Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10926 |
| ensemblid | ENSG00000006634.8 |
| hgncid | 17364 |
| symbol | DBF4 |
| name | DBF4 zinc finger |
| refseq_nuc | NM_006716.4 |
| refseq_prot | NP_006707.1 |
| ensembl_nuc | ENST00000265728.6 |
| ensembl_prot | ENSP00000265728.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 87876493 |
| end | 87909553 |
| strand | + |
| ver | v1.2 |
| region | chr7:87876493-87909553 |
| region5000 | chr7:87871493-87914553 |
| regionname0 | DBF4_chr7_87876493_87909553 |
| regionname5000 | DBF4_chr7_87871493_87914553 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 674 | 243 | 63 | 46 | 96 | 12 | 24 | 70 | DBF4_chr7_87871493_87914553 | DBF4 | MNSGA others(669): Show |
chr7 | 87871493 | 87914553 |
| a0002 | 0/0 | 674 | 39 | 14 | 7 | 16 | 0 | 2 | 15 | DBF4_chr7_87871493_87914553 | DBF4 | MNSGA others(669): Show |
chr7 | 87871493 | 87914553 |
| a0003 | 0/0 | 674 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | DBF4_chr7_87871493_87914553 | DBF4 | MNSGA others(669): Show |
chr7 | 87871493 | 87914553 |
| a0004 | 0/0 | 674 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | MNSGA others(669): Show |
chr7 | 87871493 | 87914553 |
| a0005 | 0/0 | 674 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | MNSGA others(669): Show |
chr7 | 87871493 | 87914553 |
| a0006 | 0/0 | 674 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | MNSGA others(669): Show |
chr7 | 87871493 | 87914553 |
| a0007 | 0/0 | 674 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | MNSGA others(669): Show |
chr7 | 87871493 | 87914553 |
| a0008 | 0/0 | 271 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | MNSGA others(266): Show |
chr7 | 87871493 | 87914553 |
| a0009 | 0/0 | 674 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | MNSGA others(669): Show |
chr7 | 87871493 | 87914553 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2022 | 228 | 62 | 44 | 84 | 12 | 24 | DBF4_chr7_87871493_87914553 | DBF4 | ATGAA others(2017): Show |
chr7 | 87871493 | 87914553 | ||
| a0001c0003 | 0/0 | 2022 | 12 | 0 | 0 | 12 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | ATGAA others(2017): Show |
chr7 | 87871493 | 87914553 | ||
| a0001c0006 | 0/0 | 2022 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | ATGAA others(2017): Show |
chr7 | 87871493 | 87914553 | ||
| a0001c0007 | 0/0 | 2022 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | ATGAA others(2017): Show |
chr7 | 87871493 | 87914553 | ||
| a0001c0010 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | ATGAA others(2017): Show |
chr7 | 87871493 | 87914553 | ||
| a0002c0002 | 0/0 | 2022 | 39 | 14 | 7 | 16 | 0 | 2 | DBF4_chr7_87871493_87914553 | DBF4 | ATGAA others(2017): Show |
chr7 | 87871493 | 87914553 | ||
| a0003c0004 | 0/0 | 2022 | 2 | 0 | 0 | 2 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | ATGAA others(2017): Show |
chr7 | 87871493 | 87914553 | ||
| a0003c0014 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | ATGAA others(2017): Show |
chr7 | 87871493 | 87914553 | ||
| a0004c0005 | 0/0 | 2022 | 2 | 0 | 2 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | ATGAA others(2017): Show |
chr7 | 87871493 | 87914553 | ||
| a0005c0012 | 0/0 | 2022 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | ATGAA others(2017): Show |
chr7 | 87871493 | 87914553 | ||
| a0006c0009 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | ATGAA others(2017): Show |
chr7 | 87871493 | 87914553 | ||
| a0007c0011 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | ATGAA others(2017): Show |
chr7 | 87871493 | 87914553 | ||
| a0008c0008 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | ATGAA others(2030): Show |
chr7 | 87871493 | 87914553 | ||
| a0009c0013 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | ATGAA others(2017): Show |
chr7 | 87871493 | 87914553 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3655 | 128 | 21 | 24 | 61 | 9 | 11 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3650): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0002 | 0/0 | 3656 | 38 | 13 | 10 | 12 | 0 | 3 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3651): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0004 | 0/0 | 3656 | 14 | 0 | 7 | 0 | 2 | 5 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3651): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0006 | 0/0 | 3656 | 8 | 8 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3651): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0007 | 0/0 | 3655 | 6 | 6 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3650): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0008 | 0/0 | 3655 | 5 | 1 | 1 | 0 | 1 | 2 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3650): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0009 | 0/0 | 3655 | 4 | 4 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3650): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0010 | 0/0 | 3656 | 4 | 4 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3651): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0011 | 0/0 | 3655 | 3 | 0 | 0 | 3 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3650): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0012 | 0/0 | 3655 | 3 | 0 | 0 | 3 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3650): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0013 | 0/0 | 3655 | 2 | 0 | 0 | 2 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3650): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0015 | 0/0 | 3655 | 2 | 0 | 1 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3650): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0016 | 0/0 | 3656 | 2 | 2 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3651): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0017 | 0/0 | 3655 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3650): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0018 | 0/0 | 3656 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3651): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0019 | 0/0 | 3656 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3651): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0020 | 0/0 | 3656 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3651): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0022 | 0/0 | 3655 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3650): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0023 | 0/0 | 3656 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3651): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0024 | 0/0 | 3655 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3650): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0025 | 0/0 | 3655 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3650): Show |
chr7 | 87871493 | 87914553 |
| a0001c0001t0026 | 0/0 | 3655 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3650): Show |
chr7 | 87871493 | 87914553 |
| a0001c0003t0005 | 0/0 | 3656 | 12 | 0 | 0 | 12 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3651): Show |
chr7 | 87871493 | 87914553 |
| a0001c0006t0001 | 0/0 | 3655 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3650): Show |
chr7 | 87871493 | 87914553 |
| a0001c0007t0002 | 0/0 | 3656 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3651): Show |
chr7 | 87871493 | 87914553 |
| a0001c0010t0002 | 0/0 | 3656 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3651): Show |
chr7 | 87871493 | 87914553 |
| a0002c0002t0003 | 0/0 | 3645 | 38 | 14 | 7 | 15 | 0 | 2 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3640): Show |
chr7 | 87871493 | 87914553 |
| a0002c0002t0014 | 0/0 | 3645 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3640): Show |
chr7 | 87871493 | 87914553 |
| a0003c0004t0002 | 0/0 | 3656 | 2 | 0 | 0 | 2 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3651): Show |
chr7 | 87871493 | 87914553 |
| a0003c0014t0005 | 0/0 | 3656 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3651): Show |
chr7 | 87871493 | 87914553 |
| a0004c0005t0001 | 0/0 | 3655 | 2 | 0 | 2 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3650): Show |
chr7 | 87871493 | 87914553 |
| a0005c0012t0003 | 0/0 | 3645 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3640): Show |
chr7 | 87871493 | 87914553 |
| a0006c0009t0021 | 0/0 | 3656 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3651): Show |
chr7 | 87871493 | 87914553 |
| a0007c0011t0002 | 0/0 | 3656 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3651): Show |
chr7 | 87871493 | 87914553 |
| a0008c0008t0014 | 0/0 | 3658 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3653): Show |
chr7 | 87871493 | 87914553 |
| a0009c0013t0001 | 0/0 | 3655 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | AAATC others(3650): Show |
chr7 | 87871493 | 87914553 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 22 | 1 | 2 | 14 | 2 | 2 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0005 | 0/0 | 8 | 1 | 1 | 4 | 1 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0015 | 0/1 | 3 | 0 | 0 | 0 | 2 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0002 | 0/0 | 11 | 4 | 4 | 3 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0004g0008 | 0/0 | 6 | 0 | 3 | 0 | 1 | 2 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0004g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0004g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0006g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0007g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0007g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0008g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0008g0013 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0008g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0009g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0009g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0009g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0010g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0010g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0010g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0011g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0011g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0011g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0012g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0012g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0012g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0013g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0013g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0015g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0015g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0016g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0017g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0018g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0019g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0020g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0022g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0023g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0024g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0025g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0001t0026g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0003t0005g0003 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0003t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0003t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0006t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0007t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0001c0010t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0004 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0007 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0002c0002t0014g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0003c0004t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0003c0004t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0003c0014t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0004c0005t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0004c0005t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0005c0012t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0006c0009t0021g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0007c0011t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0008c0008t0014g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| a0009c0013t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | GBR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0008 | EUR | FIN | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | FIN | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00423 | hp1 | a0001 | c0003 | t0005 | g0172 | EAS | CHS | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00621 | hp1 | a0003 | c0004 | t0002 | g0109 | EAS | CHS | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00639 | hp1 | a0001 | c0006 | t0001 | g0116 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00741 | hp1 | a0001 | c0007 | t0002 | g0161 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0170 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01074 | hp1 | a0001 | c0001 | t0022 | g0026 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01081 | hp2 | a0005 | c0012 | t0003 | g0004 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0035 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0171 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01192 | hp1 | a0002 | c0002 | t0003 | g0049 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01358 | hp1 | a0002 | c0002 | t0003 | g0007 | AMR | CLM | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | CLM | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0168 | AMR | CLM | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01496 | hp1 | a0002 | c0002 | t0003 | g0007 | AMR | CLM | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01496 | hp2 | a0001 | c0001 | t0008 | g0013 | AMR | CLM | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | IBS | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01928 | hp1 | a0004 | c0005 | t0001 | g0097 | AMR | PEL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01952 | hp1 | a0002 | c0002 | t0003 | g0007 | AMR | PEL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PEL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01978 | hp2 | a0002 | c0002 | t0003 | g0007 | AMR | PEL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01981 | hp2 | a0002 | c0002 | t0003 | g0051 | AMR | PEL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01993 | hp1 | a0001 | c0001 | t0015 | g0001 | AMR | PEL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01993 | hp2 | a0004 | c0005 | t0001 | g0005 | AMR | PEL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02071 | hp2 | a0001 | c0001 | t0017 | g0006 | EAS | KHV | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02129 | hp2 | a0002 | c0002 | t0003 | g0011 | EAS | KHV | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CDX | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CDX | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | ACB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02258 | hp1 | a0001 | c0001 | t0018 | g0064 | AFR | ACB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0001 | AFR | ACB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0071 | AFR | ACB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02572 | hp1 | a0001 | c0001 | t0023 | g0039 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0095 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0159 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0133 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02622 | hp2 | a0002 | c0002 | t0003 | g0004 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02647 | hp1 | a0001 | c0010 | t0002 | g0156 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02698 | hp1 | a0001 | c0001 | t0008 | g0013 | SAS | PJL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02717 | hp1 | a0001 | c0001 | t0016 | g0020 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02717 | hp2 | a0002 | c0002 | t0003 | g0164 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0072 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02818 | hp1 | a0002 | c0002 | t0003 | g0045 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02895 | hp2 | a0002 | c0002 | t0003 | g0004 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0033 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02965 | hp2 | a0002 | c0002 | t0003 | g0004 | AFR | ESN | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02970 | hp2 | a0002 | c0002 | t0003 | g0061 | AFR | ESN | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0008 | SAS | PJL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03041 | hp1 | a0001 | c0001 | t0009 | g0122 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | MSL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | MSL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03130 | hp1 | a0002 | c0002 | t0003 | g0004 | AFR | ESN | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0146 | AFR | ESN | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0149 | AFR | ESN | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | ESN | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03209 | hp1 | a0001 | c0001 | t0016 | g0020 | AFR | MSL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03209 | hp2 | a0002 | c0002 | t0003 | g0062 | AFR | MSL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03225 | hp1 | a0002 | c0002 | t0003 | g0004 | AFR | MSL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0134 | AFR | MSL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03453 | hp2 | a0006 | c0009 | t0021 | g0066 | AFR | MSL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0036 | SAS | PJL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0036 | SAS | PJL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03492 | hp2 | a0001 | c0001 | t0019 | g0002 | SAS | PJL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0147 | AFR | ESN | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0019 | AFR | MSL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03654 | hp2 | a0002 | c0002 | t0003 | g0052 | SAS | PJL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0008 | SAS | PJL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03942 | hp1 | a0001 | c0001 | t0024 | g0005 | SAS | BEB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0167 | SAS | BEB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG04184 | hp2 | a0001 | c0001 | t0008 | g0128 | SAS | BEB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG04199 | hp1 | a0002 | c0002 | t0003 | g0048 | SAS | STU | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG04228 | hp2 | a0001 | c0001 | t0026 | g0169 | SAS | STU | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0019 | AFR | YRI | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18522 | hp2 | a0002 | c0002 | t0003 | g0004 | AFR | YRI | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18612 | hp1 | a0001 | c0001 | t0012 | g0044 | EAS | CHB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0088 | AFR | YRI | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18906 | hp2 | a0002 | c0002 | t0003 | g0004 | AFR | YRI | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18939 | hp2 | a0001 | c0001 | t0013 | g0140 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18940 | hp1 | a0002 | c0002 | t0003 | g0055 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18952 | hp1 | a0001 | c0003 | t0005 | g0003 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18959 | hp1 | a0003 | c0004 | t0002 | g0142 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18963 | hp1 | a0003 | c0014 | t0005 | g0040 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18970 | hp1 | a0001 | c0003 | t0005 | g0003 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18973 | hp1 | a0002 | c0002 | t0003 | g0017 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18974 | hp1 | a0002 | c0002 | t0014 | g0018 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18975 | hp1 | a0001 | c0001 | t0012 | g0043 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18975 | hp2 | a0008 | c0008 | t0014 | g0054 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18977 | hp1 | a0002 | c0002 | t0003 | g0056 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18979 | hp2 | a0002 | c0002 | t0003 | g0050 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18983 | hp1 | a0001 | c0001 | t0015 | g0131 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18984 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18984 | hp2 | a0001 | c0001 | t0025 | g0030 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18988 | hp1 | a0001 | c0003 | t0005 | g0003 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18990 | hp2 | a0001 | c0003 | t0005 | g0003 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18992 | hp1 | a0001 | c0003 | t0005 | g0003 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18994 | hp2 | a0002 | c0002 | t0003 | g0018 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18998 | hp2 | a0001 | c0003 | t0005 | g0003 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18999 | hp2 | a0009 | c0013 | t0001 | g0010 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19001 | hp1 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19001 | hp2 | a0002 | c0002 | t0003 | g0017 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19003 | hp1 | a0001 | c0003 | t0005 | g0041 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19005 | hp1 | a0002 | c0002 | t0003 | g0058 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19011 | hp2 | a0001 | c0001 | t0012 | g0042 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19012 | hp2 | a0001 | c0001 | t0013 | g0139 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19030 | hp1 | a0002 | c0002 | t0003 | g0063 | AFR | LWK | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0033 | AFR | LWK | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | LWK | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19043 | hp2 | a0001 | c0001 | t0020 | g0065 | AFR | LWK | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19056 | hp2 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19057 | hp1 | a0002 | c0002 | t0003 | g0060 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19060 | hp2 | a0001 | c0003 | t0005 | g0003 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19062 | hp2 | a0001 | c0003 | t0005 | g0003 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19063 | hp2 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19072 | hp1 | a0002 | c0002 | t0003 | g0057 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19074 | hp2 | a0001 | c0001 | t0011 | g0123 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19082 | hp2 | a0001 | c0003 | t0005 | g0003 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19083 | hp1 | a0002 | c0002 | t0003 | g0059 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19083 | hp2 | a0001 | c0001 | t0011 | g0127 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19087 | hp2 | a0001 | c0003 | t0005 | g0003 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19091 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0001 | AFR | YRI | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA20129 | hp1 | a0002 | c0002 | t0003 | g0004 | AFR | ASW | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | ASW | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0035 | EUR | TSI | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA20805 | hp2 | a0001 | c0001 | t0008 | g0013 | EUR | TSI | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01123 | hp1 | a0002 | c0002 | t0003 | g0053 | AMR | CLM | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0099 | AFR | ACB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG02559 | hp2 | a0002 | c0002 | t0003 | g0004 | AFR | ACB | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | USA | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | USA | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18955 | hp1 | a0007 | c0011 | t0002 | g0002 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0090 | AFR | USA | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0015 | REF | REF | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | DBF4_chr7_87871493_87914553 | DBF4 | chr7 | 87871493 | 87914553 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87888034 | A | C | 1 | a0004 | 2 | HG01928.hp1 HG01993.hp2 |
missense_variant | MODERATE | c.572A>C | p.Lys191Thr | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/12 | 812/3655 | 572/2025 | 191/674 | chr7 | 87888034 | |||
| chr7:87900222 | C | A | 1 | a0008 | 1 | NA18975.hp2 | missense_variant&splice_region_variant | MODERATE | c.682C>A | p.Leu228Ile | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 9/12 | 922/3655 | 682/2025 | 228/674 | chr7 | 87900222 | |||
| chr7:87900228 | A | T | 1 | a0008 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.688A>T | p.Arg230Trp | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 9/12 | 928/3655 | 688/2025 | 230/674 | chr7 | 87900228 | |||
| chr7:87900230 | G | T | 1 | a0008 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.690G>T | p.Arg230Ser | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 9/12 | 930/3655 | 690/2025 | 230/674 | chr7 | 87900230 | |||
| chr7:87900232 | C | T | 1 | a0008 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.692C>T | p.Pro231Leu | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 9/12 | 932/3655 | 692/2025 | 231/674 | chr7 | 87900232 | |||
| chr7:87900237 | T | A | 1 | a0008 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.697T>A | p.Tyr233Asn | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 9/12 | 937/3655 | 697/2025 | 233/674 | chr7 | 87900237 | |||
| chr7:87900238 | A | T | 1 | a0008 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.698A>T | p.Tyr233Phe | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 9/12 | 938/3655 | 698/2025 | 233/674 | chr7 | 87900238 | |||
| chr7:87900289 | G | A | 1 | a0006 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.749G>A | p.Cys250Tyr | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 9/12 | 989/3655 | 749/2025 | 250/674 | chr7 | 87900289 | |||
| chr7:87900321 | A | AGACAAGC others(6): Show |
1 | a0008 | 1 | NA18975.hp2 | frameshift_variant | HIGH | c.781_782insGACAAGCA others(5): Show |
p.Met261fs | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 9/12 | 1022/3655 | 782/2025 | 261/674 | chr7 | 87900321 | |||
| chr7:87900322 | T | A | 1 | a0008 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.782T>A | p.Met261Lys | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 9/12 | 1022/3655 | 782/2025 | 261/674 | chr7 | 87900322 | |||
| chr7:87900334 | C | G | 1 | a0003 | 3 | HG00621.hp1 NA18959.hp1 NA18963.hp1 |
missense_variant | MODERATE | c.794C>G | p.Thr265Ser | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 9/12 | 1034/3655 | 794/2025 | 265/674 | chr7 | 87900334 | |||
| chr7:87900786 | T | C | 1 | a0008 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.832T>C | p.Tyr278His | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/12 | 1072/3655 | 832/2025 | 278/674 | chr7 | 87900786 | |||
| chr7:87900790 | G | T | 1 | a0008 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.836G>T | p.Gly279Val | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/12 | 1076/3655 | 836/2025 | 279/674 | chr7 | 87900790 | |||
| chr7:87900792 | G | C | 1 | a0008 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.838G>C | p.Gly280Arg | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/12 | 1078/3655 | 838/2025 | 280/674 | chr7 | 87900792 | |||
| chr7:87900793 | G | T | 1 | a0008 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.839G>T | p.Gly280Val | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/12 | 1079/3655 | 839/2025 | 280/674 | chr7 | 87900793 | |||
| chr7:87900801 | A | G | 1 | a0008 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.847A>G | p.Ile283Val | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/12 | 1087/3655 | 847/2025 | 283/674 | chr7 | 87900801 | |||
| chr7:87900804 | C | G | 1 | a0008 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.850C>G | p.Gln284Glu | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/12 | 1090/3655 | 850/2025 | 284/674 | chr7 | 87900804 | |||
| chr7:87900825 | A | G | 1 | a0008 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.871A>G | p.Lys291Glu | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/12 | 1111/3655 | 871/2025 | 291/674 | chr7 | 87900825 | |||
| chr7:87900839 | T | A | 1 | a0008 | 1 | NA18975.hp2 | stop_gained | HIGH | c.885T>A | p.Tyr295* | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/12 | 1125/3655 | 885/2025 | 295/674 | chr7 | 87900839 | |||
| chr7:87907328 | T | G | 1 | a0006 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.1190T>G | p.Phe397Cys | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 1430/3655 | 1190/2025 | 397/674 | chr7 | 87907328 | |||
| chr7:87907382 | C | T | 1 | a0009 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.1244C>T | p.Pro415Leu | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 1484/3655 | 1244/2025 | 415/674 | chr7 | 87907382 | |||
| chr7:87907595 | T | A | 1 | a0007 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.1457T>A | p.Ile486Lys | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 1697/3655 | 1457/2025 | 486/674 | chr7 | 87907595 | |||
| chr7:87907756 | C | A | 1 | a0005 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.1618C>A | p.Gln540Lys | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 1858/3655 | 1618/2025 | 540/674 | chr7 | 87907756 | |||
| chr7:87907862 | A | G | 4 | a0002 a0005 a0006 others(1): Show |
42 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(39): Show |
missense_variant | MODERATE | c.1724A>G | p.His575Arg | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 1964/3655 | 1724/2025 | 575/674 | chr7 | 87907862 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87878060 | C | A | 1 | a0001c0006 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.54C>A | p.Ile18Ile | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/12 | 294/3655 | 54/2025 | 18/674 | chr7 | 87878060 | |||
| chr7:87897322 | G | A | 1 | a0001c0007 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.663G>A | p.Lys221Lys | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/12 | 903/3655 | 663/2025 | 221/674 | chr7 | 87897322 | |||
| chr7:87900224 | T | G | 1 | a0008c0008 | 1 | NA18975.hp2 | synonymous_variant | LOW | c.684T>G | p.Leu228Leu | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 9/12 | 924/3655 | 684/2025 | 228/674 | chr7 | 87900224 | |||
| chr7:87900233 | A | T | 1 | a0008c0008 | 1 | NA18975.hp2 | synonymous_variant | LOW | c.693A>T | p.Pro231Pro | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 9/12 | 933/3655 | 693/2025 | 231/674 | chr7 | 87900233 | |||
| chr7:87900791 | T | G | 1 | a0008c0008 | 1 | NA18975.hp2 | synonymous_variant | LOW | c.837T>G | p.Gly279Gly | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/12 | 1077/3655 | 837/2025 | 279/674 | chr7 | 87900791 | |||
| chr7:87900824 | G | A | 1 | a0008c0008 | 1 | NA18975.hp2 | synonymous_variant | LOW | c.870G>A | p.Lys290Lys | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/12 | 1110/3655 | 870/2025 | 290/674 | chr7 | 87900824 | |||
| chr7:87900830 | A | G | 1 | a0008c0008 | 1 | NA18975.hp2 | synonymous_variant | LOW | c.876A>G | p.Lys292Lys | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/12 | 1116/3655 | 876/2025 | 292/674 | chr7 | 87900830 | |||
| chr7:87907353 | T | G | 1 | a0001c0010 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.1215T>G | p.Thr405Thr | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 1455/3655 | 1215/2025 | 405/674 | chr7 | 87907353 | |||
| chr7:87907875 | A | G | 2 | a0001c0003 a0003c0014 |
13 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(10): Show |
synonymous_variant | LOW | c.1737A>G | p.Lys579Lys | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 1977/3655 | 1737/2025 | 579/674 | chr7 | 87907875 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87876555 | G | A | 1 | a0001c0001t0013 | 2 | NA18939.hp2 NA19012.hp2 |
5_prime_UTR_variant | MODIFIER | c.-178G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 1/12 | 178 | chr7 | 87876555 | ||||||
| chr7:87876566 | C | G | 2 | a0001c0001t0004 a0001c0001t0026 |
15 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-167C>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 1/12 | 167 | chr7 | 87876566 | ||||||
| chr7:87876591 | G | A | 1 | a0001c0001t0011 | 3 | NA19001.hp1 NA19074.hp2 NA19083.hp2 |
5_prime_UTR_variant | MODIFIER | c.-142G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 1/12 | 142 | chr7 | 87876591 | ||||||
| chr7:87876600 | A | G | 1 | a0001c0001t0025 | 1 | NA18984.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-133A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 1/12 | chr7 | 87876600 | |||||||
| chr7:87876607 | A | G | 1 | a0001c0001t0024 | 1 | HG03942.hp1 | 5_prime_UTR_variant | MODIFIER | c.-126A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 1/12 | 126 | chr7 | 87876607 | ||||||
| chr7:87876653 | G | A | 1 | a0001c0001t0017 | 1 | HG02071.hp2 | 5_prime_UTR_variant | MODIFIER | c.-80G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 1/12 | 80 | chr7 | 87876653 | ||||||
| chr7:87876657 | G | A | 5 | a0001c0001t0018 a0002c0002t0003 a0002c0002t0014 others(2): Show |
42 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(39): Show |
5_prime_UTR_variant | MODIFIER | c.-76G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 1/12 | 76 | chr7 | 87876657 | ||||||
| chr7:87876686 | G | A | 1 | a0001c0001t0009 | 4 | HG02622.hp1 HG03041.hp1 HG03453.hp1 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-47G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 1/12 | chr7 | 87876686 | |||||||
| chr7:87908196 | A | G | 1 | a0001c0001t0010 | 4 | HG02280.hp2 HG02723.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*33A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 33 | chr7 | 87908196 | ||||||
| chr7:87908218 | T | C | 1 | a0001c0001t0008 | 5 | HG01496.hp2 HG02280.hp1 HG02698.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*55T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 55 | chr7 | 87908218 | ||||||
| chr7:87908388 | G | A | 1 | a0001c0001t0012 | 3 | NA18612.hp1 NA18975.hp1 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*225G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 225 | chr7 | 87908388 | ||||||
| chr7:87908426 | C | G | 2 | a0001c0003t0005 a0003c0014t0005 |
13 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*263C>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 263 | chr7 | 87908426 | ||||||
| chr7:87908530 | G | A | 4 | a0002c0002t0003 a0002c0002t0014 a0005c0012t0003 others(1): Show |
41 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*367G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 367 | chr7 | 87908530 | ||||||
| chr7:87908542 | C | T | 1 | a0001c0001t0007 | 6 | HG02615.hp2 HG02896.hp1 HG03130.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*379C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 379 | chr7 | 87908542 | ||||||
| chr7:87908573 | A | G | 1 | a0001c0001t0016 | 2 | HG02717.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*410A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 410 | chr7 | 87908573 | ||||||
| chr7:87908615 | G | T | 1 | a0001c0001t0023 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*452G>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 452 | chr7 | 87908615 | ||||||
| chr7:87908712 | G | A | 20 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(17): Show |
130 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*549G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 549 | chr7 | 87908712 | ||||||
| chr7:87908748 | C | G | 5 | a0002c0002t0003 a0002c0002t0014 a0005c0012t0003 others(2): Show |
42 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*585C>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 585 | chr7 | 87908748 | ||||||
| chr7:87908769 | C | CT | 20 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(17): Show |
130 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*608dupT | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 609 | INFO_REALIGN_3_PRIME | chr7 | 87908769 | |||||
| chr7:87908779 | A | G | 1 | a0001c0001t0015 | 2 | HG01993.hp1 NA18983.hp1 |
3_prime_UTR_variant | MODIFIER | c.*616A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 616 | chr7 | 87908779 | ||||||
| chr7:87908784 | A | G | 20 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(17): Show |
130 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*621A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 621 | chr7 | 87908784 | ||||||
| chr7:87908806 | TCCTGTGG others(4): Show |
T | 4 | a0002c0002t0003 a0002c0002t0014 a0005c0012t0003 others(1): Show |
41 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*644_*654delCCTGTG others(5): Show |
DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 644 | chr7 | 87908806 | ||||||
| chr7:87908818 | T | A | 4 | a0002c0002t0003 a0002c0002t0014 a0005c0012t0003 others(1): Show |
41 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*655T>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 655 | chr7 | 87908818 | ||||||
| chr7:87909049 | C | T | 1 | a0001c0001t0006 | 8 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*886C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 886 | chr7 | 87909049 | ||||||
| chr7:87909070 | C | T | 1 | a0001c0001t0022 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*907C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 907 | chr7 | 87909070 | ||||||
| chr7:87909268 | T | C | 1 | a0001c0001t0019 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1105T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 1105 | chr7 | 87909268 | ||||||
| chr7:87909326 | C | A | 1 | a0001c0001t0023 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1163C>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 1163 | chr7 | 87909326 | ||||||
| chr7:87909340 | A | C | 1 | a0001c0001t0023 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1177A>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 1177 | chr7 | 87909340 | ||||||
| chr7:87909430 | C | T | 1 | a0001c0001t0023 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1267C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 1267 | chr7 | 87909430 | ||||||
| chr7:87909434 | A | C | 2 | a0002c0002t0014 a0008c0008t0014 |
2 | NA18974.hp1 NA18975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1271A>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 1271 | chr7 | 87909434 | ||||||
| chr7:87909480 | T | G | 1 | a0001c0001t0020 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1317T>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 12/12 | 1317 | chr7 | 87909480 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87876781 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG00438.hp1 | splice_region_variant&intron_variant | LOW | c.46+3A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 1/11 | chr7 | 87876781 | |||||||
| chr7:87877133 | C | T | 1 | a0001c0003t0005g0172 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.46+355C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 1/11 | chr7 | 87877133 | |||||||
| chr7:87877171 | G | C | 1 | a0001c0001t0002g0037 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.46+393G>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 1/11 | chr7 | 87877171 | |||||||
| chr7:87877296 | T | C | 1 | a0001c0001t0001g0016 | 2 | HG01099.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.46+518T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 1/11 | chr7 | 87877296 | |||||||
| chr7:87877796 | A | G | 8 | a0001c0001t0004g0008 a0001c0001t0004g0035 a0001c0001t0004g0036 others(5): Show |
15 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.47-257A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 1/11 | chr7 | 87877796 | |||||||
| chr7:87877885 | G | C | 1 | a0001c0001t0001g0038 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.47-168G>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 1/11 | chr7 | 87877885 | |||||||
| chr7:87877921 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.47-132A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 1/11 | chr7 | 87877921 | |||||||
| chr7:87877931 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.47-122A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 1/11 | chr7 | 87877931 | |||||||
| chr7:87878349 | C | T | 1 | a0002c0002t0003g0164 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.219+124C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87878349 | |||||||
| chr7:87878441 | G | C | 1 | a0001c0001t0023g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.219+216G>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87878441 | |||||||
| chr7:87878534 | T | G | 4 | a0001c0003t0005g0003 a0001c0003t0005g0041 a0001c0003t0005g0172 others(1): Show |
13 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(10): Show |
intron_variant | MODIFIER | c.219+309T>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87878534 | |||||||
| chr7:87878829 | T | A | 3 | a0001c0001t0012g0042 a0001c0001t0012g0043 a0001c0001t0012g0044 |
3 | NA18612.hp1 NA18975.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.219+604T>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87878829 | |||||||
| chr7:87878977 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.219+752A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87878977 | |||||||
| chr7:87879025 | C | T | 2 | a0001c0001t0002g0162 a0001c0007t0002g0161 |
2 | HG00741.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.219+800C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87879025 | |||||||
| chr7:87879149 | G | A | 41 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0067 others(38): Show |
64 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.219+924G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87879149 | |||||||
| chr7:87879163 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.219+938G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87879163 | |||||||
| chr7:87879209 | A | G | 1 | a0001c0001t0002g0160 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.219+984A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87879209 | |||||||
| chr7:87879549 | A | C | 1 | a0001c0001t0007g0159 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.219+1324A>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87879549 | |||||||
| chr7:87879845 | C | T | 2 | a0001c0001t0002g0157 a0001c0001t0002g0158 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.219+1620C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87879845 | |||||||
| chr7:87879846 | G | A | 4 | a0001c0003t0005g0003 a0001c0003t0005g0041 a0001c0003t0005g0172 others(1): Show |
13 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(10): Show |
intron_variant | MODIFIER | c.219+1621G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87879846 | |||||||
| chr7:87879905 | A | T | 1 | a0001c0010t0002g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.219+1680A>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87879905 | |||||||
| chr7:87879951 | C | CA | 46 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0070 others(43): Show |
71 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(68): Show |
intron_variant | MODIFIER | c.219+1742dupA | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 87879951 | ||||||
| chr7:87879951 | C | CAA | 5 | a0001c0003t0005g0003 a0001c0003t0005g0041 a0001c0003t0005g0172 others(2): Show |
14 | HG00423.hp1 HG02818.hp1 NA18952.hp1 others(11): Show |
intron_variant | MODIFIER | c.219+1741_219+1742d others(4): Show |
DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 87879951 | ||||||
| chr7:87879969 | G | T | 1 | a0006c0009t0021g0066 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.219+1744G>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87879969 | |||||||
| chr7:87880037 | C | T | 2 | a0001c0001t0020g0065 a0001c0001t0023g0039 |
2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.219+1812C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87880037 | |||||||
| chr7:87880066 | A | G | 27 | a0001c0001t0018g0064 a0002c0002t0003g0004 a0002c0002t0003g0007 others(24): Show |
43 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.219+1841A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87880066 | |||||||
| chr7:87880082 | TTATCAG | T | 8 | a0001c0001t0004g0008 a0001c0001t0004g0035 a0001c0001t0004g0036 others(5): Show |
15 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.219+1860_219+1865d others(8): Show |
DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 87880082 | ||||||
| chr7:87880240 | G | A | 2 | a0001c0001t0020g0065 a0001c0001t0023g0039 |
2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.219+2015G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87880240 | |||||||
| chr7:87880311 | A | G | 27 | a0001c0001t0018g0064 a0002c0002t0003g0004 a0002c0002t0003g0007 others(24): Show |
43 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.219+2086A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87880311 | |||||||
| chr7:87880366 | T | C | 8 | a0001c0001t0004g0008 a0001c0001t0004g0035 a0001c0001t0004g0036 others(5): Show |
15 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.219+2141T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87880366 | |||||||
| chr7:87880530 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | NA18990.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.219+2305G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87880530 | |||||||
| chr7:87880649 | T | G | 18 | a0002c0002t0003g0007 a0002c0002t0003g0011 a0002c0002t0003g0017 others(15): Show |
26 | HG01123.hp1 HG01192.hp1 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.219+2424T>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87880649 | |||||||
| chr7:87880683 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.219+2458G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87880683 | |||||||
| chr7:87880700 | A | G | 8 | a0001c0001t0001g0015 a0001c0001t0001g0034 a0001c0001t0001g0151 others(5): Show |
10 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.219+2475A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87880700 | |||||||
| chr7:87880927 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.219+2702A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87880927 | |||||||
| chr7:87881030 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.219+2805C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87881030 | |||||||
| chr7:87881104 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+2879G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87881104 | |||||||
| chr7:87881135 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.219+2910G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87881135 | |||||||
| chr7:87881144 | C | T | 1 | a0001c0001t0016g0020 | 2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.219+2919C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87881144 | |||||||
| chr7:87881301 | G | C | 5 | a0001c0001t0002g0046 a0001c0001t0002g0067 a0001c0001t0002g0068 others(2): Show |
5 | HG02572.hp1 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+3076G>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87881301 | |||||||
| chr7:87881330 | C | T | 6 | a0001c0001t0001g0148 a0001c0001t0007g0033 a0001c0001t0007g0146 others(3): Show |
7 | HG02615.hp2 HG02896.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.219+3105C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87881330 | |||||||
| chr7:87881481 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.219+3256T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87881481 | |||||||
| chr7:87881512 | A | T | 4 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(1): Show |
4 | NA18960.hp2 NA18981.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.219+3287A>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87881512 | |||||||
| chr7:87881580 | G | T | 5 | a0001c0001t0002g0046 a0001c0001t0002g0067 a0001c0001t0002g0068 others(2): Show |
5 | HG02572.hp1 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+3355G>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87881580 | |||||||
| chr7:87881621 | G | T | 27 | a0001c0001t0018g0064 a0002c0002t0003g0004 a0002c0002t0003g0007 others(24): Show |
43 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.220-3358G>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87881621 | |||||||
| chr7:87881846 | A | T | 1 | a0003c0004t0002g0142 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.220-3133A>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87881846 | |||||||
| chr7:87881858 | T | G | 1 | a0001c0001t0007g0146 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.220-3121T>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87881858 | |||||||
| chr7:87881869 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.220-3110C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87881869 | |||||||
| chr7:87882081 | A | C | 54 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0067 others(51): Show |
88 | HG00280.hp1 HG00423.hp1 HG01069.hp2 others(85): Show |
intron_variant | MODIFIER | c.220-2898A>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87882081 | |||||||
| chr7:87882120 | A | C | 2 | a0001c0001t0013g0139 a0001c0001t0013g0140 |
2 | NA18939.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.220-2859A>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87882120 | |||||||
| chr7:87882307 | T | C | 1 | a0001c0001t0002g0070 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.220-2672T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87882307 | |||||||
| chr7:87882528 | C | T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0069 a0001c0001t0001g0136 others(3): Show |
8 | HG00544.hp1 HG02165.hp1 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.220-2451C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87882528 | |||||||
| chr7:87882804 | C | A | 2 | a0001c0001t0002g0067 a0001c0001t0002g0068 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.220-2175C>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87882804 | |||||||
| chr7:87883225 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.220-1754A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87883225 | |||||||
| chr7:87883262 | G | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0079 |
3 | HG03710.hp1 HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.220-1717G>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87883262 | |||||||
| chr7:87883421 | A | G | 1 | a0002c0002t0003g0060 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.220-1558A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87883421 | |||||||
| chr7:87883433 | A | T | 1 | a0001c0001t0004g0036 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.220-1546A>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87883433 | |||||||
| chr7:87883523 | C | T | 2 | a0001c0001t0009g0133 a0001c0001t0009g0134 |
2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.220-1456C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87883523 | |||||||
| chr7:87883735 | C | T | 3 | a0001c0001t0002g0046 a0001c0001t0002g0067 a0001c0001t0002g0068 |
3 | HG02630.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.220-1244C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87883735 | |||||||
| chr7:87883753 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.220-1226T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87883753 | |||||||
| chr7:87883808 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.220-1171A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87883808 | |||||||
| chr7:87883875 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.220-1104G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87883875 | |||||||
| chr7:87884034 | G | A | 2 | a0001c0001t0010g0071 a0001c0001t0010g0072 |
2 | HG02280.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.220-945G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87884034 | |||||||
| chr7:87884099 | G | A | 2 | a0001c0001t0002g0067 a0001c0001t0002g0068 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.220-880G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87884099 | |||||||
| chr7:87884173 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.220-806A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87884173 | |||||||
| chr7:87884252 | C | T | 28 | a0001c0001t0010g0072 a0001c0001t0018g0064 a0002c0002t0003g0004 others(25): Show |
44 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.220-727C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87884252 | |||||||
| chr7:87884485 | A | G | 2 | a0001c0001t0020g0065 a0001c0001t0023g0039 |
2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.220-494A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87884485 | |||||||
| chr7:87884677 | G | A | 1 | a0001c0001t0016g0020 | 2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.220-302G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87884677 | |||||||
| chr7:87884804 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.220-175G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 2/11 | chr7 | 87884804 | |||||||
| chr7:87885324 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0013g0139 a0001c0001t0013g0140 |
3 | NA18939.hp2 NA18950.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.399+166G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | chr7 | 87885324 | |||||||
| chr7:87885342 | C | G | 3 | a0002c0002t0003g0011 a0002c0002t0003g0058 a0002c0002t0003g0059 |
5 | HG02129.hp2 NA19005.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+184C>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | chr7 | 87885342 | |||||||
| chr7:87885348 | T | C | 6 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0067 others(3): Show |
6 | HG02572.hp1 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.399+190T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | chr7 | 87885348 | |||||||
| chr7:87885350 | A | G | 3 | a0001c0001t0002g0046 a0001c0001t0002g0067 a0001c0001t0002g0068 |
3 | HG02630.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.399+192A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | chr7 | 87885350 | |||||||
| chr7:87885517 | T | C | 47 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0067 others(44): Show |
79 | HG00280.hp1 HG00423.hp1 HG01069.hp2 others(76): Show |
intron_variant | MODIFIER | c.399+359T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | chr7 | 87885517 | |||||||
| chr7:87885689 | T | A | 1 | a0001c0001t0002g0080 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.399+531T>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | chr7 | 87885689 | |||||||
| chr7:87885690 | A | T | 1 | a0001c0001t0002g0080 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.399+532A>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | chr7 | 87885690 | |||||||
| chr7:87885700 | T | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.399+542T>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | chr7 | 87885700 | |||||||
| chr7:87885730 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.399+572C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | chr7 | 87885730 | |||||||
| chr7:87885856 | G | T | 1 | a0001c0001t0002g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.399+698G>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | chr7 | 87885856 | |||||||
| chr7:87885857 | A | T | 1 | a0001c0001t0002g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.399+699A>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | chr7 | 87885857 | |||||||
| chr7:87885978 | C | T | 1 | a0003c0004t0002g0142 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.399+820C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | chr7 | 87885978 | |||||||
| chr7:87886028 | T | C | 26 | a0001c0001t0018g0064 a0002c0002t0003g0004 a0002c0002t0003g0007 others(23): Show |
42 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.400-816T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | chr7 | 87886028 | |||||||
| chr7:87886271 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0085 a0001c0001t0001g0086 |
4 | HG00738.hp2 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-573G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | chr7 | 87886271 | |||||||
| chr7:87886446 | A | G | 1 | a0001c0001t0015g0131 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.400-398A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | chr7 | 87886446 | |||||||
| chr7:87886460 | G | A | 1 | a0001c0001t0004g0167 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.400-384G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | chr7 | 87886460 | |||||||
| chr7:87886535 | C | CA | 75 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0015 others(72): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.400-286dupA | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 87886535 | ||||||
| chr7:87886535 | C | CAA | 16 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0001g0086 others(13): Show |
16 | HG00423.hp2 HG00735.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.400-287_400-286dup others(2): Show |
DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 87886535 | ||||||
| chr7:87886535 | CAAAAAAA others(5): Show |
C | 4 | a0001c0003t0005g0003 a0001c0003t0005g0041 a0001c0003t0005g0172 others(1): Show |
13 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(10): Show |
intron_variant | MODIFIER | c.400-297_400-286del others(12): Show |
DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 87886535 | ||||||
| chr7:87886535 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0016g0020 | 2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.400-298_400-286del others(13): Show |
DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 87886535 | ||||||
| chr7:87886743 | T | G | 1 | a0001c0001t0002g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.400-101T>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | chr7 | 87886743 | |||||||
| chr7:87886771 | C | T | 1 | a0001c0001t0010g0071 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.400-73C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 3/11 | chr7 | 87886771 | |||||||
| chr7:87887212 | G | C | 27 | a0001c0001t0018g0064 a0002c0002t0003g0004 a0002c0002t0003g0007 others(24): Show |
43 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.451-117G>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 4/11 | chr7 | 87887212 | |||||||
| chr7:87887583 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.520+185T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 5/11 | chr7 | 87887583 | |||||||
| chr7:87887644 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.520+246G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 5/11 | chr7 | 87887644 | |||||||
| chr7:87887820 | G | A | 41 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0067 others(38): Show |
64 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.521-163G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 5/11 | chr7 | 87887820 | |||||||
| chr7:87888112 | C | T | 41 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0067 others(38): Show |
64 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.597+53C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87888112 | |||||||
| chr7:87888154 | G | A | 27 | a0001c0001t0018g0064 a0002c0002t0003g0004 a0002c0002t0003g0007 others(24): Show |
43 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.597+95G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87888154 | |||||||
| chr7:87888267 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.597+208G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87888267 | |||||||
| chr7:87888271 | C | T | 27 | a0001c0001t0018g0064 a0002c0002t0003g0004 a0002c0002t0003g0007 others(24): Show |
43 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.597+212C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87888271 | |||||||
| chr7:87888333 | T | A | 54 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0067 others(51): Show |
88 | HG00280.hp1 HG00423.hp1 HG01069.hp2 others(85): Show |
intron_variant | MODIFIER | c.597+274T>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87888333 | |||||||
| chr7:87888498 | T | C | 1 | a0001c0001t0006g0090 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.597+439T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87888498 | |||||||
| chr7:87889068 | A | G | 1 | a0006c0009t0021g0066 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.597+1009A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87889068 | |||||||
| chr7:87889120 | A | G | 2 | a0001c0001t0001g0130 a0001c0001t0002g0032 |
3 | HG00642.hp1 HG03654.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.597+1061A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87889120 | |||||||
| chr7:87889277 | A | AT | 21 | a0001c0001t0001g0014 a0001c0001t0001g0086 a0001c0001t0001g0129 others(18): Show |
30 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.597+1236dupT | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 87889277 | ||||||
| chr7:87889277 | AT | A | 6 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0106 others(3): Show |
6 | HG01167.hp2 HG02055.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.597+1236delT | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 87889277 | ||||||
| chr7:87889494 | G | T | 1 | a0006c0009t0021g0066 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.597+1435G>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87889494 | |||||||
| chr7:87889632 | C | T | 1 | a0001c0001t0016g0020 | 2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.597+1573C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87889632 | |||||||
| chr7:87890370 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.597+2311C>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87890370 | |||||||
| chr7:87890756 | G | A | 1 | a0001c0010t0002g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.597+2697G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87890756 | |||||||
| chr7:87890770 | A | G | 4 | a0002c0002t0003g0007 a0002c0002t0003g0051 a0002c0002t0003g0055 others(1): Show |
9 | HG01358.hp1 HG01496.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.597+2711A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87890770 | |||||||
| chr7:87890805 | A | C | 7 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0067 others(4): Show |
7 | HG02572.hp1 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.597+2746A>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87890805 | |||||||
| chr7:87890809 | C | T | 2 | a0001c0001t0020g0065 a0001c0001t0023g0039 |
2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.597+2750C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87890809 | |||||||
| chr7:87890878 | C | A | 1 | a0002c0002t0003g0059 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.597+2819C>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87890878 | |||||||
| chr7:87890879 | A | C | 1 | a0002c0002t0003g0059 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.597+2820A>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87890879 | |||||||
| chr7:87890946 | G | T | 8 | a0001c0001t0004g0008 a0001c0001t0004g0035 a0001c0001t0004g0036 others(5): Show |
15 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.597+2887G>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87890946 | |||||||
| chr7:87891263 | T | A | 8 | a0001c0001t0004g0008 a0001c0001t0004g0035 a0001c0001t0004g0036 others(5): Show |
15 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.597+3204T>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87891263 | |||||||
| chr7:87891380 | T | G | 1 | a0001c0001t0002g0092 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.597+3321T>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87891380 | |||||||
| chr7:87891404 | A | C | 27 | a0001c0001t0018g0064 a0002c0002t0003g0004 a0002c0002t0003g0007 others(24): Show |
43 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.597+3345A>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87891404 | |||||||
| chr7:87891693 | T | G | 6 | a0001c0001t0002g0070 a0001c0001t0002g0073 a0001c0001t0010g0019 others(3): Show |
7 | HG02055.hp2 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.597+3634T>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87891693 | |||||||
| chr7:87891702 | A | G | 8 | a0001c0001t0004g0008 a0001c0001t0004g0035 a0001c0001t0004g0036 others(5): Show |
15 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.597+3643A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87891702 | |||||||
| chr7:87892031 | C | G | 1 | a0001c0001t0002g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.597+3972C>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87892031 | |||||||
| chr7:87892377 | T | C | 1 | a0001c0001t0007g0159 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.598-4097T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87892377 | |||||||
| chr7:87892385 | A | G | 2 | a0001c0001t0008g0013 a0001c0001t0008g0128 |
4 | HG01496.hp2 HG02698.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.598-4089A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87892385 | |||||||
| chr7:87892550 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0107 a0001c0001t0001g0108 |
4 | HG01099.hp1 HG01123.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.598-3924G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87892550 | |||||||
| chr7:87892573 | A | G | 1 | a0002c0002t0003g0058 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.598-3901A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87892573 | |||||||
| chr7:87892807 | A | C | 3 | a0001c0001t0001g0076 a0001c0001t0008g0013 a0001c0001t0008g0128 |
5 | HG01261.hp1 HG01496.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-3667A>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87892807 | |||||||
| chr7:87892969 | G | A | 2 | a0003c0004t0002g0109 a0003c0004t0002g0142 |
2 | HG00621.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.598-3505G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87892969 | |||||||
| chr7:87893236 | C | CT | 14 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0125 others(11): Show |
16 | HG00140.hp1 HG00621.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.598-3218dupT | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 87893236 | ||||||
| chr7:87893261 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.598-3213C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87893261 | |||||||
| chr7:87893269 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.598-3205C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87893269 | |||||||
| chr7:87893315 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0173 |
4 | HG00438.hp1 HG02523.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.598-3159G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87893315 | |||||||
| chr7:87893331 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.598-3143C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87893331 | |||||||
| chr7:87893391 | G | A | 27 | a0001c0001t0018g0064 a0002c0002t0003g0004 a0002c0002t0003g0007 others(24): Show |
43 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.598-3083G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87893391 | |||||||
| chr7:87893435 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.598-3039C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87893435 | |||||||
| chr7:87893467 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0091 a0001c0001t0001g0093 |
4 | HG00099.hp2 HG01069.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.598-3007G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87893467 | |||||||
| chr7:87893496 | C | T | 2 | a0001c0001t0002g0067 a0001c0001t0002g0068 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.598-2978C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87893496 | |||||||
| chr7:87893497 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0069 a0001c0001t0001g0136 others(3): Show |
8 | HG00544.hp1 HG02165.hp1 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.598-2977G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87893497 | |||||||
| chr7:87893536 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.598-2938C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87893536 | |||||||
| chr7:87893741 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.598-2733T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87893741 | |||||||
| chr7:87893881 | GT | G | 4 | a0001c0001t0001g0026 a0001c0001t0001g0094 a0001c0001t0001g0111 others(1): Show |
4 | HG01074.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.598-2590delT | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 87893881 | ||||||
| chr7:87894001 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.598-2473A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87894001 | |||||||
| chr7:87894254 | G | A | 8 | a0001c0001t0004g0008 a0001c0001t0004g0035 a0001c0001t0004g0036 others(5): Show |
15 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.598-2220G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87894254 | |||||||
| chr7:87894297 | A | T | 1 | a0001c0001t0001g0107 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.598-2177A>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87894297 | |||||||
| chr7:87894384 | C | A | 27 | a0001c0001t0018g0064 a0002c0002t0003g0004 a0002c0002t0003g0007 others(24): Show |
43 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.598-2090C>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87894384 | |||||||
| chr7:87894473 | T | G | 1 | a0001c0001t0006g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.598-2001T>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87894473 | |||||||
| chr7:87894476 | G | C | 54 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0067 others(51): Show |
88 | HG00280.hp1 HG00423.hp1 HG01069.hp2 others(85): Show |
intron_variant | MODIFIER | c.598-1998G>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87894476 | |||||||
| chr7:87894569 | C | T | 1 | a0001c0001t0002g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.598-1905C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87894569 | |||||||
| chr7:87894617 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.598-1857C>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87894617 | |||||||
| chr7:87894650 | T | C | 1 | a0001c0001t0016g0020 | 2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.598-1824T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87894650 | |||||||
| chr7:87894698 | G | A | 4 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0004g0168 others(1): Show |
6 | HG01167.hp1 HG01169.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.598-1776G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87894698 | |||||||
| chr7:87894992 | T | C | 4 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0009g0133 others(1): Show |
4 | HG02622.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.598-1482T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87894992 | |||||||
| chr7:87895048 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.598-1426C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87895048 | |||||||
| chr7:87895086 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.598-1388A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87895086 | |||||||
| chr7:87895107 | T | G | 1 | a0006c0009t0021g0066 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.598-1367T>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87895107 | |||||||
| chr7:87895133 | T | C | 26 | a0001c0001t0018g0064 a0002c0002t0003g0004 a0002c0002t0003g0007 others(23): Show |
42 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.598-1341T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87895133 | |||||||
| chr7:87895340 | T | C | 4 | a0001c0003t0005g0003 a0001c0003t0005g0041 a0001c0003t0005g0172 others(1): Show |
13 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(10): Show |
intron_variant | MODIFIER | c.598-1134T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87895340 | |||||||
| chr7:87895545 | G | T | 54 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0067 others(51): Show |
88 | HG00280.hp1 HG00423.hp1 HG01069.hp2 others(85): Show |
intron_variant | MODIFIER | c.598-929G>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87895545 | |||||||
| chr7:87895698 | C | G | 4 | a0001c0003t0005g0003 a0001c0003t0005g0041 a0001c0003t0005g0172 others(1): Show |
13 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(10): Show |
intron_variant | MODIFIER | c.598-776C>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87895698 | |||||||
| chr7:87895786 | T | TTA | 27 | a0001c0001t0018g0064 a0002c0002t0003g0004 a0002c0002t0003g0007 others(24): Show |
43 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.598-687_598-686ins others(2): Show |
DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 87895786 | ||||||
| chr7:87895841 | C | A | 1 | a0001c0001t0002g0103 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.598-633C>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87895841 | |||||||
| chr7:87895867 | G | A | 2 | a0001c0001t0002g0067 a0001c0001t0002g0068 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.598-607G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87895867 | |||||||
| chr7:87895914 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG01099.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.598-560C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87895914 | |||||||
| chr7:87896369 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.598-105G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87896369 | |||||||
| chr7:87896462 | A | G | 27 | a0001c0001t0018g0064 a0002c0002t0003g0004 a0002c0002t0003g0007 others(24): Show |
43 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.598-12A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 6/11 | chr7 | 87896462 | |||||||
| chr7:87896621 | G | A | 1 | a0003c0004t0002g0109 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.634+111G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 7/11 | chr7 | 87896621 | |||||||
| chr7:87896695 | T | A | 27 | a0001c0001t0018g0064 a0002c0002t0003g0004 a0002c0002t0003g0007 others(24): Show |
43 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.634+185T>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 7/11 | chr7 | 87896695 | |||||||
| chr7:87896782 | T | C | 3 | a0001c0001t0002g0046 a0001c0001t0002g0067 a0001c0001t0002g0068 |
3 | HG02630.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.634+272T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 7/11 | chr7 | 87896782 | |||||||
| chr7:87897225 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.635-69G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 7/11 | chr7 | 87897225 | |||||||
| chr7:87897235 | T | TA | 93 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(90): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.635-47dupA | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 87897235 | ||||||
| chr7:87897235 | T | TAA | 24 | a0001c0001t0001g0096 a0001c0001t0001g0114 a0001c0001t0001g0115 others(21): Show |
39 | HG00280.hp1 HG00639.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.635-48_635-47dupAA | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 87897235 | ||||||
| chr7:87897235 | T | TAAA | 23 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0002c0002t0003g0007 others(20): Show |
31 | HG01123.hp1 HG01192.hp1 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.635-49_635-47dupAA others(1): Show |
DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 87897235 | ||||||
| chr7:87897440 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.680+101G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87897440 | |||||||
| chr7:87897473 | G | T | 1 | a0001c0001t0001g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.680+134G>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87897473 | |||||||
| chr7:87897474 | C | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0081 a0001c0001t0001g0104 others(2): Show |
6 | HG02132.hp1 NA18970.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.680+135C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87897474 | |||||||
| chr7:87897623 | C | G | 1 | a0001c0001t0002g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.680+284C>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87897623 | |||||||
| chr7:87897735 | A | G | 1 | a0001c0001t0006g0090 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.680+396A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87897735 | |||||||
| chr7:87897783 | T | C | 1 | a0006c0009t0021g0066 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.680+444T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87897783 | |||||||
| chr7:87897857 | G | A | 4 | a0001c0003t0005g0003 a0001c0003t0005g0041 a0001c0003t0005g0172 others(1): Show |
13 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(10): Show |
intron_variant | MODIFIER | c.680+518G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87897857 | |||||||
| chr7:87898021 | G | A | 1 | a0002c0002t0003g0055 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.680+682G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87898021 | |||||||
| chr7:87898069 | T | C | 140 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(137): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.680+730T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87898069 | |||||||
| chr7:87898379 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.680+1040C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87898379 | |||||||
| chr7:87898443 | C | A | 1 | a0001c0001t0001g0114 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.680+1104C>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87898443 | |||||||
| chr7:87898552 | G | A | 26 | a0001c0001t0018g0064 a0002c0002t0003g0004 a0002c0002t0003g0007 others(23): Show |
42 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.680+1213G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87898552 | |||||||
| chr7:87898585 | A | ATGGAGAC others(5): Show |
1 | a0001c0001t0004g0036 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.680+1250_680+1261d others(14): Show |
DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 87898585 | ||||||
| chr7:87898790 | C | CA | 11 | a0001c0001t0002g0070 a0001c0001t0002g0073 a0001c0001t0004g0008 others(8): Show |
19 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.681-1413dupA | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 87898790 | ||||||
| chr7:87898790 | CA | C | 6 | a0001c0001t0001g0101 a0001c0001t0001g0111 a0001c0001t0001g0113 others(3): Show |
6 | HG01169.hp2 HG02165.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.681-1413delA | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 87898790 | ||||||
| chr7:87899187 | G | A | 41 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0067 others(38): Show |
64 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.681-1034G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87899187 | |||||||
| chr7:87899291 | G | A | 27 | a0001c0001t0018g0064 a0002c0002t0003g0004 a0002c0002t0003g0007 others(24): Show |
43 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.681-930G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87899291 | |||||||
| chr7:87899491 | TAAGCATA others(56): Show |
T | 1 | a0008c0008t0014g0054 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.681-728_681-666del others(63): Show |
DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 87899491 | ||||||
| chr7:87899559 | A | G | 1 | a0001c0010t0002g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.681-662A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87899559 | |||||||
| chr7:87899965 | C | T | 2 | a0001c0001t0009g0133 a0001c0001t0009g0134 |
2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.681-256C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87899965 | |||||||
| chr7:87900047 | A | AAAATTTT others(19): Show |
1 | a0008c0008t0014g0054 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.681-171_681-170ins others(26): Show |
DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 87900047 | ||||||
| chr7:87900176 | T | C | 1 | a0008c0008t0014g0054 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.681-45T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87900176 | |||||||
| chr7:87900199 | A | C | 1 | a0008c0008t0014g0054 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.681-22A>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87900199 | |||||||
| chr7:87900203 | G | T | 1 | a0008c0008t0014g0054 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.681-18G>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87900203 | |||||||
| chr7:87900212 | T | A | 1 | a0008c0008t0014g0054 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.681-9T>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87900212 | |||||||
| chr7:87900215 | T | A | 1 | a0008c0008t0014g0054 | 1 | NA18975.hp2 | splice_region_variant&intron_variant | LOW | c.681-6T>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87900215 | |||||||
| chr7:87900218 | T | A | 1 | a0008c0008t0014g0054 | 1 | NA18975.hp2 | splice_region_variant&intron_variant | LOW | c.681-3T>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 8/11 | chr7 | 87900218 | |||||||
| chr7:87900636 | T | G | 1 | a0008c0008t0014g0054 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.810-128T>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 9/11 | chr7 | 87900636 | |||||||
| chr7:87900638 | A | T | 1 | a0008c0008t0014g0054 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.810-126A>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 9/11 | chr7 | 87900638 | |||||||
| chr7:87900746 | A | G | 1 | a0001c0001t0023g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.810-18A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 9/11 | chr7 | 87900746 | |||||||
| chr7:87901026 | A | T | 38 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0032 others(35): Show |
59 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.924+148A>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87901026 | |||||||
| chr7:87901041 | C | T | 1 | a0008c0008t0014g0054 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.924+163C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87901041 | |||||||
| chr7:87901045 | A | T | 1 | a0008c0008t0014g0054 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.924+167A>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87901045 | |||||||
| chr7:87901067 | A | C | 1 | a0008c0008t0014g0054 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.924+189A>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87901067 | |||||||
| chr7:87901150 | T | G | 1 | a0001c0001t0001g0115 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.924+272T>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87901150 | |||||||
| chr7:87901167 | AAAG | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0110 others(1): Show |
7 | HG01243.hp2 HG02055.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.924+295_924+297del others(3): Show |
DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr7 | 87901167 | ||||||
| chr7:87901186 | G | T | 64 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0032 others(61): Show |
101 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.924+308G>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87901186 | |||||||
| chr7:87901313 | T | C | 2 | a0001c0001t0007g0147 a0001c0001t0007g0149 |
2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.924+435T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87901313 | |||||||
| chr7:87901448 | G | T | 2 | a0001c0001t0002g0157 a0001c0001t0002g0158 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.924+570G>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87901448 | |||||||
| chr7:87901805 | T | G | 6 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0067 others(3): Show |
6 | HG02572.hp1 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.924+927T>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87901805 | |||||||
| chr7:87901944 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.924+1066T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87901944 | |||||||
| chr7:87902231 | A | T | 1 | a0001c0001t0002g0158 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.924+1353A>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87902231 | |||||||
| chr7:87902312 | T | G | 1 | a0001c0001t0002g0145 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.924+1434T>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87902312 | |||||||
| chr7:87902318 | CA | C | 4 | a0001c0001t0002g0070 a0001c0001t0002g0073 a0001c0001t0016g0020 others(1): Show |
5 | HG02055.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.924+1441delA | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87902318 | |||||||
| chr7:87902630 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.925-1662A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87902630 | |||||||
| chr7:87902667 | G | T | 1 | a0001c0001t0002g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.925-1625G>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87902667 | |||||||
| chr7:87903009 | C | G | 4 | a0001c0001t0002g0046 a0001c0001t0002g0067 a0001c0001t0002g0068 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.925-1283C>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87903009 | |||||||
| chr7:87903229 | T | C | 1 | a0001c0001t0016g0020 | 2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.925-1063T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87903229 | |||||||
| chr7:87903280 | G | T | 1 | a0001c0001t0007g0159 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.925-1012G>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87903280 | |||||||
| chr7:87903372 | C | T | 1 | a0001c0001t0020g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.925-920C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87903372 | |||||||
| chr7:87903461 | A | G | 1 | a0001c0001t0002g0120 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.925-831A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87903461 | |||||||
| chr7:87903596 | G | A | 36 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0032 others(33): Show |
57 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.925-696G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87903596 | |||||||
| chr7:87903689 | C | CT | 29 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(26): Show |
42 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(39): Show |
intron_variant | MODIFIER | c.925-580dupT | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr7 | 87903689 | ||||||
| chr7:87903689 | C | CTT | 8 | a0001c0001t0001g0022 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG00099.hp1 HG00738.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.925-581_925-580dup others(2): Show |
DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr7 | 87903689 | ||||||
| chr7:87903689 | CT | C | 47 | a0001c0001t0001g0029 a0001c0001t0001g0138 a0001c0001t0002g0002 others(44): Show |
70 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.925-580delT | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr7 | 87903689 | ||||||
| chr7:87903775 | C | G | 82 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0032 others(79): Show |
130 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.925-517C>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87903775 | |||||||
| chr7:87903826 | C | G | 4 | a0001c0003t0005g0003 a0001c0003t0005g0041 a0001c0003t0005g0172 others(1): Show |
13 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(10): Show |
intron_variant | MODIFIER | c.925-466C>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87903826 | |||||||
| chr7:87903989 | CCTGATCT others(4): Show |
C | 5 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0067 others(2): Show |
5 | HG02630.hp2 HG02723.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.925-300_925-290del others(11): Show |
DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr7 | 87903989 | ||||||
| chr7:87904060 | G | A | 1 | a0001c0001t0006g0099 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.925-232G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87904060 | |||||||
| chr7:87904072 | T | G | 1 | a0001c0001t0001g0038 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.925-220T>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 10/11 | chr7 | 87904072 | |||||||
| chr7:87904454 | A | G | 16 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0025 others(13): Show |
25 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.1049+38A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | chr7 | 87904454 | |||||||
| chr7:87904522 | T | C | 82 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0032 others(79): Show |
130 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1049+106T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | chr7 | 87904522 | |||||||
| chr7:87904753 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1049+337A>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | chr7 | 87904753 | |||||||
| chr7:87905026 | C | G | 2 | a0001c0001t0002g0157 a0001c0001t0002g0158 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1049+610C>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | chr7 | 87905026 | |||||||
| chr7:87905048 | A | G | 8 | a0001c0001t0001g0015 a0001c0001t0001g0034 a0001c0001t0001g0151 others(5): Show |
10 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1049+632A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | chr7 | 87905048 | |||||||
| chr7:87905095 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1049+679C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | chr7 | 87905095 | |||||||
| chr7:87905273 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1049+857C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | chr7 | 87905273 | |||||||
| chr7:87905301 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1049+885C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | chr7 | 87905301 | |||||||
| chr7:87905426 | A | C | 71 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0032 others(68): Show |
108 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.1049+1010A>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | chr7 | 87905426 | |||||||
| chr7:87905726 | G | C | 1 | a0001c0001t0002g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1049+1310G>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | chr7 | 87905726 | |||||||
| chr7:87905781 | T | C | 82 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0032 others(79): Show |
130 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1049+1365T>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | chr7 | 87905781 | |||||||
| chr7:87906021 | G | A | 1 | a0001c0001t0023g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1050-1167G>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | chr7 | 87906021 | |||||||
| chr7:87906037 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1050-1151A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | chr7 | 87906037 | |||||||
| chr7:87906084 | A | G | 1 | a0001c0001t0023g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1050-1104A>G | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | chr7 | 87906084 | |||||||
| chr7:87906122 | C | T | 1 | a0004c0005t0001g0097 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1050-1066C>T | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | chr7 | 87906122 | |||||||
| chr7:87906213 | T | A | 1 | a0001c0001t0009g0122 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1050-975T>A | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | chr7 | 87906213 | |||||||
| chr7:87906323 | G | GT | 8 | a0001c0001t0001g0030 a0001c0001t0001g0102 a0001c0001t0002g0037 others(5): Show |
8 | HG01433.hp1 HG01978.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.1050-848dupT | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 87906323 | ||||||
| chr7:87906323 | GT | G | 24 | a0001c0001t0020g0065 a0002c0002t0003g0004 a0002c0002t0003g0007 others(21): Show |
40 | HG01081.hp2 HG01123.hp1 HG01358.hp1 others(37): Show |
intron_variant | MODIFIER | c.1050-848delT | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 87906323 | ||||||
| chr7:87906613 | TAA | T | 4 | a0001c0003t0005g0003 a0001c0003t0005g0041 a0001c0003t0005g0172 others(1): Show |
13 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(10): Show |
intron_variant | MODIFIER | c.1050-572_1050-571d others(4): Show |
DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 87906613 | ||||||
| chr7:87906623 | A | C | 1 | a0006c0009t0021g0066 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1050-565A>C | DBF4 | ENSG00000006634.8 | transcript | ENST00000265728.6 | protein_coding | 11/11 | chr7 | 87906623 |