Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 85403 |
| ensemblid | ENSG00000144597.14 |
| hgncid | 20907 |
| symbol | EAF1 |
| name | ELL associated factor 1 |
| refseq_nuc | NM_033083.7 |
| refseq_prot | NP_149074.3 |
| ensembl_nuc | ENST00000396842.7 |
| ensembl_prot | ENSP00000380054.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 15427598 |
| end | 15442613 |
| strand | + |
| ver | v1.2 |
| region | chr3:15427598-15442613 |
| region5000 | chr3:15422598-15447613 |
| regionname0 | EAF1_chr3_15427598_15442613 |
| regionname5000 | EAF1_chr3_15422598_15447613 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 268 | 412 | 98 | 69 | 186 | 11 | 46 | 144 | EAF1_chr3_15422598_15447613 | EAF1 | MNGTA others(263): Show |
chr3 | 15422598 | 15447613 |
| a0002 | 0/0 | 268 | 4 | 0 | 0 | 3 | 1 | 0 | 3 | EAF1_chr3_15422598_15447613 | EAF1 | MNGTA others(263): Show |
chr3 | 15422598 | 15447613 |
| a0003 | 0/0 | 151 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | MNGTA others(146): Show |
chr3 | 15422598 | 15447613 |
| a0004 | 0/0 | 268 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | MNGTA others(263): Show |
chr3 | 15422598 | 15447613 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 804 | 292 | 67 | 54 | 132 | 8 | 29 | EAF1_chr3_15422598_15447613 | EAF1 | ATGAA others(799): Show |
chr3 | 15422598 | 15447613 | ||
| a0001c0002 | 0/0 | 804 | 88 | 3 | 13 | 52 | 3 | 17 | EAF1_chr3_15422598_15447613 | EAF1 | ATGAA others(799): Show |
chr3 | 15422598 | 15447613 | ||
| a0001c0003 | 0/0 | 804 | 17 | 14 | 1 | 2 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | ATGAA others(799): Show |
chr3 | 15422598 | 15447613 | ||
| a0001c0004 | 0/0 | 804 | 7 | 6 | 1 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | ATGAA others(799): Show |
chr3 | 15422598 | 15447613 | ||
| a0001c0005 | 0/0 | 804 | 5 | 5 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | ATGAA others(799): Show |
chr3 | 15422598 | 15447613 | ||
| a0001c0006 | 0/0 | 804 | 3 | 3 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | ATGAA others(799): Show |
chr3 | 15422598 | 15447613 | ||
| a0002c0007 | 0/0 | 804 | 3 | 0 | 0 | 3 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | ATGAA others(799): Show |
chr3 | 15422598 | 15447613 | ||
| a0002c0009 | 0/0 | 804 | 1 | 0 | 0 | 0 | 1 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | ATGAA others(799): Show |
chr3 | 15422598 | 15447613 | ||
| a0003c0008 | 0/0 | 779 | 1 | 0 | 1 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | ATGAA others(774): Show |
chr3 | 15422598 | 15447613 | ||
| a0004c0010 | 0/0 | 804 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | ATGAA others(799): Show |
chr3 | 15422598 | 15447613 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4447 | 51 | 9 | 19 | 20 | 1 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4442): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0002 | 0/0 | 4447 | 71 | 11 | 13 | 31 | 3 | 13 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4442): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0003 | 0/0 | 4449 | 57 | 11 | 9 | 34 | 1 | 2 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4444): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0004 | 0/0 | 4449 | 31 | 0 | 7 | 17 | 2 | 5 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4444): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0005 | 0/0 | 4449 | 21 | 2 | 3 | 11 | 1 | 4 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4444): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0006 | 0/0 | 4451 | 15 | 5 | 2 | 6 | 0 | 2 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4446): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0008 | 0/0 | 4447 | 10 | 9 | 1 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4442): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0009 | 0/0 | 4451 | 4 | 0 | 0 | 3 | 0 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4446): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0011 | 0/0 | 4447 | 3 | 3 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4442): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0013 | 0/0 | 4451 | 3 | 0 | 0 | 3 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4446): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0014 | 0/0 | 4444 | 3 | 3 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4439): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0015 | 0/0 | 4453 | 3 | 1 | 0 | 2 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4448): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0016 | 0/0 | 4449 | 2 | 0 | 0 | 2 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4444): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0019 | 0/0 | 4453 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4448): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0020 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4444): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0021 | 0/0 | 4457 | 2 | 2 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4452): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0022 | 0/0 | 4451 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4446): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0023 | 0/0 | 4451 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4446): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0024 | 0/0 | 4453 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4448): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0025 | 0/0 | 4451 | 1 | 0 | 0 | 0 | 0 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4446): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0026 | 0/0 | 4455 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4450): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0027 | 0/1 | 4446 | 1 | 0 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4441): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0028 | 0/0 | 4453 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4448): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0029 | 0/0 | 4455 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4450): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0030 | 0/0 | 4451 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4446): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0031 | 0/0 | 4455 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4450): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0034 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4441): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0035 | 0/0 | 4451 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4446): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0036 | 0/0 | 4451 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4446): Show |
chr3 | 15422598 | 15447613 |
| a0001c0001t0037 | 0/0 | 4447 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4442): Show |
chr3 | 15422598 | 15447613 |
| a0001c0002t0001 | 0/0 | 4447 | 81 | 3 | 13 | 48 | 3 | 14 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4442): Show |
chr3 | 15422598 | 15447613 |
| a0001c0002t0005 | 0/0 | 4449 | 4 | 0 | 0 | 3 | 0 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4444): Show |
chr3 | 15422598 | 15447613 |
| a0001c0002t0019 | 0/0 | 4453 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4448): Show |
chr3 | 15422598 | 15447613 |
| a0001c0002t0032 | 0/0 | 4447 | 1 | 0 | 0 | 0 | 0 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4442): Show |
chr3 | 15422598 | 15447613 |
| a0001c0002t0033 | 0/0 | 4447 | 1 | 0 | 0 | 0 | 0 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4442): Show |
chr3 | 15422598 | 15447613 |
| a0001c0003t0007 | 0/0 | 4451 | 14 | 13 | 1 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4446): Show |
chr3 | 15422598 | 15447613 |
| a0001c0003t0008 | 0/0 | 4447 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4442): Show |
chr3 | 15422598 | 15447613 |
| a0001c0003t0018 | 0/0 | 4455 | 2 | 0 | 0 | 2 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4450): Show |
chr3 | 15422598 | 15447613 |
| a0001c0004t0006 | 0/0 | 4451 | 7 | 6 | 1 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4446): Show |
chr3 | 15422598 | 15447613 |
| a0001c0005t0012 | 0/0 | 4465 | 3 | 3 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4460): Show |
chr3 | 15422598 | 15447613 |
| a0001c0005t0017 | 0/0 | 4461 | 2 | 2 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4456): Show |
chr3 | 15422598 | 15447613 |
| a0001c0006t0010 | 0/0 | 4451 | 3 | 3 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4446): Show |
chr3 | 15422598 | 15447613 |
| a0002c0007t0003 | 0/0 | 4449 | 3 | 0 | 0 | 3 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4444): Show |
chr3 | 15422598 | 15447613 |
| a0002c0009t0001 | 0/0 | 4447 | 1 | 0 | 0 | 0 | 1 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4442): Show |
chr3 | 15422598 | 15447613 |
| a0003c0008t0020 | 0/0 | 4424 | 1 | 0 | 1 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4419): Show |
chr3 | 15422598 | 15447613 |
| a0004c0010t0002 | 0/0 | 4447 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | CTCTC others(4442): Show |
chr3 | 15422598 | 15447613 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0001g0007 | 0/0 | 10 | 0 | 10 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0001g0009 | 1/0 | 9 | 0 | 7 | 0 | 0 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0001g0011 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0001g0013 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0001g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0002g0002 | 0/0 | 37 | 4 | 5 | 25 | 0 | 3 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0002g0004 | 0/0 | 19 | 3 | 4 | 0 | 3 | 9 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0002g0019 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0002g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0003g0003 | 0/0 | 34 | 2 | 5 | 25 | 1 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0003g0014 | 0/0 | 6 | 4 | 1 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0003g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0003g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0004g0002 | 0/0 | 19 | 0 | 2 | 12 | 0 | 5 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0004g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0004g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0005g0001 | 0/0 | 14 | 0 | 3 | 6 | 1 | 4 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0005g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0006g0008 | 0/0 | 6 | 4 | 0 | 2 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0006g0025 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0006g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0008g0006 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0008g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0009g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0009g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0011g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0013g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0013g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0014g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0014g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0015g0008 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0016g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0019g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0020g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0021g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0022g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0023g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0024g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0025g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0026g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0027g0093 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0028g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0029g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0030g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0031g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0034g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0035g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0036g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0001t0037g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0001g0001 | 0/0 | 52 | 0 | 8 | 32 | 2 | 10 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0001g0010 | 0/0 | 7 | 2 | 3 | 0 | 0 | 2 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0001g0016 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0001g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0005g0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0019g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0032g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0002t0033g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0003t0007g0005 | 0/0 | 11 | 11 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0003t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0003t0007g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0003t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0003t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0003t0018g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0004t0006g0012 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0005t0012g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0005t0012g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0005t0017g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0001c0006t0010g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0002c0007t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0002c0009t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0003c0008t0020g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| a0004c0010t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0001 | EUR | GBR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | GBR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | FIN | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | CHS | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00544 | hp2 | a0001 | c0001 | t0026 | g0001 | EAS | CHS | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0038 | EAS | CHS | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | CHS | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | CHS | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01081 | hp1 | a0003 | c0008 | t0020 | g0095 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01109 | hp1 | a0001 | c0003 | t0007 | g0051 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01168 | hp1 | a0001 | c0004 | t0006 | g0012 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0075 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0006 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0077 | EUR | IBS | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01884 | hp2 | a0001 | c0001 | t0030 | g0022 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0065 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0025 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0030 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0067 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0035 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02055 | hp2 | a0001 | c0003 | t0007 | g0005 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02056 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02071 | hp1 | a0001 | c0001 | t0013 | g0002 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0035 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02080 | hp1 | a0001 | c0001 | t0013 | g0002 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0030 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0025 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CDX | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CDX | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02165 | hp1 | a0001 | c0001 | t0005 | g0083 | EAS | CDX | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02165 | hp2 | a0001 | c0002 | t0005 | g0001 | EAS | CDX | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02257 | hp2 | a0001 | c0004 | t0006 | g0012 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02258 | hp2 | a0001 | c0001 | t0015 | g0008 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02280 | hp1 | a0001 | c0001 | t0035 | g0103 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02280 | hp2 | a0001 | c0001 | t0011 | g0006 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02615 | hp2 | a0001 | c0003 | t0007 | g0005 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0098 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02622 | hp2 | a0001 | c0005 | t0017 | g0018 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02647 | hp1 | a0001 | c0001 | t0034 | g0040 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02683 | hp2 | a0001 | c0002 | t0005 | g0001 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02717 | hp2 | a0001 | c0003 | t0007 | g0005 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02723 | hp1 | a0001 | c0003 | t0007 | g0005 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0048 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02809 | hp2 | a0001 | c0001 | t0011 | g0006 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02886 | hp1 | a0001 | c0001 | t0021 | g0022 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02886 | hp2 | a0001 | c0003 | t0007 | g0052 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02895 | hp1 | a0001 | c0003 | t0007 | g0005 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02896 | hp1 | a0001 | c0003 | t0007 | g0005 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02922 | hp1 | a0001 | c0003 | t0007 | g0005 | AFR | ESN | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | ESN | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02965 | hp1 | a0001 | c0001 | t0028 | g0041 | AFR | ESN | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02970 | hp1 | a0001 | c0006 | t0010 | g0024 | AFR | ESN | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02970 | hp2 | a0001 | c0001 | t0020 | g0094 | AFR | ESN | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02976 | hp2 | a0001 | c0006 | t0010 | g0024 | AFR | ESN | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0049 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03041 | hp1 | a0001 | c0003 | t0007 | g0050 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03098 | hp1 | a0001 | c0003 | t0007 | g0005 | AFR | MSL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03098 | hp2 | a0001 | c0001 | t0014 | g0047 | AFR | MSL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ESN | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03130 | hp2 | a0001 | c0004 | t0006 | g0012 | AFR | ESN | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03139 | hp1 | a0001 | c0003 | t0007 | g0005 | AFR | ESN | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03139 | hp2 | a0001 | c0001 | t0014 | g0027 | AFR | ESN | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03195 | hp1 | a0001 | c0003 | t0007 | g0005 | AFR | ESN | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03195 | hp2 | a0001 | c0001 | t0022 | g0046 | AFR | ESN | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03209 | hp1 | a0001 | c0005 | t0012 | g0018 | AFR | MSL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | MSL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03225 | hp2 | a0001 | c0001 | t0037 | g0002 | AFR | MSL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03239 | hp1 | a0001 | c0002 | t0033 | g0001 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03486 | hp1 | a0001 | c0001 | t0014 | g0027 | AFR | MSL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03516 | hp1 | a0001 | c0005 | t0012 | g0043 | AFR | ESN | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0057 | AFR | ESN | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03579 | hp2 | a0001 | c0001 | t0023 | g0039 | AFR | MSL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03704 | hp1 | a0001 | c0001 | t0006 | g0099 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0001 | SAS | BEB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03834 | hp1 | a0001 | c0002 | t0032 | g0001 | SAS | BEB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | BEB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0097 | SAS | BEB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0096 | SAS | STU | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | BEB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0001 | SAS | BEB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | STU | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | STU | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | STU | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | YRI | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18522 | hp2 | a0001 | c0005 | t0012 | g0018 | AFR | YRI | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | CHB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18906 | hp1 | a0001 | c0001 | t0021 | g0022 | AFR | YRI | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18906 | hp2 | a0001 | c0001 | t0024 | g0042 | AFR | YRI | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18951 | hp1 | a0001 | c0001 | t0019 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18951 | hp2 | a0001 | c0002 | t0019 | g0089 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18952 | hp1 | a0001 | c0001 | t0016 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18956 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18972 | hp1 | a0004 | c0010 | t0002 | g0079 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18972 | hp2 | a0001 | c0003 | t0018 | g0026 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18983 | hp2 | a0001 | c0002 | t0005 | g0100 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18986 | hp1 | a0001 | c0001 | t0036 | g0008 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18987 | hp1 | a0001 | c0001 | t0015 | g0008 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18987 | hp2 | a0002 | c0007 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18997 | hp2 | a0001 | c0001 | t0006 | g0038 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18998 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18999 | hp1 | a0001 | c0003 | t0018 | g0026 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19000 | hp1 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19006 | hp2 | a0001 | c0001 | t0006 | g0102 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19007 | hp2 | a0001 | c0001 | t0016 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19011 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | LWK | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0071 | AFR | LWK | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | LWK | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19043 | hp2 | a0001 | c0001 | t0029 | g0045 | AFR | LWK | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19054 | hp1 | a0002 | c0007 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19060 | hp1 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19077 | hp2 | a0001 | c0001 | t0013 | g0080 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19079 | hp2 | a0001 | c0001 | t0005 | g0084 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19082 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19086 | hp1 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19088 | hp1 | a0002 | c0007 | t0003 | g0003 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19089 | hp1 | a0001 | c0001 | t0009 | g0058 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19089 | hp2 | a0001 | c0001 | t0015 | g0008 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19240 | hp1 | a0001 | c0006 | t0010 | g0024 | AFR | YRI | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | YRI | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ASW | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA20752 | hp2 | a0002 | c0009 | t0001 | g0055 | EUR | TSI | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0092 | EUR | TSI | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0004 | EUR | TSI | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA20905 | hp1 | a0001 | c0001 | t0025 | g0001 | SAS | GIH | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA20905 | hp2 | a0001 | c0001 | t0009 | g0003 | SAS | GIH | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02109 | hp1 | a0001 | c0004 | t0006 | g0012 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0085 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02486 | hp2 | a0001 | c0004 | t0006 | g0012 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG02559 | hp2 | a0001 | c0004 | t0006 | g0012 | AFR | ACB | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0006 | AFR | MSL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG03471 | hp2 | a0001 | c0005 | t0017 | g0018 | AFR | MSL | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG06807 | hp1 | a0001 | c0004 | t0006 | g0012 | AFR | USA | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | USA | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA18955 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA20300 | hp2 | a0001 | c0003 | t0008 | g0053 | AFR | USA | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA21309 | hp1 | a0001 | c0001 | t0031 | g0044 | AFR | LWK | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| NA21309 | hp2 | a0001 | c0003 | t0007 | g0005 | AFR | LWK | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0027 | g0093 | REF | REF | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0009 | REF | REF | EAF1_chr3_15422598_15447613 | EAF1 | chr3 | 15422598 | 15447613 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15427796 | A | G | 1 | a0004 | 1 | NA18972.hp1 | missense_variant | MODERATE | c.17A>G | p.Asn6Ser | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/6 | 199/4447 | 17/807 | 6/268 | chr3 | 15427796 | |||
| chr3:15427876 | A | C | 1 | a0002 | 3 | NA18987.hp2 NA19054.hp1 NA19088.hp1 |
missense_variant | MODERATE | c.97A>C | p.Ile33Leu | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/6 | 279/4447 | 97/807 | 33/268 | chr3 | 15427876 | |||
| chr3:15427876 | A | G | 1 | a0002 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.97A>G | p.Ile33Val | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/6 | 279/4447 | 97/807 | 33/268 | chr3 | 15427876 | |||
| chr3:15434345 | CAGAGCTG others(20): Show |
C | 1 | a0003 | 1 | HG01081.hp1 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.336-2_360delAGAGCT others(21): Show |
p.Ala113fs | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/6 | 336/807 | 112/268 | chr3 | 15434345 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15427860 | G | T | 1 | a0001c0003 | 17 | HG01109.hp1 HG02055.hp2 HG02615.hp2 others(14): Show |
synonymous_variant | LOW | c.81G>T | p.Arg27Arg | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/6 | 263/4447 | 81/807 | 27/268 | chr3 | 15427860 | |||
| chr3:15434411 | G | A | 1 | a0001c0004 | 7 | HG01168.hp1 HG02109.hp1 HG02257.hp2 others(4): Show |
synonymous_variant | LOW | c.399G>A | p.Thr133Thr | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/6 | 581/4447 | 399/807 | 133/268 | chr3 | 15434411 | |||
| chr3:15434504 | C | G | 1 | a0001c0002 | 88 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(85): Show |
synonymous_variant | LOW | c.492C>G | p.Pro164Pro | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/6 | 674/4447 | 492/807 | 164/268 | chr3 | 15434504 | |||
| chr3:15436433 | C | T | 1 | a0001c0006 | 3 | HG02970.hp1 HG02976.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.618C>T | p.Asp206Asp | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/6 | 800/4447 | 618/807 | 206/268 | chr3 | 15436433 | |||
| chr3:15436442 | C | T | 1 | a0001c0005 | 5 | HG02622.hp2 HG03209.hp1 HG03471.hp2 others(2): Show |
synonymous_variant | LOW | c.627C>T | p.Ser209Ser | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/6 | 809/4447 | 627/807 | 209/268 | chr3 | 15436442 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15427607 | C | A | 1 | a0001c0001t0022 | 1 | HG03195.hp2 | 5_prime_UTR_variant | MODIFIER | c.-173C>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/6 | 173 | chr3 | 15427607 | ||||||
| chr3:15427711 | A | C | 1 | a0001c0001t0037 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-69A>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/6 | 69 | chr3 | 15427711 | ||||||
| chr3:15427763 | G | C | 1 | a0001c0001t0016 | 2 | NA18952.hp1 NA19007.hp2 |
5_prime_UTR_variant | MODIFIER | c.-17G>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/6 | 17 | chr3 | 15427763 | ||||||
| chr3:15439219 | C | T | 4 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0036 others(1): Show |
26 | HG00597.hp2 HG01168.hp1 HG01891.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*64C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 64 | chr3 | 15439219 | ||||||
| chr3:15439248 | A | G | 1 | a0001c0001t0035 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*93A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 93 | chr3 | 15439248 | ||||||
| chr3:15439277 | G | A | 1 | a0001c0006t0010 | 3 | HG02970.hp1 HG02976.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*122G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 122 | chr3 | 15439277 | ||||||
| chr3:15439526 | C | A | 1 | a0001c0001t0011 | 3 | HG02280.hp2 HG02809.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*371C>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 371 | chr3 | 15439526 | ||||||
| chr3:15439526 | C | T | 2 | a0001c0001t0014 a0001c0001t0034 |
4 | HG02647.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*371C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 371 | chr3 | 15439526 | ||||||
| chr3:15439532 | G | T | 1 | a0001c0002t0033 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*377G>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 377 | chr3 | 15439532 | ||||||
| chr3:15439784 | A | C | 2 | a0001c0002t0032 a0001c0002t0033 |
2 | HG03239.hp1 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*629A>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 629 | chr3 | 15439784 | ||||||
| chr3:15439814 | C | T | 5 | a0001c0001t0021 a0001c0001t0022 a0001c0001t0029 others(2): Show |
6 | HG01884.hp2 HG02886.hp1 HG03195.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*659C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 659 | chr3 | 15439814 | ||||||
| chr3:15439854 | C | T | 1 | a0001c0001t0031 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*699C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 699 | chr3 | 15439854 | ||||||
| chr3:15440097 | A | G | 2 | a0001c0001t0014 a0001c0001t0034 |
4 | HG02647.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*942A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 942 | chr3 | 15440097 | ||||||
| chr3:15440404 | A | G | 1 | a0001c0001t0035 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1249A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 1249 | chr3 | 15440404 | ||||||
| chr3:15440495 | A | G | 1 | a0001c0001t0036 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1340A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 1340 | chr3 | 15440495 | ||||||
| chr3:15440694 | G | A | 2 | a0001c0005t0012 a0001c0005t0017 |
5 | HG02622.hp2 HG03209.hp1 HG03471.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1539G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 1539 | chr3 | 15440694 | ||||||
| chr3:15440817 | T | C | 3 | a0001c0001t0008 a0001c0001t0011 a0001c0003t0008 |
14 | HG01192.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1662T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 1662 | chr3 | 15440817 | ||||||
| chr3:15440892 | A | G | 1 | a0001c0006t0010 | 3 | HG02970.hp1 HG02976.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1737A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 1737 | chr3 | 15440892 | ||||||
| chr3:15441141 | G | A | 1 | a0001c0003t0018 | 2 | NA18972.hp2 NA18999.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1986G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 1986 | chr3 | 15441141 | ||||||
| chr3:15441175 | T | C | 2 | a0001c0001t0023 a0001c0001t0024 |
2 | HG03579.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2020T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 2020 | chr3 | 15441175 | ||||||
| chr3:15441199 | A | G | 24 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0011 others(21): Show |
79 | HG00597.hp2 HG01081.hp1 HG01109.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2044A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 2044 | chr3 | 15441199 | ||||||
| chr3:15441240 | GC | G | 2 | a0001c0001t0014 a0001c0001t0034 |
4 | HG02647.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2088delC | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 2088 | INFO_REALIGN_3_PRIME | chr3 | 15441240 | |||||
| chr3:15441268 | C | G | 34 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(31): Show |
253 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*2113C>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 2113 | chr3 | 15441268 | ||||||
| chr3:15441325 | C | G | 5 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0020 others(2): Show |
16 | HG01081.hp1 HG01192.hp2 HG01884.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2170C>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 2170 | chr3 | 15441325 | ||||||
| chr3:15441332 | G | C | 2 | a0001c0003t0007 a0001c0003t0018 |
16 | HG01109.hp1 HG02055.hp2 HG02615.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2177G>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 2177 | chr3 | 15441332 | ||||||
| chr3:15441399 | C | T | 5 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0020 others(2): Show |
16 | HG01081.hp1 HG01192.hp2 HG01884.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2244C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 2244 | chr3 | 15441399 | ||||||
| chr3:15441489 | C | CT | 5 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0014 others(2): Show |
15 | HG00741.hp1 HG02071.hp2 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2356dupT | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 2357 | INFO_REALIGN_3_PRIME | chr3 | 15441489 | |||||
| chr3:15441489 | CT | C | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(12): Show |
182 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*2356delT | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 2356 | INFO_REALIGN_3_PRIME | chr3 | 15441489 | |||||
| chr3:15441489 | CTT | C | 13 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0015 others(10): Show |
41 | HG00597.hp2 HG01109.hp1 HG01168.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2355_*2356delTT | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 2355 | INFO_REALIGN_3_PRIME | chr3 | 15441489 | |||||
| chr3:15441489 | CTTT | C | 3 | a0001c0005t0012 a0001c0005t0017 a0001c0006t0010 |
8 | HG02622.hp2 HG02970.hp1 HG02976.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2354_*2356delTTT | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 2354 | INFO_REALIGN_3_PRIME | chr3 | 15441489 | |||||
| chr3:15441628 | G | A | 2 | a0001c0001t0014 a0001c0001t0034 |
4 | HG02647.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2473G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 2473 | chr3 | 15441628 | ||||||
| chr3:15441844 | G | T | 1 | a0001c0001t0021 | 2 | HG02886.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2689G>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 2689 | chr3 | 15441844 | ||||||
| chr3:15441930 | A | C | 1 | a0001c0001t0030 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2775A>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 2775 | chr3 | 15441930 | ||||||
| chr3:15442034 | CTT | C | 2 | a0001c0001t0014 a0001c0001t0034 |
4 | HG02647.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2880_*2881delTT | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 2880 | chr3 | 15442034 | ||||||
| chr3:15442115 | T | C | 1 | a0001c0001t0029 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2960T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 2960 | chr3 | 15442115 | ||||||
| chr3:15442119 | G | T | 1 | a0001c0001t0029 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2964G>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 2964 | chr3 | 15442119 | ||||||
| chr3:15442208 | G | GGT | 9 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(6): Show |
121 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*3080_*3081dupGT | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 3082 | INFO_REALIGN_3_PRIME | chr3 | 15442208 | |||||
| chr3:15442208 | G | GGTGT | 12 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0013 others(9): Show |
52 | HG00597.hp2 HG01109.hp1 HG01168.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*3078_*3081dupGTGT | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 3082 | INFO_REALIGN_3_PRIME | chr3 | 15442208 | |||||
| chr3:15442208 | G | GGTGTGT | 5 | a0001c0001t0015 a0001c0001t0019 a0001c0001t0024 others(2): Show |
7 | HG02258.hp2 HG02965.hp1 NA18906.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3076_*3081dupGTGT others(2): Show |
EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 3082 | INFO_REALIGN_3_PRIME | chr3 | 15442208 | |||||
| chr3:15442208 | G | GGTGTGTG others(1): Show |
4 | a0001c0001t0026 a0001c0001t0029 a0001c0001t0031 others(1): Show |
5 | HG00544.hp2 NA18972.hp2 NA18999.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3074_*3081dupGTGT others(4): Show |
EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 3082 | INFO_REALIGN_3_PRIME | chr3 | 15442208 | |||||
| chr3:15442208 | G | GGTGTGTG others(3): Show |
1 | a0001c0001t0021 | 2 | HG02886.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3072_*3081dupGTGT others(6): Show |
EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 3082 | INFO_REALIGN_3_PRIME | chr3 | 15442208 | |||||
| chr3:15442208 | G | GGTGTGTG others(7): Show |
1 | a0001c0005t0017 | 2 | HG02622.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3068_*3081dupGTGT others(10): Show |
EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 3082 | INFO_REALIGN_3_PRIME | chr3 | 15442208 | |||||
| chr3:15442208 | G | GGTGTGTG others(11): Show |
1 | a0001c0005t0012 | 3 | HG03209.hp1 HG03516.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3064_*3081dupGTGT others(14): Show |
EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 3082 | INFO_REALIGN_3_PRIME | chr3 | 15442208 | |||||
| chr3:15442323 | A | G | 5 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0013 others(2): Show |
107 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*3168A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 3168 | chr3 | 15442323 | ||||||
| chr3:15442324 | T | C | 1 | a0001c0001t0014 | 3 | HG03098.hp2 HG03139.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3169T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 3169 | chr3 | 15442324 | ||||||
| chr3:15442420 | C | G | 6 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0020 others(3): Show |
17 | HG01081.hp1 HG01192.hp2 HG01884.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3265C>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 6/6 | 3265 | chr3 | 15442420 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15428140 | T | C | 1 | a0001c0001t0023g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.103+258T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15428140 | |||||||
| chr3:15428199 | C | A | 1 | a0001c0003t0018g0026 | 2 | NA18972.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.103+317C>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15428199 | |||||||
| chr3:15428217 | C | G | 1 | a0001c0001t0006g0008 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.103+335C>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15428217 | |||||||
| chr3:15428243 | G | T | 1 | a0001c0001t0035g0103 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.103+361G>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15428243 | |||||||
| chr3:15428389 | A | G | 2 | a0001c0001t0006g0025 a0001c0001t0006g0102 |
4 | HG01978.hp2 HG02148.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+507A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15428389 | |||||||
| chr3:15428393 | T | C | 1 | a0001c0001t0034g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.103+511T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15428393 | |||||||
| chr3:15428567 | G | A | 1 | a0001c0001t0028g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.103+685G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15428567 | |||||||
| chr3:15428593 | G | A | 2 | a0001c0001t0023g0039 a0001c0001t0024g0042 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.103+711G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15428593 | |||||||
| chr3:15428617 | G | GCAGGC | 10 | a0001c0001t0014g0027 a0001c0001t0014g0047 a0001c0001t0021g0022 others(7): Show |
14 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.103+736_103+740dup others(5): Show |
EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 15428617 | ||||||
| chr3:15428654 | A | G | 2 | a0001c0001t0023g0039 a0001c0001t0024g0042 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.103+772A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15428654 | |||||||
| chr3:15428838 | C | G | 1 | a0001c0001t0003g0101 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.103+956C>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15428838 | |||||||
| chr3:15429025 | A | G | 1 | a0001c0002t0005g0100 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.104-888A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429025 | |||||||
| chr3:15429031 | A | T | 10 | a0001c0001t0006g0008 a0001c0001t0006g0025 a0001c0001t0006g0038 others(7): Show |
26 | HG00597.hp2 HG01168.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.104-882A>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429031 | |||||||
| chr3:15429104 | T | C | 1 | a0001c0001t0034g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.104-809T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429104 | |||||||
| chr3:15429187 | C | G | 1 | a0001c0001t0003g0096 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.104-726C>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429187 | |||||||
| chr3:15429191 | G | A | 3 | a0001c0002t0001g0010 a0001c0002t0001g0048 a0001c0002t0001g0049 |
9 | HG01256.hp1 HG01258.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.104-722G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429191 | |||||||
| chr3:15429210 | T | C | 30 | a0001c0001t0006g0008 a0001c0001t0006g0025 a0001c0001t0006g0038 others(27): Show |
73 | HG00597.hp2 HG01109.hp1 HG01168.hp1 others(70): Show |
intron_variant | MODIFIER | c.104-703T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429210 | |||||||
| chr3:15429216 | A | G | 1 | a0001c0003t0018g0026 | 2 | NA18972.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.104-697A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429216 | |||||||
| chr3:15429259 | G | T | 1 | a0001c0001t0034g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.104-654G>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429259 | |||||||
| chr3:15429273 | A | G | 36 | a0001c0001t0006g0008 a0001c0001t0006g0025 a0001c0001t0006g0038 others(33): Show |
79 | HG00597.hp2 HG01081.hp1 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.104-640A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429273 | |||||||
| chr3:15429275 | A | G | 7 | a0001c0001t0014g0027 a0001c0001t0014g0047 a0001c0001t0021g0022 others(4): Show |
9 | HG01884.hp2 HG02886.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.104-638A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429275 | |||||||
| chr3:15429316 | A | C | 1 | a0001c0001t0034g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.104-597A>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429316 | |||||||
| chr3:15429345 | A | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0005g0001 others(27): Show |
119 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.104-568A>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429345 | |||||||
| chr3:15429346 | A | C | 1 | a0001c0001t0001g0020 | 4 | HG02027.hp2 HG02080.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-567A>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429346 | |||||||
| chr3:15429349 | A | AC | 18 | a0001c0001t0002g0063 a0001c0001t0003g0003 a0001c0001t0003g0029 others(15): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.104-564_104-563ins others(1): Show |
EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429349 | |||||||
| chr3:15429349 | A | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(94): Show |
335 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(332): Show |
intron_variant | MODIFIER | c.104-564A>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429349 | |||||||
| chr3:15429353 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.104-560C>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429353 | |||||||
| chr3:15429360 | C | T | 1 | a0001c0006t0010g0024 | 3 | HG02970.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.104-553C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429360 | |||||||
| chr3:15429456 | A | G | 10 | a0001c0001t0014g0027 a0001c0001t0014g0047 a0001c0001t0021g0022 others(7): Show |
14 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.104-457A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429456 | |||||||
| chr3:15429555 | C | G | 9 | a0001c0001t0008g0006 a0001c0001t0008g0023 a0001c0001t0011g0006 others(6): Show |
30 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.104-358C>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429555 | |||||||
| chr3:15429705 | G | C | 8 | a0001c0001t0008g0006 a0001c0001t0008g0023 a0001c0001t0011g0006 others(5): Show |
28 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.104-208G>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429705 | |||||||
| chr3:15429733 | C | T | 8 | a0001c0001t0008g0006 a0001c0001t0008g0023 a0001c0001t0011g0006 others(5): Show |
28 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.104-180C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 1/5 | chr3 | 15429733 | |||||||
| chr3:15430021 | A | AT | 4 | a0001c0001t0008g0006 a0001c0001t0008g0023 a0001c0001t0011g0006 others(1): Show |
14 | HG01192.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+25dupT | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 15430021 | ||||||
| chr3:15430021 | AT | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0066 others(32): Show |
125 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(122): Show |
intron_variant | MODIFIER | c.198+25delT | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 15430021 | ||||||
| chr3:15430066 | AT | A | 3 | a0001c0003t0007g0005 a0001c0003t0007g0050 a0001c0003t0007g0051 |
13 | HG01109.hp1 HG02055.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.198+61delT | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 15430066 | ||||||
| chr3:15430235 | G | A | 1 | a0001c0001t0005g0083 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.198+228G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15430235 | |||||||
| chr3:15430288 | G | A | 1 | a0001c0001t0022g0046 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.198+281G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15430288 | |||||||
| chr3:15430288 | G | C | 1 | a0001c0001t0034g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.198+281G>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15430288 | |||||||
| chr3:15430302 | T | C | 1 | a0001c0003t0018g0026 | 2 | NA18972.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.198+295T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15430302 | |||||||
| chr3:15430417 | G | A | 1 | a0001c0001t0004g0065 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.198+410G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15430417 | |||||||
| chr3:15430456 | C | T | 79 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0019 others(76): Show |
253 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(250): Show |
intron_variant | MODIFIER | c.198+449C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15430456 | |||||||
| chr3:15430459 | C | CA | 29 | a0001c0001t0006g0008 a0001c0001t0006g0025 a0001c0001t0006g0038 others(26): Show |
71 | HG00597.hp2 HG01109.hp1 HG01168.hp1 others(68): Show |
intron_variant | MODIFIER | c.198+469dupA | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 15430459 | ||||||
| chr3:15430459 | CA | C | 46 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0019 others(43): Show |
177 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.198+469delA | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 15430459 | ||||||
| chr3:15430696 | G | A | 1 | a0001c0001t0034g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.198+689G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15430696 | |||||||
| chr3:15430882 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.198+875G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15430882 | |||||||
| chr3:15430900 | G | A | 2 | a0001c0001t0003g0073 a0001c0001t0003g0074 |
2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.198+893G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15430900 | |||||||
| chr3:15431109 | G | A | 1 | a0001c0004t0006g0012 | 7 | HG01168.hp1 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-978G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15431109 | |||||||
| chr3:15431248 | G | A | 1 | a0001c0001t0005g0084 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.199-839G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15431248 | |||||||
| chr3:15431290 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0068 |
2 | HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.199-797T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15431290 | |||||||
| chr3:15431385 | TAGCTGGC others(14): Show |
T | 2 | a0001c0001t0002g0031 a0001c0003t0007g0052 |
3 | HG02572.hp2 HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.199-677_199-657del others(21): Show |
EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 15431385 | ||||||
| chr3:15431451 | G | A | 1 | a0001c0001t0006g0097 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.199-636G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15431451 | |||||||
| chr3:15431458 | G | C | 1 | a0001c0001t0006g0038 | 2 | HG00597.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.199-629G>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15431458 | |||||||
| chr3:15431596 | C | A | 2 | a0001c0001t0020g0094 a0003c0008t0020g0095 |
2 | HG01081.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.199-491C>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15431596 | |||||||
| chr3:15431794 | A | G | 1 | a0001c0001t0001g0013 | 6 | HG01891.hp2 HG02647.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-293A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15431794 | |||||||
| chr3:15431878 | C | T | 1 | a0001c0002t0001g0091 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.199-209C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15431878 | |||||||
| chr3:15431879 | G | A | 1 | a0001c0002t0001g0085 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.199-208G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15431879 | |||||||
| chr3:15431893 | C | T | 1 | a0001c0001t0003g0064 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.199-194C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15431893 | |||||||
| chr3:15431907 | A | G | 1 | a0001c0001t0006g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.199-180A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15431907 | |||||||
| chr3:15432008 | G | A | 29 | a0001c0001t0001g0001 a0001c0001t0005g0001 a0001c0001t0005g0035 others(26): Show |
115 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.199-79G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15432008 | |||||||
| chr3:15432010 | G | A | 1 | a0001c0001t0034g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.199-77G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 2/5 | chr3 | 15432010 | |||||||
| chr3:15432257 | G | A | 1 | a0002c0009t0001g0055 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.335+34G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 3/5 | chr3 | 15432257 | |||||||
| chr3:15432439 | C | T | 1 | a0001c0001t0034g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.335+216C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 3/5 | chr3 | 15432439 | |||||||
| chr3:15432694 | G | A | 1 | a0001c0006t0010g0024 | 3 | HG02970.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.335+471G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 3/5 | chr3 | 15432694 | |||||||
| chr3:15432860 | T | C | 9 | a0001c0001t0008g0006 a0001c0001t0008g0023 a0001c0001t0011g0006 others(6): Show |
30 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.335+637T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 3/5 | chr3 | 15432860 | |||||||
| chr3:15432892 | A | G | 1 | a0001c0001t0014g0047 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.335+669A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 3/5 | chr3 | 15432892 | |||||||
| chr3:15432917 | C | T | 1 | a0001c0001t0029g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.335+694C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 3/5 | chr3 | 15432917 | |||||||
| chr3:15433124 | G | T | 7 | a0001c0001t0014g0027 a0001c0001t0014g0047 a0001c0001t0021g0022 others(4): Show |
9 | HG01884.hp2 HG02886.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.335+901G>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 3/5 | chr3 | 15433124 | |||||||
| chr3:15433198 | G | A | 1 | a0001c0001t0034g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.335+975G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 3/5 | chr3 | 15433198 | |||||||
| chr3:15433230 | A | G | 1 | a0001c0001t0035g0103 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.335+1007A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 3/5 | chr3 | 15433230 | |||||||
| chr3:15433233 | T | TA | 12 | a0001c0001t0001g0056 a0001c0001t0001g0069 a0001c0001t0002g0032 others(9): Show |
20 | HG00544.hp1 HG01175.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.335+1033dupA | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 15433233 | ||||||
| chr3:15433233 | TA | T | 30 | a0001c0001t0001g0013 a0001c0001t0002g0019 a0001c0001t0002g0082 others(27): Show |
75 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(72): Show |
intron_variant | MODIFIER | c.335+1033delA | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 15433233 | ||||||
| chr3:15433243 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0066 a0001c0001t0001g0068 |
9 | HG00597.hp1 HG02572.hp1 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.335+1020A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 3/5 | chr3 | 15433243 | |||||||
| chr3:15433835 | C | T | 1 | a0001c0001t0034g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.336-513C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 3/5 | chr3 | 15433835 | |||||||
| chr3:15433887 | A | G | 1 | a0001c0001t0035g0103 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.336-461A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 3/5 | chr3 | 15433887 | |||||||
| chr3:15434092 | A | G | 2 | a0001c0001t0020g0094 a0003c0008t0020g0095 |
2 | HG01081.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.336-256A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 3/5 | chr3 | 15434092 | |||||||
| chr3:15434108 | C | T | 1 | a0001c0001t0034g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.336-240C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 3/5 | chr3 | 15434108 | |||||||
| chr3:15434217 | A | C | 1 | a0001c0001t0013g0080 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.336-131A>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 3/5 | chr3 | 15434217 | |||||||
| chr3:15434330 | G | A | 3 | a0001c0001t0020g0094 a0001c0001t0035g0103 a0003c0008t0020g0095 |
3 | HG01081.hp1 HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.336-18G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 3/5 | chr3 | 15434330 | |||||||
| chr3:15434548 | A | G | 10 | a0001c0001t0006g0008 a0001c0001t0006g0025 a0001c0001t0006g0038 others(7): Show |
26 | HG00597.hp2 HG01168.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.526+10A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15434548 | |||||||
| chr3:15434788 | C | T | 3 | a0001c0001t0020g0094 a0001c0001t0035g0103 a0003c0008t0020g0095 |
3 | HG01081.hp1 HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.526+250C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15434788 | |||||||
| chr3:15434861 | G | A | 1 | a0003c0008t0020g0095 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.526+323G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15434861 | |||||||
| chr3:15434862 | A | G | 1 | a0003c0008t0020g0095 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.526+324A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15434862 | |||||||
| chr3:15435010 | T | C | 3 | a0001c0001t0014g0027 a0001c0001t0014g0047 a0001c0001t0034g0040 |
4 | HG02647.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+472T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435010 | |||||||
| chr3:15435075 | T | C | 1 | a0003c0008t0020g0095 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.526+537T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435075 | |||||||
| chr3:15435076 | C | G | 1 | a0003c0008t0020g0095 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.526+538C>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435076 | |||||||
| chr3:15435077 | T | G | 1 | a0003c0008t0020g0095 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.526+539T>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435077 | |||||||
| chr3:15435084 | T | G | 2 | a0001c0001t0020g0094 a0001c0001t0035g0103 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.526+546T>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435084 | |||||||
| chr3:15435135 | C | T | 1 | a0001c0003t0007g0051 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.526+597C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435135 | |||||||
| chr3:15435303 | C | G | 1 | a0001c0001t0004g0015 | 5 | NA18950.hp2 NA18955.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.526+765C>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435303 | |||||||
| chr3:15435364 | A | T | 1 | a0003c0008t0020g0095 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.526+826A>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435364 | |||||||
| chr3:15435365 | T | C | 1 | a0003c0008t0020g0095 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.526+827T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435365 | |||||||
| chr3:15435377 | G | C | 1 | a0003c0008t0020g0095 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.526+839G>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435377 | |||||||
| chr3:15435395 | T | C | 3 | a0001c0001t0020g0094 a0001c0001t0035g0103 a0003c0008t0020g0095 |
3 | HG01081.hp1 HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.526+857T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435395 | |||||||
| chr3:15435460 | A | G | 2 | a0001c0001t0005g0057 a0001c0001t0005g0071 |
2 | HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.527-882A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435460 | |||||||
| chr3:15435486 | T | C | 1 | a0001c0003t0008g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.527-856T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435486 | |||||||
| chr3:15435512 | T | C | 2 | a0001c0001t0023g0039 a0001c0001t0024g0042 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.527-830T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435512 | |||||||
| chr3:15435558 | A | G | 2 | a0001c0001t0020g0094 a0003c0008t0020g0095 |
2 | HG01081.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.527-784A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435558 | |||||||
| chr3:15435618 | A | G | 1 | a0003c0008t0020g0095 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.527-724A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435618 | |||||||
| chr3:15435633 | G | A | 20 | a0001c0001t0003g0003 a0001c0001t0003g0014 a0001c0001t0003g0028 others(17): Show |
66 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.527-709G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435633 | |||||||
| chr3:15435721 | A | G | 29 | a0001c0001t0001g0001 a0001c0001t0005g0001 a0001c0001t0005g0035 others(26): Show |
115 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.527-621A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435721 | |||||||
| chr3:15435896 | G | A | 1 | a0001c0002t0001g0017 | 5 | HG00621.hp2 NA18945.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.527-446G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435896 | |||||||
| chr3:15435934 | C | T | 3 | a0001c0001t0014g0027 a0001c0001t0014g0047 a0001c0001t0034g0040 |
4 | HG02647.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-408C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435934 | |||||||
| chr3:15435951 | T | C | 3 | a0001c0005t0012g0018 a0001c0005t0012g0043 a0001c0005t0017g0018 |
5 | HG02622.hp2 HG03209.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.527-391T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15435951 | |||||||
| chr3:15436181 | G | A | 1 | a0001c0001t0003g0060 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.527-161G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15436181 | |||||||
| chr3:15436226 | T | G | 1 | a0003c0008t0020g0095 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.527-116T>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 4/5 | chr3 | 15436226 | |||||||
| chr3:15436670 | G | A | 2 | a0001c0001t0014g0027 a0001c0001t0014g0047 |
3 | HG03098.hp2 HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.760+95G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15436670 | |||||||
| chr3:15436864 | G | A | 1 | a0001c0001t0003g0059 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.760+289G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15436864 | |||||||
| chr3:15436881 | C | T | 2 | a0001c0001t0023g0039 a0001c0001t0024g0042 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.760+306C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15436881 | |||||||
| chr3:15436919 | A | G | 4 | a0001c0001t0014g0027 a0001c0001t0014g0047 a0001c0001t0029g0045 others(1): Show |
5 | HG02647.hp1 HG03098.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.760+344A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15436919 | |||||||
| chr3:15436935 | G | A | 1 | a0001c0001t0006g0098 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.760+360G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15436935 | |||||||
| chr3:15436952 | A | G | 1 | a0001c0002t0001g0036 | 2 | NA18966.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.760+377A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15436952 | |||||||
| chr3:15436959 | A | G | 1 | a0001c0001t0005g0035 | 2 | HG02015.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.760+384A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15436959 | |||||||
| chr3:15436968 | T | C | 1 | a0001c0001t0002g0076 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.760+393T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15436968 | |||||||
| chr3:15436988 | C | T | 1 | a0001c0003t0018g0026 | 2 | NA18972.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.760+413C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15436988 | |||||||
| chr3:15437148 | G | A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0019 a0001c0001t0004g0004 |
25 | HG00140.hp2 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.760+573G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15437148 | |||||||
| chr3:15437214 | A | G | 1 | a0001c0002t0019g0089 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.760+639A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15437214 | |||||||
| chr3:15437244 | GGCTTTTT others(4): Show |
G | 1 | a0001c0006t0010g0024 | 3 | HG02970.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.760+670_760+680del others(11): Show |
EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15437244 | |||||||
| chr3:15437246 | C | CT | 8 | a0001c0001t0001g0007 a0001c0001t0006g0008 a0001c0001t0006g0025 others(5): Show |
8 | HG01106.hp2 HG03486.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.760+689dupT | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 15437246 | ||||||
| chr3:15437246 | CT | C | 17 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0034 others(14): Show |
39 | HG00621.hp1 HG01081.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.760+689delT | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 15437246 | ||||||
| chr3:15437246 | CTT | C | 42 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0019 others(39): Show |
164 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.760+688_760+689del others(2): Show |
EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 15437246 | ||||||
| chr3:15437257 | T | C | 1 | a0001c0006t0010g0024 | 3 | HG02970.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.760+682T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15437257 | |||||||
| chr3:15437318 | C | CT | 9 | a0001c0001t0003g0062 a0001c0001t0003g0101 a0001c0001t0021g0022 others(6): Show |
10 | HG01884.hp2 HG02083.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.760+757dupT | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 15437318 | ||||||
| chr3:15437350 | G | C | 1 | a0001c0001t0002g0034 | 2 | NA18983.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.760+775G>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15437350 | |||||||
| chr3:15437405 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0066 a0001c0001t0001g0068 others(2): Show |
11 | HG00597.hp1 HG01515.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.760+830G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15437405 | |||||||
| chr3:15437420 | C | T | 5 | a0001c0001t0021g0022 a0001c0001t0022g0046 a0001c0001t0029g0045 others(2): Show |
6 | HG01884.hp2 HG02886.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.760+845C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15437420 | |||||||
| chr3:15437469 | G | A | 1 | a0001c0001t0004g0077 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.760+894G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15437469 | |||||||
| chr3:15437530 | A | T | 3 | a0001c0001t0014g0027 a0001c0001t0014g0047 a0001c0001t0034g0040 |
4 | HG02647.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.760+955A>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15437530 | |||||||
| chr3:15437544 | C | T | 1 | a0001c0003t0018g0026 | 2 | NA18972.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.760+969C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15437544 | |||||||
| chr3:15437550 | G | C | 1 | a0001c0002t0001g0086 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.760+975G>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15437550 | |||||||
| chr3:15437705 | T | G | 1 | a0001c0001t0003g0061 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.760+1130T>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15437705 | |||||||
| chr3:15437789 | A | G | 2 | a0001c0001t0014g0027 a0001c0001t0014g0047 |
3 | HG03098.hp2 HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.760+1214A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15437789 | |||||||
| chr3:15437851 | A | C | 1 | a0001c0001t0001g0070 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.761-1258A>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15437851 | |||||||
| chr3:15437878 | A | C | 2 | a0001c0001t0023g0039 a0001c0001t0024g0042 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.761-1231A>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15437878 | |||||||
| chr3:15438062 | G | C | 5 | a0001c0001t0021g0022 a0001c0001t0022g0046 a0001c0001t0029g0045 others(2): Show |
6 | HG01884.hp2 HG02886.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.761-1047G>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15438062 | |||||||
| chr3:15438168 | G | T | 1 | a0001c0001t0035g0103 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.761-941G>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15438168 | |||||||
| chr3:15438197 | A | G | 2 | a0001c0001t0003g0033 a0001c0006t0010g0024 |
5 | HG00642.hp1 HG02970.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.761-912A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15438197 | |||||||
| chr3:15438428 | G | A | 1 | a0001c0006t0010g0024 | 3 | HG02970.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.761-681G>A | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15438428 | |||||||
| chr3:15438510 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.761-599C>T | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15438510 | |||||||
| chr3:15438510 | CT | C | 13 | a0001c0001t0008g0006 a0001c0001t0008g0023 a0001c0001t0011g0006 others(10): Show |
34 | HG01081.hp1 HG01109.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.761-584delT | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 15438510 | ||||||
| chr3:15438725 | A | G | 1 | a0001c0001t0008g0023 | 3 | HG02109.hp2 HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.761-384A>G | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15438725 | |||||||
| chr3:15438986 | T | C | 2 | a0001c0001t0014g0027 a0001c0001t0014g0047 |
3 | HG03098.hp2 HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.761-123T>C | EAF1 | ENSG00000144597.14 | transcript | ENST00000396842.7 | protein_coding | 5/5 | chr3 | 15438986 |