a0001c0001t0023 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1475T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 1475 | chr16 | 71731583 | ||||||
| chr16:71731634 | A | G | 1 | a0001c0001t0037 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1424T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 1424 | chr16 | 71731634 | ||||||
| chr16:71732133 | T | C | 2 | a0001c0001t0037 a0001c0001t0038 |
2 | HG02559.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*925A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 925 | chr16 | 71732133 | ||||||
| chr16:71732375 | C | T | 1 | a0001c0001t0016 | 2 | HG02257.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*683G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 683 | chr16 | 71732375 | ||||||
| chr16:71732415 | G | A | 1 | a0002c0002t0039 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*643C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 643 | chr16 | 71732415 | ||||||
| chr16:71732650 | G | T | 1 | a0001c0001t0012 | 6 | NA18952.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*408C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 408 | chr16 | 71732650 | ||||||
| chr16:71732748 | A | G | 2 | a0002c0002t0021 a0002c0002t0022 |
2 | HG03654.hp2 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*310T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 310 | chr16 | 71732748 | ||||||
| chr16:71732972 | T | C | 1 | a0001c0001t0040 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*86A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 86 | chr16 | 71732972 | ||||||
| chr16:71732980 | G | T | 2 | a0001c0001t0020 a0001c0009t0019 |
2 | HG02451.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*78C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 23/23 | 78 | chr16 | 71732980 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71733162 | A | G | 3 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0040g0238 |
3 | HG00408.hp2 HG02523.hp1 NA19056.hp2 |
splice_region_variant&intron_variant | LOW | c.2368-3T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733162 | |||||||
| chr16:71733384 | C | T | 1 | a0002c0002t0001g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2368-225G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733384 | |||||||
| chr16:71733410 | T | A | 1 | a0001c0001t0004g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2368-251A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733410 | |||||||
| chr16:71733416 | G | T | 1 | a0001c0001t0004g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2368-257C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733416 | |||||||
| chr16:71733510 | G | GGCTCACC others(68): Show |
282 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(279): Show |
283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.2368-352_2368-351i others(77): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733510 | |||||||
| chr16:71733510 | G | GGCTCACC others(68): Show |
3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2368-352_2368-351i others(77): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733510 | |||||||
| chr16:71733557 | G | A | 1 | a0001c0001t0002g0302 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2368-398C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733557 | |||||||
| chr16:71733747 | T | C | 1 | a0001c0001t0002g0278 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2368-588A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733747 | |||||||
| chr16:71733758 | C | T | 122 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(119): Show |
122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2368-599G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733758 | |||||||
| chr16:71733895 | A | G | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2367+714T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733895 | |||||||
| chr16:71733933 | G | A | 122 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(119): Show |
122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2367+676C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71733933 | |||||||
| chr16:71734135 | T | A | 1 | a0002c0002t0001g0150 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2367+474A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71734135 | |||||||
| chr16:71734148 | G | A | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2367+461C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71734148 | |||||||
| chr16:71734151 | G | A | 1 | a0002c0002t0001g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2367+458C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71734151 | |||||||
| chr16:71734422 | C | A | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2367+187G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71734422 | |||||||
| chr16:71734571 | A | C | 1 | a0002c0002t0001g0111 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2367+38T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71734571 | |||||||
| chr16:71734597 | T | C | 123 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(120): Show |
123 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.2367+12A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 22/22 | chr16 | 71734597 | |||||||
| chr16:71734748 | A | G | 2 | a0001c0001t0009g0001 a0001c0001t0009g0070 |
3 | HG00609.hp2 NA18968.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.2269-41T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71734748 | |||||||
| chr16:71734758 | G | C | 1 | a0001c0001t0004g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2269-51C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71734758 | |||||||
| chr16:71735011 | G | A | 1 | a0002c0002t0001g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2269-304C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71735011 | |||||||
| chr16:71735019 | C | G | 1 | a0002c0002t0001g0141 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2269-312G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71735019 | |||||||
| chr16:71735229 | T | C | 1 | a0001c0001t0005g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2269-522A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71735229 | |||||||
| chr16:71735420 | T | G | 27 | a0002c0002t0001g0092 a0002c0002t0001g0107 a0002c0002t0001g0108 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.2269-713A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71735420 | |||||||
| chr16:71735632 | GGCAACAG others(1): Show |
G | 12 | a0001c0001t0002g0216 a0001c0001t0002g0278 a0001c0001t0002g0279 others(9): Show |
12 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.2269-933_2269-926d others(10): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71735632 | |||||||
| chr16:71735659 | A | C | 123 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(120): Show |
123 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.2269-952T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71735659 | |||||||
| chr16:71735866 | G | A | 7 | a0001c0001t0002g0201 a0001c0001t0012g0197 a0001c0001t0012g0200 others(4): Show |
7 | NA18952.hp2 NA18954.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.2269-1159C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71735866 | |||||||
| chr16:71736011 | A | C | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2269-1304T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736011 | |||||||
| chr16:71736098 | C | CAAA | 9 | a0001c0001t0004g0040 a0001c0001t0004g0061 a0001c0001t0010g0002 others(6): Show |
9 | HG00738.hp2 HG01891.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2269-1394_2269-139 others(7): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736098 | |||||||
| chr16:71736098 | C | CAAAAAAA others(3): Show |
13 | a0001c0001t0002g0194 a0001c0001t0002g0233 a0001c0001t0002g0240 others(10): Show |
13 | HG00735.hp1 HG01169.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.2269-1401_2269-139 others(14): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736098 | |||||||
| chr16:71736098 | C | CAAAAAAA others(4): Show |
16 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0250 others(13): Show |
16 | HG00423.hp1 HG01081.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.2269-1402_2269-139 others(15): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736098 | |||||||
| chr16:71736098 | C | CAAAAAAA others(5): Show |
33 | a0001c0001t0002g0216 a0001c0001t0002g0221 a0001c0001t0002g0225 others(30): Show |
33 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.2269-1403_2269-139 others(16): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736098 | |||||||
| chr16:71736098 | C | CAAAAAAA others(6): Show |
19 | a0001c0001t0002g0198 a0001c0001t0002g0210 a0001c0001t0002g0215 others(16): Show |
19 | HG00609.hp1 HG00621.hp2 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.2269-1404_2269-139 others(17): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736098 | |||||||
| chr16:71736098 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0002g0231 a0001c0001t0002g0297 a0001c0001t0003g0277 |
3 | HG00733.hp2 HG02738.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.2269-1405_2269-139 others(18): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736098 | |||||||
| chr16:71736098 | C | CAAAAAAA others(8): Show |
4 | a0001c0001t0002g0276 a0001c0001t0002g0290 a0001c0001t0011g0199 others(1): Show |
4 | HG02148.hp2 NA18951.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.2269-1406_2269-139 others(19): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736098 | |||||||
| chr16:71736098 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0014g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2269-1407_2269-139 others(20): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736098 | |||||||
| chr16:71736115 | A | AT | 4 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0191 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2269-1409_2269-140 others(5): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736115 | |||||||
| chr16:71736115 | A | T | 2 | a0001c0003t0008g0189 a0001c0003t0008g0193 |
2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2269-1408T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736115 | |||||||
| chr16:71736115 | AAAATAT | A | 12 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(9): Show |
12 | HG00733.hp1 HG01358.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.2269-1414_2269-140 others(10): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736115 | |||||||
| chr16:71736115 | AAAATATA others(7): Show |
A | 1 | a0002c0002t0001g0092 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2269-1422_2269-140 others(18): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736115 | |||||||
| chr16:71736117 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0002g0266 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(22): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | A | AAAAAAAA others(10): Show |
1 | a0001c0001t0002g0267 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(21): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0003g0310 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(19): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0002g0316 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(27): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | A | AAAAAAAA others(7): Show |
2 | a0001c0001t0002g0242 a0001c0001t0002g0303 |
2 | HG03209.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2269-1411_2269-141 others(18): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0002g0302 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(20): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | A | AAAAAAAA others(6): Show |
2 | a0001c0001t0002g0308 a0001c0001t0011g0256 |
2 | HG02132.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2269-1411_2269-141 others(17): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | A | AAAAAAAA others(8): Show |
3 | a0001c0001t0002g0301 a0001c0001t0002g0307 a0001c0001t0011g0235 |
3 | HG02280.hp1 HG03540.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.2269-1411_2269-141 others(19): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | A | AAAAAAAA others(10): Show |
1 | a0001c0001t0040g0238 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(21): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | A | AAAAAAAA others(5): Show |
4 | a0001c0001t0002g0291 a0001c0001t0003g0270 a0001c0001t0003g0306 others(1): Show |
4 | HG02572.hp2 HG03834.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.2269-1411_2269-141 others(16): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0002g0312 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(18): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | A | AAAAAAAA others(9): Show |
2 | a0001c0001t0002g0249 a0001c0001t0002g0309 |
2 | HG00621.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2269-1411_2269-141 others(20): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | A | AAAAAAAA others(4): Show |
2 | a0001c0001t0002g0201 a0001c0001t0012g0202 |
2 | NA18952.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.2269-1411_2269-141 others(15): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | A | AAAAAAAA others(6): Show |
2 | a0001c0001t0002g0239 a0001c0001t0002g0294 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2269-1411_2269-141 others(17): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0002g0264 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(14): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0026g0304 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(18): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | A | AAAAAAAA others(4): Show |
1 | a0001c0001t0002g0313 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2269-1411_2269-141 others(15): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | A | AT | 4 | a0001c0003t0008g0185 a0001c0003t0008g0186 a0001c0003t0008g0187 others(1): Show |
4 | HG02970.hp2 NA18906.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2269-1411_2269-141 others(5): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | A | T | 11 | a0001c0001t0004g0020 a0001c0001t0004g0022 a0001c0001t0004g0023 others(8): Show |
11 | HG00099.hp2 HG00639.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.2269-1410T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | AAT | A | 9 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2269-1412_2269-141 others(6): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | AATAT | A | 14 | a0001c0001t0003g0255 a0001c0001t0004g0300 a0001c0001t0015g0035 others(11): Show |
14 | HG00642.hp2 HG02071.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.2269-1414_2269-141 others(8): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | AATATAT | A | 38 | a0001c0001t0005g0058 a0001c0001t0005g0112 a0001c0001t0005g0114 others(35): Show |
39 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.2269-1416_2269-141 others(10): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736117 | AATATATA others(5): Show |
A | 1 | a0001c0001t0004g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2269-1422_2269-141 others(16): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736117 | |||||||
| chr16:71736118 | ATAT | A | 5 | a0001c0001t0015g0037 a0001c0001t0015g0039 a0002c0002t0001g0135 others(2): Show |
5 | HG01515.hp1 HG02895.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.2269-1414_2269-141 others(7): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736118 | |||||||
| chr16:71736118 | ATATAT | A | 71 | a0001c0001t0005g0043 a0001c0001t0005g0093 a0001c0001t0005g0122 others(68): Show |
71 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.2269-1416_2269-141 others(9): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736118 | |||||||
| chr16:71736118 | ATATATAT | A | 5 | a0001c0001t0005g0113 a0001c0001t0007g0078 a0001c0001t0016g0041 others(2): Show |
5 | HG01168.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2269-1418_2269-141 others(11): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736118 | |||||||
| chr16:71736119 | T | A | 78 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(75): Show |
78 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.2269-1412A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736119 | |||||||
| chr16:71736121 | T | A | 50 | a0001c0001t0002g0198 a0001c0001t0002g0215 a0001c0001t0002g0216 others(47): Show |
50 | HG00099.hp1 HG00423.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.2269-1414A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736121 | |||||||
| chr16:71736123 | T | A | 35 | a0001c0001t0002g0279 a0001c0001t0003g0257 a0001c0001t0003g0273 others(32): Show |
35 | HG00099.hp1 HG00642.hp2 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.2269-1416A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736123 | |||||||
| chr16:71736125 | T | A | 128 | a0001c0001t0003g0257 a0001c0001t0004g0028 a0001c0001t0004g0300 others(125): Show |
129 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.2269-1418A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736125 | |||||||
| chr16:71736127 | T | A | 111 | a0001c0001t0004g0300 a0001c0001t0005g0093 a0001c0001t0005g0112 others(108): Show |
111 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.2269-1420A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736127 | |||||||
| chr16:71736129 | T | A | 61 | a0001c0001t0005g0093 a0001c0001t0005g0112 a0001c0001t0005g0113 others(58): Show |
61 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.2269-1422A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736129 | |||||||
| chr16:71736131 | T | A | 17 | a0001c0001t0004g0018 a0001c0001t0005g0093 a0001c0001t0005g0112 others(14): Show |
17 | HG02109.hp1 HG02145.hp2 HG02148.hp1 others(14): Show |
intron_variant | MODIFIER | c.2269-1424A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736131 | |||||||
| chr16:71736231 | A | G | 1 | a0001c0001t0004g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2269-1524T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736231 | |||||||
| chr16:71736350 | G | A | 1 | a0001c0001t0003g0258 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2269-1643C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736350 | |||||||
| chr16:71736384 | C | CT | 8 | a0001c0001t0003g0258 a0001c0001t0003g0277 a0001c0001t0004g0032 others(5): Show |
8 | HG01981.hp1 HG01993.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.2269-1678dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736384 | |||||||
| chr16:71736480 | A | G | 1 | a0001c0001t0014g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2269-1773T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736480 | |||||||
| chr16:71736526 | G | A | 15 | a0001c0001t0002g0133 a0001c0001t0002g0301 a0001c0001t0002g0302 others(12): Show |
15 | HG01433.hp1 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2269-1819C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736526 | |||||||
| chr16:71736541 | C | A | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2269-1834G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736541 | |||||||
| chr16:71736541 | C | T | 4 | a0001c0001t0002g0301 a0001c0001t0002g0307 a0001c0001t0002g0311 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2269-1834G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736541 | |||||||
| chr16:71736551 | A | ATTAT | 6 | a0001c0001t0003g0293 a0001c0001t0003g0306 a0001c0001t0040g0238 others(3): Show |
6 | HG02523.hp1 HG02572.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.2269-1848_2269-184 others(8): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736551 | |||||||
| chr16:71736551 | ATTAT | A | 99 | a0001c0001t0002g0232 a0001c0001t0002g0250 a0001c0001t0002g0253 others(96): Show |
99 | HG00099.hp2 HG00140.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.2269-1848_2269-184 others(8): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736551 | |||||||
| chr16:71736551 | ATTATTTA others(1): Show |
A | 59 | a0001c0001t0002g0309 a0001c0001t0004g0017 a0001c0001t0004g0026 others(56): Show |
60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2269-1852_2269-184 others(12): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736551 | |||||||
| chr16:71736551 | ATTATTTA others(5): Show |
A | 3 | a0001c0001t0002g0297 a0001c0001t0003g0206 a0002c0002t0001g0154 |
3 | HG00733.hp2 HG03710.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.2269-1856_2269-184 others(16): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736551 | |||||||
| chr16:71736551 | ATTATTTA others(9): Show |
A | 2 | a0001c0001t0004g0061 a0001c0001t0004g0315 |
2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2269-1860_2269-184 others(20): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736551 | |||||||
| chr16:71736598 | A | T | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2269-1891T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736598 | |||||||
| chr16:71736602 | T | A | 1 | a0001c0001t0002g0291 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2269-1895A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736602 | |||||||
| chr16:71736616 | C | T | 2 | a0001c0001t0015g0035 a0001c0001t0015g0039 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2269-1909G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736616 | |||||||
| chr16:71736678 | C | T | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2269-1971G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736678 | |||||||
| chr16:71736682 | C | T | 1 | a0002c0002t0001g0135 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2269-1975G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736682 | |||||||
| chr16:71736730 | C | T | 85 | a0002c0002t0001g0048 a0002c0002t0001g0092 a0002c0002t0001g0095 others(82): Show |
85 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.2269-2023G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736730 | |||||||
| chr16:71736746 | C | T | 1 | a0001c0001t0007g0080 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2269-2039G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736746 | |||||||
| chr16:71736752 | AT | A | 103 | a0001c0001t0002g0210 a0001c0001t0002g0276 a0001c0001t0003g0212 others(100): Show |
103 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.2269-2046delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736752 | |||||||
| chr16:71736752 | ATT | A | 169 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(166): Show |
170 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.2269-2047_2269-204 others(6): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736752 | |||||||
| chr16:71736875 | G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2268+2067C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736875 | |||||||
| chr16:71736933 | G | A | 122 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(119): Show |
122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2268+2009C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71736933 | |||||||
| chr16:71737053 | A | G | 12 | a0001c0001t0005g0093 a0001c0001t0005g0112 a0001c0001t0005g0113 others(9): Show |
12 | HG02109.hp1 HG02145.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2268+1889T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737053 | |||||||
| chr16:71737063 | T | C | 15 | a0001c0001t0002g0133 a0001c0001t0002g0301 a0001c0001t0002g0302 others(12): Show |
15 | HG01433.hp1 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2268+1879A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737063 | |||||||
| chr16:71737204 | T | C | 1 | a0001c0001t0027g0265 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2268+1738A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737204 | |||||||
| chr16:71737318 | C | G | 1 | a0001c0001t0015g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2268+1624G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737318 | |||||||
| chr16:71737439 | G | A | 1 | a0002c0002t0001g0092 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2268+1503C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737439 | |||||||
| chr16:71737560 | C | T | 2 | a0001c0001t0016g0041 a0001c0001t0016g0042 |
2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2268+1382G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737560 | |||||||
| chr16:71737747 | C | T | 3 | a0001c0001t0004g0061 a0001c0001t0004g0300 a0001c0001t0018g0314 |
3 | HG02647.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2268+1195G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737747 | |||||||
| chr16:71737886 | G | C | 1 | a0004c0006t0001g0132 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2268+1056C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737886 | |||||||
| chr16:71737911 | C | T | 1 | a0001c0001t0005g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2268+1031G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737911 | |||||||
| chr16:71737992 | C | T | 1 | a0001c0001t0004g0026 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2268+950G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71737992 | |||||||
| chr16:71738183 | T | C | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2268+759A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738183 | |||||||
| chr16:71738211 | C | T | 2 | a0001c0001t0020g0064 a0001c0009t0019g0010 |
2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2268+731G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738211 | |||||||
| chr16:71738212 | G | T | 150 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(147): Show |
151 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.2268+730C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738212 | |||||||
| chr16:71738217 | A | AT | 61 | a0001c0001t0009g0067 a0002c0002t0001g0048 a0002c0002t0001g0089 others(58): Show |
61 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.2268+724dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738217 | |||||||
| chr16:71738218 | T | C | 2 | a0001c0001t0020g0064 a0001c0009t0019g0010 |
2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2268+724A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738218 | |||||||
| chr16:71738350 | C | T | 2 | a0001c0001t0005g0112 a0001c0001t0005g0116 |
2 | HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2268+592G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738350 | |||||||
| chr16:71738424 | A | T | 28 | a0001c0001t0007g0066 a0001c0001t0007g0071 a0001c0001t0007g0073 others(25): Show |
29 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.2268+518T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738424 | |||||||
| chr16:71738474 | C | T | 1 | a0001c0001t0002g0201 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2268+468G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738474 | |||||||
| chr16:71738475 | G | A | 3 | a0002c0002t0006g0045 a0002c0002t0006g0046 a0002c0002t0006g0177 |
3 | NA18941.hp1 NA18990.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2268+467C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738475 | |||||||
| chr16:71738496 | T | C | 285 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(282): Show |
286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.2268+446A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738496 | |||||||
| chr16:71738519 | T | C | 2 | a0001c0001t0004g0300 a0001c0001t0018g0314 |
2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2268+423A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738519 | |||||||
| chr16:71738637 | A | G | 2 | a0001c0001t0004g0300 a0001c0001t0018g0314 |
2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2268+305T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738637 | |||||||
| chr16:71738757 | C | T | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2268+185G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738757 | |||||||
| chr16:71738821 | T | C | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2268+121A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738821 | |||||||
| chr16:71738880 | TG | T | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2268+61delC | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738880 | |||||||
| chr16:71738892 | G | A | 294 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(291): Show |
295 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.2268+50C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 21/22 | chr16 | 71738892 | |||||||
| chr16:71739151 | G | A | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2108-49C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 20/22 | chr16 | 71739151 | |||||||
| chr16:71739363 | A | T | 1 | a0001c0001t0002g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2000-22T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71739363 | |||||||
| chr16:71739381 | C | CA | 122 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(119): Show |
122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2000-41dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71739381 | |||||||
| chr16:71739388 | AAGCTTAC others(11): Show |
A | 3 | a0001c0001t0004g0061 a0001c0001t0004g0300 a0001c0001t0018g0314 |
3 | HG02647.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2000-65_2000-48del others(18): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71739388 | |||||||
| chr16:71739575 | C | T | 3 | a0002c0002t0001g0159 a0002c0002t0001g0319 a0002c0002t0039g0318 |
3 | HG01978.hp1 HG02071.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2000-234G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71739575 | |||||||
| chr16:71739804 | T | C | 1 | a0001c0001t0002g0250 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2000-463A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71739804 | |||||||
| chr16:71739886 | T | A | 1 | a0001c0001t0002g0266 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2000-545A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71739886 | |||||||
| chr16:71740196 | G | A | 1 | a0001c0001t0002g0295 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2000-855C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740196 | |||||||
| chr16:71740487 | G | A | 122 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(119): Show |
122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2000-1146C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740487 | |||||||
| chr16:71740512 | T | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2000-1171A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740512 | |||||||
| chr16:71740538 | T | C | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2000-1197A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740538 | |||||||
| chr16:71740605 | G | A | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2000-1264C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740605 | |||||||
| chr16:71740653 | G | A | 22 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(19): Show |
22 | HG00738.hp2 HG01515.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2000-1312C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740653 | |||||||
| chr16:71740794 | G | T | 122 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(119): Show |
122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2000-1453C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740794 | |||||||
| chr16:71740845 | A | G | 1 | a0002c0002t0001g0143 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2000-1504T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740845 | |||||||
| chr16:71740861 | A | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2000-1520T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740861 | |||||||
| chr16:71740863 | T | C | 3 | a0001c0001t0010g0005 a0001c0001t0010g0006 a0001c0001t0010g0007 |
3 | HG00738.hp2 HG02622.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2000-1522A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740863 | |||||||
| chr16:71740945 | G | A | 1 | a0001c0001t0035g0234 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2000-1604C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740945 | |||||||
| chr16:71740993 | T | G | 147 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(144): Show |
147 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.2000-1652A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71740993 | |||||||
| chr16:71741086 | G | T | 27 | a0002c0002t0001g0092 a0002c0002t0001g0107 a0002c0002t0001g0108 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.2000-1745C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741086 | |||||||
| chr16:71741107 | G | C | 3 | a0002c0002t0001g0096 a0002c0002t0001g0136 a0002c0002t0001g0137 |
3 | NA18965.hp2 NA19002.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.2000-1766C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741107 | |||||||
| chr16:71741117 | G | A | 4 | a0001c0001t0016g0041 a0001c0001t0016g0042 a0001c0001t0020g0064 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2000-1776C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741117 | |||||||
| chr16:71741177 | C | T | 122 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(119): Show |
122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2000-1836G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741177 | |||||||
| chr16:71741284 | T | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2000-1943A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741284 | |||||||
| chr16:71741440 | G | A | 12 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(9): Show |
12 | HG00323.hp2 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2000-2099C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741440 | |||||||
| chr16:71741493 | G | A | 86 | a0001c0001t0005g0043 a0002c0002t0001g0048 a0002c0002t0001g0092 others(83): Show |
86 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.2000-2152C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741493 | |||||||
| chr16:71741544 | T | C | 2 | a0001c0001t0004g0300 a0001c0001t0018g0314 |
2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2000-2203A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741544 | |||||||
| chr16:71741559 | G | T | 3 | a0002c0002t0006g0045 a0002c0002t0006g0046 a0002c0002t0006g0177 |
3 | NA18941.hp1 NA18990.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2000-2218C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741559 | |||||||
| chr16:71741629 | T | C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2000-2288A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741629 | |||||||
| chr16:71741742 | T | C | 6 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0014 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2000-2401A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741742 | |||||||
| chr16:71741888 | G | C | 4 | a0001c0001t0016g0041 a0001c0001t0016g0042 a0001c0001t0020g0064 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2000-2547C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71741888 | |||||||
| chr16:71742069 | A | G | 1 | a0001c0001t0024g0088 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2000-2728T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742069 | |||||||
| chr16:71742133 | T | G | 1 | a0002c0002t0001g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2000-2792A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742133 | |||||||
| chr16:71742241 | C | T | 122 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(119): Show |
122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2000-2900G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742241 | |||||||
| chr16:71742407 | T | G | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1999+2737A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742407 | |||||||
| chr16:71742439 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1999+2705G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742439 | |||||||
| chr16:71742532 | A | T | 1 | a0001c0001t0036g0271 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1999+2612T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742532 | |||||||
| chr16:71742804 | T | A | 58 | a0002c0002t0001g0048 a0002c0002t0001g0095 a0002c0002t0001g0096 others(55): Show |
58 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1999+2340A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742804 | |||||||
| chr16:71742836 | G | A | 2 | a0001c0001t0002g0249 a0001c0001t0002g0259 |
2 | HG00621.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1999+2308C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742836 | |||||||
| chr16:71742865 | C | T | 5 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0002c0002t0001g0109 others(2): Show |
5 | HG02055.hp2 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1999+2279G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742865 | |||||||
| chr16:71742866 | G | A | 122 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(119): Show |
122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1999+2278C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742866 | |||||||
| chr16:71742981 | C | CA | 18 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(15): Show |
18 | HG00738.hp2 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1999+2162dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742981 | |||||||
| chr16:71742998 | C | G | 1 | a0001c0001t0002g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1999+2146G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71742998 | |||||||
| chr16:71743165 | T | C | 2 | a0001c0001t0016g0041 a0001c0001t0016g0042 |
2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1999+1979A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743165 | |||||||
| chr16:71743188 | G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1999+1956C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743188 | |||||||
| chr16:71743227 | A | T | 1 | a0001c0001t0003g0277 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1999+1917T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743227 | |||||||
| chr16:71743300 | GA | G | 62 | a0002c0002t0001g0048 a0002c0002t0001g0095 a0002c0002t0001g0096 others(59): Show |
62 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1999+1843delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743300 | |||||||
| chr16:71743512 | A | G | 1 | a0001c0001t0003g0277 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1999+1632T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743512 | |||||||
| chr16:71743540 | T | C | 22 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(19): Show |
22 | HG00738.hp2 HG01515.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1999+1604A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743540 | |||||||
| chr16:71743545 | G | C | 122 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(119): Show |
122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1999+1599C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743545 | |||||||
| chr16:71743551 | C | A | 1 | a0001c0001t0003g0277 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1999+1593G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743551 | |||||||
| chr16:71743602 | C | CA | 29 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(26): Show |
29 | HG00738.hp2 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1999+1541dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743602 | |||||||
| chr16:71743602 | CAAAAAAA | C | 121 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(118): Show |
121 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1999+1535_1999+154 others(11): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743602 | |||||||
| chr16:71743604 | A | G | 2 | a0001c0001t0005g0112 a0001c0001t0005g0116 |
2 | HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1999+1540T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743604 | |||||||
| chr16:71743807 | G | A | 5 | a0001c0001t0004g0061 a0001c0001t0016g0041 a0001c0001t0016g0042 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1999+1337C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743807 | |||||||
| chr16:71743945 | C | CA | 33 | a0001c0001t0004g0021 a0001c0001t0004g0030 a0001c0001t0005g0053 others(30): Show |
33 | HG01123.hp1 HG01175.hp2 HG01258.hp1 others(30): Show |
intron_variant | MODIFIER | c.1999+1198dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743945 | |||||||
| chr16:71743945 | C | T | 1 | a0001c0001t0007g0078 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1999+1199G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743945 | |||||||
| chr16:71743945 | CA | C | 141 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(138): Show |
141 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1999+1198delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743945 | |||||||
| chr16:71743946 | A | C | 1 | a0001c0001t0007g0078 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1999+1198T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71743946 | |||||||
| chr16:71744131 | C | G | 1 | a0001c0001t0010g0008 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1999+1013G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744131 | |||||||
| chr16:71744169 | G | A | 151 | a0001c0001t0005g0043 a0001c0001t0005g0050 a0001c0001t0005g0051 others(148): Show |
152 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1999+975C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744169 | |||||||
| chr16:71744176 | G | A | 5 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(2): Show |
5 | HG00733.hp1 HG02602.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.1999+968C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744176 | |||||||
| chr16:71744262 | G | T | 1 | a0002c0002t0001g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1999+882C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744262 | |||||||
| chr16:71744426 | G | A | 4 | a0002c0002t0006g0100 a0002c0002t0006g0101 a0002c0002t0006g0127 others(1): Show |
4 | HG00741.hp1 HG01071.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1999+718C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744426 | |||||||
| chr16:71744571 | G | GT | 180 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(177): Show |
181 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1999+572dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744571 | |||||||
| chr16:71744571 | G | GTT | 37 | a0001c0001t0002g0264 a0001c0001t0002g0281 a0001c0001t0002g0286 others(34): Show |
37 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1999+571_1999+572d others(4): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744571 | |||||||
| chr16:71744571 | G | GTTT | 47 | a0001c0001t0002g0312 a0001c0001t0005g0043 a0001c0001t0005g0093 others(44): Show |
47 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.1999+570_1999+572d others(5): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744571 | |||||||
| chr16:71744571 | G | GTTTT | 16 | a0002c0002t0001g0048 a0002c0002t0001g0095 a0002c0002t0001g0111 others(13): Show |
16 | HG00741.hp2 HG01168.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1999+569_1999+572d others(6): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744571 | |||||||
| chr16:71744644 | C | T | 1 | a0001c0001t0040g0238 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1999+500G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744644 | |||||||
| chr16:71744737 | G | A | 122 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(119): Show |
122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1999+407C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744737 | |||||||
| chr16:71744975 | T | C | 3 | a0001c0001t0002g0245 a0001c0001t0002g0299 a0001c0001t0028g0251 |
3 | HG02129.hp1 NA18962.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1999+169A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71744975 | |||||||
| chr16:71745059 | C | T | 1 | a0001c0001t0004g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1999+85G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71745059 | |||||||
| chr16:71745062 | G | A | 1 | a0001c0001t0004g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1999+82C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 19/22 | chr16 | 71745062 | |||||||
| chr16:71745407 | G | T | 26 | a0001c0001t0007g0066 a0001c0001t0007g0071 a0001c0001t0007g0073 others(23): Show |
27 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1872+66C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 18/22 | chr16 | 71745407 | |||||||
| chr16:71745839 | C | A | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1731-225G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71745839 | |||||||
| chr16:71745845 | GCATATAT others(2): Show |
G | 149 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(146): Show |
150 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.1731-240_1731-232d others(11): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71745845 | |||||||
| chr16:71745922 | A | G | 1 | a0001c0001t0009g0067 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1731-308T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71745922 | |||||||
| chr16:71746076 | C | G | 6 | a0002c0002t0001g0096 a0002c0002t0001g0136 a0002c0002t0001g0137 others(3): Show |
6 | NA18957.hp2 NA18965.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.1731-462G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71746076 | |||||||
| chr16:71746187 | T | A | 3 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0054 |
3 | HG02602.hp2 HG02683.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1730+401A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71746187 | |||||||
| chr16:71746355 | A | G | 1 | a0001c0001t0007g0075 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1730+233T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71746355 | |||||||
| chr16:71746374 | T | G | 280 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(277): Show |
281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.1730+214A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71746374 | |||||||
| chr16:71746385 | G | C | 1 | a0001c0001t0004g0025 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1730+203C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71746385 | |||||||
| chr16:71746467 | C | T | 1 | a0002c0002t0001g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1730+121G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71746467 | |||||||
| chr16:71746582 | G | A | 122 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(119): Show |
122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
splice_region_variant&intron_variant | LOW | c.1730+6C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 17/22 | chr16 | 71746582 | |||||||
| chr16:71746696 | T | C | 123 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(120): Show |
123 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
splice_region_variant&intron_variant | LOW | c.1626-4A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71746696 | |||||||
| chr16:71746983 | T | C | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1626-291A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71746983 | |||||||
| chr16:71746993 | A | G | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1626-301T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71746993 | |||||||
| chr16:71747078 | A | G | 1 | a0001c0001t0028g0251 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1626-386T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747078 | |||||||
| chr16:71747127 | AT | A | 7 | a0001c0001t0002g0133 a0001c0001t0002g0301 a0001c0001t0002g0307 others(4): Show |
7 | HG02280.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1626-436delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747127 | |||||||
| chr16:71747199 | C | T | 24 | a0002c0002t0001g0092 a0002c0002t0001g0107 a0002c0002t0001g0108 others(21): Show |
24 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1626-507G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747199 | |||||||
| chr16:71747267 | G | A | 1 | a0001c0001t0004g0032 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1626-575C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747267 | |||||||
| chr16:71747348 | C | G | 1 | a0002c0002t0001g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1626-656G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747348 | |||||||
| chr16:71747435 | C | G | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1626-743G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747435 | |||||||
| chr16:71747618 | C | T | 7 | a0001c0001t0003g0205 a0001c0001t0003g0236 a0001c0001t0003g0255 others(4): Show |
7 | NA18957.hp1 NA18964.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.1625+633G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747618 | |||||||
| chr16:71747676 | C | A | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1625+575G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747676 | |||||||
| chr16:71747769 | C | T | 1 | a0001c0001t0009g0001 | 2 | HG00609.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1625+482G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747769 | |||||||
| chr16:71747978 | G | A | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1625+273C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71747978 | |||||||
| chr16:71748000 | C | T | 1 | a0001c0001t0002g0220 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1625+251G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 16/22 | chr16 | 71748000 | |||||||
| chr16:71748429 | A | G | 1 | a0001c0001t0036g0271 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1498-51T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71748429 | |||||||
| chr16:71748444 | T | C | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1498-66A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71748444 | |||||||
| chr16:71748541 | A | G | 124 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(121): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1498-163T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71748541 | |||||||
| chr16:71748911 | G | T | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1498-533C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71748911 | |||||||
| chr16:71749043 | A | C | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1498-665T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749043 | |||||||
| chr16:71749050 | G | C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1498-672C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749050 | |||||||
| chr16:71749173 | T | G | 138 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(135): Show |
139 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1497+721A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749173 | |||||||
| chr16:71749218 | T | C | 285 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(282): Show |
286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.1497+676A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749218 | |||||||
| chr16:71749260 | T | C | 3 | a0001c0001t0009g0001 a0001c0001t0009g0067 a0001c0001t0009g0070 |
4 | HG00609.hp2 NA18968.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497+634A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749260 | |||||||
| chr16:71749279 | C | T | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1497+615G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749279 | |||||||
| chr16:71749470 | T | A | 121 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(118): Show |
121 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1497+424A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749470 | |||||||
| chr16:71749471 | G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1497+423C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749471 | |||||||
| chr16:71749481 | T | TA | 7 | a0001c0001t0010g0003 a0001c0001t0010g0004 a0001c0001t0010g0005 others(4): Show |
7 | HG00738.hp2 HG01891.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1497+412dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749481 | |||||||
| chr16:71749481 | TA | T | 140 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(137): Show |
140 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1497+412delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749481 | |||||||
| chr16:71749495 | C | A | 1 | a0001c0001t0010g0002 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1497+399G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749495 | |||||||
| chr16:71749592 | T | A | 5 | a0001c0001t0009g0065 a0001c0001t0009g0069 a0001c0001t0009g0079 others(2): Show |
5 | HG01358.hp2 HG01516.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1497+302A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749592 | |||||||
| chr16:71749755 | C | T | 33 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0240 others(30): Show |
33 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.1497+139G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749755 | |||||||
| chr16:71749826 | T | A | 3 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0030 |
3 | HG00099.hp1 HG02257.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1497+68A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 15/22 | chr16 | 71749826 | |||||||
| chr16:71750097 | A | T | 138 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(135): Show |
139 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1407+113T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 14/22 | chr16 | 71750097 | |||||||
| chr16:71750389 | T | C | 1 | a0001c0001t0010g0007 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1285-57A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71750389 | |||||||
| chr16:71750445 | C | T | 24 | a0002c0002t0001g0092 a0002c0002t0001g0107 a0002c0002t0001g0108 others(21): Show |
24 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1285-113G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71750445 | |||||||
| chr16:71750466 | G | C | 2 | a0001c0001t0002g0301 a0001c0001t0002g0307 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1285-134C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71750466 | |||||||
| chr16:71750467 | T | A | 2 | a0001c0001t0004g0300 a0001c0001t0018g0314 |
2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1285-135A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71750467 | |||||||
| chr16:71750470 | G | A | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1285-138C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71750470 | |||||||
| chr16:71750476 | G | A | 4 | a0001c0001t0002g0198 a0001c0001t0002g0215 a0001c0001t0002g0263 others(1): Show |
4 | HG02080.hp1 NA18955.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.1285-144C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71750476 | |||||||
| chr16:71750653 | T | A | 1 | a0001c0001t0010g0004 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1285-321A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71750653 | |||||||
| chr16:71750882 | T | C | 4 | a0001c0004t0007g0068 a0001c0004t0007g0074 a0001c0004t0007g0076 others(1): Show |
4 | HG01106.hp1 HG01192.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1285-550A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71750882 | |||||||
| chr16:71751149 | C | T | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1285-817G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71751149 | |||||||
| chr16:71751154 | C | CA | 13 | a0001c0001t0003g0211 a0001c0001t0003g0213 a0001c0001t0004g0012 others(10): Show |
13 | HG00140.hp1 HG00733.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1285-823dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71751154 | |||||||
| chr16:71751154 | CA | C | 52 | a0001c0001t0002g0201 a0001c0001t0002g0215 a0001c0001t0002g0291 others(49): Show |
52 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.1285-823delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71751154 | |||||||
| chr16:71751324 | C | CAAT | 4 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 others(1): Show |
4 | HG01258.hp1 HG02257.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1285-995_1285-993d others(5): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71751324 | |||||||
| chr16:71751401 | T | C | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1285-1069A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71751401 | |||||||
| chr16:71751432 | A | G | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1285-1100T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71751432 | |||||||
| chr16:71751471 | GA | G | 29 | a0001c0001t0007g0066 a0001c0001t0007g0071 a0001c0001t0007g0073 others(26): Show |
30 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1285-1140delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71751471 | |||||||
| chr16:71751914 | A | C | 107 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(104): Show |
107 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1285-1582T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71751914 | |||||||
| chr16:71752163 | T | C | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1284+1670A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71752163 | |||||||
| chr16:71752175 | A | G | 1 | a0001c0001t0004g0020 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1284+1658T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71752175 | |||||||
| chr16:71752634 | T | C | 55 | a0001c0001t0002g0044 a0001c0001t0002g0198 a0001c0001t0002g0210 others(52): Show |
55 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1284+1199A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71752634 | |||||||
| chr16:71752797 | T | TA | 5 | a0001c0001t0015g0035 a0001c0001t0015g0036 a0001c0001t0015g0037 others(2): Show |
5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1284+1035dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71752797 | |||||||
| chr16:71752890 | T | C | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1284+943A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71752890 | |||||||
| chr16:71752950 | A | G | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1284+883T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71752950 | |||||||
| chr16:71753015 | T | C | 1 | a0001c0001t0004g0033 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1284+818A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71753015 | |||||||
| chr16:71753091 | G | A | 26 | a0001c0001t0007g0066 a0001c0001t0007g0071 a0001c0001t0007g0073 others(23): Show |
27 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1284+742C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71753091 | |||||||
| chr16:71753121 | G | A | 2 | a0001c0001t0020g0064 a0001c0009t0019g0010 |
2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1284+712C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71753121 | |||||||
| chr16:71753235 | G | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1284+598C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71753235 | |||||||
| chr16:71753535 | C | A | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1284+298G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71753535 | |||||||
| chr16:71753685 | G | A | 12 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(9): Show |
12 | HG00733.hp1 HG01361.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1284+148C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71753685 | |||||||
| chr16:71753785 | C | T | 18 | a0001c0001t0002g0194 a0001c0001t0002g0201 a0001c0001t0002g0239 others(15): Show |
18 | HG00408.hp2 HG00741.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.1284+48G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71753785 | |||||||
| chr16:71753809 | T | C | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1284+24A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 13/22 | chr16 | 71753809 | |||||||
| chr16:71754015 | G | C | 64 | a0001c0001t0002g0133 a0001c0001t0005g0050 a0001c0001t0005g0051 others(61): Show |
64 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1230-128C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71754015 | |||||||
| chr16:71754340 | AAAAG | A | 44 | a0001c0001t0005g0043 a0001c0001t0005g0050 a0001c0001t0005g0051 others(41): Show |
45 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.1230-457_1230-454d others(6): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71754340 | |||||||
| chr16:71754498 | T | C | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1230-611A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71754498 | |||||||
| chr16:71754927 | G | C | 121 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(118): Show |
121 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1230-1040C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71754927 | |||||||
| chr16:71754941 | C | T | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1230-1054G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71754941 | |||||||
| chr16:71755024 | G | T | 1 | a0001c0001t0002g0264 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1229+995C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755024 | |||||||
| chr16:71755128 | T | C | 2 | a0001c0001t0004g0300 a0001c0001t0018g0314 |
2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1229+891A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755128 | |||||||
| chr16:71755190 | C | G | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1229+829G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755190 | |||||||
| chr16:71755331 | G | T | 2 | a0001c0001t0002g0133 a0002c0002t0001g0109 |
2 | HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1229+688C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755331 | |||||||
| chr16:71755460 | C | A | 1 | a0001c0001t0002g0264 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1229+559G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755460 | |||||||
| chr16:71755559 | T | C | 35 | a0001c0001t0002g0229 a0001c0001t0002g0232 a0001c0001t0002g0233 others(32): Show |
35 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1229+460A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755559 | |||||||
| chr16:71755590 | G | T | 1 | a0002c0002t0001g0135 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1229+429C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755590 | |||||||
| chr16:71755626 | A | C | 280 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(277): Show |
281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.1229+393T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755626 | |||||||
| chr16:71755639 | AT | A | 9 | a0001c0001t0003g0208 a0001c0001t0003g0209 a0001c0001t0003g0212 others(6): Show |
9 | HG01099.hp1 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1229+379delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755639 | |||||||
| chr16:71755647 | T | G | 153 | a0001c0001t0002g0133 a0001c0001t0004g0300 a0001c0001t0005g0050 others(150): Show |
154 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.1229+372A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755647 | |||||||
| chr16:71755650 | T | G | 280 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(277): Show |
281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.1229+369A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755650 | |||||||
| chr16:71755707 | A | G | 27 | a0001c0001t0007g0066 a0001c0001t0007g0071 a0001c0001t0007g0073 others(24): Show |
28 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1229+312T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755707 | |||||||
| chr16:71755770 | C | T | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1229+249G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755770 | |||||||
| chr16:71755771 | G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1229+248C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755771 | |||||||
| chr16:71755933 | C | T | 1 | a0002c0002t0006g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1229+86G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 12/22 | chr16 | 71755933 | |||||||
| chr16:71756181 | A | G | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1089-22T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756181 | |||||||
| chr16:71756182 | AAC | A | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1089-25_1089-24del others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756182 | |||||||
| chr16:71756263 | G | A | 285 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(282): Show |
286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.1089-104C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756263 | |||||||
| chr16:71756300 | C | A | 1 | a0001c0001t0002g0225 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1089-141G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756300 | |||||||
| chr16:71756318 | A | G | 280 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(277): Show |
281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.1089-159T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756318 | |||||||
| chr16:71756454 | G | T | 1 | a0002c0002t0006g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1089-295C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756454 | |||||||
| chr16:71756664 | G | A | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1089-505C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756664 | |||||||
| chr16:71756770 | C | T | 122 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(119): Show |
122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1089-611G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756770 | |||||||
| chr16:71756850 | G | A | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG00099.hp2 HG00639.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1089-691C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756850 | |||||||
| chr16:71756855 | T | C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1089-696A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756855 | |||||||
| chr16:71756879 | T | C | 1 | a0001c0001t0004g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1089-720A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756879 | |||||||
| chr16:71756909 | A | C | 285 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(282): Show |
286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.1089-750T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756909 | |||||||
| chr16:71756930 | C | CA | 58 | a0001c0001t0002g0266 a0001c0001t0003g0275 a0001c0001t0004g0011 others(55): Show |
58 | HG00642.hp2 HG00738.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.1089-772dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756930 | |||||||
| chr16:71756930 | CA | C | 18 | a0001c0001t0002g0215 a0001c0001t0002g0240 a0001c0001t0002g0279 others(15): Show |
18 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1089-772delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71756930 | |||||||
| chr16:71757123 | A | G | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1089-964T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71757123 | |||||||
| chr16:71757370 | G | C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1089-1211C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71757370 | |||||||
| chr16:71757401 | A | AGGTCG | 122 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(119): Show |
122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1089-1247_1089-124 others(9): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71757401 | |||||||
| chr16:71757525 | G | A | 1 | a0001c0001t0005g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1088+1283C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71757525 | |||||||
| chr16:71757526 | A | T | 150 | a0001c0001t0002g0133 a0001c0001t0005g0050 a0001c0001t0005g0051 others(147): Show |
151 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.1088+1282T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71757526 | |||||||
| chr16:71757895 | C | T | 121 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(118): Show |
121 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1088+913G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71757895 | |||||||
| chr16:71757950 | GCT | G | 5 | a0001c0001t0007g0087 a0001c0001t0007g0090 a0001c0001t0009g0072 others(2): Show |
5 | HG01256.hp2 HG03942.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1088+856_1088+857d others(4): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71757950 | |||||||
| chr16:71758029 | T | C | 1 | a0001c0001t0004g0033 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1088+779A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758029 | |||||||
| chr16:71758086 | G | C | 1 | a0002c0002t0001g0141 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1088+722C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758086 | |||||||
| chr16:71758266 | C | A | 1 | a0001c0001t0003g0219 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1088+542G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758266 | |||||||
| chr16:71758287 | G | A | 97 | a0001c0001t0002g0133 a0001c0001t0005g0093 a0001c0001t0005g0112 others(94): Show |
97 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1088+521C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758287 | |||||||
| chr16:71758305 | T | C | 122 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(119): Show |
122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1088+503A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758305 | |||||||
| chr16:71758496 | T | C | 1 | a0001c0001t0005g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1088+312A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758496 | |||||||
| chr16:71758502 | C | T | 1 | a0001c0001t0007g0087 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1088+306G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758502 | |||||||
| chr16:71758516 | T | C | 1 | a0002c0002t0001g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1088+292A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758516 | |||||||
| chr16:71758579 | T | TAAAAAAA others(18): Show |
1 | a0001c0001t0013g0282 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1088+228_1088+229i others(27): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758579 | |||||||
| chr16:71758692 | T | C | 1 | a0002c0002t0001g0167 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1088+116A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758692 | |||||||
| chr16:71758793 | C | A | 41 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(38): Show |
42 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.1088+15G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 11/22 | chr16 | 71758793 | |||||||
| chr16:71759147 | T | C | 3 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0080 |
3 | HG01168.hp1 HG01169.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.975-226A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71759147 | |||||||
| chr16:71759422 | C | T | 1 | a0001c0001t0015g0038 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.975-501G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71759422 | |||||||
| chr16:71759621 | G | A | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.975-700C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71759621 | |||||||
| chr16:71759637 | G | A | 1 | a0001c0003t0008g0183 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.975-716C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71759637 | |||||||
| chr16:71759714 | C | T | 1 | a0001c0001t0005g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.975-793G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71759714 | |||||||
| chr16:71759746 | C | T | 2 | a0001c0001t0002g0232 a0001c0001t0003g0277 |
2 | HG02698.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.975-825G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71759746 | |||||||
| chr16:71759759 | C | CA | 10 | a0001c0001t0004g0032 a0001c0001t0004g0040 a0001c0001t0010g0002 others(7): Show |
10 | HG00738.hp2 HG01891.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.975-839dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71759759 | |||||||
| chr16:71759770 | A | T | 278 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(275): Show |
279 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.975-849T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71759770 | |||||||
| chr16:71759771 | A | T | 2 | a0001c0001t0004g0300 a0001c0001t0018g0314 |
2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.975-850T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71759771 | |||||||
| chr16:71760101 | G | A | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.975-1180C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760101 | |||||||
| chr16:71760158 | C | T | 41 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(38): Show |
42 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.975-1237G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760158 | |||||||
| chr16:71760165 | C | A | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.975-1244G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760165 | |||||||
| chr16:71760230 | CT | C | 269 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(266): Show |
270 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.974+1281delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760230 | |||||||
| chr16:71760230 | CTT | C | 11 | a0001c0001t0004g0061 a0001c0001t0004g0300 a0001c0001t0007g0078 others(8): Show |
11 | HG01168.hp1 HG01256.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.974+1280_974+1281d others(4): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760230 | |||||||
| chr16:71760336 | A | C | 1 | a0002c0002t0001g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.974+1176T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760336 | |||||||
| chr16:71760376 | C | T | 5 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.974+1136G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760376 | |||||||
| chr16:71760545 | C | CA | 29 | a0001c0001t0002g0044 a0001c0001t0004g0013 a0001c0001t0016g0041 others(26): Show |
29 | HG00642.hp2 HG00738.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.974+966dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760545 | |||||||
| chr16:71760579 | G | C | 2 | a0001c0001t0004g0300 a0001c0001t0018g0314 |
2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.974+933C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760579 | |||||||
| chr16:71760620 | C | T | 1 | a0001c0003t0008g0186 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.974+892G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760620 | |||||||
| chr16:71760768 | C | A | 1 | a0002c0002t0001g0130 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.974+744G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760768 | |||||||
| chr16:71760769 | G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.974+743C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760769 | |||||||
| chr16:71760831 | A | G | 302 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(299): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.974+681T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760831 | |||||||
| chr16:71760839 | G | A | 1 | a0002c0002t0001g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.974+673C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760839 | |||||||
| chr16:71760884 | C | G | 1 | a0002c0002t0001g0130 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.974+628G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760884 | |||||||
| chr16:71760987 | G | A | 1 | a0002c0002t0006g0173 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.974+525C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71760987 | |||||||
| chr16:71761063 | A | G | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.974+449T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71761063 | |||||||
| chr16:71761072 | G | A | 1 | a0001c0001t0004g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.974+440C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71761072 | |||||||
| chr16:71761098 | G | A | 1 | a0001c0001t0003g0270 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.974+414C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71761098 | |||||||
| chr16:71761226 | T | C | 1 | a0002c0002t0001g0111 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.974+286A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71761226 | |||||||
| chr16:71761366 | A | G | 1 | a0001c0001t0007g0090 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.974+146T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 10/22 | chr16 | 71761366 | |||||||
| chr16:71761645 | A | G | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.919-78T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71761645 | |||||||
| chr16:71761675 | A | G | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.919-108T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71761675 | |||||||
| chr16:71761742 | G | A | 1 | a0001c0001t0003g0274 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.919-175C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71761742 | |||||||
| chr16:71761800 | G | C | 2 | a0001c0001t0020g0064 a0001c0009t0019g0010 |
2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.919-233C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71761800 | |||||||
| chr16:71761816 | C | CA | 17 | a0001c0001t0002g0291 a0001c0001t0004g0012 a0001c0001t0004g0018 others(14): Show |
17 | HG00642.hp2 HG01123.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.919-250dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71761816 | |||||||
| chr16:71761816 | C | CAA | 12 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(9): Show |
12 | HG00738.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.919-251_919-250dup others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71761816 | |||||||
| chr16:71761816 | CA | C | 20 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0257 others(17): Show |
20 | HG00738.hp2 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.919-250delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71761816 | |||||||
| chr16:71761816 | CAA | C | 32 | a0001c0001t0002g0044 a0001c0001t0002g0198 a0001c0001t0002g0210 others(29): Show |
32 | HG00733.hp2 HG01099.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.919-251_919-250del others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71761816 | |||||||
| chr16:71761882 | G | T | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.919-315C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71761882 | |||||||
| chr16:71762225 | A | G | 1 | a0002c0002t0001g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.919-658T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71762225 | |||||||
| chr16:71762244 | G | C | 2 | a0001c0001t0004g0013 a0001c0001t0004g0018 |
2 | HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.919-677C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71762244 | |||||||
| chr16:71762501 | C | T | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.919-934G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71762501 | |||||||
| chr16:71762700 | C | T | 1 | a0002c0002t0001g0126 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.919-1133G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71762700 | |||||||
| chr16:71762840 | CCTGA | C | 26 | a0001c0001t0007g0066 a0001c0001t0007g0071 a0001c0001t0007g0073 others(23): Show |
27 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.919-1277_919-1274d others(6): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71762840 | |||||||
| chr16:71762911 | C | G | 5 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.919-1344G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71762911 | |||||||
| chr16:71762914 | C | T | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG00099.hp2 HG00639.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.919-1347G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71762914 | |||||||
| chr16:71763060 | C | A | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.918+1290G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71763060 | |||||||
| chr16:71763121 | G | C | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.918+1229C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71763121 | |||||||
| chr16:71763242 | T | C | 3 | a0001c0001t0002g0210 a0001c0001t0002g0220 a0001c0001t0002g0225 |
3 | HG02071.hp1 HG02165.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.918+1108A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71763242 | |||||||
| chr16:71763334 | G | A | 1 | a0001c0001t0007g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.918+1016C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71763334 | |||||||
| chr16:71763500 | T | A | 1 | a0001c0001t0003g0310 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.918+850A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71763500 | |||||||
| chr16:71763571 | T | C | 4 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0040g0238 others(1): Show |
4 | HG00408.hp2 HG02523.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+779A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71763571 | |||||||
| chr16:71763652 | G | A | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.918+698C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71763652 | |||||||
| chr16:71763653 | G | A | 1 | a0001c0001t0002g0299 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.918+697C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71763653 | |||||||
| chr16:71763689 | G | C | 8 | a0001c0001t0010g0002 a0001c0001t0010g0003 a0001c0001t0010g0004 others(5): Show |
8 | HG00738.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.918+661C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71763689 | |||||||
| chr16:71764047 | T | C | 12 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0281 others(9): Show |
12 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.918+303A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71764047 | |||||||
| chr16:71764140 | C | T | 5 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+210G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71764140 | |||||||
| chr16:71764264 | G | A | 2 | a0001c0001t0037g0082 a0001c0001t0038g0083 |
2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.918+86C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71764264 | |||||||
| chr16:71764321 | G | T | 5 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+29C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 9/22 | chr16 | 71764321 | |||||||
| chr16:71764551 | G | C | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.819+95C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 8/22 | chr16 | 71764551 | |||||||
| chr16:71764573 | C | A | 1 | a0001c0001t0003g0255 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.819+73G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 8/22 | chr16 | 71764573 | |||||||
| chr16:71764628 | T | C | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.819+18A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 8/22 | chr16 | 71764628 | |||||||
| chr16:71764642 | T | C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | splice_region_variant&intron_variant | LOW | c.819+4A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 8/22 | chr16 | 71764642 | |||||||
| chr16:71764918 | C | G | 24 | a0002c0002t0001g0092 a0002c0002t0001g0107 a0002c0002t0001g0108 others(21): Show |
24 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.739-192G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 7/22 | chr16 | 71764918 | |||||||
| chr16:71765197 | G | A | 23 | a0002c0002t0001g0092 a0002c0002t0001g0107 a0002c0002t0001g0108 others(20): Show |
23 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.738+292C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 7/22 | chr16 | 71765197 | |||||||
| chr16:71765444 | A | G | 138 | a0001c0001t0002g0133 a0001c0001t0005g0043 a0001c0001t0005g0050 others(135): Show |
139 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.738+45T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 7/22 | chr16 | 71765444 | |||||||
| chr16:71765455 | A | G | 7 | a0001c0001t0002g0201 a0001c0001t0012g0197 a0001c0001t0012g0200 others(4): Show |
7 | NA18952.hp2 NA18954.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.738+34T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 7/22 | chr16 | 71765455 | |||||||
| chr16:71765468 | A | G | 2 | a0001c0001t0037g0082 a0001c0001t0038g0083 |
2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.738+21T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 7/22 | chr16 | 71765468 | |||||||
| chr16:71765732 | G | C | 2 | a0001c0001t0002g0231 a0001c0001t0002g0290 |
2 | NA18977.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.643-148C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71765732 | |||||||
| chr16:71765829 | A | T | 1 | a0001c0001t0003g0270 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.643-245T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71765829 | |||||||
| chr16:71765856 | G | C | 29 | a0001c0001t0007g0066 a0001c0001t0007g0071 a0001c0001t0007g0073 others(26): Show |
30 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.643-272C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71765856 | |||||||
| chr16:71766091 | T | C | 21 | a0002c0002t0006g0045 a0002c0002t0006g0046 a0002c0002t0006g0099 others(18): Show |
21 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.643-507A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766091 | |||||||
| chr16:71766095 | C | T | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.643-511G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766095 | |||||||
| chr16:71766133 | T | C | 125 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(122): Show |
125 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.643-549A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766133 | |||||||
| chr16:71766142 | G | A | 38 | a0001c0001t0005g0052 a0001c0001t0005g0053 a0001c0001t0005g0055 others(35): Show |
39 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.643-558C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766142 | |||||||
| chr16:71766339 | T | C | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.643-755A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766339 | |||||||
| chr16:71766481 | T | A | 108 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(105): Show |
108 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.643-897A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766481 | |||||||
| chr16:71766547 | T | C | 1 | a0001c0001t0005g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.643-963A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766547 | |||||||
| chr16:71766569 | A | T | 1 | a0001c0001t0002g0303 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.643-985T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766569 | |||||||
| chr16:71766577 | C | T | 2 | a0001c0001t0020g0064 a0001c0009t0019g0010 |
2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.643-993G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766577 | |||||||
| chr16:71766633 | A | AAT | 27 | a0002c0002t0001g0092 a0002c0002t0001g0107 a0002c0002t0001g0108 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.643-1050_643-1049i others(4): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766633 | |||||||
| chr16:71766635 | C | G | 27 | a0002c0002t0001g0092 a0002c0002t0001g0107 a0002c0002t0001g0108 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.643-1051G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766635 | |||||||
| chr16:71766637 | C | G | 27 | a0002c0002t0001g0092 a0002c0002t0001g0107 a0002c0002t0001g0108 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.643-1053G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766637 | |||||||
| chr16:71766697 | G | T | 1 | a0002c0002t0001g0157 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.643-1113C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766697 | |||||||
| chr16:71766756 | A | G | 1 | a0002c0002t0001g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.643-1172T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766756 | |||||||
| chr16:71766796 | G | T | 1 | a0001c0001t0004g0033 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.643-1212C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766796 | |||||||
| chr16:71766846 | T | C | 1 | a0001c0001t0014g0268 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.643-1262A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71766846 | |||||||
| chr16:71767039 | A | G | 303 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(300): Show |
304 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.643-1455T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767039 | |||||||
| chr16:71767059 | T | G | 150 | a0001c0001t0002g0133 a0001c0001t0004g0032 a0001c0001t0005g0050 others(147): Show |
151 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.643-1475A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767059 | |||||||
| chr16:71767081 | C | A | 2 | a0001c0001t0020g0064 a0001c0009t0019g0010 |
2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.643-1497G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767081 | |||||||
| chr16:71767189 | C | G | 281 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(278): Show |
282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.643-1605G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767189 | |||||||
| chr16:71767200 | G | A | 1 | a0001c0001t0004g0025 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.643-1616C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767200 | |||||||
| chr16:71767204 | C | T | 1 | a0001c0001t0004g0025 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.643-1620G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767204 | |||||||
| chr16:71767356 | C | A | 20 | a0002c0002t0006g0045 a0002c0002t0006g0046 a0002c0002t0006g0099 others(17): Show |
20 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.643-1772G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767356 | |||||||
| chr16:71767467 | G | A | 1 | a0001c0001t0004g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.643-1883C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767467 | |||||||
| chr16:71767501 | G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.643-1917C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767501 | |||||||
| chr16:71767533 | A | G | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.643-1949T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767533 | |||||||
| chr16:71767691 | G | C | 124 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(121): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.642+1932C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767691 | |||||||
| chr16:71767955 | C | T | 1 | a0002c0002t0006g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.642+1668G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71767955 | |||||||
| chr16:71768043 | C | T | 11 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(8): Show |
11 | HG00733.hp1 HG01884.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.642+1580G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768043 | |||||||
| chr16:71768055 | T | C | 151 | a0001c0001t0002g0133 a0001c0001t0004g0032 a0001c0001t0005g0050 others(148): Show |
152 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.642+1568A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768055 | |||||||
| chr16:71768090 | C | T | 5 | a0001c0001t0009g0065 a0001c0001t0009g0069 a0001c0001t0009g0079 others(2): Show |
5 | HG01358.hp2 HG01516.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+1533G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768090 | |||||||
| chr16:71768192 | TA | T | 179 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0201 others(176): Show |
180 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.642+1430delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768192 | |||||||
| chr16:71768192 | TAA | T | 44 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0303 others(41): Show |
44 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.642+1429_642+1430d others(4): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768192 | |||||||
| chr16:71768192 | TAAA | T | 68 | a0001c0001t0002g0133 a0001c0001t0004g0032 a0001c0001t0005g0093 others(65): Show |
68 | HG00423.hp2 HG01071.hp2 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.642+1428_642+1430d others(5): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768192 | |||||||
| chr16:71768220 | G | A | 2 | a0001c0001t0009g0069 a0001c0001t0009g0079 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.642+1403C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768220 | |||||||
| chr16:71768231 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.642+1392G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768231 | |||||||
| chr16:71768358 | G | A | 124 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(121): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.642+1265C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768358 | |||||||
| chr16:71768479 | C | T | 98 | a0001c0001t0002g0133 a0001c0001t0004g0032 a0001c0001t0005g0093 others(95): Show |
98 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.642+1144G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768479 | |||||||
| chr16:71768500 | C | CAAAAAAA others(1): Show |
17 | a0002c0002t0006g0045 a0002c0002t0006g0046 a0002c0002t0006g0099 others(14): Show |
17 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.642+1115_642+1122d others(10): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768500 | |||||||
| chr16:71768500 | C | CAAAAAAA others(2): Show |
19 | a0001c0001t0002g0298 a0001c0001t0005g0043 a0001c0001t0016g0041 others(16): Show |
19 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.642+1114_642+1122d others(11): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768500 | |||||||
| chr16:71768500 | C | CAAAAAAA others(3): Show |
215 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(212): Show |
216 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.642+1113_642+1122d others(12): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768500 | |||||||
| chr16:71768500 | C | CAAAAAAA others(4): Show |
29 | a0001c0001t0002g0266 a0001c0001t0002g0308 a0001c0001t0002g0316 others(26): Show |
29 | HG01175.hp2 HG01358.hp2 HG01515.hp1 others(26): Show |
intron_variant | MODIFIER | c.642+1112_642+1122d others(13): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768500 | |||||||
| chr16:71768500 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0002g0302 a0002c0002t0001g0154 |
2 | HG01433.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.642+1111_642+1122d others(14): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768500 | |||||||
| chr16:71768500 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.642+1110_642+1122d others(15): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768500 | |||||||
| chr16:71768500 | C | CCAAAAAA others(3): Show |
2 | a0002c0002t0001g0156 a0002c0002t0001g0157 |
2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.642+1122_642+1123i others(12): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768500 | |||||||
| chr16:71768512 | A | AAAAAAAA others(3): Show |
1 | a0002c0002t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.642+1110_642+1111i others(12): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768512 | |||||||
| chr16:71768558 | G | A | 1 | a0002c0002t0031g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.642+1065C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768558 | |||||||
| chr16:71768595 | A | G | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.642+1028T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768595 | |||||||
| chr16:71768626 | T | C | 1 | a0001c0001t0016g0042 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.642+997A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768626 | |||||||
| chr16:71768655 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.642+968G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768655 | |||||||
| chr16:71768664 | A | C | 281 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(278): Show |
282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.642+959T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768664 | |||||||
| chr16:71768759 | C | CA | 74 | a0001c0001t0002g0133 a0001c0001t0004g0032 a0001c0001t0005g0093 others(71): Show |
74 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.642+863dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768759 | |||||||
| chr16:71768776 | G | A | 1 | a0001c0001t0002g0263 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.642+847C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768776 | |||||||
| chr16:71768810 | G | A | 1 | a0001c0001t0004g0017 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.642+813C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768810 | |||||||
| chr16:71768843 | G | A | 1 | a0002c0002t0006g0173 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.642+780C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768843 | |||||||
| chr16:71768904 | C | A | 123 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(120): Show |
123 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.642+719G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768904 | |||||||
| chr16:71768910 | T | C | 1 | a0001c0001t0002g0283 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.642+713A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768910 | |||||||
| chr16:71768917 | C | CA | 51 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0014 others(48): Show |
51 | HG00099.hp1 HG00642.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.642+705dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768917 | |||||||
| chr16:71768917 | C | CAA | 8 | a0001c0001t0004g0011 a0001c0001t0004g0016 a0001c0001t0004g0026 others(5): Show |
8 | HG01123.hp2 HG01981.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+704_642+705dup others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768917 | |||||||
| chr16:71768917 | CA | C | 10 | a0001c0001t0002g0261 a0001c0001t0002g0276 a0001c0001t0002g0284 others(7): Show |
10 | HG00642.hp1 HG00733.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.642+705delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768917 | |||||||
| chr16:71768917 | CAA | C | 109 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(106): Show |
109 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.642+704_642+705del others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768917 | |||||||
| chr16:71768917 | CAAA | C | 8 | a0001c0001t0002g0233 a0001c0001t0002g0240 a0001c0001t0002g0241 others(5): Show |
8 | HG00639.hp2 HG00735.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+703_642+705del others(3): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768917 | |||||||
| chr16:71768934 | A | G | 1 | a0001c0001t0004g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.642+689T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768934 | |||||||
| chr16:71768936 | A | G | 22 | a0001c0001t0002g0249 a0001c0001t0002g0259 a0001c0001t0002g0301 others(19): Show |
22 | HG00621.hp1 HG00733.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.642+687T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768936 | |||||||
| chr16:71768965 | T | TA | 272 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(269): Show |
273 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.642+657dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768965 | |||||||
| chr16:71768978 | C | CA | 93 | a0001c0001t0002g0133 a0001c0001t0002g0242 a0001c0001t0002g0244 others(90): Show |
93 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.642+644dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768978 | |||||||
| chr16:71768978 | C | CAA | 101 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(98): Show |
101 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.642+643_642+644dup others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768978 | |||||||
| chr16:71768978 | C | CAAA | 13 | a0001c0001t0002g0229 a0001c0001t0002g0233 a0001c0001t0002g0241 others(10): Show |
13 | HG00735.hp1 HG01192.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.642+642_642+644dup others(3): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768978 | |||||||
| chr16:71768978 | CA | C | 42 | a0001c0001t0004g0031 a0001c0001t0005g0051 a0001c0001t0005g0052 others(39): Show |
43 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.642+644delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768978 | |||||||
| chr16:71768988 | A | AC | 3 | a0001c0001t0002g0302 a0001c0001t0003g0310 a0002c0002t0001g0109 |
3 | HG01433.hp1 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.642+634_642+635ins others(1): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71768988 | |||||||
| chr16:71769121 | A | G | 1 | a0001c0001t0036g0271 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.642+502T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71769121 | |||||||
| chr16:71769212 | GGA | G | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.642+409_642+410del others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71769212 | |||||||
| chr16:71769232 | G | A | 8 | a0001c0001t0010g0002 a0001c0001t0010g0003 a0001c0001t0010g0004 others(5): Show |
8 | HG00738.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.642+391C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71769232 | |||||||
| chr16:71769364 | T | C | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.642+259A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 6/22 | chr16 | 71769364 | |||||||
| chr16:71769926 | G | T | 17 | a0001c0001t0002g0210 a0001c0001t0002g0220 a0001c0001t0002g0225 others(14): Show |
17 | HG01099.hp1 HG01256.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.566-227C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71769926 | |||||||
| chr16:71769964 | T | C | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.566-265A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71769964 | |||||||
| chr16:71770011 | G | T | 107 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(104): Show |
107 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.566-312C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71770011 | |||||||
| chr16:71770070 | A | C | 1 | a0002c0002t0006g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.566-371T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71770070 | |||||||
| chr16:71770071 | G | A | 124 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(121): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.566-372C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71770071 | |||||||
| chr16:71770191 | C | T | 4 | a0002c0002t0001g0111 a0002c0002t0001g0123 a0002c0002t0001g0124 others(1): Show |
4 | HG02083.hp1 HG02523.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-492G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71770191 | |||||||
| chr16:71770212 | C | T | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.566-513G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71770212 | |||||||
| chr16:71770384 | A | G | 285 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(282): Show |
286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.566-685T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71770384 | |||||||
| chr16:71770811 | T | C | 1 | a0001c0001t0016g0042 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.565+345A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71770811 | |||||||
| chr16:71770899 | C | T | 280 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(277): Show |
281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.565+257G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71770899 | |||||||
| chr16:71771015 | C | G | 3 | a0001c0001t0002g0233 a0001c0001t0002g0240 a0001c0001t0002g0241 |
3 | HG00735.hp1 HG01169.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.565+141G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71771015 | |||||||
| chr16:71771053 | C | G | 280 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(277): Show |
281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.565+103G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 5/22 | chr16 | 71771053 | |||||||
| chr16:71771257 | G | A | 286 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(283): Show |
287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
splice_region_variant&intron_variant | LOW | c.469-5C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71771257 | |||||||
| chr16:71771302 | G | A | 1 | a0002c0002t0001g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.469-50C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71771302 | |||||||
| chr16:71771496 | G | A | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.469-244C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71771496 | |||||||
| chr16:71771715 | T | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.469-463A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71771715 | |||||||
| chr16:71771839 | T | C | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.469-587A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71771839 | |||||||
| chr16:71771909 | T | C | 1 | a0002c0002t0001g0150 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.469-657A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71771909 | |||||||
| chr16:71772006 | C | T | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.469-754G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772006 | |||||||
| chr16:71772017 | A | G | 2 | a0001c0001t0020g0064 a0001c0008t0008g0181 |
2 | HG02809.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.469-765T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772017 | |||||||
| chr16:71772024 | C | T | 5 | a0001c0001t0015g0035 a0001c0001t0015g0036 a0001c0001t0015g0037 others(2): Show |
5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-772G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772024 | |||||||
| chr16:71772036 | G | C | 3 | a0002c0002t0006g0171 a0002c0002t0006g0172 a0002c0002t0006g0173 |
3 | HG00642.hp2 HG00738.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.469-784C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772036 | |||||||
| chr16:71772138 | C | CT | 285 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(282): Show |
286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.469-887dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772138 | |||||||
| chr16:71772153 | C | T | 1 | a0002c0002t0001g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.469-901G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772153 | |||||||
| chr16:71772162 | G | T | 41 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(38): Show |
42 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.469-910C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772162 | |||||||
| chr16:71772303 | G | T | 1 | a0002c0002t0001g0048 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.468+918C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772303 | |||||||
| chr16:71772350 | T | C | 1 | a0002c0002t0001g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.468+871A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772350 | |||||||
| chr16:71772411 | G | A | 149 | a0001c0001t0002g0133 a0001c0001t0005g0050 a0001c0001t0005g0051 others(146): Show |
150 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.468+810C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772411 | |||||||
| chr16:71772496 | A | G | 1 | a0001c0001t0002g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.468+725T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772496 | |||||||
| chr16:71772588 | G | A | 1 | a0002c0002t0001g0180 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.468+633C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772588 | |||||||
| chr16:71772673 | T | G | 1 | a0001c0001t0002g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.468+548A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772673 | |||||||
| chr16:71772862 | T | C | 1 | a0001c0001t0011g0248 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.468+359A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772862 | |||||||
| chr16:71772966 | G | A | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.468+255C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71772966 | |||||||
| chr16:71773053 | C | G | 2 | a0001c0001t0005g0119 a0001c0001t0005g0122 |
2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.468+168G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71773053 | |||||||
| chr16:71773128 | A | G | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.468+93T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 4/22 | chr16 | 71773128 | |||||||
| chr16:71773388 | A | G | 3 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0080 |
3 | HG01168.hp1 HG01169.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.327-26T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773388 | |||||||
| chr16:71773501 | T | C | 1 | a0001c0001t0004g0034 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.327-139A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773501 | |||||||
| chr16:71773546 | T | A | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.327-184A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773546 | |||||||
| chr16:71773651 | A | G | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.327-289T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773651 | |||||||
| chr16:71773733 | A | C | 1 | a0001c0001t0007g0090 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.327-371T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773733 | |||||||
| chr16:71773738 | T | A | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.327-376A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773738 | |||||||
| chr16:71773812 | G | A | 1 | a0002c0002t0001g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.327-450C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773812 | |||||||
| chr16:71773846 | G | C | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.327-484C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773846 | |||||||
| chr16:71773868 | T | G | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.327-506A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773868 | |||||||
| chr16:71773907 | C | T | 41 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(38): Show |
42 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.327-545G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773907 | |||||||
| chr16:71773920 | G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.326+548C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71773920 | |||||||
| chr16:71774067 | G | GA | 9 | a0001c0001t0002g0198 a0001c0001t0002g0281 a0001c0001t0003g0212 others(6): Show |
9 | HG01106.hp2 HG01978.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.326+400dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71774067 | |||||||
| chr16:71774103 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.326+365G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71774103 | |||||||
| chr16:71774244 | G | A | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.326+224C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71774244 | |||||||
| chr16:71774285 | G | A | 2 | a0001c0001t0020g0064 a0001c0008t0008g0181 |
2 | HG02809.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.326+183C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71774285 | |||||||
| chr16:71774332 | C | T | 145 | a0001c0001t0002g0133 a0001c0001t0005g0050 a0001c0001t0005g0051 others(142): Show |
146 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.326+136G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 3/22 | chr16 | 71774332 | |||||||
| chr16:71774919 | CCATGTTG others(304): Show |
C | 2 | a0001c0001t0002g0249 a0001c0001t0002g0259 |
2 | HG00621.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.202-638_202-328del | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71774919 | |||||||
| chr16:71775019 | C | CT | 39 | a0001c0001t0002g0194 a0001c0001t0002g0201 a0001c0001t0002g0210 others(36): Show |
39 | HG00408.hp1 HG00408.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.202-428dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775019 | |||||||
| chr16:71775019 | CT | C | 18 | a0001c0001t0004g0315 a0001c0001t0005g0050 a0001c0001t0005g0114 others(15): Show |
18 | HG00423.hp2 HG00741.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.202-428delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775019 | |||||||
| chr16:71775019 | CTT | C | 133 | a0001c0001t0002g0133 a0001c0001t0005g0043 a0001c0001t0005g0051 others(130): Show |
134 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.202-429_202-428del others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775019 | |||||||
| chr16:71775120 | G | T | 1 | a0001c0001t0003g0205 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.202-528C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775120 | |||||||
| chr16:71775125 | C | T | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.202-533G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775125 | |||||||
| chr16:71775185 | C | T | 119 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(116): Show |
119 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.202-593G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775185 | |||||||
| chr16:71775233 | T | C | 6 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0014 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-641A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775233 | |||||||
| chr16:71775294 | A | G | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.202-702T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775294 | |||||||
| chr16:71775335 | C | T | 27 | a0002c0002t0001g0092 a0002c0002t0001g0107 a0002c0002t0001g0108 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.202-743G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775335 | |||||||
| chr16:71775495 | A | G | 1 | a0001c0001t0004g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.202-903T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775495 | |||||||
| chr16:71775566 | C | T | 1 | a0001c0001t0005g0112 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.202-974G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775566 | |||||||
| chr16:71775631 | C | T | 124 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(121): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.202-1039G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775631 | |||||||
| chr16:71775758 | C | T | 1 | a0002c0002t0001g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.202-1166G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71775758 | |||||||
| chr16:71776058 | C | A | 2 | a0001c0001t0009g0069 a0001c0001t0009g0079 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.202-1466G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776058 | |||||||
| chr16:71776061 | T | G | 1 | a0001c0003t0008g0192 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.202-1469A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776061 | |||||||
| chr16:71776085 | C | T | 1 | a0001c0001t0002g0278 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.202-1493G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776085 | |||||||
| chr16:71776113 | G | C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.202-1521C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776113 | |||||||
| chr16:71776182 | G | A | 1 | a0002c0002t0001g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.202-1590C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776182 | |||||||
| chr16:71776297 | G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.202-1705C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776297 | |||||||
| chr16:71776431 | A | G | 1 | a0002c0002t0001g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.202-1839T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776431 | |||||||
| chr16:71776591 | T | C | 2 | a0002c0002t0001g0319 a0002c0002t0039g0318 |
2 | HG02071.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.202-1999A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776591 | |||||||
| chr16:71776685 | T | C | 3 | a0002c0002t0001g0134 a0002c0002t0001g0162 a0002c0002t0033g0152 |
3 | NA18951.hp2 NA19003.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.202-2093A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776685 | |||||||
| chr16:71776725 | C | A | 1 | a0001c0001t0002g0216 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.202-2133G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776725 | |||||||
| chr16:71776778 | T | C | 4 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-2186A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776778 | |||||||
| chr16:71776793 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.202-2201G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776793 | |||||||
| chr16:71776850 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.202-2258G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776850 | |||||||
| chr16:71776860 | A | G | 41 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(38): Show |
42 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.202-2268T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71776860 | |||||||
| chr16:71777101 | T | C | 2 | a0002c0002t0001g0048 a0002c0002t0001g0144 |
2 | NA18966.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.202-2509A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777101 | |||||||
| chr16:71777106 | C | CA | 43 | a0001c0001t0002g0198 a0001c0001t0002g0225 a0001c0001t0002g0227 others(40): Show |
43 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.202-2515dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777106 | |||||||
| chr16:71777106 | C | CAA | 11 | a0001c0001t0002g0216 a0001c0001t0002g0233 a0001c0001t0002g0241 others(8): Show |
11 | HG00735.hp1 HG01192.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.202-2516_202-2515d others(4): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777106 | |||||||
| chr16:71777106 | CA | C | 89 | a0001c0001t0002g0133 a0001c0001t0004g0013 a0001c0001t0004g0017 others(86): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.202-2515delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777106 | |||||||
| chr16:71777106 | CAA | C | 58 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0015 others(55): Show |
59 | HG00609.hp2 HG00733.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.202-2516_202-2515d others(4): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777106 | |||||||
| chr16:71777195 | C | A | 151 | a0001c0001t0002g0133 a0001c0001t0005g0050 a0001c0001t0005g0051 others(148): Show |
152 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.202-2603G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777195 | |||||||
| chr16:71777272 | C | A | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.202-2680G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777272 | |||||||
| chr16:71777371 | G | A | 4 | a0002c0002t0001g0111 a0002c0002t0001g0123 a0002c0002t0001g0124 others(1): Show |
4 | HG02083.hp1 HG02523.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-2779C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777371 | |||||||
| chr16:71777471 | G | C | 27 | a0002c0002t0001g0092 a0002c0002t0001g0107 a0002c0002t0001g0108 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.202-2879C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777471 | |||||||
| chr16:71777791 | T | C | 4 | a0001c0001t0002g0233 a0001c0001t0002g0240 a0001c0001t0002g0241 others(1): Show |
4 | HG00735.hp1 HG01169.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-3199A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777791 | |||||||
| chr16:71777891 | C | G | 1 | a0002c0002t0001g0154 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.202-3299G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777891 | |||||||
| chr16:71777982 | T | C | 4 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-3390A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71777982 | |||||||
| chr16:71778092 | G | A | 41 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(38): Show |
42 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.202-3500C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778092 | |||||||
| chr16:71778280 | C | A | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.202-3688G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778280 | |||||||
| chr16:71778393 | A | G | 302 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(299): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.202-3801T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778393 | |||||||
| chr16:71778493 | C | T | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG00099.hp2 HG00639.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.202-3901G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778493 | |||||||
| chr16:71778500 | C | T | 1 | a0001c0001t0004g0032 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.202-3908G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778500 | |||||||
| chr16:71778543 | C | T | 2 | a0001c0001t0013g0287 a0001c0001t0013g0288 |
2 | NA18612.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.202-3951G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778543 | |||||||
| chr16:71778576 | G | A | 1 | a0001c0001t0004g0032 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.202-3984C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778576 | |||||||
| chr16:71778637 | C | T | 2 | a0001c0001t0009g0069 a0001c0001t0009g0079 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.202-4045G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778637 | |||||||
| chr16:71778640 | G | A | 1 | a0002c0002t0001g0156 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.202-4048C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778640 | |||||||
| chr16:71778682 | TA | T | 284 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(281): Show |
285 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.202-4091delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778682 | |||||||
| chr16:71778768 | G | A | 294 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(291): Show |
295 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.202-4176C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778768 | |||||||
| chr16:71778965 | C | T | 1 | a0002c0002t0033g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.202-4373G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778965 | |||||||
| chr16:71778988 | C | T | 1 | a0001c0001t0005g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.202-4396G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71778988 | |||||||
| chr16:71779073 | G | T | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.202-4481C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779073 | |||||||
| chr16:71779098 | T | A | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.202-4506A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779098 | |||||||
| chr16:71779177 | T | C | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.202-4585A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779177 | |||||||
| chr16:71779180 | C | G | 4 | a0001c0001t0002g0233 a0001c0001t0002g0240 a0001c0001t0002g0241 others(1): Show |
4 | HG00735.hp1 HG01169.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-4588G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779180 | |||||||
| chr16:71779377 | AC | A | 4 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-4786delG | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779377 | |||||||
| chr16:71779456 | T | C | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.202-4864A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779456 | |||||||
| chr16:71779623 | A | G | 1 | a0001c0001t0004g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.202-5031T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779623 | |||||||
| chr16:71779773 | T | C | 1 | a0001c0001t0004g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.202-5181A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779773 | |||||||
| chr16:71779848 | T | C | 123 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(120): Show |
123 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.202-5256A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779848 | |||||||
| chr16:71779877 | G | T | 12 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(9): Show |
12 | HG00733.hp1 HG01361.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-5285C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779877 | |||||||
| chr16:71779973 | A | C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.202-5381T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779973 | |||||||
| chr16:71779984 | AGTTTTTT others(3): Show |
A | 1 | a0001c0001t0004g0300 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.202-5402_202-5393d others(12): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779984 | |||||||
| chr16:71779995 | G | GT | 38 | a0001c0001t0002g0309 a0001c0001t0003g0211 a0001c0001t0004g0315 others(35): Show |
38 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.202-5404dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779995 | |||||||
| chr16:71779995 | G | T | 12 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-5403C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71779995 | |||||||
| chr16:71780017 | G | C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.202-5425C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780017 | |||||||
| chr16:71780056 | C | T | 124 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(121): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.202-5464G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780056 | |||||||
| chr16:71780141 | G | A | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.202-5549C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780141 | |||||||
| chr16:71780154 | C | T | 151 | a0001c0001t0002g0133 a0001c0001t0005g0050 a0001c0001t0005g0051 others(148): Show |
152 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.202-5562G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780154 | |||||||
| chr16:71780178 | G | A | 1 | a0001c0001t0005g0117 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.202-5586C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780178 | |||||||
| chr16:71780228 | A | T | 1 | a0002c0002t0001g0144 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.202-5636T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780228 | |||||||
| chr16:71780241 | G | A | 1 | a0001c0001t0014g0268 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.202-5649C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780241 | |||||||
| chr16:71780271 | G | A | 1 | a0001c0001t0002g0316 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.202-5679C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780271 | |||||||
| chr16:71780463 | C | T | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.202-5871G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780463 | |||||||
| chr16:71780497 | T | A | 2 | a0001c0001t0020g0064 a0001c0008t0008g0181 |
2 | HG02809.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.202-5905A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780497 | |||||||
| chr16:71780497 | T | TA | 120 | a0001c0001t0002g0133 a0001c0001t0003g0277 a0001c0001t0004g0040 others(117): Show |
121 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.202-5906dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780497 | |||||||
| chr16:71780497 | T | TAA | 10 | a0001c0001t0005g0093 a0001c0001t0005g0114 a0001c0001t0005g0115 others(7): Show |
10 | HG01358.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.202-5907_202-5906d others(4): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780497 | |||||||
| chr16:71780497 | TA | T | 14 | a0001c0001t0002g0244 a0001c0001t0002g0303 a0001c0001t0002g0308 others(11): Show |
14 | HG00323.hp1 HG01496.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.202-5906delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780497 | |||||||
| chr16:71780757 | T | G | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.202-6165A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780757 | |||||||
| chr16:71780820 | C | CT | 6 | a0001c0001t0004g0034 a0001c0001t0015g0035 a0001c0001t0015g0036 others(3): Show |
6 | HG01515.hp1 HG01934.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-6229dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780820 | |||||||
| chr16:71780925 | C | T | 1 | a0002c0002t0017g0129 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.202-6333G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780925 | |||||||
| chr16:71780951 | G | A | 1 | a0002c0002t0001g0147 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.202-6359C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71780951 | |||||||
| chr16:71781231 | C | A | 1 | a0001c0001t0002g0312 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.202-6639G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71781231 | |||||||
| chr16:71781275 | T | C | 1 | a0002c0002t0001g0095 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.202-6683A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71781275 | |||||||
| chr16:71781380 | C | G | 2 | a0001c0001t0002g0249 a0001c0001t0002g0259 |
2 | HG00621.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.202-6788G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71781380 | |||||||
| chr16:71781381 | T | C | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.202-6789A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71781381 | |||||||
| chr16:71781423 | C | T | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.202-6831G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71781423 | |||||||
| chr16:71781487 | T | C | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.202-6895A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71781487 | |||||||
| chr16:71781799 | T | C | 60 | a0001c0001t0002g0133 a0002c0002t0001g0048 a0002c0002t0001g0095 others(57): Show |
60 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.202-7207A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71781799 | |||||||
| chr16:71782010 | C | T | 285 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(282): Show |
286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.201+7269G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782010 | |||||||
| chr16:71782208 | G | C | 1 | a0001c0001t0010g0002 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.201+7071C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782208 | |||||||
| chr16:71782250 | G | A | 1 | a0001c0001t0015g0038 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.201+7029C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782250 | |||||||
| chr16:71782288 | G | A | 41 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(38): Show |
42 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.201+6991C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782288 | |||||||
| chr16:71782466 | A | AATT | 59 | a0001c0001t0002g0133 a0002c0002t0001g0048 a0002c0002t0001g0095 others(56): Show |
59 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.201+6810_201+6812d others(5): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782466 | |||||||
| chr16:71782466 | A | AATTATTA others(2): Show |
11 | a0001c0001t0005g0093 a0001c0001t0005g0112 a0001c0001t0005g0114 others(8): Show |
11 | HG02109.hp1 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.201+6804_201+6812d others(11): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782466 | |||||||
| chr16:71782466 | A | AATTATTA others(5): Show |
1 | a0001c0001t0005g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.201+6801_201+6812d others(14): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782466 | |||||||
| chr16:71782479 | ATTATTAT others(5): Show |
A | 1 | a0002c0002t0022g0094 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.201+6788_201+6799d others(14): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782479 | |||||||
| chr16:71782488 | A | T | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.201+6791T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782488 | |||||||
| chr16:71782491 | T | A | 1 | a0002c0002t0039g0318 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.201+6788A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782491 | |||||||
| chr16:71782762 | AG | A | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.201+6516delC | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782762 | |||||||
| chr16:71782996 | G | A | 280 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(277): Show |
281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.201+6283C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71782996 | |||||||
| chr16:71783068 | G | C | 2 | a0002c0002t0001g0096 a0002c0002t0001g0137 |
2 | NA19002.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.201+6211C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783068 | |||||||
| chr16:71783077 | CTTTAT | C | 3 | a0001c0001t0002g0301 a0001c0001t0002g0307 a0001c0001t0002g0311 |
3 | HG02280.hp1 HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.201+6197_201+6201d others(7): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783077 | |||||||
| chr16:71783104 | T | C | 1 | a0001c0001t0009g0067 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.201+6175A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783104 | |||||||
| chr16:71783115 | G | A | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.201+6164C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783115 | |||||||
| chr16:71783230 | T | A | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.201+6049A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783230 | |||||||
| chr16:71783267 | A | C | 138 | a0001c0001t0002g0133 a0001c0001t0005g0050 a0001c0001t0005g0051 others(135): Show |
139 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.201+6012T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783267 | |||||||
| chr16:71783270 | A | G | 2 | a0001c0001t0004g0300 a0001c0001t0018g0314 |
2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.201+6009T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783270 | |||||||
| chr16:71783309 | T | C | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.201+5970A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783309 | |||||||
| chr16:71783396 | A | G | 1 | a0001c0003t0008g0184 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.201+5883T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783396 | |||||||
| chr16:71783574 | T | G | 1 | a0002c0002t0001g0131 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.201+5705A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783574 | |||||||
| chr16:71783682 | G | A | 1 | a0001c0001t0011g0248 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.201+5597C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783682 | |||||||
| chr16:71783831 | T | G | 1 | a0002c0002t0001g0138 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.201+5448A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71783831 | |||||||
| chr16:71784018 | C | A | 3 | a0002c0002t0001g0095 a0002c0002t0001g0125 a0004c0006t0001g0132 |
3 | HG01168.hp2 HG02074.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.201+5261G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71784018 | |||||||
| chr16:71784246 | T | C | 2 | a0001c0001t0004g0031 a0001c0001t0004g0032 |
2 | NA18954.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.201+5033A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71784246 | |||||||
| chr16:71784281 | A | T | 1 | a0002c0002t0006g0172 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.201+4998T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71784281 | |||||||
| chr16:71784528 | C | G | 41 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(38): Show |
42 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.201+4751G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71784528 | |||||||
| chr16:71784597 | C | T | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.201+4682G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71784597 | |||||||
| chr16:71784643 | C | T | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.201+4636G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71784643 | |||||||
| chr16:71784725 | A | C | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.201+4554T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71784725 | |||||||
| chr16:71784787 | G | T | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.201+4492C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71784787 | |||||||
| chr16:71784928 | T | G | 1 | a0001c0001t0002g0302 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.201+4351A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71784928 | |||||||
| chr16:71785135 | G | T | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.201+4144C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785135 | |||||||
| chr16:71785243 | G | T | 2 | a0001c0001t0020g0064 a0001c0009t0019g0010 |
2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.201+4036C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785243 | |||||||
| chr16:71785348 | G | A | 1 | a0001c0001t0014g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.201+3931C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785348 | |||||||
| chr16:71785384 | T | C | 2 | a0001c0001t0002g0231 a0001c0001t0002g0290 |
2 | NA18977.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.201+3895A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785384 | |||||||
| chr16:71785425 | A | C | 1 | a0002c0002t0001g0048 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.201+3854T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785425 | |||||||
| chr16:71785575 | C | CA | 27 | a0001c0001t0002g0229 a0001c0001t0002g0239 a0001c0001t0002g0241 others(24): Show |
27 | HG00735.hp1 HG00741.hp2 HG01358.hp1 others(24): Show |
intron_variant | MODIFIER | c.201+3703dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785575 | |||||||
| chr16:71785575 | CA | C | 127 | a0001c0001t0002g0133 a0001c0001t0002g0216 a0001c0001t0002g0232 others(124): Show |
128 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.201+3703delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785575 | |||||||
| chr16:71785575 | CAAA | C | 24 | a0002c0002t0001g0092 a0002c0002t0001g0107 a0002c0002t0001g0108 others(21): Show |
24 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.201+3701_201+3703d others(5): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785575 | |||||||
| chr16:71785577 | A | G | 3 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0040g0238 |
3 | HG00408.hp2 HG02523.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.201+3702T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785577 | |||||||
| chr16:71785678 | G | A | 40 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(37): Show |
41 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.201+3601C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785678 | |||||||
| chr16:71785744 | T | C | 5 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+3535A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785744 | |||||||
| chr16:71785787 | A | C | 1 | a0001c0001t0013g0287 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.201+3492T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71785787 | |||||||
| chr16:71786006 | G | A | 1 | a0001c0001t0009g0067 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.201+3273C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786006 | |||||||
| chr16:71786008 | G | C | 1 | a0002c0002t0001g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.201+3271C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786008 | |||||||
| chr16:71786045 | T | C | 6 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 others(3): Show |
6 | HG02074.hp1 HG02257.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.201+3234A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786045 | |||||||
| chr16:71786139 | G | A | 1 | a0001c0001t0002g0259 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.201+3140C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786139 | |||||||
| chr16:71786172 | C | T | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.201+3107G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786172 | |||||||
| chr16:71786202 | T | C | 1 | a0001c0001t0023g0121 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.201+3077A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786202 | |||||||
| chr16:71786301 | GTCTTAAA others(5): Show |
G | 2 | a0001c0001t0016g0041 a0001c0001t0016g0042 |
2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.201+2966_201+2977d others(14): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786301 | |||||||
| chr16:71786390 | T | C | 1 | a0001c0001t0004g0025 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.201+2889A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786390 | |||||||
| chr16:71786608 | G | A | 3 | a0001c0001t0009g0065 a0001c0001t0009g0085 a0001c0001t0009g0086 |
3 | HG01358.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.201+2671C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786608 | |||||||
| chr16:71786633 | G | C | 1 | a0001c0001t0004g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.201+2646C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786633 | |||||||
| chr16:71786724 | T | G | 285 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(282): Show |
286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.201+2555A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786724 | |||||||
| chr16:71786748 | C | T | 11 | a0002c0002t0001g0111 a0002c0002t0001g0123 a0002c0002t0001g0124 others(8): Show |
11 | HG00323.hp1 HG00323.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.201+2531G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786748 | |||||||
| chr16:71786893 | T | C | 1 | a0001c0001t0015g0038 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.201+2386A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786893 | |||||||
| chr16:71786940 | C | T | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.201+2339G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71786940 | |||||||
| chr16:71787175 | C | T | 1 | a0001c0001t0004g0030 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.201+2104G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787175 | |||||||
| chr16:71787224 | C | A | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.201+2055G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787224 | |||||||
| chr16:71787245 | G | C | 1 | a0002c0002t0031g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.201+2034C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787245 | |||||||
| chr16:71787267 | C | T | 3 | a0002c0002t0001g0139 a0002c0002t0001g0148 a0002c0002t0031g0160 |
3 | HG03017.hp1 HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.201+2012G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787267 | |||||||
| chr16:71787318 | CA | C | 15 | a0001c0001t0004g0040 a0001c0001t0010g0002 a0001c0001t0010g0003 others(12): Show |
15 | HG00738.hp2 HG01515.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.201+1960delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787318 | |||||||
| chr16:71787318 | CAAAA | C | 25 | a0001c0001t0002g0233 a0001c0001t0002g0266 a0001c0001t0002g0267 others(22): Show |
25 | HG00140.hp1 HG00408.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.201+1957_201+1960d others(6): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787318 | |||||||
| chr16:71787318 | CAAAAA | C | 214 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(211): Show |
215 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.201+1956_201+1960d others(7): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787318 | |||||||
| chr16:71787318 | CAAAAAA | C | 37 | a0001c0001t0002g0316 a0001c0003t0008g0183 a0001c0003t0008g0184 others(34): Show |
37 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.201+1955_201+1960d others(8): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787318 | |||||||
| chr16:71787356 | T | C | 6 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0014 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.201+1923A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787356 | |||||||
| chr16:71787392 | G | T | 1 | a0001c0001t0003g0214 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.201+1887C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787392 | |||||||
| chr16:71787474 | C | T | 124 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(121): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.201+1805G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787474 | |||||||
| chr16:71787656 | T | C | 1 | a0001c0001t0002g0194 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.201+1623A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787656 | |||||||
| chr16:71787897 | A | T | 11 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(8): Show |
11 | HG00733.hp1 HG01884.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.201+1382T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71787897 | |||||||
| chr16:71788075 | C | G | 1 | a0002c0002t0031g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.201+1204G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788075 | |||||||
| chr16:71788119 | T | A | 1 | a0002c0002t0001g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.201+1160A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788119 | |||||||
| chr16:71788120 | A | C | 1 | a0002c0002t0001g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.201+1159T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788120 | |||||||
| chr16:71788198 | T | A | 280 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(277): Show |
281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.201+1081A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788198 | |||||||
| chr16:71788328 | C | T | 124 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(121): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.201+951G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788328 | |||||||
| chr16:71788347 | A | C | 280 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(277): Show |
281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.201+932T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788347 | |||||||
| chr16:71788616 | C | T | 1 | a0001c0001t0002g0278 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.201+663G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788616 | |||||||
| chr16:71788638 | T | C | 1 | a0001c0001t0002g0261 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.201+641A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788638 | |||||||
| chr16:71788657 | CTT | C | 267 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(264): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.201+620_201+621del others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788657 | |||||||
| chr16:71788667 | T | A | 100 | a0001c0001t0002g0133 a0001c0001t0002g0216 a0001c0001t0002g0303 others(97): Show |
100 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.201+612A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788667 | |||||||
| chr16:71788667 | TA | T | 5 | a0001c0001t0015g0035 a0001c0001t0015g0036 a0001c0001t0015g0037 others(2): Show |
5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+611delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788667 | |||||||
| chr16:71788686 | A | C | 3 | a0002c0002t0001g0096 a0002c0002t0001g0136 a0002c0002t0001g0137 |
3 | NA18965.hp2 NA19002.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.201+593T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788686 | |||||||
| chr16:71788765 | A | C | 2 | a0001c0001t0009g0001 a0001c0001t0009g0070 |
3 | HG00609.hp2 NA18968.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.201+514T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788765 | |||||||
| chr16:71788771 | C | G | 3 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0080 |
3 | HG01168.hp1 HG01169.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.201+508G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788771 | |||||||
| chr16:71788825 | CT | C | 268 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(265): Show |
269 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.201+453delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71788825 | |||||||
| chr16:71789100 | T | C | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.201+179A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71789100 | |||||||
| chr16:71789214 | T | C | 18 | a0001c0001t0002g0194 a0001c0001t0002g0201 a0001c0001t0002g0239 others(15): Show |
18 | HG00408.hp2 HG00741.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.201+65A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 2/22 | chr16 | 71789214 | |||||||
| chr16:71789541 | A | T | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-59T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71789541 | |||||||
| chr16:71789787 | T | C | 1 | a0001c0001t0002g0194 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-3-305A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71789787 | |||||||
| chr16:71789944 | A | G | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-3-462T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71789944 | |||||||
| chr16:71790051 | A | G | 5 | a0001c0001t0015g0035 a0001c0001t0015g0036 a0001c0001t0015g0037 others(2): Show |
5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-569T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790051 | |||||||
| chr16:71790100 | TA | T | 282 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(279): Show |
283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.-3-619delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790100 | |||||||
| chr16:71790130 | A | G | 1 | a0001c0001t0012g0292 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-3-648T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790130 | |||||||
| chr16:71790210 | G | C | 1 | a0001c0001t0010g0003 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-3-728C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790210 | |||||||
| chr16:71790268 | C | T | 124 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(121): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.-3-786G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790268 | |||||||
| chr16:71790293 | C | A | 4 | a0001c0003t0008g0184 a0001c0003t0008g0189 a0001c0003t0008g0190 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-811G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790293 | |||||||
| chr16:71790339 | G | A | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-3-857C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790339 | |||||||
| chr16:71790359 | G | A | 1 | a0002c0002t0033g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-3-877C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790359 | |||||||
| chr16:71790480 | T | C | 1 | a0001c0001t0002g0244 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-3-998A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790480 | |||||||
| chr16:71790527 | C | CA | 123 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(120): Show |
123 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.-3-1046dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790527 | |||||||
| chr16:71790664 | C | A | 8 | a0001c0001t0010g0002 a0001c0001t0010g0003 a0001c0001t0010g0004 others(5): Show |
8 | HG00738.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3-1182G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790664 | |||||||
| chr16:71790682 | G | A | 5 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-1200C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790682 | |||||||
| chr16:71790769 | A | G | 12 | a0002c0002t0001g0111 a0002c0002t0001g0123 a0002c0002t0001g0124 others(9): Show |
12 | HG00323.hp1 HG00323.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3-1287T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790769 | |||||||
| chr16:71790811 | C | T | 41 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(38): Show |
42 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.-3-1329G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71790811 | |||||||
| chr16:71791010 | C | G | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-3-1528G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791010 | |||||||
| chr16:71791040 | G | C | 1 | a0001c0001t0003g0230 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-3-1558C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791040 | |||||||
| chr16:71791225 | C | CA | 12 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3-1744dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791225 | |||||||
| chr16:71791238 | C | CA | 6 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0014 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-1757dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791238 | |||||||
| chr16:71791247 | C | A | 1 | a0001c0001t0005g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-3-1765G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791247 | |||||||
| chr16:71791400 | T | C | 2 | a0001c0001t0013g0287 a0001c0001t0013g0288 |
2 | NA18612.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-3-1918A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791400 | |||||||
| chr16:71791424 | C | T | 2 | a0001c0001t0009g0069 a0001c0001t0009g0079 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-3-1942G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791424 | |||||||
| chr16:71791539 | G | T | 1 | a0001c0001t0007g0080 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-3-2057C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791539 | |||||||
| chr16:71791542 | A | G | 280 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(277): Show |
281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.-3-2060T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791542 | |||||||
| chr16:71791673 | CA | C | 267 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(264): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.-3-2192delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791673 | |||||||
| chr16:71791728 | C | T | 7 | a0001c0001t0004g0017 a0001c0001t0004g0026 a0001c0001t0004g0027 others(4): Show |
7 | HG00099.hp1 HG01123.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3-2246G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791728 | |||||||
| chr16:71791763 | C | CT | 170 | a0001c0001t0002g0044 a0001c0001t0002g0198 a0001c0001t0002g0201 others(167): Show |
171 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.-3-2282dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791763 | |||||||
| chr16:71791763 | C | CTT | 16 | a0001c0001t0002g0194 a0001c0001t0002g0244 a0001c0001t0002g0245 others(13): Show |
16 | HG00741.hp2 HG01175.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.-3-2283_-3-2282dup others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791763 | |||||||
| chr16:71791763 | CT | C | 11 | a0001c0001t0005g0093 a0001c0001t0005g0112 a0001c0001t0005g0113 others(8): Show |
11 | HG02109.hp1 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-2282delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791763 | |||||||
| chr16:71791876 | C | T | 5 | a0001c0001t0015g0035 a0001c0001t0015g0036 a0001c0001t0015g0037 others(2): Show |
5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-2394G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791876 | |||||||
| chr16:71791948 | G | C | 41 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(38): Show |
42 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.-3-2466C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791948 | |||||||
| chr16:71791990 | G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3-2508C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71791990 | |||||||
| chr16:71792095 | G | A | 124 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(121): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.-3-2613C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792095 | |||||||
| chr16:71792122 | T | C | 7 | a0001c0001t0004g0017 a0001c0001t0004g0026 a0001c0001t0004g0027 others(4): Show |
7 | HG00099.hp1 HG01123.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3-2640A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792122 | |||||||
| chr16:71792162 | G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3-2680C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792162 | |||||||
| chr16:71792185 | T | A | 1 | a0002c0002t0001g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-3-2703A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792185 | |||||||
| chr16:71792425 | T | G | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3-2943A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792425 | |||||||
| chr16:71792618 | T | C | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-3-3136A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792618 | |||||||
| chr16:71792704 | A | C | 3 | a0002c0002t0006g0045 a0002c0002t0006g0046 a0002c0002t0017g0047 |
3 | NA18941.hp2 NA18990.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-3-3222T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792704 | |||||||
| chr16:71792708 | G | T | 41 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(38): Show |
42 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.-3-3226C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792708 | |||||||
| chr16:71792773 | T | C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-3-3291A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792773 | |||||||
| chr16:71792833 | G | A | 1 | a0002c0002t0001g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-3-3351C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792833 | |||||||
| chr16:71792980 | C | T | 42 | a0001c0001t0002g0242 a0001c0001t0005g0050 a0001c0001t0005g0051 others(39): Show |
43 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.-3-3498G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71792980 | |||||||
| chr16:71793086 | C | A | 5 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-3604G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793086 | |||||||
| chr16:71793162 | G | C | 1 | a0001c0001t0010g0004 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-3-3680C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793162 | |||||||
| chr16:71793291 | T | C | 3 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0080 |
3 | HG01168.hp1 HG01169.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.-3-3809A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793291 | |||||||
| chr16:71793357 | A | G | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3-3875T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793357 | |||||||
| chr16:71793747 | C | G | 1 | a0002c0002t0001g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-3-4265G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793747 | |||||||
| chr16:71793753 | CGGCTCAC others(18): Show |
C | 5 | a0001c0001t0015g0035 a0001c0001t0015g0036 a0001c0001t0015g0037 others(2): Show |
5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-4296_-3-4272del others(25): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793753 | |||||||
| chr16:71793847 | C | T | 3 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0054 |
3 | HG02602.hp2 HG02683.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-3-4365G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793847 | |||||||
| chr16:71793870 | A | C | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-4388T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793870 | |||||||
| chr16:71793889 | T | C | 27 | a0002c0002t0001g0092 a0002c0002t0001g0107 a0002c0002t0001g0108 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.-3-4407A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793889 | |||||||
| chr16:71793896 | T | C | 71 | a0001c0001t0002g0133 a0001c0001t0005g0093 a0001c0001t0005g0112 others(68): Show |
71 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-3-4414A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71793896 | |||||||
| chr16:71794025 | T | G | 3 | a0001c0001t0009g0065 a0001c0001t0009g0085 a0001c0001t0009g0086 |
3 | HG01358.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-3-4543A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794025 | |||||||
| chr16:71794298 | G | T | 1 | a0002c0002t0001g0169 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-3-4816C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794298 | |||||||
| chr16:71794494 | G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3-5012C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794494 | |||||||
| chr16:71794574 | C | G | 1 | a0001c0001t0002g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-3-5092G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794574 | |||||||
| chr16:71794630 | T | C | 3 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0030 |
3 | HG00099.hp1 HG02257.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-3-5148A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794630 | |||||||
| chr16:71794671 | A | G | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3-5189T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794671 | |||||||
| chr16:71794713 | C | T | 41 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(38): Show |
42 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.-3-5231G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794713 | |||||||
| chr16:71794835 | C | CT | 7 | a0001c0001t0002g0233 a0001c0001t0004g0012 a0001c0001t0004g0030 others(4): Show |
7 | HG01192.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3-5354dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794835 | C | CTTT | 7 | a0001c0001t0004g0061 a0001c0008t0008g0181 a0002c0002t0001g0092 others(4): Show |
7 | HG02055.hp2 HG02165.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3-5356_-3-5354dup others(3): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794835 | C | CTTTT | 8 | a0001c0001t0004g0040 a0002c0002t0006g0104 a0002c0002t0006g0105 others(5): Show |
8 | HG00738.hp1 HG01123.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3-5357_-3-5354dup others(4): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794835 | C | CTTTTCTT others(4): Show |
2 | a0001c0003t0008g0191 a0001c0003t0008g0192 |
2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-3-5354_-3-5353ins others(11): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794835 | C | CTTTTCTT others(5): Show |
8 | a0001c0003t0008g0183 a0001c0003t0008g0185 a0001c0003t0008g0186 others(5): Show |
8 | HG01891.hp1 HG02258.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3-5354_-3-5353ins others(12): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794835 | C | CTTTTCTT others(6): Show |
1 | a0001c0003t0008g0184 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-3-5354_-3-5353ins others(13): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794835 | C | CTTTTT | 13 | a0001c0001t0009g0065 a0001c0001t0009g0086 a0002c0002t0001g0153 others(10): Show |
13 | HG00642.hp2 HG00741.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-3-5358_-3-5354dup others(5): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794835 | C | CTTTTTT | 14 | a0001c0001t0009g0085 a0002c0002t0001g0048 a0002c0002t0001g0126 others(11): Show |
14 | HG00323.hp1 HG00323.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3-5359_-3-5354dup others(6): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794835 | C | CTTTTTTT | 33 | a0002c0002t0001g0095 a0002c0002t0001g0096 a0002c0002t0001g0111 others(30): Show |
33 | HG00423.hp2 HG01168.hp2 HG02071.hp2 others(30): Show |
intron_variant | MODIFIER | c.-3-5360_-3-5354dup others(7): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794835 | C | CTTTTTTT others(1): Show |
8 | a0001c0001t0007g0080 a0001c0001t0007g0087 a0001c0001t0009g0001 others(5): Show |
9 | HG00609.hp2 HG01257.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3-5361_-3-5354dup others(8): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794835 | C | CTTTTTTT others(2): Show |
18 | a0001c0001t0005g0122 a0001c0001t0007g0071 a0001c0001t0007g0073 others(15): Show |
18 | HG00140.hp1 HG01168.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.-3-5362_-3-5354dup others(9): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794835 | C | CTTTTTTT others(3): Show |
8 | a0001c0001t0002g0133 a0001c0001t0005g0060 a0001c0001t0005g0118 others(5): Show |
8 | HG01106.hp1 HG02486.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3-5363_-3-5354dup others(10): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794835 | C | CTTTTTTT others(4): Show |
9 | a0001c0001t0005g0058 a0001c0001t0005g0059 a0001c0001t0005g0093 others(6): Show |
9 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3-5364_-3-5354dup others(11): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794835 | C | CTTTTTTT others(5): Show |
8 | a0001c0001t0005g0051 a0001c0001t0005g0054 a0001c0001t0005g0055 others(5): Show |
8 | HG02683.hp2 HG02970.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3-5365_-3-5354dup others(12): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794835 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0005g0050 a0002c0002t0001g0167 a0004c0006t0001g0132 |
3 | HG02074.hp2 HG02602.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.-3-5366_-3-5354dup others(13): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794835 | CT | C | 99 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(96): Show |
99 | HG00140.hp2 HG00408.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.-3-5354delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794835 | CTTTTTTT others(5): Show |
C | 1 | a0002c0002t0001g0089 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-3-5365_-3-5354del others(12): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794835 | CTTTTTTT others(7): Show |
C | 1 | a0002c0002t0001g0158 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-3-5367_-3-5354del others(14): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794835 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-3-5368_-3-5354del others(15): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794835 | CTTTTTTT others(11): Show |
C | 1 | a0002c0002t0006g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-3-5371_-3-5354del others(18): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794835 | |||||||
| chr16:71794916 | C | A | 1 | a0001c0001t0004g0030 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-3-5434G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794916 | |||||||
| chr16:71794958 | C | T | 2 | a0002c0002t0001g0126 a0002c0002t0001g0131 |
2 | HG00323.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-3-5476G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71794958 | |||||||
| chr16:71795426 | T | C | 41 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(38): Show |
42 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.-3-5944A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71795426 | |||||||
| chr16:71795962 | C | T | 1 | a0001c0001t0004g0011 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-3-6480G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71795962 | |||||||
| chr16:71796007 | C | G | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-3-6525G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796007 | |||||||
| chr16:71796093 | T | C | 2 | a0001c0001t0004g0300 a0001c0001t0018g0314 |
2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-3-6611A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796093 | |||||||
| chr16:71796485 | G | A | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-3-7003C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796485 | |||||||
| chr16:71796530 | A | G | 1 | a0001c0001t0015g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-3-7048T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796530 | |||||||
| chr16:71796636 | C | T | 1 | a0001c0001t0003g0205 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-3-7154G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796636 | |||||||
| chr16:71796744 | T | C | 1 | a0001c0001t0029g0269 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-3-7262A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796744 | |||||||
| chr16:71796768 | T | C | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-3-7286A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796768 | |||||||
| chr16:71796785 | T | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-3-7303A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796785 | |||||||
| chr16:71796855 | A | G | 4 | a0002c0002t0006g0045 a0002c0002t0006g0046 a0002c0002t0017g0047 others(1): Show |
4 | HG03017.hp1 NA18941.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-7373T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796855 | |||||||
| chr16:71796893 | G | A | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-7411C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71796893 | |||||||
| chr16:71797016 | T | TTA | 10 | a0001c0001t0004g0023 a0001c0001t0004g0040 a0001c0001t0010g0002 others(7): Show |
10 | HG00738.hp2 HG01361.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3-7536_-3-7535dup others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797016 | |||||||
| chr16:71797016 | TTA | T | 125 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(122): Show |
125 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-3-7536_-3-7535del others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797016 | |||||||
| chr16:71797018 | A | T | 1 | a0001c0001t0003g0272 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-3-7536T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797018 | |||||||
| chr16:71797019 | T | C | 137 | a0001c0001t0002g0133 a0001c0001t0005g0050 a0001c0001t0005g0051 others(134): Show |
138 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.-3-7537A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797019 | |||||||
| chr16:71797101 | C | T | 1 | a0002c0002t0001g0130 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-3-7619G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797101 | |||||||
| chr16:71797440 | T | A | 124 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(121): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.-3-7958A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797440 | |||||||
| chr16:71797538 | C | T | 5 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-8056G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797538 | |||||||
| chr16:71797629 | T | A | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-8147A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797629 | |||||||
| chr16:71797656 | G | A | 5 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-8174C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797656 | |||||||
| chr16:71797674 | C | T | 2 | a0001c0001t0003g0208 a0001c0001t0003g0209 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-3-8192G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797674 | |||||||
| chr16:71797696 | G | A | 1 | a0001c0001t0002g0296 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-3-8214C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797696 | |||||||
| chr16:71797736 | T | C | 1 | a0001c0001t0003g0275 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-3-8254A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797736 | |||||||
| chr16:71797810 | G | T | 6 | a0001c0001t0005g0055 a0001c0001t0005g0056 a0001c0001t0005g0057 others(3): Show |
6 | HG01884.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-8328C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797810 | |||||||
| chr16:71797828 | G | C | 1 | a0002c0002t0001g0159 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-3-8346C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797828 | |||||||
| chr16:71797850 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-3-8368G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797850 | |||||||
| chr16:71797947 | A | C | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-3-8465T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797947 | |||||||
| chr16:71797974 | T | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-3-8492A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71797974 | |||||||
| chr16:71798052 | C | A | 1 | a0001c0001t0038g0083 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-3-8570G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798052 | |||||||
| chr16:71798120 | G | T | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3-8638C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798120 | |||||||
| chr16:71798145 | TATC | T | 4 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 others(1): Show |
4 | HG00099.hp2 HG00639.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-8666_-3-8664del others(3): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798145 | |||||||
| chr16:71798173 | C | T | 5 | a0001c0001t0015g0035 a0001c0001t0015g0036 a0001c0001t0015g0037 others(2): Show |
5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-8691G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798173 | |||||||
| chr16:71798211 | A | G | 5 | a0001c0001t0015g0035 a0001c0001t0015g0036 a0001c0001t0015g0037 others(2): Show |
5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-8729T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798211 | |||||||
| chr16:71798313 | C | T | 8 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(5): Show |
8 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3-8831G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798313 | |||||||
| chr16:71798339 | T | C | 1 | a0001c0001t0004g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-3-8857A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798339 | |||||||
| chr16:71798439 | T | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-3-8957A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798439 | |||||||
| chr16:71798451 | G | A | 2 | a0001c0001t0037g0082 a0001c0001t0038g0083 |
2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-3-8969C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798451 | |||||||
| chr16:71798849 | C | T | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-9367G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798849 | |||||||
| chr16:71798878 | G | C | 2 | a0001c0001t0020g0064 a0001c0009t0019g0010 |
2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-3-9396C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71798878 | |||||||
| chr16:71799429 | C | T | 281 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(278): Show |
282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.-4+9334G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799429 | |||||||
| chr16:71799606 | T | TAAAAAAC others(344): Show |
1 | a0001c0001t0004g0031 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-4+9156_-4+9157ins others(351): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799606 | |||||||
| chr16:71799606 | T | TAAAAAAC others(349): Show |
1 | a0001c0001t0004g0032 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-4+9156_-4+9157ins others(356): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799606 | |||||||
| chr16:71799625 | G | A | 2 | a0001c0001t0004g0061 a0001c0008t0008g0181 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-4+9138C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799625 | |||||||
| chr16:71799754 | C | G | 1 | a0002c0002t0001g0111 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-4+9009G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799754 | |||||||
| chr16:71799755 | G | C | 286 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(283): Show |
287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.-4+9008C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799755 | |||||||
| chr16:71799772 | G | A | 1 | a0001c0001t0003g0270 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-4+8991C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799772 | |||||||
| chr16:71799816 | G | A | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-4+8947C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799816 | |||||||
| chr16:71799901 | AAAT | A | 41 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(38): Show |
42 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.-4+8859_-4+8861del others(3): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799901 | |||||||
| chr16:71799928 | A | T | 128 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(125): Show |
128 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.-4+8835T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799928 | |||||||
| chr16:71799959 | G | A | 2 | a0003c0005t0001g0165 a0003c0005t0001g0166 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-4+8804C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799959 | |||||||
| chr16:71799990 | G | A | 1 | a0002c0002t0006g0172 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-4+8773C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71799990 | |||||||
| chr16:71800080 | T | C | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-4+8683A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800080 | |||||||
| chr16:71800137 | G | A | 1 | a0001c0001t0007g0084 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-4+8626C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800137 | |||||||
| chr16:71800139 | T | G | 6 | a0001c0001t0005g0055 a0001c0001t0005g0056 a0001c0001t0005g0057 others(3): Show |
6 | HG01884.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+8624A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800139 | |||||||
| chr16:71800200 | T | TA | 7 | a0001c0001t0004g0033 a0001c0001t0005g0043 a0001c0001t0009g0065 others(4): Show |
7 | HG01358.hp2 HG01516.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+8562dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800200 | |||||||
| chr16:71800224 | AG | A | 151 | a0001c0001t0002g0133 a0001c0001t0004g0061 a0001c0001t0005g0050 others(148): Show |
152 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.-4+8538delC | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800224 | |||||||
| chr16:71800228 | G | A | 2 | a0001c0001t0007g0087 a0001c0001t0007g0090 |
2 | NA18971.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-4+8535C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800228 | |||||||
| chr16:71800243 | CGCCTGTA others(423): Show |
C | 6 | a0001c0001t0005g0055 a0001c0001t0005g0056 a0001c0001t0005g0057 others(3): Show |
6 | HG01884.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+8090_-4+8519del | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800243 | |||||||
| chr16:71800319 | C | T | 5 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4+8444G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800319 | |||||||
| chr16:71800372 | C | CA | 18 | a0001c0001t0002g0261 a0001c0001t0002g0263 a0001c0003t0008g0183 others(15): Show |
18 | HG01891.hp1 HG02109.hp2 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.-4+8390dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800372 | |||||||
| chr16:71800372 | CA | C | 18 | a0001c0001t0002g0301 a0001c0001t0002g0302 a0001c0001t0002g0303 others(15): Show |
18 | HG01433.hp1 HG02280.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.-4+8390delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800372 | |||||||
| chr16:71800508 | C | A | 143 | a0001c0001t0002g0133 a0001c0001t0005g0050 a0001c0001t0005g0051 others(140): Show |
144 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.-4+8255G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800508 | |||||||
| chr16:71800530 | G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-4+8233C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800530 | |||||||
| chr16:71800540 | G | A | 1 | a0001c0001t0005g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-4+8223C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800540 | |||||||
| chr16:71800551 | T | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-4+8212A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800551 | |||||||
| chr16:71800756 | G | A | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+8007C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800756 | |||||||
| chr16:71800780 | A | G | 6 | a0001c0001t0005g0055 a0001c0001t0005g0056 a0001c0001t0005g0057 others(3): Show |
6 | HG01884.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+7983T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800780 | |||||||
| chr16:71800788 | G | C | 1 | a0002c0002t0001g0319 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-4+7975C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800788 | |||||||
| chr16:71800833 | T | C | 1 | a0001c0001t0005g0054 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-4+7930A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800833 | |||||||
| chr16:71800861 | G | A | 1 | a0001c0001t0036g0271 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-4+7902C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800861 | |||||||
| chr16:71800939 | G | A | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-4+7824C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71800939 | |||||||
| chr16:71801031 | G | A | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-4+7732C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801031 | |||||||
| chr16:71801050 | T | C | 151 | a0001c0001t0002g0133 a0001c0001t0004g0061 a0001c0001t0005g0050 others(148): Show |
152 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.-4+7713A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801050 | |||||||
| chr16:71801128 | G | A | 1 | a0001c0001t0020g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-4+7635C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801128 | |||||||
| chr16:71801174 | G | A | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+7589C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801174 | |||||||
| chr16:71801274 | C | T | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+7489G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801274 | |||||||
| chr16:71801284 | A | C | 32 | a0001c0001t0002g0198 a0001c0001t0002g0210 a0001c0001t0002g0215 others(29): Show |
32 | HG00733.hp2 HG01099.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.-4+7479T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801284 | |||||||
| chr16:71801300 | A | C | 1 | a0002c0002t0021g0097 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-4+7463T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801300 | |||||||
| chr16:71801330 | T | C | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+7433A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801330 | |||||||
| chr16:71801333 | T | TA | 12 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-4+7429dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801333 | |||||||
| chr16:71801333 | TA | T | 187 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(184): Show |
187 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.-4+7429delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801333 | |||||||
| chr16:71801340 | A | C | 41 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(38): Show |
42 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.-4+7423T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801340 | |||||||
| chr16:71801419 | G | A | 2 | a0001c0001t0024g0088 a0002c0002t0001g0089 |
2 | HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-4+7344C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801419 | |||||||
| chr16:71801510 | A | T | 1 | a0002c0002t0001g0175 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-4+7253T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801510 | |||||||
| chr16:71801608 | G | T | 6 | a0001c0001t0005g0043 a0001c0001t0012g0207 a0001c0001t0016g0041 others(3): Show |
6 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+7155C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801608 | |||||||
| chr16:71801707 | G | A | 124 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(121): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.-4+7056C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801707 | |||||||
| chr16:71801781 | G | C | 6 | a0001c0001t0005g0055 a0001c0001t0005g0056 a0001c0001t0005g0057 others(3): Show |
6 | HG01884.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+6982C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801781 | |||||||
| chr16:71801853 | C | T | 1 | a0001c0001t0003g0206 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-4+6910G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801853 | |||||||
| chr16:71801858 | C | G | 1 | a0001c0001t0003g0206 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-4+6905G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801858 | |||||||
| chr16:71801878 | C | CGCCACTG others(7): Show |
1 | a0001c0001t0003g0196 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-4+6871_-4+6884dup others(14): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801878 | |||||||
| chr16:71801922 | C | CA | 14 | a0001c0001t0002g0276 a0001c0001t0002g0278 a0001c0001t0002g0312 others(11): Show |
14 | HG00621.hp2 HG01175.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.-4+6840dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801922 | |||||||
| chr16:71801936 | A | G | 5 | a0001c0001t0015g0035 a0001c0001t0015g0036 a0001c0001t0015g0037 others(2): Show |
5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+6827T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801936 | |||||||
| chr16:71801961 | C | T | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-4+6802G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71801961 | |||||||
| chr16:71802045 | T | C | 11 | a0001c0001t0002g0279 a0001c0001t0002g0281 a0001c0001t0002g0283 others(8): Show |
11 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.-4+6718A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71802045 | |||||||
| chr16:71802403 | G | C | 1 | a0001c0001t0014g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-4+6360C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71802403 | |||||||
| chr16:71802479 | C | T | 1 | a0001c0001t0003g0205 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-4+6284G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71802479 | |||||||
| chr16:71802488 | G | A | 1 | a0001c0001t0004g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-4+6275C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71802488 | |||||||
| chr16:71802524 | G | A | 5 | a0001c0001t0015g0035 a0001c0001t0015g0036 a0001c0001t0015g0037 others(2): Show |
5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+6239C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71802524 | |||||||
| chr16:71802541 | C | G | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-4+6222G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71802541 | |||||||
| chr16:71802569 | A | G | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-4+6194T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71802569 | |||||||
| chr16:71802842 | A | G | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-4+5921T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71802842 | |||||||
| chr16:71803108 | G | A | 1 | a0002c0002t0001g0167 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-4+5655C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803108 | |||||||
| chr16:71803177 | G | C | 1 | a0002c0002t0001g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-4+5586C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803177 | |||||||
| chr16:71803390 | T | A | 1 | a0001c0001t0002g0291 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-4+5373A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803390 | |||||||
| chr16:71803514 | T | G | 1 | a0001c0001t0014g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-4+5249A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803514 | |||||||
| chr16:71803574 | T | G | 149 | a0001c0001t0002g0133 a0001c0001t0005g0050 a0001c0001t0005g0051 others(146): Show |
150 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.-4+5189A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803574 | |||||||
| chr16:71803634 | CT | C | 3 | a0002c0002t0001g0164 a0003c0005t0001g0165 a0003c0005t0001g0166 |
3 | HG03491.hp1 HG03492.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-4+5128delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803634 | |||||||
| chr16:71803789 | G | C | 1 | a0001c0009t0019g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-4+4974C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803789 | |||||||
| chr16:71803794 | G | A | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-4+4969C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803794 | |||||||
| chr16:71803800 | C | A | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-4+4963G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803800 | |||||||
| chr16:71803883 | C | T | 1 | a0002c0002t0001g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-4+4880G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803883 | |||||||
| chr16:71803923 | C | CA | 23 | a0001c0001t0002g0290 a0001c0001t0002g0298 a0001c0001t0005g0093 others(20): Show |
23 | HG01071.hp1 HG01071.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.-4+4839dupT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803923 | |||||||
| chr16:71803923 | C | CAA | 49 | a0001c0001t0002g0133 a0002c0002t0001g0048 a0002c0002t0001g0095 others(46): Show |
49 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.-4+4838_-4+4839dup others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803923 | |||||||
| chr16:71803923 | CA | C | 13 | a0001c0001t0002g0198 a0001c0001t0004g0011 a0001c0001t0004g0012 others(10): Show |
13 | HG01496.hp2 HG02055.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.-4+4839delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803923 | |||||||
| chr16:71803946 | C | T | 1 | a0002c0002t0001g0095 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-4+4817G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803946 | |||||||
| chr16:71803977 | T | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-4+4786A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71803977 | |||||||
| chr16:71804053 | A | AT | 6 | a0001c0001t0002g0201 a0001c0001t0012g0197 a0001c0001t0012g0200 others(3): Show |
6 | NA18952.hp2 NA18954.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+4709dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804053 | |||||||
| chr16:71804053 | A | T | 4 | a0001c0001t0010g0002 a0001c0001t0010g0003 a0001c0001t0010g0004 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+4710T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804053 | |||||||
| chr16:71804057 | T | A | 1 | a0002c0002t0001g0167 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-4+4706A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804057 | |||||||
| chr16:71804087 | C | G | 1 | a0001c0001t0011g0199 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-4+4676G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804087 | |||||||
| chr16:71804172 | G | A | 5 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4+4591C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804172 | |||||||
| chr16:71804274 | C | T | 1 | a0002c0002t0022g0094 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-4+4489G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804274 | |||||||
| chr16:71804298 | G | A | 1 | a0001c0001t0002g0291 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-4+4465C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804298 | |||||||
| chr16:71804408 | A | AT | 7 | a0001c0001t0002g0294 a0001c0001t0002g0295 a0001c0001t0002g0296 others(4): Show |
7 | HG00639.hp2 HG01515.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4+4354dupA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804408 | |||||||
| chr16:71804408 | A | ATT | 117 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(114): Show |
117 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-4+4353_-4+4354dup others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804408 | |||||||
| chr16:71804408 | AT | A | 49 | a0001c0001t0004g0040 a0001c0001t0005g0050 a0001c0001t0005g0051 others(46): Show |
50 | HG00140.hp1 HG00609.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.-4+4354delA | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804408 | |||||||
| chr16:71804555 | A | G | 285 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(282): Show |
286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.-4+4208T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804555 | |||||||
| chr16:71804568 | C | T | 14 | a0001c0001t0002g0301 a0001c0001t0002g0302 a0001c0001t0002g0303 others(11): Show |
14 | HG01433.hp1 HG02280.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-4+4195G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804568 | |||||||
| chr16:71804578 | T | C | 149 | a0001c0001t0002g0133 a0001c0001t0005g0050 a0001c0001t0005g0051 others(146): Show |
150 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.-4+4185A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804578 | |||||||
| chr16:71804678 | G | T | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+4085C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804678 | |||||||
| chr16:71804756 | C | A | 1 | a0001c0001t0007g0090 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-4+4007G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804756 | |||||||
| chr16:71804778 | A | G | 1 | a0001c0001t0002g0198 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-4+3985T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804778 | |||||||
| chr16:71804874 | G | A | 1 | a0001c0004t0007g0091 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-4+3889C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804874 | |||||||
| chr16:71804965 | T | C | 97 | a0001c0001t0002g0133 a0001c0001t0005g0093 a0001c0001t0005g0112 others(94): Show |
97 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.-4+3798A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71804965 | |||||||
| chr16:71805014 | C | A | 3 | a0002c0002t0006g0171 a0002c0002t0006g0172 a0002c0002t0006g0173 |
3 | HG00642.hp2 HG00738.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.-4+3749G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805014 | |||||||
| chr16:71805060 | G | A | 1 | a0001c0001t0012g0197 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-4+3703C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805060 | |||||||
| chr16:71805061 | G | T | 1 | a0001c0001t0012g0197 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-4+3702C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805061 | |||||||
| chr16:71805171 | G | A | 2 | a0001c0001t0020g0064 a0001c0009t0019g0010 |
2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-4+3592C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805171 | |||||||
| chr16:71805207 | G | A | 1 | a0002c0002t0006g0173 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-4+3556C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805207 | |||||||
| chr16:71805312 | G | T | 5 | a0001c0001t0015g0035 a0001c0001t0015g0036 a0001c0001t0015g0037 others(2): Show |
5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+3451C>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805312 | |||||||
| chr16:71805341 | G | A | 3 | a0001c0001t0002g0316 a0001c0001t0020g0064 a0001c0009t0019g0010 |
3 | HG02451.hp2 HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-4+3422C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805341 | |||||||
| chr16:71805387 | T | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-4+3376A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805387 | |||||||
| chr16:71805571 | T | C | 1 | a0002c0002t0001g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-4+3192A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805571 | |||||||
| chr16:71805709 | A | T | 1 | a0002c0002t0001g0092 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-4+3054T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805709 | |||||||
| chr16:71805734 | T | G | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-4+3029A>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805734 | |||||||
| chr16:71805792 | T | C | 6 | a0001c0001t0005g0055 a0001c0001t0005g0056 a0001c0001t0005g0057 others(3): Show |
6 | HG01884.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+2971A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805792 | |||||||
| chr16:71805794 | C | T | 1 | a0001c0001t0003g0196 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-4+2969G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805794 | |||||||
| chr16:71805821 | G | A | 5 | a0001c0001t0015g0035 a0001c0001t0015g0036 a0001c0001t0015g0037 others(2): Show |
5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+2942C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805821 | |||||||
| chr16:71805899 | T | C | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-4+2864A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71805899 | |||||||
| chr16:71806007 | C | A | 28 | a0001c0001t0007g0066 a0001c0001t0007g0071 a0001c0001t0007g0073 others(25): Show |
29 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-4+2756G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806007 | |||||||
| chr16:71806012 | T | C | 124 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(121): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.-4+2751A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806012 | |||||||
| chr16:71806031 | T | A | 1 | a0001c0001t0004g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-4+2732A>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806031 | |||||||
| chr16:71806031 | TA | T | 7 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0008t0008g0181 others(4): Show |
7 | HG00733.hp2 HG02809.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+2731delT | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806031 | |||||||
| chr16:71806031 | TAA | T | 271 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(268): Show |
272 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.-4+2730_-4+2731del others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806031 | |||||||
| chr16:71806034 | A | T | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-4+2729T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806034 | |||||||
| chr16:71806035 | A | T | 2 | a0001c0001t0002g0297 a0001c0001t0002g0298 |
2 | HG00733.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-4+2728T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806035 | |||||||
| chr16:71806036 | A | T | 122 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(119): Show |
122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-4+2727T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806036 | |||||||
| chr16:71806160 | C | A | 97 | a0001c0001t0002g0133 a0001c0001t0005g0093 a0001c0001t0005g0112 others(94): Show |
97 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.-4+2603G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806160 | |||||||
| chr16:71806170 | A | T | 280 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(277): Show |
281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.-4+2593T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806170 | |||||||
| chr16:71806476 | T | C | 1 | a0001c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-4+2287A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806476 | |||||||
| chr16:71806623 | C | T | 1 | a0001c0001t0014g0195 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-4+2140G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806623 | |||||||
| chr16:71806775 | C | T | 1 | a0001c0001t0004g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-4+1988G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806775 | |||||||
| chr16:71806936 | A | T | 8 | a0001c0001t0010g0002 a0001c0001t0010g0003 a0001c0001t0010g0004 others(5): Show |
8 | HG00738.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-4+1827T>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806936 | |||||||
| chr16:71806982 | T | C | 1 | a0002c0002t0001g0182 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-4+1781A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71806982 | |||||||
| chr16:71807032 | T | C | 1 | a0001c0001t0002g0299 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-4+1731A>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807032 | |||||||
| chr16:71807105 | C | A | 11 | a0001c0003t0008g0183 a0001c0003t0008g0184 a0001c0003t0008g0185 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+1658G>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807105 | |||||||
| chr16:71807125 | A | G | 1 | a0001c0001t0004g0300 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-4+1638T>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807125 | |||||||
| chr16:71807185 | GGAGGCC | G | 107 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(104): Show |
107 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.-4+1572_-4+1577del others(6): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807185 | |||||||
| chr16:71807196 | C | G | 1 | a0001c0001t0002g0194 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-4+1567G>C | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807196 | |||||||
| chr16:71807354 | C | T | 11 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(8): Show |
11 | HG00733.hp1 HG01884.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+1409G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807354 | |||||||
| chr16:71807381 | G | A | 124 | a0001c0001t0002g0044 a0001c0001t0002g0194 a0001c0001t0002g0198 others(121): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.-4+1382C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807381 | |||||||
| chr16:71807386 | C | T | 1 | a0002c0002t0001g0048 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-4+1377G>A | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807386 | |||||||
| chr16:71807433 | A | C | 3 | a0002c0002t0006g0045 a0002c0002t0006g0046 a0002c0002t0017g0047 |
3 | NA18941.hp2 NA18990.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-4+1330T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807433 | |||||||
| chr16:71807471 | A | C | 1 | a0001c0001t0002g0044 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-4+1292T>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807471 | |||||||
| chr16:71807598 | G | C | 1 | a0002c0002t0001g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-4+1165C>G | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807598 | |||||||
| chr16:71807919 | G | A | 2 | a0002c0002t0001g0319 a0002c0002t0039g0318 |
2 | HG02071.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-4+844C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71807919 | |||||||
| chr16:71808104 | G | A | 3 | a0001c0001t0005g0043 a0001c0001t0016g0041 a0001c0001t0016g0042 |
3 | HG02257.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-4+659C>T | AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71808104 | |||||||
| chr16:71808204 | C | CAACA | 276 | a0001c0001t0002g0044 a0001c0001t0002g0133 a0001c0001t0002g0194 others(273): Show |
277 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.-4+555_-4+558dupTG others(2): Show |
AP1G1 | ENSG00000166747.13 | transcript | ENST00000299980.9 | protein_coding | 1/22 | chr16 | 71808204 |