Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1633 |
| ensemblid | ENSG00000156136.10 |
| hgncid | 2704 |
| symbol | DCK |
| name | deoxycytidine kinase |
| refseq_nuc | NM_000788.3 |
| refseq_prot | NP_000779.1 |
| ensembl_nuc | ENST00000286648.10 |
| ensembl_prot | ENSP00000286648.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 70993649 |
| end | 71030914 |
| strand | + |
| ver | v1.2 |
| region | chr4:70993649-71030914 |
| region5000 | chr4:70988649-71035914 |
| regionname0 | DCK_chr4_70993649_71030914 |
| regionname5000 | DCK_chr4_70988649_71035914 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 260 | 260 | 84 | 55 | 77 | 10 | 32 | 49 | DCK_chr4_70988649_71035914 | DCK | MATPP others(255): Show |
chr4 | 70988649 | 71035914 |
| a0002 | 0/0 | 260 | 16 | 2 | 1 | 11 | 0 | 2 | 9 | DCK_chr4_70988649_71035914 | DCK | MATPP others(255): Show |
chr4 | 70988649 | 71035914 |
| a0003 | 0/0 | 260 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | MATPP others(255): Show |
chr4 | 70988649 | 71035914 |
| a0004 | 0/0 | 260 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | MATPP others(255): Show |
chr4 | 70988649 | 71035914 |
| a0005 | 0/0 | 260 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | MATPP others(255): Show |
chr4 | 70988649 | 71035914 |
| a0006 | 0/0 | 260 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | MATPP others(255): Show |
chr4 | 70988649 | 71035914 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 780 | 254 | 83 | 53 | 77 | 8 | 32 | DCK_chr4_70988649_71035914 | DCK | ATGGC others(775): Show |
chr4 | 70988649 | 71035914 | ||
| a0001c0003 | 0/1 | 780 | 6 | 1 | 2 | 0 | 2 | 0 | DCK_chr4_70988649_71035914 | DCK | ATGGC others(775): Show |
chr4 | 70988649 | 71035914 | ||
| a0002c0002 | 0/0 | 780 | 16 | 2 | 1 | 11 | 0 | 2 | DCK_chr4_70988649_71035914 | DCK | ATGGC others(775): Show |
chr4 | 70988649 | 71035914 | ||
| a0003c0005 | 0/0 | 780 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | ATGGC others(775): Show |
chr4 | 70988649 | 71035914 | ||
| a0004c0004 | 0/0 | 780 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | ATGGC others(775): Show |
chr4 | 70988649 | 71035914 | ||
| a0005c0006 | 0/0 | 780 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | ATGGC others(775): Show |
chr4 | 70988649 | 71035914 | ||
| a0006c0007 | 0/0 | 780 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | ATGGC others(775): Show |
chr4 | 70988649 | 71035914 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2506 | 184 | 29 | 45 | 76 | 5 | 29 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0001c0001t0002 | 1/0 | 2506 | 31 | 23 | 4 | 0 | 3 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0001c0001t0003 | 0/0 | 2506 | 12 | 10 | 0 | 0 | 0 | 2 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0001c0001t0004 | 0/0 | 2504 | 9 | 9 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2499): Show |
chr4 | 70988649 | 71035914 |
| a0001c0001t0005 | 0/0 | 2506 | 4 | 4 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0001c0001t0006 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0001c0001t0008 | 0/0 | 2506 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0001c0001t0009 | 0/0 | 2506 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0001c0001t0010 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0001c0001t0011 | 0/0 | 2506 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0001c0001t0012 | 0/0 | 2506 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0001c0001t0013 | 0/0 | 2506 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0001c0001t0014 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0001c0001t0015 | 0/0 | 2506 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0001c0001t0016 | 0/0 | 2506 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0001c0001t0017 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0001c0001t0018 | 0/0 | 2506 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0001c0003t0001 | 0/0 | 2506 | 3 | 1 | 0 | 0 | 2 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0001c0003t0007 | 0/1 | 2506 | 3 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0002c0002t0002 | 0/0 | 2506 | 15 | 1 | 1 | 11 | 0 | 2 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0002c0002t0019 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0003c0005t0002 | 0/0 | 2506 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0004c0004t0006 | 0/0 | 2506 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0005c0006t0001 | 0/0 | 2506 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| a0006c0007t0001 | 0/0 | 2506 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | AGTGT others(2501): Show |
chr4 | 70988649 | 71035914 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 8 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 1 | 5 | 0 | 2 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0008 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0015 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0003g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0004g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0008g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0008g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0009g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0009g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0011g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0012g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0013g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0014g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0015g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0016g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0017g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0001t0018g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0003t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0003t0007g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0001c0003t0007g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0002c0002t0002g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0002c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0002c0002t0019g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0003c0005t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0004c0004t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0004c0004t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0005c0006t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| a0006c0007t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | GBR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00140 | hp1 | a0005 | c0006 | t0001 | g0013 | EUR | GBR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0040 | EUR | FIN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00735 | hp1 | a0001 | c0001 | t0015 | g0131 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01106 | hp2 | a0001 | c0001 | t0011 | g0018 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01109 | hp2 | a0001 | c0001 | t0013 | g0174 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01255 | hp2 | a0001 | c0001 | t0018 | g0134 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01256 | hp2 | a0001 | c0003 | t0007 | g0036 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01258 | hp2 | a0001 | c0003 | t0007 | g0036 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01515 | hp1 | a0006 | c0007 | t0001 | g0091 | EUR | IBS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0021 | EUR | IBS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0032 | EUR | IBS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0032 | EUR | IBS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0021 | EUR | IBS | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0165 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0166 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01891 | hp2 | a0003 | c0005 | t0002 | g0039 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02083 | hp2 | a0001 | c0001 | t0016 | g0097 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0180 | EAS | KHV | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02145 | hp1 | a0001 | c0001 | t0010 | g0019 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CDX | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CDX | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0129 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0062 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0179 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02723 | hp1 | a0002 | c0002 | t0019 | g0059 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02723 | hp2 | a0003 | c0005 | t0002 | g0039 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02886 | hp2 | a0004 | c0004 | t0006 | g0172 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0075 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0076 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03130 | hp1 | a0001 | c0001 | t0014 | g0051 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0064 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0054 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03453 | hp1 | a0001 | c0001 | t0017 | g0012 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ESN | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0023 | SAS | STU | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03710 | hp1 | a0001 | c0001 | t0012 | g0026 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0187 | SAS | PJL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0020 | SAS | BEB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | STU | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | YRI | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | YRI | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | YRI | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | YRI | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18997 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | LWK | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0063 | AFR | LWK | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0053 | AFR | LWK | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19240 | hp1 | a0004 | c0004 | t0006 | g0173 | AFR | YRI | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | YRI | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | ASW | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | GIH | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | GIH | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0186 | AMR | CLM | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0052 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0099 | AFR | USA | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | USA | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | USA | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | USA | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0007 | g0160 | REF | REF | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0067 | REF | REF | DCK_chr4_70988649_71035914 | DCK | chr4 | 70988649 | 71035914 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70993905 | A | G | 1 | a0003 | 2 | HG01891.hp2 HG02723.hp2 |
missense_variant | MODERATE | c.70A>G | p.Ile24Val | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/7 | 257/2506 | 70/783 | 24/260 | chr4 | 70993905 | |||
| chr4:71022428 | A | G | 1 | a0006 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.269A>G | p.Glu90Gly | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/7 | 456/2506 | 269/783 | 90/260 | chr4 | 71022428 | |||
| chr4:71022515 | C | G | 1 | a0004 | 2 | HG02886.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.356C>G | p.Ala119Gly | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/7 | 543/2506 | 356/783 | 119/260 | chr4 | 71022515 | |||
| chr4:71022523 | C | T | 1 | a0002 | 16 | HG00673.hp1 HG01123.hp2 HG02129.hp2 others(13): Show |
missense_variant | MODERATE | c.364C>T | p.Pro122Ser | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/7 | 551/2506 | 364/783 | 122/260 | chr4 | 71022523 | |||
| chr4:71023570 | C | T | 1 | a0005 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.413C>T | p.Ala138Val | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/7 | 600/2506 | 413/783 | 138/260 | chr4 | 71023570 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:71022459 | C | T | 2 | a0001c0003 a0006c0007 |
6 | HG01256.hp2 HG01258.hp2 HG01515.hp1 others(3): Show |
synonymous_variant | LOW | c.300C>T | p.Ala100Ala | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/7 | 487/2506 | 300/783 | 100/260 | chr4 | 71022459 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70993694 | C | G | 1 | a0002c0002t0019 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-142C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/7 | 142 | chr4 | 70993694 | ||||||
| chr4:70993784 | G | A | 3 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0010 |
7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-52G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/7 | 52 | chr4 | 70993784 | ||||||
| chr4:70993807 | C | A | 1 | a0001c0001t0011 | 1 | HG01106.hp2 | 5_prime_UTR_variant | MODIFIER | c.-29C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/7 | 29 | chr4 | 70993807 | ||||||
| chr4:70993824 | C | G | 1 | a0001c0001t0018 | 1 | HG01255.hp2 | 5_prime_UTR_variant | MODIFIER | c.-12C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/7 | 12 | chr4 | 70993824 | ||||||
| chr4:71029523 | T | A | 1 | a0001c0001t0012 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*145T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 145 | chr4 | 71029523 | ||||||
| chr4:71029543 | C | T | 13 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(10): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*165C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 165 | chr4 | 71029543 | ||||||
| chr4:71029923 | C | A | 1 | a0001c0001t0005 | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*545C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 545 | chr4 | 71029923 | ||||||
| chr4:71029925 | T | G | 1 | a0001c0001t0015 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*547T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 547 | chr4 | 71029925 | ||||||
| chr4:71029948 | C | T | 1 | a0001c0001t0005 | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*570C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 570 | chr4 | 71029948 | ||||||
| chr4:71029951 | T | C | 1 | a0001c0001t0004 | 9 | HG02280.hp2 HG02615.hp2 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*573T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 573 | chr4 | 71029951 | ||||||
| chr4:71030118 | A | G | 1 | a0001c0001t0017 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*740A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 740 | chr4 | 71030118 | ||||||
| chr4:71030303 | T | C | 1 | a0001c0001t0013 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*925T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 925 | chr4 | 71030303 | ||||||
| chr4:71030333 | G | A | 1 | a0001c0001t0014 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*955G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 955 | chr4 | 71030333 | ||||||
| chr4:71030503 | C | T | 4 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0013 others(1): Show |
8 | HG01109.hp2 HG01884.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1125C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 1125 | chr4 | 71030503 | ||||||
| chr4:71030572 | C | A | 1 | a0001c0003t0007 | 2 | HG01256.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1194C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 1194 | chr4 | 71030572 | ||||||
| chr4:71030649 | T | C | 1 | a0001c0001t0016 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1271T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 1271 | chr4 | 71030649 | ||||||
| chr4:71030700 | A | T | 1 | a0001c0001t0003 | 12 | HG02055.hp1 HG02602.hp1 HG02818.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1322A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 1322 | chr4 | 71030700 | ||||||
| chr4:71030750 | T | C | 1 | a0001c0001t0009 | 2 | HG01891.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1372T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 1372 | chr4 | 71030750 | ||||||
| chr4:71030804 | A | G | 1 | a0001c0001t0013 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1426A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 1426 | chr4 | 71030804 | ||||||
| chr4:71030848 | CTT | C | 1 | a0001c0001t0004 | 9 | HG02280.hp2 HG02615.hp2 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1473_*1474delTT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 7/7 | 1473 | INFO_REALIGN_3_PRIME | chr4 | 71030848 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70993963 | G | C | 3 | a0001c0001t0002g0021 a0001c0001t0002g0040 a0001c0001t0002g0041 |
4 | HG00323.hp2 HG00735.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+37G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70993963 | |||||||
| chr4:70994180 | G | T | 1 | a0003c0005t0002g0039 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.91+254G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994180 | |||||||
| chr4:70994202 | G | A | 1 | a0001c0001t0001g0022 | 2 | NA19005.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.91+276G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994202 | |||||||
| chr4:70994249 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.91+323A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994249 | |||||||
| chr4:70994438 | A | G | 1 | a0001c0001t0002g0192 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.91+512A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994438 | |||||||
| chr4:70994594 | A | G | 24 | a0001c0001t0001g0190 a0001c0001t0002g0019 a0001c0001t0002g0175 others(21): Show |
28 | HG00673.hp1 HG01109.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.91+668A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994594 | |||||||
| chr4:70994642 | G | C | 1 | a0001c0001t0002g0042 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.91+716G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994642 | |||||||
| chr4:70994688 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.91+762A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994688 | |||||||
| chr4:70994791 | T | C | 1 | a0001c0001t0005g0043 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.91+865T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994791 | |||||||
| chr4:70994807 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.91+881A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994807 | |||||||
| chr4:70994882 | A | C | 1 | a0001c0001t0001g0170 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.91+956A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994882 | |||||||
| chr4:70994925 | T | A | 3 | a0001c0001t0013g0174 a0004c0004t0006g0172 a0004c0004t0006g0173 |
3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.91+999T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994925 | |||||||
| chr4:70994944 | A | T | 1 | a0001c0001t0001g0170 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.91+1018A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994944 | |||||||
| chr4:70994950 | A | T | 9 | a0001c0001t0002g0019 a0001c0001t0002g0056 a0001c0001t0002g0065 others(6): Show |
11 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.91+1024A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994950 | |||||||
| chr4:70994958 | A | T | 4 | a0001c0001t0001g0170 a0001c0001t0013g0174 a0004c0004t0006g0172 others(1): Show |
4 | HG01109.hp2 HG02165.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+1032A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70994958 | |||||||
| chr4:70995036 | C | T | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 |
3 | HG02109.hp1 HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.91+1110C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70995036 | |||||||
| chr4:70995037 | T | G | 9 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0003g0005 others(6): Show |
14 | HG01243.hp2 HG02055.hp1 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.91+1111T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70995037 | |||||||
| chr4:70995093 | A | C | 1 | a0001c0001t0009g0166 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.91+1167A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70995093 | |||||||
| chr4:70995168 | A | G | 3 | a0001c0001t0013g0174 a0004c0004t0006g0172 a0004c0004t0006g0173 |
3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.91+1242A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70995168 | |||||||
| chr4:70995387 | G | C | 1 | a0001c0001t0002g0192 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.91+1461G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70995387 | |||||||
| chr4:70995469 | A | G | 1 | a0001c0001t0001g0038 | 2 | HG00673.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.91+1543A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70995469 | |||||||
| chr4:70995553 | T | C | 6 | a0001c0001t0002g0021 a0001c0001t0002g0024 a0001c0001t0002g0040 others(3): Show |
8 | HG00323.hp2 HG00735.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+1627T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70995553 | |||||||
| chr4:70995783 | A | G | 4 | a0001c0001t0006g0165 a0001c0001t0013g0174 a0004c0004t0006g0172 others(1): Show |
4 | HG01109.hp2 HG01884.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+1857A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70995783 | |||||||
| chr4:70995997 | G | A | 4 | a0001c0001t0005g0043 a0001c0001t0005g0052 a0001c0001t0005g0053 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-2070G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70995997 | |||||||
| chr4:70996204 | CA | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.92-1848delA | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 70996204 | ||||||
| chr4:70996377 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.92-1690T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70996377 | |||||||
| chr4:70996886 | T | A | 2 | a0004c0004t0006g0172 a0004c0004t0006g0173 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.92-1181T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70996886 | |||||||
| chr4:70996957 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.92-1110T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70996957 | |||||||
| chr4:70997287 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG00140.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.92-780C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997287 | |||||||
| chr4:70997351 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0012g0026 |
2 | HG03710.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.92-716T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997351 | |||||||
| chr4:70997382 | C | T | 3 | a0001c0001t0013g0174 a0004c0004t0006g0172 a0004c0004t0006g0173 |
3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.92-685C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997382 | |||||||
| chr4:70997393 | T | C | 31 | a0001c0001t0002g0019 a0001c0001t0002g0056 a0001c0001t0002g0057 others(28): Show |
40 | HG00673.hp1 HG01123.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.92-674T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997393 | |||||||
| chr4:70997399 | G | A | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.92-668G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997399 | |||||||
| chr4:70997479 | T | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
7 | HG00738.hp1 HG01069.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-588T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997479 | |||||||
| chr4:70997580 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.92-487A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997580 | |||||||
| chr4:70997806 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.92-261C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997806 | |||||||
| chr4:70997893 | G | A | 37 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0024 others(34): Show |
48 | HG00323.hp2 HG00673.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.92-174G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997893 | |||||||
| chr4:70997957 | T | G | 1 | a0001c0001t0002g0164 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.92-110T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | chr4 | 70997957 | |||||||
| chr4:70998016 | CT | C | 5 | a0001c0001t0002g0066 a0001c0001t0002g0167 a0001c0001t0002g0168 others(2): Show |
5 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-44delT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 70998016 | ||||||
| chr4:70998296 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.207+114A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998296 | |||||||
| chr4:70998329 | A | G | 1 | a0001c0001t0002g0169 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.207+147A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998329 | |||||||
| chr4:70998362 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.207+180A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998362 | |||||||
| chr4:70998367 | G | A | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+185G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998367 | |||||||
| chr4:70998368 | A | T | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.207+186A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998368 | |||||||
| chr4:70998455 | G | A | 2 | a0004c0004t0006g0172 a0004c0004t0006g0173 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.207+273G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998455 | |||||||
| chr4:70998525 | A | C | 1 | a0001c0003t0007g0036 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.207+343A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998525 | |||||||
| chr4:70998527 | A | G | 4 | a0001c0001t0005g0043 a0001c0001t0005g0052 a0001c0001t0005g0053 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+345A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998527 | |||||||
| chr4:70998548 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.207+366G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998548 | |||||||
| chr4:70998588 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0008g0075 a0001c0001t0008g0076 |
5 | HG02647.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+406G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998588 | |||||||
| chr4:70998638 | T | C | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.207+456T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998638 | |||||||
| chr4:70998671 | C | T | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+489C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998671 | |||||||
| chr4:70998733 | C | G | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+551C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998733 | |||||||
| chr4:70998751 | C | T | 1 | a0001c0001t0002g0065 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.207+569C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998751 | |||||||
| chr4:70998812 | G | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.207+630G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998812 | |||||||
| chr4:70998816 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA18975.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.207+634G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998816 | |||||||
| chr4:70998824 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.207+642G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998824 | |||||||
| chr4:70998859 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.207+677G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998859 | |||||||
| chr4:70998879 | C | A | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+697C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70998879 | |||||||
| chr4:70998925 | C | CA | 13 | a0001c0001t0001g0055 a0001c0001t0001g0161 a0001c0001t0002g0019 others(10): Show |
15 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.207+756dupA | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 70998925 | ||||||
| chr4:70999023 | T | G | 1 | a0001c0001t0001g0081 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.207+841T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70999023 | |||||||
| chr4:70999185 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.207+1003G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70999185 | |||||||
| chr4:70999418 | T | C | 2 | a0001c0001t0002g0057 a0001c0001t0002g0058 |
2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.207+1236T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70999418 | |||||||
| chr4:70999591 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.207+1409C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70999591 | |||||||
| chr4:70999591 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.207+1409C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70999591 | |||||||
| chr4:70999701 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | NA18968.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.207+1519A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70999701 | |||||||
| chr4:70999766 | T | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0084 |
6 | HG00609.hp2 HG02027.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.207+1584T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70999766 | |||||||
| chr4:70999798 | G | T | 1 | a0001c0001t0002g0042 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.207+1616G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 70999798 | |||||||
| chr4:71000096 | T | C | 4 | a0001c0001t0006g0165 a0001c0001t0013g0174 a0004c0004t0006g0172 others(1): Show |
4 | HG01109.hp2 HG01884.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+1914T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71000096 | |||||||
| chr4:71000161 | T | G | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+1979T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71000161 | |||||||
| chr4:71000336 | G | A | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+2154G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71000336 | |||||||
| chr4:71000453 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(137): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.207+2271A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71000453 | |||||||
| chr4:71001164 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.207+2982A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71001164 | |||||||
| chr4:71001256 | G | C | 1 | a0002c0002t0002g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.207+3074G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71001256 | |||||||
| chr4:71001421 | T | TC | 4 | a0001c0001t0004g0004 a0001c0001t0004g0062 a0001c0001t0004g0063 others(1): Show |
9 | HG02280.hp2 HG02615.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.207+3240dupC | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71001421 | ||||||
| chr4:71001535 | A | G | 5 | a0001c0001t0005g0043 a0001c0001t0005g0052 a0001c0001t0005g0053 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+3353A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71001535 | |||||||
| chr4:71001586 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.207+3404G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71001586 | |||||||
| chr4:71001669 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0087 others(1): Show |
8 | HG01192.hp2 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+3487T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71001669 | |||||||
| chr4:71001694 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.207+3512C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71001694 | |||||||
| chr4:71001714 | A | C | 4 | a0001c0001t0003g0005 a0001c0001t0003g0048 a0001c0001t0003g0049 others(1): Show |
8 | HG02055.hp1 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+3532A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71001714 | |||||||
| chr4:71001855 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | NA18968.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.207+3673C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71001855 | |||||||
| chr4:71001964 | A | G | 2 | a0001c0001t0002g0066 a0001c0001t0002g0192 |
2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.207+3782A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71001964 | |||||||
| chr4:71002220 | C | T | 3 | a0001c0001t0004g0004 a0001c0001t0004g0063 a0001c0001t0004g0064 |
8 | HG02615.hp2 HG02965.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+4038C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002220 | |||||||
| chr4:71002239 | A | C | 1 | a0001c0001t0002g0042 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.207+4057A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002239 | |||||||
| chr4:71002402 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.207+4220G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002402 | |||||||
| chr4:71002411 | C | T | 4 | a0001c0001t0006g0165 a0001c0001t0013g0174 a0004c0004t0006g0172 others(1): Show |
4 | HG01109.hp2 HG01884.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+4229C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002411 | |||||||
| chr4:71002462 | C | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.207+4280C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002462 | |||||||
| chr4:71002654 | G | A | 1 | a0001c0001t0002g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.207+4472G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002654 | |||||||
| chr4:71002669 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.207+4487A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002669 | |||||||
| chr4:71002716 | C | T | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | NA18968.hp2 NA18977.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+4534C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002716 | |||||||
| chr4:71002868 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.207+4686C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002868 | |||||||
| chr4:71002934 | C | T | 4 | a0001c0001t0001g0081 a0001c0001t0001g0086 a0001c0001t0001g0152 others(1): Show |
4 | HG00423.hp2 NA19056.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+4752C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002934 | |||||||
| chr4:71002985 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.207+4803T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71002985 | |||||||
| chr4:71003082 | C | T | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+4900C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003082 | |||||||
| chr4:71003193 | T | C | 1 | a0006c0007t0001g0091 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.207+5011T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003193 | |||||||
| chr4:71003264 | T | G | 1 | a0001c0001t0001g0092 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.207+5082T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003264 | |||||||
| chr4:71003348 | C | A | 1 | a0001c0001t0001g0028 | 2 | HG01261.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.207+5166C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003348 | |||||||
| chr4:71003428 | A | G | 3 | a0001c0001t0013g0174 a0004c0004t0006g0172 a0004c0004t0006g0173 |
3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.207+5246A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003428 | |||||||
| chr4:71003440 | G | A | 4 | a0001c0001t0005g0043 a0001c0001t0005g0052 a0001c0001t0005g0053 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+5258G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003440 | |||||||
| chr4:71003457 | C | G | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.207+5275C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003457 | |||||||
| chr4:71003697 | A | T | 9 | a0001c0001t0002g0019 a0001c0001t0002g0056 a0001c0001t0002g0065 others(6): Show |
11 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.207+5515A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003697 | |||||||
| chr4:71003724 | C | G | 1 | a0001c0001t0001g0027 | 2 | HG01192.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.207+5542C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003724 | |||||||
| chr4:71003802 | C | A | 1 | a0001c0001t0002g0066 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.207+5620C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003802 | |||||||
| chr4:71003901 | T | A | 1 | a0001c0001t0001g0037 | 2 | HG00140.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.207+5719T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71003901 | |||||||
| chr4:71004010 | T | C | 2 | a0001c0001t0005g0052 a0001c0001t0005g0053 |
2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.207+5828T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71004010 | |||||||
| chr4:71004036 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.207+5854A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71004036 | |||||||
| chr4:71004169 | A | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0087 others(1): Show |
8 | HG01192.hp2 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+5987A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71004169 | |||||||
| chr4:71004235 | A | G | 4 | a0001c0001t0005g0043 a0001c0001t0005g0052 a0001c0001t0005g0053 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+6053A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71004235 | |||||||
| chr4:71004484 | G | A | 1 | a0002c0002t0019g0059 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.207+6302G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71004484 | |||||||
| chr4:71004564 | C | G | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+6382C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71004564 | |||||||
| chr4:71004815 | A | T | 1 | a0001c0001t0002g0068 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.207+6633A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71004815 | |||||||
| chr4:71004906 | G | GGGATCTG others(20): Show |
1 | a0002c0002t0002g0189 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.207+6725_207+6751d others(29): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71004906 | ||||||
| chr4:71004926 | ACTTGGCT others(16): Show |
A | 6 | a0001c0001t0002g0019 a0001c0001t0005g0043 a0001c0001t0005g0052 others(3): Show |
7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+6771_207+6793d others(25): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71004926 | ||||||
| chr4:71005067 | A | G | 13 | a0001c0001t0002g0058 a0002c0002t0002g0020 a0002c0002t0002g0180 others(10): Show |
15 | HG00673.hp1 HG01123.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.207+6885A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005067 | |||||||
| chr4:71005170 | T | C | 1 | a0001c0001t0001g0015 | 3 | HG01167.hp1 HG01169.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.207+6988T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005170 | |||||||
| chr4:71005171 | C | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.207+6989C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005171 | |||||||
| chr4:71005211 | A | G | 4 | a0001c0001t0005g0043 a0001c0001t0005g0052 a0001c0001t0005g0053 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+7029A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005211 | |||||||
| chr4:71005240 | C | T | 3 | a0001c0001t0013g0174 a0004c0004t0006g0172 a0004c0004t0006g0173 |
3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.207+7058C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005240 | |||||||
| chr4:71005490 | C | T | 1 | a0001c0001t0002g0178 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.207+7308C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005490 | |||||||
| chr4:71005599 | C | T | 4 | a0001c0001t0005g0043 a0001c0001t0005g0052 a0001c0001t0005g0053 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+7417C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005599 | |||||||
| chr4:71005827 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0002g0069 |
2 | HG02258.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.207+7645T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005827 | |||||||
| chr4:71005861 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.207+7679C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005861 | |||||||
| chr4:71005960 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.207+7778C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71005960 | |||||||
| chr4:71006051 | G | A | 1 | a0002c0002t0019g0059 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.207+7869G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006051 | |||||||
| chr4:71006100 | C | CA | 4 | a0001c0001t0004g0004 a0001c0001t0004g0062 a0001c0001t0004g0063 others(1): Show |
9 | HG02280.hp2 HG02615.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.207+7932dupA | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71006100 | ||||||
| chr4:71006114 | A | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.207+7932A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006114 | |||||||
| chr4:71006133 | C | CA | 15 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0066 others(12): Show |
20 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.207+7969dupA | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71006133 | ||||||
| chr4:71006133 | CAA | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.207+7968_207+7969d others(4): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71006133 | ||||||
| chr4:71006133 | CAAA | C | 5 | a0001c0001t0002g0019 a0001c0001t0004g0004 a0001c0001t0004g0063 others(2): Show |
11 | HG02145.hp1 HG02615.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.207+7967_207+7969d others(5): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71006133 | ||||||
| chr4:71006153 | C | T | 1 | a0001c0001t0003g0023 | 2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.207+7971C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006153 | |||||||
| chr4:71006246 | G | T | 1 | a0002c0002t0002g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.207+8064G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006246 | |||||||
| chr4:71006262 | G | T | 5 | a0001c0001t0002g0066 a0001c0001t0002g0167 a0001c0001t0002g0168 others(2): Show |
5 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+8080G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006262 | |||||||
| chr4:71006293 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.207+8111C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006293 | |||||||
| chr4:71006462 | T | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.207+8280T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006462 | |||||||
| chr4:71006478 | T | G | 7 | a0001c0001t0002g0021 a0001c0001t0002g0024 a0001c0001t0002g0040 others(4): Show |
9 | HG00323.hp2 HG00735.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.207+8296T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006478 | |||||||
| chr4:71006637 | G | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.207+8455G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006637 | |||||||
| chr4:71006697 | A | T | 3 | a0001c0001t0013g0174 a0004c0004t0006g0172 a0004c0004t0006g0173 |
3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.207+8515A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006697 | |||||||
| chr4:71006768 | A | G | 13 | a0002c0002t0002g0020 a0002c0002t0002g0180 a0002c0002t0002g0181 others(10): Show |
15 | HG00673.hp1 HG01123.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.207+8586A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006768 | |||||||
| chr4:71006809 | G | GA | 5 | a0001c0001t0001g0029 a0001c0001t0001g0055 a0001c0001t0001g0096 others(2): Show |
6 | HG00438.hp1 HG00438.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+8634dupA | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71006809 | ||||||
| chr4:71006866 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.207+8684A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71006866 | |||||||
| chr4:71007011 | T | C | 1 | a0002c0002t0002g0181 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.207+8829T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71007011 | |||||||
| chr4:71007025 | A | G | 1 | a0001c0001t0003g0049 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.207+8843A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71007025 | |||||||
| chr4:71007106 | C | T | 2 | a0004c0004t0006g0172 a0004c0004t0006g0173 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.207+8924C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71007106 | |||||||
| chr4:71007300 | A | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | NA19002.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.207+9118A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71007300 | |||||||
| chr4:71007459 | G | T | 1 | a0001c0001t0001g0149 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.207+9277G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71007459 | |||||||
| chr4:71007470 | G | A | 2 | a0004c0004t0006g0172 a0004c0004t0006g0173 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.207+9288G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71007470 | |||||||
| chr4:71007661 | A | G | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+9479A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71007661 | |||||||
| chr4:71007776 | C | T | 4 | a0001c0001t0005g0043 a0001c0001t0005g0052 a0001c0001t0005g0053 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+9594C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71007776 | |||||||
| chr4:71007846 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.207+9664A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71007846 | |||||||
| chr4:71008028 | A | G | 66 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(63): Show |
104 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.207+9846A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71008028 | |||||||
| chr4:71008047 | G | A | 4 | a0001c0001t0005g0043 a0001c0001t0005g0052 a0001c0001t0005g0053 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+9865G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71008047 | |||||||
| chr4:71008413 | AT | A | 2 | a0001c0001t0002g0019 a0001c0001t0010g0019 |
3 | HG02145.hp1 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.207+10236delT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71008413 | ||||||
| chr4:71008421 | A | G | 2 | a0002c0002t0002g0020 a0002c0002t0002g0188 |
4 | HG03834.hp1 NA18962.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+10239A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71008421 | |||||||
| chr4:71008500 | C | T | 4 | a0001c0001t0005g0043 a0001c0001t0005g0052 a0001c0001t0005g0053 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+10318C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71008500 | |||||||
| chr4:71008614 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.207+10432A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71008614 | |||||||
| chr4:71008842 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.207+10660C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71008842 | |||||||
| chr4:71008893 | A | G | 1 | a0001c0001t0002g0065 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.207+10711A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71008893 | |||||||
| chr4:71008972 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.207+10790G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71008972 | |||||||
| chr4:71009257 | C | T | 1 | a0001c0001t0002g0178 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.207+11075C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71009257 | |||||||
| chr4:71009393 | A | C | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.207+11211A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71009393 | |||||||
| chr4:71009476 | A | G | 4 | a0001c0001t0004g0004 a0001c0001t0004g0062 a0001c0001t0004g0063 others(1): Show |
9 | HG02280.hp2 HG02615.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.207+11294A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71009476 | |||||||
| chr4:71009520 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.207+11338A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71009520 | |||||||
| chr4:71009622 | C | T | 1 | a0001c0001t0003g0049 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.207+11440C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71009622 | |||||||
| chr4:71009853 | A | C | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+11671A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71009853 | |||||||
| chr4:71009967 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0120 others(5): Show |
17 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.207+11785A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71009967 | |||||||
| chr4:71010033 | T | G | 4 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0060 others(1): Show |
4 | HG01167.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+11851T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71010033 | |||||||
| chr4:71010166 | C | CT | 59 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(56): Show |
78 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.207+12001dupT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71010166 | ||||||
| chr4:71010166 | C | CTT | 42 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0002g0019 others(39): Show |
53 | HG00099.hp1 HG00323.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.207+12000_207+1200 others(6): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71010166 | ||||||
| chr4:71010183 | T | A | 2 | a0004c0004t0006g0172 a0004c0004t0006g0173 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.207+12001T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71010183 | |||||||
| chr4:71010232 | T | C | 4 | a0001c0001t0006g0165 a0001c0001t0013g0174 a0004c0004t0006g0172 others(1): Show |
4 | HG01109.hp2 HG01884.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+12050T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71010232 | |||||||
| chr4:71010524 | A | T | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208-11843A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71010524 | |||||||
| chr4:71010569 | T | A | 1 | a0001c0001t0001g0127 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.208-11798T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71010569 | |||||||
| chr4:71010638 | C | A | 2 | a0004c0004t0006g0172 a0004c0004t0006g0173 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-11729C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71010638 | |||||||
| chr4:71010648 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.208-11719G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71010648 | |||||||
| chr4:71010719 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.208-11648A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71010719 | |||||||
| chr4:71010722 | A | G | 3 | a0001c0001t0002g0021 a0001c0001t0002g0040 a0001c0001t0002g0041 |
4 | HG00323.hp2 HG00735.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-11645A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71010722 | |||||||
| chr4:71010939 | CT | C | 5 | a0001c0001t0001g0154 a0001c0001t0006g0165 a0001c0001t0013g0174 others(2): Show |
5 | HG01109.hp2 HG01884.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.208-11413delT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71010939 | ||||||
| chr4:71011204 | AAGGGCTG others(7): Show |
A | 1 | a0001c0001t0002g0164 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.208-11159_208-1114 others(18): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71011204 | ||||||
| chr4:71011232 | CT | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.208-11111delT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71011232 | ||||||
| chr4:71011232 | CTT | C | 8 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0077 others(5): Show |
8 | HG00738.hp1 HG01070.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.208-11112_208-1111 others(6): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71011232 | ||||||
| chr4:71011232 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0005g0043 a0001c0001t0005g0052 a0001c0001t0005g0053 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-11120_208-1111 others(14): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71011232 | ||||||
| chr4:71011234 | T | C | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208-11133T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011234 | |||||||
| chr4:71011235 | T | C | 2 | a0004c0004t0006g0172 a0004c0004t0006g0173 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-11132T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011235 | |||||||
| chr4:71011288 | T | C | 4 | a0001c0003t0001g0032 a0001c0003t0001g0129 a0001c0003t0007g0036 others(1): Show |
6 | HG01256.hp2 HG01258.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-11079T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011288 | |||||||
| chr4:71011351 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.208-11016T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011351 | |||||||
| chr4:71011443 | G | A | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.208-10924G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011443 | |||||||
| chr4:71011460 | G | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0071 a0001c0001t0001g0072 others(7): Show |
13 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.208-10907G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011460 | |||||||
| chr4:71011475 | G | A | 31 | a0001c0001t0002g0019 a0001c0001t0002g0056 a0001c0001t0002g0057 others(28): Show |
40 | HG00673.hp1 HG01123.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.208-10892G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011475 | |||||||
| chr4:71011506 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.208-10861A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011506 | |||||||
| chr4:71011515 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.208-10852C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011515 | |||||||
| chr4:71011569 | A | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.208-10798A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011569 | |||||||
| chr4:71011606 | C | T | 7 | a0001c0001t0003g0005 a0001c0001t0003g0023 a0001c0001t0003g0044 others(4): Show |
12 | HG02055.hp1 HG02602.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.208-10761C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011606 | |||||||
| chr4:71011717 | A | T | 1 | a0002c0002t0002g0187 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.208-10650A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011717 | |||||||
| chr4:71011722 | A | G | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208-10645A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011722 | |||||||
| chr4:71011872 | ATATAT | A | 14 | a0002c0002t0002g0020 a0002c0002t0002g0179 a0002c0002t0002g0180 others(11): Show |
16 | HG00673.hp1 HG01123.hp2 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.208-10490_208-1048 others(9): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71011872 | ||||||
| chr4:71011912 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.208-10455A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011912 | |||||||
| chr4:71011913 | C | A | 1 | a0001c0001t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.208-10454C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011913 | |||||||
| chr4:71011955 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.208-10412A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71011955 | |||||||
| chr4:71012019 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.208-10348C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71012019 | |||||||
| chr4:71012201 | C | T | 5 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0060 others(2): Show |
5 | HG01167.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-10166C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71012201 | |||||||
| chr4:71012377 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.208-9990A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71012377 | |||||||
| chr4:71012625 | CA | C | 1 | a0001c0001t0001g0017 | 3 | HG00099.hp2 HG00323.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.208-9741delA | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71012625 | |||||||
| chr4:71012709 | G | T | 7 | a0001c0001t0002g0021 a0001c0001t0002g0024 a0001c0001t0002g0040 others(4): Show |
9 | HG00323.hp2 HG00735.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-9658G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71012709 | |||||||
| chr4:71012762 | C | A | 1 | a0001c0001t0001g0118 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.208-9605C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71012762 | |||||||
| chr4:71012809 | A | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0117 |
2 | NA18982.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.208-9558A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71012809 | |||||||
| chr4:71012988 | C | A | 1 | a0001c0001t0001g0146 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.208-9379C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71012988 | |||||||
| chr4:71012993 | G | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.208-9374G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71012993 | |||||||
| chr4:71013077 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.208-9290G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013077 | |||||||
| chr4:71013129 | C | T | 2 | a0004c0004t0006g0172 a0004c0004t0006g0173 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-9238C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013129 | |||||||
| chr4:71013168 | G | C | 5 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0177 others(2): Show |
6 | HG01891.hp2 HG02723.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-9199G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013168 | |||||||
| chr4:71013201 | T | A | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208-9166T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013201 | |||||||
| chr4:71013402 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.208-8965C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013402 | |||||||
| chr4:71013599 | A | G | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208-8768A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013599 | |||||||
| chr4:71013622 | C | A | 4 | a0001c0001t0005g0043 a0001c0001t0005g0052 a0001c0001t0005g0053 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-8745C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013622 | |||||||
| chr4:71013629 | G | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.208-8738G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013629 | |||||||
| chr4:71013634 | C | A | 4 | a0001c0001t0005g0043 a0001c0001t0005g0052 a0001c0001t0005g0053 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-8733C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013634 | |||||||
| chr4:71013641 | A | T | 5 | a0001c0001t0001g0153 a0001c0001t0005g0043 a0001c0001t0005g0052 others(2): Show |
5 | HG00423.hp2 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-8726A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013641 | |||||||
| chr4:71013642 | T | A | 4 | a0001c0001t0005g0043 a0001c0001t0005g0052 a0001c0001t0005g0053 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-8725T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013642 | |||||||
| chr4:71013661 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.208-8706A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013661 | |||||||
| chr4:71013670 | G | C | 3 | a0001c0001t0013g0174 a0004c0004t0006g0172 a0004c0004t0006g0173 |
3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-8697G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013670 | |||||||
| chr4:71013725 | C | T | 1 | a0001c0001t0002g0024 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.208-8642C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013725 | |||||||
| chr4:71013755 | G | A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(28): Show |
51 | HG00140.hp2 HG00621.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.208-8612G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013755 | |||||||
| chr4:71013783 | C | G | 1 | a0001c0001t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.208-8584C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013783 | |||||||
| chr4:71013827 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.208-8540G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013827 | |||||||
| chr4:71013833 | A | G | 2 | a0001c0001t0003g0044 a0001c0001t0003g0045 |
2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.208-8534A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013833 | |||||||
| chr4:71013873 | A | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0074 others(2): Show |
7 | HG01106.hp2 HG01175.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-8494A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013873 | |||||||
| chr4:71013890 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.208-8477A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013890 | |||||||
| chr4:71013942 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.208-8425C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71013942 | |||||||
| chr4:71014072 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.208-8295G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71014072 | |||||||
| chr4:71014257 | A | G | 1 | a0001c0003t0001g0129 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.208-8110A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71014257 | |||||||
| chr4:71014278 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.208-8089A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71014278 | |||||||
| chr4:71014484 | T | C | 1 | a0002c0002t0002g0180 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.208-7883T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71014484 | |||||||
| chr4:71014486 | G | A | 1 | a0002c0002t0002g0180 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.208-7881G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71014486 | |||||||
| chr4:71014592 | AC | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.208-7773delC | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71014592 | ||||||
| chr4:71014605 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0015g0131 |
2 | HG00735.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.208-7762G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71014605 | |||||||
| chr4:71014728 | C | A | 3 | a0002c0002t0002g0182 a0002c0002t0002g0183 a0002c0002t0002g0184 |
3 | NA18995.hp1 NA18997.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.208-7639C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71014728 | |||||||
| chr4:71014845 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.208-7522A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71014845 | |||||||
| chr4:71014970 | A | G | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208-7397A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71014970 | |||||||
| chr4:71015054 | A | C | 7 | a0001c0001t0002g0021 a0001c0001t0002g0024 a0001c0001t0002g0040 others(4): Show |
9 | HG00323.hp2 HG00735.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-7313A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015054 | |||||||
| chr4:71015083 | G | C | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208-7284G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015083 | |||||||
| chr4:71015136 | TAAACACC others(5): Show |
T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.208-7218_208-7207d others(14): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71015136 | ||||||
| chr4:71015160 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.208-7207C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015160 | |||||||
| chr4:71015350 | C | A | 3 | a0001c0001t0013g0174 a0004c0004t0006g0172 a0004c0004t0006g0173 |
3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-7017C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015350 | |||||||
| chr4:71015351 | A | G | 3 | a0001c0001t0013g0174 a0004c0004t0006g0172 a0004c0004t0006g0173 |
3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-7016A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015351 | |||||||
| chr4:71015399 | T | C | 3 | a0002c0002t0002g0182 a0002c0002t0002g0183 a0002c0002t0002g0184 |
3 | NA18995.hp1 NA18997.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.208-6968T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015399 | |||||||
| chr4:71015705 | C | A | 7 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0066 others(4): Show |
7 | HG01243.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-6662C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015705 | |||||||
| chr4:71015879 | C | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0123 |
9 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.208-6488C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015879 | |||||||
| chr4:71015879 | C | T | 1 | a0001c0001t0001g0016 | 3 | HG02717.hp1 HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.208-6488C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015879 | |||||||
| chr4:71015946 | T | G | 4 | a0001c0001t0006g0165 a0001c0001t0013g0174 a0004c0004t0006g0172 others(1): Show |
4 | HG01109.hp2 HG01884.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-6421T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015946 | |||||||
| chr4:71015969 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.208-6398A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015969 | |||||||
| chr4:71015982 | G | A | 3 | a0001c0001t0013g0174 a0004c0004t0006g0172 a0004c0004t0006g0173 |
3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-6385G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71015982 | |||||||
| chr4:71016022 | A | T | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 |
3 | HG02109.hp1 HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.208-6345A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016022 | |||||||
| chr4:71016024 | T | C | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 |
3 | HG02109.hp1 HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.208-6343T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016024 | |||||||
| chr4:71016039 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.208-6328G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016039 | |||||||
| chr4:71016137 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.208-6230T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016137 | |||||||
| chr4:71016230 | T | C | 7 | a0001c0001t0003g0005 a0001c0001t0003g0023 a0001c0001t0003g0044 others(4): Show |
12 | HG02055.hp1 HG02602.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.208-6137T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016230 | |||||||
| chr4:71016242 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.208-6125C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016242 | |||||||
| chr4:71016365 | A | C | 1 | a0001c0001t0002g0177 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.208-6002A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016365 | |||||||
| chr4:71016517 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.208-5850T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016517 | |||||||
| chr4:71016518 | A | G | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208-5849A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016518 | |||||||
| chr4:71016631 | A | G | 4 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0060 others(1): Show |
4 | HG01167.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-5736A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016631 | |||||||
| chr4:71016706 | G | A | 9 | a0001c0001t0002g0019 a0001c0001t0002g0056 a0001c0001t0002g0065 others(6): Show |
11 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.208-5661G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016706 | |||||||
| chr4:71016718 | A | C | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208-5649A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016718 | |||||||
| chr4:71016721 | G | T | 4 | a0001c0001t0001g0115 a0001c0001t0001g0119 a0001c0001t0001g0171 others(1): Show |
4 | HG02602.hp2 HG03490.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-5646G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016721 | |||||||
| chr4:71016747 | T | A | 1 | a0001c0001t0001g0135 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.208-5620T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016747 | |||||||
| chr4:71016840 | A | T | 1 | a0001c0001t0002g0168 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.208-5527A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016840 | |||||||
| chr4:71016878 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.208-5489G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016878 | |||||||
| chr4:71016887 | T | A | 5 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0177 others(2): Show |
6 | HG01891.hp2 HG02723.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-5480T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016887 | |||||||
| chr4:71016910 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.208-5457A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016910 | |||||||
| chr4:71016918 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0006g0165 |
2 | HG01884.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.208-5449C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016918 | |||||||
| chr4:71016933 | G | C | 7 | a0001c0001t0003g0005 a0001c0001t0003g0023 a0001c0001t0003g0044 others(4): Show |
12 | HG02055.hp1 HG02602.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.208-5434G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016933 | |||||||
| chr4:71016968 | A | G | 2 | a0004c0004t0006g0172 a0004c0004t0006g0173 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-5399A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016968 | |||||||
| chr4:71016974 | A | G | 2 | a0001c0001t0002g0056 a0001c0001t0002g0065 |
2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.208-5393A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71016974 | |||||||
| chr4:71017004 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.208-5363G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017004 | |||||||
| chr4:71017008 | G | A | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208-5359G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017008 | |||||||
| chr4:71017134 | C | T | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208-5233C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017134 | |||||||
| chr4:71017135 | T | G | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208-5232T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017135 | |||||||
| chr4:71017322 | A | G | 2 | a0001c0001t0005g0043 a0001c0001t0005g0054 |
2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.208-5045A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017322 | |||||||
| chr4:71017392 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.208-4975C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017392 | |||||||
| chr4:71017409 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.208-4958C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017409 | |||||||
| chr4:71017424 | A | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | NA18986.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.208-4943A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017424 | |||||||
| chr4:71017468 | A | G | 3 | a0001c0001t0013g0174 a0004c0004t0006g0172 a0004c0004t0006g0173 |
3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-4899A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017468 | |||||||
| chr4:71017762 | C | T | 4 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0060 others(1): Show |
4 | HG01167.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-4605C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017762 | |||||||
| chr4:71017777 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.208-4590T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017777 | |||||||
| chr4:71017790 | G | A | 4 | a0001c0001t0005g0043 a0001c0001t0005g0052 a0001c0001t0005g0053 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-4577G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017790 | |||||||
| chr4:71017836 | A | C | 1 | a0001c0001t0001g0110 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.208-4531A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017836 | |||||||
| chr4:71017875 | A | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0142 |
2 | HG02056.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.208-4492A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71017875 | |||||||
| chr4:71018072 | C | G | 1 | a0001c0001t0001g0128 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.208-4295C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018072 | |||||||
| chr4:71018126 | C | CT | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.208-4223dupT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71018126 | ||||||
| chr4:71018126 | C | CTT | 5 | a0001c0001t0001g0106 a0001c0001t0001g0119 a0001c0001t0001g0141 others(2): Show |
5 | HG01109.hp1 HG02027.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.208-4224_208-4223d others(4): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71018126 | ||||||
| chr4:71018251 | C | G | 5 | a0001c0001t0002g0066 a0001c0001t0002g0167 a0001c0001t0002g0168 others(2): Show |
5 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-4116C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018251 | |||||||
| chr4:71018374 | C | T | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208-3993C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018374 | |||||||
| chr4:71018423 | C | T | 2 | a0001c0001t0002g0046 a0001c0001t0002g0047 |
2 | HG01243.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.208-3944C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018423 | |||||||
| chr4:71018488 | T | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.208-3879T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018488 | |||||||
| chr4:71018497 | T | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0074 others(2): Show |
7 | HG01106.hp2 HG01175.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-3870T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018497 | |||||||
| chr4:71018666 | AT | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.208-3679delT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71018666 | ||||||
| chr4:71018666 | ATT | A | 10 | a0001c0001t0001g0109 a0001c0001t0001g0155 a0001c0001t0002g0019 others(7): Show |
11 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.208-3680_208-3679d others(4): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71018666 | ||||||
| chr4:71018911 | A | G | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208-3456A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018911 | |||||||
| chr4:71018911 | A | T | 1 | a0001c0001t0001g0122 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.208-3456A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018911 | |||||||
| chr4:71018915 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.208-3452G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018915 | |||||||
| chr4:71018923 | C | T | 3 | a0001c0003t0001g0032 a0001c0003t0007g0036 a0006c0007t0001g0091 |
5 | HG01256.hp2 HG01258.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-3444C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71018923 | |||||||
| chr4:71019021 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0123 |
9 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.208-3346T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019021 | |||||||
| chr4:71019043 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.208-3324T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019043 | |||||||
| chr4:71019150 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.208-3217A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019150 | |||||||
| chr4:71019192 | A | G | 2 | a0001c0001t0002g0057 a0001c0001t0002g0058 |
2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.208-3175A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019192 | |||||||
| chr4:71019258 | G | A | 1 | a0002c0002t0002g0187 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.208-3109G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019258 | |||||||
| chr4:71019392 | G | T | 1 | a0001c0001t0002g0066 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.208-2975G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019392 | |||||||
| chr4:71019592 | C | G | 4 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0060 others(1): Show |
4 | HG01167.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-2775C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019592 | |||||||
| chr4:71019782 | A | AT | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.208-2576dupT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71019782 | ||||||
| chr4:71019791 | T | TA | 1 | a0001c0001t0001g0016 | 3 | HG02717.hp1 HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.208-2573dupA | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71019791 | ||||||
| chr4:71019792 | A | T | 2 | a0001c0001t0002g0069 a0001c0001t0016g0097 |
2 | HG02083.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.208-2575A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019792 | |||||||
| chr4:71019932 | G | T | 1 | a0001c0001t0001g0088 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.208-2435G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019932 | |||||||
| chr4:71019980 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.208-2387G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71019980 | |||||||
| chr4:71020343 | A | G | 1 | a0002c0002t0002g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.208-2024A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71020343 | |||||||
| chr4:71020347 | G | T | 9 | a0001c0001t0002g0019 a0001c0001t0002g0056 a0001c0001t0002g0065 others(6): Show |
11 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.208-2020G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71020347 | |||||||
| chr4:71020355 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.208-2012T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71020355 | |||||||
| chr4:71020377 | T | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.208-1990T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71020377 | |||||||
| chr4:71020695 | T | TTTTG | 3 | a0001c0001t0013g0174 a0004c0004t0006g0172 a0004c0004t0006g0173 |
3 | HG01109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-1660_208-1657d others(6): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71020695 | ||||||
| chr4:71020844 | C | T | 2 | a0004c0004t0006g0172 a0004c0004t0006g0173 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-1523C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71020844 | |||||||
| chr4:71020858 | A | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0117 |
2 | NA18982.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.208-1509A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71020858 | |||||||
| chr4:71021038 | A | G | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208-1329A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021038 | |||||||
| chr4:71021066 | CT | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.208-1281delT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71021066 | ||||||
| chr4:71021066 | CTT | C | 14 | a0001c0001t0001g0107 a0001c0001t0001g0136 a0001c0001t0001g0158 others(11): Show |
14 | HG01243.hp2 HG02109.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.208-1282_208-1281d others(4): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71021066 | ||||||
| chr4:71021069 | T | C | 1 | a0002c0002t0002g0187 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.208-1298T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021069 | |||||||
| chr4:71021099 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.208-1268C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021099 | |||||||
| chr4:71021107 | C | T | 1 | a0001c0001t0002g0065 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.208-1260C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021107 | |||||||
| chr4:71021108 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.208-1259G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021108 | |||||||
| chr4:71021124 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.208-1243G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021124 | |||||||
| chr4:71021124 | G | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | NA18968.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.208-1243G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021124 | |||||||
| chr4:71021136 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0080 others(2): Show |
9 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(6): Show |
intron_variant | MODIFIER | c.208-1231C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021136 | |||||||
| chr4:71021177 | G | A | 1 | a0002c0002t0019g0059 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.208-1190G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021177 | |||||||
| chr4:71021232 | C | T | 1 | a0001c0001t0015g0131 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.208-1135C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021232 | |||||||
| chr4:71021280 | T | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.208-1087T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021280 | |||||||
| chr4:71021366 | C | T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0140 a0001c0001t0001g0163 others(1): Show |
4 | HG00438.hp2 HG03195.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-1001C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021366 | |||||||
| chr4:71021542 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.208-825A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021542 | |||||||
| chr4:71021744 | C | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.208-623C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021744 | |||||||
| chr4:71021769 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.208-598A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021769 | |||||||
| chr4:71021784 | TGAGGTCA others(1): Show |
T | 4 | a0001c0001t0005g0043 a0001c0001t0005g0052 a0001c0001t0005g0053 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-579_208-572del others(8): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 71021784 | ||||||
| chr4:71021798 | G | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.208-569G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021798 | |||||||
| chr4:71021799 | G | A | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208-568G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021799 | |||||||
| chr4:71021829 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.208-538C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021829 | |||||||
| chr4:71021929 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.208-438T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021929 | |||||||
| chr4:71021953 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.208-414A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71021953 | |||||||
| chr4:71022163 | G | T | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208-204G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 2/6 | chr4 | 71022163 | |||||||
| chr4:71022613 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.401+53G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/6 | chr4 | 71022613 | |||||||
| chr4:71022650 | T | G | 2 | a0004c0004t0006g0172 a0004c0004t0006g0173 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.401+90T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/6 | chr4 | 71022650 | |||||||
| chr4:71022775 | G | C | 1 | a0001c0001t0002g0021 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.401+215G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/6 | chr4 | 71022775 | |||||||
| chr4:71022846 | C | T | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.401+286C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/6 | chr4 | 71022846 | |||||||
| chr4:71022921 | G | A | 1 | a0002c0002t0002g0185 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.401+361G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/6 | chr4 | 71022921 | |||||||
| chr4:71023075 | A | G | 1 | a0001c0001t0001g0034 | 2 | HG01255.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.402-484A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/6 | chr4 | 71023075 | |||||||
| chr4:71023212 | C | T | 4 | a0001c0001t0005g0043 a0001c0001t0005g0052 a0001c0001t0005g0053 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.402-347C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/6 | chr4 | 71023212 | |||||||
| chr4:71023394 | A | C | 2 | a0004c0004t0006g0172 a0004c0004t0006g0173 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.402-165A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 3/6 | chr4 | 71023394 | |||||||
| chr4:71023718 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.549+12T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71023718 | |||||||
| chr4:71023746 | G | T | 1 | a0001c0001t0001g0154 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.549+40G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71023746 | |||||||
| chr4:71023913 | T | G | 1 | a0001c0001t0001g0033 | 2 | NA18950.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.549+207T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71023913 | |||||||
| chr4:71023953 | C | T | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.549+247C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71023953 | |||||||
| chr4:71024069 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.549+363T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71024069 | |||||||
| chr4:71024242 | G | A | 4 | a0001c0001t0002g0021 a0001c0001t0002g0040 a0001c0001t0002g0041 others(1): Show |
5 | HG00323.hp2 HG00735.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.549+536G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71024242 | |||||||
| chr4:71024395 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.549+689C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71024395 | |||||||
| chr4:71024448 | C | T | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.549+742C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71024448 | |||||||
| chr4:71024596 | C | T | 38 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0024 others(35): Show |
49 | HG00323.hp2 HG00673.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.549+890C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71024596 | |||||||
| chr4:71024683 | A | G | 1 | a0001c0001t0008g0075 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.549+977A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71024683 | |||||||
| chr4:71025003 | A | G | 1 | a0001c0001t0002g0061 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.550-813A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71025003 | |||||||
| chr4:71025057 | T | C | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.550-759T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71025057 | |||||||
| chr4:71025239 | T | G | 1 | a0001c0001t0002g0047 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.550-577T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71025239 | |||||||
| chr4:71025330 | G | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0105 a0001c0001t0001g0157 others(4): Show |
9 | HG01891.hp1 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.550-486G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71025330 | |||||||
| chr4:71025380 | T | C | 2 | a0001c0001t0001g0105 a0001c0001t0006g0165 |
2 | HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.550-436T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71025380 | |||||||
| chr4:71025466 | A | G | 1 | a0001c0001t0002g0041 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.550-350A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71025466 | |||||||
| chr4:71025777 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0008g0075 a0001c0001t0008g0076 |
5 | HG02647.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.550-39C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 4/6 | chr4 | 71025777 | |||||||
| chr4:71026258 | G | A | 1 | a0001c0001t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.665+327G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026258 | |||||||
| chr4:71026312 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.666-353T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026312 | |||||||
| chr4:71026319 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.666-346T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026319 | |||||||
| chr4:71026418 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.666-247T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026418 | |||||||
| chr4:71026441 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-224G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026441 | |||||||
| chr4:71026443 | T | G | 1 | a0001c0001t0001g0078 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-222T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026443 | |||||||
| chr4:71026444 | A | ATTCTCTT others(7): Show |
1 | a0001c0001t0001g0078 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-221_666-220ins others(14): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026444 | |||||||
| chr4:71026445 | C | A | 1 | a0001c0001t0001g0078 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-220C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026445 | |||||||
| chr4:71026450 | C | G | 1 | a0001c0001t0001g0078 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-215C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026450 | |||||||
| chr4:71026452 | C | A | 1 | a0001c0001t0001g0078 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-213C>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026452 | |||||||
| chr4:71026453 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-212A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026453 | |||||||
| chr4:71026454 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-211G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026454 | |||||||
| chr4:71026456 | T | A | 1 | a0001c0001t0001g0078 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-209T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026456 | |||||||
| chr4:71026457 | G | C | 1 | a0001c0001t0001g0078 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-208G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026457 | |||||||
| chr4:71026462 | T | A | 1 | a0001c0001t0001g0078 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-203T>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026462 | |||||||
| chr4:71026464 | T | G | 1 | a0001c0001t0001g0078 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-201T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026464 | |||||||
| chr4:71026471 | C | G | 1 | a0001c0001t0001g0078 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-194C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026471 | |||||||
| chr4:71026473 | T | G | 1 | a0001c0001t0001g0078 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-192T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026473 | |||||||
| chr4:71026493 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-172G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026493 | |||||||
| chr4:71026494 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-171G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026494 | |||||||
| chr4:71026498 | A | C | 1 | a0001c0001t0001g0078 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.666-167A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 5/6 | chr4 | 71026498 | |||||||
| chr4:71026796 | A | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.756+41A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71026796 | |||||||
| chr4:71026892 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.756+137A>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71026892 | |||||||
| chr4:71026912 | T | G | 4 | a0001c0001t0004g0004 a0001c0001t0004g0062 a0001c0001t0004g0063 others(1): Show |
9 | HG02280.hp2 HG02615.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.756+157T>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71026912 | |||||||
| chr4:71026935 | C | T | 2 | a0001c0001t0002g0046 a0001c0001t0002g0047 |
2 | HG01243.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.756+180C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71026935 | |||||||
| chr4:71027037 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.756+282G>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027037 | |||||||
| chr4:71027092 | T | C | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.756+337T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027092 | |||||||
| chr4:71027112 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.756+357A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027112 | |||||||
| chr4:71027124 | C | T | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.756+369C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027124 | |||||||
| chr4:71027206 | A | G | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.756+451A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027206 | |||||||
| chr4:71027304 | A | G | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.756+549A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027304 | |||||||
| chr4:71027394 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.756+639A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027394 | |||||||
| chr4:71027486 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.756+731T>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027486 | |||||||
| chr4:71027688 | G | A | 1 | a0001c0003t0001g0129 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.756+933G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027688 | |||||||
| chr4:71027745 | A | G | 3 | a0001c0001t0001g0105 a0001c0001t0009g0099 a0001c0001t0009g0166 |
3 | HG01891.hp1 HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.756+990A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027745 | |||||||
| chr4:71027782 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.756+1027G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71027782 | |||||||
| chr4:71028075 | A | C | 1 | a0001c0001t0001g0137 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.757-1277A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028075 | |||||||
| chr4:71028110 | A | G | 9 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0003g0005 others(6): Show |
14 | HG01243.hp2 HG02055.hp1 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.757-1242A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028110 | |||||||
| chr4:71028147 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(74): Show |
120 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.757-1205C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028147 | |||||||
| chr4:71028178 | A | G | 3 | a0001c0001t0004g0064 a0004c0004t0006g0172 a0004c0004t0006g0173 |
3 | HG02886.hp2 HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.757-1174A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028178 | |||||||
| chr4:71028350 | G | C | 4 | a0001c0001t0005g0043 a0001c0001t0005g0052 a0001c0001t0005g0053 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.757-1002G>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028350 | |||||||
| chr4:71028604 | C | CTTTT | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.757-743_757-740dup others(4): Show |
DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr4 | 71028604 | ||||||
| chr4:71028759 | A | AT | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.757-578dupT | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr4 | 71028759 | ||||||
| chr4:71028837 | A | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0028 others(11): Show |
25 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.757-515A>C | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028837 | |||||||
| chr4:71028846 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(74): Show |
120 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.757-506C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028846 | |||||||
| chr4:71028856 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(74): Show |
120 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.757-496C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028856 | |||||||
| chr4:71028976 | C | G | 1 | a0001c0001t0001g0143 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.757-376C>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028976 | |||||||
| chr4:71028989 | G | A | 1 | a0001c0001t0002g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.757-363G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71028989 | |||||||
| chr4:71029105 | G | A | 1 | a0001c0001t0013g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.757-247G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71029105 | |||||||
| chr4:71029189 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.757-163C>T | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71029189 | |||||||
| chr4:71029224 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.757-128A>G | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71029224 | |||||||
| chr4:71029286 | G | A | 2 | a0001c0001t0002g0060 a0001c0001t0002g0061 |
2 | HG01167.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.757-66G>A | DCK | ENSG00000156136.10 | transcript | ENST00000286648.10 | protein_coding | 6/6 | chr4 | 71029286 |