Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26094 |
| ensemblid | ENSG00000119599.17 |
| hgncid | 20229 |
| symbol | DCAF4 |
| name | DDB1 and CUL4 associated factor 4 |
| refseq_nuc | NM_015604.4 |
| refseq_prot | NP_056419.2 |
| ensembl_nuc | ENST00000358377.7 |
| ensembl_prot | ENSP00000351147.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 72926464 |
| end | 72959703 |
| strand | + |
| ver | v1.2 |
| region | chr14:72926464-72959703 |
| region5000 | chr14:72921464-72964703 |
| regionname0 | DCAF4_chr14_72926464_72959703 |
| regionname5000 | DCAF4_chr14_72921464_72964703 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 495 | 329 | 78 | 59 | 147 | 8 | 36 | 113 | DCAF4_chr14_72921464_72964703 | DCAF4 | MNKSR others(490): Show |
chr14 | 72921464 | 72964703 |
| a0002 | 0/0 | 495 | 44 | 4 | 7 | 31 | 0 | 2 | 25 | DCAF4_chr14_72921464_72964703 | DCAF4 | MNKSR others(490): Show |
chr14 | 72921464 | 72964703 |
| a0003 | 0/0 | 495 | 6 | 0 | 2 | 2 | 1 | 1 | 2 | DCAF4_chr14_72921464_72964703 | DCAF4 | MNKSR others(490): Show |
chr14 | 72921464 | 72964703 |
| a0004 | 0/0 | 495 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | DCAF4_chr14_72921464_72964703 | DCAF4 | MNKSR others(490): Show |
chr14 | 72921464 | 72964703 |
| a0005 | 0/0 | 495 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | MNKSR others(490): Show |
chr14 | 72921464 | 72964703 |
| a0006 | 0/0 | 495 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | MNKSR others(490): Show |
chr14 | 72921464 | 72964703 |
| a0007 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | MNKSR others(490): Show |
chr14 | 72921464 | 72964703 |
| a0008 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | MNKSR others(490): Show |
chr14 | 72921464 | 72964703 |
| a0009 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | MNKSR others(490): Show |
chr14 | 72921464 | 72964703 |
| a0010 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | MNKSR others(490): Show |
chr14 | 72921464 | 72964703 |
| a0011 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | MNKSR others(490): Show |
chr14 | 72921464 | 72964703 |
| a0012 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | MNKSR others(490): Show |
chr14 | 72921464 | 72964703 |
| a0013 | 0/1 | 495 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | MNKSR others(490): Show |
chr14 | 72921464 | 72964703 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1485 | 193 | 49 | 43 | 80 | 3 | 17 | DCAF4_chr14_72921464_72964703 | DCAF4 | ATGAA others(1480): Show |
chr14 | 72921464 | 72964703 | ||
| a0001c0002 | 0/0 | 1485 | 69 | 16 | 12 | 28 | 4 | 9 | DCAF4_chr14_72921464_72964703 | DCAF4 | ATGAA others(1480): Show |
chr14 | 72921464 | 72964703 | ||
| a0001c0003 | 0/0 | 1485 | 59 | 8 | 4 | 37 | 1 | 9 | DCAF4_chr14_72921464_72964703 | DCAF4 | ATGAA others(1480): Show |
chr14 | 72921464 | 72964703 | ||
| a0001c0007 | 0/0 | 1485 | 5 | 5 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | ATGAA others(1480): Show |
chr14 | 72921464 | 72964703 | ||
| a0001c0014 | 0/0 | 1485 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | ATGAA others(1480): Show |
chr14 | 72921464 | 72964703 | ||
| a0001c0015 | 0/0 | 1485 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | ATGAA others(1480): Show |
chr14 | 72921464 | 72964703 | ||
| a0001c0017 | 0/0 | 1485 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | ATGAA others(1480): Show |
chr14 | 72921464 | 72964703 | ||
| a0002c0004 | 0/0 | 1485 | 44 | 4 | 7 | 31 | 0 | 2 | DCAF4_chr14_72921464_72964703 | DCAF4 | ATGAA others(1480): Show |
chr14 | 72921464 | 72964703 | ||
| a0003c0006 | 0/0 | 1485 | 6 | 0 | 2 | 2 | 1 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | ATGAA others(1480): Show |
chr14 | 72921464 | 72964703 | ||
| a0004c0005 | 0/0 | 1485 | 6 | 0 | 0 | 6 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | ATGAA others(1480): Show |
chr14 | 72921464 | 72964703 | ||
| a0005c0009 | 0/0 | 1485 | 2 | 0 | 0 | 0 | 1 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | ATGAA others(1480): Show |
chr14 | 72921464 | 72964703 | ||
| a0006c0008 | 0/0 | 1485 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | ATGAA others(1480): Show |
chr14 | 72921464 | 72964703 | ||
| a0007c0018 | 0/0 | 1485 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | ATGAA others(1480): Show |
chr14 | 72921464 | 72964703 | ||
| a0008c0013 | 0/0 | 1485 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | ATGAA others(1480): Show |
chr14 | 72921464 | 72964703 | ||
| a0009c0016 | 0/0 | 1485 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | ATGAA others(1480): Show |
chr14 | 72921464 | 72964703 | ||
| a0010c0011 | 0/0 | 1485 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | ATGAA others(1480): Show |
chr14 | 72921464 | 72964703 | ||
| a0011c0010 | 0/0 | 1485 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | ATGAA others(1480): Show |
chr14 | 72921464 | 72964703 | ||
| a0012c0019 | 0/0 | 1485 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | ATGAA others(1480): Show |
chr14 | 72921464 | 72964703 | ||
| a0013c0012 | 0/1 | 1485 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | ATGAA others(1480): Show |
chr14 | 72921464 | 72964703 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2474 | 36 | 16 | 5 | 11 | 0 | 3 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0001c0001t0002 | 0/0 | 2474 | 88 | 2 | 20 | 56 | 2 | 8 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0001c0001t0003 | 0/0 | 2474 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0001c0001t0004 | 0/0 | 2474 | 27 | 24 | 3 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0001c0001t0005 | 0/0 | 2474 | 28 | 2 | 13 | 6 | 1 | 6 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0001c0001t0009 | 0/0 | 2474 | 8 | 1 | 1 | 6 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0001c0001t0010 | 0/0 | 2474 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0001c0001t0011 | 0/0 | 2474 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0001c0001t0013 | 0/0 | 2474 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0001c0002t0001 | 0/0 | 2474 | 56 | 5 | 10 | 28 | 4 | 9 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0001c0002t0004 | 0/0 | 2474 | 13 | 11 | 2 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0001c0003t0003 | 0/0 | 2474 | 52 | 2 | 4 | 36 | 1 | 9 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0001c0003t0008 | 0/0 | 2474 | 7 | 6 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0001c0007t0008 | 0/0 | 2474 | 5 | 5 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0001c0014t0002 | 0/0 | 2474 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0001c0015t0003 | 0/0 | 2474 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0001c0017t0003 | 0/0 | 2474 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0002c0004t0006 | 0/0 | 2474 | 26 | 3 | 4 | 19 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0002c0004t0007 | 0/0 | 2474 | 18 | 1 | 3 | 12 | 0 | 2 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0003c0006t0001 | 0/0 | 2474 | 6 | 0 | 2 | 2 | 1 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0004c0005t0002 | 0/0 | 2474 | 6 | 0 | 0 | 6 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0005c0009t0001 | 0/0 | 2474 | 2 | 0 | 0 | 0 | 1 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0006c0008t0001 | 0/0 | 2474 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0007c0018t0001 | 0/0 | 2474 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0008c0013t0012 | 0/0 | 2474 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0009c0016t0006 | 0/0 | 2474 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0010c0011t0004 | 0/0 | 2474 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0011c0010t0004 | 0/0 | 2474 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0012c0019t0008 | 0/0 | 2474 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| a0013c0012t0001 | 0/1 | 2474 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | CTTTC others(2469): Show |
chr14 | 72921464 | 72964703 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0123 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0005 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0002 | 0/0 | 6 | 0 | 5 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0009g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0009g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0009g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0009g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0009g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0009g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0009g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0010g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0010g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0011g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0011g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0001t0013g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0004g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0004g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0004g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0004g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0004g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0004g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0002t0004g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0006 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0008g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0008g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0008g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0008g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0008g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0003t0008g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0007t0008g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0007t0008g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0007t0008g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0007t0008g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0014t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0015t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0001c0017t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0006g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0007g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0007g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0007g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0007g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0007g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0007g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0007g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0007g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0002c0004t0007g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0003c0006t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0003c0006t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0003c0006t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0003c0006t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0003c0006t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0004c0005t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0004c0005t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0004c0005t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0004c0005t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0004c0005t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0004c0005t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0005c0009t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0005c0009t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0006c0008t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0006c0008t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0007c0018t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0008c0013t0012g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0009c0016t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0010c0011t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0011c0010t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0012c0019t0008g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| a0013c0012t0001g0334 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0311 | EUR | GBR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0319 | EUR | GBR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00140 | hp1 | a0001 | c0003 | t0003 | g0006 | EUR | GBR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0093 | EUR | GBR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00323 | hp1 | a0005 | c0009 | t0001 | g0183 | EUR | FIN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0333 | EUR | FIN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | CHS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00423 | hp1 | a0002 | c0004 | t0006 | g0282 | EAS | CHS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00423 | hp2 | a0001 | c0003 | t0003 | g0017 | EAS | CHS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00544 | hp1 | a0001 | c0001 | t0005 | g0215 | EAS | CHS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | CHS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00639 | hp2 | a0001 | c0003 | t0003 | g0001 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00642 | hp1 | a0001 | c0003 | t0003 | g0030 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0323 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00735 | hp2 | a0002 | c0004 | t0007 | g0203 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00738 | hp1 | a0002 | c0004 | t0007 | g0118 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0223 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0342 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0298 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01069 | hp2 | a0002 | c0004 | t0006 | g0024 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0331 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01071 | hp2 | a0002 | c0004 | t0006 | g0024 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0229 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0211 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0239 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0234 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01167 | hp2 | a0001 | c0002 | t0004 | g0273 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0250 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01168 | hp2 | a0003 | c0006 | t0001 | g0026 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0248 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0329 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01175 | hp2 | a0001 | c0001 | t0009 | g0255 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0262 | AMR | PUR | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0301 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0325 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01261 | hp1 | a0003 | c0006 | t0001 | g0026 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01261 | hp2 | a0002 | c0004 | t0006 | g0284 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01346 | hp1 | a0001 | c0003 | t0003 | g0155 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0332 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01358 | hp2 | a0002 | c0004 | t0007 | g0207 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0216 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0218 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01433 | hp2 | a0001 | c0003 | t0003 | g0159 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01496 | hp1 | a0001 | c0002 | t0004 | g0345 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0212 | EUR | IBS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0254 | EUR | IBS | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01891 | hp2 | a0001 | c0002 | t0004 | g0350 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0219 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0249 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02015 | hp2 | a0001 | c0015 | t0003 | g0164 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02027 | hp2 | a0002 | c0004 | t0006 | g0287 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0217 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02040 | hp2 | a0001 | c0003 | t0003 | g0144 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02055 | hp1 | a0002 | c0004 | t0007 | g0205 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02074 | hp1 | a0001 | c0003 | t0003 | g0001 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02083 | hp1 | a0001 | c0003 | t0003 | g0148 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02129 | hp2 | a0001 | c0003 | t0003 | g0117 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0051 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02135 | hp1 | a0002 | c0004 | t0006 | g0279 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0206 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02148 | hp2 | a0002 | c0004 | t0006 | g0274 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | CDX | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02155 | hp2 | a0001 | c0003 | t0003 | g0165 | EAS | CDX | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02165 | hp1 | a0002 | c0004 | t0006 | g0288 | EAS | CDX | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0324 | EAS | CDX | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02257 | hp1 | a0007 | c0018 | t0001 | g0187 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0220 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02280 | hp1 | a0001 | c0003 | t0003 | g0116 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0267 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0221 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02451 | hp1 | a0006 | c0008 | t0001 | g0124 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02523 | hp2 | a0002 | c0004 | t0006 | g0294 | EAS | KHV | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02602 | hp2 | a0001 | c0017 | t0003 | g0128 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0240 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02622 | hp1 | a0002 | c0004 | t0006 | g0277 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02622 | hp2 | a0008 | c0013 | t0012 | g0306 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02630 | hp1 | a0001 | c0003 | t0003 | g0153 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0266 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02647 | hp1 | a0001 | c0003 | t0008 | g0243 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0318 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0326 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02698 | hp2 | a0001 | c0003 | t0003 | g0161 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0265 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02723 | hp1 | a0001 | c0001 | t0011 | g0228 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02735 | hp1 | a0005 | c0009 | t0001 | g0182 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0343 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0189 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02809 | hp2 | a0001 | c0007 | t0008 | g0315 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02818 | hp1 | a0009 | c0016 | t0006 | g0242 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0272 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02886 | hp2 | a0001 | c0002 | t0004 | g0271 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02895 | hp1 | a0001 | c0002 | t0004 | g0348 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0237 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0263 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02922 | hp2 | a0001 | c0007 | t0008 | g0258 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0304 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02970 | hp1 | a0001 | c0002 | t0004 | g0259 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02970 | hp2 | a0001 | c0002 | t0004 | g0296 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02976 | hp1 | a0001 | c0003 | t0008 | g0023 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0231 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03017 | hp1 | a0002 | c0004 | t0007 | g0202 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03098 | hp1 | a0001 | c0001 | t0010 | g0256 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03098 | hp2 | a0010 | c0011 | t0004 | g0244 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0264 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03130 | hp2 | a0001 | c0003 | t0008 | g0023 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03139 | hp2 | a0001 | c0003 | t0008 | g0246 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03195 | hp1 | a0001 | c0003 | t0008 | g0241 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0232 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03209 | hp2 | a0001 | c0002 | t0004 | g0349 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03225 | hp1 | a0011 | c0010 | t0004 | g0209 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03239 | hp1 | a0001 | c0003 | t0003 | g0172 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03239 | hp2 | a0001 | c0003 | t0003 | g0131 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03453 | hp1 | a0001 | c0001 | t0011 | g0247 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03453 | hp2 | a0002 | c0004 | t0006 | g0020 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03486 | hp1 | a0001 | c0002 | t0004 | g0351 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0257 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03490 | hp1 | a0001 | c0003 | t0003 | g0127 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03490 | hp2 | a0001 | c0003 | t0003 | g0006 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03491 | hp1 | a0001 | c0003 | t0003 | g0031 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0040 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03492 | hp1 | a0001 | c0003 | t0003 | g0006 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0041 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03540 | hp1 | a0002 | c0004 | t0006 | g0020 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03540 | hp2 | a0001 | c0002 | t0004 | g0347 | AFR | GWD | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0295 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0339 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0226 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0320 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03688 | hp1 | a0001 | c0003 | t0003 | g0032 | SAS | STU | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0224 | SAS | STU | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0322 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0002 | SAS | PJL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0253 | SAS | BEB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03831 | hp2 | a0003 | c0006 | t0001 | g0352 | SAS | BEB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0327 | SAS | BEB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | BEB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0225 | SAS | BEB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | STU | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0227 | SAS | STU | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG04204 | hp1 | a0001 | c0003 | t0003 | g0160 | SAS | STU | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | STU | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0213 | SAS | STU | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG04228 | hp2 | a0002 | c0004 | t0007 | g0115 | SAS | STU | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0268 | AFR | YRI | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18522 | hp2 | a0001 | c0002 | t0004 | g0245 | AFR | YRI | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18612 | hp2 | a0002 | c0004 | t0007 | g0308 | EAS | CHB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18747 | hp2 | a0001 | c0003 | t0003 | g0130 | EAS | CHB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18939 | hp1 | a0001 | c0003 | t0003 | g0086 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18940 | hp2 | a0001 | c0003 | t0003 | g0169 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18941 | hp1 | a0002 | c0004 | t0006 | g0305 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18941 | hp2 | a0001 | c0003 | t0003 | g0017 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18942 | hp2 | a0002 | c0004 | t0006 | g0278 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18944 | hp1 | a0003 | c0006 | t0001 | g0198 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18944 | hp2 | a0004 | c0005 | t0002 | g0089 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18946 | hp2 | a0001 | c0003 | t0003 | g0001 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18947 | hp2 | a0002 | c0004 | t0007 | g0015 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18950 | hp2 | a0002 | c0004 | t0006 | g0280 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18952 | hp2 | a0002 | c0004 | t0006 | g0281 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18953 | hp1 | a0001 | c0003 | t0003 | g0162 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18953 | hp2 | a0002 | c0004 | t0007 | g0141 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18954 | hp1 | a0001 | c0003 | t0003 | g0149 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18956 | hp1 | a0002 | c0004 | t0007 | g0132 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18956 | hp2 | a0001 | c0001 | t0013 | g0019 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18959 | hp1 | a0002 | c0004 | t0007 | g0142 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18960 | hp1 | a0001 | c0003 | t0003 | g0147 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18960 | hp2 | a0002 | c0004 | t0007 | g0143 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18961 | hp1 | a0001 | c0001 | t0009 | g0285 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18961 | hp2 | a0001 | c0003 | t0003 | g0145 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18962 | hp2 | a0001 | c0003 | t0003 | g0150 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18964 | hp2 | a0002 | c0004 | t0007 | g0134 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18965 | hp1 | a0001 | c0001 | t0009 | g0317 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18969 | hp2 | a0001 | c0003 | t0003 | g0146 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18971 | hp2 | a0004 | c0005 | t0002 | g0068 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0330 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18974 | hp1 | a0002 | c0004 | t0006 | g0290 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18979 | hp1 | a0001 | c0003 | t0003 | g0001 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18979 | hp2 | a0001 | c0001 | t0009 | g0028 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18980 | hp2 | a0002 | c0004 | t0007 | g0133 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18983 | hp2 | a0004 | c0005 | t0002 | g0071 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18984 | hp1 | a0002 | c0004 | t0006 | g0292 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18984 | hp2 | a0001 | c0001 | t0009 | g0028 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18985 | hp2 | a0002 | c0004 | t0007 | g0015 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18986 | hp2 | a0004 | c0005 | t0002 | g0163 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18988 | hp1 | a0001 | c0003 | t0003 | g0158 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18994 | hp2 | a0002 | c0004 | t0006 | g0291 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18995 | hp1 | a0001 | c0003 | t0003 | g0167 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18995 | hp2 | a0001 | c0003 | t0003 | g0168 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18997 | hp1 | a0001 | c0001 | t0009 | g0338 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18997 | hp2 | a0001 | c0003 | t0003 | g0156 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18998 | hp2 | a0002 | c0004 | t0006 | g0286 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18999 | hp1 | a0004 | c0005 | t0002 | g0081 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18999 | hp2 | a0001 | c0003 | t0003 | g0016 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19004 | hp2 | a0001 | c0003 | t0003 | g0016 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19005 | hp2 | a0001 | c0003 | t0008 | g0283 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19007 | hp1 | a0001 | c0003 | t0003 | g0050 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19009 | hp1 | a0004 | c0005 | t0002 | g0113 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19009 | hp2 | a0001 | c0003 | t0003 | g0177 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19012 | hp1 | a0001 | c0003 | t0003 | g0152 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19012 | hp2 | a0001 | c0001 | t0005 | g0252 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19030 | hp1 | a0001 | c0007 | t0008 | g0316 | AFR | LWK | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19056 | hp1 | a0001 | c0003 | t0003 | g0208 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19056 | hp2 | a0002 | c0004 | t0006 | g0025 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19060 | hp1 | a0001 | c0003 | t0003 | g0001 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19062 | hp1 | a0001 | c0001 | t0005 | g0214 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19063 | hp1 | a0002 | c0004 | t0006 | g0289 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19064 | hp1 | a0002 | c0004 | t0007 | g0135 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19065 | hp2 | a0003 | c0006 | t0001 | g0199 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19066 | hp1 | a0001 | c0014 | t0002 | g0053 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19066 | hp2 | a0001 | c0003 | t0003 | g0001 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19067 | hp1 | a0002 | c0004 | t0006 | g0275 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19070 | hp1 | a0002 | c0004 | t0007 | g0049 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19074 | hp2 | a0001 | c0003 | t0003 | g0157 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19075 | hp2 | a0001 | c0003 | t0003 | g0176 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19077 | hp2 | a0002 | c0004 | t0006 | g0293 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19082 | hp1 | a0001 | c0001 | t0009 | g0195 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19082 | hp2 | a0001 | c0003 | t0003 | g0154 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0222 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19085 | hp2 | a0002 | c0004 | t0006 | g0025 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19087 | hp1 | a0001 | c0003 | t0003 | g0082 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19090 | hp1 | a0001 | c0003 | t0003 | g0151 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19091 | hp2 | a0002 | c0004 | t0007 | g0034 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19240 | hp1 | a0001 | c0002 | t0004 | g0346 | AFR | YRI | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0238 | AFR | YRI | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | ASW | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA20129 | hp2 | a0006 | c0008 | t0001 | g0122 | AFR | ASW | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0114 | EUR | TSI | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA20805 | hp2 | a0003 | c0006 | t0001 | g0328 | EUR | TSI | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0341 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02109 | hp1 | a0001 | c0003 | t0008 | g0307 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0270 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02486 | hp1 | a0001 | c0007 | t0008 | g0027 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0260 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0235 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0269 | AFR | ACB | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03471 | hp1 | a0001 | c0007 | t0008 | g0027 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0233 | AFR | MSL | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | USA | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | USA | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18955 | hp1 | a0001 | c0003 | t0003 | g0210 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA18955 | hp2 | a0002 | c0004 | t0006 | g0276 | EAS | JPT | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA20300 | hp1 | a0001 | c0002 | t0004 | g0340 | AFR | USA | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0251 | AFR | USA | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| NA21309 | hp2 | a0012 | c0019 | t0008 | g0344 | AFR | LWK | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| homoSapiens | chm13v2 | a0013 | c0012 | t0001 | g0334 | REF | REF | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0123 | REF | REF | DCAF4_chr14_72921464_72964703 | DCAF4 | chr14 | 72921464 | 72964703 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:72937972 | A | C | 2 | a0001 a0004 |
104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
splice_region_variant | LOW | c.-7A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/14 | chr14 | 72937972 | |||||||
| chr14:72938010 | G | T | 1 | a0012 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.32G>T | p.Arg11Leu | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/14 | 120/2474 | 32/1488 | 11/495 | chr14 | 72938010 | |||
| chr14:72938044 | G | C | 2 | a0002 a0011 |
45 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(42): Show |
missense_variant | MODERATE | c.66G>C | p.Trp22Cys | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/14 | 154/2474 | 66/1488 | 22/495 | chr14 | 72938044 | |||
| chr14:72939813 | G | A | 1 | a0004 | 6 | NA18944.hp2 NA18971.hp2 NA18983.hp2 others(3): Show |
missense_variant | MODERATE | c.104G>A | p.Arg35Gln | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 3/14 | 192/2474 | 104/1488 | 35/495 | chr14 | 72939813 | |||
| chr14:72945927 | A | C | 2 | a0003 a0005 |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
missense_variant | MODERATE | c.578A>C | p.Lys193Thr | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/14 | 666/2474 | 578/1488 | 193/495 | chr14 | 72945927 | |||
| chr14:72951866 | A | G | 1 | a0007 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.797A>G | p.Asn266Ser | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/14 | 885/2474 | 797/1488 | 266/495 | chr14 | 72951866 | |||
| chr14:72954442 | G | A | 1 | a0008 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.964G>A | p.Gly322Arg | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/14 | 1052/2474 | 964/1488 | 322/495 | chr14 | 72954442 | |||
| chr14:72954478 | C | T | 1 | a0003 | 6 | HG01168.hp2 HG01261.hp1 HG03831.hp2 others(3): Show |
missense_variant | MODERATE | c.1000C>T | p.Leu334Phe | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/14 | 1088/2474 | 1000/1488 | 334/495 | chr14 | 72954478 | |||
| chr14:72955551 | C | G | 2 | a0002 a0009 |
45 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(42): Show |
missense_variant | MODERATE | c.1034C>G | p.Ser345Cys | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/14 | 1122/2474 | 1034/1488 | 345/495 | chr14 | 72955551 | |||
| chr14:72958656 | C | T | 1 | a0010 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.1339C>T | p.Arg447Cys | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 1427/2474 | 1339/1488 | 447/495 | chr14 | 72958656 | |||
| chr14:72958770 | G | A | 1 | a0006 | 2 | HG02451.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.1453G>A | p.Val485Ile | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 1541/2474 | 1453/1488 | 485/495 | chr14 | 72958770 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:72938062 | T | C | 1 | a0001c0007 | 5 | HG02486.hp1 HG02809.hp2 HG02922.hp2 others(2): Show |
synonymous_variant | LOW | c.84T>C | p.Ser28Ser | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/14 | 172/2474 | 84/1488 | 28/495 | chr14 | 72938062 | |||
| chr14:72939874 | T | G | 1 | a0010c0011 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.165T>G | p.Ser55Ser | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 3/14 | 253/2474 | 165/1488 | 55/495 | chr14 | 72939874 | |||
| chr14:72954243 | A | G | 1 | a0001c0017 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.888A>G | p.Ala296Ala | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 10/14 | 976/2474 | 888/1488 | 296/495 | chr14 | 72954243 | |||
| chr14:72955642 | T | G | 1 | a0001c0002 | 69 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(66): Show |
synonymous_variant | LOW | c.1125T>G | p.Ser375Ser | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/14 | 1213/2474 | 1125/1488 | 375/495 | chr14 | 72955642 | |||
| chr14:72956490 | C | A | 1 | a0001c0014 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.1284C>A | p.Ile428Ile | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/14 | 1372/2474 | 1284/1488 | 428/495 | chr14 | 72956490 | |||
| chr14:72958724 | G | A | 1 | a0001c0015 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.1407G>A | p.Ser469Ser | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 1495/2474 | 1407/1488 | 469/495 | chr14 | 72958724 | |||
| chr14:72958754 | G | A | 3 | a0001c0003 a0001c0015 a0001c0017 |
61 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(58): Show |
synonymous_variant | LOW | c.1437G>A | p.Pro479Pro | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 1525/2474 | 1437/1488 | 479/495 | chr14 | 72958754 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:72926538 | G | C | 11 | a0001c0001t0004 a0001c0001t0009 a0001c0002t0004 others(8): Show |
91 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(88): Show |
5_prime_UTR_variant | MODIFIER | c.-14G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/14 | 11441 | chr14 | 72926538 | ||||||
| chr14:72958886 | G | T | 1 | a0001c0001t0011 | 2 | HG02723.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*81G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 81 | chr14 | 72958886 | ||||||
| chr14:72958973 | A | C | 8 | a0001c0001t0003 a0001c0001t0005 a0001c0003t0003 others(5): Show |
96 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*168A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 168 | chr14 | 72958973 | ||||||
| chr14:72959130 | C | T | 1 | a0001c0001t0013 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*325C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 325 | chr14 | 72959130 | ||||||
| chr14:72959331 | C | G | 2 | a0001c0001t0010 a0008c0013t0012 |
3 | HG02622.hp2 HG03098.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*526C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 526 | chr14 | 72959331 | ||||||
| chr14:72959359 | C | G | 1 | a0001c0001t0005 | 28 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*554C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 554 | chr14 | 72959359 | ||||||
| chr14:72959582 | C | T | 3 | a0002c0004t0006 a0002c0004t0007 a0009c0016t0006 |
45 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*777C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 14/14 | 777 | chr14 | 72959582 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:72926576 | A | G | 155 | a0001c0001t0001g0230 a0001c0001t0001g0261 a0001c0001t0001g0309 others(152): Show |
173 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.-9+33A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72926576 | |||||||
| chr14:72926593 | C | T | 1 | a0001c0003t0003g0208 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-9+50C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72926593 | |||||||
| chr14:72926650 | AAGGGGCG others(3): Show |
A | 3 | a0001c0003t0003g0030 a0001c0003t0003g0031 a0001c0003t0003g0032 |
3 | HG00642.hp1 HG03491.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-9+121_-9+130delGG others(8): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72926650 | ||||||
| chr14:72926682 | C | T | 1 | a0003c0006t0001g0352 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-9+139C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72926682 | |||||||
| chr14:72926683 | G | A | 90 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0061 others(87): Show |
101 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.-9+140G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72926683 | |||||||
| chr14:72926715 | A | C | 2 | a0001c0002t0004g0350 a0001c0002t0004g0351 |
2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-9+172A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72926715 | |||||||
| chr14:72926849 | A | C | 335 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0061 others(332): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.-9+306A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72926849 | |||||||
| chr14:72926851 | C | T | 1 | a0001c0002t0001g0114 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-9+308C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72926851 | |||||||
| chr14:72926882 | G | A | 1 | a0001c0002t0001g0014 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-9+339G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72926882 | |||||||
| chr14:72926962 | T | A | 1 | a0001c0003t0003g0130 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-9+419T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72926962 | |||||||
| chr14:72927019 | A | G | 1 | a0002c0004t0007g0207 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-9+476A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927019 | |||||||
| chr14:72927170 | G | A | 132 | a0001c0001t0001g0033 a0001c0001t0001g0136 a0001c0001t0001g0137 others(129): Show |
151 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.-9+627G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927170 | |||||||
| chr14:72927319 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-9+776G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927319 | |||||||
| chr14:72927343 | C | CT | 12 | a0001c0001t0001g0013 a0001c0001t0001g0129 a0001c0002t0001g0206 others(9): Show |
13 | HG00323.hp1 HG00733.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9+828dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72927343 | ||||||
| chr14:72927343 | CTTTTTTT | C | 7 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0002g0112 others(4): Show |
7 | HG00408.hp1 HG00741.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+822_-9+828delTT others(5): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72927343 | ||||||
| chr14:72927343 | CTTTTTTT others(1): Show |
C | 134 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(131): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.-9+821_-9+828delTT others(6): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72927343 | ||||||
| chr14:72927343 | CTTTTTTT others(2): Show |
C | 157 | a0001c0001t0001g0033 a0001c0001t0001g0136 a0001c0001t0001g0137 others(154): Show |
189 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.-9+820_-9+828delTT others(7): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72927343 | ||||||
| chr14:72927343 | CTTTTTTT others(3): Show |
C | 18 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(15): Show |
18 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-9+819_-9+828delTT others(8): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72927343 | ||||||
| chr14:72927371 | T | G | 4 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0002c0004t0007g0115 others(1): Show |
4 | HG01358.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+828T>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927371 | |||||||
| chr14:72927371 | T | TG | 3 | a0001c0001t0001g0204 a0002c0004t0007g0203 a0002c0004t0007g0205 |
3 | HG00735.hp2 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-9+829dupG | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72927371 | ||||||
| chr14:72927413 | A | G | 1 | a0002c0004t0007g0205 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-9+870A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927413 | |||||||
| chr14:72927414 | C | T | 264 | a0001c0001t0001g0087 a0001c0001t0001g0178 a0001c0001t0001g0181 others(261): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.-9+871C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927414 | |||||||
| chr14:72927453 | G | A | 1 | a0001c0002t0001g0189 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-9+910G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927453 | |||||||
| chr14:72927483 | C | T | 1 | a0001c0001t0011g0247 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-9+940C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927483 | |||||||
| chr14:72927572 | C | T | 3 | a0003c0006t0001g0026 a0003c0006t0001g0199 a0003c0006t0001g0352 |
4 | HG01168.hp2 HG01261.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1029C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927572 | |||||||
| chr14:72927602 | C | T | 1 | a0001c0003t0003g0127 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-9+1059C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927602 | |||||||
| chr14:72927629 | G | C | 4 | a0002c0004t0007g0132 a0002c0004t0007g0133 a0002c0004t0007g0134 others(1): Show |
4 | NA18956.hp1 NA18964.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1086G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927629 | |||||||
| chr14:72927630 | C | A | 4 | a0002c0004t0007g0132 a0002c0004t0007g0133 a0002c0004t0007g0134 others(1): Show |
4 | NA18956.hp1 NA18964.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1087C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927630 | |||||||
| chr14:72927631 | G | C | 4 | a0002c0004t0007g0132 a0002c0004t0007g0133 a0002c0004t0007g0134 others(1): Show |
4 | NA18956.hp1 NA18964.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1088G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927631 | |||||||
| chr14:72927633 | G | T | 4 | a0002c0004t0007g0132 a0002c0004t0007g0133 a0002c0004t0007g0134 others(1): Show |
4 | NA18956.hp1 NA18964.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1090G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927633 | |||||||
| chr14:72927634 | AGCCACCG others(20): Show |
A | 4 | a0002c0004t0007g0132 a0002c0004t0007g0133 a0002c0004t0007g0134 others(1): Show |
4 | NA18956.hp1 NA18964.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1092_-9+1118del others(27): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927634 | |||||||
| chr14:72927640 | C | T | 2 | a0001c0001t0002g0005 a0001c0001t0009g0255 |
2 | HG01175.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-9+1097C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927640 | |||||||
| chr14:72927641 | G | A | 1 | a0001c0001t0002g0112 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-9+1098G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927641 | |||||||
| chr14:72927662 | T | C | 4 | a0002c0004t0007g0132 a0002c0004t0007g0133 a0002c0004t0007g0134 others(1): Show |
4 | NA18956.hp1 NA18964.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1119T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927662 | |||||||
| chr14:72927906 | G | C | 91 | a0001c0001t0001g0033 a0001c0001t0001g0230 a0001c0001t0001g0309 others(88): Show |
108 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-9+1363G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927906 | |||||||
| chr14:72927972 | G | A | 156 | a0001c0001t0001g0087 a0001c0001t0001g0178 a0001c0001t0001g0181 others(153): Show |
176 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.-9+1429G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927972 | |||||||
| chr14:72927994 | T | C | 52 | a0001c0001t0002g0166 a0001c0001t0002g0171 a0001c0002t0001g0170 others(49): Show |
62 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.-9+1451T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72927994 | |||||||
| chr14:72928054 | G | C | 1 | a0001c0001t0009g0317 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-9+1511G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928054 | |||||||
| chr14:72928060 | C | G | 57 | a0001c0001t0002g0166 a0001c0001t0002g0171 a0001c0002t0001g0170 others(54): Show |
68 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.-9+1517C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928060 | |||||||
| chr14:72928117 | A | C | 1 | a0001c0003t0003g0172 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-9+1574A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928117 | |||||||
| chr14:72928187 | C | CT | 13 | a0001c0001t0001g0012 a0001c0001t0001g0125 a0001c0001t0001g0126 others(10): Show |
15 | HG00323.hp1 HG01168.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+1667dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | ||||||
| chr14:72928187 | C | CTTTTT | 53 | a0001c0001t0001g0201 a0001c0001t0001g0261 a0001c0001t0004g0260 others(50): Show |
62 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.-9+1663_-9+1667dup others(5): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | ||||||
| chr14:72928187 | C | CTTTTTT | 10 | a0001c0001t0001g0033 a0001c0001t0001g0186 a0001c0001t0002g0166 others(7): Show |
11 | HG00423.hp2 HG02055.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9+1662_-9+1667dup others(6): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | ||||||
| chr14:72928187 | C | CTTTTTTT others(3): Show |
2 | a0001c0003t0008g0023 a0001c0003t0008g0241 |
3 | HG02976.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-9+1658_-9+1667dup others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | ||||||
| chr14:72928187 | C | CTTTTTTT others(4): Show |
8 | a0001c0001t0001g0060 a0001c0001t0004g0295 a0001c0002t0001g0189 others(5): Show |
8 | HG01081.hp1 HG01891.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+1657_-9+1667dup others(11): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | ||||||
| chr14:72928187 | C | CTTTTTTT others(5): Show |
32 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0231 others(29): Show |
36 | HG00099.hp2 HG00733.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.-9+1656_-9+1667dup others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | ||||||
| chr14:72928187 | C | CTTTTTTT others(6): Show |
27 | a0001c0001t0001g0061 a0001c0001t0002g0042 a0001c0001t0002g0052 others(24): Show |
30 | HG00323.hp2 HG00558.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.-9+1655_-9+1667dup others(13): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | ||||||
| chr14:72928187 | C | CTTTTTTT others(7): Show |
39 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(36): Show |
47 | HG00738.hp2 HG00741.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.-9+1654_-9+1667dup others(14): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | ||||||
| chr14:72928187 | C | CTTTTTTT others(8): Show |
38 | a0001c0001t0001g0087 a0001c0001t0001g0178 a0001c0001t0001g0181 others(35): Show |
40 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.-9+1653_-9+1667dup others(15): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | ||||||
| chr14:72928187 | C | CTTTTTTT others(9): Show |
15 | a0001c0001t0002g0008 a0001c0001t0002g0019 a0001c0001t0002g0029 others(12): Show |
17 | HG00642.hp2 HG00735.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.-9+1652_-9+1667dup others(16): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | ||||||
| chr14:72928187 | C | CTTTTTTT others(10): Show |
4 | a0001c0001t0001g0230 a0001c0001t0002g0005 a0001c0001t0002g0105 others(1): Show |
6 | HG02004.hp2 HG02074.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+1651_-9+1667dup others(17): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | ||||||
| chr14:72928187 | C | CTTTTTTT others(11): Show |
3 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0002g0109 |
3 | NA18970.hp1 NA18970.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-9+1650_-9+1667dup others(18): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | ||||||
| chr14:72928187 | C | CTTTTTTT others(12): Show |
4 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0001c0002t0004g0296 others(1): Show |
4 | HG02132.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1649_-9+1667dup others(19): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | ||||||
| chr14:72928187 | C | CTTTTTTT others(13): Show |
4 | a0001c0002t0004g0345 a0001c0002t0004g0346 a0001c0002t0004g0347 others(1): Show |
4 | HG01496.hp1 HG02895.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+1648_-9+1667dup others(20): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | ||||||
| chr14:72928187 | C | CTTTTTTT others(14): Show |
3 | a0001c0002t0004g0245 a0001c0002t0004g0340 a0001c0002t0004g0349 |
3 | HG03209.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-9+1647_-9+1667dup others(21): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | ||||||
| chr14:72928187 | C | CTTTTTTT others(19): Show |
1 | a0001c0002t0004g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-9+1667_-9+1668ins others(26): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | ||||||
| chr14:72928187 | CT | C | 37 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(34): Show |
40 | HG00423.hp1 HG00544.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-9+1667delT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928187 | ||||||
| chr14:72928279 | C | T | 1 | a0001c0001t0002g0098 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-9+1736C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928279 | |||||||
| chr14:72928280 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-9+1737G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928280 | |||||||
| chr14:72928312 | G | C | 1 | a0001c0001t0001g0337 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-9+1769G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928312 | |||||||
| chr14:72928334 | C | T | 3 | a0001c0001t0001g0188 a0001c0001t0001g0200 a0001c0001t0001g0204 |
3 | HG02258.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+1791C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928334 | |||||||
| chr14:72928361 | C | T | 336 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0061 others(333): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.-9+1818C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928361 | |||||||
| chr14:72928382 | C | T | 1 | a0001c0001t0005g0226 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-9+1839C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928382 | |||||||
| chr14:72928406 | A | C | 1 | a0001c0003t0003g0165 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-9+1863A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928406 | |||||||
| chr14:72928408 | G | C | 1 | a0001c0001t0005g0227 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-9+1865G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928408 | |||||||
| chr14:72928416 | A | G | 9 | a0001c0001t0001g0186 a0001c0001t0004g0263 a0001c0001t0004g0264 others(6): Show |
9 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+1873A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928416 | |||||||
| chr14:72928438 | G | T | 3 | a0001c0007t0008g0027 a0001c0007t0008g0315 a0001c0007t0008g0316 |
4 | HG02486.hp1 HG02809.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+1895G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928438 | |||||||
| chr14:72928452 | C | T | 1 | a0001c0002t0001g0067 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-9+1909C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928452 | |||||||
| chr14:72928465 | G | T | 1 | a0001c0002t0001g0190 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-9+1922G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928465 | |||||||
| chr14:72928511 | C | A | 1 | a0001c0001t0001g0013 | 2 | HG00733.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-9+1968C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928511 | |||||||
| chr14:72928556 | C | T | 2 | a0002c0004t0007g0141 a0002c0004t0007g0143 |
2 | NA18953.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-9+2013C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928556 | |||||||
| chr14:72928562 | C | T | 34 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0312 others(31): Show |
40 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.-9+2019C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928562 | |||||||
| chr14:72928585 | T | TTATATAT others(41): Show |
1 | a0001c0007t0008g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-9+2074_-9+2075ins others(48): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | ||||||
| chr14:72928585 | T | TTTTATAT others(1): Show |
4 | a0001c0001t0003g0229 a0001c0007t0008g0027 a0001c0007t0008g0315 others(1): Show |
5 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+2043_-9+2044ins others(8): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | ||||||
| chr14:72928585 | T | TTTTATAT others(3): Show |
23 | a0001c0001t0001g0310 a0001c0001t0005g0002 a0001c0001t0005g0051 others(20): Show |
28 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.-9+2043_-9+2044ins others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | ||||||
| chr14:72928585 | T | TTTTATAT others(5): Show |
6 | a0001c0001t0001g0309 a0001c0001t0001g0312 a0001c0001t0001g0313 others(3): Show |
6 | HG02723.hp1 HG03942.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+2043_-9+2044ins others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | ||||||
| chr14:72928585 | T | TTTTATAT others(13): Show |
1 | a0001c0003t0008g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-9+2043_-9+2044ins others(20): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | ||||||
| chr14:72928585 | TTA | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0121 a0001c0001t0001g0126 others(2): Show |
6 | HG00733.hp2 HG01106.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+2073_-9+2074del others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | ||||||
| chr14:72928585 | TTATA | T | 6 | a0001c0001t0001g0180 a0001c0001t0001g0188 a0001c0001t0001g0200 others(3): Show |
6 | HG02258.hp2 HG02647.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+2071_-9+2074del others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | ||||||
| chr14:72928585 | TTATATA | T | 7 | a0001c0001t0001g0033 a0001c0001t0010g0256 a0001c0001t0010g0257 others(4): Show |
8 | HG02109.hp1 HG02615.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+2069_-9+2074del others(6): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | ||||||
| chr14:72928585 | TTATATAT others(1): Show |
T | 12 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0140 others(9): Show |
12 | HG01081.hp1 HG01106.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9+2067_-9+2074del others(8): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | ||||||
| chr14:72928585 | TTATATAT others(3): Show |
T | 65 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(62): Show |
75 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-9+2065_-9+2074del others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | ||||||
| chr14:72928585 | TTATATAT others(5): Show |
T | 213 | a0001c0001t0001g0087 a0001c0001t0001g0178 a0001c0001t0001g0181 others(210): Show |
237 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.-9+2063_-9+2074del others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928585 | ||||||
| chr14:72928587 | A | T | 2 | a0001c0001t0005g0214 a0001c0003t0003g0145 |
2 | NA18961.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-9+2044A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928587 | |||||||
| chr14:72928591 | A | T | 3 | a0001c0001t0001g0180 a0001c0001t0004g0295 a0001c0003t0008g0243 |
3 | HG02647.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-9+2048A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928591 | |||||||
| chr14:72928593 | A | T | 5 | a0001c0001t0001g0033 a0001c0003t0008g0023 a0001c0003t0008g0241 others(2): Show |
6 | HG02109.hp1 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+2050A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928593 | |||||||
| chr14:72928594 | T | A | 5 | a0001c0001t0001g0309 a0001c0001t0001g0312 a0001c0001t0001g0313 others(2): Show |
5 | HG03942.hp1 NA18947.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+2051T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928594 | |||||||
| chr14:72928594 | T | TATATATA others(4): Show |
1 | a0001c0001t0005g0214 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-9+2052_-9+2062dup others(11): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928594 | ||||||
| chr14:72928595 | A | T | 12 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0140 others(9): Show |
12 | HG01081.hp1 HG01106.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9+2052A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928595 | |||||||
| chr14:72928596 | T | A | 24 | a0001c0001t0001g0310 a0001c0001t0005g0002 a0001c0001t0005g0051 others(21): Show |
29 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.-9+2053T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928596 | |||||||
| chr14:72928597 | A | T | 63 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(60): Show |
73 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-9+2054A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928597 | |||||||
| chr14:72928598 | T | A | 4 | a0001c0001t0003g0229 a0001c0007t0008g0027 a0001c0007t0008g0315 others(1): Show |
5 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+2055T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928598 | |||||||
| chr14:72928599 | A | T | 213 | a0001c0001t0001g0087 a0001c0001t0001g0178 a0001c0001t0001g0181 others(210): Show |
237 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.-9+2056A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928599 | |||||||
| chr14:72928611 | A | G | 2 | a0005c0009t0001g0182 a0005c0009t0001g0183 |
2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-9+2068A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928611 | |||||||
| chr14:72928627 | C | A | 3 | a0001c0007t0008g0027 a0001c0007t0008g0315 a0001c0007t0008g0316 |
4 | HG02486.hp1 HG02809.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+2084C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928627 | |||||||
| chr14:72928777 | A | T | 1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-9+2234A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928777 | |||||||
| chr14:72928874 | C | G | 1 | a0001c0001t0004g0295 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9+2331C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928874 | |||||||
| chr14:72928971 | C | T | 5 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0085 others(2): Show |
5 | NA18939.hp1 NA18961.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+2428C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928971 | |||||||
| chr14:72928976 | C | T | 2 | a0005c0009t0001g0182 a0005c0009t0001g0183 |
2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-9+2433C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72928976 | |||||||
| chr14:72928977 | A | AG | 195 | a0001c0001t0001g0033 a0001c0001t0001g0136 a0001c0001t0001g0137 others(192): Show |
216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.-9+2438dupG | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72928977 | ||||||
| chr14:72929079 | C | A | 291 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0136 others(288): Show |
325 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.-9+2536C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929079 | |||||||
| chr14:72929108 | C | G | 2 | a0001c0003t0008g0246 a0001c0007t0008g0258 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-9+2565C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929108 | |||||||
| chr14:72929127 | C | T | 2 | a0001c0003t0008g0246 a0001c0007t0008g0258 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-9+2584C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929127 | |||||||
| chr14:72929216 | G | T | 3 | a0001c0001t0001g0188 a0001c0001t0001g0200 a0001c0001t0001g0204 |
3 | HG02258.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+2673G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929216 | |||||||
| chr14:72929295 | A | G | 1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-9+2752A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929295 | |||||||
| chr14:72929298 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-9+2755C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929298 | |||||||
| chr14:72929312 | C | T | 1 | a0002c0004t0006g0284 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-9+2769C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929312 | |||||||
| chr14:72929423 | C | T | 1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-9+2880C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929423 | |||||||
| chr14:72929532 | T | C | 1 | a0010c0011t0004g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-9+2989T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929532 | |||||||
| chr14:72929533 | C | G | 93 | a0001c0001t0001g0087 a0001c0001t0001g0230 a0001c0001t0002g0003 others(90): Show |
106 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.-9+2990C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929533 | |||||||
| chr14:72929739 | A | G | 344 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0060 others(341): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.-9+3196A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929739 | |||||||
| chr14:72929779 | C | T | 1 | a0002c0004t0007g0135 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-9+3236C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929779 | |||||||
| chr14:72929836 | CGCCCGCG others(11): Show |
C | 1 | a0010c0011t0004g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-9+3297_-9+3314del others(18): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72929836 | ||||||
| chr14:72929956 | G | A | 6 | a0002c0004t0007g0115 a0002c0004t0007g0118 a0002c0004t0007g0202 others(3): Show |
6 | HG00735.hp2 HG00738.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+3413G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72929956 | |||||||
| chr14:72930112 | G | A | 1 | a0001c0014t0002g0053 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-9+3569G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72930112 | |||||||
| chr14:72930113 | G | T | 2 | a0001c0001t0010g0256 a0001c0001t0010g0257 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-9+3570G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72930113 | |||||||
| chr14:72930154 | G | A | 1 | a0001c0001t0009g0272 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-9+3611G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72930154 | |||||||
| chr14:72930155 | T | C | 9 | a0001c0002t0004g0245 a0001c0002t0004g0259 a0001c0002t0004g0296 others(6): Show |
9 | HG01496.hp1 HG02895.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+3612T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72930155 | |||||||
| chr14:72930246 | C | CT | 81 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0180 others(78): Show |
88 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.-9+3715dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72930246 | ||||||
| chr14:72930246 | C | CTT | 72 | a0001c0001t0001g0139 a0001c0001t0001g0186 a0001c0001t0001g0201 others(69): Show |
82 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.-9+3714_-9+3715dup others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72930246 | ||||||
| chr14:72930254 | T | C | 92 | a0001c0001t0001g0087 a0001c0001t0001g0230 a0001c0001t0002g0003 others(89): Show |
105 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.-9+3711T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72930254 | |||||||
| chr14:72930259 | G | C | 1 | a0001c0001t0002g0105 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-9+3716G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72930259 | |||||||
| chr14:72930309 | C | A | 1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-9+3766C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72930309 | |||||||
| chr14:72930511 | C | T | 1 | a0001c0001t0002g0039 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-9+3968C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72930511 | |||||||
| chr14:72930641 | G | GTA | 120 | a0001c0001t0001g0033 a0001c0001t0001g0139 a0001c0001t0001g0186 others(117): Show |
136 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-9+4110_-9+4111dup others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72930641 | ||||||
| chr14:72930713 | G | A | 3 | a0001c0001t0003g0229 a0001c0001t0011g0228 a0001c0001t0011g0247 |
3 | HG01074.hp2 HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-9+4170G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72930713 | |||||||
| chr14:72931263 | C | CT | 221 | a0001c0001t0001g0033 a0001c0001t0001g0138 a0001c0001t0001g0186 others(218): Show |
251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.-9+4738dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72931263 | ||||||
| chr14:72931263 | C | CTT | 9 | a0001c0001t0002g0048 a0001c0001t0002g0080 a0001c0001t0002g0106 others(6): Show |
9 | HG02074.hp2 HG02970.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+4737_-9+4738dup others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72931263 | ||||||
| chr14:72931263 | C | CTTT | 40 | a0001c0003t0008g0283 a0002c0004t0006g0020 a0002c0004t0006g0024 others(37): Show |
43 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.-9+4736_-9+4738dup others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72931263 | ||||||
| chr14:72931263 | C | CTTTT | 7 | a0002c0004t0006g0025 a0002c0004t0006g0293 a0003c0006t0001g0198 others(4): Show |
8 | HG00323.hp1 HG02735.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+4735_-9+4738dup others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72931263 | ||||||
| chr14:72931263 | C | T | 1 | a0001c0002t0001g0036 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-9+4720C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72931263 | |||||||
| chr14:72931265 | T | C | 1 | a0001c0007t0008g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-9+4722T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72931265 | |||||||
| chr14:72931737 | A | C | 1 | a0001c0003t0003g0165 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-9+5194A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72931737 | |||||||
| chr14:72931738 | G | A | 42 | a0001c0003t0008g0283 a0002c0004t0006g0020 a0002c0004t0006g0024 others(39): Show |
46 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.-9+5195G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72931738 | |||||||
| chr14:72931873 | G | A | 2 | a0003c0006t0001g0198 a0003c0006t0001g0199 |
2 | NA18944.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-9+5330G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72931873 | |||||||
| chr14:72931883 | G | A | 1 | a0001c0002t0004g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-9+5340G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72931883 | |||||||
| chr14:72931951 | CTG | C | 5 | a0003c0006t0001g0026 a0003c0006t0001g0198 a0003c0006t0001g0199 others(2): Show |
6 | HG01168.hp2 HG01261.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+5410_-9+5411del others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72931951 | ||||||
| chr14:72931985 | CTTCT | C | 13 | a0001c0001t0003g0229 a0001c0001t0011g0228 a0001c0001t0011g0247 others(10): Show |
15 | HG01074.hp2 HG02109.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+5445_-9+5448del others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72931985 | ||||||
| chr14:72931987 | TC | T | 28 | a0001c0001t0001g0178 a0001c0001t0001g0181 a0001c0001t0001g0309 others(25): Show |
33 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.-9+5445delC | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72931987 | |||||||
| chr14:72931988 | C | T | 2 | a0001c0001t0001g0314 a0001c0001t0005g0253 |
2 | HG03831.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-9+5445C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72931988 | |||||||
| chr14:72931988 | CT | C | 128 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0060 others(125): Show |
144 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.-9+5461delT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72931988 | ||||||
| chr14:72932007 | G | A | 1 | a0010c0011t0004g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-9+5464G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72932007 | |||||||
| chr14:72932191 | A | G | 1 | a0001c0003t0003g0144 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-9+5648A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72932191 | |||||||
| chr14:72932477 | C | A | 3 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0039 |
3 | NA18950.hp1 NA18963.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-8-5494C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72932477 | |||||||
| chr14:72932710 | T | C | 91 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(88): Show |
104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-8-5261T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72932710 | |||||||
| chr14:72932810 | C | T | 1 | a0001c0001t0002g0079 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-8-5161C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72932810 | |||||||
| chr14:72932880 | TTTTC | T | 64 | a0001c0002t0001g0004 a0001c0002t0001g0014 a0001c0002t0001g0018 others(61): Show |
69 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.-8-5071_-8-5068del others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72932880 | ||||||
| chr14:72932946 | G | A | 1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8-5025G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72932946 | |||||||
| chr14:72932998 | C | T | 116 | a0001c0001t0001g0033 a0001c0001t0001g0178 a0001c0001t0001g0181 others(113): Show |
134 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-8-4973C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72932998 | |||||||
| chr14:72933129 | A | G | 42 | a0001c0003t0008g0283 a0002c0004t0006g0020 a0002c0004t0006g0024 others(39): Show |
46 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.-8-4842A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72933129 | |||||||
| chr14:72933140 | A | AC | 45 | a0001c0003t0003g0001 a0001c0003t0003g0006 a0001c0003t0003g0016 others(42): Show |
54 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.-8-4827dupC | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72933140 | ||||||
| chr14:72933142 | C | T | 64 | a0001c0002t0001g0004 a0001c0002t0001g0014 a0001c0002t0001g0018 others(61): Show |
69 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.-8-4829C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72933142 | |||||||
| chr14:72933330 | A | G | 322 | a0001c0001t0001g0033 a0001c0001t0001g0178 a0001c0001t0001g0181 others(319): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.-8-4641A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72933330 | |||||||
| chr14:72933558 | CA | C | 120 | a0001c0001t0001g0033 a0001c0001t0001g0186 a0001c0001t0001g0201 others(117): Show |
135 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.-8-4397delA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72933558 | ||||||
| chr14:72933664 | C | T | 7 | a0003c0006t0001g0026 a0003c0006t0001g0198 a0003c0006t0001g0199 others(4): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-4307C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72933664 | |||||||
| chr14:72933816 | C | T | 1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8-4155C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72933816 | |||||||
| chr14:72933922 | G | A | 1 | a0001c0002t0001g0104 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-8-4049G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72933922 | |||||||
| chr14:72933973 | C | T | 11 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(8): Show |
11 | HG00544.hp2 HG01081.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-3998C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72933973 | |||||||
| chr14:72934132 | C | T | 230 | a0001c0001t0001g0033 a0001c0001t0001g0178 a0001c0001t0001g0181 others(227): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-8-3839C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934132 | |||||||
| chr14:72934156 | C | CT | 16 | a0001c0001t0003g0229 a0001c0001t0004g0264 a0001c0001t0011g0228 others(13): Show |
18 | HG01074.hp2 HG02109.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8-3801dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72934156 | ||||||
| chr14:72934156 | C | CTT | 56 | a0001c0001t0001g0033 a0001c0001t0001g0178 a0001c0001t0001g0181 others(53): Show |
63 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.-8-3802_-8-3801dup others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72934156 | ||||||
| chr14:72934156 | C | CTTT | 46 | a0001c0001t0001g0314 a0001c0001t0005g0224 a0001c0003t0003g0001 others(43): Show |
55 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.-8-3803_-8-3801dup others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72934156 | ||||||
| chr14:72934239 | C | A | 91 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(88): Show |
104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-8-3732C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934239 | |||||||
| chr14:72934266 | G | A | 1 | a0001c0001t0004g0234 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-8-3705G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934266 | |||||||
| chr14:72934298 | C | T | 1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8-3673C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934298 | |||||||
| chr14:72934388 | A | G | 1 | a0012c0019t0008g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8-3583A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934388 | |||||||
| chr14:72934447 | C | T | 1 | a0001c0001t0002g0078 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-8-3524C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934447 | |||||||
| chr14:72934449 | C | T | 64 | a0001c0002t0001g0004 a0001c0002t0001g0014 a0001c0002t0001g0018 others(61): Show |
69 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.-8-3522C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934449 | |||||||
| chr14:72934487 | G | A | 1 | a0001c0002t0001g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-8-3484G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934487 | |||||||
| chr14:72934488 | T | C | 322 | a0001c0001t0001g0033 a0001c0001t0001g0178 a0001c0001t0001g0181 others(319): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.-8-3483T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934488 | |||||||
| chr14:72934496 | G | T | 2 | a0001c0002t0001g0189 a0001c0002t0004g0271 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-8-3475G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934496 | |||||||
| chr14:72934584 | C | T | 1 | a0001c0001t0004g0239 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-8-3387C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934584 | |||||||
| chr14:72934886 | C | T | 1 | a0002c0004t0007g0133 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-8-3085C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934886 | |||||||
| chr14:72934912 | C | A | 1 | a0010c0011t0004g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-8-3059C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934912 | |||||||
| chr14:72934943 | A | C | 91 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(88): Show |
104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-8-3028A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72934943 | |||||||
| chr14:72935059 | A | G | 1 | a0001c0003t0008g0283 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-8-2912A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935059 | |||||||
| chr14:72935158 | T | A | 7 | a0003c0006t0001g0026 a0003c0006t0001g0198 a0003c0006t0001g0199 others(4): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-2813T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935158 | |||||||
| chr14:72935197 | T | C | 231 | a0001c0001t0001g0033 a0001c0001t0001g0178 a0001c0001t0001g0181 others(228): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.-8-2774T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935197 | |||||||
| chr14:72935261 | A | ATTT | 310 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0061 others(307): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.-8-2701_-8-2699dup others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72935261 | ||||||
| chr14:72935261 | A | ATTTT | 19 | a0001c0001t0005g0223 a0001c0001t0009g0317 a0001c0002t0001g0194 others(16): Show |
19 | HG00423.hp1 HG00741.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8-2702_-8-2699dup others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72935261 | ||||||
| chr14:72935278 | G | A | 4 | a0001c0002t0001g0014 a0001c0002t0001g0206 a0001c0002t0004g0350 others(1): Show |
5 | HG01891.hp2 HG02145.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-2693G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935278 | |||||||
| chr14:72935344 | A | T | 231 | a0001c0001t0001g0033 a0001c0001t0001g0178 a0001c0001t0001g0181 others(228): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.-8-2627A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935344 | |||||||
| chr14:72935443 | C | T | 91 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(88): Show |
104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-8-2528C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935443 | |||||||
| chr14:72935502 | G | A | 2 | a0001c0003t0003g0148 a0007c0018t0001g0187 |
2 | HG02083.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-8-2469G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935502 | |||||||
| chr14:72935619 | G | A | 1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8-2352G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935619 | |||||||
| chr14:72935643 | G | A | 230 | a0001c0001t0001g0033 a0001c0001t0001g0178 a0001c0001t0001g0181 others(227): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-8-2328G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935643 | |||||||
| chr14:72935766 | T | C | 91 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(88): Show |
104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-8-2205T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72935766 | |||||||
| chr14:72935958 | CTT | C | 6 | a0001c0003t0008g0023 a0001c0003t0008g0241 a0001c0003t0008g0243 others(3): Show |
7 | HG02109.hp1 HG02647.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-2009_-8-2008del others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72935958 | ||||||
| chr14:72936119 | G | A | 91 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(88): Show |
104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-8-1852G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936119 | |||||||
| chr14:72936225 | C | G | 166 | a0001c0001t0001g0033 a0001c0001t0001g0178 a0001c0001t0001g0181 others(163): Show |
189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.-8-1746C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936225 | |||||||
| chr14:72936306 | G | T | 1 | a0012c0019t0008g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8-1665G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936306 | |||||||
| chr14:72936409 | C | G | 1 | a0001c0003t0003g0161 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-8-1562C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936409 | |||||||
| chr14:72936420 | T | C | 1 | a0012c0019t0008g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8-1551T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936420 | |||||||
| chr14:72936444 | G | T | 1 | a0001c0003t0003g0161 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-8-1527G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936444 | |||||||
| chr14:72936563 | C | CA | 241 | a0001c0001t0001g0033 a0001c0001t0001g0136 a0001c0001t0001g0178 others(238): Show |
276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.-8-1392dupA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72936563 | ||||||
| chr14:72936613 | T | C | 91 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(88): Show |
104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-8-1358T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936613 | |||||||
| chr14:72936699 | G | A | 1 | a0004c0005t0002g0071 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-8-1272G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936699 | |||||||
| chr14:72936823 | A | C | 3 | a0001c0007t0008g0027 a0001c0007t0008g0315 a0001c0007t0008g0316 |
4 | HG02486.hp1 HG02809.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1148A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936823 | |||||||
| chr14:72936840 | A | G | 1 | a0001c0002t0001g0070 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-8-1131A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936840 | |||||||
| chr14:72936849 | G | T | 1 | a0010c0011t0004g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-8-1122G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936849 | |||||||
| chr14:72936858 | A | G | 10 | a0001c0002t0001g0004 a0001c0002t0001g0036 a0001c0002t0001g0069 others(7): Show |
13 | NA18943.hp2 NA18963.hp1 NA18971.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8-1113A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936858 | |||||||
| chr14:72936879 | T | C | 335 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0061 others(332): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.-8-1092T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72936879 | |||||||
| chr14:72937001 | T | TG | 9 | a0001c0002t0004g0245 a0001c0002t0004g0259 a0001c0002t0004g0296 others(6): Show |
9 | HG01496.hp1 HG02895.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-970_-8-969insG | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937001 | |||||||
| chr14:72937129 | A | G | 1 | a0008c0013t0012g0306 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-8-842A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937129 | |||||||
| chr14:72937199 | GAGA | G | 64 | a0001c0002t0001g0004 a0001c0002t0001g0014 a0001c0002t0001g0018 others(61): Show |
69 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.-8-769_-8-767delAA others(1): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72937199 | ||||||
| chr14:72937220 | G | C | 2 | a0002c0004t0006g0274 a0002c0004t0006g0284 |
2 | HG01261.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.-8-751G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937220 | |||||||
| chr14:72937227 | CAGAT | C | 337 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0061 others(334): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.-8-739_-8-736delAG others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72937227 | ||||||
| chr14:72937410 | C | CT | 137 | a0001c0001t0001g0178 a0001c0001t0001g0181 a0001c0001t0001g0309 others(134): Show |
158 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.-8-541dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72937410 | ||||||
| chr14:72937410 | C | CTT | 58 | a0001c0001t0001g0314 a0001c0001t0002g0048 a0001c0001t0002g0063 others(55): Show |
62 | HG00323.hp2 HG00558.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.-8-542_-8-541dupTT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72937410 | ||||||
| chr14:72937410 | CT | C | 46 | a0001c0003t0003g0146 a0001c0003t0003g0150 a0002c0004t0006g0020 others(43): Show |
51 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.-8-541delT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 72937410 | ||||||
| chr14:72937570 | G | A | 1 | a0002c0004t0007g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-8-401G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937570 | |||||||
| chr14:72937582 | G | A | 64 | a0001c0002t0001g0004 a0001c0002t0001g0014 a0001c0002t0001g0018 others(61): Show |
69 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.-8-389G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937582 | |||||||
| chr14:72937661 | C | T | 1 | a0001c0003t0003g0160 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-8-310C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937661 | |||||||
| chr14:72937685 | C | T | 1 | a0001c0002t0004g0349 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-8-286C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937685 | |||||||
| chr14:72937730 | G | A | 91 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(88): Show |
104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-8-241G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937730 | |||||||
| chr14:72937822 | A | G | 1 | a0001c0002t0001g0189 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-8-149A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937822 | |||||||
| chr14:72937826 | A | C | 1 | a0001c0002t0001g0193 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-8-145A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937826 | |||||||
| chr14:72937891 | G | A | 4 | a0001c0003t0008g0023 a0001c0003t0008g0241 a0001c0003t0008g0243 others(1): Show |
5 | HG02647.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-80G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937891 | |||||||
| chr14:72937930 | AC | A | 11 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(8): Show |
11 | HG00544.hp2 HG01081.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-40delC | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937930 | |||||||
| chr14:72937968 | T | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG02572.hp2 HG06807.hp1 |
splice_region_variant&intron_variant | LOW | c.-8-3T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 1/13 | chr14 | 72937968 | |||||||
| chr14:72938077 | G | A | 1 | a0004c0005t0002g0071 | 1 | NA18983.hp2 | splice_region_variant&intron_variant | LOW | c.92+7G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938077 | |||||||
| chr14:72938087 | G | A | 64 | a0001c0002t0001g0004 a0001c0002t0001g0014 a0001c0002t0001g0018 others(61): Show |
69 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.92+17G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938087 | |||||||
| chr14:72938117 | G | C | 91 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(88): Show |
104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.92+47G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938117 | |||||||
| chr14:72938260 | G | A | 1 | a0002c0004t0006g0020 | 2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.92+190G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938260 | |||||||
| chr14:72938369 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0121 a0001c0001t0001g0188 others(2): Show |
6 | HG00733.hp2 HG01106.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.92+299G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938369 | |||||||
| chr14:72938393 | G | A | 2 | a0001c0003t0003g0149 a0001c0003t0003g0151 |
2 | NA18954.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.92+323G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938393 | |||||||
| chr14:72938524 | T | A | 7 | a0003c0006t0001g0026 a0003c0006t0001g0198 a0003c0006t0001g0199 others(4): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.92+454T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938524 | |||||||
| chr14:72938533 | G | A | 1 | a0010c0011t0004g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.92+463G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938533 | |||||||
| chr14:72938607 | A | G | 1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.92+537A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938607 | |||||||
| chr14:72938732 | T | C | 1 | a0001c0001t0004g0265 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.92+662T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938732 | |||||||
| chr14:72938754 | T | C | 8 | a0001c0001t0001g0178 a0001c0001t0001g0181 a0001c0001t0001g0309 others(5): Show |
8 | HG00408.hp1 HG01975.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.92+684T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938754 | |||||||
| chr14:72938759 | G | A | 1 | a0001c0003t0008g0307 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.92+689G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938759 | |||||||
| chr14:72938765 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.92+695C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938765 | |||||||
| chr14:72938863 | T | C | 91 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(88): Show |
104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.92+793T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938863 | |||||||
| chr14:72938928 | C | G | 1 | a0001c0001t0002g0072 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.92+858C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72938928 | |||||||
| chr14:72939070 | T | C | 2 | a0001c0003t0003g0152 a0001c0003t0003g0167 |
2 | NA18995.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.93-732T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72939070 | |||||||
| chr14:72939460 | C | G | 2 | a0001c0001t0002g0055 a0001c0001t0002g0057 |
2 | NA19081.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.93-342C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72939460 | |||||||
| chr14:72939524 | A | G | 1 | a0001c0001t0002g0038 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.93-278A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72939524 | |||||||
| chr14:72939540 | A | G | 1 | a0002c0004t0006g0282 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.93-262A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 2/13 | chr14 | 72939540 | |||||||
| chr14:72939960 | C | T | 90 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(87): Show |
103 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.193+58C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 3/13 | chr14 | 72939960 | |||||||
| chr14:72939999 | C | T | 1 | a0001c0007t0008g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.193+97C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 3/13 | chr14 | 72939999 | |||||||
| chr14:72940022 | G | T | 1 | a0001c0001t0005g0221 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.193+120G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 3/13 | chr14 | 72940022 | |||||||
| chr14:72940054 | C | T | 1 | a0001c0001t0004g0022 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.193+152C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 3/13 | chr14 | 72940054 | |||||||
| chr14:72940147 | G | A | 10 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(7): Show |
10 | HG00544.hp2 HG01081.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-73G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 3/13 | chr14 | 72940147 | |||||||
| chr14:72940413 | G | A | 7 | a0003c0006t0001g0026 a0003c0006t0001g0198 a0003c0006t0001g0199 others(4): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.351+36G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940413 | |||||||
| chr14:72940550 | G | A | 2 | a0001c0002t0001g0040 a0001c0002t0001g0041 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.351+173G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940550 | |||||||
| chr14:72940582 | C | G | 1 | a0002c0004t0007g0207 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.351+205C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940582 | |||||||
| chr14:72940588 | G | GT | 61 | a0001c0001t0002g0103 a0001c0001t0009g0255 a0001c0002t0001g0004 others(58): Show |
66 | HG00099.hp2 HG00558.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.351+213dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 72940588 | ||||||
| chr14:72940588 | G | GTT | 4 | a0001c0002t0001g0041 a0001c0002t0001g0192 a0001c0002t0001g0303 others(1): Show |
4 | HG00323.hp2 HG03492.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+212_351+213dup others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 72940588 | ||||||
| chr14:72940590 | TG | T | 10 | a0001c0001t0001g0087 a0001c0001t0001g0137 a0001c0001t0001g0139 others(7): Show |
10 | HG00544.hp2 HG02056.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.351+214delG | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940590 | |||||||
| chr14:72940591 | G | GT | 26 | a0001c0001t0001g0188 a0001c0001t0001g0200 a0001c0001t0001g0204 others(23): Show |
31 | HG00140.hp1 HG00323.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.351+231dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 72940591 | ||||||
| chr14:72940591 | G | GTT | 35 | a0002c0004t0006g0024 a0002c0004t0006g0025 a0002c0004t0006g0274 others(32): Show |
38 | HG00423.hp1 HG00738.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.351+230_351+231dup others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 72940591 | ||||||
| chr14:72940591 | G | GTTT | 6 | a0002c0004t0006g0020 a0002c0004t0006g0287 a0002c0004t0006g0289 others(3): Show |
6 | HG00735.hp2 HG01358.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+229_351+231dup others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 72940591 | ||||||
| chr14:72940591 | G | T | 161 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0136 others(158): Show |
179 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.351+214G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940591 | |||||||
| chr14:72940596 | T | G | 3 | a0001c0001t0002g0088 a0001c0001t0002g0106 a0007c0018t0001g0187 |
3 | HG02074.hp2 HG02155.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.351+219T>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940596 | |||||||
| chr14:72940686 | A | G | 334 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0061 others(331): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.351+309A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940686 | |||||||
| chr14:72940692 | G | A | 1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.351+315G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940692 | |||||||
| chr14:72940791 | A | C | 1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.351+414A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940791 | |||||||
| chr14:72940881 | A | G | 337 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0061 others(334): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.351+504A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940881 | |||||||
| chr14:72940906 | A | G | 3 | a0001c0003t0008g0023 a0001c0003t0008g0241 a0001c0003t0008g0243 |
4 | HG02647.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+529A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72940906 | |||||||
| chr14:72940974 | G | GT | 321 | a0001c0001t0001g0033 a0001c0001t0001g0178 a0001c0001t0001g0181 others(318): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.351+604dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 72940974 | ||||||
| chr14:72941138 | A | AT | 3 | a0001c0003t0003g0006 a0001c0003t0003g0159 a0001c0003t0003g0172 |
5 | HG00140.hp1 HG01433.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.352-599dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 72941138 | ||||||
| chr14:72941148 | T | C | 93 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(90): Show |
106 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.352-597T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72941148 | |||||||
| chr14:72941186 | G | A | 93 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(90): Show |
106 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.352-559G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72941186 | |||||||
| chr14:72941208 | C | A | 2 | a0001c0001t0004g0235 a0001c0001t0004g0304 |
2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.352-537C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72941208 | |||||||
| chr14:72941426 | G | A | 115 | a0001c0001t0001g0033 a0001c0001t0001g0178 a0001c0001t0001g0181 others(112): Show |
133 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.352-319G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72941426 | |||||||
| chr14:72941578 | C | T | 1 | a0010c0011t0004g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.352-167C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72941578 | |||||||
| chr14:72941589 | G | T | 1 | a0001c0001t0002g0103 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.352-156G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72941589 | |||||||
| chr14:72941611 | A | AT | 91 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(88): Show |
104 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.352-129dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 72941611 | ||||||
| chr14:72941647 | G | A | 232 | a0001c0001t0001g0033 a0001c0001t0001g0178 a0001c0001t0001g0181 others(229): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.352-98G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | chr14 | 72941647 | |||||||
| chr14:72941661 | A | AT | 64 | a0001c0002t0001g0004 a0001c0002t0001g0014 a0001c0002t0001g0018 others(61): Show |
69 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.352-83dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 72941661 | ||||||
| chr14:72941908 | G | C | 36 | a0002c0004t0006g0020 a0002c0004t0006g0024 a0002c0004t0006g0025 others(33): Show |
40 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.431+84G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72941908 | |||||||
| chr14:72942002 | C | T | 1 | a0010c0011t0004g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.431+178C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942002 | |||||||
| chr14:72942063 | C | T | 7 | a0003c0006t0001g0026 a0003c0006t0001g0198 a0003c0006t0001g0199 others(4): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.431+239C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942063 | |||||||
| chr14:72942181 | A | G | 1 | a0001c0002t0004g0296 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.431+357A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942181 | |||||||
| chr14:72942309 | C | A | 1 | a0006c0008t0001g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.431+485C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942309 | |||||||
| chr14:72942415 | A | C | 1 | a0001c0001t0002g0096 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.432-579A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942415 | |||||||
| chr14:72942456 | C | T | 2 | a0003c0006t0001g0198 a0003c0006t0001g0199 |
2 | NA18944.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.432-538C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942456 | |||||||
| chr14:72942477 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0004g0263 |
2 | HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.432-517C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942477 | |||||||
| chr14:72942603 | G | GGCCGTAT others(19): Show |
1 | a0003c0006t0001g0328 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.432-368_432-343dup others(26): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr14 | 72942603 | ||||||
| chr14:72942603 | GGCCGTAT others(19): Show |
G | 65 | a0001c0002t0001g0004 a0001c0002t0001g0014 a0001c0002t0001g0018 others(62): Show |
70 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.432-368_432-343del others(26): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr14 | 72942603 | ||||||
| chr14:72942638 | C | T | 2 | a0001c0001t0011g0228 a0001c0001t0011g0247 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.432-356C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942638 | |||||||
| chr14:72942687 | C | T | 1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.432-307C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942687 | |||||||
| chr14:72942814 | T | C | 1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.432-180T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942814 | |||||||
| chr14:72942832 | C | T | 1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.432-162C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942832 | |||||||
| chr14:72942905 | G | A | 65 | a0001c0002t0001g0004 a0001c0002t0001g0014 a0001c0002t0001g0018 others(62): Show |
70 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.432-89G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942905 | |||||||
| chr14:72942933 | C | T | 9 | a0001c0002t0004g0245 a0001c0002t0004g0259 a0001c0002t0004g0296 others(6): Show |
9 | HG01496.hp1 HG02895.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.432-61C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942933 | |||||||
| chr14:72942953 | G | A | 1 | a0001c0001t0002g0107 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.432-41G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942953 | |||||||
| chr14:72942975 | C | G | 134 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(131): Show |
151 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.432-19C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 5/13 | chr14 | 72942975 | |||||||
| chr14:72943182 | G | A | 1 | a0001c0003t0003g0153 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.534+86G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943182 | |||||||
| chr14:72943249 | G | C | 23 | a0001c0001t0005g0002 a0001c0001t0005g0051 a0001c0001t0005g0214 others(20): Show |
28 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.534+153G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943249 | |||||||
| chr14:72943268 | A | C | 4 | a0001c0002t0001g0014 a0001c0002t0001g0206 a0001c0002t0004g0350 others(1): Show |
5 | HG01891.hp2 HG02145.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.534+172A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943268 | |||||||
| chr14:72943328 | G | A | 1 | a0001c0001t0002g0335 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.534+232G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943328 | |||||||
| chr14:72943490 | C | T | 94 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(91): Show |
107 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.534+394C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943490 | |||||||
| chr14:72943514 | G | A | 9 | a0001c0002t0004g0245 a0001c0002t0004g0259 a0001c0002t0004g0296 others(6): Show |
9 | HG01496.hp1 HG02895.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.534+418G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943514 | |||||||
| chr14:72943750 | C | T | 1 | a0001c0001t0004g0238 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.534+654C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943750 | |||||||
| chr14:72943795 | G | A | 1 | a0001c0001t0005g0252 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.534+699G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943795 | |||||||
| chr14:72943859 | G | A | 7 | a0003c0006t0001g0026 a0003c0006t0001g0198 a0003c0006t0001g0199 others(4): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.534+763G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943859 | |||||||
| chr14:72943913 | C | T | 64 | a0001c0002t0001g0004 a0001c0002t0001g0014 a0001c0002t0001g0018 others(61): Show |
69 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.534+817C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943913 | |||||||
| chr14:72943934 | T | G | 1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.534+838T>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943934 | |||||||
| chr14:72943942 | G | A | 1 | a0001c0001t0005g0249 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.534+846G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943942 | |||||||
| chr14:72943961 | C | T | 7 | a0003c0006t0001g0026 a0003c0006t0001g0198 a0003c0006t0001g0199 others(4): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.534+865C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943961 | |||||||
| chr14:72943989 | G | T | 2 | a0001c0001t0002g0109 a0001c0001t0002g0111 |
2 | NA18970.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.534+893G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72943989 | |||||||
| chr14:72944085 | C | T | 4 | a0001c0003t0003g0116 a0001c0003t0003g0117 a0001c0003t0003g0127 others(1): Show |
4 | HG02129.hp2 HG02280.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.534+989C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72944085 | |||||||
| chr14:72944337 | C | A | 23 | a0001c0001t0005g0002 a0001c0001t0005g0051 a0001c0001t0005g0214 others(20): Show |
28 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.534+1241C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72944337 | |||||||
| chr14:72944389 | C | T | 4 | a0001c0007t0008g0027 a0001c0007t0008g0258 a0001c0007t0008g0315 others(1): Show |
5 | HG02486.hp1 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.534+1293C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72944389 | |||||||
| chr14:72944690 | G | C | 94 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(91): Show |
107 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.535-1194G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72944690 | |||||||
| chr14:72944736 | G | C | 3 | a0001c0001t0001g0188 a0001c0001t0001g0200 a0001c0001t0001g0204 |
3 | HG02258.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.535-1148G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72944736 | |||||||
| chr14:72944782 | A | T | 23 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(20): Show |
23 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.535-1102A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72944782 | |||||||
| chr14:72944816 | T | C | 229 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(226): Show |
252 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.535-1068T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72944816 | |||||||
| chr14:72944851 | G | A | 1 | a0002c0004t0006g0275 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.535-1033G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72944851 | |||||||
| chr14:72945068 | G | A | 1 | a0001c0003t0003g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.535-816G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945068 | |||||||
| chr14:72945305 | A | G | 1 | a0001c0001t0002g0054 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.535-579A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945305 | |||||||
| chr14:72945395 | T | TA | 7 | a0003c0006t0001g0026 a0003c0006t0001g0198 a0003c0006t0001g0199 others(4): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.535-480dupA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 72945395 | ||||||
| chr14:72945463 | T | G | 34 | a0002c0004t0006g0020 a0002c0004t0006g0024 a0002c0004t0006g0025 others(31): Show |
38 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.535-421T>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945463 | |||||||
| chr14:72945474 | T | TA | 41 | a0001c0001t0003g0229 a0002c0004t0006g0020 a0002c0004t0006g0024 others(38): Show |
45 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.535-395dupA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 72945474 | ||||||
| chr14:72945474 | TA | T | 69 | a0001c0001t0001g0188 a0001c0001t0002g0095 a0001c0002t0001g0004 others(66): Show |
75 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.535-395delA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 72945474 | ||||||
| chr14:72945491 | A | T | 23 | a0001c0001t0005g0002 a0001c0001t0005g0051 a0001c0001t0005g0214 others(20): Show |
28 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.535-393A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945491 | |||||||
| chr14:72945528 | C | T | 1 | a0001c0003t0003g0032 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.535-356C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945528 | |||||||
| chr14:72945531 | C | T | 92 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(89): Show |
105 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.535-353C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945531 | |||||||
| chr14:72945727 | G | A | 1 | a0002c0004t0007g0133 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.535-157G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945727 | |||||||
| chr14:72945753 | C | A | 1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.535-131C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945753 | |||||||
| chr14:72945756 | A | C | 94 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(91): Show |
107 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.535-128A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945756 | |||||||
| chr14:72945779 | G | A | 1 | a0002c0004t0006g0277 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.535-105G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 6/13 | chr14 | 72945779 | |||||||
| chr14:72946031 | C | A | 2 | a0001c0001t0002g0103 a0001c0001t0002g0105 |
2 | HG02602.hp1 HG04204.hp2 |
splice_region_variant&intron_variant | LOW | c.678+4C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72946031 | |||||||
| chr14:72946031 | C | T | 64 | a0001c0002t0001g0004 a0001c0002t0001g0014 a0001c0002t0001g0018 others(61): Show |
69 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(66): Show |
splice_region_variant&intron_variant | LOW | c.678+4C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72946031 | |||||||
| chr14:72946056 | G | A | 3 | a0002c0004t0006g0282 a0002c0004t0006g0291 a0002c0004t0006g0292 |
3 | HG00423.hp1 NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.678+29G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72946056 | |||||||
| chr14:72946072 | GGGTAGTT | G | 40 | a0002c0004t0006g0020 a0002c0004t0006g0024 a0002c0004t0006g0025 others(37): Show |
44 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.678+48_678+54delTA others(5): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr14 | 72946072 | ||||||
| chr14:72946227 | C | CA | 9 | a0001c0001t0001g0138 a0001c0001t0002g0035 a0001c0001t0002g0054 others(6): Show |
9 | HG01175.hp1 HG01891.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.678+218dupA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr14 | 72946227 | ||||||
| chr14:72946227 | CAAAAAAA others(1): Show |
C | 7 | a0003c0006t0001g0026 a0003c0006t0001g0198 a0003c0006t0001g0199 others(4): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.678+211_678+218del others(8): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr14 | 72946227 | ||||||
| chr14:72946265 | C | T | 3 | a0001c0001t0010g0256 a0001c0001t0010g0257 a0008c0013t0012g0306 |
3 | HG02622.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.678+238C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72946265 | |||||||
| chr14:72946562 | G | A | 2 | a0002c0004t0007g0115 a0002c0004t0007g0202 |
2 | HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.678+535G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72946562 | |||||||
| chr14:72946573 | A | G | 1 | a0002c0004t0007g0142 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.678+546A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72946573 | |||||||
| chr14:72946660 | G | C | 2 | a0001c0001t0010g0256 a0001c0001t0010g0257 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.679-482G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72946660 | |||||||
| chr14:72946667 | G | A | 1 | a0008c0013t0012g0306 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.679-475G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72946667 | |||||||
| chr14:72946820 | T | C | 1 | a0002c0004t0006g0020 | 2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.679-322T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72946820 | |||||||
| chr14:72947060 | G | A | 3 | a0001c0002t0001g0206 a0001c0002t0004g0350 a0001c0002t0004g0351 |
3 | HG01891.hp2 HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.679-82G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72947060 | |||||||
| chr14:72947122 | G | A | 23 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(20): Show |
23 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.679-20G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 7/13 | chr14 | 72947122 | |||||||
| chr14:72947217 | T | G | 2 | a0001c0002t0001g0321 a0001c0002t0001g0330 |
2 | NA18951.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.728+26T>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947217 | |||||||
| chr14:72947252 | T | C | 1 | a0001c0003t0003g0131 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.728+61T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947252 | |||||||
| chr14:72947257 | G | C | 64 | a0001c0002t0001g0004 a0001c0002t0001g0014 a0001c0002t0001g0018 others(61): Show |
69 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.728+66G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947257 | |||||||
| chr14:72947438 | G | T | 1 | a0001c0001t0010g0257 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.728+247G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947438 | |||||||
| chr14:72947526 | C | G | 1 | a0001c0003t0003g0032 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.728+335C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947526 | |||||||
| chr14:72947592 | G | A | 1 | a0001c0003t0008g0307 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.728+401G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947592 | |||||||
| chr14:72947608 | A | G | 218 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(215): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.728+417A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947608 | |||||||
| chr14:72947613 | A | G | 263 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(260): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.728+422A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947613 | |||||||
| chr14:72947729 | G | A | 2 | a0001c0002t0001g0189 a0001c0002t0004g0271 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.728+538G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947729 | |||||||
| chr14:72947810 | C | T | 1 | a0001c0001t0002g0094 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.728+619C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947810 | |||||||
| chr14:72947839 | A | G | 1 | a0001c0001t0004g0231 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.728+648A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947839 | |||||||
| chr14:72947853 | G | T | 1 | a0001c0001t0004g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.728+662G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947853 | |||||||
| chr14:72947878 | G | A | 1 | a0001c0001t0004g0304 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.728+687G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947878 | |||||||
| chr14:72947904 | G | C | 2 | a0001c0001t0010g0256 a0001c0001t0010g0257 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.728+713G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947904 | |||||||
| chr14:72947939 | A | G | 178 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(175): Show |
196 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.728+748A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72947939 | |||||||
| chr14:72948076 | G | C | 1 | a0012c0019t0008g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.728+885G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72948076 | |||||||
| chr14:72948119 | A | T | 3 | a0001c0001t0010g0256 a0001c0001t0010g0257 a0008c0013t0012g0306 |
3 | HG02622.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.728+928A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72948119 | |||||||
| chr14:72948187 | G | T | 84 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(81): Show |
89 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.728+996G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72948187 | |||||||
| chr14:72948188 | G | T | 10 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0190 others(7): Show |
10 | HG02071.hp2 HG02080.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.728+997G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72948188 | |||||||
| chr14:72948357 | T | C | 64 | a0001c0002t0001g0004 a0001c0002t0001g0014 a0001c0002t0001g0018 others(61): Show |
69 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.728+1166T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72948357 | |||||||
| chr14:72948525 | G | A | 64 | a0001c0002t0001g0004 a0001c0002t0001g0014 a0001c0002t0001g0018 others(61): Show |
69 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.728+1334G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72948525 | |||||||
| chr14:72948819 | T | A | 1 | a0002c0004t0007g0141 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.728+1628T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72948819 | |||||||
| chr14:72948838 | G | A | 6 | a0004c0005t0002g0068 a0004c0005t0002g0071 a0004c0005t0002g0081 others(3): Show |
6 | NA18944.hp2 NA18971.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.728+1647G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72948838 | |||||||
| chr14:72948955 | T | C | 1 | a0001c0001t0002g0098 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.728+1764T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72948955 | |||||||
| chr14:72949109 | T | C | 263 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(260): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.728+1918T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72949109 | |||||||
| chr14:72949119 | G | C | 1 | a0008c0013t0012g0306 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.728+1928G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72949119 | |||||||
| chr14:72949145 | C | T | 5 | a0001c0001t0002g0093 a0001c0001t0002g0099 a0001c0001t0002g0102 others(2): Show |
5 | HG00140.hp2 HG01496.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.728+1954C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72949145 | |||||||
| chr14:72949156 | G | A | 1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.728+1965G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72949156 | |||||||
| chr14:72949221 | G | T | 5 | a0003c0006t0001g0026 a0003c0006t0001g0198 a0003c0006t0001g0199 others(2): Show |
6 | HG01168.hp2 HG01261.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.728+2030G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72949221 | |||||||
| chr14:72949366 | G | A | 1 | a0001c0001t0004g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.728+2175G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72949366 | |||||||
| chr14:72949378 | C | T | 1 | a0001c0002t0001g0104 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.728+2187C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72949378 | |||||||
| chr14:72949416 | A | G | 114 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(111): Show |
127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.728+2225A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72949416 | |||||||
| chr14:72949426 | A | G | 1 | a0001c0002t0001g0114 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.728+2235A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72949426 | |||||||
| chr14:72950052 | A | G | 1 | a0002c0004t0006g0291 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.729-1746A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950052 | |||||||
| chr14:72950243 | C | T | 19 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(16): Show |
19 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.729-1555C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950243 | |||||||
| chr14:72950399 | G | C | 2 | a0001c0001t0002g0119 a0001c0001t0002g0120 |
2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.729-1399G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950399 | |||||||
| chr14:72950599 | G | C | 1 | a0001c0002t0004g0273 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.729-1199G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950599 | |||||||
| chr14:72950614 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.729-1184C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950614 | |||||||
| chr14:72950684 | G | C | 2 | a0001c0001t0005g0051 a0001c0001t0005g0215 |
2 | HG00544.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.729-1114G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950684 | |||||||
| chr14:72950795 | A | C | 1 | a0001c0002t0001g0330 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.729-1003A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950795 | |||||||
| chr14:72950810 | GT | G | 259 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(256): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.729-979delT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr14 | 72950810 | ||||||
| chr14:72950830 | T | C | 1 | a0001c0001t0002g0095 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.729-968T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950830 | |||||||
| chr14:72950858 | T | A | 1 | a0001c0003t0003g0165 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.729-940T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950858 | |||||||
| chr14:72950958 | C | T | 1 | a0010c0011t0004g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.729-840C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950958 | |||||||
| chr14:72950972 | T | G | 1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.729-826T>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950972 | |||||||
| chr14:72950983 | A | G | 1 | a0001c0001t0001g0012 | 2 | HG02717.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.729-815A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72950983 | |||||||
| chr14:72951036 | G | A | 114 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(111): Show |
127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.729-762G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951036 | |||||||
| chr14:72951155 | A | G | 64 | a0001c0002t0001g0004 a0001c0002t0001g0014 a0001c0002t0001g0018 others(61): Show |
69 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.729-643A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951155 | |||||||
| chr14:72951214 | C | G | 1 | a0001c0001t0004g0265 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.729-584C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951214 | |||||||
| chr14:72951269 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.729-529C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951269 | |||||||
| chr14:72951295 | T | C | 1 | a0001c0001t0004g0266 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.729-503T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951295 | |||||||
| chr14:72951377 | C | T | 4 | a0001c0007t0008g0027 a0001c0007t0008g0258 a0001c0007t0008g0315 others(1): Show |
5 | HG02486.hp1 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.729-421C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951377 | |||||||
| chr14:72951387 | G | A | 40 | a0002c0004t0006g0020 a0002c0004t0006g0024 a0002c0004t0006g0025 others(37): Show |
44 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.729-411G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951387 | |||||||
| chr14:72951492 | T | C | 64 | a0001c0002t0001g0004 a0001c0002t0001g0014 a0001c0002t0001g0018 others(61): Show |
69 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.729-306T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951492 | |||||||
| chr14:72951669 | T | C | 3 | a0001c0001t0010g0256 a0001c0001t0010g0257 a0008c0013t0012g0306 |
3 | HG02622.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.729-129T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951669 | |||||||
| chr14:72951715 | G | A | 2 | a0001c0001t0011g0228 a0001c0001t0011g0247 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.729-83G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951715 | |||||||
| chr14:72951782 | T | C | 1 | a0001c0001t0002g0110 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.729-16T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 8/13 | chr14 | 72951782 | |||||||
| chr14:72952024 | GT | G | 262 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(259): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.808+155delT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952024 | ||||||
| chr14:72952065 | C | T | 1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.808+188C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952065 | |||||||
| chr14:72952136 | G | A | 19 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(16): Show |
19 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.808+259G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952136 | |||||||
| chr14:72952143 | C | T | 2 | a0001c0001t0002g0077 a0001c0001t0002g0112 |
2 | NA18986.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.808+266C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952143 | |||||||
| chr14:72952206 | T | G | 10 | a0001c0001t0003g0229 a0001c0003t0008g0023 a0001c0003t0008g0241 others(7): Show |
12 | HG01074.hp2 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.808+329T>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952206 | |||||||
| chr14:72952229 | C | T | 1 | a0001c0002t0001g0191 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.808+352C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952229 | |||||||
| chr14:72952303 | C | G | 1 | a0002c0004t0006g0025 | 2 | NA19056.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.808+426C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952303 | |||||||
| chr14:72952418 | T | C | 1 | a0001c0002t0004g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.808+541T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952418 | |||||||
| chr14:72952552 | A | G | 114 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(111): Show |
127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.808+675A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952552 | |||||||
| chr14:72952577 | A | T | 2 | a0005c0009t0001g0182 a0005c0009t0001g0183 |
2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.808+700A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952577 | |||||||
| chr14:72952661 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.808+784G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952661 | |||||||
| chr14:72952691 | C | CT | 118 | a0001c0001t0001g0033 a0001c0001t0001g0125 a0001c0001t0001g0184 others(115): Show |
129 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.808+834dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952691 | ||||||
| chr14:72952691 | CT | C | 92 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(89): Show |
105 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.808+834delT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952691 | ||||||
| chr14:72952752 | T | A | 40 | a0002c0004t0006g0020 a0002c0004t0006g0024 a0002c0004t0006g0025 others(37): Show |
44 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.808+875T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952752 | |||||||
| chr14:72952907 | C | T | 40 | a0002c0004t0006g0020 a0002c0004t0006g0024 a0002c0004t0006g0025 others(37): Show |
44 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.808+1030C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952907 | |||||||
| chr14:72952928 | C | T | 47 | a0002c0004t0006g0020 a0002c0004t0006g0024 a0002c0004t0006g0025 others(44): Show |
52 | HG00323.hp1 HG00423.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.808+1051C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952928 | |||||||
| chr14:72952944 | C | T | 1 | a0001c0003t0003g0167 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.808+1067C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952944 | |||||||
| chr14:72952972 | T | A | 1 | a0001c0001t0002g0043 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.808+1095T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952972 | |||||||
| chr14:72952972 | T | C | 160 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(157): Show |
178 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.808+1095T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952972 | |||||||
| chr14:72952982 | A | G | 1 | a0002c0004t0007g0205 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.808+1105A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72952982 | |||||||
| chr14:72952992 | C | CT | 87 | a0001c0001t0001g0138 a0001c0001t0001g0180 a0001c0001t0001g0186 others(84): Show |
100 | HG00408.hp2 HG00544.hp1 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.808+1140dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | ||||||
| chr14:72952992 | C | CTT | 44 | a0001c0001t0002g0007 a0001c0001t0002g0043 a0001c0001t0002g0044 others(41): Show |
52 | HG00099.hp1 HG00639.hp1 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.808+1139_808+1140d others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | ||||||
| chr14:72952992 | C | CTTT | 9 | a0001c0001t0002g0042 a0001c0001t0005g0219 a0001c0001t0005g0220 others(6): Show |
9 | HG00741.hp1 HG01123.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.808+1138_808+1140d others(5): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | ||||||
| chr14:72952992 | C | CTTTTT | 18 | a0001c0001t0001g0230 a0002c0004t0006g0025 a0002c0004t0006g0274 others(15): Show |
20 | HG02135.hp1 HG02148.hp2 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.808+1136_808+1140d others(7): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | ||||||
| chr14:72952992 | C | CTTTTTT | 13 | a0002c0004t0006g0024 a0002c0004t0006g0275 a0002c0004t0006g0281 others(10): Show |
14 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.808+1135_808+1140d others(8): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | ||||||
| chr14:72952992 | C | CTTTTTTT others(3): Show |
2 | a0002c0004t0007g0118 a0002c0004t0007g0203 |
2 | HG00735.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.808+1131_808+1140d others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | ||||||
| chr14:72952992 | C | CTTTTTTT others(4): Show |
2 | a0002c0004t0007g0115 a0002c0004t0007g0207 |
2 | HG01358.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.808+1130_808+1140d others(13): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | ||||||
| chr14:72952992 | C | CTTTTTTT others(5): Show |
1 | a0002c0004t0007g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.808+1129_808+1140d others(14): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | ||||||
| chr14:72952992 | C | CTTTTTTT others(7): Show |
1 | a0002c0004t0007g0205 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.808+1127_808+1140d others(16): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | ||||||
| chr14:72952992 | CTTT | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
6 | HG01243.hp1 HG02717.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.808+1138_808+1140d others(5): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72952992 | ||||||
| chr14:72953184 | A | G | 5 | a0003c0006t0001g0026 a0003c0006t0001g0198 a0003c0006t0001g0199 others(2): Show |
6 | HG01168.hp2 HG01261.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.809-980A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953184 | |||||||
| chr14:72953247 | G | A | 19 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(16): Show |
19 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.809-917G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953247 | |||||||
| chr14:72953253 | G | A | 40 | a0002c0004t0006g0020 a0002c0004t0006g0024 a0002c0004t0006g0025 others(37): Show |
44 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.809-911G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953253 | |||||||
| chr14:72953289 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.809-875C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953289 | |||||||
| chr14:72953621 | G | A | 23 | a0001c0001t0005g0002 a0001c0001t0005g0051 a0001c0001t0005g0214 others(20): Show |
28 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.809-543G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953621 | |||||||
| chr14:72953709 | T | TA | 21 | a0001c0001t0001g0012 a0001c0002t0001g0084 a0001c0002t0001g0192 others(18): Show |
23 | HG00735.hp2 HG00738.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.809-431dupA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953709 | ||||||
| chr14:72953709 | T | TAA | 11 | a0001c0002t0001g0083 a0001c0002t0001g0190 a0002c0004t0006g0276 others(8): Show |
12 | HG02055.hp1 HG02071.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.809-432_809-431dup others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953709 | ||||||
| chr14:72953709 | T | TAAA | 7 | a0001c0001t0002g0103 a0001c0002t0001g0194 a0002c0004t0006g0282 others(4): Show |
7 | HG00423.hp1 HG02818.hp1 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.809-433_809-431dup others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953709 | ||||||
| chr14:72953709 | T | TAAAAAAA others(3): Show |
1 | a0001c0002t0001g0041 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.809-440_809-431dup others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953709 | ||||||
| chr14:72953709 | T | TAAAAAAA others(7): Show |
1 | a0002c0004t0007g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.809-444_809-431dup others(14): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953709 | ||||||
| chr14:72953709 | TAA | T | 22 | a0001c0001t0001g0013 a0001c0001t0001g0121 a0001c0001t0001g0200 others(19): Show |
25 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.809-432_809-431del others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953709 | ||||||
| chr14:72953709 | TAAAAAAA others(5): Show |
T | 1 | a0010c0011t0004g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.809-442_809-431del others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953709 | ||||||
| chr14:72953721 | AAAAAAAA others(16): Show |
A | 3 | a0001c0001t0010g0256 a0001c0001t0010g0257 a0008c0013t0012g0306 |
3 | HG02622.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.809-441_809-419del others(23): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953721 | ||||||
| chr14:72953725 | AAAAAAAA others(4): Show |
A | 2 | a0005c0009t0001g0182 a0005c0009t0001g0183 |
2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.809-437_809-427del others(11): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953725 | ||||||
| chr14:72953725 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0004g0238 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.809-437_809-423del others(15): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953725 | ||||||
| chr14:72953726 | A | T | 1 | a0001c0003t0008g0243 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.809-438A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953726 | |||||||
| chr14:72953726 | AAAAAAAA others(3): Show |
A | 2 | a0001c0002t0004g0259 a0003c0006t0001g0328 |
2 | HG02970.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.809-436_809-427del others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953726 | ||||||
| chr14:72953726 | AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0004g0234 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.809-436_809-421del others(16): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953726 | ||||||
| chr14:72953728 | A | AAT | 9 | a0001c0001t0001g0129 a0001c0001t0001g0313 a0001c0001t0004g0269 others(6): Show |
9 | HG02129.hp2 HG02155.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.809-435_809-434ins others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953728 | ||||||
| chr14:72953728 | A | T | 10 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0309 others(7): Show |
10 | HG01975.hp1 HG02109.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.809-436A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953728 | |||||||
| chr14:72953728 | AAAAAATA others(9): Show |
A | 8 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0232 others(5): Show |
10 | HG01109.hp1 HG01891.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.809-434_809-419del others(16): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953728 | ||||||
| chr14:72953730 | A | AAT | 9 | a0001c0001t0001g0138 a0001c0003t0003g0001 a0001c0003t0003g0016 others(6): Show |
10 | HG02738.hp1 NA18946.hp2 NA18961.hp2 others(7): Show |
intron_variant | MODIFIER | c.809-433_809-432ins others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953730 | ||||||
| chr14:72953730 | A | AATATATA others(11): Show |
1 | a0001c0001t0002g0098 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.809-433_809-432ins others(18): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953730 | ||||||
| chr14:72953730 | A | T | 43 | a0001c0001t0001g0060 a0001c0001t0001g0087 a0001c0001t0001g0126 others(40): Show |
48 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.809-434A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953730 | |||||||
| chr14:72953730 | AAAATATA others(9): Show |
A | 3 | a0001c0001t0004g0231 a0001c0001t0004g0235 a0001c0001t0004g0304 |
3 | HG02559.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.809-432_809-417del others(16): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953730 | ||||||
| chr14:72953731 | AAAT | A | 6 | a0001c0001t0005g0253 a0001c0002t0004g0245 a0001c0002t0004g0340 others(3): Show |
6 | HG01496.hp1 HG03209.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-431_809-429del others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953731 | ||||||
| chr14:72953731 | AAATATAT others(8): Show |
A | 2 | a0001c0001t0011g0228 a0001c0001t0011g0247 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.809-431_809-417del others(15): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953731 | ||||||
| chr14:72953732 | A | AAAAAAAA others(12): Show |
2 | a0001c0001t0002g0005 a0001c0007t0008g0315 |
2 | HG02004.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.809-431_809-430ins others(19): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAAAAA others(18): Show |
1 | a0001c0002t0001g0343 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.809-431_809-430ins others(25): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAAAAA others(3): Show |
3 | a0001c0002t0001g0018 a0001c0002t0001g0191 a0001c0002t0001g0321 |
3 | HG00558.hp2 HG02135.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.809-431_809-430ins others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAAAAA others(7): Show |
1 | a0001c0002t0001g0170 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.809-431_809-430ins others(14): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0002g0119 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.809-431_809-430ins others(15): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAAAAA others(10): Show |
1 | a0001c0001t0002g0059 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.809-431_809-430ins others(17): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0002g0011 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.809-431_809-430ins others(21): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAAAAA others(3): Show |
1 | a0001c0002t0001g0004 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.809-431_809-430ins others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0002g0120 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.809-431_809-430ins others(14): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAAAAA others(9): Show |
2 | a0001c0001t0002g0105 a0001c0002t0001g0330 |
2 | HG02602.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.809-431_809-430ins others(16): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAAAAA others(11): Show |
2 | a0001c0001t0002g0029 a0001c0007t0008g0316 |
2 | HG00735.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.809-431_809-430ins others(18): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAAAAA others(13): Show |
2 | a0001c0001t0002g0065 a0001c0001t0002g0066 |
2 | HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.809-431_809-430ins others(20): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAAAAA others(15): Show |
1 | a0001c0007t0008g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.809-431_809-430ins others(22): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAAAAA others(17): Show |
1 | a0001c0007t0008g0027 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.809-431_809-430ins others(24): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAAAAT others(8): Show |
3 | a0001c0001t0002g0005 a0001c0001t0002g0037 a0001c0001t0002g0095 |
3 | NA18946.hp1 NA18950.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.809-431_809-430ins others(15): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAAAAT others(10): Show |
3 | a0001c0001t0002g0029 a0001c0001t0002g0058 a0001c0001t0002g0094 |
3 | HG00558.hp1 HG00642.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.809-431_809-430ins others(17): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAAAAT others(12): Show |
2 | a0001c0001t0009g0255 a0001c0007t0008g0027 |
2 | HG01175.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.809-431_809-430ins others(19): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAAAAT others(16): Show |
1 | a0001c0001t0002g0110 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.809-431_809-430ins others(23): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAAATA others(3): Show |
1 | a0001c0002t0001g0004 | 3 | NA18971.hp1 NA18988.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.809-431_809-430ins others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAAATA others(13): Show |
1 | a0001c0001t0002g0166 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.809-431_809-430ins others(20): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAATAT others(8): Show |
2 | a0001c0002t0001g0069 a0001c0002t0004g0351 |
2 | HG03486.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.809-431_809-430ins others(15): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAAAATAT others(12): Show |
1 | a0001c0001t0002g0039 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.809-431_809-430ins others(19): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAATATAT others(4): Show |
2 | a0001c0002t0001g0014 a0001c0002t0004g0350 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.809-431_809-430ins others(11): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | AAATATAT others(10): Show |
5 | a0001c0001t0002g0005 a0001c0001t0002g0038 a0001c0001t0002g0171 others(2): Show |
5 | HG02027.hp1 HG02145.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.809-431_809-430ins others(17): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | A | ATATATAT others(4): Show |
1 | a0001c0002t0001g0014 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.809-432_809-431ins others(11): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953732 | |||||||
| chr14:72953732 | A | ATATATAT others(12): Show |
1 | a0001c0001t0002g0107 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.809-432_809-431ins others(19): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953732 | |||||||
| chr14:72953732 | A | T | 85 | a0001c0001t0001g0013 a0001c0001t0001g0033 a0001c0001t0001g0060 others(82): Show |
95 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.809-432A>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953732 | |||||||
| chr14:72953732 | AATAT | A | 12 | a0001c0001t0005g0002 a0001c0001t0005g0051 a0001c0001t0005g0215 others(9): Show |
12 | HG00544.hp1 HG00741.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.809-404_809-401del others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953732 | AATATAT | A | 14 | a0001c0001t0002g0019 a0001c0001t0002g0046 a0001c0001t0002g0062 others(11): Show |
14 | HG01071.hp1 HG01361.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.809-406_809-401del others(6): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953732 | ||||||
| chr14:72953733 | ATAT | A | 3 | a0001c0002t0004g0296 a0001c0002t0004g0347 a0001c0002t0004g0348 |
3 | HG02895.hp1 HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.809-430_809-428del others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953733 | |||||||
| chr14:72953733 | ATATAT | A | 6 | a0001c0001t0002g0010 a0001c0001t0005g0002 a0001c0001t0005g0311 others(3): Show |
6 | HG00099.hp1 HG01175.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.809-430_809-426del others(5): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953733 | |||||||
| chr14:72953733 | ATATATAT | A | 56 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(53): Show |
65 | HG00323.hp2 HG00408.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.809-430_809-424del others(7): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953733 | |||||||
| chr14:72953734 | T | A | 53 | a0001c0001t0002g0103 a0001c0002t0001g0083 a0001c0002t0001g0084 others(50): Show |
57 | HG00099.hp2 HG00423.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.809-430T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953734 | |||||||
| chr14:72953736 | T | A | 37 | a0001c0001t0002g0101 a0001c0002t0001g0083 a0001c0002t0001g0084 others(34): Show |
37 | HG00099.hp2 HG00733.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.809-428T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953736 | |||||||
| chr14:72953738 | T | A | 12 | a0001c0001t0002g0101 a0001c0002t0001g0083 a0001c0002t0001g0084 others(9): Show |
12 | HG01070.hp1 HG01928.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.809-426T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953738 | |||||||
| chr14:72953740 | T | A | 13 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0046 others(10): Show |
14 | HG01071.hp1 HG01175.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.809-424T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953740 | |||||||
| chr14:72953742 | T | A | 59 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(56): Show |
66 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.809-422T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953742 | |||||||
| chr14:72953744 | T | A | 11 | a0001c0001t0002g0100 a0001c0001t0002g0197 a0001c0002t0001g0097 others(8): Show |
11 | HG00323.hp2 HG01069.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.809-420T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953744 | |||||||
| chr14:72953746 | T | A | 3 | a0001c0002t0001g0211 a0001c0002t0001g0322 a0001c0002t0001g0333 |
3 | HG00323.hp2 HG01106.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.809-418T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953746 | |||||||
| chr14:72953755 | ATATATAT others(5): Show |
A | 2 | a0001c0002t0001g0323 a0001c0002t0001g0331 |
2 | HG00733.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.809-408_809-397del others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953755 | |||||||
| chr14:72953757 | ATATATAG others(3): Show |
A | 7 | a0001c0002t0001g0114 a0001c0002t0001g0213 a0001c0002t0001g0319 others(4): Show |
7 | HG00099.hp2 HG00741.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.809-406_809-397del others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953757 | |||||||
| chr14:72953762 | T | A | 2 | a0001c0002t0004g0345 a0001c0002t0004g0349 |
2 | HG01496.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.809-402T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953762 | |||||||
| chr14:72953763 | A | AT | 17 | a0001c0002t0001g0004 a0001c0002t0001g0018 a0001c0002t0001g0036 others(14): Show |
21 | HG00558.hp2 HG02135.hp2 HG02165.hp2 others(18): Show |
intron_variant | MODIFIER | c.809-401_809-400ins others(1): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953763 | |||||||
| chr14:72953763 | A | ATATATAT others(6): Show |
1 | a0001c0003t0008g0023 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.809-401_809-400ins others(13): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953763 | |||||||
| chr14:72953763 | A | G | 30 | a0001c0001t0003g0229 a0001c0001t0005g0002 a0001c0001t0005g0051 others(27): Show |
36 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.809-401A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953763 | |||||||
| chr14:72953763 | AG | A | 6 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0067 others(3): Show |
6 | HG01123.hp1 HG02647.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.809-400delG | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953763 | |||||||
| chr14:72953764 | G | A | 37 | a0001c0002t0001g0004 a0001c0002t0001g0018 a0001c0002t0001g0036 others(34): Show |
42 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.809-400G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953764 | |||||||
| chr14:72953764 | G | T | 14 | a0001c0002t0001g0014 a0001c0002t0001g0070 a0001c0002t0001g0083 others(11): Show |
15 | HG01891.hp2 HG02015.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.809-400G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953764 | |||||||
| chr14:72953765 | T | A | 14 | a0001c0002t0001g0014 a0001c0002t0001g0070 a0001c0002t0001g0083 others(11): Show |
15 | HG01891.hp2 HG02015.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.809-399T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953765 | |||||||
| chr14:72953766 | T | A | 24 | a0001c0002t0001g0004 a0001c0002t0001g0018 a0001c0002t0001g0036 others(21): Show |
29 | HG00558.hp2 HG01123.hp1 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.809-398T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953766 | |||||||
| chr14:72953767 | T | A | 14 | a0001c0002t0001g0014 a0001c0002t0001g0070 a0001c0002t0001g0083 others(11): Show |
15 | HG01891.hp2 HG02015.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.809-397T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953767 | |||||||
| chr14:72953768 | A | ATGG | 2 | a0001c0003t0008g0023 a0001c0003t0008g0241 |
3 | HG02976.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.809-395_809-394ins others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953768 | ||||||
| chr14:72953770 | T | A | 22 | a0001c0002t0001g0004 a0001c0002t0001g0018 a0001c0002t0001g0036 others(19): Show |
26 | HG00558.hp2 HG01123.hp1 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.809-394T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953770 | |||||||
| chr14:72953774 | T | A | 21 | a0001c0002t0001g0004 a0001c0002t0001g0018 a0001c0002t0001g0036 others(18): Show |
25 | HG00558.hp2 HG01123.hp1 HG02135.hp2 others(22): Show |
intron_variant | MODIFIER | c.809-390T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953774 | |||||||
| chr14:72953777 | T | TA | 17 | a0001c0002t0001g0004 a0001c0002t0001g0018 a0001c0002t0001g0036 others(14): Show |
21 | HG02135.hp2 HG02165.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.809-387_809-386ins others(1): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953777 | |||||||
| chr14:72953778 | T | A | 4 | a0001c0002t0001g0067 a0001c0002t0001g0191 a0001c0002t0001g0327 others(1): Show |
4 | HG00558.hp2 HG01123.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-386T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953778 | |||||||
| chr14:72953778 | TTATTTG | T | 4 | a0001c0001t0001g0261 a0001c0001t0004g0265 a0001c0001t0004g0269 others(1): Show |
4 | HG02109.hp2 HG02451.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.809-384_809-379del others(6): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953778 | ||||||
| chr14:72953778 | TTATTTGT others(1): Show |
T | 3 | a0001c0001t0004g0260 a0001c0001t0004g0262 a0001c0001t0004g0268 |
3 | HG01243.hp2 HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.809-384_809-377del others(8): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953778 | ||||||
| chr14:72953778 | TTATTTGT others(3): Show |
T | 6 | a0001c0001t0001g0033 a0001c0001t0001g0201 a0001c0001t0002g0010 others(3): Show |
7 | HG00738.hp2 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.809-384_809-375del others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953778 | ||||||
| chr14:72953778 | TTATTTGT others(5): Show |
T | 8 | a0001c0001t0002g0091 a0001c0002t0001g0322 a0001c0002t0001g0333 others(5): Show |
9 | HG00323.hp2 HG01361.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.809-384_809-373del others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953778 | ||||||
| chr14:72953778 | TTATTTGT others(7): Show |
T | 12 | a0001c0002t0001g0211 a0001c0002t0001g0212 a0001c0002t0001g0298 others(9): Show |
12 | HG01069.hp1 HG01106.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.809-384_809-371del others(14): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953778 | ||||||
| chr14:72953778 | TTATTTGT others(9): Show |
T | 39 | a0001c0002t0001g0097 a0002c0004t0006g0020 a0002c0004t0006g0024 others(36): Show |
42 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.809-384_809-369del others(16): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953778 | ||||||
| chr14:72953779 | T | A | 17 | a0001c0002t0001g0004 a0001c0002t0001g0018 a0001c0002t0001g0036 others(14): Show |
21 | HG02135.hp2 HG02165.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.809-385T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953779 | |||||||
| chr14:72953780 | A | AATT | 3 | a0001c0002t0001g0067 a0001c0002t0001g0327 a0001c0002t0001g0341 |
3 | HG01123.hp1 HG03834.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.809-384_809-383ins others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953780 | |||||||
| chr14:72953780 | A | ATGTGTGT others(5): Show |
1 | a0001c0001t0003g0229 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.809-383_809-382ins others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953780 | ||||||
| chr14:72953780 | A | G | 2 | a0001c0003t0003g0030 a0001c0003t0003g0031 |
2 | HG00642.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.809-384A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953780 | |||||||
| chr14:72953780 | ATTTGTGT others(3): Show |
A | 1 | a0001c0003t0008g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.809-382_809-373del others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953780 | ||||||
| chr14:72953782 | T | A | 4 | a0001c0002t0001g0067 a0001c0002t0001g0191 a0001c0002t0001g0327 others(1): Show |
4 | HG00558.hp2 HG01123.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-382T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953782 | |||||||
| chr14:72953782 | T | G | 5 | a0001c0001t0001g0186 a0001c0001t0003g0229 a0001c0003t0003g0030 others(2): Show |
5 | HG00642.hp1 HG01074.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.809-382T>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953782 | |||||||
| chr14:72953782 | T | TTG | 14 | a0001c0001t0004g0021 a0001c0001t0004g0232 a0001c0003t0003g0001 others(11): Show |
18 | HG00140.hp1 HG01433.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.809-336_809-335dup others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953782 | ||||||
| chr14:72953782 | T | TTGTG | 17 | a0001c0003t0003g0001 a0001c0003t0003g0016 a0001c0003t0003g0017 others(14): Show |
19 | HG00423.hp2 HG02015.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.809-338_809-335dup others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953782 | ||||||
| chr14:72953782 | TTG | T | 23 | a0001c0001t0001g0060 a0001c0001t0001g0087 a0001c0001t0001g0136 others(20): Show |
26 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.809-336_809-335del others(2): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953782 | ||||||
| chr14:72953782 | TTGTG | T | 27 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0037 others(24): Show |
28 | HG00099.hp1 HG00741.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.809-338_809-335del others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953782 | ||||||
| chr14:72953782 | TTGTGTG | T | 90 | a0001c0001t0001g0121 a0001c0001t0001g0180 a0001c0001t0002g0003 others(87): Show |
101 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.809-340_809-335del others(6): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953782 | ||||||
| chr14:72953782 | TTGTGTGT others(1): Show |
T | 19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0125 others(16): Show |
21 | HG00323.hp1 HG00733.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.809-342_809-335del others(8): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953782 | ||||||
| chr14:72953782 | TTGTGTGT others(3): Show |
T | 18 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0200 others(15): Show |
18 | HG00099.hp2 HG00741.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.809-344_809-335del others(10): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953782 | ||||||
| chr14:72953782 | TTGTGTGT others(5): Show |
T | 12 | a0001c0001t0005g0215 a0001c0002t0001g0070 a0001c0002t0001g0083 others(9): Show |
12 | HG00544.hp1 HG02015.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.809-346_809-335del others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953782 | ||||||
| chr14:72953782 | TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0001g0061 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.809-348_809-335del others(14): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953782 | ||||||
| chr14:72953784 | G | A | 19 | a0001c0002t0001g0004 a0001c0002t0001g0018 a0001c0002t0001g0036 others(16): Show |
24 | HG02135.hp2 HG02165.hp2 HG02976.hp1 others(21): Show |
intron_variant | MODIFIER | c.809-380G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953784 | |||||||
| chr14:72953784 | G | T | 4 | a0001c0002t0001g0067 a0001c0002t0001g0191 a0001c0002t0001g0327 others(1): Show |
4 | HG00558.hp2 HG01123.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-380G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953784 | |||||||
| chr14:72953786 | G | A | 5 | a0001c0002t0001g0067 a0001c0002t0001g0191 a0001c0002t0001g0327 others(2): Show |
5 | HG00558.hp2 HG01123.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.809-378G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953786 | |||||||
| chr14:72953786 | G | T | 17 | a0001c0002t0001g0004 a0001c0002t0001g0018 a0001c0002t0001g0036 others(14): Show |
21 | HG02135.hp2 HG02165.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.809-378G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953786 | |||||||
| chr14:72953788 | G | A | 17 | a0001c0002t0001g0004 a0001c0002t0001g0018 a0001c0002t0001g0036 others(14): Show |
21 | HG02135.hp2 HG02165.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.809-376G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953788 | |||||||
| chr14:72953788 | G | T | 5 | a0001c0002t0001g0067 a0001c0002t0001g0191 a0001c0002t0001g0327 others(2): Show |
5 | HG00558.hp2 HG01123.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.809-376G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953788 | |||||||
| chr14:72953790 | G | A | 5 | a0001c0002t0001g0067 a0001c0002t0001g0191 a0001c0002t0001g0327 others(2): Show |
5 | HG00558.hp2 HG01123.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.809-374G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953790 | |||||||
| chr14:72953790 | G | T | 17 | a0001c0002t0001g0004 a0001c0002t0001g0018 a0001c0002t0001g0036 others(14): Show |
21 | HG02135.hp2 HG02165.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.809-374G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953790 | |||||||
| chr14:72953792 | G | A | 17 | a0001c0002t0001g0004 a0001c0002t0001g0018 a0001c0002t0001g0036 others(14): Show |
21 | HG02135.hp2 HG02165.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.809-372G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953792 | |||||||
| chr14:72953792 | G | T | 4 | a0001c0002t0001g0067 a0001c0002t0001g0191 a0001c0002t0001g0327 others(1): Show |
4 | HG00558.hp2 HG01123.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-372G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953792 | |||||||
| chr14:72953794 | G | A | 1 | a0001c0002t0001g0191 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.809-370G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953794 | |||||||
| chr14:72953794 | G | T | 17 | a0001c0002t0001g0004 a0001c0002t0001g0018 a0001c0002t0001g0036 others(14): Show |
21 | HG02135.hp2 HG02165.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.809-370G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953794 | |||||||
| chr14:72953796 | G | T | 1 | a0001c0002t0001g0191 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.809-368G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953796 | |||||||
| chr14:72953800 | GTGTGTGT others(23): Show |
G | 1 | a0002c0004t0006g0277 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.809-362_809-333del others(30): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953800 | ||||||
| chr14:72953808 | G | A | 1 | a0002c0004t0006g0025 | 2 | NA19056.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.809-356G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953808 | |||||||
| chr14:72953812 | G | A | 39 | a0002c0004t0006g0020 a0002c0004t0006g0024 a0002c0004t0006g0274 others(36): Show |
42 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.809-352G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953812 | |||||||
| chr14:72953814 | GTGTGTGT others(9): Show |
G | 1 | a0001c0003t0003g0154 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.809-348_809-333del others(16): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953814 | ||||||
| chr14:72953818 | GTGTGTGT others(5): Show |
G | 4 | a0001c0003t0003g0210 a0001c0007t0008g0027 a0001c0007t0008g0315 others(1): Show |
5 | HG02486.hp1 HG02809.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.809-344_809-333del others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953818 | ||||||
| chr14:72953819 | T | A | 1 | a0001c0001t0004g0234 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.809-345T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953819 | |||||||
| chr14:72953820 | G | A | 2 | a0001c0001t0010g0256 a0001c0001t0010g0257 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.809-344G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953820 | |||||||
| chr14:72953826 | G | A | 163 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(160): Show |
181 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.809-338G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953826 | |||||||
| chr14:72953826 | G | GTGTGTGT others(5): Show |
1 | a0001c0001t0001g0138 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.809-335_809-334ins others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 72953826 | ||||||
| chr14:72953828 | G | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0230 |
2 | HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.809-336G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953828 | |||||||
| chr14:72953830 | A | G | 4 | a0001c0001t0001g0261 a0001c0003t0003g0153 a0001c0003t0008g0246 others(1): Show |
4 | HG02109.hp1 HG02451.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-334A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953830 | |||||||
| chr14:72953934 | G | A | 64 | a0001c0002t0001g0004 a0001c0002t0001g0014 a0001c0002t0001g0018 others(61): Show |
69 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.809-230G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72953934 | |||||||
| chr14:72954025 | C | A | 1 | a0001c0001t0002g0095 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.809-139C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 9/13 | chr14 | 72954025 | |||||||
| chr14:72954307 | C | T | 1 | a0001c0015t0003g0164 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.907+45C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 10/13 | chr14 | 72954307 | |||||||
| chr14:72954353 | A | G | 2 | a0001c0001t0010g0256 a0001c0001t0010g0257 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.908-33A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 10/13 | chr14 | 72954353 | |||||||
| chr14:72954381 | G | A | 1 | a0001c0001t0004g0304 | 1 | HG02965.hp1 | splice_region_variant&intron_variant | LOW | c.908-5G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 10/13 | chr14 | 72954381 | |||||||
| chr14:72954554 | ACTC | A | 95 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(92): Show |
108 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.1005+75_1005+77del others(3): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 72954554 | ||||||
| chr14:72954576 | A | C | 114 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(111): Show |
127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1005+93A>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | chr14 | 72954576 | |||||||
| chr14:72954643 | G | A | 9 | a0001c0002t0004g0245 a0001c0002t0004g0259 a0001c0002t0004g0296 others(6): Show |
9 | HG01496.hp1 HG02895.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1005+160G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | chr14 | 72954643 | |||||||
| chr14:72955035 | C | T | 1 | a0001c0003t0003g0155 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1006-488C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | chr14 | 72955035 | |||||||
| chr14:72955110 | C | CA | 22 | a0001c0001t0001g0138 a0001c0001t0002g0095 a0001c0001t0002g0106 others(19): Show |
24 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1006-398dupA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 72955110 | ||||||
| chr14:72955110 | C | CAAAAA | 40 | a0002c0004t0006g0020 a0002c0004t0006g0024 a0002c0004t0006g0025 others(37): Show |
44 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1006-402_1006-398d others(7): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 72955110 | ||||||
| chr14:72955126 | T | C | 9 | a0001c0002t0004g0245 a0001c0002t0004g0259 a0001c0002t0004g0296 others(6): Show |
9 | HG01496.hp1 HG02895.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1006-397T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | chr14 | 72955126 | |||||||
| chr14:72955171 | G | A | 1 | a0001c0001t0005g0216 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1006-352G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | chr14 | 72955171 | |||||||
| chr14:72955191 | G | T | 41 | a0002c0004t0006g0020 a0002c0004t0006g0024 a0002c0004t0006g0025 others(38): Show |
45 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1006-332G>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | chr14 | 72955191 | |||||||
| chr14:72955204 | T | C | 1 | a0001c0001t0002g0099 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1006-319T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | chr14 | 72955204 | |||||||
| chr14:72955258 | C | G | 343 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0060 others(340): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.1006-265C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | chr14 | 72955258 | |||||||
| chr14:72955277 | G | C | 5 | a0001c0001t0003g0229 a0001c0007t0008g0027 a0001c0007t0008g0258 others(2): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006-246G>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 11/13 | chr14 | 72955277 | |||||||
| chr14:72955734 | G | A | 2 | a0001c0001t0002g0065 a0001c0001t0002g0066 |
2 | HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1179+38G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | chr14 | 72955734 | |||||||
| chr14:72955831 | AGGCCCTG others(3): Show |
A | 1 | a0001c0002t0001g0299 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1179+138_1179+147d others(12): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955831 | ||||||
| chr14:72955846 | A | G | 1 | a0001c0001t0004g0295 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1179+150A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | chr14 | 72955846 | |||||||
| chr14:72955854 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1179+158G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | chr14 | 72955854 | |||||||
| chr14:72955914 | C | CT | 40 | a0001c0001t0001g0012 a0001c0002t0001g0206 a0001c0002t0001g0299 others(37): Show |
44 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1179+244dupT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955914 | ||||||
| chr14:72955914 | C | CTT | 12 | a0001c0007t0008g0027 a0002c0004t0006g0274 a0002c0004t0006g0280 others(9): Show |
13 | HG01168.hp2 HG01261.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1179+243_1179+244d others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955914 | ||||||
| chr14:72955914 | C | CTTT | 6 | a0001c0001t0001g0139 a0001c0001t0001g0310 a0001c0001t0011g0228 others(3): Show |
6 | HG00323.hp1 HG00544.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1179+242_1179+244d others(5): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955914 | ||||||
| chr14:72955914 | C | CTTTT | 6 | a0001c0001t0001g0087 a0001c0001t0001g0136 a0001c0001t0001g0140 others(3): Show |
6 | HG02735.hp1 HG03579.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1179+241_1179+244d others(6): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955914 | ||||||
| chr14:72955914 | C | CTTTTT | 7 | a0001c0001t0001g0137 a0001c0001t0001g0178 a0001c0001t0001g0181 others(4): Show |
7 | HG00408.hp1 HG02056.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179+240_1179+244d others(7): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955914 | ||||||
| chr14:72955914 | C | CTTTTTTT others(10): Show |
1 | a0007c0018t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1179+228_1179+244d others(19): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955914 | ||||||
| chr14:72955914 | CT | C | 148 | a0001c0001t0001g0201 a0001c0001t0001g0261 a0001c0001t0002g0003 others(145): Show |
166 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1179+244delT | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955914 | ||||||
| chr14:72955914 | CTT | C | 92 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(89): Show |
103 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.1179+243_1179+244d others(4): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955914 | ||||||
| chr14:72955914 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0138 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1179+233_1179+244d others(14): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 72955914 | ||||||
| chr14:72955944 | A | G | 2 | a0001c0001t0002g0088 a0001c0001t0002g0106 |
2 | HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1179+248A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | chr14 | 72955944 | |||||||
| chr14:72955946 | G | A | 35 | a0002c0004t0006g0020 a0002c0004t0006g0024 a0002c0004t0006g0025 others(32): Show |
39 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.1179+250G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | chr14 | 72955946 | |||||||
| chr14:72955975 | T | G | 1 | a0001c0001t0005g0249 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1179+279T>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | chr14 | 72955975 | |||||||
| chr14:72956264 | A | G | 3 | a0001c0001t0010g0256 a0001c0001t0010g0257 a0008c0013t0012g0306 |
3 | HG02622.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1180-122A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 12/13 | chr14 | 72956264 | |||||||
| chr14:72956679 | G | A | 1 | a0001c0003t0003g0160 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1294+179G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72956679 | |||||||
| chr14:72956867 | C | T | 1 | a0001c0001t0003g0229 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1294+367C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72956867 | |||||||
| chr14:72956885 | G | A | 4 | a0001c0002t0001g0211 a0001c0002t0001g0212 a0001c0002t0001g0213 others(1): Show |
4 | HG01106.hp2 HG01257.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1294+385G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72956885 | |||||||
| chr14:72956952 | C | T | 7 | a0003c0006t0001g0026 a0003c0006t0001g0198 a0003c0006t0001g0199 others(4): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1294+452C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72956952 | |||||||
| chr14:72957104 | C | G | 114 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(111): Show |
127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1294+604C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72957104 | |||||||
| chr14:72957119 | G | A | 113 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(110): Show |
126 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1294+619G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72957119 | |||||||
| chr14:72957143 | C | T | 2 | a0001c0003t0003g0006 a0001c0003t0003g0159 |
4 | HG00140.hp1 HG01433.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1294+643C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72957143 | |||||||
| chr14:72957161 | G | A | 5 | a0001c0001t0004g0339 a0001c0002t0001g0014 a0001c0002t0001g0206 others(2): Show |
6 | HG01891.hp2 HG02145.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1294+661G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72957161 | |||||||
| chr14:72957163 | T | C | 9 | a0001c0002t0004g0245 a0001c0002t0004g0259 a0001c0002t0004g0296 others(6): Show |
9 | HG01496.hp1 HG02895.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1294+663T>C | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72957163 | |||||||
| chr14:72957211 | AAAAT | A | 19 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(16): Show |
19 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1294+727_1294+730d others(6): Show |
DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr14 | 72957211 | ||||||
| chr14:72957399 | A | G | 13 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0231 others(10): Show |
15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1294+899A>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72957399 | |||||||
| chr14:72957584 | C | G | 5 | a0003c0006t0001g0026 a0003c0006t0001g0198 a0003c0006t0001g0199 others(2): Show |
6 | HG01168.hp2 HG01261.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.1295-1028C>G | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72957584 | |||||||
| chr14:72957701 | G | A | 23 | a0001c0001t0005g0002 a0001c0001t0005g0051 a0001c0001t0005g0214 others(20): Show |
28 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1295-911G>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72957701 | |||||||
| chr14:72957875 | T | A | 3 | a0001c0001t0002g0008 a0001c0001t0002g0035 a0001c0001t0002g0056 |
4 | NA19003.hp1 NA19007.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1295-737T>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72957875 | |||||||
| chr14:72958106 | C | T | 145 | a0001c0001t0003g0229 a0001c0001t0004g0339 a0001c0001t0005g0002 others(142): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.1295-506C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72958106 | |||||||
| chr14:72958112 | C | CA | 24 | a0001c0001t0001g0012 a0001c0001t0001g0060 a0001c0001t0001g0061 others(21): Show |
25 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1295-486dupA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr14 | 72958112 | ||||||
| chr14:72958112 | CA | C | 8 | a0001c0001t0002g0120 a0001c0001t0005g0217 a0001c0001t0005g0248 others(5): Show |
8 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1295-486delA | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr14 | 72958112 | ||||||
| chr14:72958345 | C | T | 114 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(111): Show |
127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1295-267C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72958345 | |||||||
| chr14:72958516 | C | A | 1 | a0001c0001t0009g0195 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1295-96C>A | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72958516 | |||||||
| chr14:72958607 | C | T | 114 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(111): Show |
127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
splice_region_variant&intron_variant | LOW | c.1295-5C>T | DCAF4 | ENSG00000119599.17 | transcript | ENST00000358377.7 | protein_coding | 13/13 | chr14 | 72958607 |