Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64756 |
| ensemblid | ENSG00000123472.13 |
| hgncid | 18803 |
| symbol | ATPAF1 |
| name | ATP synthase mitochondrial F1 complex assembly factor 1 |
| refseq_nuc | NM_001394565.1 |
| refseq_prot | NP_001381494.1 |
| ensembl_nuc | ENST00000574428.6 |
| ensembl_prot | ENSP00000459167.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 46632737 |
| end | 46668364 |
| strand | - |
| ver | v1.2 |
| region | chr1:46632737-46668364 |
| region5000 | chr1:46627737-46673364 |
| regionname0 | ATPAF1_chr1_46632737_46668364 |
| regionname5000 | ATPAF1_chr1_46627737_46673364 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 328 | 359 | 85 | 51 | 183 | 8 | 32 | 142 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | MAAVV others(323): Show |
chr1 | 46627737 | 46673364 |
| a0002 | 1/1 | 328 | 51 | 9 | 7 | 15 | 4 | 14 | 10 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | MAAVV others(323): Show |
chr1 | 46627737 | 46673364 |
| a0003 | 0/0 | 328 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | MAAVV others(323): Show |
chr1 | 46627737 | 46673364 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 984 | 358 | 84 | 51 | 183 | 8 | 32 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | ATGGC others(979): Show |
chr1 | 46627737 | 46673364 | ||
| a0001c0004 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | ATGGC others(979): Show |
chr1 | 46627737 | 46673364 | ||
| a0002c0002 | 1/1 | 984 | 51 | 9 | 7 | 15 | 4 | 14 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | ATGGC others(979): Show |
chr1 | 46627737 | 46673364 | ||
| a0003c0003 | 0/0 | 984 | 2 | 0 | 2 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | ATGGC others(979): Show |
chr1 | 46627737 | 46673364 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4068 | 110 | 34 | 4 | 63 | 0 | 9 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0002 | 0/0 | 4068 | 105 | 9 | 20 | 64 | 1 | 11 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0003 | 0/0 | 4069 | 75 | 12 | 21 | 31 | 4 | 7 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4064): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0004 | 0/0 | 4069 | 10 | 9 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4064): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0005 | 0/0 | 4068 | 15 | 0 | 2 | 11 | 0 | 2 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0006 | 0/0 | 4068 | 6 | 0 | 0 | 6 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0008 | 0/0 | 4071 | 4 | 4 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4066): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0009 | 0/0 | 4068 | 4 | 4 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0010 | 0/0 | 4068 | 3 | 3 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0011 | 0/0 | 4068 | 3 | 0 | 0 | 3 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0012 | 0/0 | 4069 | 3 | 0 | 0 | 0 | 2 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4064): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0013 | 0/0 | 4068 | 2 | 0 | 0 | 1 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0014 | 0/0 | 4068 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0015 | 0/0 | 4068 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0016 | 0/0 | 4068 | 2 | 1 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0017 | 0/0 | 4068 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0018 | 0/0 | 4069 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4064): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0019 | 0/0 | 4068 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0020 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4064): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0021 | 0/0 | 4068 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0022 | 0/0 | 4068 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0023 | 0/0 | 4068 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0024 | 0/0 | 4068 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0026 | 0/0 | 4068 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0028 | 0/0 | 4069 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4064): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0029 | 0/0 | 4068 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0001t0030 | 0/0 | 4068 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0001c0004t0002 | 0/0 | 4068 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0002c0002t0001 | 1/0 | 4068 | 1 | 0 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| a0002c0002t0004 | 0/1 | 4069 | 42 | 9 | 6 | 9 | 3 | 14 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4064): Show |
chr1 | 46627737 | 46673364 |
| a0002c0002t0007 | 0/0 | 4069 | 6 | 0 | 0 | 6 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4064): Show |
chr1 | 46627737 | 46673364 |
| a0002c0002t0025 | 0/0 | 4069 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4064): Show |
chr1 | 46627737 | 46673364 |
| a0002c0002t0027 | 0/0 | 4069 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4064): Show |
chr1 | 46627737 | 46673364 |
| a0003c0003t0002 | 0/0 | 4068 | 2 | 0 | 2 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | GAGGC others(4063): Show |
chr1 | 46627737 | 46673364 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 22 | 2 | 1 | 18 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0002 | 0/0 | 18 | 1 | 7 | 7 | 0 | 3 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0004 | 0/0 | 14 | 0 | 4 | 8 | 0 | 2 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0012 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0003 | 0/0 | 16 | 1 | 9 | 3 | 2 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0004g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0004g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0005g0006 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0006g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0006g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0008g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0009g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0009g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0009g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0010g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0010g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0010g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0011g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0012g0052 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0012g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0013g0039 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0014g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0014g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0015g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0015g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0016g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0016g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0017g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0018g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0019g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0020g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0021g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0022g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0023g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0024g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0026g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0028g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0029g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0001t0030g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0001c0004t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0001g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0007 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0010 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0004g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0007g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0007g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0007g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0007g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0025g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0002c0002t0027g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| a0003c0003t0002g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0004 | g0086 | EUR | GBR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0219 | EUR | GBR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00280 | hp1 | a0001 | c0001 | t0013 | g0039 | EUR | FIN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0101 | EUR | FIN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00323 | hp1 | a0002 | c0002 | t0027 | g0070 | EUR | FIN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00323 | hp2 | a0002 | c0002 | t0004 | g0082 | EUR | FIN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00438 | hp1 | a0002 | c0002 | t0004 | g0007 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00544 | hp1 | a0001 | c0001 | t0006 | g0042 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0236 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00597 | hp2 | a0002 | c0002 | t0007 | g0024 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00642 | hp1 | a0001 | c0001 | t0016 | g0188 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00673 | hp1 | a0001 | c0001 | t0019 | g0148 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0111 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01069 | hp1 | a0001 | c0001 | t0022 | g0218 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01070 | hp2 | a0003 | c0003 | t0002 | g0048 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01071 | hp2 | a0003 | c0003 | t0002 | g0048 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0131 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01243 | hp2 | a0002 | c0002 | t0004 | g0063 | AMR | PUR | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01256 | hp2 | a0002 | c0002 | t0025 | g0083 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01257 | hp2 | a0002 | c0002 | t0004 | g0007 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0105 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01358 | hp1 | a0002 | c0002 | t0004 | g0010 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0117 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0120 | EUR | IBS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01515 | hp2 | a0001 | c0001 | t0012 | g0052 | EUR | IBS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01517 | hp2 | a0001 | c0001 | t0012 | g0052 | EUR | IBS | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01884 | hp1 | a0002 | c0002 | t0004 | g0025 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01943 | hp2 | a0002 | c0002 | t0004 | g0067 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01952 | hp1 | a0001 | c0001 | t0029 | g0216 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0106 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01981 | hp2 | a0002 | c0002 | t0004 | g0062 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02027 | hp1 | a0002 | c0002 | t0007 | g0023 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02074 | hp1 | a0001 | c0001 | t0006 | g0207 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02074 | hp2 | a0002 | c0002 | t0004 | g0074 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02145 | hp1 | a0001 | c0001 | t0015 | g0248 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CDX | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | CDX | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02165 | hp1 | a0001 | c0001 | t0006 | g0043 | EAS | CDX | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | CDX | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02280 | hp2 | a0001 | c0004 | t0002 | g0223 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0034 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02451 | hp2 | a0002 | c0002 | t0004 | g0060 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02602 | hp1 | a0002 | c0002 | t0004 | g0076 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0235 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02615 | hp1 | a0001 | c0001 | t0026 | g0133 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0013 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02683 | hp1 | a0002 | c0002 | t0004 | g0010 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02698 | hp2 | a0002 | c0002 | t0004 | g0084 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02723 | hp2 | a0002 | c0002 | t0004 | g0056 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02735 | hp1 | a0002 | c0002 | t0004 | g0078 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0122 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0034 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02895 | hp1 | a0002 | c0002 | t0004 | g0061 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02896 | hp2 | a0002 | c0002 | t0004 | g0066 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02922 | hp2 | a0001 | c0001 | t0017 | g0143 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02965 | hp1 | a0001 | c0001 | t0014 | g0144 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0146 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02970 | hp2 | a0002 | c0002 | t0004 | g0064 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02976 | hp1 | a0001 | c0001 | t0010 | g0212 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02976 | hp2 | a0001 | c0001 | t0015 | g0247 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03017 | hp1 | a0002 | c0002 | t0004 | g0072 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0147 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03139 | hp2 | a0002 | c0002 | t0004 | g0054 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03195 | hp1 | a0001 | c0001 | t0016 | g0187 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0129 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0089 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0110 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03490 | hp1 | a0001 | c0001 | t0024 | g0221 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0126 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03491 | hp1 | a0002 | c0002 | t0004 | g0007 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0013 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03516 | hp2 | a0002 | c0002 | t0004 | g0025 | AFR | ESN | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03540 | hp1 | a0001 | c0001 | t0010 | g0211 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | GWD | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0121 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03704 | hp1 | a0002 | c0002 | t0004 | g0077 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03704 | hp2 | a0002 | c0002 | t0004 | g0057 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03710 | hp1 | a0002 | c0002 | t0004 | g0010 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0006 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0220 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03834 | hp2 | a0002 | c0002 | t0004 | g0010 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03942 | hp1 | a0001 | c0001 | t0012 | g0112 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03942 | hp2 | a0002 | c0002 | t0004 | g0068 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0224 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG04199 | hp1 | a0001 | c0001 | t0023 | g0232 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG04199 | hp2 | a0002 | c0002 | t0004 | g0073 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG04204 | hp1 | a0002 | c0002 | t0004 | g0058 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0107 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG04228 | hp2 | a0002 | c0002 | t0004 | g0079 | SAS | STU | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | YRI | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | CHB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18747 | hp1 | a0002 | c0002 | t0007 | g0024 | EAS | CHB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | CHB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18906 | hp2 | a0001 | c0001 | t0030 | g0213 | AFR | YRI | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18939 | hp1 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18946 | hp2 | a0002 | c0002 | t0007 | g0071 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18947 | hp2 | a0002 | c0002 | t0004 | g0080 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18952 | hp1 | a0001 | c0001 | t0006 | g0042 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18961 | hp1 | a0001 | c0001 | t0011 | g0019 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18967 | hp2 | a0001 | c0001 | t0028 | g0113 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18971 | hp2 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18973 | hp2 | a0001 | c0001 | t0006 | g0043 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0239 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18988 | hp2 | a0002 | c0002 | t0007 | g0023 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18993 | hp1 | a0002 | c0002 | t0004 | g0075 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18997 | hp1 | a0001 | c0001 | t0005 | g0237 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18997 | hp2 | a0001 | c0001 | t0018 | g0164 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0234 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18998 | hp2 | a0001 | c0001 | t0006 | g0205 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18999 | hp1 | a0001 | c0001 | t0005 | g0238 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19005 | hp2 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19006 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19006 | hp2 | a0002 | c0002 | t0007 | g0081 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19010 | hp1 | a0001 | c0001 | t0011 | g0019 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19030 | hp1 | a0001 | c0001 | t0010 | g0243 | AFR | LWK | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19030 | hp2 | a0001 | c0001 | t0014 | g0145 | AFR | LWK | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | LWK | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19054 | hp2 | a0002 | c0002 | t0004 | g0010 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19055 | hp2 | a0002 | c0002 | t0004 | g0059 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0240 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19056 | hp2 | a0001 | c0001 | t0013 | g0039 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19087 | hp1 | a0001 | c0001 | t0021 | g0241 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19090 | hp2 | a0001 | c0001 | t0011 | g0019 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA20805 | hp2 | a0002 | c0002 | t0004 | g0085 | EUR | TSI | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01123 | hp1 | a0002 | c0002 | t0004 | g0069 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0132 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | USA | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | USA | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | USA | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | USA | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA21309 | hp1 | a0002 | c0002 | t0004 | g0055 | AFR | LWK | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| NA21309 | hp2 | a0001 | c0001 | t0020 | g0130 | AFR | LWK | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0004 | g0087 | REF | REF | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0065 | REF | REF | ATPAF1_chr1_46627737_46673364 | ATPAF1 | chr1 | 46627737 | 46673364 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:46635868 | T | G | 1 | a0003 | 2 | HG01070.hp2 HG01071.hp2 |
missense_variant | MODERATE | c.895A>C | p.Asn299His | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 937/4068 | 895/987 | 299/328 | chr1 | 46635868 | |||
| chr1:46668139 | T | C | 2 | a0001 a0003 |
361 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(358): Show |
missense_variant | MODERATE | c.184A>G | p.Ser62Gly | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/9 | 226/4068 | 184/987 | 62/328 | chr1 | 46668139 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:46635884 | G | C | 1 | a0001c0004 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.879C>G | p.Thr293Thr | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 921/4068 | 879/987 | 293/328 | chr1 | 46635884 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:46632819 | G | A | 1 | a0002c0002t0027 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2957C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2957 | chr1 | 46632819 | ||||||
| chr1:46632997 | T | G | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2779A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2779 | chr1 | 46632997 | ||||||
| chr1:46632999 | C | T | 1 | a0001c0001t0020 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2777G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2777 | chr1 | 46632999 | ||||||
| chr1:46633151 | C | T | 1 | a0001c0001t0012 | 3 | HG01515.hp2 HG01517.hp2 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2625G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2625 | chr1 | 46633151 | ||||||
| chr1:46633238 | G | A | 1 | a0001c0001t0016 | 2 | HG00642.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2538C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2538 | chr1 | 46633238 | ||||||
| chr1:46633418 | G | GA | 10 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0012 others(7): Show |
140 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*2357dupT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2357 | chr1 | 46633418 | ||||||
| chr1:46633426 | A | C | 2 | a0001c0001t0009 a0001c0001t0014 |
6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2350T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2350 | chr1 | 46633426 | ||||||
| chr1:46633487 | C | T | 2 | a0001c0001t0009 a0001c0001t0014 |
6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2289G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2289 | chr1 | 46633487 | ||||||
| chr1:46633498 | A | C | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2278T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2278 | chr1 | 46633498 | ||||||
| chr1:46633499 | C | A | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2277G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2277 | chr1 | 46633499 | ||||||
| chr1:46633525 | G | A | 1 | a0001c0001t0024 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2251C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2251 | chr1 | 46633525 | ||||||
| chr1:46633563 | A | C | 6 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0012 others(3): Show |
84 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*2213T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2213 | chr1 | 46633563 | ||||||
| chr1:46633674 | C | A | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(20): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*2102G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 2102 | chr1 | 46633674 | ||||||
| chr1:46633792 | T | A | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1984A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1984 | chr1 | 46633792 | ||||||
| chr1:46633794 | T | C | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1982A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1982 | chr1 | 46633794 | ||||||
| chr1:46633797 | A | T | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1979T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1979 | chr1 | 46633797 | ||||||
| chr1:46633801 | A | T | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1975T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1975 | chr1 | 46633801 | ||||||
| chr1:46633802 | C | T | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1974G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1974 | chr1 | 46633802 | ||||||
| chr1:46633803 | T | A | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1973A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1973 | chr1 | 46633803 | ||||||
| chr1:46633805 | T | A | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1971A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1971 | chr1 | 46633805 | ||||||
| chr1:46633806 | G | T | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1970C>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1970 | chr1 | 46633806 | ||||||
| chr1:46633807 | T | C | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1969A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1969 | chr1 | 46633807 | ||||||
| chr1:46633810 | G | T | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1966C>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1966 | chr1 | 46633810 | ||||||
| chr1:46633811 | G | C | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1965C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1965 | chr1 | 46633811 | ||||||
| chr1:46633814 | A | G | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1962T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1962 | chr1 | 46633814 | ||||||
| chr1:46633817 | A | G | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1959T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1959 | chr1 | 46633817 | ||||||
| chr1:46633818 | A | T | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1958T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1958 | chr1 | 46633818 | ||||||
| chr1:46633819 | C | A | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1957G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1957 | chr1 | 46633819 | ||||||
| chr1:46633831 | G | C | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1945C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1945 | chr1 | 46633831 | ||||||
| chr1:46633835 | A | G | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1941T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1941 | chr1 | 46633835 | ||||||
| chr1:46633837 | A | C | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1939T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1939 | chr1 | 46633837 | ||||||
| chr1:46633843 | A | C | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1933T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1933 | chr1 | 46633843 | ||||||
| chr1:46633851 | C | T | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1925G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1925 | chr1 | 46633851 | ||||||
| chr1:46633852 | T | G | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1924A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1924 | chr1 | 46633852 | ||||||
| chr1:46633856 | T | G | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1920A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1920 | chr1 | 46633856 | ||||||
| chr1:46633894 | T | G | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1882A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1882 | chr1 | 46633894 | ||||||
| chr1:46633897 | G | A | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1879C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1879 | chr1 | 46633897 | ||||||
| chr1:46633898 | A | C | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1878T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1878 | chr1 | 46633898 | ||||||
| chr1:46634049 | T | C | 11 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0011 others(8): Show |
143 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*1727A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1727 | chr1 | 46634049 | ||||||
| chr1:46634255 | C | T | 1 | a0001c0001t0013 | 2 | HG00280.hp1 NA19056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1521G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1521 | chr1 | 46634255 | ||||||
| chr1:46634377 | C | T | 24 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(21): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1399G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1399 | chr1 | 46634377 | ||||||
| chr1:46634403 | G | A | 1 | a0001c0001t0019 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1373C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1373 | chr1 | 46634403 | ||||||
| chr1:46634410 | G | C | 1 | a0001c0001t0015 | 2 | HG02145.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1366C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1366 | chr1 | 46634410 | ||||||
| chr1:46634427 | C | A | 4 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0012 others(1): Show |
82 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1349G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1349 | chr1 | 46634427 | ||||||
| chr1:46634487 | C | T | 10 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0016 others(7): Show |
121 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*1289G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1289 | chr1 | 46634487 | ||||||
| chr1:46634654 | G | A | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1122C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1122 | chr1 | 46634654 | ||||||
| chr1:46634665 | C | T | 1 | a0001c0001t0022 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1111G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1111 | chr1 | 46634665 | ||||||
| chr1:46634704 | C | A | 1 | a0001c0001t0014 | 2 | HG02965.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1072G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 1072 | chr1 | 46634704 | ||||||
| chr1:46634818 | T | G | 1 | a0002c0002t0007 | 6 | HG00597.hp2 HG02027.hp1 NA18747.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*958A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 958 | chr1 | 46634818 | ||||||
| chr1:46634911 | T | C | 1 | a0001c0001t0015 | 2 | HG02145.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*865A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 865 | chr1 | 46634911 | ||||||
| chr1:46634956 | C | T | 1 | a0001c0001t0021 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*820G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 820 | chr1 | 46634956 | ||||||
| chr1:46635128 | C | T | 1 | a0001c0001t0020 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*648G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 648 | chr1 | 46635128 | ||||||
| chr1:46635186 | T | C | 1 | a0001c0001t0005 | 15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*590A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 590 | chr1 | 46635186 | ||||||
| chr1:46635299 | T | C | 1 | a0001c0001t0015 | 2 | HG02145.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*477A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 477 | chr1 | 46635299 | ||||||
| chr1:46635343 | C | A | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(20): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*433G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 433 | chr1 | 46635343 | ||||||
| chr1:46635501 | G | C | 1 | a0001c0001t0029 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*275C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 275 | chr1 | 46635501 | ||||||
| chr1:46635692 | T | C | 1 | a0001c0001t0030 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*84A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 9/9 | 84 | chr1 | 46635692 | ||||||
| chr1:46668333 | G | GCCT | 1 | a0001c0001t0008 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-14_-12dupAGG | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/9 | 12 | chr1 | 46668333 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:46636075 | C | T | 1 | a0002c0002t0004g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.793-105G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46636075 | |||||||
| chr1:46636124 | C | T | 1 | a0001c0001t0003g0089 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.793-154G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46636124 | |||||||
| chr1:46636731 | T | TA | 5 | a0001c0001t0009g0034 a0001c0001t0009g0146 a0001c0001t0009g0147 others(2): Show |
6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.793-762dupT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46636731 | |||||||
| chr1:46636859 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.793-889T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46636859 | |||||||
| chr1:46636890 | G | A | 1 | a0001c0001t0014g0144 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.793-920C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46636890 | |||||||
| chr1:46636927 | T | C | 1 | a0001c0001t0009g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.793-957A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46636927 | |||||||
| chr1:46637027 | C | T | 1 | a0001c0001t0002g0050 | 2 | NA19058.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.793-1057G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637027 | |||||||
| chr1:46637140 | G | C | 1 | a0001c0001t0003g0093 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.793-1170C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637140 | |||||||
| chr1:46637284 | A | G | 173 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(170): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.793-1314T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637284 | |||||||
| chr1:46637293 | T | A | 1 | a0001c0001t0001g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.793-1323A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637293 | |||||||
| chr1:46637423 | C | T | 2 | a0001c0001t0010g0243 a0001c0001t0030g0213 |
2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.793-1453G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637423 | |||||||
| chr1:46637483 | C | G | 2 | a0001c0001t0010g0211 a0001c0001t0010g0212 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.793-1513G>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637483 | |||||||
| chr1:46637500 | C | T | 173 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(170): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.793-1530G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637500 | |||||||
| chr1:46637517 | C | T | 1 | a0002c0002t0004g0079 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.793-1547G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637517 | |||||||
| chr1:46637743 | T | C | 7 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0031 others(4): Show |
10 | HG01167.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.793-1773A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637743 | |||||||
| chr1:46637945 | T | G | 173 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(170): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.793-1975A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46637945 | |||||||
| chr1:46638082 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(49): Show |
95 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.793-2112G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638082 | |||||||
| chr1:46638120 | A | G | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-2150T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638120 | |||||||
| chr1:46638151 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.793-2181C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638151 | |||||||
| chr1:46638159 | T | A | 78 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(75): Show |
140 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.793-2189A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638159 | |||||||
| chr1:46638198 | A | T | 66 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(63): Show |
121 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.793-2228T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638198 | |||||||
| chr1:46638214 | C | A | 28 | a0002c0002t0004g0007 a0002c0002t0004g0010 a0002c0002t0004g0057 others(25): Show |
39 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.793-2244G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638214 | |||||||
| chr1:46638219 | T | G | 173 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(170): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.793-2249A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638219 | |||||||
| chr1:46638400 | T | C | 173 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(170): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.793-2430A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638400 | |||||||
| chr1:46638479 | G | C | 1 | a0002c0002t0004g0084 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.793-2509C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638479 | |||||||
| chr1:46638488 | G | T | 1 | a0001c0001t0009g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.793-2518C>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638488 | |||||||
| chr1:46638621 | CA | C | 166 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0002 others(163): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.793-2652delT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638621 | |||||||
| chr1:46638658 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.793-2688G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638658 | |||||||
| chr1:46638659 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(240): Show |
402 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(399): Show |
intron_variant | MODIFIER | c.793-2689T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638659 | |||||||
| chr1:46638700 | A | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(49): Show |
95 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.793-2730T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638700 | |||||||
| chr1:46638718 | T | C | 1 | a0001c0001t0002g0202 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.793-2748A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638718 | |||||||
| chr1:46638798 | C | T | 1 | a0001c0001t0002g0220 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.793-2828G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638798 | |||||||
| chr1:46638828 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.793-2858G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638828 | |||||||
| chr1:46638912 | G | A | 1 | a0001c0001t0030g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.793-2942C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638912 | |||||||
| chr1:46638949 | T | C | 1 | a0002c0002t0004g0068 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.793-2979A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46638949 | |||||||
| chr1:46639036 | T | C | 78 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(75): Show |
140 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.793-3066A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639036 | |||||||
| chr1:46639112 | A | C | 8 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0235 others(5): Show |
15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.793-3142T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639112 | |||||||
| chr1:46639235 | T | TAC | 73 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(70): Show |
135 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.793-3267_793-3266d others(4): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639235 | |||||||
| chr1:46639235 | T | TACAC | 95 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0018 others(92): Show |
143 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.793-3269_793-3266d others(6): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639235 | |||||||
| chr1:46639328 | G | A | 38 | a0001c0001t0004g0129 a0002c0002t0004g0007 a0002c0002t0004g0010 others(35): Show |
50 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.793-3358C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639328 | |||||||
| chr1:46639412 | C | A | 1 | a0001c0001t0030g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.793-3442G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639412 | |||||||
| chr1:46639487 | T | A | 1 | a0001c0001t0005g0236 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.793-3517A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639487 | |||||||
| chr1:46639553 | G | A | 1 | a0001c0001t0003g0111 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.793-3583C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639553 | |||||||
| chr1:46639697 | T | A | 3 | a0001c0001t0002g0215 a0001c0001t0002g0217 a0001c0001t0029g0216 |
3 | HG00639.hp1 HG01952.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.792+3497A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639697 | |||||||
| chr1:46639790 | A | G | 8 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0235 others(5): Show |
15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.792+3404T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639790 | |||||||
| chr1:46639807 | A | G | 11 | a0001c0001t0001g0033 a0001c0001t0001g0135 a0001c0001t0001g0136 others(8): Show |
12 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.792+3387T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46639807 | |||||||
| chr1:46640278 | G | A | 86 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0018 others(83): Show |
130 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.792+2916C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46640278 | |||||||
| chr1:46640386 | G | A | 1 | a0001c0001t0020g0130 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.792+2808C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46640386 | |||||||
| chr1:46640427 | T | C | 4 | a0001c0001t0001g0140 a0001c0001t0015g0247 a0001c0001t0015g0248 others(1): Show |
4 | HG02145.hp1 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.792+2767A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46640427 | |||||||
| chr1:46640627 | C | CT | 2 | a0001c0001t0004g0031 a0001c0001t0004g0132 |
3 | HG02559.hp1 HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.792+2566dupA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46640627 | |||||||
| chr1:46640635 | A | AAAAC | 91 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0018 others(88): Show |
139 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.792+2555_792+2558d others(6): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46640635 | |||||||
| chr1:46640635 | A | AAAACAAA others(1): Show |
3 | a0001c0001t0003g0109 a0001c0001t0003g0110 a0002c0002t0004g0069 |
3 | HG01123.hp1 HG03239.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.792+2551_792+2558d others(10): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46640635 | |||||||
| chr1:46640683 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.792+2511A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46640683 | |||||||
| chr1:46640948 | T | C | 1 | a0001c0001t0010g0212 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.792+2246A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46640948 | |||||||
| chr1:46641253 | A | AT | 28 | a0002c0002t0004g0007 a0002c0002t0004g0010 a0002c0002t0004g0057 others(25): Show |
39 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.792+1940dupA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641253 | |||||||
| chr1:46641277 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(240): Show |
402 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(399): Show |
intron_variant | MODIFIER | c.792+1917A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641277 | |||||||
| chr1:46641344 | G | A | 78 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(75): Show |
140 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.792+1850C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641344 | |||||||
| chr1:46641370 | T | TG | 173 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(170): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.792+1823_792+1824i others(3): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641370 | |||||||
| chr1:46641442 | C | G | 1 | a0001c0001t0001g0158 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.792+1752G>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641442 | |||||||
| chr1:46641451 | G | A | 1 | a0001c0001t0002g0050 | 2 | NA19058.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.792+1743C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641451 | |||||||
| chr1:46641505 | C | G | 2 | a0001c0001t0010g0211 a0001c0001t0010g0212 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.792+1689G>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641505 | |||||||
| chr1:46641535 | C | T | 3 | a0001c0001t0003g0128 a0002c0002t0004g0074 a0002c0002t0004g0075 |
3 | HG02074.hp2 HG02622.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.792+1659G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641535 | |||||||
| chr1:46641537 | G | C | 1 | a0001c0001t0001g0176 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.792+1657C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641537 | |||||||
| chr1:46641539 | G | A | 1 | a0001c0001t0020g0130 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.792+1655C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641539 | |||||||
| chr1:46641647 | T | C | 173 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(170): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.792+1547A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641647 | |||||||
| chr1:46641718 | A | G | 79 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(76): Show |
142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.792+1476T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641718 | |||||||
| chr1:46641877 | TG | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0154 a0001c0001t0001g0184 |
5 | HG02055.hp2 HG02647.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.792+1316delC | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46641877 | |||||||
| chr1:46642074 | G | C | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.792+1120C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642074 | |||||||
| chr1:46642317 | A | G | 7 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0031 others(4): Show |
10 | HG01167.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.792+877T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642317 | |||||||
| chr1:46642460 | C | A | 5 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(2): Show |
5 | HG01256.hp1 HG01515.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.792+734G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642460 | |||||||
| chr1:46642535 | A | T | 1 | a0001c0001t0014g0144 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.792+659T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642535 | |||||||
| chr1:46642671 | A | G | 94 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0018 others(91): Show |
141 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.792+523T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642671 | |||||||
| chr1:46642693 | G | A | 79 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(76): Show |
142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.792+501C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642693 | |||||||
| chr1:46642786 | TAAC | T | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.792+405_792+407del others(3): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642786 | |||||||
| chr1:46642821 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.792+373A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642821 | |||||||
| chr1:46642874 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.792+320A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642874 | |||||||
| chr1:46642961 | C | A | 1 | a0001c0001t0001g0153 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.792+233G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642961 | |||||||
| chr1:46642962 | A | C | 1 | a0001c0001t0001g0153 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.792+232T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642962 | |||||||
| chr1:46642963 | T | A | 1 | a0001c0001t0001g0153 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.792+231A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46642963 | |||||||
| chr1:46643030 | A | C | 1 | a0001c0001t0003g0122 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.792+164T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46643030 | |||||||
| chr1:46643031 | T | C | 1 | a0001c0001t0001g0014 | 4 | NA18612.hp2 NA18963.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+163A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46643031 | |||||||
| chr1:46643041 | T | C | 1 | a0002c0002t0004g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.792+153A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46643041 | |||||||
| chr1:46643156 | T | C | 173 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(170): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.792+38A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46643156 | |||||||
| chr1:46643157 | G | A | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.792+37C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 8/8 | chr1 | 46643157 | |||||||
| chr1:46643348 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.685-47G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46643348 | |||||||
| chr1:46643417 | A | G | 94 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0018 others(91): Show |
141 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.685-116T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46643417 | |||||||
| chr1:46643579 | A | G | 179 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(176): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.685-278T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46643579 | |||||||
| chr1:46643656 | C | T | 191 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0135 others(188): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.685-355G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46643656 | |||||||
| chr1:46643801 | G | A | 67 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(64): Show |
123 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.685-500C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46643801 | |||||||
| chr1:46643812 | G | C | 1 | a0001c0001t0003g0115 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.685-511C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46643812 | |||||||
| chr1:46643838 | A | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0154 a0001c0001t0001g0184 |
5 | HG02055.hp2 HG02647.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.685-537T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46643838 | |||||||
| chr1:46644072 | A | G | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-771T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644072 | |||||||
| chr1:46644126 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.685-825A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644126 | |||||||
| chr1:46644156 | A | T | 178 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(175): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.685-855T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644156 | |||||||
| chr1:46644158 | G | C | 178 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(175): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.685-857C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644158 | |||||||
| chr1:46644220 | T | C | 1 | a0002c0002t0004g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.685-919A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644220 | |||||||
| chr1:46644244 | T | C | 94 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0018 others(91): Show |
141 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.684+917A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644244 | |||||||
| chr1:46644311 | T | TG | 190 | a0001c0001t0001g0033 a0001c0001t0001g0135 a0001c0001t0001g0136 others(187): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.684+849_684+850ins others(1): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644311 | |||||||
| chr1:46644466 | G | A | 1 | a0002c0002t0004g0060 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.684+695C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644466 | |||||||
| chr1:46644559 | G | A | 173 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(170): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.684+602C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644559 | |||||||
| chr1:46644565 | G | GT | 71 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(68): Show |
127 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.684+595dupA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644565 | |||||||
| chr1:46644624 | ATT | A | 5 | a0001c0001t0009g0034 a0001c0001t0009g0146 a0001c0001t0009g0147 others(2): Show |
6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.684+535_684+536del others(2): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644624 | |||||||
| chr1:46644742 | C | CATTT | 243 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(240): Show |
402 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(399): Show |
intron_variant | MODIFIER | c.684+418_684+419ins others(4): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644742 | |||||||
| chr1:46644838 | C | T | 1 | a0001c0001t0002g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.684+323G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644838 | |||||||
| chr1:46644996 | G | C | 94 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0018 others(91): Show |
141 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.684+165C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46644996 | |||||||
| chr1:46645040 | C | T | 94 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0018 others(91): Show |
141 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.684+121G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46645040 | |||||||
| chr1:46645079 | T | C | 2 | a0001c0001t0004g0031 a0001c0001t0004g0132 |
3 | HG02559.hp1 HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.684+82A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46645079 | |||||||
| chr1:46645094 | G | GC | 173 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(170): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.684+66dupG | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46645094 | |||||||
| chr1:46645136 | T | C | 1 | a0001c0001t0003g0116 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.684+25A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 7/8 | chr1 | 46645136 | |||||||
| chr1:46645365 | TA | T | 3 | a0001c0001t0009g0034 a0001c0001t0014g0144 a0001c0001t0014g0145 |
4 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-110delT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46645365 | |||||||
| chr1:46645501 | C | T | 1 | a0002c0002t0004g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.589-245G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46645501 | |||||||
| chr1:46645590 | C | T | 2 | a0001c0001t0002g0222 a0001c0001t0002g0230 |
2 | NA18968.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.589-334G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46645590 | |||||||
| chr1:46645591 | G | A | 1 | a0001c0001t0020g0130 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.589-335C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46645591 | |||||||
| chr1:46645634 | A | G | 4 | a0001c0001t0002g0047 a0001c0001t0002g0193 a0001c0001t0002g0219 others(1): Show |
5 | HG00099.hp2 HG01109.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.589-378T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46645634 | |||||||
| chr1:46645753 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.589-497A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46645753 | |||||||
| chr1:46645804 | T | C | 1 | a0002c0002t0004g0073 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.589-548A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46645804 | |||||||
| chr1:46645946 | C | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0017 others(38): Show |
74 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.589-690G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46645946 | |||||||
| chr1:46645998 | G | C | 8 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0235 others(5): Show |
15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.589-742C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46645998 | |||||||
| chr1:46646078 | G | A | 79 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(76): Show |
142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.589-822C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646078 | |||||||
| chr1:46646151 | A | T | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-895T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646151 | |||||||
| chr1:46646205 | TG | T | 8 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0235 others(5): Show |
15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.589-950delC | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646205 | |||||||
| chr1:46646314 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(149): Show |
269 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.589-1058A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646314 | |||||||
| chr1:46646400 | A | G | 1 | a0001c0001t0004g0129 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.589-1144T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646400 | |||||||
| chr1:46646413 | C | T | 1 | a0002c0002t0004g0082 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.589-1157G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646413 | |||||||
| chr1:46646435 | C | CTGATA | 3 | a0001c0001t0003g0124 a0001c0001t0003g0125 a0002c0002t0004g0066 |
3 | HG02896.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.589-1184_589-1180d others(7): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646435 | |||||||
| chr1:46646467 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.589-1211G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646467 | |||||||
| chr1:46646523 | G | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(49): Show |
95 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.589-1267C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646523 | |||||||
| chr1:46646845 | A | C | 1 | a0002c0002t0004g0064 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.589-1589T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646845 | |||||||
| chr1:46646877 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.589-1621T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646877 | |||||||
| chr1:46646904 | T | G | 1 | a0001c0001t0001g0155 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.589-1648A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46646904 | |||||||
| chr1:46647182 | G | C | 1 | a0001c0001t0002g0200 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.589-1926C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647182 | |||||||
| chr1:46647188 | A | C | 1 | a0001c0001t0003g0114 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.589-1932T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647188 | |||||||
| chr1:46647238 | T | C | 67 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(64): Show |
123 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.589-1982A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647238 | |||||||
| chr1:46647503 | TAC | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(123): Show |
212 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.589-2249_589-2248d others(4): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647503 | |||||||
| chr1:46647523 | CAT | C | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-2269_589-2268d others(4): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647523 | |||||||
| chr1:46647587 | A | T | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-2331T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647587 | |||||||
| chr1:46647610 | C | T | 5 | a0001c0001t0009g0034 a0001c0001t0009g0146 a0001c0001t0009g0147 others(2): Show |
6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-2354G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647610 | |||||||
| chr1:46647623 | G | A | 1 | a0001c0001t0002g0225 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.589-2367C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647623 | |||||||
| chr1:46647870 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0166 |
2 | NA18987.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.589-2614C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647870 | |||||||
| chr1:46647946 | T | A | 1 | a0001c0001t0001g0167 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.589-2690A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46647946 | |||||||
| chr1:46648239 | G | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.589-2983C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46648239 | |||||||
| chr1:46648265 | C | T | 1 | a0001c0001t0020g0130 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.589-3009G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46648265 | |||||||
| chr1:46648339 | G | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(148): Show |
267 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.589-3083C>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46648339 | |||||||
| chr1:46648391 | C | T | 2 | a0001c0001t0003g0121 a0002c0002t0004g0085 |
2 | HG03654.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.589-3135G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46648391 | |||||||
| chr1:46648815 | C | T | 7 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0031 others(4): Show |
10 | HG01167.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.589-3559G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46648815 | |||||||
| chr1:46648873 | C | T | 95 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(92): Show |
171 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.589-3617G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46648873 | |||||||
| chr1:46648893 | C | T | 79 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(76): Show |
142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.589-3637G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46648893 | |||||||
| chr1:46648948 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0018g0164 |
2 | NA18988.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.588+3633G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46648948 | |||||||
| chr1:46649113 | G | A | 79 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(76): Show |
142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.588+3468C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649113 | |||||||
| chr1:46649140 | C | T | 2 | a0001c0001t0002g0222 a0001c0001t0002g0230 |
2 | NA18968.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.588+3441G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649140 | |||||||
| chr1:46649157 | C | CA | 76 | a0001c0001t0001g0150 a0001c0001t0001g0153 a0001c0001t0001g0168 others(73): Show |
130 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.588+3423dupT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649157 | |||||||
| chr1:46649157 | C | CAA | 11 | a0001c0001t0002g0022 a0001c0001t0002g0189 a0001c0001t0002g0201 others(8): Show |
20 | HG01255.hp1 HG01496.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.588+3422_588+3423d others(4): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649157 | |||||||
| chr1:46649157 | CA | C | 44 | a0001c0001t0001g0032 a0001c0001t0003g0003 a0001c0001t0003g0005 others(41): Show |
76 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.588+3423delT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649157 | |||||||
| chr1:46649191 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.588+3390A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649191 | |||||||
| chr1:46649193 | A | G | 1 | a0001c0001t0005g0236 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.588+3388T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649193 | |||||||
| chr1:46649214 | A | G | 1 | a0001c0001t0005g0236 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.588+3367T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649214 | |||||||
| chr1:46649272 | T | C | 1 | a0001c0001t0002g0226 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.588+3309A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649272 | |||||||
| chr1:46649307 | A | G | 79 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(76): Show |
142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.588+3274T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649307 | |||||||
| chr1:46649313 | A | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.588+3268T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649313 | |||||||
| chr1:46649342 | CAT | C | 4 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0205 others(1): Show |
6 | HG00544.hp1 HG02074.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+3237_588+3238d others(4): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649342 | |||||||
| chr1:46649379 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.588+3202G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649379 | |||||||
| chr1:46649380 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(53): Show |
105 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.588+3201T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649380 | |||||||
| chr1:46649542 | C | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.588+3039G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649542 | |||||||
| chr1:46649830 | G | A | 1 | a0001c0001t0009g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.588+2751C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649830 | |||||||
| chr1:46649868 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.588+2713C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46649868 | |||||||
| chr1:46650051 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0151 others(3): Show |
10 | HG00597.hp1 HG02135.hp2 NA18612.hp2 others(7): Show |
intron_variant | MODIFIER | c.588+2530G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650051 | |||||||
| chr1:46650363 | G | GA | 58 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(55): Show |
107 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.588+2217dupT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650363 | |||||||
| chr1:46650363 | G | GAA | 14 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0135 others(11): Show |
19 | HG01891.hp1 HG01891.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.588+2216_588+2217d others(4): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650363 | |||||||
| chr1:46650392 | GGAGA | G | 2 | a0001c0001t0002g0049 a0001c0001t0002g0227 |
3 | NA18962.hp1 NA18970.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.588+2185_588+2188d others(6): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650392 | |||||||
| chr1:46650456 | AT | A | 79 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(76): Show |
142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.588+2124delA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650456 | |||||||
| chr1:46650465 | T | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.588+2116A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650465 | |||||||
| chr1:46650500 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.588+2081T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650500 | |||||||
| chr1:46650602 | C | T | 6 | a0001c0001t0009g0034 a0001c0001t0009g0146 a0001c0001t0009g0147 others(3): Show |
7 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.588+1979G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650602 | |||||||
| chr1:46650603 | G | A | 6 | a0001c0001t0001g0033 a0001c0001t0001g0140 a0001c0001t0001g0142 others(3): Show |
7 | HG02145.hp1 HG02258.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+1978C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650603 | |||||||
| chr1:46650643 | T | C | 3 | a0001c0001t0002g0190 a0001c0001t0002g0245 a0001c0001t0002g0246 |
3 | HG02486.hp2 HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.588+1938A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650643 | |||||||
| chr1:46650767 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.588+1814G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650767 | |||||||
| chr1:46650810 | T | TA | 17 | a0001c0001t0001g0032 a0001c0001t0001g0138 a0001c0001t0001g0170 others(14): Show |
20 | HG01109.hp2 HG02027.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.588+1770dupT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650810 | |||||||
| chr1:46650885 | T | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(149): Show |
269 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.588+1696A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650885 | |||||||
| chr1:46650951 | G | T | 11 | a0001c0001t0001g0033 a0001c0001t0001g0135 a0001c0001t0001g0136 others(8): Show |
12 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.588+1630C>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650951 | |||||||
| chr1:46650996 | T | G | 8 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0235 others(5): Show |
15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.588+1585A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46650996 | |||||||
| chr1:46651046 | T | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(53): Show |
105 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.588+1535A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651046 | |||||||
| chr1:46651156 | C | A | 1 | a0001c0001t0001g0141 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.588+1425G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651156 | |||||||
| chr1:46651328 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(64): Show |
117 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.588+1253G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651328 | |||||||
| chr1:46651334 | A | AT | 52 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(49): Show |
95 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.588+1246dupA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651334 | |||||||
| chr1:46651341 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0037 |
4 | NA18951.hp1 NA19063.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.588+1240T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651341 | |||||||
| chr1:46651462 | G | A | 1 | a0001c0001t0001g0016 | 4 | HG02486.hp1 HG02717.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+1119C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651462 | |||||||
| chr1:46651512 | C | T | 2 | a0001c0001t0002g0017 a0001c0001t0002g0192 |
5 | NA18979.hp2 NA18986.hp2 NA19076.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+1069G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651512 | |||||||
| chr1:46651581 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+1000A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651581 | |||||||
| chr1:46651582 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+999A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651582 | |||||||
| chr1:46651585 | A | C | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+996T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651585 | |||||||
| chr1:46651586 | CAATGGTT others(45): Show |
C | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+943_588+994del others(52): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651586 | |||||||
| chr1:46651640 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+941A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651640 | |||||||
| chr1:46651643 | A | C | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+938T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651643 | |||||||
| chr1:46651645 | A | C | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+936T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651645 | |||||||
| chr1:46651646 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+935A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651646 | |||||||
| chr1:46651649 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+932A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651649 | |||||||
| chr1:46651650 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.588+931G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651650 | |||||||
| chr1:46651651 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+930A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651651 | |||||||
| chr1:46651654 | A | C | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+927T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651654 | |||||||
| chr1:46651655 | G | C | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+926C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651655 | |||||||
| chr1:46651657 | A | C | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+924T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651657 | |||||||
| chr1:46651659 | C | CCCCCCCC others(45): Show |
1 | a0001c0001t0001g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+921_588+922ins others(52): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651659 | |||||||
| chr1:46651665 | T | C | 1 | a0002c0002t0004g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.588+916A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651665 | |||||||
| chr1:46651735 | T | G | 2 | a0001c0001t0003g0126 a0001c0001t0003g0127 |
2 | HG01256.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.588+846A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651735 | |||||||
| chr1:46651896 | G | T | 7 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0031 others(4): Show |
10 | HG01167.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.588+685C>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46651896 | |||||||
| chr1:46652072 | G | A | 8 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0235 others(5): Show |
15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.588+509C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652072 | |||||||
| chr1:46652205 | C | CA | 11 | a0001c0001t0003g0114 a0001c0001t0004g0029 a0001c0001t0004g0030 others(8): Show |
14 | HG01109.hp2 HG01167.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.588+375dupT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652205 | |||||||
| chr1:46652205 | CA | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(129): Show |
241 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(238): Show |
intron_variant | MODIFIER | c.588+375delT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652205 | |||||||
| chr1:46652205 | CAA | C | 6 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0174 others(3): Show |
7 | HG02280.hp1 HG02738.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+374_588+375del others(2): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652205 | |||||||
| chr1:46652272 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.588+309G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652272 | |||||||
| chr1:46652375 | CACTTATT others(48): Show |
C | 5 | a0001c0001t0009g0034 a0001c0001t0009g0146 a0001c0001t0009g0147 others(2): Show |
6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+151_588+205del others(55): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652375 | |||||||
| chr1:46652395 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(144): Show |
263 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.588+186C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652395 | |||||||
| chr1:46652424 | C | A | 79 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(76): Show |
142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.588+157G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652424 | |||||||
| chr1:46652496 | C | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0017 others(38): Show |
74 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.588+85G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652496 | |||||||
| chr1:46652517 | G | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(149): Show |
269 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.588+64C>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652517 | |||||||
| chr1:46652570 | C | T | 5 | a0001c0001t0009g0034 a0001c0001t0009g0146 a0001c0001t0009g0147 others(2): Show |
6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+11G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 6/8 | chr1 | 46652570 | |||||||
| chr1:46652900 | A | G | 1 | a0001c0001t0001g0036 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.541-272T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 5/8 | chr1 | 46652900 | |||||||
| chr1:46652929 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(149): Show |
269 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.541-301A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 5/8 | chr1 | 46652929 | |||||||
| chr1:46652972 | C | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(237): Show |
404 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(401): Show |
intron_variant | MODIFIER | c.541-344G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 5/8 | chr1 | 46652972 | |||||||
| chr1:46652990 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0186 a0001c0001t0001g0244 |
8 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.541-362G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 5/8 | chr1 | 46652990 | |||||||
| chr1:46653026 | G | A | 4 | a0001c0001t0010g0211 a0001c0001t0010g0212 a0001c0001t0010g0243 others(1): Show |
4 | HG02976.hp1 HG03540.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-398C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 5/8 | chr1 | 46653026 | |||||||
| chr1:46653246 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(157): Show |
280 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.540+571T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 5/8 | chr1 | 46653246 | |||||||
| chr1:46653352 | A | G | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+465T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 5/8 | chr1 | 46653352 | |||||||
| chr1:46653676 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(53): Show |
105 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.540+141G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 5/8 | chr1 | 46653676 | |||||||
| chr1:46654011 | G | C | 1 | a0001c0001t0005g0239 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.490-144C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654011 | |||||||
| chr1:46654091 | G | A | 1 | a0001c0001t0005g0240 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.490-224C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654091 | |||||||
| chr1:46654154 | C | T | 8 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0235 others(5): Show |
15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-287G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654154 | |||||||
| chr1:46654161 | T | C | 2 | a0001c0001t0003g0126 a0001c0001t0003g0127 |
2 | HG01256.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.490-294A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654161 | |||||||
| chr1:46654243 | G | C | 1 | a0001c0001t0004g0129 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.490-376C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654243 | |||||||
| chr1:46654280 | T | C | 8 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0235 others(5): Show |
15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-413A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654280 | |||||||
| chr1:46654300 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.490-433T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654300 | |||||||
| chr1:46654501 | C | A | 1 | a0001c0001t0002g0053 | 2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.490-634G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654501 | |||||||
| chr1:46654527 | A | ATTTAT | 45 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(42): Show |
88 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.490-665_490-661dup others(5): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654527 | |||||||
| chr1:46654528 | T | TTTA | 33 | a0001c0001t0002g0004 a0001c0001t0002g0017 a0001c0001t0002g0022 others(30): Show |
56 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.490-664_490-662dup others(3): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654528 | |||||||
| chr1:46654528 | T | TTTATTA | 58 | a0001c0001t0002g0002 a0001c0001t0002g0044 a0001c0001t0002g0047 others(55): Show |
109 | HG00280.hp2 HG00408.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.490-667_490-662dup others(6): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654528 | |||||||
| chr1:46654528 | T | TTTATTAT others(2): Show |
12 | a0001c0001t0002g0012 a0001c0001t0002g0049 a0001c0001t0002g0050 others(9): Show |
20 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.490-670_490-662dup others(9): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654528 | |||||||
| chr1:46654528 | T | TTTATTAT others(5): Show |
2 | a0001c0001t0002g0051 a0001c0001t0002g0227 |
3 | HG00408.hp1 HG02523.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.490-673_490-662dup others(12): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654528 | |||||||
| chr1:46654528 | T | TTTATTTA others(3): Show |
1 | a0001c0001t0020g0130 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.490-662_490-661ins others(10): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654528 | |||||||
| chr1:46654528 | T | TTTATTTT others(1): Show |
8 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0156 others(5): Show |
14 | HG00544.hp2 HG01243.hp1 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.490-662_490-661ins others(8): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654528 | |||||||
| chr1:46654528 | T | TTTATTTT others(4): Show |
6 | a0001c0001t0001g0140 a0001c0001t0001g0142 a0001c0001t0001g0152 others(3): Show |
6 | HG01884.hp2 HG02040.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-662_490-661ins others(11): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654528 | |||||||
| chr1:46654528 | T | TTTATTTT others(10): Show |
1 | a0001c0001t0001g0141 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.490-662_490-661ins others(17): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654528 | |||||||
| chr1:46654528 | TTTA | T | 4 | a0001c0001t0003g0126 a0002c0002t0004g0010 a0002c0002t0004g0067 others(1): Show |
8 | HG01358.hp1 HG01943.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-664_490-662del others(3): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654528 | |||||||
| chr1:46654531 | A | ATT | 9 | a0001c0001t0001g0032 a0001c0001t0001g0150 a0001c0001t0001g0158 others(6): Show |
14 | HG01891.hp2 HG02080.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.490-666_490-665dup others(2): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654531 | |||||||
| chr1:46654532 | TTA | T | 8 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0235 others(5): Show |
15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-667_490-666del others(2): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654532 | |||||||
| chr1:46654561 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(146): Show |
265 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.490-694C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654561 | |||||||
| chr1:46654563 | A | T | 8 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0235 others(5): Show |
15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-696T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654563 | |||||||
| chr1:46654564 | C | A | 8 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0235 others(5): Show |
15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-697G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654564 | |||||||
| chr1:46654567 | T | A | 8 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0235 others(5): Show |
15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-700A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654567 | |||||||
| chr1:46654702 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.490-835G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654702 | |||||||
| chr1:46654786 | C | T | 2 | a0001c0001t0010g0211 a0001c0001t0010g0212 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.490-919G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654786 | |||||||
| chr1:46654997 | G | A | 4 | a0001c0001t0010g0211 a0001c0001t0010g0212 a0001c0001t0010g0243 others(1): Show |
4 | HG02976.hp1 HG03540.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-1130C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46654997 | |||||||
| chr1:46655001 | A | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.490-1134T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655001 | |||||||
| chr1:46655112 | G | A | 1 | a0001c0001t0004g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.490-1245C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655112 | |||||||
| chr1:46655271 | C | T | 1 | a0001c0001t0019g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.490-1404G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655271 | |||||||
| chr1:46655289 | TA | T | 3 | a0001c0001t0002g0215 a0001c0001t0002g0217 a0001c0001t0029g0216 |
3 | HG00639.hp1 HG01952.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.490-1423delT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655289 | |||||||
| chr1:46655294 | T | C | 4 | a0001c0001t0010g0211 a0001c0001t0010g0212 a0001c0001t0010g0243 others(1): Show |
4 | HG02976.hp1 HG03540.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-1427A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655294 | |||||||
| chr1:46655694 | T | C | 2 | a0001c0001t0002g0193 a0001c0001t0002g0228 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.490-1827A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655694 | |||||||
| chr1:46655747 | T | C | 49 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0018 others(46): Show |
82 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.490-1880A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655747 | |||||||
| chr1:46655790 | C | T | 1 | a0001c0001t0003g0094 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.490-1923G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655790 | |||||||
| chr1:46655830 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(64): Show |
117 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.490-1963G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655830 | |||||||
| chr1:46655869 | A | T | 1 | a0001c0001t0004g0132 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.490-2002T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655869 | |||||||
| chr1:46655977 | T | C | 1 | a0001c0001t0002g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.490-2110A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46655977 | |||||||
| chr1:46656060 | G | A | 78 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(75): Show |
140 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.489+2067C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656060 | |||||||
| chr1:46656124 | T | A | 7 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0031 others(4): Show |
10 | HG01167.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+2003A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656124 | |||||||
| chr1:46656138 | T | C | 1 | a0001c0001t0001g0032 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.489+1989A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656138 | |||||||
| chr1:46656266 | G | A | 1 | a0002c0002t0004g0082 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.489+1861C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656266 | |||||||
| chr1:46656269 | G | A | 1 | a0001c0001t0023g0232 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.489+1858C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656269 | |||||||
| chr1:46656359 | G | T | 1 | a0001c0001t0002g0245 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.489+1768C>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656359 | |||||||
| chr1:46656443 | C | T | 3 | a0001c0001t0002g0190 a0001c0001t0002g0245 a0001c0001t0002g0246 |
3 | HG02486.hp2 HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.489+1684G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656443 | |||||||
| chr1:46656453 | T | C | 1 | a0001c0001t0002g0230 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.489+1674A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656453 | |||||||
| chr1:46656460 | T | C | 1 | a0001c0001t0006g0207 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.489+1667A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656460 | |||||||
| chr1:46656861 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0244 |
7 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+1266A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656861 | |||||||
| chr1:46656870 | C | T | 1 | a0001c0001t0003g0104 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.489+1257G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656870 | |||||||
| chr1:46656924 | C | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.489+1203G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46656924 | |||||||
| chr1:46657049 | G | C | 1 | a0001c0001t0006g0043 | 2 | HG02165.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.489+1078C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657049 | |||||||
| chr1:46657153 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.489+974C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657153 | |||||||
| chr1:46657184 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(52): Show |
103 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.489+943A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657184 | |||||||
| chr1:46657261 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.489+866C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657261 | |||||||
| chr1:46657300 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.489+827G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657300 | |||||||
| chr1:46657344 | C | A | 1 | a0001c0001t0004g0129 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.489+783G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657344 | |||||||
| chr1:46657410 | C | T | 5 | a0001c0001t0009g0034 a0001c0001t0009g0146 a0001c0001t0009g0147 others(2): Show |
6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+717G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657410 | |||||||
| chr1:46657606 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(148): Show |
267 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.489+521C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657606 | |||||||
| chr1:46657891 | C | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.489+236G>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657891 | |||||||
| chr1:46657891 | C | T | 1 | a0001c0001t0002g0214 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.489+236G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657891 | |||||||
| chr1:46657927 | C | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.489+200G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 4/8 | chr1 | 46657927 | |||||||
| chr1:46658226 | T | TA | 40 | a0001c0001t0002g0230 a0001c0001t0005g0006 a0001c0001t0005g0234 others(37): Show |
58 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.427-38dupT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 3/8 | chr1 | 46658226 | |||||||
| chr1:46658226 | TA | T | 11 | a0001c0001t0002g0088 a0001c0001t0002g0192 a0001c0001t0002g0196 others(8): Show |
15 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.427-38delT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 3/8 | chr1 | 46658226 | |||||||
| chr1:46658226 | TAA | T | 15 | a0001c0001t0001g0009 a0001c0001t0001g0032 a0001c0001t0001g0033 others(12): Show |
22 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.427-39_427-38delTT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 3/8 | chr1 | 46658226 | |||||||
| chr1:46658226 | TAAA | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(49): Show |
95 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.427-40_427-38delTT others(1): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 3/8 | chr1 | 46658226 | |||||||
| chr1:46658239 | A | C | 1 | a0001c0001t0003g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.427-50T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 3/8 | chr1 | 46658239 | |||||||
| chr1:46658478 | G | A | 1 | a0001c0001t0003g0101 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.426+209C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 3/8 | chr1 | 46658478 | |||||||
| chr1:46658532 | C | CA | 151 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(148): Show |
267 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.426+154dupT | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 3/8 | chr1 | 46658532 | |||||||
| chr1:46658642 | C | T | 5 | a0001c0001t0009g0034 a0001c0001t0009g0146 a0001c0001t0009g0147 others(2): Show |
6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.426+45G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 3/8 | chr1 | 46658642 | |||||||
| chr1:46658807 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(148): Show |
267 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.376-70T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46658807 | |||||||
| chr1:46658882 | T | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.376-145A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46658882 | |||||||
| chr1:46658930 | A | G | 1 | a0001c0001t0001g0036 | 2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.376-193T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46658930 | |||||||
| chr1:46659018 | C | T | 2 | a0001c0001t0010g0211 a0001c0001t0010g0212 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.376-281G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659018 | |||||||
| chr1:46659106 | G | A | 8 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0235 others(5): Show |
15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.376-369C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659106 | |||||||
| chr1:46659116 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(205): Show |
360 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(357): Show |
intron_variant | MODIFIER | c.376-379T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659116 | |||||||
| chr1:46659212 | A | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(64): Show |
117 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.376-475T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659212 | |||||||
| chr1:46659327 | C | T | 78 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(75): Show |
140 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.376-590G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659327 | |||||||
| chr1:46659365 | TC | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.376-629delG | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659365 | |||||||
| chr1:46659419 | C | T | 8 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0235 others(5): Show |
15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.376-682G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659419 | |||||||
| chr1:46659513 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0186 a0001c0001t0001g0244 |
8 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-776G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659513 | |||||||
| chr1:46659535 | AT | A | 49 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0018 others(46): Show |
82 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.376-799delA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659535 | |||||||
| chr1:46659611 | G | A | 21 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0022 others(18): Show |
43 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.376-874C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659611 | |||||||
| chr1:46659900 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.376-1163A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659900 | |||||||
| chr1:46659902 | C | T | 2 | a0001c0001t0001g0032 a0002c0002t0004g0057 |
3 | HG02559.hp2 HG03209.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.376-1165G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659902 | |||||||
| chr1:46659916 | C | T | 1 | a0001c0001t0009g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.376-1179G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659916 | |||||||
| chr1:46659979 | C | CT | 11 | a0001c0001t0003g0102 a0001c0001t0005g0006 a0001c0001t0005g0234 others(8): Show |
18 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.376-1243dupA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659979 | |||||||
| chr1:46659979 | CT | C | 41 | a0001c0001t0001g0177 a0001c0001t0002g0002 a0001c0001t0002g0012 others(38): Show |
73 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.376-1243delA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46659979 | |||||||
| chr1:46660101 | C | T | 3 | a0002c0002t0004g0025 a0002c0002t0004g0060 a0002c0002t0004g0061 |
4 | HG01884.hp1 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.376-1364G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660101 | |||||||
| chr1:46660225 | C | A | 1 | a0001c0001t0006g0207 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.376-1488G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660225 | |||||||
| chr1:46660294 | C | A | 78 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(75): Show |
140 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.376-1557G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660294 | |||||||
| chr1:46660328 | A | G | 5 | a0001c0001t0002g0044 a0001c0001t0002g0191 a0001c0001t0002g0208 others(2): Show |
6 | NA18951.hp2 NA18969.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.376-1591T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660328 | |||||||
| chr1:46660351 | T | G | 1 | a0001c0001t0004g0029 | 2 | HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.376-1614A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660351 | |||||||
| chr1:46660716 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0182 a0001c0001t0001g0183 |
6 | NA18945.hp2 NA18950.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.376-1979C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660716 | |||||||
| chr1:46660719 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(148): Show |
267 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.376-1982T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660719 | |||||||
| chr1:46660720 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(148): Show |
267 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.376-1983A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660720 | |||||||
| chr1:46660853 | T | A | 1 | a0001c0001t0003g0100 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.376-2116A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660853 | |||||||
| chr1:46660860 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0178 |
3 | NA18979.hp1 NA18984.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.376-2123G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660860 | |||||||
| chr1:46660953 | CT | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.376-2217delA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660953 | |||||||
| chr1:46660955 | T | C | 49 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0018 others(46): Show |
82 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.376-2218A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46660955 | |||||||
| chr1:46661076 | G | GT | 12 | a0001c0001t0001g0157 a0001c0001t0001g0244 a0001c0001t0002g0191 others(9): Show |
13 | HG01168.hp1 HG01243.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.376-2340dupA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661076 | |||||||
| chr1:46661104 | A | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.376-2367T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661104 | |||||||
| chr1:46661111 | C | T | 80 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(77): Show |
143 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.376-2374G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661111 | |||||||
| chr1:46661120 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0186 a0001c0001t0001g0244 |
8 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-2383A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661120 | |||||||
| chr1:46661159 | G | A | 1 | a0002c0002t0004g0025 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.376-2422C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661159 | |||||||
| chr1:46661165 | C | T | 11 | a0001c0001t0001g0033 a0001c0001t0001g0135 a0001c0001t0001g0136 others(8): Show |
12 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.376-2428G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661165 | |||||||
| chr1:46661268 | G | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.376-2531C>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661268 | |||||||
| chr1:46661370 | C | T | 1 | a0001c0001t0003g0101 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.376-2633G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661370 | |||||||
| chr1:46661499 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0186 a0001c0001t0001g0244 |
8 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-2762C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661499 | |||||||
| chr1:46661505 | G | A | 1 | a0001c0001t0003g0090 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.376-2768C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661505 | |||||||
| chr1:46661518 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.376-2781A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661518 | |||||||
| chr1:46661594 | C | A | 21 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0022 others(18): Show |
43 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.376-2857G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661594 | |||||||
| chr1:46661680 | T | A | 6 | a0001c0001t0001g0033 a0001c0001t0001g0140 a0001c0001t0001g0142 others(3): Show |
7 | HG02145.hp1 HG02258.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.376-2943A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661680 | |||||||
| chr1:46661709 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(52): Show |
103 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.376-2972C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661709 | |||||||
| chr1:46661776 | G | A | 10 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0041 others(7): Show |
18 | HG00673.hp1 HG02132.hp1 HG02155.hp1 others(15): Show |
intron_variant | MODIFIER | c.376-3039C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661776 | |||||||
| chr1:46661893 | C | CT | 5 | a0001c0001t0003g0093 a0001c0001t0003g0099 a0001c0001t0003g0100 others(2): Show |
5 | HG03130.hp1 NA18970.hp1 NA19078.hp1 others(2): Show |
intron_variant | MODIFIER | c.376-3157dupA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661893 | |||||||
| chr1:46661893 | C | CTT | 4 | a0001c0001t0009g0034 a0001c0001t0009g0146 a0001c0001t0014g0144 others(1): Show |
5 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.376-3158_376-3157d others(4): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661893 | |||||||
| chr1:46661896 | TC | T | 33 | a0001c0001t0001g0035 a0001c0001t0001g0140 a0001c0001t0001g0154 others(30): Show |
56 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.376-3160delG | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661896 | |||||||
| chr1:46661897 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(173): Show |
305 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.376-3160G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661897 | |||||||
| chr1:46661934 | G | A | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.376-3197C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46661934 | |||||||
| chr1:46662092 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.375+3164G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662092 | |||||||
| chr1:46662116 | A | G | 1 | a0001c0001t0002g0191 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.375+3140T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662116 | |||||||
| chr1:46662164 | C | G | 1 | a0001c0001t0001g0153 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.375+3092G>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662164 | |||||||
| chr1:46662312 | CTA | C | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.375+2942_375+2943d others(4): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662312 | |||||||
| chr1:46662383 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.375+2873C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662383 | |||||||
| chr1:46662396 | T | C | 79 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(76): Show |
142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.375+2860A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662396 | |||||||
| chr1:46662451 | A | AT | 80 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(77): Show |
142 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.375+2804dupA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662451 | |||||||
| chr1:46662706 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG01884.hp2 HG03225.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.375+2550G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662706 | |||||||
| chr1:46662720 | C | T | 2 | a0001c0001t0003g0118 a0001c0001t0003g0128 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.375+2536G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662720 | |||||||
| chr1:46662923 | C | A | 1 | a0001c0001t0002g0053 | 2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.375+2333G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46662923 | |||||||
| chr1:46663002 | G | A | 2 | a0001c0001t0003g0124 a0001c0001t0003g0125 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.375+2254C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663002 | |||||||
| chr1:46663009 | A | C | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.375+2247T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663009 | |||||||
| chr1:46663012 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.375+2244G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663012 | |||||||
| chr1:46663014 | T | A | 2 | a0001c0001t0003g0126 a0001c0001t0003g0127 |
2 | HG01256.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.375+2242A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663014 | |||||||
| chr1:46663043 | T | C | 79 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(76): Show |
142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.375+2213A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663043 | |||||||
| chr1:46663107 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.375+2149A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663107 | |||||||
| chr1:46663148 | T | C | 11 | a0001c0001t0001g0033 a0001c0001t0001g0135 a0001c0001t0001g0136 others(8): Show |
12 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.375+2108A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663148 | |||||||
| chr1:46663150 | T | C | 1 | a0002c0002t0004g0084 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.375+2106A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663150 | |||||||
| chr1:46663355 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(65): Show |
121 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.375+1901G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663355 | |||||||
| chr1:46663602 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.375+1654A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663602 | |||||||
| chr1:46663627 | GT | G | 79 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(76): Show |
142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.375+1628delA | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663627 | |||||||
| chr1:46663747 | C | G | 1 | a0001c0001t0003g0094 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.375+1509G>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46663747 | |||||||
| chr1:46664078 | T | G | 8 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0235 others(5): Show |
15 | HG00558.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.375+1178A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664078 | |||||||
| chr1:46664187 | T | C | 1 | a0001c0001t0003g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.375+1069A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664187 | |||||||
| chr1:46664189 | T | A | 1 | a0001c0001t0009g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.375+1067A>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664189 | |||||||
| chr1:46664336 | C | T | 1 | a0001c0001t0003g0093 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.375+920G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664336 | |||||||
| chr1:46664407 | G | A | 1 | a0002c0002t0004g0085 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.375+849C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664407 | |||||||
| chr1:46664435 | C | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.375+821G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664435 | |||||||
| chr1:46664460 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.375+796G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664460 | |||||||
| chr1:46664645 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.375+611C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664645 | |||||||
| chr1:46664776 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.375+480C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664776 | |||||||
| chr1:46664861 | T | C | 1 | a0001c0001t0023g0232 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.375+395A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664861 | |||||||
| chr1:46664865 | T | G | 1 | a0001c0001t0003g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.375+391A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664865 | |||||||
| chr1:46664922 | C | T | 37 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0018 others(34): Show |
69 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.375+334G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664922 | |||||||
| chr1:46664956 | C | T | 136 | a0001c0001t0001g0150 a0001c0001t0002g0002 a0001c0001t0002g0004 others(133): Show |
234 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.375+300G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664956 | |||||||
| chr1:46664972 | C | G | 1 | a0001c0001t0001g0149 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.375+284G>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46664972 | |||||||
| chr1:46665042 | G | A | 1 | a0001c0001t0002g0233 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.375+214C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46665042 | |||||||
| chr1:46665201 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(151): Show |
264 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.375+55T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 2/8 | chr1 | 46665201 | |||||||
| chr1:46665435 | T | G | 2 | a0001c0001t0002g0242 a0001c0001t0021g0241 |
2 | NA18964.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.267-71A>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46665435 | |||||||
| chr1:46665534 | A | G | 2 | a0001c0001t0016g0187 a0001c0001t0016g0188 |
2 | HG00642.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.267-170T>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46665534 | |||||||
| chr1:46665576 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.267-212C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46665576 | |||||||
| chr1:46665647 | A | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.267-283T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46665647 | |||||||
| chr1:46665738 | C | G | 1 | a0001c0001t0019g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.267-374G>C | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46665738 | |||||||
| chr1:46665858 | G | A | 1 | a0001c0001t0001g0016 | 4 | HG02486.hp1 HG02717.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.267-494C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46665858 | |||||||
| chr1:46665923 | A | T | 2 | a0001c0001t0003g0091 a0001c0001t0003g0092 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.267-559T>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46665923 | |||||||
| chr1:46666062 | C | T | 2 | a0001c0001t0003g0089 a0001c0001t0003g0090 |
2 | HG00642.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.267-698G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666062 | |||||||
| chr1:46666108 | C | A | 5 | a0001c0001t0009g0034 a0001c0001t0009g0146 a0001c0001t0009g0147 others(2): Show |
6 | HG02451.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.267-744G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666108 | |||||||
| chr1:46666237 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0186 a0001c0001t0001g0244 |
8 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.267-873C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666237 | |||||||
| chr1:46666310 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(70): Show |
127 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.267-946C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666310 | |||||||
| chr1:46666345 | C | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(52): Show |
103 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.267-981G>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666345 | |||||||
| chr1:46666350 | G | A | 8 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0031 others(5): Show |
11 | HG01167.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.267-986C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666350 | |||||||
| chr1:46666548 | A | C | 1 | a0001c0001t0001g0139 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.267-1184T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666548 | |||||||
| chr1:46666571 | T | C | 79 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(76): Show |
142 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.267-1207A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666571 | |||||||
| chr1:46666642 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(149): Show |
269 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.267-1278A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666642 | |||||||
| chr1:46666774 | G | A | 1 | a0002c0002t0004g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.266+1283C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666774 | |||||||
| chr1:46666848 | C | T | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.266+1209G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46666848 | |||||||
| chr1:46667050 | T | C | 1 | a0001c0001t0010g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.266+1007A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667050 | |||||||
| chr1:46667232 | TGGA | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0244 |
7 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.266+822_266+824del others(3): Show |
ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667232 | |||||||
| chr1:46667236 | A | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0244 |
7 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.266+821T>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667236 | |||||||
| chr1:46667237 | G | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0244 |
7 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.266+820C>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667237 | |||||||
| chr1:46667342 | T | C | 7 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0031 others(4): Show |
10 | HG01167.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.266+715A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667342 | |||||||
| chr1:46667388 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(149): Show |
269 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.266+669A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667388 | |||||||
| chr1:46667617 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.266+440G>A | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667617 | |||||||
| chr1:46667743 | T | C | 2 | a0001c0001t0002g0245 a0001c0001t0002g0246 |
2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.266+314A>G | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667743 | |||||||
| chr1:46667803 | G | A | 1 | a0001c0001t0008g0013 | 4 | HG01891.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.266+254C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667803 | |||||||
| chr1:46667910 | G | A | 2 | a0001c0001t0015g0247 a0001c0001t0015g0248 |
2 | HG02145.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.266+147C>T | ATPAF1 | ENSG00000123472.13 | transcript | ENST00000574428.6 | protein_coding | 1/8 | chr1 | 46667910 |