Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80174 |
| ensemblid | ENSG00000161692.18 |
| hgncid | 17883 |
| symbol | DBF4B |
| name | DBF4 zinc finger B |
| refseq_nuc | NM_145663.3 |
| refseq_prot | NP_663696.1 |
| ensembl_nuc | ENST00000315005.8 |
| ensembl_prot | ENSP00000323663.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 44708665 |
| end | 44752264 |
| strand | + |
| ver | v1.2 |
| region | chr17:44708665-44752264 |
| region5000 | chr17:44703665-44757264 |
| regionname0 | DBF4B_chr17_44708665_44752264 |
| regionname5000 | DBF4B_chr17_44703665_44757264 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 615 | 275 | 81 | 56 | 102 | 10 | 24 | 72 | DBF4B_chr17_44703665_44757264 | DBF4B | MSEPG others(610): Show |
chr17 | 44703665 | 44757264 |
| a0002 | 0/0 | 615 | 8 | 6 | 2 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | MSEPG others(610): Show |
chr17 | 44703665 | 44757264 |
| a0003 | 0/0 | 615 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | MSEPG others(610): Show |
chr17 | 44703665 | 44757264 |
| a0004 | 0/0 | 615 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | MSEPG others(610): Show |
chr17 | 44703665 | 44757264 |
| a0005 | 0/0 | 615 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | MSEPG others(610): Show |
chr17 | 44703665 | 44757264 |
| a0006 | 0/0 | 615 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | MSEPG others(610): Show |
chr17 | 44703665 | 44757264 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1845 | 263 | 74 | 55 | 98 | 10 | 24 | DBF4B_chr17_44703665_44757264 | DBF4B | ATGAG others(1840): Show |
chr17 | 44703665 | 44757264 | ||
| a0001c0003 | 0/0 | 1845 | 8 | 7 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | ATGAG others(1840): Show |
chr17 | 44703665 | 44757264 | ||
| a0001c0005 | 0/0 | 1845 | 2 | 0 | 0 | 2 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | ATGAG others(1840): Show |
chr17 | 44703665 | 44757264 | ||
| a0001c0006 | 0/0 | 1845 | 2 | 0 | 0 | 2 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | ATGAG others(1840): Show |
chr17 | 44703665 | 44757264 | ||
| a0002c0002 | 0/0 | 1845 | 8 | 6 | 2 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | ATGAG others(1840): Show |
chr17 | 44703665 | 44757264 | ||
| a0003c0004 | 0/0 | 1845 | 2 | 2 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | ATGAG others(1840): Show |
chr17 | 44703665 | 44757264 | ||
| a0004c0007 | 0/0 | 1845 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | ATGAG others(1840): Show |
chr17 | 44703665 | 44757264 | ||
| a0005c0008 | 0/0 | 1845 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | ATGAG others(1840): Show |
chr17 | 44703665 | 44757264 | ||
| a0006c0009 | 0/0 | 1845 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | ATGAG others(1840): Show |
chr17 | 44703665 | 44757264 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3015 | 204 | 55 | 36 | 85 | 7 | 20 | DBF4B_chr17_44703665_44757264 | DBF4B | AAACT others(3010): Show |
chr17 | 44703665 | 44757264 |
| a0001c0001t0002 | 0/1 | 3015 | 51 | 14 | 16 | 13 | 3 | 4 | DBF4B_chr17_44703665_44757264 | DBF4B | AAACT others(3010): Show |
chr17 | 44703665 | 44757264 |
| a0001c0001t0003 | 0/0 | 3015 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | AAACT others(3010): Show |
chr17 | 44703665 | 44757264 |
| a0001c0001t0004 | 0/0 | 3015 | 2 | 2 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | AAACT others(3010): Show |
chr17 | 44703665 | 44757264 |
| a0001c0001t0006 | 0/0 | 3015 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | AAACT others(3010): Show |
chr17 | 44703665 | 44757264 |
| a0001c0001t0007 | 0/0 | 3015 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | AAACT others(3010): Show |
chr17 | 44703665 | 44757264 |
| a0001c0001t0008 | 0/0 | 3015 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | AAACT others(3010): Show |
chr17 | 44703665 | 44757264 |
| a0001c0001t0009 | 0/0 | 3015 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | AAACT others(3010): Show |
chr17 | 44703665 | 44757264 |
| a0001c0001t0010 | 0/0 | 3015 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | AAACT others(3010): Show |
chr17 | 44703665 | 44757264 |
| a0001c0003t0001 | 0/0 | 3015 | 8 | 7 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | AAACT others(3010): Show |
chr17 | 44703665 | 44757264 |
| a0001c0005t0001 | 0/0 | 3015 | 2 | 0 | 0 | 2 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | AAACT others(3010): Show |
chr17 | 44703665 | 44757264 |
| a0001c0006t0001 | 0/0 | 3015 | 2 | 0 | 0 | 2 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | AAACT others(3010): Show |
chr17 | 44703665 | 44757264 |
| a0002c0002t0003 | 0/0 | 3015 | 8 | 6 | 2 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | AAACT others(3010): Show |
chr17 | 44703665 | 44757264 |
| a0003c0004t0002 | 0/0 | 3015 | 2 | 2 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | AAACT others(3010): Show |
chr17 | 44703665 | 44757264 |
| a0004c0007t0001 | 0/0 | 3015 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | AAACT others(3010): Show |
chr17 | 44703665 | 44757264 |
| a0005c0008t0002 | 0/0 | 3015 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | AAACT others(3010): Show |
chr17 | 44703665 | 44757264 |
| a0006c0009t0005 | 0/0 | 3015 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | AAACT others(3010): Show |
chr17 | 44703665 | 44757264 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0249 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0046 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0006g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0007g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0008g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0009g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0001t0010g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0003t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0003t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0003t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0005t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0005t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0006t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0001c0006t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0002c0002t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0002c0002t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0002c0002t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0002c0002t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0002c0002t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0002c0002t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0002c0002t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0002c0002t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0003c0004t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0003c0004t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0004c0007t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0005c0008t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| a0006c0009t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | GBR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | GBR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | GBR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0029 | EUR | FIN | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0242 | EUR | FIN | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01099 | hp1 | a0004 | c0007 | t0001 | g0160 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01167 | hp1 | a0002 | c0002 | t0003 | g0263 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01169 | hp1 | a0002 | c0002 | t0003 | g0260 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0208 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01256 | hp2 | a0001 | c0001 | t0009 | g0119 | AMR | CLM | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0055 | EUR | IBS | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | IBS | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0054 | EUR | IBS | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | IBS | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01891 | hp1 | a0002 | c0002 | t0003 | g0265 | AFR | ACB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01952 | hp1 | a0005 | c0008 | t0002 | g0032 | AMR | PEL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01978 | hp2 | a0001 | c0001 | t0008 | g0168 | AMR | PEL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02148 | hp2 | a0001 | c0001 | t0007 | g0267 | AMR | PEL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CDX | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CDX | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CDX | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CDX | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0206 | AFR | ACB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0268 | AFR | ACB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0211 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02615 | hp1 | a0002 | c0002 | t0003 | g0264 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02615 | hp2 | a0003 | c0004 | t0002 | g0007 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02622 | hp1 | a0002 | c0002 | t0003 | g0259 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02809 | hp2 | a0002 | c0002 | t0003 | g0257 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0258 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0205 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0269 | AFR | ESN | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02976 | hp2 | a0002 | c0002 | t0003 | g0262 | AFR | ESN | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03098 | hp2 | a0003 | c0004 | t0002 | g0005 | AFR | MSL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | ESN | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0271 | AFR | ESN | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | MSL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | ESN | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0204 | AFR | ESN | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | MSL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0207 | AFR | YRI | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | YRI | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | YRI | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18940 | hp2 | a0001 | c0005 | t0001 | g0102 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18974 | hp1 | a0001 | c0006 | t0001 | g0066 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19009 | hp2 | a0001 | c0005 | t0001 | g0096 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | LWK | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19030 | hp2 | a0006 | c0009 | t0005 | g0272 | AFR | LWK | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19043 | hp1 | a0002 | c0002 | t0003 | g0261 | AFR | LWK | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | LWK | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19059 | hp2 | a0001 | c0006 | t0001 | g0065 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | YRI | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | YRI | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ASW | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ASW | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | GIH | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | GIH | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | USA | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | USA | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | USA | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | LWK | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0273 | AFR | LWK | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0046 | REF | REF | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0249 | REF | REF | DBF4B_chr17_44703665_44757264 | DBF4B | chr17 | 44703665 | 44757264 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44709343 | G | A | 1 | a0004 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.59G>A | p.Ser20Asn | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/14 | 215/3015 | 59/1848 | 20/615 | chr17 | 44709343 | |||
| chr17:44732206 | G | A | 1 | a0003 | 2 | HG02615.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.497G>A | p.Gly166Asp | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 6/14 | 653/3015 | 497/1848 | 166/615 | chr17 | 44732206 | |||
| chr17:44734129 | T | C | 1 | a0002 | 8 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(5): Show |
missense_variant | MODERATE | c.596T>C | p.Leu199Ser | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/14 | 752/3015 | 596/1848 | 199/615 | chr17 | 44734129 | |||
| chr17:44751047 | C | T | 1 | a0006 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1642C>T | p.Leu548Phe | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 14/14 | 1798/3015 | 1642/1848 | 548/615 | chr17 | 44751047 | |||
| chr17:44751116 | T | A | 1 | a0005 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.1711T>A | p.Ser571Thr | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 14/14 | 1867/3015 | 1711/1848 | 571/615 | chr17 | 44751116 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44722944 | C | T | 1 | a0001c0003 | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
synonymous_variant | LOW | c.147C>T | p.Ser49Ser | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/14 | 303/3015 | 147/1848 | 49/615 | chr17 | 44722944 | |||
| chr17:44734115 | G | A | 1 | a0001c0005 | 2 | NA18940.hp2 NA19009.hp2 |
synonymous_variant | LOW | c.582G>A | p.Leu194Leu | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/14 | 738/3015 | 582/1848 | 194/615 | chr17 | 44734115 | |||
| chr17:44747429 | A | G | 1 | a0001c0006 | 2 | NA18974.hp1 NA19059.hp2 |
synonymous_variant | LOW | c.978A>G | p.Glu326Glu | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 12/14 | 1134/3015 | 978/1848 | 326/615 | chr17 | 44747429 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44708697 | T | G | 2 | a0001c0001t0003 a0002c0002t0003 |
9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-124T>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 1/14 | 124 | chr17 | 44708697 | ||||||
| chr17:44708740 | G | C | 1 | a0001c0001t0004 | 2 | HG02451.hp2 HG02970.hp1 |
5_prime_UTR_variant | MODIFIER | c.-81G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 1/14 | 81 | chr17 | 44708740 | ||||||
| chr17:44708755 | G | C | 2 | a0001c0001t0006 a0006c0009t0005 |
2 | NA19030.hp2 NA21309.hp2 |
5_prime_UTR_variant | MODIFIER | c.-66G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 1/14 | 66 | chr17 | 44708755 | ||||||
| chr17:44708802 | G | A | 1 | a0001c0001t0007 | 1 | HG02148.hp2 | 5_prime_UTR_variant | MODIFIER | c.-19G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 1/14 | 19 | chr17 | 44708802 | ||||||
| chr17:44751711 | C | T | 1 | a0001c0001t0010 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*458C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 14/14 | 458 | chr17 | 44751711 | ||||||
| chr17:44751930 | G | A | 1 | a0001c0001t0008 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*677G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 14/14 | 677 | chr17 | 44751930 | ||||||
| chr17:44751985 | G | A | 1 | a0001c0001t0009 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*732G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 14/14 | 732 | chr17 | 44751985 | ||||||
| chr17:44752115 | G | A | 1 | a0006c0009t0005 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*862G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 14/14 | 862 | chr17 | 44752115 | ||||||
| chr17:44752259 | C | G | 3 | a0001c0001t0002 a0003c0004t0002 a0005c0008t0002 |
53 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1006C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 14/14 | 1006 | chr17 | 44752259 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44708840 | G | T | 11 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(8): Show |
11 | HG00558.hp2 HG02145.hp2 HG02630.hp2 others(8): Show |
splice_donor_variant&intron_variant | HIGH | c.19+1G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 1/13 | chr17 | 44708840 | |||||||
| chr17:44708845 | G | C | 51 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(48): Show |
51 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(48): Show |
splice_region_variant&intron_variant | LOW | c.19+6G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 1/13 | chr17 | 44708845 | |||||||
| chr17:44708910 | G | T | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.19+71G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 1/13 | chr17 | 44708910 | |||||||
| chr17:44708917 | G | C | 1 | a0001c0001t0001g0057 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.19+78G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 1/13 | chr17 | 44708917 | |||||||
| chr17:44708927 | A | G | 1 | a0001c0001t0010g0271 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.19+88A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 1/13 | chr17 | 44708927 | |||||||
| chr17:44708982 | C | T | 3 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0056 |
3 | HG01515.hp1 HG01517.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.19+143C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 1/13 | chr17 | 44708982 | |||||||
| chr17:44709031 | G | A | 1 | a0003c0004t0002g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.19+192G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 1/13 | chr17 | 44709031 | |||||||
| chr17:44709094 | C | T | 1 | a0001c0001t0006g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.20-210C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 1/13 | chr17 | 44709094 | |||||||
| chr17:44709144 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.20-160C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 1/13 | chr17 | 44709144 | |||||||
| chr17:44709195 | C | T | 3 | a0001c0001t0001g0284 a0001c0001t0004g0268 a0001c0001t0004g0269 |
3 | HG02145.hp2 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.20-109C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 1/13 | chr17 | 44709195 | |||||||
| chr17:44709262 | G | C | 47 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 others(44): Show |
47 | HG00140.hp2 HG01167.hp2 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.20-42G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 1/13 | chr17 | 44709262 | |||||||
| chr17:44709293 | T | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | NA18967.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.20-11T>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 1/13 | chr17 | 44709293 | |||||||
| chr17:44709294 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | NA18967.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.20-10C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 1/13 | chr17 | 44709294 | |||||||
| chr17:44709586 | G | T | 1 | a0001c0001t0007g0267 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.82+220G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44709586 | |||||||
| chr17:44709590 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.82+224G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44709590 | |||||||
| chr17:44709644 | T | A | 3 | a0001c0001t0002g0006 a0003c0004t0002g0005 a0003c0004t0002g0007 |
3 | HG02615.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.82+278T>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44709644 | |||||||
| chr17:44709646 | T | C | 1 | a0006c0009t0005g0272 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.82+280T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44709646 | |||||||
| chr17:44709944 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.82+578C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44709944 | |||||||
| chr17:44709955 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.82+589C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44709955 | |||||||
| chr17:44709965 | A | G | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.82+599A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44709965 | |||||||
| chr17:44710001 | A | G | 15 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(12): Show |
15 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.82+635A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44710001 | |||||||
| chr17:44710710 | C | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0104 others(91): Show |
95 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.82+1344C>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44710710 | |||||||
| chr17:44710728 | G | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
164 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.82+1362G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44710728 | |||||||
| chr17:44710972 | T | C | 7 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(4): Show |
7 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.82+1606T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44710972 | |||||||
| chr17:44710976 | A | AT | 34 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(31): Show |
34 | HG00673.hp2 HG01099.hp2 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.82+1637dupT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44710976 | ||||||
| chr17:44710976 | AT | A | 55 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 others(52): Show |
55 | HG00140.hp2 HG00323.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.82+1637delT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44710976 | ||||||
| chr17:44710976 | ATT | A | 8 | a0001c0001t0003g0258 a0002c0002t0003g0257 a0002c0002t0003g0259 others(5): Show |
8 | HG01167.hp1 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.82+1636_82+1637del others(2): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44710976 | ||||||
| chr17:44710976 | ATTTTTTT | A | 15 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(12): Show |
15 | HG00621.hp2 HG00639.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.82+1631_82+1637del others(7): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44710976 | ||||||
| chr17:44710976 | ATTTTTTT others(3): Show |
A | 3 | a0001c0001t0001g0105 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG03239.hp1 NA18940.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.82+1628_82+1637del others(10): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44710976 | ||||||
| chr17:44710976 | ATTTTTTT others(4): Show |
A | 67 | a0001c0001t0001g0057 a0001c0001t0001g0104 a0001c0001t0001g0109 others(64): Show |
67 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.82+1627_82+1637del others(11): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44710976 | ||||||
| chr17:44710976 | ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | NA19005.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.82+1626_82+1637del others(12): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44710976 | ||||||
| chr17:44711003 | T | G | 1 | a0001c0001t0001g0090 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.82+1637T>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44711003 | |||||||
| chr17:44711004 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.82+1638G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44711004 | |||||||
| chr17:44711005 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.82+1639A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44711005 | |||||||
| chr17:44711034 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.82+1668G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44711034 | |||||||
| chr17:44711222 | G | A | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG01074.hp1 HG01358.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+1856G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44711222 | |||||||
| chr17:44711289 | A | T | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.82+1923A>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44711289 | |||||||
| chr17:44711456 | C | G | 1 | a0001c0001t0010g0271 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.82+2090C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44711456 | |||||||
| chr17:44711541 | G | T | 1 | a0002c0002t0003g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.82+2175G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44711541 | |||||||
| chr17:44711571 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.82+2205G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44711571 | |||||||
| chr17:44711594 | C | CT | 13 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(10): Show |
13 | HG00621.hp2 HG00639.hp1 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.82+2229dupT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44711594 | ||||||
| chr17:44711811 | C | T | 2 | a0001c0001t0002g0037 a0001c0001t0002g0038 |
2 | HG00642.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.82+2445C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44711811 | |||||||
| chr17:44711888 | T | A | 1 | a0001c0001t0002g0012 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.82+2522T>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44711888 | |||||||
| chr17:44711957 | C | T | 9 | a0001c0001t0003g0258 a0002c0002t0003g0257 a0002c0002t0003g0259 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.82+2591C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44711957 | |||||||
| chr17:44712104 | G | GA | 15 | a0001c0001t0001g0105 a0001c0001t0001g0111 a0001c0001t0001g0112 others(12): Show |
15 | HG01167.hp1 HG01169.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.82+2752dupA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44712104 | ||||||
| chr17:44712145 | G | A | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.82+2779G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44712145 | |||||||
| chr17:44712153 | A | G | 43 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(40): Show |
43 | HG00140.hp2 HG01167.hp2 HG01943.hp1 others(40): Show |
intron_variant | MODIFIER | c.82+2787A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44712153 | |||||||
| chr17:44712219 | A | G | 1 | a0001c0001t0006g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.82+2853A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44712219 | |||||||
| chr17:44712301 | C | CT | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0057 others(98): Show |
103 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.82+2958dupT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44712301 | ||||||
| chr17:44712301 | C | CTT | 9 | a0001c0001t0001g0105 a0001c0001t0001g0170 a0001c0001t0001g0171 others(6): Show |
9 | HG00642.hp2 HG01109.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.82+2957_82+2958dup others(2): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44712301 | ||||||
| chr17:44712301 | CT | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0195 others(78): Show |
81 | HG00323.hp1 HG00323.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.82+2958delT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44712301 | ||||||
| chr17:44712301 | CTT | C | 45 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 others(42): Show |
45 | HG00140.hp2 HG01167.hp2 HG01943.hp1 others(42): Show |
intron_variant | MODIFIER | c.82+2957_82+2958del others(2): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44712301 | ||||||
| chr17:44712336 | ACT | A | 3 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 |
3 | HG03041.hp1 HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.82+2974_82+2975del others(2): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44712336 | ||||||
| chr17:44712341 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.82+2975C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44712341 | |||||||
| chr17:44712407 | C | T | 5 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+3041C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44712407 | |||||||
| chr17:44712414 | C | T | 1 | a0006c0009t0005g0272 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.82+3048C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44712414 | |||||||
| chr17:44712735 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0103 |
2 | NA18948.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.82+3369G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44712735 | |||||||
| chr17:44712745 | C | CT | 47 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 others(44): Show |
47 | HG00140.hp2 HG01167.hp2 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.82+3389dupT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44712745 | ||||||
| chr17:44712854 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0104 others(91): Show |
95 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.82+3488C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44712854 | |||||||
| chr17:44712855 | G | A | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.82+3489G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44712855 | |||||||
| chr17:44712872 | G | A | 53 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0002g0006 others(50): Show |
53 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.82+3506G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44712872 | |||||||
| chr17:44713034 | C | CT | 26 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(23): Show |
26 | HG00558.hp2 HG00639.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.82+3691dupT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44713034 | ||||||
| chr17:44713034 | CT | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0057 others(23): Show |
26 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.82+3691delT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44713034 | ||||||
| chr17:44713083 | A | G | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.82+3717A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713083 | |||||||
| chr17:44713088 | G | A | 47 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 others(44): Show |
47 | HG00140.hp2 HG01167.hp2 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.82+3722G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713088 | |||||||
| chr17:44713101 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.82+3735G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713101 | |||||||
| chr17:44713132 | C | T | 1 | a0001c0003t0001g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.82+3766C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713132 | |||||||
| chr17:44713142 | C | A | 10 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(7): Show |
10 | HG00642.hp1 HG01069.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.82+3776C>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713142 | |||||||
| chr17:44713191 | G | A | 7 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(4): Show |
7 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.82+3825G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713191 | |||||||
| chr17:44713214 | G | GT | 5 | a0001c0001t0001g0167 a0001c0001t0001g0173 a0001c0001t0001g0175 others(2): Show |
5 | HG01081.hp1 HG02056.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+3856dupT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44713214 | ||||||
| chr17:44713214 | G | T | 1 | a0001c0001t0002g0021 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.82+3848G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713214 | |||||||
| chr17:44713233 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0062 |
2 | HG00140.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.82+3867G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713233 | |||||||
| chr17:44713255 | A | G | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.82+3889A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713255 | |||||||
| chr17:44713269 | C | T | 2 | a0001c0001t0001g0254 a0001c0001t0001g0256 |
2 | HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.82+3903C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713269 | |||||||
| chr17:44713340 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.82+3974C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713340 | |||||||
| chr17:44713365 | T | A | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.82+3999T>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713365 | |||||||
| chr17:44713418 | T | G | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.82+4052T>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713418 | |||||||
| chr17:44713448 | T | A | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.82+4082T>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713448 | |||||||
| chr17:44713482 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.82+4116G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713482 | |||||||
| chr17:44713496 | T | A | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.82+4130T>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713496 | |||||||
| chr17:44713505 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.82+4139C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713505 | |||||||
| chr17:44713508 | T | A | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.82+4142T>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713508 | |||||||
| chr17:44713509 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.82+4143A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713509 | |||||||
| chr17:44713521 | A | T | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.82+4155A>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713521 | |||||||
| chr17:44713522 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.82+4156C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713522 | |||||||
| chr17:44713538 | T | G | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.82+4172T>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713538 | |||||||
| chr17:44713542 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.82+4176T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713542 | |||||||
| chr17:44713543 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.82+4177G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713543 | |||||||
| chr17:44713556 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.82+4190A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713556 | |||||||
| chr17:44713575 | G | A | 32 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0024 others(29): Show |
32 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.82+4209G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713575 | |||||||
| chr17:44713586 | G | T | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.82+4220G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713586 | |||||||
| chr17:44713617 | C | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG01074.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.82+4251C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713617 | |||||||
| chr17:44713627 | C | T | 47 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 others(44): Show |
47 | HG00140.hp2 HG01167.hp2 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.82+4261C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713627 | |||||||
| chr17:44713714 | GT | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
182 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.82+4355delT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44713714 | ||||||
| chr17:44713889 | C | T | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.82+4523C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44713889 | |||||||
| chr17:44714079 | C | T | 1 | a0001c0001t0004g0269 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.82+4713C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44714079 | |||||||
| chr17:44714118 | G | A | 2 | a0001c0001t0002g0014 a0001c0001t0002g0022 |
2 | HG00639.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.82+4752G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44714118 | |||||||
| chr17:44714119 | C | A | 2 | a0001c0001t0002g0014 a0001c0001t0002g0022 |
2 | HG00639.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.82+4753C>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44714119 | |||||||
| chr17:44714275 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | NA18946.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.82+4909G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44714275 | |||||||
| chr17:44714462 | G | C | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.82+5096G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44714462 | |||||||
| chr17:44714544 | A | G | 5 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+5178A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44714544 | |||||||
| chr17:44714585 | TGTAACTG others(9): Show |
T | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.82+5220_82+5235del others(16): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44714585 | |||||||
| chr17:44714604 | A | T | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.82+5238A>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44714604 | |||||||
| chr17:44714802 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.82+5436A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44714802 | |||||||
| chr17:44715138 | C | G | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.82+5772C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44715138 | |||||||
| chr17:44715194 | G | C | 2 | a0001c0001t0002g0014 a0001c0001t0002g0022 |
2 | HG00639.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.82+5828G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44715194 | |||||||
| chr17:44715323 | C | T | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.82+5957C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44715323 | |||||||
| chr17:44715581 | G | A | 51 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(48): Show |
51 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.82+6215G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44715581 | |||||||
| chr17:44715669 | T | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG01074.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.82+6303T>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44715669 | |||||||
| chr17:44715812 | C | CT | 23 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0107 others(20): Show |
23 | HG00099.hp1 HG00621.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.82+6474dupT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44715812 | ||||||
| chr17:44715812 | CT | C | 19 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0155 others(16): Show |
19 | HG00621.hp2 HG00642.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.82+6474delT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44715812 | ||||||
| chr17:44715812 | CTT | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0062 others(51): Show |
54 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.82+6473_82+6474del others(2): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44715812 | ||||||
| chr17:44715812 | CTTT | C | 85 | a0001c0001t0001g0003 a0001c0001t0001g0058 a0001c0001t0001g0060 others(82): Show |
86 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.82+6472_82+6474del others(3): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44715812 | ||||||
| chr17:44715818 | T | C | 8 | a0001c0001t0003g0258 a0002c0002t0003g0257 a0002c0002t0003g0259 others(5): Show |
8 | HG01169.hp1 HG01891.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.82+6452T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44715818 | |||||||
| chr17:44715819 | T | C | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0002c0002t0003g0263 |
3 | HG01109.hp1 HG01167.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.82+6453T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44715819 | |||||||
| chr17:44715879 | A | C | 1 | a0001c0001t0002g0025 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.82+6513A>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44715879 | |||||||
| chr17:44715901 | C | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG02109.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.82+6535C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44715901 | |||||||
| chr17:44716051 | C | A | 1 | a0002c0002t0003g0257 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.82+6685C>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44716051 | |||||||
| chr17:44716052 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.82+6686G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44716052 | |||||||
| chr17:44716069 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0164 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.82+6703C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44716069 | |||||||
| chr17:44716075 | C | G | 1 | a0001c0001t0001g0173 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.82+6709C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44716075 | |||||||
| chr17:44716075 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.82+6709C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44716075 | |||||||
| chr17:44716271 | G | A | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.83-6609G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44716271 | |||||||
| chr17:44716314 | G | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
182 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.83-6566G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44716314 | |||||||
| chr17:44716380 | T | C | 3 | a0001c0001t0001g0177 a0001c0001t0001g0185 a0001c0001t0001g0187 |
3 | HG00642.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.83-6500T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44716380 | |||||||
| chr17:44716580 | C | T | 9 | a0001c0001t0003g0258 a0002c0002t0003g0257 a0002c0002t0003g0259 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.83-6300C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44716580 | |||||||
| chr17:44716599 | T | G | 47 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 others(44): Show |
47 | HG00140.hp2 HG01167.hp2 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.83-6281T>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44716599 | |||||||
| chr17:44716877 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.83-6003A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44716877 | |||||||
| chr17:44716953 | T | C | 3 | a0001c0001t0001g0177 a0001c0001t0001g0185 a0001c0001t0001g0187 |
3 | HG00642.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.83-5927T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44716953 | |||||||
| chr17:44717429 | G | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0209 others(9): Show |
12 | HG01243.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.83-5451G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44717429 | |||||||
| chr17:44717444 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.83-5436C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44717444 | |||||||
| chr17:44717502 | T | C | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.83-5378T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44717502 | |||||||
| chr17:44717663 | C | T | 1 | a0001c0003t0001g0207 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.83-5217C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44717663 | |||||||
| chr17:44717707 | C | CA | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(65): Show |
69 | HG00099.hp2 HG00609.hp1 HG01074.hp1 others(66): Show |
intron_variant | MODIFIER | c.83-5155dupA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44717707 | ||||||
| chr17:44717707 | CA | C | 7 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0162 others(4): Show |
7 | HG01069.hp1 HG01109.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.83-5155delA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44717707 | ||||||
| chr17:44717788 | G | A | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.83-5092G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44717788 | |||||||
| chr17:44717870 | G | A | 5 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0118 others(2): Show |
5 | HG02523.hp1 NA18941.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-5010G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44717870 | |||||||
| chr17:44717891 | C | T | 9 | a0001c0001t0003g0258 a0002c0002t0003g0257 a0002c0002t0003g0259 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.83-4989C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44717891 | |||||||
| chr17:44717931 | G | C | 1 | a0001c0001t0009g0119 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.83-4949G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44717931 | |||||||
| chr17:44718029 | A | G | 11 | a0001c0001t0003g0258 a0001c0001t0004g0268 a0001c0001t0004g0269 others(8): Show |
11 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.83-4851A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44718029 | |||||||
| chr17:44718033 | AGAAAG | A | 15 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(12): Show |
15 | HG00099.hp2 HG00609.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.83-4846_83-4842del others(5): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44718033 | |||||||
| chr17:44718051 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.83-4829G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44718051 | |||||||
| chr17:44718061 | G | A | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.83-4819G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44718061 | |||||||
| chr17:44718139 | T | C | 6 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0094 others(3): Show |
6 | HG02083.hp2 HG02132.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.83-4741T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44718139 | |||||||
| chr17:44718182 | A | G | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.83-4698A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44718182 | |||||||
| chr17:44718422 | C | CA | 6 | a0001c0001t0001g0109 a0001c0001t0001g0116 a0001c0001t0001g0120 others(3): Show |
6 | HG01192.hp2 HG01346.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-4441dupA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44718422 | ||||||
| chr17:44718422 | CA | C | 19 | a0001c0001t0001g0057 a0001c0001t0001g0061 a0001c0001t0001g0083 others(16): Show |
19 | HG00621.hp2 HG00639.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.83-4441delA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44718422 | ||||||
| chr17:44718539 | C | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0209 others(9): Show |
12 | HG01243.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.83-4341C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44718539 | |||||||
| chr17:44718654 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.83-4226A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44718654 | |||||||
| chr17:44718677 | G | A | 3 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0056 |
3 | HG01515.hp1 HG01517.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.83-4203G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44718677 | |||||||
| chr17:44718696 | G | C | 1 | a0001c0001t0004g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.83-4184G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44718696 | |||||||
| chr17:44718718 | G | A | 3 | a0001c0001t0001g0058 a0001c0001t0002g0059 a0001c0001t0002g0091 |
3 | HG03130.hp2 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.83-4162G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44718718 | |||||||
| chr17:44718720 | A | G | 102 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 others(99): Show |
102 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.83-4160A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44718720 | |||||||
| chr17:44719029 | C | T | 9 | a0001c0001t0003g0258 a0002c0002t0003g0257 a0002c0002t0003g0259 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.83-3851C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44719029 | |||||||
| chr17:44719153 | G | C | 1 | a0001c0001t0002g0051 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.83-3727G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44719153 | |||||||
| chr17:44719310 | C | T | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.83-3570C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44719310 | |||||||
| chr17:44719521 | A | G | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.83-3359A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44719521 | |||||||
| chr17:44719534 | C | A | 1 | a0001c0001t0006g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.83-3346C>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44719534 | |||||||
| chr17:44719542 | G | A | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.83-3338G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44719542 | |||||||
| chr17:44719577 | A | G | 37 | a0001c0001t0001g0003 a0001c0001t0001g0198 a0001c0001t0001g0199 others(34): Show |
38 | HG00099.hp2 HG00609.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.83-3303A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44719577 | |||||||
| chr17:44719667 | C | T | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.83-3213C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44719667 | |||||||
| chr17:44719687 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.83-3193A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44719687 | |||||||
| chr17:44719932 | TCACCTTC others(18): Show |
T | 13 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(10): Show |
13 | HG00621.hp2 HG00639.hp1 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.83-2940_83-2916del others(25): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44719932 | ||||||
| chr17:44719987 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.83-2893G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44719987 | |||||||
| chr17:44720150 | G | T | 7 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(4): Show |
7 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.83-2730G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44720150 | |||||||
| chr17:44720161 | T | C | 13 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(10): Show |
13 | HG00621.hp2 HG00639.hp1 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.83-2719T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44720161 | |||||||
| chr17:44720209 | G | C | 1 | a0001c0005t0001g0096 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.83-2671G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44720209 | |||||||
| chr17:44720380 | G | A | 47 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 others(44): Show |
47 | HG00140.hp2 HG01167.hp2 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.83-2500G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44720380 | |||||||
| chr17:44720399 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.83-2481G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44720399 | |||||||
| chr17:44720530 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
183 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.83-2350A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44720530 | |||||||
| chr17:44720864 | C | CT | 11 | a0001c0001t0001g0159 a0001c0001t0001g0274 a0001c0001t0001g0275 others(8): Show |
11 | HG00558.hp2 HG00609.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.83-2002dupT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44720864 | ||||||
| chr17:44720889 | C | T | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0042 |
3 | HG01891.hp2 HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.83-1991C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44720889 | |||||||
| chr17:44720952 | A | G | 3 | a0001c0001t0002g0006 a0003c0004t0002g0005 a0003c0004t0002g0007 |
3 | HG02615.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.83-1928A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44720952 | |||||||
| chr17:44720990 | C | T | 1 | a0001c0001t0002g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-1890C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44720990 | |||||||
| chr17:44721026 | C | T | 1 | a0001c0001t0002g0012 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.83-1854C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44721026 | |||||||
| chr17:44721054 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.83-1826C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44721054 | |||||||
| chr17:44721216 | T | TC | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
154 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.83-1655dupC | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44721216 | ||||||
| chr17:44721216 | T | TCC | 19 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(16): Show |
19 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.83-1656_83-1655dup others(2): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44721216 | ||||||
| chr17:44721352 | G | T | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.83-1528G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44721352 | |||||||
| chr17:44721447 | G | C | 1 | a0001c0001t0004g0269 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.83-1433G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44721447 | |||||||
| chr17:44721618 | C | A | 1 | a0001c0001t0008g0168 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.83-1262C>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44721618 | |||||||
| chr17:44721702 | T | C | 11 | a0001c0001t0003g0258 a0001c0001t0004g0268 a0001c0001t0004g0269 others(8): Show |
11 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.83-1178T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44721702 | |||||||
| chr17:44721795 | C | T | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.83-1085C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44721795 | |||||||
| chr17:44721806 | C | A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.83-1074C>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44721806 | |||||||
| chr17:44721856 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.83-1024C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44721856 | |||||||
| chr17:44721901 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG01070.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.83-979G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44721901 | |||||||
| chr17:44721905 | C | T | 45 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 others(42): Show |
45 | HG00140.hp2 HG01167.hp2 HG01943.hp1 others(42): Show |
intron_variant | MODIFIER | c.83-975C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44721905 | |||||||
| chr17:44722092 | C | T | 1 | a0001c0001t0004g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.83-788C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44722092 | |||||||
| chr17:44722114 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.83-766A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44722114 | |||||||
| chr17:44722186 | G | C | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.83-694G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44722186 | |||||||
| chr17:44722198 | A | G | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.83-682A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44722198 | |||||||
| chr17:44722209 | A | G | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.83-671A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44722209 | |||||||
| chr17:44722235 | A | AAC | 19 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(16): Show |
19 | HG00621.hp2 HG00639.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.83-632_83-631dupAC | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44722235 | ||||||
| chr17:44722235 | A | AACACACA others(25): Show |
1 | a0006c0009t0005g0272 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.83-631_83-630insAC others(30): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44722235 | ||||||
| chr17:44722235 | A | AACACACA others(29): Show |
1 | a0001c0001t0006g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.83-631_83-630insAC others(34): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 44722235 | ||||||
| chr17:44722397 | C | T | 51 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(48): Show |
51 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.83-483C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44722397 | |||||||
| chr17:44722591 | G | A | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.83-289G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44722591 | |||||||
| chr17:44722636 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.83-244T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44722636 | |||||||
| chr17:44722743 | G | A | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.83-137G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44722743 | |||||||
| chr17:44722795 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.83-85A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44722795 | |||||||
| chr17:44722837 | T | C | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.83-43T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 2/13 | chr17 | 44722837 | |||||||
| chr17:44723030 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02165.hp1 | splice_region_variant&intron_variant | LOW | c.225+8A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44723030 | |||||||
| chr17:44723046 | C | T | 5 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(2): Show |
5 | HG00099.hp1 HG01074.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+24C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44723046 | |||||||
| chr17:44723054 | T | C | 3 | a0001c0001t0002g0006 a0003c0004t0002g0005 a0003c0004t0002g0007 |
3 | HG02615.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.225+32T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44723054 | |||||||
| chr17:44723182 | C | T | 3 | a0001c0001t0002g0006 a0003c0004t0002g0005 a0003c0004t0002g0007 |
3 | HG02615.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.225+160C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44723182 | |||||||
| chr17:44723341 | A | C | 5 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(2): Show |
5 | HG02922.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+319A>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44723341 | |||||||
| chr17:44723345 | T | C | 47 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 others(44): Show |
47 | HG00140.hp2 HG01167.hp2 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.225+323T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44723345 | |||||||
| chr17:44723412 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.225+390G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44723412 | |||||||
| chr17:44723541 | G | A | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.225+519G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44723541 | |||||||
| chr17:44723579 | A | G | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.225+557A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44723579 | |||||||
| chr17:44723700 | A | G | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.225+678A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44723700 | |||||||
| chr17:44723736 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.225+714G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44723736 | |||||||
| chr17:44723758 | A | C | 102 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 others(99): Show |
102 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.225+736A>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44723758 | |||||||
| chr17:44723771 | T | A | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG00323.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.225+749T>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44723771 | |||||||
| chr17:44723784 | A | G | 47 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 others(44): Show |
47 | HG00140.hp2 HG01167.hp2 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.225+762A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44723784 | |||||||
| chr17:44723939 | G | A | 3 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 |
3 | HG03041.hp1 HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.225+917G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44723939 | |||||||
| chr17:44724006 | T | G | 1 | a0001c0001t0001g0280 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.225+984T>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44724006 | |||||||
| chr17:44724009 | G | A | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.225+987G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44724009 | |||||||
| chr17:44724064 | G | C | 1 | a0001c0001t0010g0271 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.225+1042G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44724064 | |||||||
| chr17:44724188 | A | T | 8 | a0002c0002t0003g0257 a0002c0002t0003g0259 a0002c0002t0003g0260 others(5): Show |
8 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.225+1166A>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44724188 | |||||||
| chr17:44724523 | G | T | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.225+1501G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44724523 | |||||||
| chr17:44724580 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.225+1558C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44724580 | |||||||
| chr17:44724581 | G | A | 5 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+1559G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44724581 | |||||||
| chr17:44724785 | G | A | 2 | a0001c0006t0001g0065 a0001c0006t0001g0066 |
2 | NA18974.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.225+1763G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44724785 | |||||||
| chr17:44724857 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.225+1835C>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44724857 | |||||||
| chr17:44724866 | C | T | 29 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(26): Show |
29 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.225+1844C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44724866 | |||||||
| chr17:44724907 | A | T | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.225+1885A>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44724907 | |||||||
| chr17:44725035 | A | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.225+2013A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44725035 | |||||||
| chr17:44725104 | A | G | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.225+2082A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44725104 | |||||||
| chr17:44725116 | C | CA | 75 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(72): Show |
75 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.225+2117dupA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725116 | ||||||
| chr17:44725116 | C | CAA | 15 | a0001c0001t0001g0061 a0001c0001t0001g0069 a0001c0001t0001g0070 others(12): Show |
15 | HG00621.hp2 HG00642.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.225+2116_225+2117d others(4): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725116 | ||||||
| chr17:44725527 | A | G | 1 | a0001c0001t0006g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.225+2505A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44725527 | |||||||
| chr17:44725552 | A | G | 1 | a0001c0001t0002g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.225+2530A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44725552 | |||||||
| chr17:44725662 | C | T | 1 | a0001c0001t0006g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.225+2640C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44725662 | |||||||
| chr17:44725684 | C | CT | 10 | a0001c0001t0001g0078 a0001c0001t0001g0105 a0001c0001t0001g0106 others(7): Show |
10 | HG01167.hp2 HG01978.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.225+2682dupT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTT | 42 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(39): Show |
42 | HG00140.hp2 HG01943.hp1 HG02004.hp1 others(39): Show |
intron_variant | MODIFIER | c.225+2681_225+2682d others(4): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTCTTTT others(6): Show |
5 | a0001c0001t0003g0258 a0002c0002t0003g0257 a0002c0002t0003g0259 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+2664_225+2665i others(15): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTTTT | 11 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0209 others(8): Show |
11 | HG01243.hp1 HG02280.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.225+2678_225+2682d others(7): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTTTTT | 9 | a0001c0001t0001g0197 a0001c0001t0001g0278 a0001c0001t0002g0008 others(6): Show |
9 | HG01952.hp1 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.225+2677_225+2682d others(8): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTTTTTT | 11 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(8): Show |
11 | HG00558.hp2 HG02723.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.225+2676_225+2682d others(9): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0002g0047 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.225+2670_225+2682d others(15): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTTTTTT others(9): Show |
2 | a0001c0001t0001g0195 a0001c0001t0002g0043 |
2 | HG00673.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.225+2667_225+2682d others(18): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0002g0027 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.225+2666_225+2682d others(19): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTTTTTT others(11): Show |
4 | a0001c0001t0001g0196 a0001c0001t0002g0044 a0001c0001t0002g0050 others(1): Show |
4 | HG03579.hp2 NA18944.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+2665_225+2682d others(20): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTTTTTT others(12): Show |
2 | a0001c0001t0002g0006 a0003c0004t0002g0007 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.225+2664_225+2682d others(21): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTTTTTT others(13): Show |
1 | a0003c0004t0002g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.225+2663_225+2682d others(22): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0001g0227 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.225+2682_225+2683i others(24): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTTTTTT others(16): Show |
3 | a0001c0001t0001g0212 a0001c0001t0001g0231 a0001c0001t0002g0028 |
3 | HG01168.hp2 HG01884.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.225+2682_225+2683i others(25): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTTTTTT others(17): Show |
15 | a0001c0001t0001g0003 a0001c0001t0001g0198 a0001c0001t0001g0213 others(12): Show |
16 | HG00609.hp1 HG01169.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.225+2682_225+2683i others(26): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTTTTTT others(18): Show |
8 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(5): Show |
8 | HG00099.hp2 HG01243.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.225+2682_225+2683i others(27): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTTTTTT others(19): Show |
2 | a0001c0001t0001g0235 a0001c0001t0001g0240 |
2 | HG02572.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.225+2682_225+2683i others(28): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTTTTTT others(20): Show |
3 | a0001c0001t0002g0038 a0001c0001t0002g0054 a0001c0001t0002g0055 |
3 | HG01069.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.225+2682_225+2683i others(29): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTTTTTT others(21): Show |
3 | a0001c0001t0001g0236 a0001c0001t0002g0023 a0001c0001t0002g0041 |
3 | HG02735.hp2 NA19000.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.225+2682_225+2683i others(30): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTTTTTT others(22): Show |
4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(1): Show |
4 | HG00642.hp1 HG01074.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+2682_225+2683i others(31): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTTTTTT others(23): Show |
11 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0001t0002g0026 others(8): Show |
11 | HG00323.hp1 HG01071.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.225+2682_225+2683i others(32): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | C | CTTTTTTT others(24): Show |
6 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0034 others(3): Show |
6 | HG01070.hp1 HG01081.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+2682_225+2683i others(33): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | CT | C | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG01256.hp2 HG02080.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+2682delT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725684 | CTT | C | 6 | a0001c0001t0001g0241 a0001c0001t0001g0243 a0001c0001t0001g0244 others(3): Show |
6 | HG00639.hp2 HG01081.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+2681_225+2682d others(4): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44725684 | ||||||
| chr17:44725870 | G | A | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.225+2848G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44725870 | |||||||
| chr17:44726088 | CA | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(46): Show |
50 | HG00099.hp2 HG00609.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.225+3068delA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44726088 | ||||||
| chr17:44726178 | G | A | 5 | a0001c0001t0003g0258 a0002c0002t0003g0257 a0002c0002t0003g0259 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+3156G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44726178 | |||||||
| chr17:44726229 | A | T | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.225+3207A>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44726229 | |||||||
| chr17:44726266 | G | A | 37 | a0001c0001t0001g0003 a0001c0001t0001g0198 a0001c0001t0001g0199 others(34): Show |
38 | HG00099.hp2 HG00609.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.225+3244G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44726266 | |||||||
| chr17:44726292 | T | TTTTA | 37 | a0001c0001t0001g0003 a0001c0001t0001g0112 a0001c0001t0001g0149 others(34): Show |
38 | HG00099.hp2 HG00609.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.225+3310_225+3313d others(6): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44726292 | ||||||
| chr17:44726292 | T | TTTTATGT others(5): Show |
1 | a0001c0001t0001g0188 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.225+3275_225+3276i others(14): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44726292 | ||||||
| chr17:44726292 | T | TTTTATGT others(9): Show |
1 | a0001c0001t0001g0186 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.225+3275_225+3276i others(18): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44726292 | ||||||
| chr17:44726292 | T | TTTTATTT others(1): Show |
150 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0058 others(147): Show |
150 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.225+3306_225+3313d others(10): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44726292 | ||||||
| chr17:44726292 | T | TTTTATTT others(5): Show |
46 | a0001c0001t0001g0057 a0001c0001t0001g0067 a0001c0001t0001g0069 others(43): Show |
46 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.225+3302_225+3313d others(14): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44726292 | ||||||
| chr17:44726292 | T | TTTTATTT others(9): Show |
2 | a0001c0001t0001g0162 a0001c0001t0002g0041 |
2 | HG02735.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.225+3298_225+3313d others(18): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44726292 | ||||||
| chr17:44726292 | T | TTTTATTT others(13): Show |
1 | a0001c0001t0001g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.225+3294_225+3313d others(22): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44726292 | ||||||
| chr17:44726292 | T | TTTTTTTT others(1): Show |
18 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0002g0008 others(15): Show |
18 | HG00621.hp2 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.225+3273_225+3274i others(10): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44726292 | ||||||
| chr17:44726292 | T | TTTTTTTT others(5): Show |
3 | a0001c0001t0001g0001 a0001c0001t0002g0011 a0001c0001t0002g0016 |
4 | HG03098.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+3273_225+3274i others(14): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44726292 | ||||||
| chr17:44726292 | TTTTA | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0010g0271 |
3 | HG01109.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.225+3310_225+3313d others(6): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44726292 | ||||||
| chr17:44726292 | TTTTATTT others(5): Show |
T | 1 | a0006c0009t0005g0272 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.225+3302_225+3313d others(14): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44726292 | ||||||
| chr17:44726323 | T | TATTTATT others(6): Show |
4 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0277 others(1): Show |
4 | HG00558.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+3313_225+3314i others(15): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44726323 | ||||||
| chr17:44726323 | T | TATTTATT others(10): Show |
1 | a0001c0001t0001g0284 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.225+3313_225+3314i others(19): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44726323 | ||||||
| chr17:44726456 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0233 |
2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.225+3434C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44726456 | |||||||
| chr17:44726459 | G | A | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.225+3437G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44726459 | |||||||
| chr17:44726747 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.226-3158A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44726747 | |||||||
| chr17:44726768 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.226-3137T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44726768 | |||||||
| chr17:44726875 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.226-3030G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44726875 | |||||||
| chr17:44726990 | T | C | 5 | a0001c0001t0003g0258 a0002c0002t0003g0257 a0002c0002t0003g0259 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.226-2915T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44726990 | |||||||
| chr17:44727098 | CA | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0073 a0001c0001t0001g0092 others(121): Show |
125 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.226-2783delA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44727098 | ||||||
| chr17:44727098 | CAA | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
109 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.226-2784_226-2783d others(4): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44727098 | ||||||
| chr17:44727102 | A | G | 3 | a0001c0001t0001g0115 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | HG01069.hp2 HG01071.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.226-2803A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44727102 | |||||||
| chr17:44727263 | A | T | 5 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0230 others(2): Show |
5 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.226-2642A>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44727263 | |||||||
| chr17:44727311 | C | T | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.226-2594C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44727311 | |||||||
| chr17:44727393 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.226-2512C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44727393 | |||||||
| chr17:44727424 | GA | G | 6 | a0001c0001t0001g0057 a0001c0001t0001g0108 a0001c0001t0001g0137 others(3): Show |
6 | NA18942.hp1 NA18946.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.226-2471delA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44727424 | ||||||
| chr17:44727595 | C | G | 1 | a0001c0001t0001g0135 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.226-2310C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44727595 | |||||||
| chr17:44727786 | T | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
178 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.226-2119T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44727786 | |||||||
| chr17:44727800 | C | T | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.226-2105C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44727800 | |||||||
| chr17:44727816 | G | A | 1 | a0001c0001t0002g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.226-2089G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44727816 | |||||||
| chr17:44727864 | A | AT | 36 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(33): Show |
36 | HG00140.hp1 HG00558.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.226-2016dupT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44727864 | ||||||
| chr17:44727864 | AT | A | 49 | a0001c0001t0001g0062 a0001c0001t0001g0073 a0001c0001t0001g0088 others(46): Show |
49 | HG00323.hp1 HG00639.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.226-2016delT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44727864 | ||||||
| chr17:44727864 | ATT | A | 38 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 others(35): Show |
38 | HG00140.hp2 HG01167.hp2 HG01943.hp1 others(35): Show |
intron_variant | MODIFIER | c.226-2017_226-2016d others(4): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44727864 | ||||||
| chr17:44727864 | ATTTTTTT | A | 9 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(6): Show |
9 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.226-2022_226-2016d others(9): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44727864 | ||||||
| chr17:44727869 | T | C | 35 | a0001c0001t0001g0003 a0001c0001t0001g0198 a0001c0001t0001g0199 others(32): Show |
36 | HG00099.hp2 HG00609.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.226-2036T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44727869 | |||||||
| chr17:44727916 | C | T | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.226-1989C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44727916 | |||||||
| chr17:44727925 | C | T | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.226-1980C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44727925 | |||||||
| chr17:44728018 | A | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0209 others(9): Show |
12 | HG01243.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.226-1887A>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44728018 | |||||||
| chr17:44728022 | C | G | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.226-1883C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44728022 | |||||||
| chr17:44728117 | C | T | 37 | a0001c0001t0001g0003 a0001c0001t0001g0198 a0001c0001t0001g0199 others(34): Show |
38 | HG00099.hp2 HG00609.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.226-1788C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44728117 | |||||||
| chr17:44728204 | A | G | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.226-1701A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44728204 | |||||||
| chr17:44728268 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.226-1637G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44728268 | |||||||
| chr17:44728456 | T | A | 1 | a0001c0001t0006g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.226-1449T>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44728456 | |||||||
| chr17:44728569 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.226-1336A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44728569 | |||||||
| chr17:44728573 | CT | C | 19 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(16): Show |
19 | HG00621.hp2 HG00639.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.226-1329delT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44728573 | ||||||
| chr17:44728648 | C | T | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.226-1257C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44728648 | |||||||
| chr17:44728733 | C | A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.226-1172C>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44728733 | |||||||
| chr17:44728749 | G | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0209 others(9): Show |
12 | HG01243.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.226-1156G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44728749 | |||||||
| chr17:44728798 | A | G | 9 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(6): Show |
9 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.226-1107A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44728798 | |||||||
| chr17:44728804 | A | C | 1 | a0001c0001t0002g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.226-1101A>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44728804 | |||||||
| chr17:44728844 | C | T | 37 | a0001c0001t0001g0003 a0001c0001t0001g0198 a0001c0001t0001g0199 others(34): Show |
38 | HG00099.hp2 HG00609.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.226-1061C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44728844 | |||||||
| chr17:44729105 | AAAG | A | 51 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(48): Show |
51 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.226-797_226-795del others(3): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44729105 | ||||||
| chr17:44729263 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.226-642G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44729263 | |||||||
| chr17:44729264 | T | C | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.226-641T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44729264 | |||||||
| chr17:44729333 | C | G | 1 | a0001c0001t0010g0271 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.226-572C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44729333 | |||||||
| chr17:44729403 | A | G | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.226-502A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44729403 | |||||||
| chr17:44729419 | A | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(46): Show |
50 | HG00099.hp2 HG00609.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.226-486A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44729419 | |||||||
| chr17:44729574 | G | A | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.226-331G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44729574 | |||||||
| chr17:44729669 | A | G | 1 | a0001c0001t0004g0269 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.226-236A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44729669 | |||||||
| chr17:44729677 | TACACATA others(7): Show |
T | 1 | a0001c0001t0006g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.226-222_226-209del others(14): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44729677 | ||||||
| chr17:44729683 | T | TAC | 37 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0120 others(34): Show |
38 | HG00099.hp1 HG00609.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.226-179_226-178dup others(2): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44729683 | ||||||
| chr17:44729683 | T | TACAC | 26 | a0001c0001t0001g0109 a0001c0001t0001g0113 a0001c0001t0001g0114 others(23): Show |
26 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.226-181_226-178dup others(4): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44729683 | ||||||
| chr17:44729683 | T | TACACAC | 11 | a0001c0001t0001g0130 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
11 | HG00099.hp2 HG00609.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.226-183_226-178dup others(6): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44729683 | ||||||
| chr17:44729683 | T | TACACACA others(3): Show |
7 | a0001c0001t0001g0004 a0001c0001t0001g0193 a0001c0001t0001g0209 others(4): Show |
7 | HG02486.hp2 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.226-187_226-178dup others(10): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44729683 | ||||||
| chr17:44729683 | TAC | T | 9 | a0001c0001t0001g0110 a0001c0001t0001g0184 a0001c0001t0001g0185 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.226-179_226-178del others(2): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44729683 | ||||||
| chr17:44729683 | TACAC | T | 19 | a0001c0001t0001g0135 a0001c0001t0001g0202 a0001c0001t0001g0248 others(16): Show |
19 | HG00323.hp1 HG00558.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.226-181_226-178del others(4): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44729683 | ||||||
| chr17:44729683 | TACACAC | T | 8 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(5): Show |
8 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.226-183_226-178del others(6): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44729683 | ||||||
| chr17:44729683 | TACACACA others(1): Show |
T | 8 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0023 others(5): Show |
8 | HG01081.hp2 HG01261.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.226-185_226-178del others(8): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44729683 | ||||||
| chr17:44729683 | TACACACA others(3): Show |
T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0063 others(39): Show |
43 | HG00621.hp2 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.226-187_226-178del others(10): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44729683 | ||||||
| chr17:44729683 | TACACACA others(5): Show |
T | 43 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0062 others(40): Show |
43 | HG00140.hp2 HG01167.hp2 HG01943.hp1 others(40): Show |
intron_variant | MODIFIER | c.226-189_226-178del others(12): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44729683 | ||||||
| chr17:44729683 | TACACACA others(7): Show |
T | 1 | a0001c0001t0001g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.226-191_226-178del others(14): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44729683 | ||||||
| chr17:44729683 | TACACACA others(9): Show |
T | 1 | a0001c0001t0001g0075 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.226-193_226-178del others(16): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44729683 | ||||||
| chr17:44729683 | TACACACA others(11): Show |
T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.226-195_226-178del others(18): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 44729683 | ||||||
| chr17:44729724 | A | C | 1 | a0001c0001t0003g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.226-181A>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44729724 | |||||||
| chr17:44729727 | C | CACA | 3 | a0001c0001t0001g0147 a0001c0001t0001g0182 a0001c0001t0001g0237 |
3 | HG02602.hp1 HG02622.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.226-178_226-177ins others(3): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44729727 | |||||||
| chr17:44729728 | C | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0006g0273 others(9): Show |
12 | HG01243.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.226-177C>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44729728 | |||||||
| chr17:44729776 | G | C | 1 | a0005c0008t0002g0032 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.226-129G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 3/13 | chr17 | 44729776 | |||||||
| chr17:44730122 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.417+26T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 4/13 | chr17 | 44730122 | |||||||
| chr17:44730382 | T | C | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.417+286T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 4/13 | chr17 | 44730382 | |||||||
| chr17:44730747 | A | G | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.418-218A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 4/13 | chr17 | 44730747 | |||||||
| chr17:44730834 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0224 a0001c0001t0001g0229 others(2): Show |
6 | HG01884.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.418-131C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 4/13 | chr17 | 44730834 | |||||||
| chr17:44730912 | T | G | 1 | a0001c0001t0001g0219 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.418-53T>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 4/13 | chr17 | 44730912 | |||||||
| chr17:44731123 | G | A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(53): Show |
57 | HG00099.hp2 HG00609.hp1 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.468+108G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 5/13 | chr17 | 44731123 | |||||||
| chr17:44731348 | G | T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0091 |
2 | HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.468+333G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 5/13 | chr17 | 44731348 | |||||||
| chr17:44731494 | G | T | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.468+479G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 5/13 | chr17 | 44731494 | |||||||
| chr17:44731608 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.469-570A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 5/13 | chr17 | 44731608 | |||||||
| chr17:44731753 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0233 |
2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.469-425G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 5/13 | chr17 | 44731753 | |||||||
| chr17:44731871 | C | T | 1 | a0001c0001t0006g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.469-307C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 5/13 | chr17 | 44731871 | |||||||
| chr17:44731888 | C | T | 4 | a0001c0001t0002g0028 a0001c0001t0002g0044 a0001c0001t0002g0050 others(1): Show |
4 | HG02083.hp1 NA18944.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-290C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 5/13 | chr17 | 44731888 | |||||||
| chr17:44732022 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.469-156T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 5/13 | chr17 | 44732022 | |||||||
| chr17:44732443 | C | T | 1 | a0001c0001t0010g0271 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.556+178C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 6/13 | chr17 | 44732443 | |||||||
| chr17:44732638 | C | T | 1 | a0001c0001t0007g0267 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.556+373C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 6/13 | chr17 | 44732638 | |||||||
| chr17:44732695 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0001g0085 |
3 | HG02135.hp1 HG02155.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.556+430G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 6/13 | chr17 | 44732695 | |||||||
| chr17:44732726 | C | T | 37 | a0001c0001t0001g0003 a0001c0001t0001g0198 a0001c0001t0001g0199 others(34): Show |
38 | HG00099.hp2 HG00609.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.556+461C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 6/13 | chr17 | 44732726 | |||||||
| chr17:44732802 | G | A | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.556+537G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 6/13 | chr17 | 44732802 | |||||||
| chr17:44732852 | C | T | 1 | a0001c0001t0006g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.556+587C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 6/13 | chr17 | 44732852 | |||||||
| chr17:44732865 | C | CA | 6 | a0001c0001t0001g0126 a0001c0001t0001g0170 a0001c0001t0002g0027 others(3): Show |
6 | HG01361.hp2 HG02738.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.556+615dupA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 44732865 | ||||||
| chr17:44733009 | C | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(46): Show |
50 | HG00099.hp2 HG00609.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.556+744C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 6/13 | chr17 | 44733009 | |||||||
| chr17:44733089 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.556+824T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 6/13 | chr17 | 44733089 | |||||||
| chr17:44733122 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.556+857G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 6/13 | chr17 | 44733122 | |||||||
| chr17:44733164 | C | CAA | 48 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(45): Show |
49 | HG00099.hp2 HG00609.hp1 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.557-910_557-909dup others(2): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 44733164 | ||||||
| chr17:44733423 | A | G | 7 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(4): Show |
7 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.557-667A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 6/13 | chr17 | 44733423 | |||||||
| chr17:44733706 | G | A | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.557-384G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 6/13 | chr17 | 44733706 | |||||||
| chr17:44734043 | A | G | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.557-47A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 6/13 | chr17 | 44734043 | |||||||
| chr17:44734171 | A | C | 1 | a0001c0005t0001g0102 | 1 | NA18940.hp2 | splice_region_variant&intron_variant | LOW | c.630+8A>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734171 | |||||||
| chr17:44734201 | T | G | 1 | a0001c0005t0001g0102 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.630+38T>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734201 | |||||||
| chr17:44734251 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.630+88C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734251 | |||||||
| chr17:44734294 | C | G | 1 | a0001c0001t0007g0267 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.630+131C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734294 | |||||||
| chr17:44734375 | A | G | 1 | a0001c0001t0002g0059 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.630+212A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734375 | |||||||
| chr17:44734400 | C | G | 1 | a0003c0004t0002g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.630+237C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734400 | |||||||
| chr17:44734575 | G | T | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+412G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734575 | |||||||
| chr17:44734588 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+425T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734588 | |||||||
| chr17:44734595 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+432T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734595 | |||||||
| chr17:44734599 | T | A | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+436T>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734599 | |||||||
| chr17:44734601 | T | G | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+438T>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734601 | |||||||
| chr17:44734605 | T | A | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+442T>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734605 | |||||||
| chr17:44734608 | T | G | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+445T>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734608 | |||||||
| chr17:44734611 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+448G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734611 | |||||||
| chr17:44734613 | T | A | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+450T>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734613 | |||||||
| chr17:44734615 | G | T | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+452G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734615 | |||||||
| chr17:44734617 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.630+454G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734617 | |||||||
| chr17:44734623 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+460A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734623 | |||||||
| chr17:44734624 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+461C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734624 | |||||||
| chr17:44734625 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+462T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734625 | |||||||
| chr17:44734626 | G | T | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+463G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734626 | |||||||
| chr17:44734634 | T | A | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+471T>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734634 | |||||||
| chr17:44734636 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+473C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734636 | |||||||
| chr17:44734637 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+474A>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734637 | |||||||
| chr17:44734640 | A | C | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+477A>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734640 | |||||||
| chr17:44734644 | G | T | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+481G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734644 | |||||||
| chr17:44734652 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+489C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734652 | |||||||
| chr17:44734659 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+496T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734659 | |||||||
| chr17:44734661 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+498A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734661 | |||||||
| chr17:44734662 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+499A>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734662 | |||||||
| chr17:44734668 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+505A>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734668 | |||||||
| chr17:44734670 | T | G | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+507T>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734670 | |||||||
| chr17:44734671 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+508A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734671 | |||||||
| chr17:44734672 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+509T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734672 | |||||||
| chr17:44734673 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+510C>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734673 | |||||||
| chr17:44734676 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+513C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734676 | |||||||
| chr17:44734678 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+515C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734678 | |||||||
| chr17:44734679 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+516C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734679 | |||||||
| chr17:44734680 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+517C>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734680 | |||||||
| chr17:44734687 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+524C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734687 | |||||||
| chr17:44734688 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+525A>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734688 | |||||||
| chr17:44734696 | G | T | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+533G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734696 | |||||||
| chr17:44734697 | A | C | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+534A>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734697 | |||||||
| chr17:44734700 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+537G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734700 | |||||||
| chr17:44734702 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+539T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734702 | |||||||
| chr17:44734706 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+543A>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734706 | |||||||
| chr17:44734707 | T | G | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+544T>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734707 | |||||||
| chr17:44734711 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+548C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734711 | |||||||
| chr17:44734712 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+549A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734712 | |||||||
| chr17:44734715 | T | G | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+552T>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734715 | |||||||
| chr17:44734724 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+561A>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734724 | |||||||
| chr17:44734728 | T | A | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.630+565T>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734728 | |||||||
| chr17:44734822 | A | G | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.630+659A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734822 | |||||||
| chr17:44734842 | A | G | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.630+679A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734842 | |||||||
| chr17:44734932 | C | T | 2 | a0001c0001t0002g0036 a0001c0001t0002g0053 |
2 | HG01099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.630+769C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734932 | |||||||
| chr17:44734960 | C | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | NA18964.hp2 NA18973.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.630+797C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44734960 | |||||||
| chr17:44735007 | G | T | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.630+844G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44735007 | |||||||
| chr17:44735190 | T | A | 1 | a0001c0005t0001g0102 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.630+1027T>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44735190 | |||||||
| chr17:44735193 | A | C | 1 | a0001c0001t0002g0052 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.630+1030A>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44735193 | |||||||
| chr17:44735238 | C | T | 6 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0184 others(3): Show |
6 | HG02280.hp2 HG02976.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.630+1075C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44735238 | |||||||
| chr17:44735354 | T | C | 7 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(4): Show |
7 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.630+1191T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44735354 | |||||||
| chr17:44735388 | G | C | 1 | a0001c0001t0001g0216 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.630+1225G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44735388 | |||||||
| chr17:44735409 | A | G | 51 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(48): Show |
51 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.630+1246A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44735409 | |||||||
| chr17:44735410 | C | T | 1 | a0001c0001t0002g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.630+1247C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44735410 | |||||||
| chr17:44735446 | G | A | 5 | a0001c0001t0003g0258 a0002c0002t0003g0257 a0002c0002t0003g0259 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.630+1283G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44735446 | |||||||
| chr17:44735538 | C | T | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.631-1292C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44735538 | |||||||
| chr17:44735708 | G | C | 15 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(12): Show |
15 | HG00621.hp2 HG00639.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.631-1122G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44735708 | |||||||
| chr17:44736020 | C | T | 1 | a0006c0009t0005g0272 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.631-810C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44736020 | |||||||
| chr17:44736021 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.631-809G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44736021 | |||||||
| chr17:44736027 | GC | G | 3 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0001g0085 |
3 | HG02135.hp1 HG02155.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.631-802delC | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44736027 | |||||||
| chr17:44736091 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.631-739C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44736091 | |||||||
| chr17:44736136 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.631-694C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44736136 | |||||||
| chr17:44736148 | A | AT | 21 | a0001c0001t0001g0085 a0001c0001t0001g0170 a0001c0001t0001g0197 others(18): Show |
21 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.631-664dupT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 44736148 | ||||||
| chr17:44736148 | AT | A | 13 | a0001c0001t0001g0154 a0001c0001t0001g0194 a0001c0001t0001g0250 others(10): Show |
13 | HG00099.hp1 HG01167.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.631-664delT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 44736148 | ||||||
| chr17:44736222 | A | G | 2 | a0002c0002t0003g0260 a0002c0002t0003g0263 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.631-608A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44736222 | |||||||
| chr17:44736235 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.631-595C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44736235 | |||||||
| chr17:44736388 | A | G | 1 | a0001c0001t0006g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.631-442A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44736388 | |||||||
| chr17:44736425 | G | A | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.631-405G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44736425 | |||||||
| chr17:44736650 | G | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0209 others(8): Show |
11 | HG01243.hp1 HG02280.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.631-180G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 7/13 | chr17 | 44736650 | |||||||
| chr17:44736945 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0103 |
2 | NA18948.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.667+79C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 8/13 | chr17 | 44736945 | |||||||
| chr17:44737148 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.667+282G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 8/13 | chr17 | 44737148 | |||||||
| chr17:44737285 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.667+419G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 8/13 | chr17 | 44737285 | |||||||
| chr17:44737308 | T | C | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.667+442T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 8/13 | chr17 | 44737308 | |||||||
| chr17:44737586 | C | T | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.667+720C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 8/13 | chr17 | 44737586 | |||||||
| chr17:44737587 | G | A | 7 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(4): Show |
7 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.667+721G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 8/13 | chr17 | 44737587 | |||||||
| chr17:44737716 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.668-663C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 8/13 | chr17 | 44737716 | |||||||
| chr17:44737776 | A | G | 6 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(3): Show |
6 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.668-603A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 8/13 | chr17 | 44737776 | |||||||
| chr17:44738017 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0007g0267 |
2 | HG00733.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.668-362G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 8/13 | chr17 | 44738017 | |||||||
| chr17:44738047 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.668-332C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 8/13 | chr17 | 44738047 | |||||||
| chr17:44738122 | G | A | 1 | a0001c0001t0006g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.668-257G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 8/13 | chr17 | 44738122 | |||||||
| chr17:44738155 | G | A | 2 | a0001c0005t0001g0096 a0001c0005t0001g0102 |
2 | NA18940.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.668-224G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 8/13 | chr17 | 44738155 | |||||||
| chr17:44738718 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.713+294G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 9/13 | chr17 | 44738718 | |||||||
| chr17:44738775 | A | T | 7 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
7 | HG00558.hp2 HG02145.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.713+351A>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 9/13 | chr17 | 44738775 | |||||||
| chr17:44738978 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.713+554A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 9/13 | chr17 | 44738978 | |||||||
| chr17:44739253 | A | C | 1 | a0001c0001t0001g0274 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.713+829A>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 9/13 | chr17 | 44739253 | |||||||
| chr17:44740034 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.714-1302T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 9/13 | chr17 | 44740034 | |||||||
| chr17:44740038 | A | G | 8 | a0001c0001t0001g0129 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
8 | HG00733.hp2 HG01074.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.714-1298A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 9/13 | chr17 | 44740038 | |||||||
| chr17:44740168 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.714-1168A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 9/13 | chr17 | 44740168 | |||||||
| chr17:44740416 | C | A | 1 | a0001c0001t0002g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.714-920C>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 9/13 | chr17 | 44740416 | |||||||
| chr17:44740564 | G | A | 11 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(8): Show |
11 | HG00558.hp2 HG02145.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.714-772G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 9/13 | chr17 | 44740564 | |||||||
| chr17:44740686 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.714-650G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 9/13 | chr17 | 44740686 | |||||||
| chr17:44740991 | C | T | 4 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0098 others(1): Show |
4 | HG00140.hp2 HG01943.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.714-345C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 9/13 | chr17 | 44740991 | |||||||
| chr17:44741027 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0104 others(99): Show |
103 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.714-309C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 9/13 | chr17 | 44741027 | |||||||
| chr17:44741051 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.714-285T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 9/13 | chr17 | 44741051 | |||||||
| chr17:44741120 | G | A | 3 | a0001c0001t0002g0006 a0003c0004t0002g0005 a0003c0004t0002g0007 |
3 | HG02615.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.714-216G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 9/13 | chr17 | 44741120 | |||||||
| chr17:44741518 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0224 a0001c0001t0001g0229 others(2): Show |
6 | HG01884.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.830+66C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44741518 | |||||||
| chr17:44741767 | G | A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.830+315G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44741767 | |||||||
| chr17:44741797 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.830+345C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44741797 | |||||||
| chr17:44742088 | C | CA | 10 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(7): Show |
10 | HG01952.hp1 HG02615.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.830+642dupA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44742088 | ||||||
| chr17:44742095 | T | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.830+643T>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44742095 | |||||||
| chr17:44742101 | T | A | 51 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(48): Show |
51 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.830+649T>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44742101 | |||||||
| chr17:44742228 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.830+776C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44742228 | |||||||
| chr17:44742250 | CA | C | 19 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(16): Show |
19 | HG00621.hp2 HG00639.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.830+808delA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44742250 | ||||||
| chr17:44742409 | C | CA | 22 | a0001c0001t0001g0090 a0001c0001t0001g0093 a0001c0001t0001g0107 others(19): Show |
22 | HG00673.hp2 HG01192.hp2 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.830+979dupA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44742409 | ||||||
| chr17:44742409 | CA | C | 17 | a0001c0001t0001g0071 a0001c0001t0001g0075 a0001c0001t0001g0101 others(14): Show |
17 | HG01070.hp2 HG01109.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.830+979delA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44742409 | ||||||
| chr17:44742755 | G | A | 4 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(1): Show |
4 | HG02922.hp1 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.830+1303G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44742755 | |||||||
| chr17:44743017 | G | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0104 others(94): Show |
98 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.830+1565G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44743017 | |||||||
| chr17:44743291 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.830+1839C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44743291 | |||||||
| chr17:44743422 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.830+1970G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44743422 | |||||||
| chr17:44743607 | C | CT | 28 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0110 others(25): Show |
28 | HG00621.hp2 HG00639.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.830+2176dupT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44743607 | ||||||
| chr17:44743607 | CT | C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
64 | HG00099.hp2 HG00609.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.830+2176delT | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44743607 | ||||||
| chr17:44743640 | C | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.830+2188C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44743640 | |||||||
| chr17:44743652 | C | G | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | NA18964.hp2 NA18973.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.830+2200C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44743652 | |||||||
| chr17:44743764 | C | G | 1 | a0001c0001t0010g0271 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.830+2312C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44743764 | |||||||
| chr17:44743878 | G | C | 3 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0228 |
3 | HG01168.hp2 HG01169.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.830+2426G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44743878 | |||||||
| chr17:44744077 | G | T | 1 | a0001c0001t0001g0221 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.830+2625G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44744077 | |||||||
| chr17:44744081 | A | AC | 102 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(99): Show |
103 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.830+2644dupC | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44744081 | ||||||
| chr17:44744081 | A | ACC | 38 | a0001c0001t0001g0003 a0001c0001t0001g0068 a0001c0001t0001g0079 others(35): Show |
39 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.830+2643_830+2644d others(4): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44744081 | ||||||
| chr17:44744081 | AC | A | 31 | a0001c0001t0001g0072 a0001c0001t0001g0077 a0001c0001t0001g0093 others(28): Show |
31 | HG00558.hp2 HG00642.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.830+2644delC | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44744081 | ||||||
| chr17:44744081 | ACC | A | 25 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0073 others(22): Show |
25 | HG00323.hp2 HG01069.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.830+2643_830+2644d others(4): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44744081 | ||||||
| chr17:44744086 | C | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0147 |
2 | HG02602.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.830+2634C>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44744086 | |||||||
| chr17:44744094 | C | A | 1 | a0001c0001t0004g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.830+2642C>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44744094 | |||||||
| chr17:44744094 | C | G | 1 | a0001c0001t0001g0217 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.830+2642C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44744094 | |||||||
| chr17:44744096 | C | G | 7 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
7 | HG00558.hp2 HG02145.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.830+2644C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44744096 | |||||||
| chr17:44744097 | G | A | 51 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(48): Show |
51 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.830+2645G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44744097 | |||||||
| chr17:44744410 | C | CA | 7 | a0001c0001t0001g0098 a0001c0001t0001g0112 a0001c0001t0001g0182 others(4): Show |
7 | HG01175.hp2 HG02300.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.831-2657dupA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44744410 | ||||||
| chr17:44744410 | CA | C | 11 | a0001c0001t0001g0095 a0001c0001t0001g0099 a0001c0001t0001g0147 others(8): Show |
11 | HG01167.hp1 HG01515.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.831-2657delA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44744410 | ||||||
| chr17:44744819 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.831-2264A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44744819 | |||||||
| chr17:44744889 | T | C | 1 | a0001c0001t0002g0024 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.831-2194T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44744889 | |||||||
| chr17:44745003 | G | C | 2 | a0001c0001t0006g0273 a0006c0009t0005g0272 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.831-2080G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44745003 | |||||||
| chr17:44745199 | A | G | 4 | a0002c0002t0003g0261 a0002c0002t0003g0262 a0002c0002t0003g0264 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.831-1884A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44745199 | |||||||
| chr17:44745237 | A | C | 5 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(2): Show |
5 | HG02922.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.831-1846A>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44745237 | |||||||
| chr17:44745392 | G | GGGTAATT others(17): Show |
1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.831-1690_831-1667d others(26): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44745392 | ||||||
| chr17:44745580 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.831-1503C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44745580 | |||||||
| chr17:44745843 | G | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.831-1240G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44745843 | |||||||
| chr17:44745979 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0104 others(115): Show |
119 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.831-1104G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44745979 | |||||||
| chr17:44746053 | CA | C | 7 | a0001c0001t0001g0082 a0001c0001t0001g0195 a0001c0001t0001g0196 others(4): Show |
7 | HG01109.hp1 HG01175.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.831-1010delA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44746053 | ||||||
| chr17:44746053 | CAA | C | 61 | a0001c0001t0001g0104 a0001c0001t0001g0150 a0001c0001t0001g0180 others(58): Show |
61 | HG00323.hp1 HG00323.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.831-1011_831-1010d others(4): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44746053 | ||||||
| chr17:44746053 | CAAA | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0057 others(151): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.831-1012_831-1010d others(5): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44746053 | ||||||
| chr17:44746053 | CAAAA | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0139 others(13): Show |
16 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.831-1013_831-1010d others(6): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44746053 | ||||||
| chr17:44746231 | CA | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
190 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(187): Show |
intron_variant | MODIFIER | c.831-833delA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44746231 | ||||||
| chr17:44746231 | CAA | C | 21 | a0001c0001t0001g0104 a0001c0001t0001g0145 a0001c0001t0001g0146 others(18): Show |
21 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.831-834_831-833del others(2): Show |
DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44746231 | ||||||
| chr17:44746687 | C | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0070 others(1): Show |
4 | NA18946.hp1 NA18971.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.831-396C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44746687 | |||||||
| chr17:44746691 | C | A | 1 | a0001c0001t0002g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.831-392C>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44746691 | |||||||
| chr17:44746707 | T | A | 1 | a0001c0001t0001g0283 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.831-376T>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44746707 | |||||||
| chr17:44746718 | C | T | 2 | a0001c0001t0002g0026 a0001c0001t0002g0043 |
2 | HG00673.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.831-365C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44746718 | |||||||
| chr17:44746729 | G | C | 1 | a0001c0001t0002g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.831-354G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44746729 | |||||||
| chr17:44746816 | C | CA | 12 | a0001c0001t0001g0170 a0001c0001t0001g0177 a0001c0001t0001g0185 others(9): Show |
12 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.831-251dupA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44746816 | ||||||
| chr17:44746816 | CA | C | 58 | a0001c0001t0001g0061 a0001c0001t0001g0123 a0001c0001t0001g0132 others(55): Show |
58 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.831-251delA | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 44746816 | ||||||
| chr17:44746882 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.831-201C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44746882 | |||||||
| chr17:44746899 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.831-184C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44746899 | |||||||
| chr17:44747034 | C | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0104 others(103): Show |
107 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.831-49C>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44747034 | |||||||
| chr17:44747034 | C | G | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.831-49C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 10/13 | chr17 | 44747034 | |||||||
| chr17:44747280 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.939+89T>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 11/13 | chr17 | 44747280 | |||||||
| chr17:44747363 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0104 others(103): Show |
107 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.940-28G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 11/13 | chr17 | 44747363 | |||||||
| chr17:44747526 | C | T | 2 | a0001c0001t0002g0037 a0001c0001t0002g0038 |
2 | HG00642.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.1064+11C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 12/13 | chr17 | 44747526 | |||||||
| chr17:44747592 | T | A | 1 | a0001c0001t0002g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1064+77T>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 12/13 | chr17 | 44747592 | |||||||
| chr17:44747679 | G | A | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0140 others(1): Show |
4 | NA18986.hp2 NA19004.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+164G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 12/13 | chr17 | 44747679 | |||||||
| chr17:44747988 | C | G | 1 | a0001c0001t0001g0243 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1065-353C>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 12/13 | chr17 | 44747988 | |||||||
| chr17:44748175 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1065-166C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 12/13 | chr17 | 44748175 | |||||||
| chr17:44748181 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0188 |
2 | HG02738.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1065-160G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 12/13 | chr17 | 44748181 | |||||||
| chr17:44748255 | G | A | 19 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(16): Show |
19 | HG00621.hp2 HG00639.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.1065-86G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 12/13 | chr17 | 44748255 | |||||||
| chr17:44748962 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1189+497C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 13/13 | chr17 | 44748962 | |||||||
| chr17:44749046 | G | A | 4 | a0002c0002t0003g0261 a0002c0002t0003g0262 a0002c0002t0003g0264 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1189+581G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 13/13 | chr17 | 44749046 | |||||||
| chr17:44749288 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1189+823A>G | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 13/13 | chr17 | 44749288 | |||||||
| chr17:44749299 | G | C | 1 | a0001c0001t0001g0242 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1189+834G>C | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 13/13 | chr17 | 44749299 | |||||||
| chr17:44749742 | C | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG00323.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1190-853C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 13/13 | chr17 | 44749742 | |||||||
| chr17:44749787 | G | A | 7 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(4): Show |
7 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1190-808G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 13/13 | chr17 | 44749787 | |||||||
| chr17:44749903 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1190-692C>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 13/13 | chr17 | 44749903 | |||||||
| chr17:44750242 | C | A | 1 | a0001c0001t0001g0123 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1190-353C>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 13/13 | chr17 | 44750242 | |||||||
| chr17:44750277 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1190-318G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 13/13 | chr17 | 44750277 | |||||||
| chr17:44750305 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.1190-290G>A | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 13/13 | chr17 | 44750305 | |||||||
| chr17:44750387 | G | T | 1 | a0001c0001t0006g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1190-208G>T | DBF4B | ENSG00000161692.18 | transcript | ENST00000315005.8 | protein_coding | 13/13 | chr17 | 44750387 |