Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 286148 |
|---|---|
| ensemblid | ENSG00000156162.16 |
| hgncid | 27829 |
| symbol | DPY19L4 |
| name | dpy-19 like 4 |
| refseq_nuc | NM_181787.3 |
| refseq_prot | NP_861452.2 |
| ensembl_nuc | ENST00000414645.6 |
| ensembl_prot | ENSP00000389630.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 94719900 |
| end | 94793836 |
| strand | + |
| ver | v1.2 |
| region | chr8:94719900-94793836 |
| region5000 | chr8:94714900-94798836 |
| regionname0 | DPY19L4_chr8_94719900_94793836 |
| regionname5000 | DPY19L4_chr8_94714900_94798836 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 723 | 275 | 85 | 51 | 105 | 6 | 26 | 78 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0002 | 0/0 | 723 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0003 | 0/0 | 723 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0004 | 0/0 | 723 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0005 | 0/0 | 723 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0006 | 0/0 | 723 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0007 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0008 | 0/0 | 723 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0009 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2172 | 262 | 74 | 50 | 104 | 6 | 26 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| c0002 | 0/0 | 2172 | 9 | 9 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| c0003 | 0/0 | 2172 | 5 | 5 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| c0004 | 0/0 | 2172 | 3 | 0 | 0 | 3 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| c0005 | 0/0 | 2172 | 2 | 2 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| c0006 | 0/0 | 2172 | 2 | 2 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| c0007 | 0/0 | 2172 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| c0008 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| c0009 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| c0010 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| c0011 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| c0012 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| c0013 | 0/0 | 2172 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 4026 | 190 | 49 | 46 | 73 | 5 | 16 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0002 | 0/0 | 4026 | 32 | 0 | 0 | 26 | 1 | 5 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0003 | 0/0 | 4025 | 13 | 11 | 2 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0004 | 0/0 | 4028 | 6 | 5 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0005 | 0/0 | 4026 | 5 | 5 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0006 | 0/0 | 4026 | 4 | 0 | 0 | 4 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0007 | 0/0 | 4027 | 3 | 3 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0008 | 0/0 | 4026 | 3 | 3 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0009 | 0/0 | 4026 | 3 | 0 | 0 | 0 | 0 | 3 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0010 | 0/0 | 4026 | 3 | 3 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0011 | 0/0 | 4026 | 3 | 0 | 0 | 3 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0012 | 0/0 | 4026 | 3 | 2 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0013 | 0/0 | 4026 | 2 | 2 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0014 | 0/1 | 4026 | 2 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0015 | 0/0 | 4026 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0016 | 0/0 | 4026 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0017 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0018 | 0/0 | 4026 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0019 | 0/0 | 4026 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0020 | 0/0 | 4026 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0021 | 0/0 | 4026 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0022 | 0/0 | 4026 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0023 | 0/0 | 4026 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0024 | 0/0 | 4026 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0025 | 0/0 | 4028 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0026 | 0/0 | 4026 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0027 | 0/0 | 4028 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0028 | 0/0 | 4026 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0029 | 0/0 | 4026 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0030 | 0/0 | 4028 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0031 | 0/0 | 4025 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| t0032 | 0/0 | 4026 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0230 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0237 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2172 | 262 | 74 | 50 | 104 | 6 | 26 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0002 | 0/0 | 2172 | 9 | 9 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0006 | 0/0 | 2172 | 2 | 2 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0007 | 0/0 | 2172 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0009 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0002c0003 | 0/0 | 2172 | 5 | 5 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0003c0004 | 0/0 | 2172 | 3 | 0 | 0 | 3 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0004c0005 | 0/0 | 2172 | 2 | 2 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0005c0013 | 0/0 | 2172 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0006c0011 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0007c0008 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0008c0010 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0009c0012 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6197 | 172 | 35 | 45 | 70 | 5 | 16 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0002 | 0/0 | 6197 | 32 | 0 | 0 | 26 | 1 | 5 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0003 | 0/0 | 6196 | 13 | 11 | 2 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0004 | 0/0 | 6199 | 3 | 2 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0005 | 0/0 | 6197 | 5 | 5 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0006 | 0/0 | 6197 | 4 | 0 | 0 | 4 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0007 | 0/0 | 6198 | 3 | 3 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0008 | 0/0 | 6197 | 3 | 3 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0009 | 0/0 | 6197 | 3 | 0 | 0 | 0 | 0 | 3 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0010 | 0/0 | 6197 | 3 | 3 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0012 | 0/0 | 6197 | 3 | 2 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0013 | 0/0 | 6197 | 2 | 2 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0014 | 0/1 | 6197 | 2 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0015 | 0/0 | 6197 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0016 | 0/0 | 6197 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0018 | 0/0 | 6197 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0019 | 0/0 | 6197 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0020 | 0/0 | 6197 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0021 | 0/0 | 6197 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0022 | 0/0 | 6197 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0023 | 0/0 | 6197 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0025 | 0/0 | 6199 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0028 | 0/0 | 6197 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0029 | 0/0 | 6197 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0030 | 0/0 | 6199 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0031 | 0/0 | 6196 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0001t0032 | 0/0 | 6197 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0002t0001 | 0/0 | 6197 | 8 | 8 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0002t0017 | 0/0 | 6181 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0006t0001 | 0/0 | 6197 | 2 | 2 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0007t0001 | 0/0 | 6197 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0001c0009t0001 | 0/0 | 6197 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0002c0003t0004 | 0/0 | 6199 | 3 | 3 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0002c0003t0026 | 0/0 | 6197 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0002c0003t0027 | 0/0 | 6199 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0003c0004t0011 | 0/0 | 6197 | 3 | 0 | 0 | 3 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0004c0005t0001 | 0/0 | 6197 | 2 | 2 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0005c0013t0024 | 0/0 | 6197 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0006c0011t0001 | 0/0 | 6197 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0007c0008t0001 | 0/0 | 6197 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0008c0010t0001 | 0/0 | 6197 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| a0009c0012t0001 | 0/0 | 6197 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | copy fasta | chr8 | 94714900 | 94798836 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0230 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0003g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0006g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0008g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0008g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0009g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0009g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0009g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0012g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0012g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0012g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0013g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0013g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0014g0237 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0014g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0015g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0016g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0018g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0019g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0020g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0021g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0022g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0023g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0025g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0028g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0029g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0030g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0031g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0001t0032g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0002t0017g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0006t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0006t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0007t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0001c0009t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0002c0003t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0002c0003t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0002c0003t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0002c0003t0026g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0002c0003t0027g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0003c0004t0011g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0003c0004t0011g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0003c0004t0011g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0004c0005t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0004c0005t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0005c0013t0024g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0006c0011t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0007c0008t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0008c0010t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| a0009c0012t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0100 | EUR | GBR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | CHS | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | CHS | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00738 | hp1 | a0001 | c0001 | t0014 | g0238 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01069 | hp1 | a0001 | c0007 | t0001 | g0158 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01070 | hp1 | a0001 | c0001 | t0012 | g0014 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01109 | hp2 | a0005 | c0013 | t0024 | g0059 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0163 | AMR | CLM | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0270 | EUR | IBS | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | IBS | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | IBS | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01884 | hp1 | a0007 | c0008 | t0001 | g0009 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01884 | hp2 | a0002 | c0003 | t0027 | g0207 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02027 | hp2 | a0001 | c0001 | t0020 | g0186 | EAS | KHV | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02145 | hp1 | a0001 | c0001 | t0018 | g0077 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CDX | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CDX | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02257 | hp1 | a0001 | c0001 | t0013 | g0182 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0219 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02258 | hp2 | a0001 | c0001 | t0030 | g0119 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02280 | hp1 | a0002 | c0003 | t0004 | g0166 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02280 | hp2 | a0001 | c0001 | t0013 | g0178 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02451 | hp2 | a0001 | c0001 | t0012 | g0013 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02523 | hp1 | a0008 | c0010 | t0001 | g0212 | EAS | KHV | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0116 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02615 | hp1 | a0004 | c0005 | t0001 | g0221 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02622 | hp1 | a0002 | c0003 | t0026 | g0165 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0217 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0078 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0216 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0057 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02723 | hp2 | a0001 | c0001 | t0028 | g0070 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02735 | hp1 | a0001 | c0001 | t0009 | g0261 | SAS | PJL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0067 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0065 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02895 | hp1 | a0002 | c0003 | t0004 | g0168 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02896 | hp2 | a0009 | c0012 | t0001 | g0214 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0083 | AFR | ESN | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02976 | hp2 | a0001 | c0001 | t0025 | g0068 | AFR | ESN | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03098 | hp1 | a0001 | c0001 | t0010 | g0017 | AFR | MSL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0164 | AFR | MSL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03130 | hp1 | a0001 | c0001 | t0021 | g0025 | AFR | ESN | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | ESN | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0018 | AFR | ESN | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | ESN | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0215 | AFR | MSL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0080 | AFR | MSL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | MSL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03491 | hp2 | a0001 | c0001 | t0009 | g0262 | SAS | PJL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0222 | AFR | ESN | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03516 | hp2 | a0001 | c0001 | t0016 | g0082 | AFR | ESN | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03540 | hp1 | a0004 | c0005 | t0001 | g0220 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03579 | hp1 | a0002 | c0003 | t0004 | g0167 | AFR | MSL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | MSL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | STU | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | STU | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03831 | hp1 | a0001 | c0001 | t0009 | g0234 | SAS | BEB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | BEB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | STU | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG04184 | hp1 | a0001 | c0001 | t0032 | g0223 | SAS | BEB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG04228 | hp1 | a0001 | c0001 | t0023 | g0263 | SAS | STU | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | STU | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | YRI | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0079 | AFR | YRI | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18906 | hp1 | a0001 | c0002 | t0017 | g0218 | AFR | YRI | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18947 | hp1 | a0001 | c0001 | t0015 | g0206 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18956 | hp2 | a0001 | c0001 | t0022 | g0205 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18960 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18981 | hp2 | a0001 | c0001 | t0006 | g0184 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18985 | hp1 | a0001 | c0001 | t0029 | g0254 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18994 | hp2 | a0003 | c0004 | t0011 | g0101 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA18999 | hp2 | a0001 | c0001 | t0006 | g0185 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19002 | hp1 | a0006 | c0011 | t0001 | g0177 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19002 | hp2 | a0003 | c0004 | t0011 | g0112 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | LWK | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | LWK | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19043 | hp2 | a0001 | c0001 | t0019 | g0175 | AFR | LWK | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19074 | hp1 | a0003 | c0004 | t0011 | g0113 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19088 | hp1 | a0001 | c0009 | t0001 | g0003 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19088 | hp2 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | YRI | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ASW | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ASW | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02109 | hp1 | a0001 | c0001 | t0010 | g0019 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02109 | hp2 | a0001 | c0006 | t0001 | g0020 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0081 | AFR | ACB | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG03471 | hp2 | a0001 | c0006 | t0001 | g0021 | AFR | MSL | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | USA | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | USA | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | USA | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| NA20300 | hp2 | a0001 | c0001 | t0031 | g0072 | AFR | USA | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0014 | g0237 | REF | REF | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0230 | REF | REF | DPY19L4_chr8_94714900_94798836 | DPY19L4 | chr8 | 94714900 | 94798836 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:94720003
|
C | T | 1 | a0003 | 3 | NA18994.hp2 NA19002.hp2 NA19074.hp1 |
missense_variant | MODERATE | c.5C>T | p.Ala2Val | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/19 | 104/6197 | 5/2172 | 2/723 | chr8 | 94720003 | ||
| chr8:94726334
|
C | T | 1 | a0005 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.20C>T | p.Pro7Leu | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/19 | 119/6197 | 20/2172 | 7/723 | chr8 | 94726334 | ||
| chr8:94734747
|
A | G | 1 | a0009 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.245A>G | p.Asn82Ser | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/19 | 344/6197 | 245/2172 | 82/723 | chr8 | 94734747 | ||
| chr8:94738453
|
G | C | 1 | a0004 | 2 | HG02615.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.337G>C | p.Glu113Gln | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 4/19 | 436/6197 | 337/2172 | 113/723 | chr8 | 94738453 | ||
| chr8:94739496
|
C | T | 1 | a0006 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.427C>T | p.Leu143Phe | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 5/19 | 526/6197 | 427/2172 | 143/723 | chr8 | 94739496 | ||
| chr8:94739706
|
T | C | 1 | a0002 | 5 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(2): Show |
missense_variant | MODERATE | c.527T>C | p.Val176Ala | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/19 | 626/6197 | 527/2172 | 176/723 | chr8 | 94739706 | ||
| chr8:94768510
|
A | G | 1 | a0008 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1291A>G | p.Ile431Val | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/19 | 1390/6197 | 1291/2172 | 431/723 | chr8 | 94768510 | ||
| chr8:94770517
|
T | C | 1 | a0007 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1400T>C | p.Ile467Thr | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/19 | 1499/6197 | 1400/2172 | 467/723 | chr8 | 94770517 | ||
| chr8:94788025
|
A | C | 1 | a0005 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.1980A>C | p.Lys660Asn | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/19 | 2079/6197 | 1980/2172 | 660/723 | chr8 | 94788025 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:94734679
|
G | A | 1 | a0001c0007 | 1 | HG01069.hp1 | synonymous_variant | LOW | c.177G>A | p.Ala59Ala | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/19 | 276/6197 | 177/2172 | 59/723 | chr8 | 94734679 | ||
| chr8:94756126
|
C | G | 3 | a0001c0002a0004c0005a0009c0012 | 12 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
synonymous_variant | LOW | c.702C>G | p.Gly234Gly | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/19 | 801/6197 | 702/2172 | 234/723 | chr8 | 94756126 | ||
| chr8:94768428
|
A | G | 1 | a0001c0006 | 2 | HG02109.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.1209A>G | p.Glu403Glu | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/19 | 1308/6197 | 1209/2172 | 403/723 | chr8 | 94768428 | ||
| chr8:94770462
|
C | T | 3 | a0001c0002a0004c0005a0009c0012 | 12 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
synonymous_variant | LOW | c.1345C>T | p.Leu449Leu | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/19 | 1444/6197 | 1345/2172 | 449/723 | chr8 | 94770462 | ||
| chr8:94788052
|
C | T | 1 | a0001c0009 | 1 | NA19088.hp1 | splice_region_variant&synonymous_variant | LOW | c.2007C>T | p.His669His | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/19 | 2106/6197 | 2007/2172 | 669/723 | chr8 | 94788052 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:94790206
|
C | A | 1 | a0001c0001t0007 | 3 | HG02723.hp1 HG02818.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*296C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 296 | chr8 | 94790206 | |||||
| chr8:94790233
|
A | G | 1 | a0001c0001t0032 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*323A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 323 | chr8 | 94790233 | |||||
| chr8:94790353
|
A | G | 2 | a0001c0001t0003a0001c0001t0031 | 14 | HG01081.hp1 HG01167.hp1 HG02486.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*443A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 443 | chr8 | 94790353 | |||||
| chr8:94790383
|
A | C | 1 | a0001c0001t0012 | 3 | HG01070.hp1 HG02451.hp2 HG02572.hp2 |
3_prime_UTR_variant | MODIFIER | c.*473A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 473 | chr8 | 94790383 | |||||
| chr8:94790496
|
TCTC | T | 2 | a0001c0001t0003a0001c0001t0031 | 14 | HG01081.hp1 HG01167.hp1 HG02486.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*590_*592delCTC | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 590 | INFO_REALIGN_3_PRIME | chr8 | 94790496 | ||||
| chr8:94790545
|
A | G | 2 | a0001c0001t0007a0001c0001t0030 | 4 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*635A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 635 | chr8 | 94790545 | |||||
| chr8:94790705
|
T | A | 2 | a0001c0001t0007a0001c0001t0030 | 4 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*795T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 795 | chr8 | 94790705 | |||||
| chr8:94790854
|
T | A | 2 | a0001c0001t0007a0001c0001t0030 | 4 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*944T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 944 | chr8 | 94790854 | |||||
| chr8:94790906
|
G | A | 1 | a0001c0001t0031 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*996G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 996 | chr8 | 94790906 | |||||
| chr8:94791156
|
T | C | 1 | a0001c0001t0015 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1246T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 1246 | chr8 | 94791156 | |||||
| chr8:94791311
|
G | C | 1 | a0001c0001t0013 | 2 | HG02257.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1401G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 1401 | chr8 | 94791311 | |||||
| chr8:94791406
|
A | G | 1 | a0001c0001t0014 | 2 | HG00738.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1496A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 1496 | chr8 | 94791406 | |||||
| chr8:94791522
|
A | G | 2 | a0001c0001t0002a0003c0004t0011 | 35 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1612A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 1612 | chr8 | 94791522 | |||||
| chr8:94791557
|
A | G | 1 | a0001c0001t0029 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1647A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 1647 | chr8 | 94791557 | |||||
| chr8:94791669
|
G | T | 1 | a0001c0001t0006 | 4 | NA18960.hp1 NA18981.hp2 NA18999.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1759G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 1759 | chr8 | 94791669 | |||||
| chr8:94791685
|
A | T | 1 | a0001c0001t0028 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1775A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 1775 | chr8 | 94791685 | |||||
| chr8:94791706
|
C | G | 10 | a0001c0001t0003a0001c0001t0004a0001c0001t0012others(7): Show | 28 | HG01070.hp1 HG01081.hp1 HG01109.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1796C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 1796 | chr8 | 94791706 | |||||
| chr8:94791738
|
T | C | 1 | a0001c0001t0007 | 3 | HG02723.hp1 HG02818.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1828T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 1828 | chr8 | 94791738 | |||||
| chr8:94792231
|
A | T | 1 | a0002c0003t0027 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2321A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 2321 | chr8 | 94792231 | |||||
| chr8:94792234
|
A | T | 9 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(6): Show | 29 | HG01081.hp1 HG01167.hp1 HG01261.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2324A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 2324 | chr8 | 94792234 | |||||
| chr8:94792237
|
T | A | 1 | a0001c0001t0016 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2327T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 2327 | chr8 | 94792237 | |||||
| chr8:94792265
|
C | T | 1 | a0001c0001t0005 | 5 | HG02572.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2355C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 2355 | chr8 | 94792265 | |||||
| chr8:94792306
|
ACTGCAAC others(9): Show |
A | 1 | a0001c0002t0017 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2410_*2425delTCGC others(12): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 2410 | INFO_REALIGN_3_PRIME | chr8 | 94792306 | ||||
| chr8:94792388
|
C | T | 3 | a0001c0001t0004a0002c0003t0004a0002c0003t0027 | 7 | HG01261.hp2 HG01884.hp2 HG02055.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2478C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 2478 | chr8 | 94792388 | |||||
| chr8:94792445
|
G | T | 7 | a0001c0001t0003a0001c0001t0004a0001c0001t0025others(4): Show | 23 | HG01081.hp1 HG01167.hp1 HG01261.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2535G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 2535 | chr8 | 94792445 | |||||
| chr8:94792796
|
G | A | 10 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(7): Show | 28 | HG01081.hp1 HG01167.hp1 HG01261.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2886G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 2886 | chr8 | 94792796 | |||||
| chr8:94792861
|
A | C | 1 | a0001c0001t0023 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2951A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 2951 | chr8 | 94792861 | |||||
| chr8:94792927
|
G | T | 1 | a0001c0001t0009 | 3 | HG02735.hp1 HG03491.hp2 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3017G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 3017 | chr8 | 94792927 | |||||
| chr8:94793191
|
T | C | 2 | a0001c0001t0008a0001c0001t0016 | 4 | HG02559.hp2 HG03225.hp2 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3281T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 3281 | chr8 | 94793191 | |||||
| chr8:94793224
|
G | C | 7 | a0001c0001t0003a0001c0001t0004a0001c0001t0025others(4): Show | 23 | HG01081.hp1 HG01167.hp1 HG01261.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3314G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 3314 | chr8 | 94793224 | |||||
| chr8:94793226
|
G | A | 1 | a0003c0004t0011 | 3 | NA18994.hp2 NA19002.hp2 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3316G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 3316 | chr8 | 94793226 | |||||
| chr8:94793286
|
G | A | 1 | a0001c0001t0019 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3376G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 3376 | chr8 | 94793286 | |||||
| chr8:94793298
|
T | C | 1 | a0001c0001t0007 | 3 | HG02723.hp1 HG02818.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3388T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 3388 | chr8 | 94793298 | |||||
| chr8:94793421
|
G | GTA | 8 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(5): Show | 26 | HG01081.hp1 HG01167.hp1 HG01261.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3512_*3513insAT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 3513 | INFO_REALIGN_3_PRIME | chr8 | 94793421 | ||||
| chr8:94793431
|
C | T | 1 | a0001c0001t0013 | 2 | HG02257.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3521C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 3521 | chr8 | 94793431 | |||||
| chr8:94793437
|
T | C | 1 | a0001c0001t0020 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3527T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 3527 | chr8 | 94793437 | |||||
| chr8:94793658
|
T | G | 1 | a0001c0001t0021 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3748T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 3748 | chr8 | 94793658 | |||||
| chr8:94793659
|
T | G | 1 | a0001c0001t0021 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3749T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 3749 | chr8 | 94793659 | |||||
| chr8:94793660
|
T | G | 1 | a0001c0001t0021 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3750T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 3750 | chr8 | 94793660 | |||||
| chr8:94793699
|
T | G | 1 | a0001c0001t0022 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3789T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 3789 | chr8 | 94793699 | |||||
| chr8:94793723
|
TA | T | 1 | a0001c0001t0007 | 3 | HG02723.hp1 HG02818.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3817delA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 3817 | INFO_REALIGN_3_PRIME | chr8 | 94793723 | ||||
| chr8:94793735
|
G | T | 3 | a0001c0001t0004a0002c0003t0004a0002c0003t0027 | 7 | HG01261.hp2 HG01884.hp2 HG02055.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3825G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 19/19 | 3825 | chr8 | 94793735 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:94720034
|
G | A | 4 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+20G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94720034 | ||||||
| chr8:94720043
|
C | A | 1 | a0001c0002t0001g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.16+29C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94720043 | ||||||
| chr8:94720055
|
G | C | 213 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.16+41G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94720055 | ||||||
| chr8:94720102
|
CTGGTGGC others(11): Show |
C | 10 | a0001c0002t0001g0008a0001c0002t0001g0215a0001c0002t0001g0216others(7): Show | 10 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.16+92_16+109delTGG others(15): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 94720102 | |||||
| chr8:94720284
|
G | A | 9 | a0001c0001t0001g0011a0001c0001t0003g0001a0001c0001t0003g0010others(6): Show | 11 | HG01070.hp1 HG01081.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.16+270G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94720284 | ||||||
| chr8:94720418
|
A | G | 10 | a0001c0002t0001g0008a0001c0002t0001g0215a0001c0002t0001g0216others(7): Show | 10 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.16+404A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94720418 | ||||||
| chr8:94720486
|
C | A | 1 | a0001c0001t0032g0223 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.16+472C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94720486 | ||||||
| chr8:94720488
|
T | A | 1 | a0001c0001t0032g0223 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.16+474T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94720488 | ||||||
| chr8:94720538
|
A | G | 39 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0187others(36): Show | 39 | HG00609.hp1 HG00741.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.16+524A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94720538 | ||||||
| chr8:94720691
|
T | C | 3 | a0001c0001t0010g0017a0001c0001t0010g0018a0001c0001t0010g0019 | 3 | HG02109.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.16+677T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94720691 | ||||||
| chr8:94720777
|
A | C | 1 | a0001c0001t0001g0176 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.16+763A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94720777 | ||||||
| chr8:94720949
|
G | T | 1 | a0001c0001t0019g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.16+935G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94720949 | ||||||
| chr8:94720951
|
C | CT | 10 | a0001c0001t0001g0213a0001c0001t0001g0281a0001c0001t0001g0283others(7): Show | 10 | HG01934.hp1 HG02523.hp1 HG03516.hp1 others(7): Show |
intron_variant | MODIFIER | c.16+949dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 94720951 | |||||
| chr8:94721007
|
C | T | 7 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276others(4): Show | 7 | HG00438.hp1 HG00609.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.16+993C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94721007 | ||||||
| chr8:94721035
|
T | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(197): Show | 203 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.16+1021T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94721035 | ||||||
| chr8:94721115
|
G | A | 2 | a0001c0006t0001g0020a0001c0006t0001g0021 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.16+1101G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94721115 | ||||||
| chr8:94721135
|
G | A | 42 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(39): Show | 42 | HG00423.hp1 HG00544.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.16+1121G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94721135 | ||||||
| chr8:94721235
|
G | C | 1 | a0001c0001t0019g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.16+1221G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94721235 | ||||||
| chr8:94721240
|
C | T | 3 | a0001c0001t0010g0017a0001c0001t0010g0018a0001c0001t0010g0019 | 3 | HG02109.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.16+1226C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94721240 | ||||||
| chr8:94721323
|
A | G | 9 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0172others(6): Show | 9 | HG01167.hp1 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.16+1309A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94721323 | ||||||
| chr8:94721421
|
T | C | 1 | a0009c0012t0001g0214 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.16+1407T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94721421 | ||||||
| chr8:94721732
|
T | G | 1 | a0001c0001t0002g0064 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.16+1718T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94721732 | ||||||
| chr8:94721771
|
A | AGATCTGT others(9): Show |
1 | a0008c0010t0001g0212 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.16+1757_16+1758ins others(16): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94721771 | ||||||
| chr8:94721772
|
T | A | 1 | a0008c0010t0001g0212 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.16+1758T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94721772 | ||||||
| chr8:94721774
|
A | T | 1 | a0008c0010t0001g0212 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.16+1760A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94721774 | ||||||
| chr8:94721996
|
C | A | 213 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(210): Show | 216 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.16+1982C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94721996 | ||||||
| chr8:94722033
|
C | T | 2 | a0001c0001t0001g0272a0001c0001t0001g0273 | 2 | HG00733.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.16+2019C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94722033 | ||||||
| chr8:94722189
|
C | T | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG00438.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.16+2175C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94722189 | ||||||
| chr8:94722284
|
A | G | 3 | a0001c0001t0010g0017a0001c0001t0010g0018a0001c0001t0010g0019 | 3 | HG02109.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.16+2270A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94722284 | ||||||
| chr8:94722486
|
C | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0026others(148): Show | 152 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.16+2472C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94722486 | ||||||
| chr8:94722491
|
G | T | 4 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(1): Show | 4 | HG01934.hp2 HG01978.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+2477G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94722491 | ||||||
| chr8:94722533
|
A | C | 3 | a0001c0001t0004g0162a0001c0001t0004g0163a0001c0001t0004g0164 | 3 | HG01261.hp2 HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.16+2519A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94722533 | ||||||
| chr8:94722751
|
G | A | 1 | a0006c0011t0001g0177 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.16+2737G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94722751 | ||||||
| chr8:94722847
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.16+2833C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94722847 | ||||||
| chr8:94722951
|
A | G | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(1): Show | 4 | HG00609.hp2 NA18939.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+2937A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94722951 | ||||||
| chr8:94723180
|
T | A | 9 | a0001c0002t0001g0008a0001c0002t0001g0215a0001c0002t0001g0216others(6): Show | 9 | HG02257.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.17-3151T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94723180 | ||||||
| chr8:94723198
|
C | A | 1 | a0001c0001t0013g0178 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.17-3133C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94723198 | ||||||
| chr8:94723334
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0005g0065 | 2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.17-2997G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94723334 | ||||||
| chr8:94723383
|
G | A | 1 | a0001c0001t0007g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.17-2948G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94723383 | ||||||
| chr8:94723404
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.17-2927C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94723404 | ||||||
| chr8:94723422
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.17-2909G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94723422 | ||||||
| chr8:94723469
|
G | A | 6 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0003g0179others(3): Show | 6 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.17-2862G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94723469 | ||||||
| chr8:94723516
|
C | T | 13 | a0001c0001t0001g0011a0001c0001t0001g0066a0001c0001t0001g0118others(10): Show | 15 | HG01070.hp1 HG01081.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.17-2815C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94723516 | ||||||
| chr8:94723598
|
C | T | 1 | a0001c0001t0005g0007 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.17-2733C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94723598 | ||||||
| chr8:94723750
|
A | G | 222 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(219): Show | 225 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.17-2581A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94723750 | ||||||
| chr8:94723832
|
A | T | 4 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-2499A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94723832 | ||||||
| chr8:94724020
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.17-2311C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94724020 | ||||||
| chr8:94724046
|
G | A | 1 | a0001c0001t0007g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.17-2285G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94724046 | ||||||
| chr8:94724251
|
A | G | 3 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0213 | 3 | HG01934.hp1 HG02165.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.17-2080A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94724251 | ||||||
| chr8:94724657
|
CG | C | 42 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(39): Show | 42 | HG00423.hp1 HG00544.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.17-1671delG | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 94724657 | |||||
| chr8:94724670
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.17-1661C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94724670 | ||||||
| chr8:94724738
|
C | A | 1 | a0001c0001t0001g0225 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.17-1593C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94724738 | ||||||
| chr8:94724749
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0120others(90): Show | 94 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.17-1582G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94724749 | ||||||
| chr8:94725008
|
C | CT | 154 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0026others(151): Show | 155 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.17-1314dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 94725008 | |||||
| chr8:94725008
|
C | CTT | 66 | a0001c0001t0001g0011a0001c0001t0001g0066a0001c0001t0001g0069others(63): Show | 68 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.17-1315_17-1314dup others(2): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 94725008 | |||||
| chr8:94725192
|
A | G | 1 | a0001c0001t0002g0117 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.17-1139A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94725192 | ||||||
| chr8:94725222
|
A | G | 1 | a0001c0001t0012g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.17-1109A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94725222 | ||||||
| chr8:94725335
|
T | C | 1 | a0001c0001t0006g0022 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.17-996T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94725335 | ||||||
| chr8:94725609
|
G | T | 34 | a0001c0001t0001g0090a0001c0001t0001g0104a0001c0001t0001g0107others(31): Show | 34 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.17-722G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94725609 | ||||||
| chr8:94725643
|
A | AT | 11 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198others(8): Show | 11 | HG01928.hp1 HG01993.hp2 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.17-678dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 94725643 | |||||
| chr8:94725709
|
C | G | 1 | a0001c0001t0007g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.17-622C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94725709 | ||||||
| chr8:94725873
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.17-458G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94725873 | ||||||
| chr8:94726135
|
A | G | 219 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(216): Show | 222 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.17-196A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94726135 | ||||||
| chr8:94726218
|
A | T | 1 | a0004c0005t0001g0220 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.17-113A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 1/18 | chr8 | 94726218 | ||||||
| chr8:94726489
|
A | G | 219 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(216): Show | 222 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.127+48A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94726489 | ||||||
| chr8:94726651
|
G | A | 10 | a0001c0002t0001g0008a0001c0002t0001g0215a0001c0002t0001g0216others(7): Show | 10 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.127+210G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94726651 | ||||||
| chr8:94726707
|
C | T | 1 | a0001c0001t0019g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127+266C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94726707 | ||||||
| chr8:94726749
|
T | C | 6 | a0001c0001t0001g0160a0002c0003t0004g0166a0002c0003t0004g0167others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+308T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94726749 | ||||||
| chr8:94726770
|
A | G | 3 | a0001c0001t0002g0284a0001c0001t0002g0285a0001c0001t0002g0286 | 3 | NA18984.hp1 NA19007.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.127+329A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94726770 | ||||||
| chr8:94726823
|
C | T | 1 | a0001c0001t0012g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.127+382C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94726823 | ||||||
| chr8:94727066
|
A | G | 3 | a0001c0001t0001g0204a0001c0001t0015g0206a0001c0001t0022g0205 | 3 | NA18947.hp1 NA18950.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.127+625A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94727066 | ||||||
| chr8:94727068
|
C | G | 10 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(7): Show | 10 | HG01109.hp2 HG01891.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.127+627C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94727068 | ||||||
| chr8:94727102
|
C | T | 4 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+661C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94727102 | ||||||
| chr8:94727219
|
ATGATTGA others(5): Show |
A | 2 | a0001c0006t0001g0020a0001c0006t0001g0021 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.127+796_127+807del others(12): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94727219 | |||||
| chr8:94727414
|
G | T | 53 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(50): Show | 53 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.127+973G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94727414 | ||||||
| chr8:94727438
|
T | G | 11 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0076others(8): Show | 11 | HG01167.hp1 HG02145.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.127+997T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94727438 | ||||||
| chr8:94727462
|
G | A | 43 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(40): Show | 43 | HG00423.hp1 HG00544.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.127+1021G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94727462 | ||||||
| chr8:94727487
|
A | G | 92 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0120others(89): Show | 93 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.127+1046A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94727487 | ||||||
| chr8:94727514
|
A | G | 13 | a0001c0001t0001g0011a0001c0001t0001g0066a0001c0001t0001g0118others(10): Show | 15 | HG01070.hp1 HG01081.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.127+1073A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94727514 | ||||||
| chr8:94727600
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.127+1159G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94727600 | ||||||
| chr8:94727832
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.127+1391A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94727832 | ||||||
| chr8:94728024
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.127+1583C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94728024 | ||||||
| chr8:94728039
|
G | A | 43 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(40): Show | 43 | HG00423.hp1 HG00544.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.127+1598G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94728039 | ||||||
| chr8:94728056
|
G | A | 3 | a0001c0001t0010g0017a0001c0001t0010g0018a0001c0001t0010g0019 | 3 | HG02109.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.127+1615G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94728056 | ||||||
| chr8:94728086
|
C | T | 3 | a0001c0001t0010g0017a0001c0001t0010g0018a0001c0001t0010g0019 | 3 | HG02109.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.127+1645C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94728086 | ||||||
| chr8:94728087
|
G | C | 1 | a0002c0003t0026g0165 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.127+1646G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94728087 | ||||||
| chr8:94728150
|
C | T | 4 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(1): Show | 4 | HG01934.hp2 HG01978.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+1709C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94728150 | ||||||
| chr8:94728162
|
A | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0120others(36): Show | 40 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.127+1721A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94728162 | ||||||
| chr8:94728273
|
C | G | 33 | a0001c0001t0001g0002a0001c0001t0001g0120a0001c0001t0001g0121others(30): Show | 34 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.127+1832C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94728273 | ||||||
| chr8:94728390
|
T | G | 7 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086others(4): Show | 7 | HG00438.hp2 HG02071.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.127+1949T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94728390 | ||||||
| chr8:94728415
|
A | G | 222 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(219): Show | 225 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.127+1974A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94728415 | ||||||
| chr8:94728589
|
G | T | 3 | a0001c0001t0010g0017a0001c0001t0010g0018a0001c0001t0010g0019 | 3 | HG02109.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.127+2148G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94728589 | ||||||
| chr8:94728600
|
C | T | 65 | a0001c0001t0001g0011a0001c0001t0001g0066a0001c0001t0001g0069others(62): Show | 67 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.127+2159C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94728600 | ||||||
| chr8:94728830
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.127+2389G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94728830 | ||||||
| chr8:94728884
|
G | C | 1 | a0001c0001t0001g0026 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.127+2443G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94728884 | ||||||
| chr8:94728918
|
G | A | 2 | a0001c0001t0001g0027a0007c0008t0001g0009 | 2 | HG01884.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.127+2477G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94728918 | ||||||
| chr8:94728957
|
G | A | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(1): Show | 4 | HG00140.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+2516G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94728957 | ||||||
| chr8:94728988
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.127+2547C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94728988 | ||||||
| chr8:94729003
|
A | G | 2 | a0001c0001t0001g0170a0005c0013t0024g0059 | 2 | HG01109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.127+2562A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94729003 | ||||||
| chr8:94729023
|
GA | G | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+2594delA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94729023 | |||||
| chr8:94729099
|
G | A | 40 | a0001c0001t0001g0090a0001c0001t0001g0104a0001c0001t0001g0107others(37): Show | 40 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.127+2658G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94729099 | ||||||
| chr8:94729166
|
C | G | 12 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0076others(9): Show | 12 | HG01167.hp1 HG02145.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.127+2725C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94729166 | ||||||
| chr8:94729271
|
C | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0120others(90): Show | 94 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.127+2830C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94729271 | ||||||
| chr8:94729358
|
T | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(212): Show | 218 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.127+2917T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94729358 | ||||||
| chr8:94729367
|
G | A | 6 | a0001c0001t0001g0160a0002c0003t0004g0166a0002c0003t0004g0167others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+2926G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94729367 | ||||||
| chr8:94729402
|
G | A | 10 | a0001c0001t0002g0064a0001c0001t0002g0091a0001c0001t0002g0092others(7): Show | 10 | HG00544.hp2 HG00673.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.127+2961G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94729402 | ||||||
| chr8:94729415
|
G | C | 1 | a0001c0001t0019g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127+2974G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94729415 | ||||||
| chr8:94729460
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.127+3019G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94729460 | ||||||
| chr8:94729555
|
TGCCACTG others(225): Show |
T | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.127+3135_127+3366d others(2): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94729555 | |||||
| chr8:94729597
|
C | CA | 30 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0090others(27): Show | 30 | HG00140.hp2 HG02027.hp1 HG02071.hp1 others(27): Show |
intron_variant | MODIFIER | c.127+3180dupA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94729597 | |||||
| chr8:94729597
|
C | CAA | 53 | a0001c0001t0001g0011a0001c0001t0001g0118a0001c0001t0001g0149others(50): Show | 55 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.127+3179_127+3180d others(4): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94729597 | |||||
| chr8:94729597
|
C | CAAA | 13 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0147others(10): Show | 13 | HG02056.hp1 HG02523.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.127+3178_127+3180d others(5): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94729597 | |||||
| chr8:94729597
|
C | CAAAA | 48 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0031others(45): Show | 48 | HG00423.hp1 HG00544.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.127+3177_127+3180d others(6): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94729597 | |||||
| chr8:94729597
|
C | CAAAAA | 31 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(28): Show | 32 | HG00140.hp1 HG01168.hp2 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.127+3176_127+3180d others(7): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94729597 | |||||
| chr8:94729667
|
T | A | 1 | a0002c0003t0027g0207 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.127+3226T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94729667 | ||||||
| chr8:94729786
|
A | G | 285 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(282): Show | 288 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.127+3345A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94729786 | ||||||
| chr8:94729833
|
A | AAAAC | 10 | a0001c0002t0001g0008a0001c0002t0001g0215a0001c0002t0001g0216others(7): Show | 10 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.127+3404_127+3407d others(6): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94729833 | |||||
| chr8:94729911
|
T | C | 222 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(219): Show | 225 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.127+3470T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94729911 | ||||||
| chr8:94729966
|
G | A | 1 | a0008c0010t0001g0212 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.127+3525G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94729966 | ||||||
| chr8:94730020
|
A | T | 1 | a0001c0001t0001g0194 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.127+3579A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94730020 | ||||||
| chr8:94730046
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.127+3605G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94730046 | ||||||
| chr8:94730067
|
A | G | 53 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(50): Show | 53 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.127+3626A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94730067 | ||||||
| chr8:94730166
|
C | A | 34 | a0001c0001t0001g0090a0001c0001t0001g0104a0001c0001t0001g0107others(31): Show | 34 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.127+3725C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94730166 | ||||||
| chr8:94730168
|
A | G | 2 | a0001c0001t0006g0003a0001c0009t0001g0003 | 2 | NA18960.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.127+3727A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94730168 | ||||||
| chr8:94730362
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.127+3921A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94730362 | ||||||
| chr8:94730567
|
T | G | 33 | a0001c0001t0001g0002a0001c0001t0001g0120a0001c0001t0001g0121others(30): Show | 34 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.128-4063T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94730567 | ||||||
| chr8:94730686
|
A | G | 6 | a0001c0001t0001g0160a0002c0003t0004g0166a0002c0003t0004g0167others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-3944A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94730686 | ||||||
| chr8:94730739
|
CTG | C | 3 | a0001c0001t0010g0017a0001c0001t0010g0018a0001c0001t0010g0019 | 3 | HG02109.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.128-3889_128-3888d others(4): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94730739 | |||||
| chr8:94730745
|
C | CT | 14 | a0001c0001t0001g0011a0001c0001t0001g0066a0001c0001t0001g0118others(11): Show | 16 | HG01070.hp1 HG01081.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.128-3868dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94730745 | |||||
| chr8:94730823
|
G | A | 158 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(155): Show | 161 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.128-3807G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94730823 | ||||||
| chr8:94730870
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.128-3760C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94730870 | ||||||
| chr8:94730871
|
G | A | 6 | a0001c0001t0001g0160a0002c0003t0004g0166a0002c0003t0004g0167others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-3759G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94730871 | ||||||
| chr8:94730917
|
G | T | 1 | a0001c0001t0005g0006 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.128-3713G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94730917 | ||||||
| chr8:94730946
|
T | C | 4 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-3684T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94730946 | ||||||
| chr8:94731040
|
C | T | 1 | a0009c0012t0001g0214 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.128-3590C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94731040 | ||||||
| chr8:94731043
|
C | A | 1 | a0001c0001t0001g0231 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.128-3587C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94731043 | ||||||
| chr8:94731055
|
C | CA | 9 | a0001c0001t0001g0224a0001c0001t0001g0232a0001c0001t0001g0233others(6): Show | 9 | HG01358.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.128-3555dupA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94731055 | |||||
| chr8:94731055
|
CA | C | 162 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(159): Show | 164 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.128-3555delA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94731055 | |||||
| chr8:94731055
|
CAA | C | 10 | a0001c0001t0001g0050a0001c0001t0001g0160a0001c0001t0001g0169others(7): Show | 10 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.128-3556_128-3555d others(4): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94731055 | |||||
| chr8:94731055
|
CAAA | C | 10 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0076others(7): Show | 10 | HG01167.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.128-3557_128-3555d others(5): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94731055 | |||||
| chr8:94731079
|
G | C | 1 | a0001c0001t0001g0135 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.128-3551G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94731079 | ||||||
| chr8:94731402
|
T | A | 1 | a0001c0001t0025g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.128-3228T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94731402 | ||||||
| chr8:94731564
|
C | T | 43 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(40): Show | 43 | HG00423.hp1 HG00544.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.128-3066C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94731564 | ||||||
| chr8:94731719
|
C | T | 1 | a0001c0001t0002g0098 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.128-2911C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94731719 | ||||||
| chr8:94731798
|
C | T | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0058others(3): Show | 6 | HG01891.hp2 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-2832C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94731798 | ||||||
| chr8:94731903
|
G | A | 1 | a0001c0001t0009g0234 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.128-2727G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94731903 | ||||||
| chr8:94731903
|
G | T | 1 | a0001c0001t0001g0225 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.128-2727G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94731903 | ||||||
| chr8:94731905
|
C | G | 3 | a0001c0001t0010g0017a0001c0001t0010g0018a0001c0001t0010g0019 | 3 | HG02109.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.128-2725C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94731905 | ||||||
| chr8:94731917
|
G | A | 40 | a0001c0001t0001g0090a0001c0001t0001g0104a0001c0001t0001g0107others(37): Show | 40 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.128-2713G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94731917 | ||||||
| chr8:94732066
|
C | T | 43 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(40): Show | 43 | HG00423.hp1 HG00544.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.128-2564C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94732066 | ||||||
| chr8:94732124
|
G | T | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0058others(3): Show | 6 | HG01891.hp2 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-2506G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94732124 | ||||||
| chr8:94732147
|
AC | A | 25 | a0001c0001t0001g0011a0001c0001t0001g0066a0001c0001t0001g0069others(22): Show | 27 | HG01070.hp1 HG01081.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.128-2482delC | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94732147 | ||||||
| chr8:94732148
|
C | A | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0058others(3): Show | 6 | HG01891.hp2 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-2482C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94732148 | ||||||
| chr8:94732225
|
T | TA | 10 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0076others(7): Show | 10 | HG01167.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.128-2396dupA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94732225 | |||||
| chr8:94732238
|
A | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(156): Show | 162 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.128-2392A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94732238 | ||||||
| chr8:94732290
|
C | A | 1 | a0001c0001t0001g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.128-2340C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94732290 | ||||||
| chr8:94732690
|
GA | G | 10 | a0001c0002t0001g0008a0001c0002t0001g0215a0001c0002t0001g0216others(7): Show | 10 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.128-1930delA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94732690 | |||||
| chr8:94732756
|
CT | C | 40 | a0001c0001t0001g0090a0001c0001t0001g0104a0001c0001t0001g0107others(37): Show | 40 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.128-1869delT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94732756 | |||||
| chr8:94732811
|
C | CT | 155 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(152): Show | 158 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.128-1802dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94732811 | |||||
| chr8:94732811
|
C | CTT | 54 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(51): Show | 54 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.128-1803_128-1802d others(4): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94732811 | |||||
| chr8:94732837
|
A | G | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0058others(3): Show | 6 | HG01891.hp2 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-1793A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94732837 | ||||||
| chr8:94732959
|
C | T | 1 | a0001c0001t0002g0229 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.128-1671C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94732959 | ||||||
| chr8:94733034
|
A | G | 223 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(220): Show | 226 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.128-1596A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94733034 | ||||||
| chr8:94733118
|
C | CT | 81 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0047others(78): Show | 83 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.128-1487dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94733118 | |||||
| chr8:94733118
|
C | CTT | 7 | a0001c0001t0001g0090a0001c0001t0001g0115a0001c0001t0002g0064others(4): Show | 7 | HG02145.hp1 HG02258.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-1488_128-1487d others(4): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94733118 | |||||
| chr8:94733118
|
CT | C | 67 | a0001c0001t0001g0055a0001c0001t0001g0125a0001c0001t0001g0147others(64): Show | 67 | HG00609.hp1 HG00733.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.128-1487delT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94733118 | |||||
| chr8:94733121
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.128-1509T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94733121 | ||||||
| chr8:94733204
|
C | T | 10 | a0001c0002t0001g0008a0001c0002t0001g0215a0001c0002t0001g0216others(7): Show | 10 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.128-1426C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94733204 | ||||||
| chr8:94733262
|
C | T | 1 | a0001c0001t0025g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.128-1368C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94733262 | ||||||
| chr8:94733283
|
C | G | 1 | a0001c0001t0001g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.128-1347C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94733283 | ||||||
| chr8:94733371
|
C | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0120others(90): Show | 94 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.128-1259C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94733371 | ||||||
| chr8:94733458
|
G | T | 1 | a0001c0001t0002g0114 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.128-1172G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94733458 | ||||||
| chr8:94733604
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0159 | 2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.128-1026C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94733604 | ||||||
| chr8:94733643
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0120others(90): Show | 94 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.128-987G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94733643 | ||||||
| chr8:94733655
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.128-975C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94733655 | ||||||
| chr8:94733709
|
T | C | 4 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-921T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94733709 | ||||||
| chr8:94733808
|
G | C | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.128-822G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94733808 | ||||||
| chr8:94733821
|
C | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0159 | 2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.128-809C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94733821 | ||||||
| chr8:94733822
|
G | A | 2 | a0001c0001t0002g0084a0001c0001t0002g0089 | 2 | NA18939.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.128-808G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94733822 | ||||||
| chr8:94733888
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.128-742C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94733888 | ||||||
| chr8:94733912
|
C | T | 2 | a0001c0006t0001g0020a0001c0006t0001g0021 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.128-718C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94733912 | ||||||
| chr8:94733922
|
T | C | 33 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(30): Show | 33 | HG00423.hp1 HG00544.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.128-708T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94733922 | ||||||
| chr8:94733996
|
A | T | 1 | a0001c0001t0001g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.128-634A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94733996 | ||||||
| chr8:94734004
|
T | G | 1 | a0001c0001t0005g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.128-626T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94734004 | ||||||
| chr8:94734061
|
C | CT | 16 | a0001c0001t0001g0033a0001c0001t0001g0054a0001c0001t0001g0055others(13): Show | 16 | HG01168.hp2 HG01169.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.128-553dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94734061 | |||||
| chr8:94734061
|
C | CTT | 41 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(38): Show | 41 | HG00423.hp1 HG00544.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.128-554_128-553dup others(2): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 94734061 | |||||
| chr8:94734137
|
G | A | 1 | a0001c0001t0007g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.128-493G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94734137 | ||||||
| chr8:94734138
|
C | A | 1 | a0001c0001t0007g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.128-492C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94734138 | ||||||
| chr8:94734184
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.128-446G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94734184 | ||||||
| chr8:94734220
|
A | G | 1 | a0001c0001t0007g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.128-410A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94734220 | ||||||
| chr8:94734280
|
C | G | 51 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(48): Show | 51 | HG00423.hp1 HG00544.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.128-350C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94734280 | ||||||
| chr8:94734307
|
A | C | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.128-323A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94734307 | ||||||
| chr8:94734605
|
C | G | 156 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0026others(153): Show | 157 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.128-25C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 2/18 | chr8 | 94734605 | ||||||
| chr8:94734946
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 5 | NA18971.hp2 NA19062.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+192G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94734946 | ||||||
| chr8:94735227
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.252+473C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94735227 | ||||||
| chr8:94735232
|
A | C | 33 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(30): Show | 33 | HG00423.hp1 HG00544.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.252+478A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94735232 | ||||||
| chr8:94735271
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.252+517A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94735271 | ||||||
| chr8:94735313
|
T | A | 45 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(42): Show | 45 | HG00423.hp1 HG00544.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.252+559T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94735313 | ||||||
| chr8:94735401
|
C | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0002g0200 | 3 | NA18962.hp1 NA19090.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.252+647C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94735401 | ||||||
| chr8:94735457
|
A | G | 1 | a0001c0001t0001g0274 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.252+703A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94735457 | ||||||
| chr8:94735600
|
G | A | 1 | a0001c0001t0032g0223 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.252+846G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94735600 | ||||||
| chr8:94735662
|
A | G | 1 | a0001c0001t0023g0263 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.252+908A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94735662 | ||||||
| chr8:94735792
|
G | T | 1 | a0001c0001t0006g0022 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.252+1038G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94735792 | ||||||
| chr8:94735902
|
TA | T | 6 | a0001c0001t0001g0160a0002c0003t0004g0166a0002c0003t0004g0167others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.252+1156delA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 94735902 | |||||
| chr8:94735910
|
A | T | 33 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(30): Show | 33 | HG00423.hp1 HG00544.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.252+1156A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94735910 | ||||||
| chr8:94735978
|
A | G | 9 | a0001c0001t0001g0011a0001c0001t0003g0001a0001c0001t0003g0010others(6): Show | 11 | HG01070.hp1 HG01081.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.252+1224A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94735978 | ||||||
| chr8:94735992
|
A | C | 1 | a0001c0001t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.252+1238A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94735992 | ||||||
| chr8:94736026
|
A | G | 40 | a0001c0001t0001g0090a0001c0001t0001g0104a0001c0001t0001g0107others(37): Show | 40 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.252+1272A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94736026 | ||||||
| chr8:94736066
|
C | G | 2 | a0001c0001t0001g0169a0001c0001t0007g0067 | 2 | HG02486.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.252+1312C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94736066 | ||||||
| chr8:94736133
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.252+1379A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94736133 | ||||||
| chr8:94736371
|
T | C | 1 | a0001c0001t0012g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.252+1617T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94736371 | ||||||
| chr8:94736417
|
G | C | 34 | a0001c0001t0001g0090a0001c0001t0001g0104a0001c0001t0001g0107others(31): Show | 34 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.252+1663G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94736417 | ||||||
| chr8:94736629
|
A | C | 33 | a0001c0001t0001g0002a0001c0001t0001g0120a0001c0001t0001g0121others(30): Show | 34 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.253-1740A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94736629 | ||||||
| chr8:94736795
|
A | G | 54 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(51): Show | 54 | HG00609.hp1 HG00733.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.253-1574A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94736795 | ||||||
| chr8:94736934
|
G | C | 1 | a0001c0001t0002g0102 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.253-1435G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94736934 | ||||||
| chr8:94736946
|
A | T | 10 | a0001c0002t0001g0008a0001c0002t0001g0215a0001c0002t0001g0216others(7): Show | 10 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.253-1423A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94736946 | ||||||
| chr8:94736954
|
C | T | 4 | a0001c0001t0001g0272a0001c0001t0009g0234a0001c0001t0009g0261others(1): Show | 4 | HG02451.hp1 HG02735.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-1415C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94736954 | ||||||
| chr8:94736966
|
A | G | 53 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(50): Show | 53 | HG00423.hp1 HG00544.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.253-1403A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94736966 | ||||||
| chr8:94737510
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0159 | 2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.253-859C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94737510 | ||||||
| chr8:94737782
|
CAAACA | C | 184 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(181): Show | 187 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.253-563_253-559del others(5): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 94737782 | |||||
| chr8:94737792
|
A | G | 11 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0076others(8): Show | 11 | HG01167.hp1 HG02145.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.253-577A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94737792 | ||||||
| chr8:94737845
|
G | A | 25 | a0001c0001t0001g0011a0001c0001t0001g0066a0001c0001t0001g0069others(22): Show | 27 | HG01070.hp1 HG01081.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.253-524G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94737845 | ||||||
| chr8:94738104
|
G | A | 65 | a0001c0001t0001g0011a0001c0001t0001g0066a0001c0001t0001g0069others(62): Show | 67 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.253-265G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94738104 | ||||||
| chr8:94738159
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.253-210A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94738159 | ||||||
| chr8:94738193
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.253-176C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94738193 | ||||||
| chr8:94738251
|
G | A | 1 | a0001c0001t0007g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.253-118G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94738251 | ||||||
| chr8:94738263
|
G | T | 40 | a0001c0001t0001g0090a0001c0001t0001g0104a0001c0001t0001g0107others(37): Show | 40 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.253-106G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | chr8 | 94738263 | ||||||
| chr8:94738318
|
CA | C | 218 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(215): Show | 221 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.253-35delA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 94738318 | |||||
| chr8:94738516
|
CT | C | 12 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0076others(9): Show | 12 | HG01069.hp2 HG01167.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.343+71delT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 94738516 | |||||
| chr8:94738570
|
A | G | 1 | a0001c0001t0007g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.343+111A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 4/18 | chr8 | 94738570 | ||||||
| chr8:94738734
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.343+275G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 4/18 | chr8 | 94738734 | ||||||
| chr8:94738800
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0120a0001c0001t0001g0121others(28): Show | 32 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.343+341C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 4/18 | chr8 | 94738800 | ||||||
| chr8:94738869
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.343+410C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 4/18 | chr8 | 94738869 | ||||||
| chr8:94739011
|
T | C | 1 | a0001c0001t0012g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.344-402T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 4/18 | chr8 | 94739011 | ||||||
| chr8:94739048
|
T | G | 1 | a0001c0001t0005g0006 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.344-365T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 4/18 | chr8 | 94739048 | ||||||
| chr8:94739062
|
G | C | 1 | a0001c0001t0001g0126 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.344-351G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 4/18 | chr8 | 94739062 | ||||||
| chr8:94739116
|
C | T | 36 | a0001c0001t0001g0011a0001c0001t0001g0066a0001c0001t0001g0069others(33): Show | 38 | HG01070.hp1 HG01081.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.344-297C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 4/18 | chr8 | 94739116 | ||||||
| chr8:94739215
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.344-198C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 4/18 | chr8 | 94739215 | ||||||
| chr8:94739274
|
T | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0026others(162): Show | 166 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.344-139T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 4/18 | chr8 | 94739274 | ||||||
| chr8:94739832
|
G | C | 1 | a0001c0001t0005g0005 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.611+42G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94739832 | ||||||
| chr8:94739866
|
T | TC | 95 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0104others(92): Show | 95 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.611+80dupC | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94739866 | |||||
| chr8:94739921
|
T | C | 5 | a0001c0001t0001g0054a0001c0001t0001g0267a0001c0001t0019g0175others(2): Show | 5 | HG01109.hp2 HG01358.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.611+131T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94739921 | ||||||
| chr8:94740160
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.611+370G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94740160 | ||||||
| chr8:94740447
|
G | T | 37 | a0001c0001t0001g0011a0001c0001t0001g0066a0001c0001t0001g0069others(34): Show | 39 | HG01070.hp1 HG01081.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.611+657G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94740447 | ||||||
| chr8:94740471
|
T | C | 15 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0003g0001others(12): Show | 17 | HG01070.hp1 HG01081.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.611+681T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94740471 | ||||||
| chr8:94740545
|
C | G | 1 | a0001c0001t0009g0262 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.611+755C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94740545 | ||||||
| chr8:94740733
|
G | C | 1 | a0001c0001t0001g0236 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.611+943G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94740733 | ||||||
| chr8:94740771
|
T | A | 8 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0201others(5): Show | 8 | HG01928.hp1 HG01993.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.611+981T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94740771 | ||||||
| chr8:94740813
|
T | A | 164 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(161): Show | 167 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.611+1023T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94740813 | ||||||
| chr8:94740869
|
C | T | 7 | a0001c0001t0001g0170a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG02109.hp2 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.611+1079C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94740869 | ||||||
| chr8:94740887
|
C | A | 1 | a0001c0001t0001g0264 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.611+1097C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94740887 | ||||||
| chr8:94741192
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.611+1402A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94741192 | ||||||
| chr8:94741239
|
A | G | 1 | a0001c0001t0007g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.611+1449A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94741239 | ||||||
| chr8:94741242
|
G | C | 1 | a0001c0001t0007g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.611+1452G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94741242 | ||||||
| chr8:94741343
|
AC | A | 10 | a0001c0002t0001g0008a0001c0002t0001g0215a0001c0002t0001g0216others(7): Show | 10 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.611+1555delC | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94741343 | |||||
| chr8:94741437
|
A | G | 70 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0032others(67): Show | 73 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.611+1647A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94741437 | ||||||
| chr8:94741494
|
G | A | 7 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0172others(4): Show | 7 | HG01109.hp2 HG01358.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.611+1704G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94741494 | ||||||
| chr8:94741626
|
T | G | 69 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(66): Show | 69 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.611+1836T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94741626 | ||||||
| chr8:94742063
|
A | G | 171 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(168): Show | 174 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.611+2273A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94742063 | ||||||
| chr8:94742080
|
C | T | 1 | a0001c0001t0007g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.611+2290C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94742080 | ||||||
| chr8:94742183
|
G | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0032others(72): Show | 78 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(75): Show |
intron_variant | MODIFIER | c.611+2393G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94742183 | ||||||
| chr8:94742224
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.611+2434G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94742224 | ||||||
| chr8:94742250
|
C | T | 9 | a0001c0001t0001g0024a0001c0001t0001g0160a0001c0001t0019g0175others(6): Show | 9 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.611+2460C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94742250 | ||||||
| chr8:94742290
|
A | G | 169 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(166): Show | 172 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.611+2500A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94742290 | ||||||
| chr8:94742344
|
C | T | 2 | a0001c0001t0001g0281a0001c0001t0001g0283 | 2 | NA19001.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.611+2554C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94742344 | ||||||
| chr8:94742353
|
G | A | 1 | a0001c0001t0012g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.611+2563G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94742353 | ||||||
| chr8:94742387
|
AT | A | 7 | a0001c0001t0001g0170a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG02109.hp2 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.611+2609delT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94742387 | |||||
| chr8:94742391
|
T | A | 164 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(161): Show | 167 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.611+2601T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94742391 | ||||||
| chr8:94742402
|
T | C | 3 | a0001c0001t0004g0162a0001c0001t0004g0163a0001c0001t0004g0164 | 3 | HG01261.hp2 HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.611+2612T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94742402 | ||||||
| chr8:94742559
|
A | AT | 11 | a0001c0001t0001g0028a0001c0001t0001g0063a0001c0001t0001g0148others(8): Show | 11 | HG00735.hp2 HG01069.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.611+2786dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94742559 | |||||
| chr8:94742559
|
AT | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0125a0001c0001t0001g0130others(6): Show | 10 | HG01069.hp2 HG01255.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.611+2786delT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94742559 | |||||
| chr8:94742559
|
ATT | A | 77 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0032others(74): Show | 79 | HG00140.hp1 HG00423.hp2 HG01070.hp1 others(76): Show |
intron_variant | MODIFIER | c.611+2785_611+2786d others(4): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94742559 | |||||
| chr8:94742621
|
C | T | 2 | a0001c0001t0001g0257a0001c0001t0002g0088 | 2 | NA19007.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.611+2831C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94742621 | ||||||
| chr8:94742709
|
C | A | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.611+2919C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94742709 | ||||||
| chr8:94742732
|
T | C | 10 | a0001c0002t0001g0008a0001c0002t0001g0215a0001c0002t0001g0216others(7): Show | 10 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.611+2942T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94742732 | ||||||
| chr8:94742851
|
C | G | 1 | a0001c0001t0001g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.611+3061C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94742851 | ||||||
| chr8:94743219
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0051 | 2 | NA18949.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.611+3429G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94743219 | ||||||
| chr8:94743247
|
C | G | 69 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(66): Show | 69 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.611+3457C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94743247 | ||||||
| chr8:94743248
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(35): Show | 39 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.611+3458T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94743248 | ||||||
| chr8:94743266
|
G | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(35): Show | 39 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.611+3476G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94743266 | ||||||
| chr8:94743276
|
C | T | 1 | a0005c0013t0024g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.611+3486C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94743276 | ||||||
| chr8:94743326
|
A | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(92): Show | 98 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(95): Show |
intron_variant | MODIFIER | c.611+3536A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94743326 | ||||||
| chr8:94743442
|
G | A | 2 | a0001c0006t0001g0020a0001c0006t0001g0021 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.611+3652G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94743442 | ||||||
| chr8:94743463
|
CCTCATCA others(1): Show |
C | 3 | a0001c0001t0001g0132a0001c0001t0001g0138a0001c0001t0001g0140 | 3 | NA18950.hp1 NA18961.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.611+3677_611+3684d others(10): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94743463 | |||||
| chr8:94743479
|
T | TA | 43 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(40): Show | 44 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.611+3705dupA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94743479 | |||||
| chr8:94743494
|
A | G | 10 | a0001c0001t0001g0024a0001c0001t0001g0160a0001c0001t0001g0169others(7): Show | 10 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.611+3704A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94743494 | ||||||
| chr8:94743550
|
A | G | 15 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0003g0001others(12): Show | 17 | HG01070.hp1 HG01081.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.611+3760A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94743550 | ||||||
| chr8:94743734
|
A | G | 37 | a0001c0001t0001g0032a0001c0001t0001g0050a0001c0001t0001g0115others(34): Show | 37 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.611+3944A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94743734 | ||||||
| chr8:94743809
|
T | C | 164 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(161): Show | 167 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.611+4019T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94743809 | ||||||
| chr8:94743883
|
A | G | 5 | a0001c0001t0001g0169a0001c0001t0001g0236a0001c0001t0010g0017others(2): Show | 5 | HG01081.hp2 HG02109.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.611+4093A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94743883 | ||||||
| chr8:94743962
|
T | A | 70 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0032others(67): Show | 73 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.611+4172T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94743962 | ||||||
| chr8:94743978
|
C | T | 9 | a0001c0001t0001g0024a0001c0001t0001g0160a0001c0001t0019g0175others(6): Show | 9 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.611+4188C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94743978 | ||||||
| chr8:94744080
|
G | A | 1 | a0001c0001t0002g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.611+4290G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94744080 | ||||||
| chr8:94744121
|
G | T | 164 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(161): Show | 167 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.611+4331G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94744121 | ||||||
| chr8:94744176
|
A | G | 4 | a0001c0001t0008g0079a0001c0001t0008g0080a0001c0001t0008g0081others(1): Show | 4 | HG02559.hp2 HG03225.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+4386A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94744176 | ||||||
| chr8:94744222
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0010g0017a0001c0001t0010g0018others(1): Show | 4 | HG01081.hp2 HG02109.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.611+4432C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94744222 | ||||||
| chr8:94744260
|
T | A | 7 | a0001c0001t0001g0170a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG02109.hp2 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.611+4470T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94744260 | ||||||
| chr8:94744500
|
G | A | 1 | a0001c0001t0007g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.611+4710G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94744500 | ||||||
| chr8:94744765
|
C | A | 3 | a0001c0001t0001g0024a0001c0001t0019g0175a0001c0002t0001g0023 | 3 | HG03209.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.611+4975C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94744765 | ||||||
| chr8:94744795
|
T | C | 70 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0032others(67): Show | 73 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.611+5005T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94744795 | ||||||
| chr8:94744944
|
A | T | 4 | a0001c0001t0006g0003a0001c0001t0006g0184a0001c0001t0006g0185others(1): Show | 4 | NA18960.hp1 NA18981.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+5154A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94744944 | ||||||
| chr8:94745091
|
G | A | 1 | a0001c0001t0002g0098 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.611+5301G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94745091 | ||||||
| chr8:94745227
|
T | C | 2 | a0001c0001t0014g0237a0001c0001t0014g0238 | 2 | HG00738.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.611+5437T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94745227 | ||||||
| chr8:94745346
|
A | AG | 164 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(161): Show | 167 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.611+5556_611+5557i others(3): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94745346 | ||||||
| chr8:94745513
|
A | G | 5 | a0001c0001t0001g0181a0001c0001t0003g0179a0001c0001t0003g0180others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.611+5723A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94745513 | ||||||
| chr8:94745569
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.611+5779A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94745569 | ||||||
| chr8:94745617
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.611+5827C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94745617 | ||||||
| chr8:94745679
|
G | A | 2 | a0001c0001t0001g0024a0001c0002t0001g0023 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.611+5889G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94745679 | ||||||
| chr8:94745688
|
C | A | 62 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(59): Show | 62 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.611+5898C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94745688 | ||||||
| chr8:94745694
|
A | G | 4 | a0001c0001t0001g0236a0001c0001t0010g0017a0001c0001t0010g0018others(1): Show | 4 | HG01081.hp2 HG02109.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.611+5904A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94745694 | ||||||
| chr8:94745776
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0010g0017a0001c0001t0010g0018others(1): Show | 4 | HG01081.hp2 HG02109.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.611+5986C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94745776 | ||||||
| chr8:94746043
|
C | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0236a0001c0001t0010g0017others(2): Show | 5 | HG01081.hp2 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.611+6253C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94746043 | ||||||
| chr8:94746054
|
A | AT | 70 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0031others(67): Show | 70 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.611+6289dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94746054 | |||||
| chr8:94746054
|
A | ATT | 19 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0037others(16): Show | 19 | HG00673.hp1 HG00733.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.611+6288_611+6289d others(4): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94746054 | |||||
| chr8:94746054
|
AT | A | 32 | a0001c0001t0001g0011a0001c0001t0001g0069a0001c0001t0001g0071others(29): Show | 34 | HG01070.hp1 HG01081.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.611+6289delT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94746054 | |||||
| chr8:94746054
|
ATT | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(33): Show | 37 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.611+6288_611+6289d others(4): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94746054 | |||||
| chr8:94746094
|
C | G | 1 | a0001c0001t0004g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.611+6304C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94746094 | ||||||
| chr8:94746274
|
T | C | 4 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(1): Show | 4 | HG01934.hp2 HG01978.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.611+6484T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94746274 | ||||||
| chr8:94746388
|
G | A | 1 | a0001c0001t0002g0089 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.611+6598G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94746388 | ||||||
| chr8:94746538
|
T | C | 157 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(154): Show | 160 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.611+6748T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94746538 | ||||||
| chr8:94746573
|
C | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0032others(68): Show | 74 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.611+6783C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94746573 | ||||||
| chr8:94746672
|
A | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0076 | 2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.611+6882A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94746672 | ||||||
| chr8:94746738
|
A | G | 4 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 4 | HG00738.hp2 HG01099.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+6948A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94746738 | ||||||
| chr8:94746835
|
A | G | 19 | a0001c0001t0001g0024a0001c0001t0001g0054a0001c0001t0001g0055others(16): Show | 19 | HG01109.hp2 HG01358.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.611+7045A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94746835 | ||||||
| chr8:94746878
|
G | T | 3 | a0001c0001t0010g0017a0001c0001t0010g0018a0001c0001t0010g0019 | 3 | HG02109.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.611+7088G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94746878 | ||||||
| chr8:94746879
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.611+7089C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94746879 | ||||||
| chr8:94746932
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.611+7142C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94746932 | ||||||
| chr8:94746971
|
C | G | 2 | a0001c0006t0001g0020a0001c0006t0001g0021 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.611+7181C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94746971 | ||||||
| chr8:94747013
|
A | AT | 61 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(58): Show | 61 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.611+7234dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94747013 | |||||
| chr8:94747070
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.611+7280G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94747070 | ||||||
| chr8:94747156
|
A | C | 1 | a0001c0001t0012g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.611+7366A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94747156 | ||||||
| chr8:94747249
|
C | T | 1 | a0001c0001t0002g0102 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.611+7459C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94747249 | ||||||
| chr8:94747272
|
C | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(31): Show | 35 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.611+7482C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94747272 | ||||||
| chr8:94747323
|
G | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0236a0001c0001t0010g0017others(2): Show | 5 | HG01081.hp2 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.611+7533G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94747323 | ||||||
| chr8:94747381
|
G | T | 164 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(161): Show | 167 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.611+7591G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94747381 | ||||||
| chr8:94747404
|
A | AT | 157 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(154): Show | 160 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.611+7620dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94747404 | |||||
| chr8:94747440
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.611+7650C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94747440 | ||||||
| chr8:94747441
|
C | T | 10 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(7): Show | 10 | HG01109.hp2 HG01358.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.611+7651C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94747441 | ||||||
| chr8:94747445
|
T | C | 3 | a0001c0001t0010g0017a0001c0001t0010g0018a0001c0001t0010g0019 | 3 | HG02109.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.611+7655T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94747445 | ||||||
| chr8:94747470
|
C | T | 61 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(58): Show | 61 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.611+7680C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94747470 | ||||||
| chr8:94747554
|
C | CT | 28 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0066others(25): Show | 28 | HG02055.hp1 HG02056.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.611+7786dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94747554 | |||||
| chr8:94747566
|
T | G | 1 | a0001c0001t0012g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.611+7776T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94747566 | ||||||
| chr8:94747645
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.611+7855G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94747645 | ||||||
| chr8:94747719
|
T | A | 61 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(58): Show | 61 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.611+7929T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94747719 | ||||||
| chr8:94747782
|
G | A | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.611+7992G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94747782 | ||||||
| chr8:94747849
|
C | T | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.611+8059C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94747849 | ||||||
| chr8:94747855
|
G | A | 1 | a0001c0001t0004g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.611+8065G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94747855 | ||||||
| chr8:94747902
|
TAAACTC | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0236a0001c0001t0010g0017others(2): Show | 5 | HG01081.hp2 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.611+8116_611+8121d others(8): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94747902 | |||||
| chr8:94747906
|
C | T | 10 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(7): Show | 10 | HG01109.hp2 HG01358.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.611+8116C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94747906 | ||||||
| chr8:94747923
|
G | C | 71 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0032others(68): Show | 74 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.612-8113G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94747923 | ||||||
| chr8:94747982
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.612-8054G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94747982 | ||||||
| chr8:94748037
|
G | A | 15 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0003g0001others(12): Show | 17 | HG01070.hp1 HG01081.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.612-7999G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94748037 | ||||||
| chr8:94748058
|
C | G | 7 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0172others(4): Show | 7 | HG01109.hp2 HG01358.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.612-7978C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94748058 | ||||||
| chr8:94748095
|
A | G | 96 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(93): Show | 99 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(96): Show |
intron_variant | MODIFIER | c.612-7941A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94748095 | ||||||
| chr8:94748107
|
G | A | 1 | a0001c0001t0012g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.612-7929G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94748107 | ||||||
| chr8:94748342
|
T | A | 1 | a0008c0010t0001g0212 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.612-7694T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94748342 | ||||||
| chr8:94748476
|
A | T | 1 | a0001c0001t0007g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.612-7560A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94748476 | ||||||
| chr8:94748499
|
A | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0236a0001c0001t0010g0017others(2): Show | 5 | HG01081.hp2 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-7537A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94748499 | ||||||
| chr8:94748508
|
C | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0236a0001c0001t0010g0017others(2): Show | 5 | HG01081.hp2 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-7528C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94748508 | ||||||
| chr8:94748600
|
G | GGCA | 6 | a0001c0001t0001g0160a0002c0003t0004g0166a0002c0003t0004g0167others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.612-7422_612-7420d others(5): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94748600 | |||||
| chr8:94748620
|
CAAT | C | 3 | a0001c0001t0010g0017a0001c0001t0010g0018a0001c0001t0010g0019 | 3 | HG02109.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.612-7415_612-7413d others(5): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94748620 | ||||||
| chr8:94748621
|
A | AATG | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0007g0057 | 3 | HG02723.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.612-7401_612-7399d others(5): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94748621 | |||||
| chr8:94748621
|
AATGATGA others(11): Show |
A | 1 | a0001c0001t0001g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.612-7397_612-7380d others(20): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94748621 | |||||
| chr8:94748621
|
AATGATGA others(14): Show |
A | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG01070.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.612-7401_612-7381d others(23): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94748621 | |||||
| chr8:94748638
|
C | T | 1 | a0001c0001t0023g0263 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.612-7398C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94748638 | ||||||
| chr8:94748763
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.612-7273G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94748763 | ||||||
| chr8:94748924
|
T | C | 164 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(161): Show | 167 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.612-7112T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94748924 | ||||||
| chr8:94748928
|
A | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(31): Show | 35 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.612-7108A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94748928 | ||||||
| chr8:94749124
|
G | GA | 11 | a0001c0002t0001g0008a0001c0002t0001g0078a0001c0002t0001g0215others(8): Show | 11 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.612-6909dupA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94749124 | |||||
| chr8:94749235
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.612-6801A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94749235 | ||||||
| chr8:94749325
|
C | T | 38 | a0001c0001t0001g0011a0001c0001t0001g0066a0001c0001t0001g0069others(35): Show | 40 | HG01070.hp1 HG01081.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.612-6711C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94749325 | ||||||
| chr8:94749471
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(36): Show | 40 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.612-6565A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94749471 | ||||||
| chr8:94749554
|
C | T | 7 | a0001c0001t0001g0170a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG02109.hp2 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.612-6482C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94749554 | ||||||
| chr8:94749654
|
G | A | 9 | a0001c0001t0001g0024a0001c0001t0001g0160a0001c0001t0019g0175others(6): Show | 9 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.612-6382G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94749654 | ||||||
| chr8:94749658
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.612-6378G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94749658 | ||||||
| chr8:94749762
|
C | G | 7 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0172others(4): Show | 7 | HG01109.hp2 HG01358.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.612-6274C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94749762 | ||||||
| chr8:94749803
|
C | T | 5 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0172others(2): Show | 5 | HG02723.hp1 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.612-6233C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94749803 | ||||||
| chr8:94750072
|
C | T | 11 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(8): Show | 11 | HG01109.hp2 HG01358.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.612-5964C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750072 | ||||||
| chr8:94750101
|
G | A | 2 | a0001c0006t0001g0020a0001c0006t0001g0021 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.612-5935G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750101 | ||||||
| chr8:94750148
|
G | T | 1 | a0001c0001t0006g0022 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.612-5888G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750148 | ||||||
| chr8:94750232
|
G | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0236a0001c0001t0010g0017others(2): Show | 5 | HG01081.hp2 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-5804G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750232 | ||||||
| chr8:94750266
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0043 | 2 | HG00738.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.612-5770G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750266 | ||||||
| chr8:94750352
|
G | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0236a0001c0001t0010g0017others(2): Show | 5 | HG01081.hp2 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-5684G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750352 | ||||||
| chr8:94750361
|
G | A | 11 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(8): Show | 11 | HG00738.hp1 HG01070.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.612-5675G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750361 | ||||||
| chr8:94750433
|
A | C | 2 | a0001c0001t0013g0178a0001c0001t0013g0182 | 2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.612-5603A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750433 | ||||||
| chr8:94750443
|
A | C | 11 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(8): Show | 11 | HG01109.hp2 HG01358.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.612-5593A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750443 | ||||||
| chr8:94750457
|
A | G | 3 | a0001c0001t0010g0017a0001c0001t0010g0018a0001c0001t0010g0019 | 3 | HG02109.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.612-5579A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750457 | ||||||
| chr8:94750466
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.612-5570A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750466 | ||||||
| chr8:94750490
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.612-5546G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750490 | ||||||
| chr8:94750561
|
CTG | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0236a0001c0001t0010g0017others(2): Show | 5 | HG01081.hp2 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-5459_612-5458d others(4): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94750561 | |||||
| chr8:94750577
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.612-5459G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750577 | ||||||
| chr8:94750613
|
T | C | 11 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(8): Show | 11 | HG01109.hp2 HG01358.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.612-5423T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750613 | ||||||
| chr8:94750785
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0002g0097 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.612-5247_612-5236d others(14): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94750785 | |||||
| chr8:94750806
|
A | G | 1 | a0001c0001t0002g0097 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.612-5230A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750806 | ||||||
| chr8:94750808
|
G | A | 1 | a0001c0001t0002g0097 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.612-5228G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750808 | ||||||
| chr8:94750809
|
A | G | 1 | a0001c0001t0002g0097 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.612-5227A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750809 | ||||||
| chr8:94750814
|
A | G | 1 | a0001c0001t0002g0097 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.612-5222A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750814 | ||||||
| chr8:94750822
|
A | G | 1 | a0001c0001t0002g0097 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.612-5214A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750822 | ||||||
| chr8:94750834
|
G | C | 1 | a0001c0001t0002g0097 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.612-5202G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750834 | ||||||
| chr8:94750843
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0019g0175 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.612-5193C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750843 | ||||||
| chr8:94750973
|
G | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(31): Show | 35 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.612-5063G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750973 | ||||||
| chr8:94750997
|
T | C | 1 | a0001c0001t0016g0082 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.612-5039T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94750997 | ||||||
| chr8:94751028
|
G | C | 3 | a0001c0001t0010g0017a0001c0001t0010g0018a0001c0001t0010g0019 | 3 | HG02109.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.612-5008G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751028 | ||||||
| chr8:94751118
|
C | CTTTCTT | 5 | a0001c0001t0001g0029a0001c0001t0001g0236a0001c0001t0010g0017others(2): Show | 5 | HG01081.hp2 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-4915_612-4914i others(8): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94751118 | |||||
| chr8:94751120
|
T | TTC | 31 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(28): Show | 32 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.612-4915_612-4914i others(4): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94751120 | |||||
| chr8:94751123
|
C | CT | 12 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0104others(9): Show | 12 | HG00741.hp2 HG01109.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.612-4900dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94751123 | |||||
| chr8:94751123
|
C | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(36): Show | 40 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.612-4913C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751123 | ||||||
| chr8:94751128
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.612-4908T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751128 | ||||||
| chr8:94751192
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.612-4844C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751192 | ||||||
| chr8:94751263
|
C | T | 14 | a0001c0001t0001g0134a0001c0001t0001g0149a0001c0001t0001g0150others(11): Show | 14 | HG00735.hp1 HG00741.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.612-4773C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751263 | ||||||
| chr8:94751267
|
C | T | 37 | a0001c0001t0001g0011a0001c0001t0001g0066a0001c0001t0001g0071others(34): Show | 39 | HG01070.hp1 HG01081.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.612-4769C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751267 | ||||||
| chr8:94751275
|
C | T | 12 | a0001c0002t0001g0008a0001c0002t0001g0023a0001c0002t0001g0078others(9): Show | 12 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.612-4761C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751275 | ||||||
| chr8:94751319
|
T | A | 1 | a0001c0001t0001g0196 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.612-4717T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751319 | ||||||
| chr8:94751367
|
C | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(31): Show | 35 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.612-4669C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751367 | ||||||
| chr8:94751484
|
C | A | 6 | a0001c0001t0001g0160a0002c0003t0004g0166a0002c0003t0004g0167others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.612-4552C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751484 | ||||||
| chr8:94751495
|
A | T | 2 | a0001c0006t0001g0020a0001c0006t0001g0021 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.612-4541A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751495 | ||||||
| chr8:94751531
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.612-4505G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751531 | ||||||
| chr8:94751566
|
A | G | 5 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | NA18985.hp1 NA18985.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.612-4470A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751566 | ||||||
| chr8:94751584
|
C | T | 3 | a0001c0001t0010g0017a0001c0001t0010g0018a0001c0001t0010g0019 | 3 | HG02109.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.612-4452C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751584 | ||||||
| chr8:94751636
|
C | T | 3 | a0001c0001t0001g0176a0001c0006t0001g0020a0001c0006t0001g0021 | 3 | HG01978.hp2 HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.612-4400C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751636 | ||||||
| chr8:94751646
|
C | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(31): Show | 35 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.612-4390C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751646 | ||||||
| chr8:94751664
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(36): Show | 40 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.612-4372A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751664 | ||||||
| chr8:94751713
|
C | T | 2 | a0001c0001t0004g0162a0001c0001t0004g0163 | 2 | HG01261.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.612-4323C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751713 | ||||||
| chr8:94751734
|
G | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(36): Show | 40 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.612-4302G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751734 | ||||||
| chr8:94751813
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(36): Show | 40 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.612-4223A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751813 | ||||||
| chr8:94751920
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.612-4116A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751920 | ||||||
| chr8:94751926
|
T | G | 156 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(153): Show | 159 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.612-4110T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94751926 | ||||||
| chr8:94752046
|
A | G | 3 | a0001c0001t0010g0017a0001c0001t0010g0018a0001c0001t0010g0019 | 3 | HG02109.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.612-3990A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94752046 | ||||||
| chr8:94752088
|
T | A | 156 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(153): Show | 159 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.612-3948T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94752088 | ||||||
| chr8:94752138
|
C | T | 7 | a0001c0002t0001g0008a0001c0002t0001g0215a0001c0002t0001g0216others(4): Show | 7 | HG02257.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.612-3898C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94752138 | ||||||
| chr8:94752139
|
G | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.612-3897G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94752139 | ||||||
| chr8:94752380
|
C | T | 8 | a0001c0001t0001g0024a0001c0001t0001g0160a0001c0001t0019g0175others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.612-3656C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94752380 | ||||||
| chr8:94752442
|
C | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0236a0001c0001t0010g0017others(2): Show | 5 | HG01081.hp2 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-3594C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94752442 | ||||||
| chr8:94752447
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(36): Show | 40 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.612-3589A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94752447 | ||||||
| chr8:94752458
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.612-3578C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94752458 | ||||||
| chr8:94752490
|
G | A | 5 | a0001c0001t0001g0181a0001c0001t0003g0179a0001c0001t0003g0180others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.612-3546G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94752490 | ||||||
| chr8:94752585
|
C | CA | 22 | a0001c0001t0001g0150a0001c0001t0001g0153a0001c0001t0001g0159others(19): Show | 22 | HG00544.hp2 HG00735.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.612-3429dupA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94752585 | |||||
| chr8:94752585
|
CA | C | 48 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(45): Show | 48 | HG00140.hp2 HG00558.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.612-3429delA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94752585 | |||||
| chr8:94752585
|
CAAAAAA | C | 9 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(6): Show | 9 | HG01109.hp2 HG01358.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.612-3434_612-3429d others(8): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94752585 | |||||
| chr8:94752585
|
CAAAAAAA others(2): Show |
C | 69 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0050others(66): Show | 72 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.612-3437_612-3429d others(11): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94752585 | |||||
| chr8:94752585
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0032 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.612-3438_612-3429d others(12): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94752585 | |||||
| chr8:94752669
|
A | AT | 16 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0050others(13): Show | 16 | HG01081.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.612-3356dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94752669 | |||||
| chr8:94752718
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.612-3318G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94752718 | ||||||
| chr8:94752810
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.612-3226G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94752810 | ||||||
| chr8:94752869
|
G | T | 1 | a0001c0001t0021g0025 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.612-3167G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94752869 | ||||||
| chr8:94753008
|
C | CA | 24 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(21): Show | 24 | HG01261.hp2 HG01358.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.612-3013dupA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94753008 | |||||
| chr8:94753008
|
CA | C | 26 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0066others(23): Show | 28 | HG01070.hp1 HG01081.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.612-3013delA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94753008 | |||||
| chr8:94753283
|
G | A | 1 | a0001c0001t0007g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.612-2753G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94753283 | ||||||
| chr8:94753597
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0159 | 2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.612-2439G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94753597 | ||||||
| chr8:94753613
|
C | T | 12 | a0001c0002t0001g0008a0001c0002t0001g0023a0001c0002t0001g0078others(9): Show | 12 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.612-2423C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94753613 | ||||||
| chr8:94753638
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.612-2398C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94753638 | ||||||
| chr8:94753706
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.612-2330A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94753706 | ||||||
| chr8:94753786
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.612-2250C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94753786 | ||||||
| chr8:94753868
|
G | A | 3 | a0001c0001t0001g0076a0001c0001t0018g0077a0001c0001t0028g0070 | 3 | HG02145.hp1 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.612-2168G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94753868 | ||||||
| chr8:94753899
|
C | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(36): Show | 40 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.612-2137C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94753899 | ||||||
| chr8:94753922
|
C | G | 1 | a0001c0001t0007g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.612-2114C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94753922 | ||||||
| chr8:94753976
|
G | A | 1 | a0001c0001t0012g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.612-2060G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94753976 | ||||||
| chr8:94754139
|
G | A | 3 | a0001c0001t0001g0076a0001c0001t0018g0077a0001c0001t0028g0070 | 3 | HG02145.hp1 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.612-1897G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94754139 | ||||||
| chr8:94754186
|
T | C | 1 | a0001c0001t0025g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.612-1850T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94754186 | ||||||
| chr8:94754356
|
T | G | 1 | a0001c0001t0007g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.612-1680T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94754356 | ||||||
| chr8:94754374
|
T | TTATTGCT others(38): Show |
1 | a0001c0001t0029g0254 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.612-1660_612-1616d others(47): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 94754374 | |||||
| chr8:94754425
|
A | T | 3 | a0001c0001t0001g0076a0001c0001t0018g0077a0001c0001t0028g0070 | 3 | HG02145.hp1 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.612-1611A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94754425 | ||||||
| chr8:94754827
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.612-1209C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94754827 | ||||||
| chr8:94754852
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.612-1184G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94754852 | ||||||
| chr8:94754937
|
C | T | 11 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(8): Show | 11 | HG01109.hp2 HG01358.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.612-1099C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94754937 | ||||||
| chr8:94755070
|
G | T | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG01070.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.612-966G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94755070 | ||||||
| chr8:94755077
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.612-959C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94755077 | ||||||
| chr8:94755091
|
C | T | 5 | a0001c0001t0001g0170a0001c0001t0005g0004a0001c0001t0005g0005others(2): Show | 5 | HG02572.hp1 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-945C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94755091 | ||||||
| chr8:94755329
|
A | G | 34 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(31): Show | 35 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.612-707A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94755329 | ||||||
| chr8:94755345
|
G | A | 12 | a0001c0002t0001g0008a0001c0002t0001g0023a0001c0002t0001g0078others(9): Show | 12 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.612-691G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94755345 | ||||||
| chr8:94755421
|
T | G | 1 | a0001c0001t0002g0098 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.612-615T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94755421 | ||||||
| chr8:94755591
|
T | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0140 | 2 | NA18950.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.612-445T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94755591 | ||||||
| chr8:94755622
|
C | T | 12 | a0001c0002t0001g0008a0001c0002t0001g0023a0001c0002t0001g0078others(9): Show | 12 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.612-414C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94755622 | ||||||
| chr8:94755637
|
G | A | 5 | a0001c0001t0001g0170a0001c0001t0005g0004a0001c0001t0005g0005others(2): Show | 5 | HG02572.hp1 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-399G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94755637 | ||||||
| chr8:94755665
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.612-371C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94755665 | ||||||
| chr8:94755756
|
G | A | 1 | a0001c0001t0018g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.612-280G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94755756 | ||||||
| chr8:94755814
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.612-222G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94755814 | ||||||
| chr8:94755839
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0236 | 2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.612-197C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94755839 | ||||||
| chr8:94755924
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.612-112C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 6/18 | chr8 | 94755924 | ||||||
| chr8:94756321
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.735+162A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94756321 | ||||||
| chr8:94756568
|
G | A | 27 | a0001c0001t0001g0011a0001c0001t0001g0066a0001c0001t0001g0071others(24): Show | 29 | HG01070.hp1 HG01081.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.735+409G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94756568 | ||||||
| chr8:94756610
|
T | A | 1 | a0001c0001t0001g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.735+451T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94756610 | ||||||
| chr8:94756636
|
G | A | 5 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0172others(2): Show | 5 | HG02723.hp1 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.735+477G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94756636 | ||||||
| chr8:94756710
|
C | T | 4 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0006g0003others(1): Show | 4 | HG01167.hp2 HG01169.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.735+551C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94756710 | ||||||
| chr8:94756801
|
AC | A | 50 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0054others(47): Show | 52 | HG01070.hp1 HG01081.hp1 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.735+645delC | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 94756801 | |||||
| chr8:94756816
|
G | A | 1 | a0001c0001t0002g0052 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.735+657G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94756816 | ||||||
| chr8:94756850
|
C | T | 5 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0172others(2): Show | 5 | HG02723.hp1 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.735+691C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94756850 | ||||||
| chr8:94756936
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.735+777G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94756936 | ||||||
| chr8:94757003
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.735+844C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94757003 | ||||||
| chr8:94757107
|
G | C | 66 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(63): Show | 66 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.735+948G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94757107 | ||||||
| chr8:94757255
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.735+1096T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94757255 | ||||||
| chr8:94757379
|
A | G | 2 | a0001c0001t0002g0092a0001c0001t0002g0093 | 2 | HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.735+1220A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94757379 | ||||||
| chr8:94757397
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.735+1238C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94757397 | ||||||
| chr8:94757497
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.735+1338C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94757497 | ||||||
| chr8:94757502
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.735+1343C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94757502 | ||||||
| chr8:94757513
|
G | T | 1 | a0001c0001t0001g0029 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.735+1354G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94757513 | ||||||
| chr8:94757599
|
G | A | 7 | a0001c0001t0002g0064a0001c0001t0002g0092a0001c0001t0002g0093others(4): Show | 7 | HG00673.hp1 HG02074.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.735+1440G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94757599 | ||||||
| chr8:94757626
|
C | T | 1 | a0001c0001t0032g0223 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.735+1467C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94757626 | ||||||
| chr8:94757737
|
T | G | 163 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(160): Show | 166 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.735+1578T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94757737 | ||||||
| chr8:94757753
|
A | G | 12 | a0001c0002t0001g0008a0001c0002t0001g0023a0001c0002t0001g0078others(9): Show | 12 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.735+1594A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94757753 | ||||||
| chr8:94757769
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0058 | 2 | HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.735+1610G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94757769 | ||||||
| chr8:94757820
|
A | G | 163 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(160): Show | 166 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.735+1661A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94757820 | ||||||
| chr8:94757931
|
T | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0032others(70): Show | 76 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.735+1772T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94757931 | ||||||
| chr8:94758107
|
T | A | 7 | a0001c0001t0002g0064a0001c0001t0002g0092a0001c0001t0002g0093others(4): Show | 7 | HG00673.hp1 HG02074.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.735+1948T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94758107 | ||||||
| chr8:94758247
|
T | C | 1 | a0001c0001t0001g0002 | 2 | HG01255.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.735+2088T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94758247 | ||||||
| chr8:94758359
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.735+2200C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94758359 | ||||||
| chr8:94758531
|
C | G | 1 | a0009c0012t0001g0214 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.735+2372C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94758531 | ||||||
| chr8:94758549
|
A | G | 1 | a0001c0001t0002g0282 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.735+2390A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94758549 | ||||||
| chr8:94758578
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.735+2419G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94758578 | ||||||
| chr8:94758686
|
C | T | 163 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(160): Show | 166 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.735+2527C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94758686 | ||||||
| chr8:94758735
|
A | AT | 63 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(60): Show | 64 | HG00140.hp1 HG00423.hp2 HG01168.hp2 others(61): Show |
intron_variant | MODIFIER | c.735+2591dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 94758735 | |||||
| chr8:94758736
|
T | A | 2 | a0001c0001t0001g0228a0001c0001t0001g0276 | 2 | HG02071.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.735+2577T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94758736 | ||||||
| chr8:94758838
|
G | T | 1 | a0001c0001t0001g0090 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.735+2679G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94758838 | ||||||
| chr8:94758859
|
C | T | 2 | a0001c0006t0001g0020a0001c0006t0001g0021 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.735+2700C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94758859 | ||||||
| chr8:94758945
|
A | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0032others(70): Show | 76 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.736-2755A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94758945 | ||||||
| chr8:94759038
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.736-2662C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94759038 | ||||||
| chr8:94759042
|
G | T | 5 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0087others(2): Show | 5 | HG00438.hp2 HG02071.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.736-2658G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94759042 | ||||||
| chr8:94759062
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.736-2638G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94759062 | ||||||
| chr8:94759067
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.736-2633C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94759067 | ||||||
| chr8:94759078
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.736-2622T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94759078 | ||||||
| chr8:94759119
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.736-2581C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94759119 | ||||||
| chr8:94759130
|
T | C | 1 | a0002c0003t0027g0207 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.736-2570T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94759130 | ||||||
| chr8:94759140
|
C | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0032others(70): Show | 76 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.736-2560C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94759140 | ||||||
| chr8:94759224
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.736-2476C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94759224 | ||||||
| chr8:94759266
|
C | T | 1 | a0001c0001t0003g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.736-2434C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94759266 | ||||||
| chr8:94759267
|
G | A | 12 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(9): Show | 12 | HG01109.hp2 HG01358.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.736-2433G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94759267 | ||||||
| chr8:94759335
|
C | T | 1 | a0001c0001t0001g0274 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.736-2365C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94759335 | ||||||
| chr8:94759336
|
G | GCTGATTG others(17): Show |
1 | a0001c0001t0001g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.736-2350_736-2327d others(26): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 94759336 | |||||
| chr8:94759416
|
A | G | 1 | a0001c0001t0018g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.736-2284A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94759416 | ||||||
| chr8:94759500
|
C | CT | 12 | a0001c0001t0001g0169a0001c0002t0001g0008a0001c0002t0001g0023others(9): Show | 12 | HG02257.hp2 HG02486.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.736-2177dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 94759500 | |||||
| chr8:94759500
|
C | CTTT | 22 | a0001c0001t0001g0011a0001c0001t0001g0066a0001c0001t0001g0071others(19): Show | 24 | HG01069.hp2 HG01070.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.736-2179_736-2177d others(5): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 94759500 | |||||
| chr8:94759500
|
C | CTTTT | 28 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(25): Show | 29 | HG00140.hp1 HG00423.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.736-2180_736-2177d others(6): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 94759500 | |||||
| chr8:94759500
|
C | CTTTTT | 6 | a0001c0001t0001g0138a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG02055.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.736-2181_736-2177d others(7): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 94759500 | |||||
| chr8:94759500
|
CT | C | 128 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0038others(125): Show | 128 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.736-2177delT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 94759500 | |||||
| chr8:94759500
|
CTT | C | 68 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(65): Show | 68 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.736-2178_736-2177d others(4): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 94759500 | |||||
| chr8:94759500
|
CTTT | C | 9 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0170others(6): Show | 9 | HG01257.hp2 HG01358.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.736-2179_736-2177d others(5): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 94759500 | |||||
| chr8:94759731
|
G | A | 1 | a0001c0001t0001g0279 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.736-1969G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94759731 | ||||||
| chr8:94759746
|
G | A | 15 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0003g0001others(12): Show | 17 | HG01070.hp1 HG01081.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.736-1954G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94759746 | ||||||
| chr8:94759863
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.736-1837C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94759863 | ||||||
| chr8:94760079
|
A | G | 12 | a0001c0002t0001g0008a0001c0002t0001g0023a0001c0002t0001g0078others(9): Show | 12 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.736-1621A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94760079 | ||||||
| chr8:94760161
|
G | C | 1 | a0001c0001t0001g0076 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.736-1539G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94760161 | ||||||
| chr8:94760304
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.736-1396G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94760304 | ||||||
| chr8:94760343
|
G | A | 18 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0001g0118others(15): Show | 20 | HG01070.hp1 HG01081.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.736-1357G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94760343 | ||||||
| chr8:94760527
|
T | G | 1 | a0001c0001t0007g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.736-1173T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94760527 | ||||||
| chr8:94760534
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.736-1166G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94760534 | ||||||
| chr8:94760605
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.736-1095G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94760605 | ||||||
| chr8:94760647
|
C | G | 5 | a0001c0001t0001g0181a0001c0001t0003g0179a0001c0001t0003g0180others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.736-1053C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94760647 | ||||||
| chr8:94760724
|
C | T | 60 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(57): Show | 60 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.736-976C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94760724 | ||||||
| chr8:94760777
|
T | G | 34 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(31): Show | 35 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.736-923T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94760777 | ||||||
| chr8:94760786
|
C | T | 90 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(87): Show | 90 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.736-914C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94760786 | ||||||
| chr8:94760938
|
G | T | 6 | a0001c0001t0001g0160a0002c0003t0004g0166a0002c0003t0004g0167others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.736-762G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94760938 | ||||||
| chr8:94760998
|
G | C | 1 | a0001c0001t0003g0075 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.736-702G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94760998 | ||||||
| chr8:94761061
|
T | G | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.736-639T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94761061 | ||||||
| chr8:94761101
|
T | C | 7 | a0001c0001t0001g0227a0001c0001t0001g0233a0001c0001t0001g0243others(4): Show | 7 | HG02132.hp2 HG02523.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.736-599T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94761101 | ||||||
| chr8:94761189
|
T | G | 12 | a0001c0002t0001g0008a0001c0002t0001g0023a0001c0002t0001g0078others(9): Show | 12 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.736-511T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94761189 | ||||||
| chr8:94761380
|
G | A | 163 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(160): Show | 166 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.736-320G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | chr8 | 94761380 | ||||||
| chr8:94761658
|
TAA | T | 3 | a0001c0001t0001g0242a0001c0001t0014g0237a0001c0001t0014g0238 | 3 | HG00738.hp1 HG03239.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.736-40_736-39delAA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 94761658 | |||||
| chr8:94761879
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.870+45A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94761879 | ||||||
| chr8:94762174
|
T | C | 104 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(101): Show | 104 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.870+340T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94762174 | ||||||
| chr8:94762285
|
T | TTCTTGAT others(4): Show |
100 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(97): Show | 100 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.870+457_870+458ins others(11): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94762285 | |||||
| chr8:94762342
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.870+508C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94762342 | ||||||
| chr8:94762410
|
G | C | 60 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(57): Show | 60 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.870+576G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94762410 | ||||||
| chr8:94762426
|
C | T | 2 | a0001c0006t0001g0020a0001c0006t0001g0021 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.870+592C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94762426 | ||||||
| chr8:94762491
|
T | C | 4 | a0001c0001t0001g0029a0001c0001t0001g0236a0001c0006t0001g0020others(1): Show | 4 | HG01081.hp2 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+657T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94762491 | ||||||
| chr8:94762498
|
C | T | 88 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(85): Show | 88 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.870+664C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94762498 | ||||||
| chr8:94762499
|
A | G | 2 | a0001c0006t0001g0020a0001c0006t0001g0021 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.870+665A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94762499 | ||||||
| chr8:94762538
|
A | G | 104 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(101): Show | 104 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.870+704A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94762538 | ||||||
| chr8:94762578
|
G | A | 60 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(57): Show | 60 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.870+744G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94762578 | ||||||
| chr8:94762619
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.870+785G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94762619 | ||||||
| chr8:94762842
|
G | A | 1 | a0001c0001t0019g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.870+1008G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94762842 | ||||||
| chr8:94762954
|
C | CT | 100 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(97): Show | 100 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.870+1132dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94762954 | |||||
| chr8:94762990
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.870+1156C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94762990 | ||||||
| chr8:94763003
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.870+1169C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763003 | ||||||
| chr8:94763084
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.870+1250G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763084 | ||||||
| chr8:94763168
|
C | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0050a0001c0001t0001g0128others(5): Show | 8 | HG00423.hp2 NA18944.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.870+1334C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763168 | ||||||
| chr8:94763169
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.870+1335G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763169 | ||||||
| chr8:94763171
|
A | G | 1 | a0001c0001t0006g0022 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.870+1337A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763171 | ||||||
| chr8:94763179
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.870+1345C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763179 | ||||||
| chr8:94763193
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.870+1359C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763193 | ||||||
| chr8:94763236
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.870+1402C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763236 | ||||||
| chr8:94763254
|
C | CT | 11 | a0001c0001t0001g0149a0001c0001t0001g0155a0001c0001t0001g0210others(8): Show | 11 | HG01099.hp1 HG01346.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.870+1442dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94763254 | |||||
| chr8:94763254
|
CT | C | 93 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(90): Show | 93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.870+1442delT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94763254 | |||||
| chr8:94763254
|
CTT | C | 15 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0058others(12): Show | 15 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.870+1441_870+1442d others(4): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94763254 | |||||
| chr8:94763254
|
CTTT | C | 13 | a0001c0001t0001g0056a0001c0002t0001g0008a0001c0002t0001g0023others(10): Show | 13 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.870+1440_870+1442d others(5): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94763254 | |||||
| chr8:94763283
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0236 | 2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.870+1449C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763283 | ||||||
| chr8:94763377
|
G | A | 12 | a0001c0002t0001g0008a0001c0002t0001g0023a0001c0002t0001g0078others(9): Show | 12 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.870+1543G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763377 | ||||||
| chr8:94763518
|
CT | C | 89 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(86): Show | 89 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.871-1653delT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94763518 | |||||
| chr8:94763523
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.871-1660T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763523 | ||||||
| chr8:94763589
|
C | T | 5 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0172others(2): Show | 5 | HG02723.hp1 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-1594C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763589 | ||||||
| chr8:94763601
|
G | C | 1 | a0001c0001t0001g0202 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.871-1582G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763601 | ||||||
| chr8:94763602
|
C | G | 1 | a0001c0001t0001g0202 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.871-1581C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763602 | ||||||
| chr8:94763607
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.871-1576G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763607 | ||||||
| chr8:94763621
|
A | G | 2 | a0001c0006t0001g0020a0001c0006t0001g0021 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.871-1562A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763621 | ||||||
| chr8:94763687
|
AT | A | 16 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0002g0286others(13): Show | 18 | HG01070.hp1 HG01081.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.871-1484delT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94763687 | |||||
| chr8:94763718
|
G | A | 3 | a0001c0001t0010g0017a0001c0001t0010g0018a0001c0001t0010g0019 | 3 | HG02109.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.871-1465G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763718 | ||||||
| chr8:94763768
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.871-1415C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763768 | ||||||
| chr8:94763843
|
G | A | 17 | a0001c0001t0001g0029a0001c0001t0001g0169a0001c0001t0001g0236others(14): Show | 17 | HG01081.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.871-1340G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763843 | ||||||
| chr8:94763935
|
G | A | 163 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(160): Show | 166 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.871-1248G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94763935 | ||||||
| chr8:94764105
|
C | G | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.871-1078C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764105 | ||||||
| chr8:94764291
|
A | G | 2 | a0001c0006t0001g0020a0001c0006t0001g0021 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.871-892A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764291 | ||||||
| chr8:94764562
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.871-621C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764562 | ||||||
| chr8:94764575
|
C | CA | 32 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(29): Show | 32 | HG00735.hp2 HG01109.hp2 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.871-591dupA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764575 | |||||
| chr8:94764610
|
A | C | 4 | a0001c0001t0001g0029a0001c0001t0001g0236a0001c0006t0001g0020others(1): Show | 4 | HG01081.hp2 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-573A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764610 | ||||||
| chr8:94764667
|
G | GTGTGTGT others(9): Show |
2 | a0001c0001t0001g0069a0001c0001t0021g0025 | 2 | HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.871-503_871-502ins others(16): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764667 | |||||
| chr8:94764669
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0001g0034 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.871-505_871-504ins others(10): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764669 | |||||
| chr8:94764681
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0001g0031 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.871-493_871-492ins others(12): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764681 | |||||
| chr8:94764681
|
C | CTGTGTGT others(7): Show |
4 | a0001c0001t0001g0046a0001c0001t0002g0110a0001c0001t0007g0057others(1): Show | 4 | HG01109.hp2 HG01928.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.871-493_871-492ins others(14): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764681 | |||||
| chr8:94764681
|
C | CTGTGTGT others(9): Show |
1 | a0001c0001t0001g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.871-493_871-492ins others(16): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764681 | |||||
| chr8:94764681
|
C | CTGTGTGT others(11): Show |
1 | a0001c0001t0001g0054 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.871-493_871-492ins others(18): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764681 | |||||
| chr8:94764681
|
C | G | 20 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0034others(17): Show | 20 | HG01081.hp2 HG01257.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.871-502C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764681 | ||||||
| chr8:94764683
|
G | GTGTGTGT others(1): Show |
11 | a0001c0002t0001g0008a0001c0002t0001g0078a0001c0002t0001g0215others(8): Show | 11 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.871-493_871-492ins others(8): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764683 | |||||
| chr8:94764687
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.871-496G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764687 | ||||||
| chr8:94764687
|
G | C | 2 | a0001c0006t0001g0020a0001c0006t0001g0021 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.871-496G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764687 | ||||||
| chr8:94764689
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.871-494G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764689 | ||||||
| chr8:94764689
|
G | GTA | 3 | a0001c0001t0001g0144a0001c0001t0002g0174a0001c0001t0004g0163 | 3 | HG01261.hp2 HG02622.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.871-466_871-465dup others(2): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
G | GTGTGTAT others(3): Show |
1 | a0001c0001t0010g0018 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.871-493_871-492ins others(10): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
G | GTGTGTGT others(11): Show |
3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007 | 3 | HG02572.hp1 HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.871-493_871-492ins others(18): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
G | GTGTGTGT others(13): Show |
1 | a0001c0001t0005g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.871-493_871-492ins others(20): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
G | GTGTGTGT others(21): Show |
1 | a0001c0001t0001g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.871-493_871-492ins others(28): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
G | GTGTGTGT others(5): Show |
4 | a0001c0001t0002g0106a0001c0001t0008g0080a0001c0001t0008g0081others(1): Show | 4 | HG02559.hp2 HG02698.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-493_871-492ins others(12): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
G | GTGTGTGT others(7): Show |
8 | a0001c0001t0002g0089a0001c0001t0002g0091a0001c0001t0002g0094others(5): Show | 8 | HG00140.hp2 HG00673.hp1 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.871-493_871-492ins others(14): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
G | GTGTGTGT others(9): Show |
9 | a0001c0001t0002g0064a0001c0001t0002g0085a0001c0001t0002g0086others(6): Show | 9 | HG00544.hp2 HG00558.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.871-493_871-492ins others(16): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
G | GTGTGTGT others(11): Show |
7 | a0001c0001t0002g0084a0001c0001t0002g0087a0001c0001t0002g0088others(4): Show | 7 | HG00438.hp2 HG02071.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.871-493_871-492ins others(18): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
G | GTGTGTGT others(13): Show |
2 | a0001c0001t0002g0093a0001c0001t0008g0079 | 2 | HG02129.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.871-493_871-492ins others(20): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
G | GTGTGTGT others(7): Show |
10 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0041others(7): Show | 10 | HG01934.hp2 HG02004.hp2 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.871-493_871-492ins others(14): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
G | GTGTGTGT others(9): Show |
9 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01167.hp2 HG01169.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.871-493_871-492ins others(16): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
G | GTGTGTGT others(11): Show |
5 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0043others(2): Show | 5 | HG00733.hp1 HG00738.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-493_871-492ins others(18): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
G | GTGTGTGT others(13): Show |
2 | a0001c0001t0001g0047a0001c0001t0001g0051 | 2 | NA18949.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.871-493_871-492ins others(20): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
G | GTGTGTGT others(19): Show |
1 | a0001c0006t0001g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.871-493_871-492ins others(26): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
G | GTGTGTGT others(25): Show |
1 | a0001c0006t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.871-493_871-492ins others(32): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
G | GTGTGTGT others(9): Show |
1 | a0001c0001t0001g0111 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.871-493_871-492ins others(16): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
G | GTGTGTGT others(11): Show |
2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.871-493_871-492ins others(18): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
G | GTGTGTGT others(27): Show |
1 | a0001c0001t0007g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.871-493_871-492ins others(34): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
GTA | G | 74 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0076others(71): Show | 74 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.871-466_871-465del others(2): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764689
|
GTATATA | G | 6 | a0001c0001t0001g0118a0002c0003t0004g0166a0002c0003t0004g0167others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.871-470_871-465del others(6): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764689 | |||||
| chr8:94764691
|
A | C | 1 | a0001c0002t0001g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.871-492A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764691 | ||||||
| chr8:94764691
|
A | G | 20 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0029others(17): Show | 22 | HG00423.hp1 HG01081.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.871-492A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764691 | ||||||
| chr8:94764693
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0069a0001c0001t0001g0208others(2): Show | 5 | HG01081.hp2 HG02055.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-490A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764693 | ||||||
| chr8:94764695
|
A | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0236a0001c0002t0001g0023 | 3 | HG01081.hp2 HG02055.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.871-488A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764695 | ||||||
| chr8:94764697
|
A | G | 1 | a0001c0002t0001g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.871-486A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764697 | ||||||
| chr8:94764713
|
A | T | 9 | a0001c0002t0001g0008a0001c0002t0001g0215a0001c0002t0001g0216others(6): Show | 9 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.871-470A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764713 | ||||||
| chr8:94764713
|
ATATATTT others(6): Show |
A | 1 | a0001c0001t0019g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.871-468_871-456del others(13): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764713 | |||||
| chr8:94764715
|
A | T | 11 | a0001c0001t0001g0033a0001c0002t0001g0008a0001c0002t0001g0078others(8): Show | 11 | HG01257.hp2 HG02257.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.871-468A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764715 | ||||||
| chr8:94764715
|
ATATTTTT others(3): Show |
A | 1 | a0001c0001t0001g0024 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.871-466_871-457del others(10): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764715 | |||||
| chr8:94764716
|
TA | T | 13 | a0001c0001t0001g0027a0001c0001t0001g0039a0001c0001t0001g0196others(10): Show | 13 | HG00423.hp1 HG00438.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.871-466delA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764716 | ||||||
| chr8:94764717
|
A | ATTT | 8 | a0001c0001t0001g0026a0001c0001t0001g0062a0001c0001t0001g0111others(5): Show | 8 | HG00438.hp2 HG00733.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.871-443_871-441dup others(3): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764717 | |||||
| chr8:94764717
|
A | ATTTT | 12 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0037others(9): Show | 12 | HG00140.hp2 HG00738.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.871-444_871-441dup others(4): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764717 | |||||
| chr8:94764717
|
A | ATTTTT | 16 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0041others(13): Show | 16 | HG02056.hp1 HG02074.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.871-445_871-441dup others(5): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764717 | |||||
| chr8:94764717
|
A | ATTTTTT | 9 | a0001c0001t0001g0036a0001c0001t0001g0044a0001c0001t0001g0045others(6): Show | 9 | HG01167.hp2 HG01169.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.871-446_871-441dup others(6): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764717 | |||||
| chr8:94764717
|
A | ATTTTTTT others(1): Show |
6 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0097others(3): Show | 6 | HG00544.hp2 HG00558.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.871-448_871-441dup others(8): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764717 | |||||
| chr8:94764717
|
A | T | 23 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0047others(20): Show | 23 | HG01257.hp2 HG01928.hp2 HG02165.hp2 others(20): Show |
intron_variant | MODIFIER | c.871-466A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764717 | ||||||
| chr8:94764717
|
AT | A | 15 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0137others(12): Show | 15 | HG01167.hp1 HG01261.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.871-441delT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764717 | |||||
| chr8:94764717
|
ATT | A | 9 | a0001c0001t0001g0151a0001c0001t0001g0169a0001c0001t0001g0255others(6): Show | 9 | HG01069.hp1 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.871-442_871-441del others(2): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764717 | |||||
| chr8:94764718
|
T | TA | 18 | a0001c0001t0001g0011a0001c0001t0001g0120a0001c0001t0001g0127others(15): Show | 20 | HG01884.hp1 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.871-465_871-464ins others(1): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764718 | ||||||
| chr8:94764718
|
T | TATA | 8 | a0001c0001t0001g0050a0001c0001t0001g0115a0001c0001t0001g0202others(5): Show | 8 | HG01081.hp1 HG02451.hp2 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.871-465_871-464ins others(3): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764718 | ||||||
| chr8:94764719
|
T | A | 39 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(36): Show | 40 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.871-464T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764719 | ||||||
| chr8:94764720
|
T | A | 26 | a0001c0001t0001g0011a0001c0001t0001g0069a0001c0001t0001g0071others(23): Show | 28 | HG01081.hp1 HG01167.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.871-463T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764720 | ||||||
| chr8:94764721
|
T | A | 17 | a0001c0001t0001g0029a0001c0001t0001g0055a0001c0001t0001g0056others(14): Show | 17 | HG00140.hp1 HG01070.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.871-462T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764721 | ||||||
| chr8:94764722
|
T | A | 6 | a0001c0001t0005g0065a0001c0001t0008g0080a0001c0001t0008g0081others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.871-461T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764722 | ||||||
| chr8:94764723
|
T | A | 6 | a0001c0001t0001g0029a0001c0001t0001g0172a0001c0001t0001g0173others(3): Show | 6 | HG01081.hp2 HG01109.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.871-460T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764723 | ||||||
| chr8:94764725
|
T | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0236 | 2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.871-458T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764725 | ||||||
| chr8:94764727
|
T | A | 1 | a0001c0001t0001g0029 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.871-456T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764727 | ||||||
| chr8:94764728
|
T | TTTTTC | 10 | a0001c0002t0001g0008a0001c0002t0001g0078a0001c0002t0001g0215others(7): Show | 10 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.871-451_871-450ins others(5): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764728 | |||||
| chr8:94764728
|
T | TTTTTTTT others(3): Show |
1 | a0001c0002t0001g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.871-446_871-445ins others(10): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 94764728 | |||||
| chr8:94764831
|
C | T | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(1): Show | 4 | HG01070.hp2 HG01168.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-352C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764831 | ||||||
| chr8:94764845
|
C | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0169a0001c0001t0001g0236others(2): Show | 5 | HG01081.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-338C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764845 | ||||||
| chr8:94764878
|
G | C | 1 | a0001c0001t0001g0107 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.871-305G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764878 | ||||||
| chr8:94764898
|
T | C | 13 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(10): Show | 13 | HG00735.hp1 HG00741.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.871-285T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 8/18 | chr8 | 94764898 | ||||||
| chr8:94765327
|
A | G | 6 | a0001c0001t0001g0029a0001c0001t0001g0169a0001c0001t0001g0236others(3): Show | 6 | HG01081.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1002+13A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 9/18 | chr8 | 94765327 | ||||||
| chr8:94765350
|
A | AT | 13 | a0001c0001t0002g0286a0001c0002t0001g0023a0001c0002t0001g0078others(10): Show | 13 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1002+48dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 94765350 | |||||
| chr8:94765381
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1002+67G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 9/18 | chr8 | 94765381 | ||||||
| chr8:94765429
|
G | A | 27 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(24): Show | 27 | HG00733.hp1 HG00738.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.1002+115G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 9/18 | chr8 | 94765429 | ||||||
| chr8:94765448
|
G | T | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1002+134G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 9/18 | chr8 | 94765448 | ||||||
| chr8:94765449
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1002+135C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 9/18 | chr8 | 94765449 | ||||||
| chr8:94765546
|
G | A | 1 | a0001c0001t0012g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1003-165G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 9/18 | chr8 | 94765546 | ||||||
| chr8:94765578
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1003-133C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 9/18 | chr8 | 94765578 | ||||||
| chr8:94765817
|
ACT | A | 12 | a0001c0002t0001g0008a0001c0002t0001g0023a0001c0002t0001g0078others(9): Show | 12 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1101+13_1101+14del others(2): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 94765817 | |||||
| chr8:94765899
|
G | A | 12 | a0001c0002t0001g0008a0001c0002t0001g0023a0001c0002t0001g0078others(9): Show | 12 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1101+90G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 10/18 | chr8 | 94765899 | ||||||
| chr8:94765918
|
A | G | 11 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(8): Show | 11 | HG01109.hp2 HG01891.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1101+109A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 10/18 | chr8 | 94765918 | ||||||
| chr8:94766067
|
T | A | 2 | a0001c0006t0001g0020a0001c0006t0001g0021 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1101+258T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 10/18 | chr8 | 94766067 | ||||||
| chr8:94766233
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1102-379G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 10/18 | chr8 | 94766233 | ||||||
| chr8:94766300
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1102-312G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 10/18 | chr8 | 94766300 | ||||||
| chr8:94766408
|
G | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0169a0001c0001t0001g0236others(2): Show | 5 | HG01081.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1102-204G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 10/18 | chr8 | 94766408 | ||||||
| chr8:94766439
|
A | G | 11 | a0001c0001t0001g0024a0001c0001t0001g0160a0001c0001t0010g0017others(8): Show | 11 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1102-173A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 10/18 | chr8 | 94766439 | ||||||
| chr8:94766443
|
G | A | 71 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(68): Show | 71 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1102-169G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 10/18 | chr8 | 94766443 | ||||||
| chr8:94766718
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1175+33C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94766718 | ||||||
| chr8:94766759
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0236a0001c0006t0001g0020others(1): Show | 4 | HG01081.hp2 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175+74C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94766759 | ||||||
| chr8:94766762
|
G | C | 1 | a0001c0001t0001g0120 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1175+77G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94766762 | ||||||
| chr8:94766919
|
A | T | 12 | a0001c0002t0001g0008a0001c0002t0001g0023a0001c0002t0001g0078others(9): Show | 12 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1175+234A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94766919 | ||||||
| chr8:94766934
|
G | T | 12 | a0001c0002t0001g0008a0001c0002t0001g0023a0001c0002t0001g0078others(9): Show | 12 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1175+249G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94766934 | ||||||
| chr8:94767038
|
C | G | 5 | a0002c0003t0004g0166a0002c0003t0004g0167a0002c0003t0004g0168others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1175+353C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94767038 | ||||||
| chr8:94767039
|
C | T | 2 | a0001c0001t0002g0092a0001c0001t0002g0093 | 2 | HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1175+354C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94767039 | ||||||
| chr8:94767066
|
T | TA | 8 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0118others(5): Show | 8 | HG02056.hp2 HG02071.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1175+400dupA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 94767066 | |||||
| chr8:94767066
|
TA | T | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0173others(3): Show | 6 | HG02723.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1175+400delA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 94767066 | |||||
| chr8:94767197
|
C | T | 1 | a0002c0003t0027g0207 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1175+512C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94767197 | ||||||
| chr8:94767295
|
C | CT | 96 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0028others(93): Show | 97 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1175+626dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 94767295 | |||||
| chr8:94767295
|
C | CTT | 14 | a0001c0001t0001g0060a0001c0001t0001g0157a0001c0002t0001g0008others(11): Show | 14 | HG01257.hp1 HG02257.hp2 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.1175+625_1175+626d others(4): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 94767295 | |||||
| chr8:94767316
|
T | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0026others(135): Show | 139 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.1175+631T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94767316 | ||||||
| chr8:94767362
|
C | T | 12 | a0001c0002t0001g0008a0001c0002t0001g0023a0001c0002t0001g0078others(9): Show | 12 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1175+677C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94767362 | ||||||
| chr8:94767363
|
G | A | 60 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(57): Show | 60 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1175+678G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94767363 | ||||||
| chr8:94767418
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1175+733C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94767418 | ||||||
| chr8:94767462
|
T | G | 1 | a0001c0001t0001g0115 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1175+777T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94767462 | ||||||
| chr8:94767491
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1175+806C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94767491 | ||||||
| chr8:94767514
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1175+829C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94767514 | ||||||
| chr8:94767539
|
G | A | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 4 | NA18985.hp2 NA18992.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175+854G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94767539 | ||||||
| chr8:94767970
|
A | T | 1 | a0001c0001t0001g0030 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1176-425A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94767970 | ||||||
| chr8:94768073
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0236a0001c0006t0001g0020others(1): Show | 4 | HG01081.hp2 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1176-322G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94768073 | ||||||
| chr8:94768153
|
C | T | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG01070.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.1176-242C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94768153 | ||||||
| chr8:94768233
|
G | A | 1 | a0001c0001t0002g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1176-162G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | chr8 | 94768233 | ||||||
| chr8:94768325
|
TA | T | 87 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(84): Show | 87 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.1176-62delA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 94768325 | |||||
| chr8:94768763
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1334+210G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94768763 | ||||||
| chr8:94768773
|
C | T | 17 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0003g0001others(14): Show | 19 | HG01070.hp1 HG01081.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.1334+220C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94768773 | ||||||
| chr8:94768778
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1334+225G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94768778 | ||||||
| chr8:94768837
|
C | A | 1 | a0001c0001t0019g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1334+284C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94768837 | ||||||
| chr8:94768853
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1334+300G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94768853 | ||||||
| chr8:94768938
|
G | A | 3 | a0001c0001t0001g0076a0001c0001t0018g0077a0001c0001t0028g0070 | 3 | HG02145.hp1 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1334+385G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94768938 | ||||||
| chr8:94769010
|
T | TA | 6 | a0001c0001t0001g0148a0001c0001t0001g0183a0001c0001t0005g0004others(3): Show | 6 | HG02572.hp1 HG02738.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1334+471dupA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 94769010 | |||||
| chr8:94769010
|
T | TAAA | 6 | a0001c0001t0001g0160a0002c0003t0004g0166a0002c0003t0004g0167others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1334+469_1334+471d others(5): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 94769010 | |||||
| chr8:94769010
|
TA | T | 12 | a0001c0001t0001g0036a0001c0001t0001g0054a0001c0001t0001g0055others(9): Show | 12 | HG01109.hp2 HG01891.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1334+471delA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 94769010 | |||||
| chr8:94769054
|
G | GT | 12 | a0001c0001t0001g0120a0001c0001t0001g0126a0001c0001t0001g0127others(9): Show | 12 | HG00423.hp2 HG01255.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1334+508dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 94769054 | |||||
| chr8:94769061
|
T | TG | 8 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0060others(5): Show | 8 | HG01978.hp1 HG02056.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1334+509dupG | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 94769061 | |||||
| chr8:94769062
|
G | GT | 13 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0198others(10): Show | 13 | HG01934.hp1 HG02027.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1334+525dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 94769062 | |||||
| chr8:94769062
|
G | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(47): Show | 51 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.1334+509G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94769062 | ||||||
| chr8:94769063
|
T | G | 56 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(53): Show | 56 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1334+510T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94769063 | ||||||
| chr8:94769084
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1334+531G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94769084 | ||||||
| chr8:94769130
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0058 | 2 | HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1334+577C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94769130 | ||||||
| chr8:94769200
|
G | T | 104 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(101): Show | 104 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1334+647G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94769200 | ||||||
| chr8:94769692
|
GA | G | 11 | a0001c0001t0001g0024a0001c0001t0001g0160a0001c0001t0010g0017others(8): Show | 11 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1335-755delA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 94769692 | |||||
| chr8:94769758
|
G | A | 12 | a0001c0002t0001g0008a0001c0002t0001g0023a0001c0002t0001g0078others(9): Show | 12 | HG02257.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1335-694G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94769758 | ||||||
| chr8:94769798
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1335-654A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94769798 | ||||||
| chr8:94769888
|
C | CT | 17 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0054others(14): Show | 17 | HG00423.hp2 HG01081.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1335-547dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 94769888 | |||||
| chr8:94769888
|
CT | C | 74 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(71): Show | 74 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.1335-547delT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 94769888 | |||||
| chr8:94770006
|
A | C | 1 | a0001c0002t0001g0219 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1335-446A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94770006 | ||||||
| chr8:94770012
|
G | T | 2 | a0001c0001t0002g0085a0001c0001t0002g0086 | 2 | NA18946.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1335-440G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94770012 | ||||||
| chr8:94770023
|
G | A | 1 | a0001c0001t0001g0276 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1335-429G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94770023 | ||||||
| chr8:94770068
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0169a0001c0001t0001g0236others(2): Show | 5 | HG01081.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1335-384A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94770068 | ||||||
| chr8:94770241
|
A | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0159 | 2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1335-211A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94770241 | ||||||
| chr8:94770259
|
G | A | 1 | a0001c0001t0019g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1335-193G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94770259 | ||||||
| chr8:94770392
|
A | G | 1 | a0001c0001t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1335-60A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 12/18 | chr8 | 94770392 | ||||||
| chr8:94770636
|
A | G | 166 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(163): Show | 169 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.1454+65A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94770636 | ||||||
| chr8:94770773
|
G | C | 1 | a0001c0001t0012g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1454+202G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94770773 | ||||||
| chr8:94770826
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0019g0175 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1454+255G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94770826 | ||||||
| chr8:94770921
|
CT | C | 101 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(98): Show | 101 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1454+366delT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94770921 | |||||
| chr8:94770945
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0159 | 2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1454+374C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94770945 | ||||||
| chr8:94771163
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0236 | 2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1454+592C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94771163 | ||||||
| chr8:94771259
|
G | A | 102 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(99): Show | 102 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1454+688G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94771259 | ||||||
| chr8:94771425
|
G | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0236 | 2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1454+854G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94771425 | ||||||
| chr8:94771441
|
T | C | 10 | a0001c0001t0001g0024a0001c0001t0010g0017a0001c0001t0010g0018others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1454+870T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94771441 | ||||||
| chr8:94771596
|
A | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(33): Show | 37 | HG00140.hp1 HG00423.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1454+1025A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94771596 | ||||||
| chr8:94771781
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0236 | 2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1454+1210A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94771781 | ||||||
| chr8:94771803
|
C | T | 11 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(8): Show | 11 | HG01109.hp2 HG01891.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1454+1232C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94771803 | ||||||
| chr8:94772034
|
G | A | 6 | a0001c0001t0001g0281a0001c0001t0001g0283a0001c0001t0002g0282others(3): Show | 6 | NA18984.hp1 NA18992.hp1 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.1454+1463G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94772034 | ||||||
| chr8:94772172
|
T | G | 3 | a0001c0001t0010g0017a0001c0001t0010g0018a0001c0001t0010g0019 | 3 | HG02109.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1454+1601T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94772172 | ||||||
| chr8:94772212
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0012g0116 | 2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1454+1641A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94772212 | ||||||
| chr8:94772306
|
C | A | 10 | a0001c0001t0001g0024a0001c0001t0010g0017a0001c0001t0010g0018others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1454+1735C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94772306 | ||||||
| chr8:94772328
|
C | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0050a0001c0001t0001g0128others(5): Show | 8 | HG00423.hp2 NA18944.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.1454+1757C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94772328 | ||||||
| chr8:94772332
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1454+1761A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94772332 | ||||||
| chr8:94772479
|
C | G | 3 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0002g0095 | 3 | HG00673.hp1 HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1454+1908C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94772479 | ||||||
| chr8:94772947
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1454+2376C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94772947 | ||||||
| chr8:94772983
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1454+2412G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94772983 | ||||||
| chr8:94772986
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1454+2415C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94772986 | ||||||
| chr8:94773041
|
G | A | 4 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454+2470G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94773041 | ||||||
| chr8:94773138
|
C | T | 3 | a0001c0001t0001g0076a0001c0001t0018g0077a0001c0001t0028g0070 | 3 | HG02145.hp1 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1454+2567C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94773138 | ||||||
| chr8:94773213
|
C | A | 2 | a0001c0006t0001g0020a0001c0006t0001g0021 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1454+2642C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94773213 | ||||||
| chr8:94773213
|
C | CA | 13 | a0001c0001t0001g0029a0001c0001t0001g0054a0001c0001t0001g0058others(10): Show | 13 | HG01081.hp2 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.1454+2660dupA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94773213 | |||||
| chr8:94773213
|
CA | C | 23 | a0001c0001t0001g0024a0001c0001t0001g0157a0001c0001t0001g0255others(20): Show | 23 | HG01257.hp1 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1454+2660delA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94773213 | |||||
| chr8:94773217
|
A | G | 8 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0201others(5): Show | 8 | HG01928.hp1 HG01993.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.1454+2646A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94773217 | ||||||
| chr8:94773343
|
TA | T | 36 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(33): Show | 37 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1454+2773delA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94773343 | ||||||
| chr8:94773467
|
TGTCGCCC others(943): Show |
T | 8 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0201others(5): Show | 8 | HG01928.hp1 HG01993.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.1454+2899_1455-324 others(4): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94773467 | |||||
| chr8:94773587
|
C | T | 1 | a0001c0001t0019g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1454+3016C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94773587 | ||||||
| chr8:94773660
|
C | T | 7 | a0001c0001t0001g0002a0001c0001t0001g0125a0001c0001t0001g0130others(4): Show | 8 | HG01069.hp2 HG01255.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1454+3089C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94773660 | ||||||
| chr8:94773721
|
T | C | 52 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(49): Show | 53 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.1454+3150T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94773721 | ||||||
| chr8:94773744
|
T | C | 1 | a0002c0003t0004g0166 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1454+3173T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94773744 | ||||||
| chr8:94773801
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(33): Show | 37 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1454+3230G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94773801 | ||||||
| chr8:94773871
|
C | CA | 108 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(105): Show | 110 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1454+3317dupA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94773871 | |||||
| chr8:94773871
|
C | CAA | 19 | a0001c0001t0001g0107a0001c0001t0001g0161a0001c0001t0001g0169others(16): Show | 19 | HG00544.hp2 HG01081.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.1454+3316_1454+331 others(6): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94773871 | |||||
| chr8:94773871
|
C | CAAA | 36 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(33): Show | 37 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1454+3315_1454+331 others(7): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94773871 | |||||
| chr8:94773907
|
C | T | 2 | a0001c0006t0001g0020a0001c0006t0001g0021 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1454+3336C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94773907 | ||||||
| chr8:94774039
|
T | TA | 42 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0115others(39): Show | 43 | HG00140.hp1 HG00423.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.1454+3492dupA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94774039 | |||||
| chr8:94774039
|
TA | T | 75 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(72): Show | 75 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1454+3492delA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94774039 | |||||
| chr8:94774039
|
TAA | T | 15 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0058others(12): Show | 15 | HG01167.hp2 HG01891.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1454+3491_1454+349 others(6): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94774039 | |||||
| chr8:94774098
|
C | T | 3 | a0003c0004t0011g0101a0003c0004t0011g0112a0003c0004t0011g0113 | 3 | NA18994.hp2 NA19002.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1454+3527C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94774098 | ||||||
| chr8:94774300
|
A | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(33): Show | 37 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1455-3366A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94774300 | ||||||
| chr8:94774377
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(33): Show | 37 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1455-3289G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94774377 | ||||||
| chr8:94774425
|
A | T | 4 | a0001c0001t0001g0076a0001c0001t0005g0065a0001c0001t0018g0077others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1455-3241A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94774425 | ||||||
| chr8:94774458
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1455-3208G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94774458 | ||||||
| chr8:94774578
|
T | TC | 3 | a0001c0001t0001g0118a0001c0001t0025g0068a0001c0001t0030g0119 | 3 | HG02145.hp2 HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1455-3087dupC | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94774578 | |||||
| chr8:94774579
|
CT | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(35): Show | 39 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.1455-3071delT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94774579 | |||||
| chr8:94774680
|
C | T | 2 | a0001c0001t0013g0178a0001c0001t0013g0182 | 2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1455-2986C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94774680 | ||||||
| chr8:94774799
|
A | G | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0145others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1455-2867A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94774799 | ||||||
| chr8:94774818
|
C | G | 88 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(85): Show | 88 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1455-2848C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94774818 | ||||||
| chr8:94774867
|
G | A | 1 | a0001c0001t0032g0223 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1455-2799G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94774867 | ||||||
| chr8:94774873
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1455-2793A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94774873 | ||||||
| chr8:94775184
|
C | CT | 71 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(68): Show | 71 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1455-2470dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94775184 | |||||
| chr8:94775184
|
C | CTT | 39 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(36): Show | 40 | HG00140.hp1 HG00423.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1455-2471_1455-247 others(6): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94775184 | |||||
| chr8:94775208
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1455-2458C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94775208 | ||||||
| chr8:94775305
|
G | A | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG01243.hp1 HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1455-2361G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94775305 | ||||||
| chr8:94775328
|
C | T | 2 | a0001c0001t0018g0077a0001c0001t0028g0070 | 2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1455-2338C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94775328 | ||||||
| chr8:94775457
|
C | G | 3 | a0001c0001t0002g0284a0001c0001t0002g0285a0001c0001t0002g0286 | 3 | NA18984.hp1 NA19007.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1455-2209C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94775457 | ||||||
| chr8:94775626
|
G | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(30): Show | 34 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.1455-2040G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94775626 | ||||||
| chr8:94775724
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1455-1942G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94775724 | ||||||
| chr8:94775899
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1455-1767G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94775899 | ||||||
| chr8:94775976
|
T | C | 3 | a0001c0001t0007g0057a0001c0001t0007g0067a0001c0001t0007g0083 | 3 | HG02723.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1455-1690T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94775976 | ||||||
| chr8:94776026
|
C | CT | 20 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0033others(17): Show | 20 | HG01081.hp2 HG01257.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1455-1616dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94776026 | |||||
| chr8:94776026
|
C | CTT | 6 | a0001c0001t0003g0073a0001c0001t0004g0164a0002c0003t0004g0166others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1455-1617_1455-161 others(6): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94776026 | |||||
| chr8:94776026
|
CT | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(33): Show | 37 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1455-1616delT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94776026 | |||||
| chr8:94776026
|
CTT | C | 64 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(61): Show | 64 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1455-1617_1455-161 others(6): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94776026 | |||||
| chr8:94776089
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0032others(61): Show | 67 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.1455-1577A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94776089 | ||||||
| chr8:94776118
|
T | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0032others(62): Show | 68 | HG00140.hp1 HG00423.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.1455-1548T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94776118 | ||||||
| chr8:94776133
|
T | C | 2 | a0001c0001t0007g0057a0001c0001t0007g0067 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1455-1533T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94776133 | ||||||
| chr8:94776158
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1455-1508G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94776158 | ||||||
| chr8:94776158
|
G | C | 4 | a0001c0001t0001g0024a0001c0001t0001g0076a0001c0001t0001g0160others(1): Show | 4 | HG02886.hp2 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1455-1508G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94776158 | ||||||
| chr8:94776323
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1455-1343G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94776323 | ||||||
| chr8:94776326
|
C | T | 4 | a0001c0001t0008g0079a0001c0001t0008g0080a0001c0001t0008g0081others(1): Show | 4 | HG02559.hp2 HG03225.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1455-1340C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94776326 | ||||||
| chr8:94776438
|
A | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0032others(60): Show | 66 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(63): Show |
intron_variant | MODIFIER | c.1455-1228A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94776438 | ||||||
| chr8:94776611
|
T | G | 1 | a0001c0001t0005g0065 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1455-1055T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94776611 | ||||||
| chr8:94776611
|
TTTG | T | 16 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0003g0001others(13): Show | 18 | HG01070.hp1 HG01081.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1455-1040_1455-103 others(7): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94776611 | |||||
| chr8:94776614
|
G | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0033others(28): Show | 32 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1455-1052G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94776614 | ||||||
| chr8:94776693
|
G | A | 3 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0002g0095 | 3 | HG00673.hp1 HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1455-973G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94776693 | ||||||
| chr8:94776713
|
T | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0029others(70): Show | 76 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.1455-953T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94776713 | ||||||
| chr8:94776779
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1455-887A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94776779 | ||||||
| chr8:94776780
|
C | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0029others(70): Show | 76 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.1455-886C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94776780 | ||||||
| chr8:94776907
|
G | A | 17 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0071others(14): Show | 17 | HG01257.hp2 HG01261.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1455-759G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94776907 | ||||||
| chr8:94776914
|
A | C | 11 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0012others(8): Show | 13 | HG01081.hp1 HG01167.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1455-752A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94776914 | ||||||
| chr8:94776922
|
A | C | 1 | a0001c0001t0002g0106 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1455-744A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94776922 | ||||||
| chr8:94776944
|
C | T | 2 | a0004c0005t0001g0220a0004c0005t0001g0221 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1455-722C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94776944 | ||||||
| chr8:94776963
|
C | CA | 104 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(101): Show | 106 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.1455-687dupA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94776963 | |||||
| chr8:94776963
|
C | CAA | 14 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0107others(11): Show | 14 | HG00544.hp2 HG01167.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1455-688_1455-687d others(4): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 94776963 | |||||
| chr8:94776982
|
C | T | 4 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1455-684C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94776982 | ||||||
| chr8:94777015
|
A | G | 16 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0003g0001others(13): Show | 18 | HG01070.hp1 HG01081.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1455-651A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94777015 | ||||||
| chr8:94777091
|
A | C | 1 | a0001c0001t0030g0119 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1455-575A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94777091 | ||||||
| chr8:94777106
|
A | T | 16 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0003g0001others(13): Show | 18 | HG01070.hp1 HG01081.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1455-560A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94777106 | ||||||
| chr8:94777286
|
C | G | 1 | a0001c0001t0005g0065 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1455-380C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94777286 | ||||||
| chr8:94777392
|
G | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0029others(72): Show | 78 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(75): Show |
intron_variant | MODIFIER | c.1455-274G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94777392 | ||||||
| chr8:94777426
|
T | G | 58 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(55): Show | 61 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1455-240T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 13/18 | chr8 | 94777426 | ||||||
| chr8:94777857
|
T | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(54): Show | 60 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.1575+71T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94777857 | ||||||
| chr8:94778028
|
C | T | 30 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(27): Show | 31 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.1575+242C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94778028 | ||||||
| chr8:94778037
|
T | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0026others(140): Show | 146 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1575+251T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94778037 | ||||||
| chr8:94778050
|
G | A | 56 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(53): Show | 59 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.1575+264G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94778050 | ||||||
| chr8:94778103
|
C | T | 56 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(53): Show | 59 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.1575+317C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94778103 | ||||||
| chr8:94778156
|
A | G | 1 | a0001c0001t0005g0065 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1575+370A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94778156 | ||||||
| chr8:94778162
|
G | T | 1 | a0001c0001t0001g0211 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1575+376G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94778162 | ||||||
| chr8:94778203
|
A | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(54): Show | 60 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.1575+417A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94778203 | ||||||
| chr8:94778234
|
C | CA | 65 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(62): Show | 65 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1575+460dupA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 94778234 | |||||
| chr8:94778330
|
G | A | 1 | a0001c0001t0002g0052 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1575+544G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94778330 | ||||||
| chr8:94778343
|
C | T | 56 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(53): Show | 59 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.1575+557C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94778343 | ||||||
| chr8:94778539
|
G | A | 30 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0050others(27): Show | 31 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.1575+753G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94778539 | ||||||
| chr8:94778605
|
T | G | 59 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(56): Show | 62 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.1575+819T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94778605 | ||||||
| chr8:94778655
|
GTTTTTC | G | 5 | a0001c0001t0001g0024a0001c0001t0001g0071a0001c0001t0001g0076others(2): Show | 5 | HG02886.hp2 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+879_1575+884d others(8): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 94778655 | |||||
| chr8:94778671
|
C | CT | 7 | a0001c0002t0001g0008a0001c0002t0001g0023a0001c0002t0001g0215others(4): Show | 7 | HG02257.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1575+895dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 94778671 | |||||
| chr8:94778741
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1575+955G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94778741 | ||||||
| chr8:94778985
|
A | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(58): Show | 64 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.1575+1199A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94778985 | ||||||
| chr8:94778999
|
C | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0032others(58): Show | 64 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.1575+1213C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94778999 | ||||||
| chr8:94779010
|
A | G | 4 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1575+1224A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94779010 | ||||||
| chr8:94779182
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1576-1177A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94779182 | ||||||
| chr8:94779184
|
G | A | 3 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0002g0095 | 3 | HG00673.hp1 HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1576-1175G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94779184 | ||||||
| chr8:94779198
|
G | A | 210 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0027others(207): Show | 210 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.1576-1161G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94779198 | ||||||
| chr8:94779219
|
T | TA | 113 | a0001c0001t0001g0027a0001c0001t0001g0038a0001c0001t0001g0039others(110): Show | 113 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.1576-1128dupA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 94779219 | |||||
| chr8:94779219
|
T | TAA | 95 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0028others(92): Show | 95 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1576-1129_1576-112 others(6): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 94779219 | |||||
| chr8:94779232
|
C | A | 141 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0038others(138): Show | 141 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.1576-1127C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94779232 | ||||||
| chr8:94779344
|
A | G | 142 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0038others(139): Show | 142 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.1576-1015A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94779344 | ||||||
| chr8:94779355
|
C | T | 1 | a0001c0001t0019g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1576-1004C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94779355 | ||||||
| chr8:94779382
|
G | A | 21 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0066others(18): Show | 21 | HG01070.hp1 HG01257.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.1576-977G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94779382 | ||||||
| chr8:94779496
|
CT | C | 241 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(238): Show | 243 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(240): Show |
intron_variant | MODIFIER | c.1576-850delT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 94779496 | |||||
| chr8:94779529
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1576-830A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94779529 | ||||||
| chr8:94779534
|
G | T | 1 | a0001c0001t0001g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1576-825G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94779534 | ||||||
| chr8:94779616
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1576-743C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94779616 | ||||||
| chr8:94779628
|
T | C | 255 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(252): Show | 257 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(254): Show |
intron_variant | MODIFIER | c.1576-731T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94779628 | ||||||
| chr8:94779699
|
G | A | 141 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0038others(138): Show | 141 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.1576-660G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94779699 | ||||||
| chr8:94779824
|
A | T | 231 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(228): Show | 231 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.1576-535A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94779824 | ||||||
| chr8:94779866
|
T | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0071a0001c0001t0019g0175 | 3 | HG03041.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1576-493T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94779866 | ||||||
| chr8:94779922
|
G | A | 255 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(252): Show | 257 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(254): Show |
intron_variant | MODIFIER | c.1576-437G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94779922 | ||||||
| chr8:94780022
|
T | C | 1 | a0001c0001t0020g0186 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1576-337T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94780022 | ||||||
| chr8:94780070
|
G | A | 231 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(228): Show | 231 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.1576-289G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94780070 | ||||||
| chr8:94780175
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1576-184A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94780175 | ||||||
| chr8:94780219
|
A | C | 66 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(63): Show | 66 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1576-140A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 14/18 | chr8 | 94780219 | ||||||
| chr8:94780651
|
A | G | 231 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(228): Show | 231 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.1632+236A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 15/18 | chr8 | 94780651 | ||||||
| chr8:94780690
|
T | C | 3 | a0001c0001t0010g0017a0001c0001t0010g0018a0001c0001t0010g0019 | 3 | HG02109.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1632+275T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 15/18 | chr8 | 94780690 | ||||||
| chr8:94780700
|
C | T | 231 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(228): Show | 231 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.1632+285C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 15/18 | chr8 | 94780700 | ||||||
| chr8:94780794
|
G | A | 231 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(228): Show | 231 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.1633-290G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 15/18 | chr8 | 94780794 | ||||||
| chr8:94780832
|
G | A | 21 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0066others(18): Show | 21 | HG01070.hp1 HG01257.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.1633-252G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 15/18 | chr8 | 94780832 | ||||||
| chr8:94780971
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1633-113A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 15/18 | chr8 | 94780971 | ||||||
| chr8:94781051
|
T | G | 1 | a0001c0001t0001g0243 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1633-33T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 15/18 | chr8 | 94781051 | ||||||
| chr8:94781056
|
A | AT | 199 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0027others(196): Show | 199 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.1633-10dupT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 94781056 | |||||
| chr8:94781056
|
A | ATT | 10 | a0001c0001t0001g0028a0001c0001t0001g0053a0001c0001t0001g0090others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.1633-11_1633-10dup others(2): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 94781056 | |||||
| chr8:94781056
|
A | ATTT | 14 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0071others(11): Show | 14 | HG01257.hp2 HG01261.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1633-12_1633-10dup others(3): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 94781056 | |||||
| chr8:94781056
|
AT | A | 7 | a0001c0001t0001g0029a0001c0001t0005g0004a0001c0001t0005g0005others(4): Show | 7 | HG02055.hp2 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1633-10delT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 94781056 | |||||
| chr8:94781287
|
G | A | 210 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0027others(207): Show | 210 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.1715+121G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94781287 | ||||||
| chr8:94781316
|
C | G | 1 | a0001c0001t0001g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1715+150C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94781316 | ||||||
| chr8:94781325
|
A | T | 255 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(252): Show | 257 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(254): Show |
intron_variant | MODIFIER | c.1715+159A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94781325 | ||||||
| chr8:94781591
|
A | G | 14 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0012others(11): Show | 16 | HG01081.hp1 HG01167.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1715+425A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94781591 | ||||||
| chr8:94781640
|
G | A | 2 | a0001c0001t0018g0077a0001c0001t0028g0070 | 2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1715+474G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94781640 | ||||||
| chr8:94781966
|
C | T | 10 | a0001c0001t0001g0029a0001c0001t0005g0004a0001c0001t0005g0005others(7): Show | 10 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1715+800C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94781966 | ||||||
| chr8:94782358
|
A | G | 231 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(228): Show | 231 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.1715+1192A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94782358 | ||||||
| chr8:94782458
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1716-1212A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94782458 | ||||||
| chr8:94782492
|
T | TTACTGTG others(305): Show |
2 | a0001c0001t0001g0024a0001c0001t0001g0071 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1716-1162_1716-116 others(316): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 94782492 | |||||
| chr8:94782492
|
T | TTACTGTG others(306): Show |
11 | a0001c0001t0001g0033a0001c0001t0004g0162a0001c0001t0004g0163others(8): Show | 11 | HG01257.hp2 HG01261.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1716-1162_1716-116 others(317): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 94782492 | |||||
| chr8:94782492
|
T | TTACTGTG others(307): Show |
1 | a0007c0008t0001g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1716-1162_1716-116 others(318): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 94782492 | |||||
| chr8:94782492
|
T | TTACTGTG others(307): Show |
6 | a0001c0001t0001g0066a0001c0001t0001g0076a0001c0001t0012g0013others(3): Show | 6 | HG01070.hp1 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1716-1162_1716-116 others(318): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 94782492 | |||||
| chr8:94782492
|
T | TTACTGTG others(309): Show |
1 | a0001c0001t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1716-1162_1716-116 others(320): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 94782492 | |||||
| chr8:94782526
|
T | G | 12 | a0001c0001t0001g0033a0001c0001t0004g0162a0001c0001t0004g0163others(9): Show | 12 | HG01257.hp2 HG01261.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1716-1144T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94782526 | ||||||
| chr8:94782534
|
A | G | 255 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(252): Show | 257 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(254): Show |
intron_variant | MODIFIER | c.1716-1136A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94782534 | ||||||
| chr8:94782663
|
AT | A | 10 | a0001c0001t0001g0029a0001c0001t0005g0004a0001c0001t0005g0005others(7): Show | 10 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1716-1004delT | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 94782663 | |||||
| chr8:94782704
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1716-966T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94782704 | ||||||
| chr8:94782747
|
T | C | 23 | a0001c0001t0001g0024a0001c0001t0001g0066a0001c0001t0001g0071others(20): Show | 25 | HG01070.hp1 HG01081.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.1716-923T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94782747 | ||||||
| chr8:94782789
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1716-881C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94782789 | ||||||
| chr8:94782802
|
T | C | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0118others(3): Show | 6 | HG02145.hp2 HG02486.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1716-868T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94782802 | ||||||
| chr8:94782860
|
A | C | 165 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0027others(162): Show | 165 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.1716-810A>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94782860 | ||||||
| chr8:94782880
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1716-790T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94782880 | ||||||
| chr8:94782963
|
G | A | 111 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(108): Show | 113 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.1716-707G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94782963 | ||||||
| chr8:94783030
|
C | A | 21 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0066others(18): Show | 21 | HG01070.hp1 HG01257.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.1716-640C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94783030 | ||||||
| chr8:94783038
|
G | A | 165 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0027others(162): Show | 165 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.1716-632G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94783038 | ||||||
| chr8:94783054
|
T | G | 21 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0066others(18): Show | 21 | HG01070.hp1 HG01257.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.1716-616T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94783054 | ||||||
| chr8:94783137
|
T | TTGCAAGT others(48): Show |
5 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(2): Show | 5 | HG02572.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1716-531_1716-477d others(57): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 94783137 | |||||
| chr8:94783344
|
A | T | 78 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(75): Show | 78 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1716-326A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94783344 | ||||||
| chr8:94783479
|
CA | C | 229 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(226): Show | 229 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.1716-189delA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 94783479 | |||||
| chr8:94783482
|
G | A | 1 | a0001c0001t0003g0179 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1716-188G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 16/18 | chr8 | 94783482 | ||||||
| chr8:94783949
|
T | A | 243 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(240): Show | 245 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(242): Show |
intron_variant | MODIFIER | c.1848+147T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94783949 | ||||||
| chr8:94784069
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0021g0025 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1848+267G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94784069 | ||||||
| chr8:94784076
|
T | C | 4 | a0001c0001t0007g0057a0001c0001t0007g0067a0001c0001t0007g0083others(1): Show | 4 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1848+274T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94784076 | ||||||
| chr8:94784237
|
A | T | 2 | a0001c0001t0001g0029a0001c0001t0021g0025 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1848+435A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94784237 | ||||||
| chr8:94784279
|
C | T | 2 | a0001c0001t0014g0237a0001c0001t0014g0238 | 2 | HG00738.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1848+477C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94784279 | ||||||
| chr8:94784280
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1848+478G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94784280 | ||||||
| chr8:94784296
|
T | C | 247 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(244): Show | 249 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(246): Show |
intron_variant | MODIFIER | c.1848+494T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94784296 | ||||||
| chr8:94784365
|
C | A | 2 | a0001c0001t0014g0237a0001c0001t0014g0238 | 2 | HG00738.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1848+563C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94784365 | ||||||
| chr8:94784431
|
A | G | 157 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0038others(154): Show | 159 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.1848+629A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94784431 | ||||||
| chr8:94784554
|
G | A | 1 | a0001c0002t0001g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1848+752G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94784554 | ||||||
| chr8:94784690
|
A | G | 1 | a0002c0003t0027g0207 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1848+888A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94784690 | ||||||
| chr8:94784813
|
T | G | 1 | a0001c0001t0001g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1848+1011T>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94784813 | ||||||
| chr8:94784861
|
G | C | 1 | a0001c0001t0007g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1848+1059G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94784861 | ||||||
| chr8:94784929
|
A | G | 256 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(253): Show | 258 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(255): Show |
intron_variant | MODIFIER | c.1848+1127A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94784929 | ||||||
| chr8:94785234
|
A | G | 4 | a0001c0001t0007g0057a0001c0001t0007g0067a0001c0001t0007g0083others(1): Show | 4 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1848+1432A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94785234 | ||||||
| chr8:94785434
|
G | A | 243 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(240): Show | 245 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(242): Show |
intron_variant | MODIFIER | c.1848+1632G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94785434 | ||||||
| chr8:94785973
|
T | TA | 7 | a0001c0001t0001g0024a0001c0001t0001g0066a0001c0001t0001g0071others(4): Show | 7 | HG01070.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1849-1920dupA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr8 | 94785973 | |||||
| chr8:94786041
|
C | T | 157 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0038others(154): Show | 159 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.1849-1853C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94786041 | ||||||
| chr8:94786166
|
G | A | 7 | a0001c0001t0001g0024a0001c0001t0001g0066a0001c0001t0001g0071others(4): Show | 7 | HG01070.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1849-1728G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94786166 | ||||||
| chr8:94786283
|
C | T | 156 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0038others(153): Show | 158 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.1849-1611C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94786283 | ||||||
| chr8:94786335
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0043 | 2 | HG00738.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.1849-1559G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94786335 | ||||||
| chr8:94786376
|
C | A | 1 | a0001c0001t0001g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1849-1518C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94786376 | ||||||
| chr8:94786390
|
G | C | 86 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(83): Show | 86 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1849-1504G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94786390 | ||||||
| chr8:94786421
|
G | A | 2 | a0001c0001t0001g0281a0001c0001t0001g0283 | 2 | NA19001.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1849-1473G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94786421 | ||||||
| chr8:94786424
|
CATTT | C | 243 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(240): Show | 245 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(242): Show |
intron_variant | MODIFIER | c.1849-1445_1849-144 others(8): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr8 | 94786424 | |||||
| chr8:94786587
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1849-1307G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94786587 | ||||||
| chr8:94786617
|
G | A | 1 | a0001c0002t0001g0219 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1849-1277G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94786617 | ||||||
| chr8:94786790
|
C | T | 5 | a0002c0003t0004g0166a0002c0003t0004g0167a0002c0003t0004g0168others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1849-1104C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94786790 | ||||||
| chr8:94786795
|
C | G | 4 | a0001c0001t0007g0057a0001c0001t0007g0067a0001c0001t0007g0083others(1): Show | 4 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1849-1099C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94786795 | ||||||
| chr8:94786833
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1849-1061A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94786833 | ||||||
| chr8:94786844
|
G | A | 86 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(83): Show | 86 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1849-1050G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94786844 | ||||||
| chr8:94786848
|
A | G | 256 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(253): Show | 258 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(255): Show |
intron_variant | MODIFIER | c.1849-1046A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94786848 | ||||||
| chr8:94786853
|
T | C | 4 | a0001c0001t0007g0057a0001c0001t0007g0067a0001c0001t0007g0083others(1): Show | 4 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1849-1041T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94786853 | ||||||
| chr8:94787185
|
G | T | 4 | a0001c0001t0007g0057a0001c0001t0007g0067a0001c0001t0007g0083others(1): Show | 4 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1849-709G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94787185 | ||||||
| chr8:94787224
|
A | G | 5 | a0001c0001t0001g0069a0001c0001t0007g0057a0001c0001t0007g0067others(2): Show | 5 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1849-670A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94787224 | ||||||
| chr8:94787588
|
G | C | 4 | a0001c0001t0001g0066a0001c0001t0012g0013a0001c0001t0012g0014others(1): Show | 4 | HG01070.hp1 HG02451.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1849-306G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94787588 | ||||||
| chr8:94787610
|
T | C | 2 | a0001c0001t0007g0057a0001c0001t0007g0067 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1849-284T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94787610 | ||||||
| chr8:94787639
|
A | G | 14 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0012others(11): Show | 16 | HG01081.hp1 HG01109.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1849-255A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94787639 | ||||||
| chr8:94787678
|
T | A | 1 | a0001c0001t0009g0262 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1849-216T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94787678 | ||||||
| chr8:94787797
|
G | T | 1 | a0001c0001t0001g0031 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1849-97G>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 17/18 | chr8 | 94787797 | ||||||
| chr8:94788083
|
G | A | 4 | a0001c0001t0007g0057a0001c0001t0007g0067a0001c0001t0007g0083others(1): Show | 4 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2007+31G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94788083 | ||||||
| chr8:94788094
|
TA | T | 15 | a0001c0001t0001g0143a0001c0001t0003g0001a0001c0001t0003g0010others(12): Show | 17 | HG01081.hp1 HG01109.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.2007+43delA | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94788094 | ||||||
| chr8:94788095
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0007g0057 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2007+44_2007+45ins others(33): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | 94788095 | |||||
| chr8:94788095
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0007g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2007+44_2007+45ins others(34): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | 94788095 | |||||
| chr8:94788095
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0030g0119 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2007+44_2007+45ins others(14): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | 94788095 | |||||
| chr8:94788095
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0007g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2007+44_2007+45ins others(10): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | 94788095 | |||||
| chr8:94788095
|
A | T | 1 | a0001c0001t0001g0031 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2007+43A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94788095 | ||||||
| chr8:94788097
|
T | A | 145 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0027others(142): Show | 145 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.2007+45T>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94788097 | ||||||
| chr8:94788141
|
T | C | 4 | a0001c0001t0007g0057a0001c0001t0007g0067a0001c0001t0007g0083others(1): Show | 4 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2007+89T>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94788141 | ||||||
| chr8:94788148
|
A | G | 19 | a0001c0001t0001g0069a0001c0001t0003g0001a0001c0001t0003g0010others(16): Show | 21 | HG01081.hp1 HG01109.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.2007+96A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94788148 | ||||||
| chr8:94788227
|
A | T | 1 | a0001c0001t0001g0251 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2007+175A>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94788227 | ||||||
| chr8:94788266
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2007+214A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94788266 | ||||||
| chr8:94788286
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0021g0025 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2007+234A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94788286 | ||||||
| chr8:94788310
|
C | T | 14 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0012others(11): Show | 16 | HG01081.hp1 HG01109.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.2007+258C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94788310 | ||||||
| chr8:94788564
|
G | C | 1 | a0001c0001t0002g0096 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2007+512G>C | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94788564 | ||||||
| chr8:94788588
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2007+536C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94788588 | ||||||
| chr8:94788636
|
GACGC | G | 113 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0034others(110): Show | 113 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.2007+589_2007+592d others(6): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | 94788636 | |||||
| chr8:94788637
|
ACGCACG | A | 4 | a0001c0001t0001g0060a0001c0001t0001g0108a0001c0001t0001g0149others(1): Show | 4 | HG01099.hp1 HG01928.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.2007+589_2007+594d others(8): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | 94788637 | |||||
| chr8:94788639
|
GCA | G | 9 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0001t0001g0076others(6): Show | 9 | HG01070.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2007+589_2007+590d others(4): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | 94788639 | |||||
| chr8:94788641
|
A | ACG | 3 | a0001c0001t0001g0029a0001c0001t0001g0147a0001c0001t0021g0025 | 3 | HG02055.hp2 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2007+599_2007+600d others(4): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | 94788641 | |||||
| chr8:94788641
|
A | G | 26 | a0001c0001t0001g0154a0001c0001t0001g0157a0001c0001t0001g0170others(23): Show | 28 | HG00738.hp1 HG01070.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.2007+589A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94788641 | ||||||
| chr8:94788641
|
ACG | A | 48 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0035others(45): Show | 48 | HG01069.hp1 HG01081.hp2 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.2007+599_2007+600d others(4): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | 94788641 | |||||
| chr8:94788641
|
ACGCG | A | 20 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0040others(17): Show | 20 | HG00423.hp2 HG00733.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.2007+597_2007+600d others(6): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | 94788641 | |||||
| chr8:94788642
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2007+590C>T | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94788642 | ||||||
| chr8:94788649
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2007+597G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94788649 | ||||||
| chr8:94788661
|
TC | T | 7 | a0001c0001t0001g0024a0001c0001t0016g0082a0001c0001t0018g0077others(4): Show | 7 | HG01109.hp2 HG02145.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2007+616delC | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | 94788661 | |||||
| chr8:94788666
|
C | G | 5 | a0001c0001t0001g0170a0001c0001t0007g0057a0001c0001t0007g0067others(2): Show | 5 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2007+614C>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94788666 | ||||||
| chr8:94788668
|
C | A | 29 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0135others(26): Show | 31 | HG01081.hp1 HG01167.hp1 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.2007+616C>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94788668 | ||||||
| chr8:94789015
|
G | A | 3 | a0001c0001t0007g0057a0001c0001t0007g0067a0001c0001t0007g0083 | 3 | HG02723.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2008-731G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94789015 | ||||||
| chr8:94789165
|
TCTC | T | 3 | a0001c0001t0007g0057a0001c0001t0007g0067a0001c0001t0007g0083 | 3 | HG02723.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2008-578_2008-576d others(5): Show |
DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | 94789165 | |||||
| chr8:94789453
|
G | A | 21 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0012others(18): Show | 23 | HG01081.hp1 HG01109.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.2008-293G>A | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94789453 | ||||||
| chr8:94789595
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2008-151A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94789595 | ||||||
| chr8:94789644
|
A | G | 26 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0012others(23): Show | 28 | HG01081.hp1 HG01109.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.2008-102A>G | DPY19L4 | ENSG00000156162.16 | transcript | ENST00000414645.6 | protein_coding | 18/18 | chr8 | 94789644 |