Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1833 |
| ensemblid | ENSG00000083782.8 |
| hgncid | 3053 |
| symbol | EPYC |
| name | epiphycan |
| refseq_nuc | NM_004950.5 |
| refseq_prot | NP_004941.2 |
| ensembl_nuc | ENST00000261172.8 |
| ensembl_prot | ENSP00000261172.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 90963682 |
| end | 91004972 |
| strand | - |
| ver | v1.2 |
| region | chr12:90963682-91004972 |
| region5000 | chr12:90958682-91009972 |
| regionname0 | EPYC_chr12_90963682_91004972 |
| regionname5000 | EPYC_chr12_90958682_91009972 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 322 | 332 | 88 | 59 | 155 | 4 | 24 | 126 | EPYC_chr12_90958682_91009972 | EPYC | MKTLA others(317): Show |
chr12 | 90958682 | 91009972 |
| a0002 | 0/0 | 322 | 8 | 0 | 5 | 1 | 0 | 2 | 0 | EPYC_chr12_90958682_91009972 | EPYC | MKTLA others(317): Show |
chr12 | 90958682 | 91009972 |
| a0003 | 0/0 | 322 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | MKTLA others(317): Show |
chr12 | 90958682 | 91009972 |
| a0004 | 0/0 | 322 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | MKTLA others(317): Show |
chr12 | 90958682 | 91009972 |
| a0005 | 0/0 | 322 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | MKTLA others(317): Show |
chr12 | 90958682 | 91009972 |
| a0006 | 0/0 | 322 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EPYC_chr12_90958682_91009972 | EPYC | MKTLA others(317): Show |
chr12 | 90958682 | 91009972 |
| a0007 | 0/0 | 322 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EPYC_chr12_90958682_91009972 | EPYC | MKTLA others(317): Show |
chr12 | 90958682 | 91009972 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 966 | 324 | 85 | 58 | 153 | 4 | 22 | EPYC_chr12_90958682_91009972 | EPYC | ATGAA others(961): Show |
chr12 | 90958682 | 91009972 | ||
| a0001c0003 | 0/0 | 966 | 6 | 3 | 1 | 0 | 0 | 2 | EPYC_chr12_90958682_91009972 | EPYC | ATGAA others(961): Show |
chr12 | 90958682 | 91009972 | ||
| a0001c0005 | 0/0 | 966 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | ATGAA others(961): Show |
chr12 | 90958682 | 91009972 | ||
| a0001c0007 | 0/0 | 966 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | ATGAA others(961): Show |
chr12 | 90958682 | 91009972 | ||
| a0002c0002 | 0/0 | 966 | 8 | 0 | 5 | 1 | 0 | 2 | EPYC_chr12_90958682_91009972 | EPYC | ATGAA others(961): Show |
chr12 | 90958682 | 91009972 | ||
| a0003c0004 | 0/0 | 966 | 2 | 2 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | ATGAA others(961): Show |
chr12 | 90958682 | 91009972 | ||
| a0004c0008 | 0/0 | 966 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | ATGAA others(961): Show |
chr12 | 90958682 | 91009972 | ||
| a0005c0009 | 0/0 | 966 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | ATGAA others(961): Show |
chr12 | 90958682 | 91009972 | ||
| a0006c0010 | 0/0 | 966 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | ATGAA others(961): Show |
chr12 | 90958682 | 91009972 | ||
| a0007c0006 | 0/0 | 966 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | ATGAA others(961): Show |
chr12 | 90958682 | 91009972 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1487 | 208 | 36 | 43 | 112 | 4 | 13 | EPYC_chr12_90958682_91009972 | EPYC | GCCAT others(1482): Show |
chr12 | 90958682 | 91009972 |
| a0001c0001t0002 | 1/1 | 1482 | 108 | 48 | 9 | 41 | 0 | 8 | EPYC_chr12_90958682_91009972 | EPYC | GCCAT others(1477): Show |
chr12 | 90958682 | 91009972 |
| a0001c0001t0003 | 0/0 | 1487 | 6 | 1 | 5 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | GCCAT others(1482): Show |
chr12 | 90958682 | 91009972 |
| a0001c0001t0004 | 0/0 | 1482 | 2 | 0 | 1 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | GCCAT others(1477): Show |
chr12 | 90958682 | 91009972 |
| a0001c0003t0002 | 0/0 | 1482 | 6 | 3 | 1 | 0 | 0 | 2 | EPYC_chr12_90958682_91009972 | EPYC | GCCAT others(1477): Show |
chr12 | 90958682 | 91009972 |
| a0001c0005t0001 | 0/0 | 1487 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | GCCAT others(1482): Show |
chr12 | 90958682 | 91009972 |
| a0001c0007t0001 | 0/0 | 1487 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | GCCAT others(1482): Show |
chr12 | 90958682 | 91009972 |
| a0002c0002t0002 | 0/0 | 1482 | 7 | 0 | 4 | 1 | 0 | 2 | EPYC_chr12_90958682_91009972 | EPYC | GCCAT others(1477): Show |
chr12 | 90958682 | 91009972 |
| a0002c0002t0005 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | GCCAT others(1477): Show |
chr12 | 90958682 | 91009972 |
| a0003c0004t0002 | 0/0 | 1482 | 2 | 2 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | GCCAT others(1477): Show |
chr12 | 90958682 | 91009972 |
| a0004c0008t0002 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | GCCAT others(1477): Show |
chr12 | 90958682 | 91009972 |
| a0005c0009t0002 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | GCCAT others(1477): Show |
chr12 | 90958682 | 91009972 |
| a0006c0010t0001 | 0/0 | 1487 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | GCCAT others(1482): Show |
chr12 | 90958682 | 91009972 |
| a0007c0006t0001 | 0/0 | 1487 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | GCCAT others(1482): Show |
chr12 | 90958682 | 91009972 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 12 | 0 | 8 | 3 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0003 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0004 | 0/0 | 8 | 3 | 1 | 4 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0011 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0012 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0022 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0002 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0009 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0025 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0003g0008 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0003t0002g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0003t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0005t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0001c0007t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0002c0002t0002g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0002c0002t0002g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0002c0002t0005g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0003c0004t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0003c0004t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0004c0008t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0005c0009t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0006c0010t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| a0007c0006t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | GBR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0062 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01192 | hp1 | a0001 | c0003 | t0002 | g0089 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01496 | hp1 | a0002 | c0002 | t0005 | g0212 | AMR | CLM | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01891 | hp1 | a0004 | c0008 | t0002 | g0200 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | KHV | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CDX | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CDX | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02258 | hp1 | a0001 | c0003 | t0002 | g0018 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02698 | hp1 | a0006 | c0010 | t0001 | g0143 | SAS | PJL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ESN | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | ESN | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02965 | hp2 | a0001 | c0003 | t0002 | g0018 | AFR | ESN | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | ESN | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0067 | SAS | PJL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | MSL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | ESN | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ESN | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | MSL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | MSL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0048 | SAS | PJL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03453 | hp1 | a0003 | c0004 | t0002 | g0091 | AFR | MSL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | MSL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03516 | hp1 | a0003 | c0004 | t0002 | g0093 | AFR | ESN | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | MSL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03710 | hp2 | a0001 | c0003 | t0002 | g0087 | SAS | PJL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | BEB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0048 | SAS | BEB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | BEB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03927 | hp2 | a0001 | c0003 | t0002 | g0088 | SAS | BEB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | STU | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | STU | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG04184 | hp2 | a0007 | c0006 | t0001 | g0113 | SAS | BEB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | YRI | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | YRI | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0217 | EAS | CHB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | YRI | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18984 | hp1 | a0001 | c0007 | t0001 | g0171 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19000 | hp1 | a0001 | c0005 | t0001 | g0137 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | LWK | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | LWK | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | LWK | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19043 | hp2 | a0001 | c0003 | t0002 | g0018 | AFR | LWK | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | YRI | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | ASW | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | ASW | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | TSI | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | TSI | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02486 | hp2 | a0005 | c0009 | t0002 | g0092 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | USA | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | USA | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | USA | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0065 | REF | REF | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0059 | REF | REF | EPYC_chr12_90958682_91009972 | EPYC | chr12 | 90958682 | 91009972 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:90964273 | C | G | 1 | a0004 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.852G>C | p.Leu284Phe | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 7/7 | 891/1482 | 852/969 | 284/322 | chr12 | 90964273 | |||
| chr12:90964295 | G | C | 1 | a0005 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.830C>G | p.Thr277Arg | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 7/7 | 869/1482 | 830/969 | 277/322 | chr12 | 90964295 | |||
| chr12:90971907 | G | A | 1 | a0006 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.595C>T | p.Arg199Cys | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/7 | 634/1482 | 595/969 | 199/322 | chr12 | 90971907 | |||
| chr12:90972869 | C | T | 1 | a0007 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.452G>A | p.Arg151His | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 4/7 | 491/1482 | 452/969 | 151/322 | chr12 | 90972869 | |||
| chr12:90972872 | G | C | 1 | a0002 | 8 | HG01074.hp1 HG01496.hp1 HG01952.hp2 others(5): Show |
missense_variant | MODERATE | c.449C>G | p.Ser150Cys | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 4/7 | 488/1482 | 449/969 | 150/322 | chr12 | 90972872 | |||
| chr12:90978180 | T | C | 1 | a0003 | 2 | HG03453.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.248A>G | p.Glu83Gly | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/7 | 287/1482 | 248/969 | 83/322 | chr12 | 90978180 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:90971997 | A | G | 1 | a0001c0007 | 1 | NA18984.hp1 | synonymous_variant | LOW | c.505T>C | p.Leu169Leu | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/7 | 544/1482 | 505/969 | 169/322 | chr12 | 90971997 | |||
| chr12:90972892 | C | T | 1 | a0001c0005 | 1 | NA19000.hp1 | synonymous_variant | LOW | c.429G>A | p.Lys143Lys | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 4/7 | 468/1482 | 429/969 | 143/322 | chr12 | 90972892 | |||
| chr12:91002470 | G | T | 1 | a0001c0003 | 6 | HG01192.hp1 HG02258.hp1 HG02965.hp2 others(3): Show |
synonymous_variant | LOW | c.96C>A | p.Thr32Thr | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/7 | 135/1482 | 96/969 | 32/322 | chr12 | 91002470 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:90963822 | T | C | 1 | a0001c0001t0004 | 2 | HG00642.hp1 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*334A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 7/7 | 334 | chr12 | 90963822 | ||||||
| chr12:90963881 | A | G | 1 | a0001c0001t0003 | 6 | HG01123.hp1 HG01928.hp2 HG01934.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*275T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 7/7 | 275 | chr12 | 90963881 | ||||||
| chr12:90964009 | C | CATTAT | 6 | a0001c0001t0001 a0001c0001t0003 a0001c0005t0001 others(3): Show |
218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*142_*146dupATAAT | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 7/7 | 146 | chr12 | 90964009 | ||||||
| chr12:90964130 | A | G | 1 | a0002c0002t0005 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*26T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 7/7 | 26 | chr12 | 90964130 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:90964392 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
200 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.799-66A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90964392 | |||||||
| chr12:90964479 | A | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
200 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.799-153T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90964479 | |||||||
| chr12:90964578 | A | G | 28 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(25): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.799-252T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90964578 | |||||||
| chr12:90964645 | A | G | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0079 others(6): Show |
11 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.799-319T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90964645 | |||||||
| chr12:90964798 | T | A | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0079 others(6): Show |
11 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.799-472A>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90964798 | |||||||
| chr12:90964860 | A | G | 23 | a0001c0001t0002g0029 a0001c0001t0002g0034 a0001c0001t0002g0047 others(20): Show |
28 | HG01109.hp2 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.799-534T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90964860 | |||||||
| chr12:90964914 | C | A | 1 | a0001c0001t0001g0163 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.799-588G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90964914 | |||||||
| chr12:90965036 | C | A | 2 | a0003c0004t0002g0091 a0003c0004t0002g0093 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.799-710G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90965036 | |||||||
| chr12:90965235 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.799-909G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90965235 | |||||||
| chr12:90965309 | T | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0133 |
2 | HG02896.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.799-983A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90965309 | |||||||
| chr12:90965789 | A | C | 1 | a0004c0008t0002g0200 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.799-1463T>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90965789 | |||||||
| chr12:90965817 | C | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.799-1491G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90965817 | |||||||
| chr12:90965854 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.799-1528A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90965854 | |||||||
| chr12:90965896 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.799-1570C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90965896 | |||||||
| chr12:90965928 | A | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.799-1602T>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90965928 | |||||||
| chr12:90966003 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.799-1677G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90966003 | |||||||
| chr12:90966017 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.799-1691T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90966017 | |||||||
| chr12:90966233 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.799-1907A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90966233 | |||||||
| chr12:90966274 | A | G | 1 | a0001c0001t0004g0067 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.799-1948T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90966274 | |||||||
| chr12:90966327 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.799-2001G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90966327 | |||||||
| chr12:90966340 | A | G | 2 | a0003c0004t0002g0091 a0003c0004t0002g0093 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.799-2014T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90966340 | |||||||
| chr12:90966388 | T | A | 10 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0051 others(7): Show |
21 | HG00642.hp1 HG01070.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.799-2062A>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90966388 | |||||||
| chr12:90966493 | C | A | 1 | a0001c0001t0001g0118 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.799-2167G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90966493 | |||||||
| chr12:90966495 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG00741.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.799-2169A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90966495 | |||||||
| chr12:90966840 | C | T | 1 | a0004c0008t0002g0200 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.799-2514G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90966840 | |||||||
| chr12:90966916 | G | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0114 a0001c0001t0001g0129 others(2): Show |
7 | HG01943.hp2 HG02148.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.799-2590C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90966916 | |||||||
| chr12:90966919 | A | G | 1 | a0004c0008t0002g0200 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.799-2593T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90966919 | |||||||
| chr12:90966928 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.799-2602G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90966928 | |||||||
| chr12:90966984 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.799-2658C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90966984 | |||||||
| chr12:90967005 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.799-2679A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90967005 | |||||||
| chr12:90967014 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
200 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.799-2688C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90967014 | |||||||
| chr12:90967019 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.799-2693T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90967019 | |||||||
| chr12:90967105 | A | G | 28 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(25): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.799-2779T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90967105 | |||||||
| chr12:90967128 | T | C | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0079 others(6): Show |
11 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.799-2802A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90967128 | |||||||
| chr12:90967137 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.799-2811A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90967137 | |||||||
| chr12:90967138 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.799-2812G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90967138 | |||||||
| chr12:90967141 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.799-2815G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90967141 | |||||||
| chr12:90967320 | A | AT | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
200 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.798+2723dupA | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90967320 | |||||||
| chr12:90967423 | G | T | 1 | a0001c0001t0001g0162 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.798+2621C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90967423 | |||||||
| chr12:90967487 | A | T | 2 | a0001c0001t0002g0030 a0001c0001t0002g0063 |
3 | HG02145.hp2 HG02451.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.798+2557T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90967487 | |||||||
| chr12:90967670 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.798+2374A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90967670 | |||||||
| chr12:90967846 | C | T | 7 | a0001c0001t0002g0006 a0001c0001t0002g0015 a0001c0001t0002g0049 others(4): Show |
16 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+2198G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90967846 | |||||||
| chr12:90967847 | T | TGGGTG | 7 | a0001c0001t0002g0006 a0001c0001t0002g0015 a0001c0001t0002g0049 others(4): Show |
16 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+2196_798+2197i others(7): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90967847 | |||||||
| chr12:90967849 | A | T | 7 | a0001c0001t0002g0006 a0001c0001t0002g0015 a0001c0001t0002g0049 others(4): Show |
16 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+2195T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90967849 | |||||||
| chr12:90967850 | A | G | 7 | a0001c0001t0002g0006 a0001c0001t0002g0015 a0001c0001t0002g0049 others(4): Show |
16 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+2194T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90967850 | |||||||
| chr12:90967995 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.798+2049T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90967995 | |||||||
| chr12:90968520 | A | G | 12 | a0001c0001t0001g0031 a0001c0001t0001g0072 a0001c0001t0001g0073 others(9): Show |
17 | HG01123.hp1 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.798+1524T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90968520 | |||||||
| chr12:90968666 | T | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0179 |
2 | HG02004.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.798+1378A>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90968666 | |||||||
| chr12:90968791 | T | C | 2 | a0001c0001t0002g0034 a0005c0009t0002g0092 |
3 | HG02486.hp2 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.798+1253A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90968791 | |||||||
| chr12:90968890 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0149 |
9 | HG00423.hp2 NA18747.hp2 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+1154T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90968890 | |||||||
| chr12:90969002 | CAT | C | 7 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0142 others(4): Show |
8 | HG02015.hp2 HG02486.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.798+1040_798+1041d others(4): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90969002 | |||||||
| chr12:90969038 | G | A | 2 | a0003c0004t0002g0091 a0003c0004t0002g0093 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.798+1006C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90969038 | |||||||
| chr12:90969241 | T | C | 23 | a0001c0001t0002g0029 a0001c0001t0002g0034 a0001c0001t0002g0047 others(20): Show |
28 | HG01109.hp2 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.798+803A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90969241 | |||||||
| chr12:90969485 | T | C | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0079 others(6): Show |
11 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.798+559A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90969485 | |||||||
| chr12:90969523 | T | TA | 158 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(155): Show |
244 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.798+520dupT | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90969523 | |||||||
| chr12:90969584 | C | T | 1 | a0001c0001t0002g0213 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.798+460G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90969584 | |||||||
| chr12:90969646 | C | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
308 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(305): Show |
intron_variant | MODIFIER | c.798+398G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90969646 | |||||||
| chr12:90969742 | C | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
297 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(294): Show |
intron_variant | MODIFIER | c.798+302G>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90969742 | |||||||
| chr12:90969824 | G | T | 1 | a0001c0001t0003g0076 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.798+220C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90969824 | |||||||
| chr12:90969911 | A | G | 2 | a0001c0003t0002g0087 a0001c0003t0002g0088 |
2 | HG03710.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.798+133T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 6/6 | chr12 | 90969911 | |||||||
| chr12:90970142 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18985.hp1 | splice_region_variant&intron_variant | LOW | c.703-3C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90970142 | |||||||
| chr12:90970161 | GAACTCAA others(4): Show |
G | 1 | a0001c0001t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.703-33_703-23delTT others(9): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90970161 | |||||||
| chr12:90970272 | T | A | 2 | a0001c0001t0002g0060 a0001c0001t0002g0066 |
2 | HG01257.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.703-133A>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90970272 | |||||||
| chr12:90970607 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.703-468A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90970607 | |||||||
| chr12:90970620 | T | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0181 a0001c0001t0001g0188 |
3 | NA18966.hp1 NA19076.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.703-481A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90970620 | |||||||
| chr12:90970830 | G | A | 6 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0003t0002g0018 others(3): Show |
8 | HG01192.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.703-691C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90970830 | |||||||
| chr12:90970866 | G | T | 1 | a0001c0001t0001g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.703-727C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90970866 | |||||||
| chr12:90970952 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.703-813C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90970952 | |||||||
| chr12:90970960 | A | T | 1 | a0001c0001t0001g0037 | 2 | NA18980.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.703-821T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90970960 | |||||||
| chr12:90971166 | T | G | 12 | a0001c0001t0001g0031 a0001c0001t0001g0072 a0001c0001t0001g0073 others(9): Show |
17 | HG01123.hp1 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.702+634A>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90971166 | |||||||
| chr12:90971180 | C | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.702+620G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90971180 | |||||||
| chr12:90971241 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0164 |
4 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+559A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90971241 | |||||||
| chr12:90971413 | T | C | 1 | a0001c0001t0001g0043 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.702+387A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90971413 | |||||||
| chr12:90971416 | T | A | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0079 others(6): Show |
11 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.702+384A>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90971416 | |||||||
| chr12:90971435 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.702+365G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90971435 | |||||||
| chr12:90971443 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.702+357C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90971443 | |||||||
| chr12:90971529 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.702+271C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90971529 | |||||||
| chr12:90971558 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.702+242C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90971558 | |||||||
| chr12:90971654 | C | G | 1 | a0001c0001t0001g0122 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.702+146G>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90971654 | |||||||
| chr12:90971672 | C | CAATA | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
197 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.702+124_702+127dup others(4): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90971672 | |||||||
| chr12:90971672 | C | CAATAAAT others(1): Show |
56 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0023 others(53): Show |
77 | HG00609.hp2 HG00741.hp2 HG01081.hp1 others(74): Show |
intron_variant | MODIFIER | c.702+120_702+127dup others(8): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90971672 | |||||||
| chr12:90971672 | C | CAATAAAT others(5): Show |
9 | a0001c0001t0001g0022 a0001c0001t0001g0071 a0001c0001t0001g0135 others(6): Show |
12 | HG00423.hp1 HG02615.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.702+116_702+127dup others(12): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90971672 | |||||||
| chr12:90971672 | C | CAATAAAT others(9): Show |
2 | a0001c0001t0002g0192 a0001c0001t0002g0199 |
2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.702+112_702+127dup others(16): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90971672 | |||||||
| chr12:90971672 | C | CTATAAAT others(5): Show |
1 | a0001c0001t0001g0122 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.702+127_702+128ins others(12): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90971672 | |||||||
| chr12:90971672 | CAATA | C | 5 | a0001c0001t0002g0064 a0001c0001t0002g0094 a0001c0001t0002g0095 others(2): Show |
5 | HG01070.hp1 HG02280.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+124_702+127del others(4): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90971672 | |||||||
| chr12:90971672 | CAATAAAT others(1): Show |
C | 10 | a0001c0001t0001g0031 a0001c0001t0001g0072 a0001c0001t0001g0073 others(7): Show |
13 | HG01192.hp1 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.702+120_702+127del others(8): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90971672 | |||||||
| chr12:90971672 | CAATAAAT others(5): Show |
C | 2 | a0001c0001t0003g0008 a0001c0001t0003g0076 |
6 | HG01123.hp1 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.702+116_702+127del others(12): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 5/6 | chr12 | 90971672 | |||||||
| chr12:90972179 | T | C | 1 | a0001c0001t0002g0222 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.500-177A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 4/6 | chr12 | 90972179 | |||||||
| chr12:90972409 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.500-407G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 4/6 | chr12 | 90972409 | |||||||
| chr12:90972800 | C | T | 1 | a0001c0001t0003g0008 | 5 | HG01123.hp1 HG01928.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.499+22G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 4/6 | chr12 | 90972800 | |||||||
| chr12:90973167 | G | A | 28 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(25): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.341-187C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90973167 | |||||||
| chr12:90973214 | C | CTATT | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
309 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.341-238_341-235dup others(4): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90973214 | |||||||
| chr12:90973321 | A | G | 2 | a0001c0001t0002g0034 a0005c0009t0002g0092 |
3 | HG02486.hp2 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.341-341T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90973321 | |||||||
| chr12:90973533 | G | A | 12 | a0001c0001t0002g0029 a0001c0001t0002g0047 a0001c0001t0002g0050 others(9): Show |
14 | HG01109.hp2 HG01433.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.341-553C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90973533 | |||||||
| chr12:90973703 | T | G | 1 | a0001c0001t0002g0080 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.341-723A>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90973703 | |||||||
| chr12:90973845 | G | A | 12 | a0001c0001t0002g0029 a0001c0001t0002g0047 a0001c0001t0002g0050 others(9): Show |
14 | HG01109.hp2 HG01433.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.341-865C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90973845 | |||||||
| chr12:90973899 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.341-919C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90973899 | |||||||
| chr12:90973913 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.341-933T>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90973913 | |||||||
| chr12:90974030 | A | ACACT | 2 | a0001c0001t0001g0035 a0001c0001t0001g0096 |
3 | HG00738.hp2 HG01081.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.341-1051_341-1050i others(6): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974030 | |||||||
| chr12:90974032 | ACACACT | A | 12 | a0001c0001t0001g0031 a0001c0001t0001g0071 a0001c0001t0001g0074 others(9): Show |
17 | HG01123.hp1 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.341-1058_341-1053d others(8): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974032 | |||||||
| chr12:90974034 | ACACT | A | 3 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0077 |
3 | HG02647.hp1 HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.341-1058_341-1055d others(6): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974034 | |||||||
| chr12:90974038 | T | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0035 others(5): Show |
10 | HG00738.hp2 HG01081.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.341-1058A>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974038 | |||||||
| chr12:90974038 | T | TCA | 6 | a0001c0001t0001g0172 a0001c0001t0002g0051 a0001c0001t0002g0090 others(3): Show |
6 | HG02818.hp1 HG03453.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-1060_341-1059d others(4): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974038 | |||||||
| chr12:90974038 | T | TCACA | 20 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(17): Show |
27 | HG00597.hp2 HG00738.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.341-1062_341-1059d others(6): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974038 | |||||||
| chr12:90974038 | T | TCACACA | 32 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(29): Show |
43 | HG00408.hp1 HG00438.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.341-1064_341-1059d others(8): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974038 | |||||||
| chr12:90974038 | T | TCACACAC others(1): Show |
49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(46): Show |
69 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.341-1066_341-1059d others(10): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974038 | |||||||
| chr12:90974038 | T | TCACACAC others(3): Show |
19 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0020 others(16): Show |
23 | HG00558.hp1 HG00639.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.341-1068_341-1059d others(12): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974038 | |||||||
| chr12:90974038 | T | TCACACAC others(5): Show |
1 | a0001c0001t0001g0003 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.341-1070_341-1059d others(14): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974038 | |||||||
| chr12:90974038 | TCA | T | 45 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(42): Show |
67 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.341-1060_341-1059d others(4): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974038 | |||||||
| chr12:90974038 | TCACA | T | 4 | a0001c0001t0001g0070 a0001c0001t0002g0030 a0001c0001t0002g0063 others(1): Show |
4 | HG02145.hp2 HG02451.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-1062_341-1059d others(6): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974038 | |||||||
| chr12:90974038 | TCACACA | T | 1 | a0001c0001t0002g0015 | 3 | NA18962.hp2 NA19060.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.341-1064_341-1059d others(8): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974038 | |||||||
| chr12:90974040 | A | T | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0218 |
3 | HG03098.hp1 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.341-1060T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974040 | |||||||
| chr12:90974066 | A | ACACACG | 8 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0042 others(5): Show |
18 | HG02040.hp2 HG02155.hp1 HG02273.hp1 others(15): Show |
intron_variant | MODIFIER | c.341-1087_341-1086i others(8): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974066 | |||||||
| chr12:90974072 | A | C | 2 | a0001c0001t0001g0098 a0001c0001t0002g0054 |
2 | HG00741.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.341-1092T>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974072 | |||||||
| chr12:90974266 | AG | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
226 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.341-1287delC | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974266 | |||||||
| chr12:90974452 | A | T | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.341-1472T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974452 | |||||||
| chr12:90974498 | G | T | 1 | a0001c0001t0001g0160 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.341-1518C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974498 | |||||||
| chr12:90974514 | A | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
309 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.341-1534T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974514 | |||||||
| chr12:90974522 | A | C | 1 | a0001c0001t0001g0159 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.341-1542T>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974522 | |||||||
| chr12:90974536 | G | T | 1 | a0001c0001t0002g0197 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.341-1556C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974536 | |||||||
| chr12:90974761 | T | C | 1 | a0001c0001t0002g0049 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.341-1781A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974761 | |||||||
| chr12:90974874 | C | A | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.341-1894G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90974874 | |||||||
| chr12:90975213 | T | C | 28 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(25): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.341-2233A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90975213 | |||||||
| chr12:90975312 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.341-2332C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90975312 | |||||||
| chr12:90975552 | T | C | 28 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(25): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.340+2536A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90975552 | |||||||
| chr12:90975848 | A | G | 4 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(1): Show |
4 | HG02895.hp2 HG02965.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.340+2240T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90975848 | |||||||
| chr12:90975997 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.340+2091T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90975997 | |||||||
| chr12:90976017 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.340+2071T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90976017 | |||||||
| chr12:90976018 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.340+2070G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90976018 | |||||||
| chr12:90976121 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.340+1967C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90976121 | |||||||
| chr12:90976139 | C | T | 1 | a0004c0008t0002g0200 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.340+1949G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90976139 | |||||||
| chr12:90976223 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.340+1865C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90976223 | |||||||
| chr12:90976309 | A | C | 1 | a0001c0001t0002g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.340+1779T>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90976309 | |||||||
| chr12:90976330 | A | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0042 others(7): Show |
20 | HG01993.hp2 HG02040.hp2 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.340+1758T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90976330 | |||||||
| chr12:90976412 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG02015.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.340+1676C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90976412 | |||||||
| chr12:90976564 | C | T | 28 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(25): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.340+1524G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90976564 | |||||||
| chr12:90976707 | A | G | 4 | a0001c0001t0002g0027 a0001c0001t0002g0086 a0001c0001t0002g0221 others(1): Show |
6 | HG02257.hp1 HG02572.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.340+1381T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90976707 | |||||||
| chr12:90976857 | C | T | 2 | a0003c0004t0002g0091 a0003c0004t0002g0093 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.340+1231G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90976857 | |||||||
| chr12:90976953 | T | A | 1 | a0001c0001t0002g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.340+1135A>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90976953 | |||||||
| chr12:90977038 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.340+1050T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90977038 | |||||||
| chr12:90977074 | A | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.340+1014T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90977074 | |||||||
| chr12:90977120 | T | C | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.340+968A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90977120 | |||||||
| chr12:90977288 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.340+800A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90977288 | |||||||
| chr12:90977338 | T | A | 12 | a0001c0001t0002g0029 a0001c0001t0002g0047 a0001c0001t0002g0050 others(9): Show |
14 | HG01109.hp2 HG01433.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.340+750A>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90977338 | |||||||
| chr12:90977439 | T | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
226 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.340+649A>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90977439 | |||||||
| chr12:90977756 | T | C | 10 | a0001c0001t0001g0031 a0001c0001t0001g0072 a0001c0001t0001g0073 others(7): Show |
15 | HG01123.hp1 HG01928.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.340+332A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90977756 | |||||||
| chr12:90977966 | C | G | 1 | a0001c0001t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.340+122G>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 3/6 | chr12 | 90977966 | |||||||
| chr12:90978265 | GA | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
248 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(245): Show |
splice_region_variant&intron_variant | LOW | c.166-4delT | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90978265 | |||||||
| chr12:90978324 | G | C | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0079 others(6): Show |
11 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.166-62C>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90978324 | |||||||
| chr12:90978392 | T | C | 4 | a0001c0003t0002g0018 a0001c0003t0002g0087 a0001c0003t0002g0088 others(1): Show |
6 | HG01192.hp1 HG02258.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-130A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90978392 | |||||||
| chr12:90978517 | A | G | 67 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(64): Show |
101 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.166-255T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90978517 | |||||||
| chr12:90978789 | T | C | 1 | a0001c0001t0002g0080 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.166-527A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90978789 | |||||||
| chr12:90978952 | C | T | 7 | a0001c0001t0002g0027 a0001c0001t0002g0086 a0001c0001t0002g0206 others(4): Show |
9 | HG02257.hp1 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-690G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90978952 | |||||||
| chr12:90978957 | T | C | 1 | a0001c0001t0002g0080 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.166-695A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90978957 | |||||||
| chr12:90979009 | GT | G | 1 | a0001c0001t0003g0008 | 5 | HG01123.hp1 HG01928.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-748delA | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90979009 | |||||||
| chr12:90979012 | T | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.166-750A>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90979012 | |||||||
| chr12:90979231 | C | A | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0079 others(6): Show |
11 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.166-969G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90979231 | |||||||
| chr12:90979467 | A | T | 28 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(25): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.166-1205T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90979467 | |||||||
| chr12:90979576 | C | A | 1 | a0005c0009t0002g0092 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.166-1314G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90979576 | |||||||
| chr12:90979607 | A | G | 28 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(25): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.166-1345T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90979607 | |||||||
| chr12:90979790 | A | T | 2 | a0001c0001t0002g0034 a0005c0009t0002g0092 |
3 | HG02486.hp2 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.166-1528T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90979790 | |||||||
| chr12:90979844 | G | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
309 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.166-1582C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90979844 | |||||||
| chr12:90980410 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.166-2148C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90980410 | |||||||
| chr12:90980701 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
309 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.166-2439A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90980701 | |||||||
| chr12:90980703 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.166-2441A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90980703 | |||||||
| chr12:90980777 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.166-2515G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90980777 | |||||||
| chr12:90980913 | G | C | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0218 |
3 | HG03098.hp1 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.166-2651C>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90980913 | |||||||
| chr12:90980946 | T | A | 1 | a0001c0001t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.166-2684A>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90980946 | |||||||
| chr12:90980963 | A | G | 11 | a0001c0001t0002g0029 a0001c0001t0002g0047 a0001c0001t0002g0050 others(8): Show |
13 | HG01109.hp2 HG01433.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.166-2701T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90980963 | |||||||
| chr12:90980976 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
298 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.166-2714T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90980976 | |||||||
| chr12:90981091 | T | A | 1 | a0001c0001t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.166-2829A>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90981091 | |||||||
| chr12:90981109 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.166-2847C>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90981109 | |||||||
| chr12:90981283 | C | A | 1 | a0001c0001t0001g0042 | 2 | HG02040.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.166-3021G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90981283 | |||||||
| chr12:90981431 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.166-3169C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90981431 | |||||||
| chr12:90981615 | T | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0077 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.166-3353A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90981615 | |||||||
| chr12:90981962 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.166-3700G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90981962 | |||||||
| chr12:90982267 | G | A | 5 | a0001c0001t0002g0047 a0001c0001t0002g0192 a0001c0001t0002g0197 others(2): Show |
6 | HG01109.hp2 HG01433.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-4005C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90982267 | |||||||
| chr12:90982291 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.166-4029C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90982291 | |||||||
| chr12:90982308 | A | G | 1 | a0001c0001t0003g0008 | 5 | HG01123.hp1 HG01928.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-4046T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90982308 | |||||||
| chr12:90982332 | A | G | 10 | a0001c0001t0001g0071 a0001c0001t0002g0032 a0001c0001t0002g0033 others(7): Show |
12 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-4070T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90982332 | |||||||
| chr12:90982367 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.166-4105G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90982367 | |||||||
| chr12:90982368 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.166-4106C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90982368 | |||||||
| chr12:90982410 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.166-4148T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90982410 | |||||||
| chr12:90982442 | A | C | 3 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0084 |
5 | HG01167.hp2 HG02280.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-4180T>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90982442 | |||||||
| chr12:90982476 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.166-4214G>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90982476 | |||||||
| chr12:90982558 | C | A | 1 | a0001c0001t0001g0185 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.166-4296G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90982558 | |||||||
| chr12:90982567 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.166-4305G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90982567 | |||||||
| chr12:90982580 | A | T | 10 | a0001c0001t0001g0071 a0001c0001t0002g0032 a0001c0001t0002g0033 others(7): Show |
12 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-4318T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90982580 | |||||||
| chr12:90982583 | C | A | 1 | a0001c0001t0001g0174 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.166-4321G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90982583 | |||||||
| chr12:90982627 | A | G | 2 | a0003c0004t0002g0091 a0003c0004t0002g0093 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.166-4365T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90982627 | |||||||
| chr12:90982771 | A | G | 2 | a0002c0002t0002g0014 a0002c0002t0005g0212 |
5 | HG01074.hp1 HG01496.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-4509T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90982771 | |||||||
| chr12:90982915 | G | A | 1 | a0001c0001t0002g0215 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.166-4653C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90982915 | |||||||
| chr12:90983004 | A | T | 1 | a0001c0001t0001g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.166-4742T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90983004 | |||||||
| chr12:90983103 | C | A | 1 | a0004c0008t0002g0200 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.166-4841G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90983103 | |||||||
| chr12:90983147 | T | C | 10 | a0001c0001t0001g0071 a0001c0001t0002g0032 a0001c0001t0002g0033 others(7): Show |
12 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-4885A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90983147 | |||||||
| chr12:90983332 | C | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | NA19000.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.166-5070G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90983332 | |||||||
| chr12:90983587 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.166-5325C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90983587 | |||||||
| chr12:90983909 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.166-5647T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90983909 | |||||||
| chr12:90984148 | A | G | 1 | a0001c0001t0002g0052 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.166-5886T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90984148 | |||||||
| chr12:90984549 | A | G | 1 | a0001c0001t0002g0211 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.166-6287T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90984549 | |||||||
| chr12:90984617 | G | A | 2 | a0003c0004t0002g0091 a0003c0004t0002g0093 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.166-6355C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90984617 | |||||||
| chr12:90984626 | T | G | 29 | a0001c0001t0001g0180 a0001c0001t0002g0006 a0001c0001t0002g0009 others(26): Show |
52 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.166-6364A>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90984626 | |||||||
| chr12:90984667 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.166-6405G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90984667 | |||||||
| chr12:90984784 | A | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0152 a0001c0001t0001g0154 others(2): Show |
8 | HG06807.hp1 NA18983.hp1 NA18987.hp2 others(5): Show |
intron_variant | MODIFIER | c.166-6522T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90984784 | |||||||
| chr12:90984877 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.166-6615A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90984877 | |||||||
| chr12:90985367 | A | C | 1 | a0001c0001t0002g0210 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.166-7105T>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90985367 | |||||||
| chr12:90985372 | A | T | 1 | a0001c0003t0002g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.166-7110T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90985372 | |||||||
| chr12:90985420 | C | T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0002g0034 others(1): Show |
5 | HG00741.hp1 HG02300.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-7158G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90985420 | |||||||
| chr12:90985428 | G | C | 1 | a0001c0001t0002g0015 | 4 | HG00408.hp2 NA18962.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-7166C>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90985428 | |||||||
| chr12:90985497 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0128 |
3 | HG02572.hp2 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.166-7235C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90985497 | |||||||
| chr12:90985519 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.166-7257G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90985519 | |||||||
| chr12:90985752 | C | G | 5 | a0001c0001t0001g0019 a0001c0001t0001g0098 a0001c0001t0001g0099 others(2): Show |
7 | HG00741.hp1 HG01081.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-7490G>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90985752 | |||||||
| chr12:90985776 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.166-7514A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90985776 | |||||||
| chr12:90985792 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.166-7530G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90985792 | |||||||
| chr12:90985794 | G | C | 1 | a0001c0001t0002g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.166-7532C>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90985794 | |||||||
| chr12:90986239 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0132 |
2 | NA18941.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.166-7977C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90986239 | |||||||
| chr12:90986317 | G | A | 28 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(25): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.166-8055C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90986317 | |||||||
| chr12:90986341 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.166-8079A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90986341 | |||||||
| chr12:90986354 | G | A | 2 | a0001c0003t0002g0018 a0001c0003t0002g0089 |
4 | HG01192.hp1 HG02258.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-8092C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90986354 | |||||||
| chr12:90986377 | A | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0077 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.166-8115T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90986377 | |||||||
| chr12:90986397 | A | G | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0079 others(6): Show |
11 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.166-8135T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90986397 | |||||||
| chr12:90986468 | T | C | 1 | a0001c0001t0002g0220 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.166-8206A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90986468 | |||||||
| chr12:90986488 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.166-8226G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90986488 | |||||||
| chr12:90986635 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.166-8373C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90986635 | |||||||
| chr12:90986742 | C | T | 18 | a0001c0001t0001g0031 a0001c0001t0001g0072 a0001c0001t0001g0073 others(15): Show |
25 | HG01123.hp1 HG01192.hp1 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.166-8480G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90986742 | |||||||
| chr12:90986819 | T | C | 1 | a0001c0001t0002g0219 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.166-8557A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90986819 | |||||||
| chr12:90986856 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(96): Show |
156 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.166-8594T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90986856 | |||||||
| chr12:90986893 | G | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
309 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.166-8631C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90986893 | |||||||
| chr12:90987072 | G | T | 1 | a0001c0001t0002g0209 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.166-8810C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90987072 | |||||||
| chr12:90987104 | A | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
309 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.166-8842T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90987104 | |||||||
| chr12:90987277 | A | G | 2 | a0001c0001t0002g0034 a0005c0009t0002g0092 |
3 | HG02486.hp2 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.166-9015T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90987277 | |||||||
| chr12:90987286 | C | G | 2 | a0001c0001t0002g0193 a0001c0001t0002g0194 |
2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.166-9024G>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90987286 | |||||||
| chr12:90987352 | G | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG00642.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.166-9090C>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90987352 | |||||||
| chr12:90987354 | T | TCACAAGC others(366): Show |
2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG00642.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.166-9093_166-9092i others(375): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90987354 | |||||||
| chr12:90987384 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.166-9122G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90987384 | |||||||
| chr12:90987419 | A | G | 10 | a0001c0001t0001g0071 a0001c0001t0002g0032 a0001c0001t0002g0033 others(7): Show |
12 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-9157T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90987419 | |||||||
| chr12:90987441 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(28): Show |
54 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.166-9179C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90987441 | |||||||
| chr12:90987515 | A | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
309 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.166-9253T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90987515 | |||||||
| chr12:90987641 | T | C | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0079 others(6): Show |
11 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.166-9379A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90987641 | |||||||
| chr12:90987647 | A | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
309 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.166-9385T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90987647 | |||||||
| chr12:90987845 | T | A | 2 | a0001c0001t0002g0060 a0001c0001t0002g0066 |
2 | HG01257.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.166-9583A>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90987845 | |||||||
| chr12:90987939 | G | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
309 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.166-9677C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90987939 | |||||||
| chr12:90988069 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0150 |
2 | HG02015.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.166-9807C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90988069 | |||||||
| chr12:90988088 | A | G | 1 | a0001c0001t0002g0208 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.166-9826T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90988088 | |||||||
| chr12:90988139 | T | C | 1 | a0001c0001t0002g0064 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.166-9877A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90988139 | |||||||
| chr12:90988460 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.166-10198C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90988460 | |||||||
| chr12:90988495 | A | G | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0079 others(6): Show |
11 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.166-10233T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90988495 | |||||||
| chr12:90988524 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.166-10262C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90988524 | |||||||
| chr12:90988762 | G | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | NA18969.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.166-10500C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90988762 | |||||||
| chr12:90989088 | A | C | 1 | a0001c0001t0001g0045 | 2 | HG02129.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.166-10826T>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90989088 | |||||||
| chr12:90989093 | A | G | 6 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0003t0002g0018 others(3): Show |
8 | HG01192.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.166-10831T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90989093 | |||||||
| chr12:90989259 | G | C | 10 | a0001c0001t0001g0071 a0001c0001t0002g0032 a0001c0001t0002g0033 others(7): Show |
12 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-10997C>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90989259 | |||||||
| chr12:90989535 | A | G | 1 | a0001c0001t0002g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.166-11273T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90989535 | |||||||
| chr12:90989583 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
247 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.166-11321G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90989583 | |||||||
| chr12:90989632 | A | G | 1 | a0001c0001t0002g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.166-11370T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90989632 | |||||||
| chr12:90989943 | T | C | 14 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0152 others(11): Show |
20 | HG00597.hp2 HG02155.hp2 HG03831.hp2 others(17): Show |
intron_variant | MODIFIER | c.166-11681A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90989943 | |||||||
| chr12:90989979 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.166-11717G>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90989979 | |||||||
| chr12:90990188 | T | G | 1 | a0001c0001t0001g0130 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.166-11926A>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90990188 | |||||||
| chr12:90990236 | G | C | 33 | a0001c0001t0001g0071 a0001c0001t0002g0029 a0001c0001t0002g0032 others(30): Show |
40 | HG01109.hp2 HG01167.hp2 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.166-11974C>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90990236 | |||||||
| chr12:90990314 | A | C | 1 | a0001c0001t0001g0078 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.166-12052T>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90990314 | |||||||
| chr12:90990690 | C | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
342 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(339): Show |
intron_variant | MODIFIER | c.165+11711G>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90990690 | |||||||
| chr12:90990798 | T | TA | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0079 others(6): Show |
11 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.165+11602dupT | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90990798 | |||||||
| chr12:90990840 | T | G | 2 | a0001c0001t0002g0060 a0001c0001t0002g0066 |
2 | HG01257.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.165+11561A>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90990840 | |||||||
| chr12:90990844 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
258 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.165+11557T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90990844 | |||||||
| chr12:90990982 | T | C | 1 | a0001c0001t0002g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.165+11419A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90990982 | |||||||
| chr12:90991139 | T | C | 1 | a0001c0001t0002g0026 | 3 | NA19059.hp2 NA19074.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.165+11262A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90991139 | |||||||
| chr12:90991158 | T | C | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0079 others(6): Show |
11 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.165+11243A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90991158 | |||||||
| chr12:90991318 | G | A | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.165+11083C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90991318 | |||||||
| chr12:90991705 | C | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
258 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.165+10696G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90991705 | |||||||
| chr12:90991766 | C | T | 1 | a0005c0009t0002g0092 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.165+10635G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90991766 | |||||||
| chr12:90991797 | G | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG00741.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.165+10604C>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90991797 | |||||||
| chr12:90991849 | T | C | 33 | a0001c0001t0001g0071 a0001c0001t0002g0029 a0001c0001t0002g0032 others(30): Show |
40 | HG01109.hp2 HG01167.hp2 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.165+10552A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90991849 | |||||||
| chr12:90991957 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
309 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.165+10444A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90991957 | |||||||
| chr12:90992181 | T | A | 12 | a0001c0001t0001g0031 a0001c0001t0001g0072 a0001c0001t0001g0073 others(9): Show |
17 | HG01123.hp1 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.165+10220A>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90992181 | |||||||
| chr12:90992397 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.165+10004C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90992397 | |||||||
| chr12:90992545 | T | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
258 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.165+9856A>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90992545 | |||||||
| chr12:90992801 | C | T | 2 | a0001c0001t0002g0029 a0001c0001t0002g0050 |
3 | HG02258.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.165+9600G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90992801 | |||||||
| chr12:90992810 | T | C | 2 | a0001c0001t0003g0008 a0001c0001t0003g0076 |
6 | HG01123.hp1 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+9591A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90992810 | |||||||
| chr12:90992989 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.165+9412G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90992989 | |||||||
| chr12:90993016 | TAA | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
309 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.165+9383_165+9384d others(4): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90993016 | |||||||
| chr12:90993048 | C | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.165+9353G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90993048 | |||||||
| chr12:90993117 | C | T | 12 | a0001c0001t0001g0031 a0001c0001t0001g0072 a0001c0001t0001g0073 others(9): Show |
17 | HG01123.hp1 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.165+9284G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90993117 | |||||||
| chr12:90993145 | A | G | 12 | a0001c0001t0002g0029 a0001c0001t0002g0047 a0001c0001t0002g0050 others(9): Show |
14 | HG01109.hp2 HG01433.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+9256T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90993145 | |||||||
| chr12:90993499 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.165+8902C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90993499 | |||||||
| chr12:90993533 | C | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
258 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.165+8868G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90993533 | |||||||
| chr12:90993640 | T | A | 1 | a0001c0001t0002g0216 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.165+8761A>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90993640 | |||||||
| chr12:90993641 | C | A | 1 | a0001c0001t0002g0216 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.165+8760G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90993641 | |||||||
| chr12:90993659 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0150 |
2 | HG02015.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.165+8742C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90993659 | |||||||
| chr12:90993741 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
258 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.165+8660C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90993741 | |||||||
| chr12:90993746 | A | G | 1 | a0006c0010t0001g0143 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.165+8655T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90993746 | |||||||
| chr12:90993747 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.165+8654G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90993747 | |||||||
| chr12:90993779 | T | C | 1 | a0001c0003t0002g0018 | 3 | HG02258.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.165+8622A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90993779 | |||||||
| chr12:90993855 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.165+8546G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90993855 | |||||||
| chr12:90993949 | A | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.165+8452T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90993949 | |||||||
| chr12:90994024 | C | G | 1 | a0001c0003t0002g0087 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.165+8377G>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90994024 | |||||||
| chr12:90994026 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.165+8375A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90994026 | |||||||
| chr12:90994098 | T | A | 1 | a0001c0001t0002g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.165+8303A>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90994098 | |||||||
| chr12:90994145 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
258 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.165+8256T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90994145 | |||||||
| chr12:90994201 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
258 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.165+8200T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90994201 | |||||||
| chr12:90994365 | G | A | 2 | a0001c0001t0002g0034 a0005c0009t0002g0092 |
3 | HG02486.hp2 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.165+8036C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90994365 | |||||||
| chr12:90994489 | A | G | 1 | a0001c0001t0002g0080 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.165+7912T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90994489 | |||||||
| chr12:90994544 | A | G | 14 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0152 others(11): Show |
20 | HG00597.hp2 HG02155.hp2 HG03831.hp2 others(17): Show |
intron_variant | MODIFIER | c.165+7857T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90994544 | |||||||
| chr12:90994558 | G | C | 12 | a0001c0001t0002g0029 a0001c0001t0002g0047 a0001c0001t0002g0050 others(9): Show |
14 | HG01109.hp2 HG01433.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+7843C>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90994558 | |||||||
| chr12:90994906 | T | C | 1 | a0002c0002t0002g0217 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.165+7495A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90994906 | |||||||
| chr12:90994980 | G | A | 1 | a0001c0001t0002g0080 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.165+7421C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90994980 | |||||||
| chr12:90995178 | A | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
258 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.165+7223T>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90995178 | |||||||
| chr12:90995179 | G | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
258 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.165+7222C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90995179 | |||||||
| chr12:90995585 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.165+6816G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90995585 | |||||||
| chr12:90995779 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0150 |
2 | HG02015.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.165+6622C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90995779 | |||||||
| chr12:90996407 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.165+5994T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90996407 | |||||||
| chr12:90996431 | A | T | 4 | a0001c0003t0002g0018 a0001c0003t0002g0087 a0001c0003t0002g0088 others(1): Show |
6 | HG01192.hp1 HG02258.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+5970T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90996431 | |||||||
| chr12:90996432 | T | C | 2 | a0001c0001t0002g0034 a0005c0009t0002g0092 |
3 | HG02486.hp2 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.165+5969A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90996432 | |||||||
| chr12:90996541 | C | T | 1 | a0001c0001t0002g0192 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.165+5860G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90996541 | |||||||
| chr12:90996659 | T | C | 7 | a0001c0001t0002g0027 a0001c0001t0002g0086 a0001c0001t0002g0206 others(4): Show |
9 | HG02257.hp1 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+5742A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90996659 | |||||||
| chr12:90996891 | T | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
258 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.165+5510A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90996891 | |||||||
| chr12:90997016 | C | A | 1 | a0001c0001t0001g0105 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.165+5385G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90997016 | |||||||
| chr12:90997340 | G | A | 2 | a0003c0004t0002g0091 a0003c0004t0002g0093 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.165+5061C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90997340 | |||||||
| chr12:90997355 | CT | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
229 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.165+5045delA | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90997355 | |||||||
| chr12:90997494 | C | T | 28 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(25): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.165+4907G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90997494 | |||||||
| chr12:90997500 | C | A | 1 | a0001c0001t0002g0219 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.165+4901G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90997500 | |||||||
| chr12:90997701 | C | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
258 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.165+4700G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90997701 | |||||||
| chr12:90997793 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
258 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.165+4608T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90997793 | |||||||
| chr12:90997866 | C | T | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.165+4535G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90997866 | |||||||
| chr12:90997965 | C | T | 28 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(25): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.165+4436G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90997965 | |||||||
| chr12:90997986 | G | T | 1 | a0001c0001t0001g0068 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.165+4415C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90997986 | |||||||
| chr12:90998062 | C | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
258 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.165+4339G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90998062 | |||||||
| chr12:90998249 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.165+4152C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90998249 | |||||||
| chr12:90998279 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.165+4122C>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90998279 | |||||||
| chr12:90998362 | G | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0074 a0001c0001t0001g0201 others(3): Show |
7 | HG02109.hp2 HG02895.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+4039C>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90998362 | |||||||
| chr12:90998440 | C | T | 24 | a0001c0001t0001g0071 a0001c0001t0002g0029 a0001c0001t0002g0034 others(21): Show |
29 | HG01109.hp2 HG01192.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.165+3961G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90998440 | |||||||
| chr12:90998447 | A | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
258 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.165+3954T>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90998447 | |||||||
| chr12:90998504 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0153 |
2 | HG01109.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.165+3897G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90998504 | |||||||
| chr12:90998592 | G | T | 1 | a0001c0001t0001g0043 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.165+3809C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90998592 | |||||||
| chr12:90998615 | C | G | 28 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(25): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.165+3786G>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90998615 | |||||||
| chr12:90998708 | T | G | 12 | a0001c0001t0002g0029 a0001c0001t0002g0047 a0001c0001t0002g0050 others(9): Show |
14 | HG01109.hp2 HG01433.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+3693A>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90998708 | |||||||
| chr12:90998841 | C | A | 1 | a0001c0001t0001g0181 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.165+3560G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90998841 | |||||||
| chr12:90999121 | T | G | 10 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0079 others(7): Show |
12 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.165+3280A>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90999121 | |||||||
| chr12:90999143 | G | T | 1 | a0001c0001t0002g0051 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.165+3258C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90999143 | |||||||
| chr12:90999367 | G | A | 2 | a0003c0004t0002g0091 a0003c0004t0002g0093 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.165+3034C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90999367 | |||||||
| chr12:90999630 | A | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0077 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.165+2771T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90999630 | |||||||
| chr12:90999656 | G | C | 2 | a0003c0004t0002g0091 a0003c0004t0002g0093 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.165+2745C>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90999656 | |||||||
| chr12:90999742 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.165+2659G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90999742 | |||||||
| chr12:90999803 | G | GT | 11 | a0001c0001t0001g0152 a0001c0001t0002g0032 a0001c0001t0002g0033 others(8): Show |
13 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+2597dupA | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90999803 | |||||||
| chr12:90999804 | T | G | 1 | a0001c0001t0001g0165 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.165+2597A>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90999804 | |||||||
| chr12:90999997 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.165+2404T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 90999997 | |||||||
| chr12:91000052 | G | A | 10 | a0001c0001t0001g0031 a0001c0001t0001g0072 a0001c0001t0001g0073 others(7): Show |
15 | HG01123.hp1 HG01928.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+2349C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000052 | |||||||
| chr12:91000120 | A | G | 1 | a0001c0001t0002g0080 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.165+2281T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000120 | |||||||
| chr12:91000147 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG00741.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.165+2254T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000147 | |||||||
| chr12:91000165 | A | G | 2 | a0001c0001t0002g0034 a0005c0009t0002g0092 |
3 | HG02486.hp2 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.165+2236T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000165 | |||||||
| chr12:91000205 | T | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
259 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.165+2196A>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000205 | |||||||
| chr12:91000275 | G | T | 1 | a0001c0001t0001g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.165+2126C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000275 | |||||||
| chr12:91000299 | C | T | 12 | a0001c0001t0002g0029 a0001c0001t0002g0047 a0001c0001t0002g0050 others(9): Show |
14 | HG01109.hp2 HG01433.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+2102G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000299 | |||||||
| chr12:91000519 | G | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
259 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.165+1882C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000519 | |||||||
| chr12:91000540 | T | C | 1 | a0001c0001t0002g0061 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.165+1861A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000540 | |||||||
| chr12:91000584 | C | G | 1 | a0001c0001t0004g0062 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.165+1817G>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000584 | |||||||
| chr12:91000669 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.165+1732T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000669 | |||||||
| chr12:91000729 | A | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.165+1672T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000729 | |||||||
| chr12:91000790 | C | CT | 7 | a0001c0001t0001g0037 a0001c0001t0001g0045 a0001c0001t0001g0097 others(4): Show |
9 | HG01258.hp2 HG01891.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+1610dupA | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000790 | |||||||
| chr12:91000798 | T | A | 1 | a0001c0001t0001g0131 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.165+1603A>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000798 | |||||||
| chr12:91000798 | T | TA | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
200 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.165+1602dupT | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000798 | |||||||
| chr12:91000799 | A | T | 1 | a0001c0001t0002g0207 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.165+1602T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000799 | |||||||
| chr12:91000831 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.165+1570C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000831 | |||||||
| chr12:91000845 | G | T | 1 | a0001c0001t0002g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.165+1556C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000845 | |||||||
| chr12:91000903 | T | C | 34 | a0001c0001t0001g0071 a0001c0001t0002g0029 a0001c0001t0002g0032 others(31): Show |
41 | HG01109.hp2 HG01167.hp2 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.165+1498A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000903 | |||||||
| chr12:91000939 | C | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0042 others(7): Show |
20 | HG01993.hp2 HG02040.hp2 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.165+1462G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91000939 | |||||||
| chr12:91001040 | T | G | 10 | a0001c0001t0001g0031 a0001c0001t0001g0072 a0001c0001t0001g0073 others(7): Show |
15 | HG01123.hp1 HG01928.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+1361A>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91001040 | |||||||
| chr12:91001370 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.165+1031C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91001370 | |||||||
| chr12:91001384 | A | G | 27 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0015 others(24): Show |
50 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.165+1017T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91001384 | |||||||
| chr12:91001398 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.165+1003C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91001398 | |||||||
| chr12:91001410 | C | A | 1 | a0001c0001t0001g0185 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.165+991G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91001410 | |||||||
| chr12:91001712 | T | G | 24 | a0001c0001t0001g0071 a0001c0001t0002g0029 a0001c0001t0002g0034 others(21): Show |
29 | HG01109.hp2 HG01192.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.165+689A>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91001712 | |||||||
| chr12:91001763 | G | A | 5 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(2): Show |
5 | HG00423.hp1 HG00597.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+638C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91001763 | |||||||
| chr12:91001953 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.165+448G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91001953 | |||||||
| chr12:91001962 | G | A | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.165+439C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91001962 | |||||||
| chr12:91002020 | C | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | NA18975.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.165+381G>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91002020 | |||||||
| chr12:91002045 | C | T | 13 | a0001c0001t0002g0029 a0001c0001t0002g0047 a0001c0001t0002g0050 others(10): Show |
15 | HG01109.hp2 HG01433.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+356G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91002045 | |||||||
| chr12:91002189 | C | CA | 14 | a0001c0001t0002g0017 a0001c0001t0002g0063 a0001c0001t0002g0064 others(11): Show |
16 | HG00642.hp1 HG01070.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.165+211dupT | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91002189 | |||||||
| chr12:91002189 | C | CAA | 7 | a0001c0001t0001g0071 a0001c0001t0002g0034 a0001c0001t0002g0094 others(4): Show |
10 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.165+210_165+211dup others(2): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91002189 | |||||||
| chr12:91002189 | C | CAAA | 13 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0201 others(10): Show |
14 | HG01109.hp2 HG01433.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+209_165+211dup others(3): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91002189 | |||||||
| chr12:91002189 | C | CAAAA | 11 | a0001c0001t0001g0031 a0001c0001t0001g0072 a0001c0001t0001g0073 others(8): Show |
16 | HG01123.hp1 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.165+208_165+211dup others(4): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91002189 | |||||||
| chr12:91002189 | C | CAAAAA | 32 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(29): Show |
54 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.165+207_165+211dup others(5): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91002189 | |||||||
| chr12:91002189 | C | CAAAAAA | 32 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(29): Show |
51 | HG00597.hp2 HG00738.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.165+206_165+211dup others(6): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91002189 | |||||||
| chr12:91002189 | C | CAAAAAAA | 7 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(4): Show |
8 | HG02572.hp1 HG02683.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.165+205_165+211dup others(7): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91002189 | |||||||
| chr12:91002189 | CA | C | 9 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0001t0001g0046 others(6): Show |
12 | HG01106.hp1 HG01261.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.165+211delT | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91002189 | |||||||
| chr12:91002189 | CAA | C | 52 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(49): Show |
82 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.165+210_165+211del others(2): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91002189 | |||||||
| chr12:91002211 | A | G | 3 | a0001c0001t0002g0009 a0001c0001t0002g0025 a0001c0001t0002g0209 |
3 | HG03490.hp1 HG03704.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.165+190T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91002211 | |||||||
| chr12:91002227 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG00642.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.165+174G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91002227 | |||||||
| chr12:91002229 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.165+172C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 2/6 | chr12 | 91002229 | |||||||
| chr12:91002596 | A | C | 10 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0079 others(7): Show |
12 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-13-18T>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91002596 | |||||||
| chr12:91002668 | T | C | 1 | a0001c0001t0001g0045 | 2 | HG02129.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-13-90A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91002668 | |||||||
| chr12:91002748 | CATTGCTG others(12): Show |
C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0078 others(7): Show |
13 | HG00099.hp2 HG00741.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.-13-189_-13-171del others(19): Show |
EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91002748 | |||||||
| chr12:91002753 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-13-175G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91002753 | |||||||
| chr12:91002784 | G | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0096 |
3 | HG00738.hp2 HG01081.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.-13-206C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91002784 | |||||||
| chr12:91002867 | C | CT | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.-13-290dupA | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91002867 | |||||||
| chr12:91002965 | G | A | 2 | a0001c0001t0002g0029 a0001c0001t0002g0050 |
3 | HG02258.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-13-387C>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91002965 | |||||||
| chr12:91003023 | G | C | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-13-445C>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91003023 | |||||||
| chr12:91003069 | G | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.-13-491C>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91003069 | |||||||
| chr12:91003125 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-13-547G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91003125 | |||||||
| chr12:91003392 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-13-814A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91003392 | |||||||
| chr12:91003402 | T | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.-13-824A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91003402 | |||||||
| chr12:91003505 | T | C | 10 | a0001c0001t0002g0047 a0001c0001t0002g0192 a0001c0001t0002g0193 others(7): Show |
11 | HG01109.hp2 HG01433.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-13-927A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91003505 | |||||||
| chr12:91003525 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-13-947G>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91003525 | |||||||
| chr12:91003659 | G | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0068 a0001c0001t0001g0069 others(1): Show |
7 | NA18944.hp1 NA18961.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13-1081C>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91003659 | |||||||
| chr12:91004164 | A | T | 12 | a0001c0001t0001g0031 a0001c0001t0001g0072 a0001c0001t0001g0073 others(9): Show |
17 | HG01123.hp1 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.-14+783T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91004164 | |||||||
| chr12:91004184 | T | A | 4 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(1): Show |
4 | HG02895.hp2 HG02965.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+763A>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91004184 | |||||||
| chr12:91004249 | C | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0068 a0001c0001t0001g0069 |
6 | NA18944.hp1 NA18961.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14+698G>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91004249 | |||||||
| chr12:91004262 | C | A | 1 | a0001c0001t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-14+685G>T | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91004262 | |||||||
| chr12:91004362 | A | C | 1 | a0001c0001t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-14+585T>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91004362 | |||||||
| chr12:91004470 | A | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
256 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.-14+477T>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91004470 | |||||||
| chr12:91004492 | A | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0068 a0001c0001t0001g0069 others(1): Show |
7 | NA18944.hp1 NA18961.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+455T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91004492 | |||||||
| chr12:91004515 | T | C | 1 | a0001c0001t0004g0067 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-14+432A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91004515 | |||||||
| chr12:91004523 | A | T | 3 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0050 |
5 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+424T>A | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91004523 | |||||||
| chr12:91004857 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
306 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.-14+90A>G | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91004857 | |||||||
| chr12:91004941 | A | G | 1 | a0001c0001t0002g0049 | 1 | HG00609.hp1 | splice_region_variant&intron_variant | LOW | c.-14+6T>C | EPYC | ENSG00000083782.8 | transcript | ENST00000261172.8 | protein_coding | 1/6 | chr12 | 91004941 |