Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23113 |
| ensemblid | ENSG00000112659.14 |
| hgncid | 15982 |
| symbol | CUL9 |
| name | cullin 9 |
| refseq_nuc | NM_015089.4 |
| refseq_prot | NP_055904.1 |
| ensembl_nuc | ENST00000252050.9 |
| ensembl_prot | ENSP00000252050.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 43182196 |
| end | 43224587 |
| strand | + |
| ver | v1.2 |
| region | chr6:43182196-43224587 |
| region5000 | chr6:43177196-43229587 |
| regionname0 | CUL9_chr6_43182196_43224587 |
| regionname5000 | CUL9_chr6_43177196_43229587 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 2517 | 135 | 50 | 17 | 54 | 2 | 11 | 44 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0002 | 1/0 | 2517 | 108 | 24 | 21 | 47 | 5 | 10 | 37 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0003 | 0/0 | 2516 | 8 | 5 | 1 | 2 | 0 | 0 | 2 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2511): Show |
chr6 | 43177196 | 43229587 |
| a0004 | 0/0 | 2517 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0005 | 0/0 | 2517 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0006 | 0/0 | 2517 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0007 | 0/0 | 2517 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0008 | 0/0 | 2517 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0009 | 0/0 | 2517 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0010 | 0/0 | 2517 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0011 | 0/0 | 2517 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0012 | 0/0 | 2517 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0013 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0014 | 0/0 | 2517 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0015 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0016 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0017 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0018 | 0/0 | 2517 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0019 | 0/0 | 2517 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0020 | 0/0 | 2517 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0021 | 0/0 | 2517 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| a0022 | 0/0 | 2517 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | MVGER others(2512): Show |
chr6 | 43177196 | 43229587 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 7551 | 63 | 3 | 6 | 47 | 1 | 6 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0001c0003 | 0/1 | 7551 | 29 | 18 | 6 | 1 | 0 | 3 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0001c0004 | 0/0 | 7551 | 9 | 2 | 2 | 4 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0001c0007 | 0/0 | 7551 | 7 | 7 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0001c0008 | 0/0 | 7551 | 6 | 6 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0001c0010 | 0/0 | 7551 | 5 | 5 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0001c0011 | 0/0 | 7551 | 5 | 3 | 2 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0001c0012 | 0/0 | 7551 | 4 | 2 | 0 | 0 | 1 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0001c0020 | 0/0 | 7551 | 2 | 2 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0001c0032 | 0/0 | 7551 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0001c0038 | 0/0 | 7551 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0001c0039 | 0/0 | 7551 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0001c0040 | 0/0 | 7551 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0001c0042 | 0/0 | 7551 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0002c0001 | 1/0 | 7551 | 88 | 15 | 18 | 42 | 4 | 8 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0002c0006 | 0/0 | 7551 | 7 | 2 | 2 | 2 | 1 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0002c0009 | 0/0 | 7551 | 6 | 6 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0002c0014 | 0/0 | 7551 | 2 | 0 | 0 | 2 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0002c0022 | 0/0 | 7551 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0002c0029 | 0/0 | 7551 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0002c0030 | 0/0 | 7551 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0002c0031 | 0/0 | 7551 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0002c0033 | 0/0 | 7551 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0003c0005 | 0/0 | 7548 | 8 | 5 | 1 | 2 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7543): Show |
chr6 | 43177196 | 43229587 | ||
| a0004c0015 | 0/0 | 7551 | 2 | 1 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0005c0019 | 0/0 | 7551 | 2 | 2 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0006c0016 | 0/0 | 7551 | 2 | 2 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0007c0013 | 0/0 | 7551 | 2 | 2 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0008c0018 | 0/0 | 7551 | 2 | 0 | 0 | 2 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0009c0017 | 0/0 | 7551 | 2 | 0 | 0 | 2 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0010c0025 | 0/0 | 7551 | 1 | 0 | 0 | 0 | 1 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0011c0036 | 0/0 | 7551 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0012c0035 | 0/0 | 7551 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0013c0028 | 0/0 | 7551 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0014c0026 | 0/0 | 7551 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0015c0041 | 0/0 | 7551 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0016c0021 | 0/0 | 7551 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0017c0037 | 0/0 | 7551 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0018c0024 | 0/0 | 7551 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0019c0043 | 0/0 | 7551 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0020c0034 | 0/0 | 7551 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0021c0023 | 0/0 | 7551 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 | ||
| a0022c0027 | 0/0 | 7551 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | ATGGT others(7546): Show |
chr6 | 43177196 | 43229587 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 7759 | 63 | 3 | 6 | 47 | 1 | 6 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0001c0003t0001 | 0/1 | 7759 | 23 | 12 | 6 | 1 | 0 | 3 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0001c0003t0002 | 0/0 | 7759 | 6 | 6 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0001c0004t0001 | 0/0 | 7759 | 4 | 2 | 2 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0001c0004t0002 | 0/0 | 7759 | 5 | 0 | 0 | 4 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0001c0007t0001 | 0/0 | 7759 | 7 | 7 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0001c0008t0001 | 0/0 | 7759 | 6 | 6 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0001c0010t0002 | 0/0 | 7759 | 5 | 5 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0001c0011t0002 | 0/0 | 7759 | 5 | 3 | 2 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0001c0012t0001 | 0/0 | 7759 | 4 | 2 | 0 | 0 | 1 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0001c0020t0002 | 0/0 | 7759 | 2 | 2 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0001c0032t0001 | 0/0 | 7759 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0001c0038t0001 | 0/0 | 7759 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0001c0039t0002 | 0/0 | 7759 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0001c0040t0001 | 0/0 | 7759 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0001c0042t0001 | 0/0 | 7759 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0002c0001t0001 | 1/0 | 7759 | 88 | 15 | 18 | 42 | 4 | 8 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0002c0006t0001 | 0/0 | 7759 | 7 | 2 | 2 | 2 | 1 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0002c0009t0001 | 0/0 | 7759 | 6 | 6 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0002c0014t0001 | 0/0 | 7759 | 2 | 0 | 0 | 2 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0002c0022t0001 | 0/0 | 7759 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0002c0029t0001 | 0/0 | 7759 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0002c0030t0001 | 0/0 | 7759 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0002c0031t0002 | 0/0 | 7759 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0002c0033t0002 | 0/0 | 7759 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0003c0005t0001 | 0/0 | 7756 | 8 | 5 | 1 | 2 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7751): Show |
chr6 | 43177196 | 43229587 |
| a0004c0015t0001 | 0/0 | 7759 | 2 | 1 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0005c0019t0001 | 0/0 | 7759 | 2 | 2 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0006c0016t0001 | 0/0 | 7759 | 2 | 2 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0007c0013t0001 | 0/0 | 7759 | 2 | 2 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0008c0018t0001 | 0/0 | 7759 | 2 | 0 | 0 | 2 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0009c0017t0001 | 0/0 | 7759 | 2 | 0 | 0 | 2 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0010c0025t0001 | 0/0 | 7759 | 1 | 0 | 0 | 0 | 1 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0011c0036t0001 | 0/0 | 7759 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0012c0035t0001 | 0/0 | 7759 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0013c0028t0001 | 0/0 | 7759 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0014c0026t0001 | 0/0 | 7759 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0015c0041t0001 | 0/0 | 7759 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0016c0021t0002 | 0/0 | 7759 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0017c0037t0001 | 0/0 | 7759 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0018c0024t0001 | 0/0 | 7759 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0019c0043t0001 | 0/0 | 7759 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0020c0034t0001 | 0/0 | 7759 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0021c0023t0001 | 0/0 | 7759 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| a0022c0027t0001 | 0/0 | 7759 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | GGACG others(7754): Show |
chr6 | 43177196 | 43229587 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0002 | 0/0 | 9 | 0 | 0 | 6 | 1 | 2 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0003t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0004t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0004t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0004t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0004t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0004t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0004t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0004t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0007t0001g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0007t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0008t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0008t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0008t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0008t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0008t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0008t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0010t0002g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0010t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0010t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0011t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0011t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0011t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0011t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0011t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0012t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0012t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0012t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0012t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0020t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0020t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0032t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0038t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0039t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0040t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0001c0042t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0001 | 1/0 | 14 | 1 | 1 | 9 | 0 | 2 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0010 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0006t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0006t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0006t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0006t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0006t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0006t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0009t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0009t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0009t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0009t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0014t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0014t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0022t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0029t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0030t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0031t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0002c0033t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0003c0005t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0003c0005t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0003c0005t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0003c0005t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0003c0005t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0003c0005t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0004c0015t0001g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0005c0019t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0005c0019t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0006c0016t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0007c0013t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0007c0013t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0008c0018t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0009c0017t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0010c0025t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0011c0036t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0012c0035t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0013c0028t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0014c0026t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0015c0041t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0016c0021t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0017c0037t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0018c0024t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0019c0043t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0020c0034t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0021c0023t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| a0022c0027t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0001 | t0001 | g0150 | EUR | GBR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG00099 | hp2 | a0010 | c0025 | t0001 | g0151 | EUR | GBR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG00323 | hp1 | a0002 | c0001 | t0001 | g0133 | EUR | FIN | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | FIN | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | CHS | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG00423 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | CHS | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG00558 | hp1 | a0002 | c0001 | t0001 | g0033 | EAS | CHS | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG00558 | hp2 | a0001 | c0004 | t0002 | g0027 | EAS | CHS | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG00639 | hp1 | a0003 | c0005 | t0001 | g0182 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG00642 | hp2 | a0002 | c0001 | t0001 | g0022 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG00733 | hp2 | a0002 | c0001 | t0001 | g0153 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG00738 | hp1 | a0004 | c0015 | t0001 | g0001 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG00738 | hp2 | a0002 | c0001 | t0001 | g0022 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0105 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG00741 | hp2 | a0001 | c0011 | t0002 | g0194 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01070 | hp1 | a0002 | c0033 | t0002 | g0110 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01070 | hp2 | a0002 | c0001 | t0001 | g0146 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01081 | hp1 | a0011 | c0036 | t0001 | g0039 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01081 | hp2 | a0002 | c0001 | t0001 | g0130 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01175 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01192 | hp1 | a0002 | c0001 | t0001 | g0030 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01192 | hp2 | a0002 | c0001 | t0001 | g0179 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01243 | hp1 | a0001 | c0011 | t0002 | g0193 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01243 | hp2 | a0012 | c0035 | t0001 | g0083 | AMR | PUR | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0101 | AMR | CLM | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01255 | hp2 | a0001 | c0040 | t0001 | g0195 | AMR | CLM | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01257 | hp1 | a0002 | c0001 | t0001 | g0131 | AMR | CLM | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0102 | AMR | CLM | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01258 | hp1 | a0002 | c0001 | t0001 | g0011 | AMR | CLM | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0104 | AMR | CLM | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0103 | AMR | CLM | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | CLM | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0023 | AMR | CLM | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01433 | hp2 | a0002 | c0001 | t0001 | g0143 | AMR | CLM | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01884 | hp1 | a0002 | c0001 | t0001 | g0171 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01884 | hp2 | a0002 | c0001 | t0001 | g0187 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01891 | hp1 | a0013 | c0028 | t0001 | g0087 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01891 | hp2 | a0002 | c0009 | t0001 | g0025 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01928 | hp1 | a0002 | c0006 | t0001 | g0017 | AMR | PEL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01928 | hp2 | a0001 | c0004 | t0001 | g0126 | AMR | PEL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01934 | hp1 | a0002 | c0001 | t0001 | g0030 | AMR | PEL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01934 | hp2 | a0002 | c0001 | t0001 | g0132 | AMR | PEL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0099 | AMR | PEL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01978 | hp2 | a0002 | c0001 | t0001 | g0010 | AMR | PEL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01981 | hp1 | a0002 | c0006 | t0001 | g0051 | AMR | PEL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01981 | hp2 | a0002 | c0001 | t0001 | g0149 | AMR | PEL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01993 | hp1 | a0002 | c0001 | t0001 | g0028 | AMR | PEL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PEL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02015 | hp1 | a0002 | c0001 | t0001 | g0180 | EAS | KHV | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | KHV | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02027 | hp1 | a0002 | c0001 | t0001 | g0181 | EAS | KHV | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02040 | hp1 | a0002 | c0001 | t0001 | g0162 | EAS | KHV | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02040 | hp2 | a0014 | c0026 | t0001 | g0167 | EAS | KHV | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02055 | hp1 | a0004 | c0015 | t0001 | g0001 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02055 | hp2 | a0001 | c0011 | t0002 | g0197 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02056 | hp1 | a0002 | c0001 | t0001 | g0173 | EAS | KHV | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | KHV | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02071 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | KHV | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02074 | hp1 | a0002 | c0001 | t0001 | g0185 | EAS | KHV | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | KHV | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02083 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | KHV | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02135 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | KHV | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02135 | hp2 | a0001 | c0004 | t0002 | g0027 | EAS | KHV | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02145 | hp1 | a0015 | c0041 | t0001 | g0040 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0092 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02257 | hp1 | a0002 | c0009 | t0001 | g0025 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02257 | hp2 | a0002 | c0001 | t0001 | g0188 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02258 | hp1 | a0001 | c0007 | t0001 | g0020 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02258 | hp2 | a0001 | c0010 | t0002 | g0009 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02280 | hp1 | a0001 | c0007 | t0001 | g0004 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02280 | hp2 | a0002 | c0001 | t0001 | g0029 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02451 | hp1 | a0002 | c0001 | t0001 | g0078 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02451 | hp2 | a0001 | c0003 | t0002 | g0021 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02572 | hp1 | a0001 | c0008 | t0001 | g0113 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02572 | hp2 | a0001 | c0003 | t0002 | g0109 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02602 | hp1 | a0002 | c0001 | t0001 | g0161 | SAS | PJL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0067 | SAS | PJL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02615 | hp2 | a0001 | c0007 | t0001 | g0020 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02622 | hp1 | a0001 | c0003 | t0002 | g0021 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02622 | hp2 | a0001 | c0012 | t0001 | g0116 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02630 | hp1 | a0002 | c0001 | t0001 | g0012 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0085 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02647 | hp1 | a0001 | c0011 | t0002 | g0183 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02647 | hp2 | a0001 | c0008 | t0001 | g0115 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02723 | hp1 | a0001 | c0003 | t0002 | g0041 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0084 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02809 | hp1 | a0002 | c0006 | t0001 | g0090 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02809 | hp2 | a0016 | c0021 | t0002 | g0094 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02818 | hp1 | a0005 | c0019 | t0001 | g0086 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02818 | hp2 | a0001 | c0003 | t0002 | g0038 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02886 | hp1 | a0001 | c0039 | t0002 | g0196 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02886 | hp2 | a0006 | c0016 | t0001 | g0011 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02896 | hp1 | a0001 | c0008 | t0001 | g0034 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02896 | hp2 | a0001 | c0007 | t0001 | g0004 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02897 | hp1 | a0002 | c0001 | t0001 | g0134 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02897 | hp2 | a0001 | c0007 | t0001 | g0004 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0073 | AFR | ESN | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02922 | hp2 | a0002 | c0001 | t0001 | g0029 | AFR | ESN | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02965 | hp1 | a0001 | c0010 | t0002 | g0009 | AFR | ESN | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02965 | hp2 | a0001 | c0008 | t0001 | g0111 | AFR | ESN | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02970 | hp1 | a0003 | c0005 | t0001 | g0013 | AFR | ESN | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | ESN | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02976 | hp1 | a0005 | c0019 | t0001 | g0082 | AFR | ESN | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02976 | hp2 | a0002 | c0001 | t0001 | g0128 | AFR | ESN | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0037 | SAS | PJL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03017 | hp2 | a0002 | c0001 | t0001 | g0189 | SAS | PJL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03098 | hp1 | a0001 | c0010 | t0002 | g0080 | AFR | MSL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0118 | AFR | MSL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03130 | hp1 | a0006 | c0016 | t0001 | g0011 | AFR | ESN | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03130 | hp2 | a0003 | c0005 | t0001 | g0013 | AFR | ESN | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03139 | hp1 | a0002 | c0001 | t0001 | g0127 | AFR | ESN | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0081 | AFR | ESN | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03195 | hp1 | a0001 | c0010 | t0002 | g0072 | AFR | ESN | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03195 | hp2 | a0003 | c0005 | t0001 | g0152 | AFR | ESN | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03209 | hp1 | a0001 | c0020 | t0002 | g0192 | AFR | MSL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03209 | hp2 | a0007 | c0013 | t0001 | g0095 | AFR | MSL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0119 | AFR | MSL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0096 | AFR | MSL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03453 | hp1 | a0002 | c0031 | t0002 | g0117 | AFR | MSL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03453 | hp2 | a0002 | c0009 | t0001 | g0142 | AFR | MSL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03486 | hp1 | a0001 | c0008 | t0001 | g0112 | AFR | MSL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03486 | hp2 | a0003 | c0005 | t0001 | g0148 | AFR | MSL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03492 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0107 | SAS | PJL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03516 | hp1 | a0001 | c0004 | t0001 | g0147 | AFR | ESN | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03516 | hp2 | a0001 | c0008 | t0001 | g0114 | AFR | ESN | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03540 | hp1 | a0001 | c0042 | t0001 | g0091 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0075 | AFR | GWD | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03579 | hp1 | a0002 | c0009 | t0001 | g0024 | AFR | MSL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03579 | hp2 | a0001 | c0011 | t0002 | g0191 | AFR | MSL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03654 | hp1 | a0002 | c0001 | t0001 | g0121 | SAS | PJL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03654 | hp2 | a0002 | c0030 | t0001 | g0177 | SAS | PJL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03669 | hp1 | a0002 | c0001 | t0001 | g0178 | SAS | PJL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0053 | SAS | PJL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0100 | SAS | PJL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03831 | hp1 | a0001 | c0012 | t0001 | g0137 | SAS | BEB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03831 | hp2 | a0002 | c0001 | t0001 | g0163 | SAS | BEB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG04199 | hp1 | a0002 | c0001 | t0001 | g0120 | SAS | STU | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG04199 | hp2 | a0001 | c0004 | t0002 | g0124 | SAS | STU | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | STU | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG04204 | hp2 | a0002 | c0022 | t0001 | g0129 | SAS | STU | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | STU | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG04228 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | STU | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0076 | AFR | YRI | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18522 | hp2 | a0017 | c0037 | t0001 | g0088 | AFR | YRI | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18747 | hp2 | a0008 | c0018 | t0001 | g0015 | EAS | CHB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0074 | AFR | YRI | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18906 | hp2 | a0002 | c0001 | t0001 | g0145 | AFR | YRI | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18939 | hp2 | a0002 | c0001 | t0001 | g0155 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18941 | hp1 | a0002 | c0001 | t0001 | g0160 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18943 | hp1 | a0001 | c0003 | t0001 | g0098 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18943 | hp2 | a0002 | c0001 | t0001 | g0158 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18945 | hp1 | a0008 | c0018 | t0001 | g0015 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18945 | hp2 | a0002 | c0001 | t0001 | g0164 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18947 | hp1 | a0018 | c0024 | t0001 | g0026 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18948 | hp2 | a0002 | c0006 | t0001 | g0052 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18950 | hp2 | a0001 | c0038 | t0001 | g0003 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18951 | hp1 | a0009 | c0017 | t0001 | g0032 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18951 | hp2 | a0002 | c0001 | t0001 | g0144 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18961 | hp1 | a0002 | c0001 | t0001 | g0172 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18961 | hp2 | a0019 | c0043 | t0001 | g0063 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18962 | hp1 | a0001 | c0032 | t0001 | g0186 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18962 | hp2 | a0020 | c0034 | t0001 | g0159 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18963 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18965 | hp2 | a0003 | c0005 | t0001 | g0122 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18968 | hp1 | a0002 | c0001 | t0001 | g0033 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18970 | hp1 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18975 | hp1 | a0002 | c0014 | t0001 | g0168 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18979 | hp1 | a0002 | c0001 | t0001 | g0169 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18981 | hp1 | a0002 | c0001 | t0001 | g0170 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18984 | hp1 | a0002 | c0001 | t0001 | g0010 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18984 | hp2 | a0021 | c0023 | t0001 | g0026 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18985 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18989 | hp1 | a0002 | c0001 | t0001 | g0166 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18998 | hp1 | a0001 | c0004 | t0002 | g0140 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18998 | hp2 | a0002 | c0001 | t0001 | g0176 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA18999 | hp2 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19000 | hp1 | a0002 | c0006 | t0001 | g0017 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19002 | hp2 | a0002 | c0001 | t0001 | g0174 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19004 | hp1 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19005 | hp1 | a0002 | c0001 | t0001 | g0175 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19010 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19011 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19012 | hp2 | a0001 | c0004 | t0002 | g0141 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19030 | hp1 | a0002 | c0006 | t0001 | g0089 | AFR | LWK | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19030 | hp2 | a0007 | c0013 | t0001 | g0093 | AFR | LWK | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19043 | hp1 | a0001 | c0010 | t0002 | g0009 | AFR | LWK | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19043 | hp2 | a0001 | c0020 | t0002 | g0190 | AFR | LWK | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19055 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19060 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19063 | hp2 | a0002 | c0001 | t0001 | g0028 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19064 | hp2 | a0002 | c0001 | t0001 | g0031 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19065 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19066 | hp2 | a0003 | c0005 | t0001 | g0123 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19068 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19070 | hp2 | a0002 | c0014 | t0001 | g0165 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19076 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19077 | hp1 | a0002 | c0001 | t0001 | g0157 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19081 | hp1 | a0002 | c0029 | t0001 | g0001 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19084 | hp2 | a0002 | c0001 | t0001 | g0156 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19089 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19091 | hp1 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19091 | hp2 | a0009 | c0017 | t0001 | g0032 | EAS | JPT | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19240 | hp1 | a0002 | c0009 | t0001 | g0135 | AFR | YRI | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA19240 | hp2 | a0001 | c0012 | t0001 | g0154 | AFR | YRI | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA20129 | hp1 | a0001 | c0007 | t0001 | g0004 | AFR | ASW | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA20129 | hp2 | a0002 | c0001 | t0001 | g0001 | AFR | ASW | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA20752 | hp1 | a0002 | c0006 | t0001 | g0049 | EUR | TSI | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA20752 | hp2 | a0001 | c0012 | t0001 | g0138 | EUR | TSI | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA20805 | hp1 | a0002 | c0001 | t0001 | g0125 | EUR | TSI | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA20805 | hp2 | a0002 | c0001 | t0001 | g0023 | EUR | TSI | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0106 | SAS | GIH | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA20905 | hp2 | a0022 | c0027 | t0001 | g0001 | SAS | GIH | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01123 | hp1 | a0002 | c0001 | t0001 | g0031 | AMR | CLM | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG01123 | hp2 | a0001 | c0004 | t0001 | g0136 | AMR | CLM | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02109 | hp1 | a0001 | c0007 | t0001 | g0004 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02109 | hp2 | a0002 | c0009 | t0001 | g0024 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02486 | hp1 | a0003 | c0005 | t0001 | g0013 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG02486 | hp2 | a0001 | c0003 | t0002 | g0108 | AFR | ACB | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0043 | AFR | MSL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG03471 | hp2 | a0002 | c0001 | t0001 | g0012 | AFR | MSL | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0077 | AFR | USA | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| HG06807 | hp2 | a0002 | c0001 | t0001 | g0012 | AFR | USA | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA20300 | hp1 | a0002 | c0001 | t0001 | g0010 | AFR | USA | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| NA20300 | hp2 | a0001 | c0004 | t0001 | g0139 | AFR | USA | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0097 | REF | REF | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| homoSapiens | grch38p0 | a0002 | c0001 | t0001 | g0001 | REF | REF | CUL9_chr6_43177196_43229587 | CUL9 | chr6 | 43177196 | 43229587 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:43184726 | C | T | 1 | a0019 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.416C>T | p.Thr139Met | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 2/41 | 479/7759 | 416/7554 | 139/2517 | chr6 | 43184726 | |||
| chr6:43185527 | C | T | 1 | a0015 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.667C>T | p.Arg223Cys | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 3/41 | 730/7759 | 667/7554 | 223/2517 | chr6 | 43185527 | |||
| chr6:43186049 | G | A | 1 | a0010 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.845G>A | p.Gly282Glu | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 4/41 | 908/7759 | 845/7554 | 282/2517 | chr6 | 43186049 | |||
| chr6:43187407 | A | G | 2 | a0009 a0020 |
3 | NA18951.hp1 NA18962.hp2 NA19091.hp2 |
missense_variant | MODERATE | c.1549A>G | p.Ile517Val | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 6/41 | 1612/7759 | 1549/7554 | 517/2517 | chr6 | 43187407 | |||
| chr6:43187720 | G | C | 1 | a0012 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.1589G>C | p.Gly530Ala | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 7/41 | 1652/7759 | 1589/7554 | 530/2517 | chr6 | 43187720 | |||
| chr6:43187881 | A | G | 1 | a0006 | 2 | HG02886.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.1750A>G | p.Thr584Ala | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 7/41 | 1813/7759 | 1750/7554 | 584/2517 | chr6 | 43187881 | |||
| chr6:43187980 | G | A | 1 | a0011 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.1849G>A | p.Glu617Lys | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 7/41 | 1912/7759 | 1849/7554 | 617/2517 | chr6 | 43187980 | |||
| chr6:43188709 | C | T | 1 | a0018 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.2174C>T | p.Ser725Leu | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/41 | 2237/7759 | 2174/7554 | 725/2517 | chr6 | 43188709 | |||
| chr6:43193002 | G | A | 1 | a0019 | 1 | NA18961.hp2 | missense_variant&splice_region_variant | MODERATE | c.2182G>A | p.Glu728Lys | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/41 | 2245/7759 | 2182/7554 | 728/2517 | chr6 | 43193002 | |||
| chr6:43193003 | A | T | 1 | a0019 | 1 | NA18961.hp2 | missense_variant&splice_region_variant | MODERATE | c.2183A>T | p.Glu728Val | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/41 | 2246/7759 | 2183/7554 | 728/2517 | chr6 | 43193003 | |||
| chr6:43196199 | G | A | 1 | a0014 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.2519G>A | p.Arg840His | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 10/41 | 2582/7759 | 2519/7554 | 840/2517 | chr6 | 43196199 | |||
| chr6:43198673 | TGGG | T | 1 | a0003 | 8 | HG00639.hp1 HG02486.hp1 HG02970.hp1 others(5): Show |
disruptive_inframe_deletion | MODERATE | c.2871_2873delGGG | p.Gly958del | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 12/41 | 2934/7759 | 2871/7554 | 957/2517 | INFO_REALIGN_3_PRIME | chr6 | 43198673 | ||
| chr6:43200698 | G | A | 1 | a0022 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.3511G>A | p.Glu1171Lys | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/41 | 3574/7759 | 3511/7554 | 1171/2517 | chr6 | 43200698 | |||
| chr6:43203502 | G | A | 1 | a0013 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.3935G>A | p.Arg1312His | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 19/41 | 3998/7759 | 3935/7554 | 1312/2517 | chr6 | 43203502 | |||
| chr6:43204843 | G | A | 1 | a0008 | 2 | NA18747.hp2 NA18945.hp1 |
missense_variant | MODERATE | c.4435G>A | p.Val1479Met | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 22/41 | 4498/7759 | 4435/7554 | 1479/2517 | chr6 | 43204843 | |||
| chr6:43205035 | C | T | 2 | a0007 a0016 |
3 | HG02809.hp2 HG03209.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.4552C>T | p.Pro1518Ser | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 23/41 | 4615/7759 | 4552/7554 | 1518/2517 | chr6 | 43205035 | |||
| chr6:43206170 | C | G | 1 | a0012 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.4957C>G | p.Gln1653Glu | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 25/41 | 5020/7759 | 4957/7554 | 1653/2517 | chr6 | 43206170 | |||
| chr6:43215250 | C | T | 1 | a0017 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.5860C>T | p.Pro1954Ser | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 30/41 | 5923/7759 | 5860/7554 | 1954/2517 | chr6 | 43215250 | |||
| chr6:43216394 | A | C | 12 | a0001 a0005 a0007 others(9): Show |
149 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(146): Show |
missense_variant | MODERATE | c.6173A>C | p.His2058Pro | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/41 | 6236/7759 | 6173/7554 | 2058/2517 | chr6 | 43216394 | |||
| chr6:43216403 | A | G | 1 | a0007 | 2 | HG03209.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.6182A>G | p.Gln2061Arg | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/41 | 6245/7759 | 6182/7554 | 2061/2517 | chr6 | 43216403 | |||
| chr6:43220862 | C | T | 1 | a0004 | 2 | HG00738.hp1 HG02055.hp1 |
missense_variant | MODERATE | c.6539C>T | p.Thr2180Ile | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 33/41 | 6602/7759 | 6539/7554 | 2180/2517 | chr6 | 43220862 | |||
| chr6:43221695 | G | A | 1 | a0005 | 2 | HG02818.hp1 HG02976.hp1 |
missense_variant | MODERATE | c.6763G>A | p.Ala2255Thr | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 35/41 | 6826/7759 | 6763/7554 | 2255/2517 | chr6 | 43221695 | |||
| chr6:43222556 | G | A | 1 | a0021 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.6947G>A | p.Arg2316Gln | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 37/41 | 7010/7759 | 6947/7554 | 2316/2517 | chr6 | 43222556 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:43184547 | G | C | 2 | a0007c0013 a0016c0021 |
3 | HG02809.hp2 HG03209.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.237G>C | p.Leu79Leu | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 2/41 | 300/7759 | 237/7554 | 79/2517 | chr6 | 43184547 | |||
| chr6:43184628 | C | A | 5 | a0001c0008 a0001c0012 a0002c0022 others(2): Show |
13 | HG02572.hp1 HG02622.hp2 HG02647.hp2 others(10): Show |
synonymous_variant | LOW | c.318C>A | p.Gly106Gly | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 2/41 | 381/7759 | 318/7554 | 106/2517 | chr6 | 43184628 | |||
| chr6:43184766 | C | T | 1 | a0001c0042 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.456C>T | p.Tyr152Tyr | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 2/41 | 519/7759 | 456/7554 | 152/2517 | chr6 | 43184766 | |||
| chr6:43184835 | A | G | 20 | a0001c0002 a0001c0003 a0001c0007 others(17): Show |
133 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(130): Show |
synonymous_variant | LOW | c.525A>G | p.Leu175Leu | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 2/41 | 588/7759 | 525/7554 | 175/2517 | chr6 | 43184835 | |||
| chr6:43186098 | G | A | 1 | a0002c0014 | 2 | NA18975.hp1 NA19070.hp2 |
synonymous_variant | LOW | c.894G>A | p.Arg298Arg | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 4/41 | 957/7759 | 894/7554 | 298/2517 | chr6 | 43186098 | |||
| chr6:43186326 | C | T | 4 | a0001c0011 a0001c0020 a0001c0039 others(1): Show |
9 | HG00741.hp2 HG01243.hp1 HG01255.hp2 others(6): Show |
synonymous_variant | LOW | c.1122C>T | p.Gly374Gly | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 4/41 | 1185/7759 | 1122/7554 | 374/2517 | chr6 | 43186326 | |||
| chr6:43187307 | C | T | 1 | a0001c0020 | 2 | HG03209.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.1449C>T | p.Pro483Pro | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 6/41 | 1512/7759 | 1449/7554 | 483/2517 | chr6 | 43187307 | |||
| chr6:43199317 | C | T | 1 | a0001c0042 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.3102C>T | p.His1034His | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 13/41 | 3165/7759 | 3102/7554 | 1034/2517 | chr6 | 43199317 | |||
| chr6:43200802 | C | A | 1 | a0002c0009 | 6 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(3): Show |
synonymous_variant | LOW | c.3615C>A | p.Ile1205Ile | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/41 | 3678/7759 | 3615/7554 | 1205/2517 | chr6 | 43200802 | |||
| chr6:43202746 | C | T | 1 | a0001c0038 | 1 | NA18950.hp2 | synonymous_variant | LOW | c.3678C>T | p.Asp1226Asp | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 17/41 | 3741/7759 | 3678/7554 | 1226/2517 | chr6 | 43202746 | |||
| chr6:43203863 | G | A | 1 | a0002c0029 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.4035G>A | p.Arg1345Arg | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 20/41 | 4098/7759 | 4035/7554 | 1345/2517 | chr6 | 43203863 | |||
| chr6:43204412 | G | A | 1 | a0001c0010 | 5 | HG02258.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
synonymous_variant | LOW | c.4212G>A | p.Gln1404Gln | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 21/41 | 4275/7759 | 4212/7554 | 1404/2517 | chr6 | 43204412 | |||
| chr6:43204440 | C | A | 1 | a0001c0039 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.4240C>A | p.Arg1414Arg | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 21/41 | 4303/7759 | 4240/7554 | 1414/2517 | chr6 | 43204440 | |||
| chr6:43204791 | G | A | 1 | a0002c0030 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.4383G>A | p.Ser1461Ser | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 22/41 | 4446/7759 | 4383/7554 | 1461/2517 | chr6 | 43204791 | |||
| chr6:43205295 | A | G | 1 | a0002c0033 | 1 | HG01070.hp1 | synonymous_variant | LOW | c.4665A>G | p.Gln1555Gln | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 24/41 | 4728/7759 | 4665/7554 | 1555/2517 | chr6 | 43205295 | |||
| chr6:43206169 | C | A | 1 | a0012c0035 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.4956C>A | p.Leu1652Leu | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 25/41 | 5019/7759 | 4956/7554 | 1652/2517 | chr6 | 43206169 | |||
| chr6:43213560 | A | G | 2 | a0001c0007 a0001c0042 |
8 | HG02109.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
synonymous_variant | LOW | c.5481A>G | p.Pro1827Pro | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 28/41 | 5544/7759 | 5481/7554 | 1827/2517 | chr6 | 43213560 | |||
| chr6:43215168 | C | T | 1 | a0004c0015 | 2 | HG00738.hp1 HG02055.hp1 |
synonymous_variant | LOW | c.5778C>T | p.Val1926Val | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 30/41 | 5841/7759 | 5778/7554 | 1926/2517 | chr6 | 43215168 | |||
| chr6:43221202 | C | T | 13 | a0001c0003 a0001c0004 a0001c0010 others(10): Show |
62 | HG00558.hp2 HG00741.hp1 HG00741.hp2 others(59): Show |
synonymous_variant | LOW | c.6633C>T | p.Asp2211Asp | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 34/41 | 6696/7759 | 6633/7554 | 2211/2517 | chr6 | 43221202 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:43224531 | T | G | 9 | a0001c0003t0002 a0001c0004t0002 a0001c0010t0002 others(6): Show |
27 | HG00558.hp2 HG00741.hp2 HG01070.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*86T>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 41/41 | 86 | chr6 | 43224531 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:43182299 | C | T | 8 | a0001c0011t0002g0191 a0001c0011t0002g0193 a0001c0011t0002g0194 others(5): Show |
8 | HG00741.hp2 HG01243.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+50C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43182299 | |||||||
| chr6:43182564 | G | C | 97 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0006 others(94): Show |
129 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.-10+315G>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43182564 | |||||||
| chr6:43182586 | C | G | 3 | a0001c0003t0002g0021 a0001c0003t0002g0108 a0001c0003t0002g0109 |
4 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+337C>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43182586 | |||||||
| chr6:43182617 | T | TA | 8 | a0001c0008t0001g0111 a0001c0008t0001g0112 a0001c0008t0001g0113 others(5): Show |
8 | HG01070.hp1 HG02572.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+370dupA | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr6 | 43182617 | ||||||
| chr6:43182782 | A | G | 31 | a0001c0002t0001g0079 a0001c0003t0001g0081 a0001c0003t0001g0084 others(28): Show |
38 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.-10+533A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43182782 | |||||||
| chr6:43182821 | C | T | 1 | a0002c0001t0001g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-10+572C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43182821 | |||||||
| chr6:43182851 | A | T | 10 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0100 others(7): Show |
10 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+602A>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43182851 | |||||||
| chr6:43183111 | A | C | 1 | a0001c0003t0001g0096 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-10+862A>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43183111 | |||||||
| chr6:43183224 | C | T | 2 | a0001c0003t0002g0108 a0001c0003t0002g0109 |
2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-10+975C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43183224 | |||||||
| chr6:43183242 | T | C | 98 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0006 others(95): Show |
130 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.-10+993T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43183242 | |||||||
| chr6:43183406 | C | T | 2 | a0002c0001t0001g0187 a0002c0001t0001g0188 |
2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-9-896C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43183406 | |||||||
| chr6:43183448 | C | T | 10 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0100 others(7): Show |
10 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9-854C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43183448 | |||||||
| chr6:43183573 | T | G | 2 | a0002c0001t0001g0120 a0002c0001t0001g0121 |
2 | HG03654.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-9-729T>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43183573 | |||||||
| chr6:43183701 | CCTTT | C | 95 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0006 others(92): Show |
126 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(123): Show |
intron_variant | MODIFIER | c.-9-597_-9-594delTC others(2): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr6 | 43183701 | ||||||
| chr6:43183705 | T | C | 1 | a0001c0011t0002g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-9-597T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43183705 | |||||||
| chr6:43183705 | T | TCTTC | 12 | a0002c0001t0001g0001 a0002c0001t0001g0005 a0002c0001t0001g0007 others(9): Show |
13 | HG01175.hp1 HG01192.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9-566_-9-563dupTC others(2): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr6 | 43183705 | ||||||
| chr6:43183705 | TCTTC | T | 23 | a0001c0002t0001g0014 a0001c0004t0001g0126 a0001c0004t0001g0139 others(20): Show |
24 | HG00558.hp2 HG01928.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.-9-566_-9-563delTC others(2): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr6 | 43183705 | ||||||
| chr6:43183706 | C | A | 2 | a0003c0005t0001g0122 a0003c0005t0001g0123 |
2 | NA18965.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-9-596C>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43183706 | |||||||
| chr6:43183709 | C | T | 1 | a0001c0011t0002g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-9-593C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43183709 | |||||||
| chr6:43183713 | C | T | 95 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0006 others(92): Show |
126 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(123): Show |
intron_variant | MODIFIER | c.-9-589C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43183713 | |||||||
| chr6:43183717 | C | T | 3 | a0001c0032t0001g0186 a0002c0001t0001g0185 a0008c0018t0001g0015 |
4 | HG02074.hp1 NA18747.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-585C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43183717 | |||||||
| chr6:43183746 | C | T | 39 | a0001c0002t0001g0073 a0001c0002t0001g0079 a0001c0003t0001g0074 others(36): Show |
46 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.-9-556C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43183746 | |||||||
| chr6:43183814 | G | A | 1 | a0001c0003t0002g0108 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-9-488G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43183814 | |||||||
| chr6:43183942 | G | C | 3 | a0001c0004t0001g0126 a0001c0004t0002g0124 a0002c0001t0001g0125 |
3 | HG01928.hp2 HG04199.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-9-360G>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43183942 | |||||||
| chr6:43184005 | C | A | 1 | a0001c0020t0002g0190 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-297C>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43184005 | |||||||
| chr6:43184281 | C | T | 3 | a0007c0013t0001g0093 a0007c0013t0001g0095 a0016c0021t0002g0094 |
3 | HG02809.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-9-21C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 1/40 | chr6 | 43184281 | |||||||
| chr6:43184985 | C | T | 61 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0006 others(58): Show |
88 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.595+80C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 2/40 | chr6 | 43184985 | |||||||
| chr6:43185055 | A | G | 1 | a0003c0005t0001g0182 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.595+150A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 2/40 | chr6 | 43185055 | |||||||
| chr6:43185213 | A | AT | 8 | a0001c0002t0001g0073 a0001c0003t0001g0074 a0001c0003t0001g0075 others(5): Show |
8 | HG02922.hp1 HG03098.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.596-236dupT | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 2/40 | INFO_REALIGN_3_PRIME | chr6 | 43185213 | ||||||
| chr6:43185671 | G | A | 11 | a0001c0002t0001g0079 a0001c0003t0001g0081 a0001c0003t0001g0084 others(8): Show |
16 | HG01243.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.750+61G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 3/40 | chr6 | 43185671 | |||||||
| chr6:43185746 | G | A | 10 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0100 others(7): Show |
10 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.750+136G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 3/40 | chr6 | 43185746 | |||||||
| chr6:43185908 | C | A | 2 | a0002c0001t0001g0127 a0002c0001t0001g0128 |
2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.751-47C>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 3/40 | chr6 | 43185908 | |||||||
| chr6:43185916 | A | G | 1 | a0002c0031t0002g0117 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.751-39A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 3/40 | chr6 | 43185916 | |||||||
| chr6:43186506 | G | A | 1 | a0002c0022t0001g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1251+51G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 4/40 | chr6 | 43186506 | |||||||
| chr6:43186587 | G | T | 3 | a0001c0003t0001g0092 a0001c0042t0001g0091 a0002c0006t0001g0090 |
3 | HG02145.hp2 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1251+132G>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 4/40 | chr6 | 43186587 | |||||||
| chr6:43186711 | A | G | 2 | a0002c0001t0001g0180 a0002c0001t0001g0181 |
2 | HG02015.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1252-249A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 4/40 | chr6 | 43186711 | |||||||
| chr6:43187694 | A | G | 27 | a0001c0002t0001g0003 a0001c0002t0001g0006 a0001c0002t0001g0008 others(24): Show |
43 | HG00423.hp1 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1582-19A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 6/40 | chr6 | 43187694 | |||||||
| chr6:43188422 | T | A | 4 | a0002c0001t0001g0022 a0002c0001t0001g0130 a0002c0001t0001g0131 others(1): Show |
5 | HG00642.hp2 HG00738.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1988-101T>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 7/40 | chr6 | 43188422 | |||||||
| chr6:43188423 | G | A | 1 | a0002c0001t0001g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1988-100G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 7/40 | chr6 | 43188423 | |||||||
| chr6:43188847 | G | A | 1 | a0001c0011t0002g0191 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2180+132G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43188847 | |||||||
| chr6:43189055 | G | A | 1 | a0002c0001t0001g0133 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2180+340G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43189055 | |||||||
| chr6:43189082 | G | T | 1 | a0001c0002t0001g0053 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2180+367G>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43189082 | |||||||
| chr6:43189137 | C | CT | 99 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0006 others(96): Show |
133 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.2180+433dupT | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43189137 | ||||||
| chr6:43189222 | G | A | 1 | a0002c0001t0001g0023 | 2 | HG01433.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2180+507G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43189222 | |||||||
| chr6:43189253 | G | A | 21 | a0001c0002t0001g0079 a0001c0003t0001g0081 a0001c0003t0001g0084 others(18): Show |
26 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.2180+538G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43189253 | |||||||
| chr6:43189265 | C | T | 1 | a0002c0001t0001g0179 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2180+550C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43189265 | |||||||
| chr6:43189282 | C | T | 10 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0100 others(7): Show |
10 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2180+567C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43189282 | |||||||
| chr6:43189407 | A | G | 1 | a0002c0001t0001g0078 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2180+692A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43189407 | |||||||
| chr6:43189484 | C | T | 10 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0100 others(7): Show |
10 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2180+769C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43189484 | |||||||
| chr6:43189694 | C | T | 1 | a0001c0003t0001g0077 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2180+979C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43189694 | |||||||
| chr6:43189919 | A | G | 2 | a0002c0001t0001g0127 a0002c0001t0001g0128 |
2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2180+1204A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43189919 | |||||||
| chr6:43190017 | CT | C | 147 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0006 others(144): Show |
191 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.2180+1314delT | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43190017 | ||||||
| chr6:43190017 | CTT | C | 6 | a0002c0001t0001g0134 a0002c0009t0001g0024 a0002c0009t0001g0025 others(3): Show |
8 | HG01070.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2180+1313_2180+131 others(6): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43190017 | ||||||
| chr6:43190088 | A | G | 22 | a0001c0003t0001g0081 a0001c0003t0001g0084 a0001c0003t0001g0085 others(19): Show |
27 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.2180+1373A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43190088 | |||||||
| chr6:43190103 | T | G | 11 | a0001c0002t0001g0003 a0001c0002t0001g0006 a0001c0002t0001g0054 others(8): Show |
20 | HG02027.hp2 HG02056.hp2 NA18747.hp1 others(17): Show |
intron_variant | MODIFIER | c.2180+1388T>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43190103 | |||||||
| chr6:43190151 | C | T | 1 | a0001c0002t0001g0019 | 2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2180+1436C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43190151 | |||||||
| chr6:43190170 | G | A | 27 | a0001c0002t0001g0073 a0001c0003t0001g0074 a0001c0003t0001g0075 others(24): Show |
28 | HG00558.hp2 HG01123.hp2 HG01928.hp2 others(25): Show |
intron_variant | MODIFIER | c.2180+1455G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43190170 | |||||||
| chr6:43190178 | A | G | 2 | a0002c0006t0001g0089 a0017c0037t0001g0088 |
2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2180+1463A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43190178 | |||||||
| chr6:43190298 | G | GT | 8 | a0001c0011t0002g0183 a0001c0011t0002g0191 a0001c0011t0002g0193 others(5): Show |
8 | HG00741.hp2 HG01243.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.2180+1594dupT | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43190298 | ||||||
| chr6:43190298 | GT | G | 63 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0006 others(60): Show |
94 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.2180+1594delT | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43190298 | ||||||
| chr6:43190331 | C | G | 1 | a0001c0039t0002g0196 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2180+1616C>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43190331 | |||||||
| chr6:43190476 | A | G | 1 | a0001c0011t0002g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2180+1761A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43190476 | |||||||
| chr6:43190543 | GA | G | 4 | a0001c0002t0001g0047 a0001c0002t0001g0048 a0001c0002t0001g0050 others(1): Show |
4 | HG06807.hp1 NA18952.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.2180+1836delA | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43190543 | ||||||
| chr6:43191252 | T | TTG | 32 | a0001c0002t0001g0054 a0001c0002t0001g0071 a0001c0003t0001g0098 others(29): Show |
41 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.2181-1710_2181-170 others(6): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191252 | ||||||
| chr6:43191252 | T | TTGTG | 28 | a0001c0002t0001g0003 a0001c0002t0001g0055 a0001c0002t0001g0056 others(25): Show |
34 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.2181-1712_2181-170 others(8): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191252 | ||||||
| chr6:43191252 | T | TTGTGTG | 3 | a0001c0002t0001g0006 a0001c0002t0001g0060 a0001c0008t0001g0034 |
6 | HG02027.hp2 HG02896.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2181-1714_2181-170 others(10): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191252 | ||||||
| chr6:43191252 | T | TTGTGTGT others(1): Show |
12 | a0001c0002t0001g0061 a0001c0002t0001g0073 a0001c0003t0001g0074 others(9): Show |
12 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.2181-1716_2181-170 others(12): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191252 | ||||||
| chr6:43191252 | T | TTGTGTGT others(3): Show |
6 | a0001c0003t0001g0075 a0001c0003t0001g0084 a0001c0003t0001g0085 others(3): Show |
6 | HG01255.hp2 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2181-1718_2181-170 others(14): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191252 | ||||||
| chr6:43191252 | T | TTGTGTGT others(5): Show |
2 | a0001c0003t0001g0077 a0005c0019t0001g0086 |
2 | HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2181-1720_2181-170 others(16): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191252 | ||||||
| chr6:43191252 | T | TTGTGTGT others(7): Show |
3 | a0001c0003t0001g0076 a0001c0003t0001g0118 a0001c0003t0001g0119 |
3 | HG03098.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2181-1722_2181-170 others(18): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191252 | ||||||
| chr6:43191252 | TTG | T | 8 | a0001c0002t0001g0035 a0001c0002t0001g0062 a0002c0001t0001g0023 others(5): Show |
11 | HG01123.hp1 HG01433.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.2181-1710_2181-170 others(6): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191252 | ||||||
| chr6:43191252 | TTGTGTG | T | 2 | a0001c0012t0001g0116 a0017c0037t0001g0088 |
2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2181-1714_2181-170 others(10): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191252 | ||||||
| chr6:43191252 | TTGTGTGT others(5): Show |
T | 20 | a0001c0032t0001g0186 a0002c0001t0001g0010 a0002c0001t0001g0011 others(17): Show |
29 | HG01070.hp1 HG01258.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.2181-1720_2181-170 others(16): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191252 | ||||||
| chr6:43191291 | T | C | 1 | a0001c0042t0001g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2181-1710T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43191291 | |||||||
| chr6:43191293 | C | T | 2 | a0001c0002t0001g0079 a0001c0003t0001g0096 |
2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2181-1708C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43191293 | |||||||
| chr6:43191295 | T | C | 1 | a0001c0002t0001g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2181-1706T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43191295 | |||||||
| chr6:43191307 | T | G | 6 | a0001c0004t0001g0139 a0002c0001t0001g0022 a0002c0001t0001g0130 others(3): Show |
7 | HG00642.hp2 HG00738.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.2181-1694T>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43191307 | |||||||
| chr6:43191307 | TTTTG | T | 7 | a0001c0002t0001g0073 a0001c0003t0001g0074 a0001c0003t0001g0075 others(4): Show |
7 | HG02922.hp1 HG03098.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.2181-1686_2181-168 others(8): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191307 | ||||||
| chr6:43191310 | T | G | 23 | a0001c0002t0001g0079 a0001c0003t0001g0081 a0001c0003t0001g0092 others(20): Show |
28 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.2181-1691T>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43191310 | |||||||
| chr6:43191311 | G | GT | 6 | a0001c0003t0001g0084 a0001c0003t0001g0085 a0001c0003t0001g0096 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2181-1687dupT | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191311 | ||||||
| chr6:43191311 | G | T | 23 | a0001c0002t0001g0079 a0001c0003t0001g0081 a0001c0003t0001g0092 others(20): Show |
28 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.2181-1690G>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43191311 | |||||||
| chr6:43191315 | G | T | 1 | a0001c0002t0001g0002 | 2 | HG03704.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2181-1686G>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43191315 | |||||||
| chr6:43191318 | T | C | 1 | a0001c0002t0001g0053 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2181-1683T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43191318 | |||||||
| chr6:43191390 | C | G | 10 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0100 others(7): Show |
10 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2181-1611C>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43191390 | |||||||
| chr6:43191481 | A | AT | 8 | a0001c0007t0001g0004 a0001c0007t0001g0020 a0001c0008t0001g0111 others(5): Show |
15 | HG02056.hp1 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2181-1496dupT | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191481 | A | ATT | 6 | a0001c0004t0002g0140 a0001c0008t0001g0034 a0001c0008t0001g0112 others(3): Show |
6 | HG02572.hp1 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2181-1497_2181-149 others(6): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191481 | A | ATTT | 12 | a0001c0004t0001g0126 a0001c0004t0001g0136 a0001c0004t0001g0139 others(9): Show |
13 | HG00558.hp2 HG01123.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.2181-1498_2181-149 others(7): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191481 | A | ATTTTTTT others(1): Show |
17 | a0001c0003t0001g0074 a0001c0003t0001g0075 a0001c0003t0001g0076 others(14): Show |
19 | HG00741.hp2 HG01243.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.2181-1503_2181-149 others(12): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191481 | A | ATTTTTTT others(3): Show |
1 | a0007c0013t0001g0095 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2181-1505_2181-149 others(14): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191481 | A | ATTTTTTT others(6): Show |
1 | a0017c0037t0001g0088 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2181-1508_2181-149 others(17): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191481 | A | ATTTTTTT others(7): Show |
1 | a0001c0002t0001g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2181-1509_2181-149 others(18): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191481 | A | ATTTTTTT others(9): Show |
1 | a0002c0006t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2181-1511_2181-149 others(20): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191481 | A | ATTTTTTT others(11): Show |
3 | a0001c0003t0001g0081 a0005c0019t0001g0082 a0005c0019t0001g0086 |
3 | HG02818.hp1 HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2181-1513_2181-149 others(22): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191481 | A | ATTTTTTT others(13): Show |
2 | a0001c0003t0001g0084 a0012c0035t0001g0083 |
2 | HG01243.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2181-1515_2181-149 others(24): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191481 | A | ATTTTTTT others(14): Show |
1 | a0001c0003t0001g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2181-1516_2181-149 others(25): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191481 | A | ATTTTTTT others(15): Show |
1 | a0001c0003t0001g0096 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2181-1517_2181-149 others(26): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191481 | A | ATTTTTTT others(17): Show |
2 | a0001c0003t0001g0101 a0001c0012t0001g0116 |
2 | HG01255.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.2181-1519_2181-149 others(28): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191481 | A | ATTTTTTT others(18): Show |
2 | a0001c0003t0001g0102 a0001c0003t0001g0103 |
2 | HG01257.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.2181-1496_2181-149 others(29): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191481 | A | ATTTTTTT others(19): Show |
5 | a0001c0003t0001g0099 a0001c0003t0001g0100 a0001c0003t0001g0104 others(2): Show |
5 | HG00741.hp1 HG01258.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.2181-1496_2181-149 others(30): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191481 | A | ATTTTTTT others(20): Show |
1 | a0001c0003t0001g0107 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2181-1496_2181-149 others(31): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191481 | A | ATTTTTTT others(22): Show |
1 | a0001c0003t0001g0092 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2181-1496_2181-149 others(33): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191481 | AT | A | 5 | a0001c0002t0001g0016 a0001c0002t0001g0046 a0002c0001t0001g0133 others(2): Show |
6 | HG00323.hp1 HG00733.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.2181-1496delT | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191481 | ATT | A | 40 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0006 others(37): Show |
65 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.2181-1497_2181-149 others(6): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191481 | ATTT | A | 6 | a0001c0002t0001g0036 a0001c0002t0001g0037 a0001c0002t0001g0055 others(3): Show |
6 | HG02015.hp2 HG03017.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.2181-1498_2181-149 others(7): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191481 | ||||||
| chr6:43191564 | T | G | 24 | a0001c0002t0001g0079 a0001c0003t0001g0081 a0001c0003t0001g0084 others(21): Show |
29 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.2181-1437T>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43191564 | |||||||
| chr6:43191607 | CAG | C | 5 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0105 others(2): Show |
5 | HG00741.hp1 HG01255.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.2181-1391_2181-139 others(6): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43191607 | ||||||
| chr6:43191681 | T | C | 1 | a0002c0001t0001g0161 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2181-1320T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43191681 | |||||||
| chr6:43192059 | C | CT | 12 | a0001c0002t0001g0059 a0001c0003t0001g0100 a0001c0003t0001g0102 others(9): Show |
16 | HG01123.hp2 HG01257.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.2181-922dupT | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43192059 | ||||||
| chr6:43192059 | C | CTT | 37 | a0001c0002t0001g0079 a0001c0003t0001g0077 a0001c0003t0001g0084 others(34): Show |
43 | HG00558.hp2 HG00741.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.2181-923_2181-922d others(4): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43192059 | ||||||
| chr6:43192059 | C | CTTT | 15 | a0001c0002t0001g0073 a0001c0003t0001g0074 a0001c0003t0001g0075 others(12): Show |
17 | HG02258.hp2 HG02809.hp2 HG02922.hp1 others(14): Show |
intron_variant | MODIFIER | c.2181-924_2181-922d others(5): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43192059 | ||||||
| chr6:43192059 | CT | C | 7 | a0001c0002t0001g0061 a0001c0002t0001g0066 a0001c0039t0002g0196 others(4): Show |
8 | HG00733.hp2 HG01257.hp1 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.2181-922delT | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43192059 | ||||||
| chr6:43192060 | T | C | 1 | a0002c0001t0001g0162 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2181-941T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43192060 | |||||||
| chr6:43192086 | G | A | 1 | a0002c0001t0001g0163 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2181-915G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43192086 | |||||||
| chr6:43192127 | T | C | 1 | a0001c0004t0001g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2181-874T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43192127 | |||||||
| chr6:43192399 | G | GT | 20 | a0001c0004t0001g0126 a0001c0004t0001g0136 a0001c0004t0001g0139 others(17): Show |
21 | HG00558.hp2 HG01123.hp2 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.2181-597dupT | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr6 | 43192399 | ||||||
| chr6:43192491 | C | T | 3 | a0007c0013t0001g0093 a0007c0013t0001g0095 a0016c0021t0002g0094 |
3 | HG02809.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2181-510C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43192491 | |||||||
| chr6:43192637 | T | C | 115 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0006 others(112): Show |
149 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(146): Show |
intron_variant | MODIFIER | c.2181-364T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43192637 | |||||||
| chr6:43192722 | A | G | 1 | a0002c0001t0001g0173 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2181-279A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43192722 | |||||||
| chr6:43192913 | A | G | 2 | a0001c0002t0001g0079 a0001c0042t0001g0091 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2181-88A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 8/40 | chr6 | 43192913 | |||||||
| chr6:43193229 | G | A | 1 | a0001c0003t0001g0092 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2388+21G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/40 | chr6 | 43193229 | |||||||
| chr6:43193265 | C | A | 7 | a0001c0002t0001g0073 a0001c0003t0001g0074 a0001c0003t0001g0075 others(4): Show |
7 | HG02922.hp1 HG03098.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.2388+57C>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/40 | chr6 | 43193265 | |||||||
| chr6:43193267 | A | G | 1 | a0007c0013t0001g0095 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2388+59A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/40 | chr6 | 43193267 | |||||||
| chr6:43193358 | A | G | 48 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0006 others(45): Show |
74 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.2388+150A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/40 | chr6 | 43193358 | |||||||
| chr6:43193395 | G | A | 10 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0100 others(7): Show |
10 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2388+187G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/40 | chr6 | 43193395 | |||||||
| chr6:43193423 | A | G | 5 | a0001c0008t0001g0034 a0001c0008t0001g0111 a0001c0008t0001g0113 others(2): Show |
5 | HG02572.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2388+215A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/40 | chr6 | 43193423 | |||||||
| chr6:43193727 | C | A | 1 | a0001c0042t0001g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2388+519C>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/40 | chr6 | 43193727 | |||||||
| chr6:43194023 | C | G | 2 | a0001c0002t0001g0069 a0001c0002t0001g0070 |
2 | NA19010.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2388+815C>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/40 | chr6 | 43194023 | |||||||
| chr6:43194023 | C | T | 11 | a0001c0003t0001g0081 a0001c0003t0001g0084 a0001c0003t0001g0085 others(8): Show |
16 | HG01243.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2388+815C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/40 | chr6 | 43194023 | |||||||
| chr6:43194297 | T | C | 2 | a0001c0020t0002g0190 a0001c0020t0002g0192 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2388+1089T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/40 | chr6 | 43194297 | |||||||
| chr6:43194510 | G | A | 2 | a0002c0031t0002g0117 a0002c0033t0002g0110 |
2 | HG01070.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2388+1302G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/40 | chr6 | 43194510 | |||||||
| chr6:43194620 | G | A | 1 | a0002c0001t0001g0164 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2388+1412G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/40 | chr6 | 43194620 | |||||||
| chr6:43194621 | G | A | 1 | a0002c0001t0001g0164 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2388+1413G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/40 | chr6 | 43194621 | |||||||
| chr6:43194752 | A | G | 66 | a0001c0002t0001g0073 a0001c0002t0001g0079 a0001c0003t0001g0074 others(63): Show |
74 | HG00558.hp2 HG00741.hp1 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.2389-1317A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/40 | chr6 | 43194752 | |||||||
| chr6:43194793 | C | T | 1 | a0002c0001t0001g0146 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2389-1276C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/40 | chr6 | 43194793 | |||||||
| chr6:43194915 | C | T | 2 | a0001c0010t0002g0009 a0001c0010t0002g0072 |
4 | HG02258.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2389-1154C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/40 | chr6 | 43194915 | |||||||
| chr6:43195134 | G | A | 24 | a0001c0002t0001g0079 a0001c0003t0001g0081 a0001c0003t0001g0084 others(21): Show |
29 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.2389-935G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/40 | chr6 | 43195134 | |||||||
| chr6:43195756 | G | A | 9 | a0001c0011t0002g0183 a0001c0011t0002g0191 a0001c0011t0002g0193 others(6): Show |
9 | HG00741.hp2 HG01243.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.2389-313G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/40 | chr6 | 43195756 | |||||||
| chr6:43196030 | C | G | 1 | a0002c0006t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2389-39C>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 9/40 | chr6 | 43196030 | |||||||
| chr6:43196354 | T | G | 1 | a0001c0003t0001g0092 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2585+89T>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 10/40 | chr6 | 43196354 | |||||||
| chr6:43196419 | C | T | 1 | a0002c0022t0001g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2585+154C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 10/40 | chr6 | 43196419 | |||||||
| chr6:43196505 | G | T | 1 | a0001c0002t0001g0045 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2586-140G>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 10/40 | chr6 | 43196505 | |||||||
| chr6:43196566 | C | T | 9 | a0001c0011t0002g0183 a0001c0011t0002g0191 a0001c0011t0002g0193 others(6): Show |
9 | HG00741.hp2 HG01243.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.2586-79C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 10/40 | chr6 | 43196566 | |||||||
| chr6:43197050 | AT | A | 11 | a0001c0002t0001g0064 a0001c0003t0001g0098 a0001c0003t0001g0099 others(8): Show |
11 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2803+201delT | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 11/40 | INFO_REALIGN_3_PRIME | chr6 | 43197050 | ||||||
| chr6:43197929 | T | C | 1 | a0001c0003t0002g0038 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2804-680T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 11/40 | chr6 | 43197929 | |||||||
| chr6:43198060 | G | C | 1 | a0001c0002t0001g0055 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2804-549G>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 11/40 | chr6 | 43198060 | |||||||
| chr6:43198499 | A | G | 1 | a0001c0003t0002g0038 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2804-110A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 11/40 | chr6 | 43198499 | |||||||
| chr6:43198939 | C | CT | 22 | a0001c0002t0001g0003 a0001c0002t0001g0006 a0001c0002t0001g0054 others(19): Show |
31 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.3050+98dupT | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 12/40 | INFO_REALIGN_3_PRIME | chr6 | 43198939 | ||||||
| chr6:43199163 | C | T | 1 | a0001c0002t0001g0044 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3051-103C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 12/40 | chr6 | 43199163 | |||||||
| chr6:43199258 | C | T | 1 | a0001c0010t0002g0080 | 1 | HG03098.hp1 | splice_region_variant&intron_variant | LOW | c.3051-8C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 12/40 | chr6 | 43199258 | |||||||
| chr6:43199560 | T | G | 1 | a0002c0006t0001g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3156+189T>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 13/40 | chr6 | 43199560 | |||||||
| chr6:43199696 | TG | T | 58 | a0001c0002t0001g0073 a0001c0002t0001g0079 a0001c0003t0001g0074 others(55): Show |
66 | HG00558.hp2 HG00741.hp1 HG01123.hp2 others(63): Show |
intron_variant | MODIFIER | c.3157-230delG | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 13/40 | INFO_REALIGN_3_PRIME | chr6 | 43199696 | ||||||
| chr6:43199840 | C | T | 50 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0006 others(47): Show |
78 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.3157-89C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 13/40 | chr6 | 43199840 | |||||||
| chr6:43199860 | C | G | 2 | a0001c0010t0002g0009 a0001c0010t0002g0072 |
4 | HG02258.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3157-69C>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 13/40 | chr6 | 43199860 | |||||||
| chr6:43199863 | C | G | 11 | a0001c0003t0001g0081 a0001c0003t0001g0084 a0001c0003t0001g0085 others(8): Show |
16 | HG01243.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3157-66C>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 13/40 | chr6 | 43199863 | |||||||
| chr6:43199917 | C | T | 11 | a0001c0003t0001g0081 a0001c0003t0001g0084 a0001c0003t0001g0085 others(8): Show |
16 | HG01243.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3157-12C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 13/40 | chr6 | 43199917 | |||||||
| chr6:43200379 | A | G | 58 | a0001c0002t0001g0073 a0001c0002t0001g0079 a0001c0003t0001g0074 others(55): Show |
66 | HG00558.hp2 HG00741.hp1 HG01123.hp2 others(63): Show |
intron_variant | MODIFIER | c.3385-57A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 14/40 | chr6 | 43200379 | |||||||
| chr6:43200640 | C | T | 2 | a0001c0010t0002g0009 a0001c0010t0002g0072 |
4 | HG02258.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476-23C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 15/40 | chr6 | 43200640 | |||||||
| chr6:43201030 | G | T | 3 | a0007c0013t0001g0093 a0007c0013t0001g0095 a0016c0021t0002g0094 |
3 | HG02809.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3647+196G>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43201030 | |||||||
| chr6:43201061 | G | A | 6 | a0001c0002t0001g0073 a0001c0003t0001g0074 a0001c0003t0001g0076 others(3): Show |
6 | HG02922.hp1 HG03098.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.3647+227G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43201061 | |||||||
| chr6:43201175 | A | G | 1 | a0001c0003t0001g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3647+341A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43201175 | |||||||
| chr6:43201415 | A | G | 67 | a0001c0002t0001g0073 a0001c0002t0001g0079 a0001c0003t0001g0074 others(64): Show |
75 | HG00558.hp2 HG00741.hp1 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.3647+581A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43201415 | |||||||
| chr6:43201442 | A | G | 8 | a0001c0003t0001g0081 a0001c0003t0001g0084 a0001c0003t0001g0085 others(5): Show |
8 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3647+608A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43201442 | |||||||
| chr6:43201461 | C | T | 2 | a0002c0006t0001g0089 a0017c0037t0001g0088 |
2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3647+627C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43201461 | |||||||
| chr6:43201572 | C | T | 1 | a0002c0001t0001g0128 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3647+738C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43201572 | |||||||
| chr6:43201661 | A | C | 1 | a0001c0003t0001g0099 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3647+827A>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43201661 | |||||||
| chr6:43201670 | G | A | 11 | a0001c0003t0001g0081 a0001c0003t0001g0084 a0001c0003t0001g0085 others(8): Show |
16 | HG01243.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3647+836G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43201670 | |||||||
| chr6:43201681 | G | A | 1 | a0002c0006t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3647+847G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43201681 | |||||||
| chr6:43201701 | G | C | 2 | a0001c0002t0001g0055 a0002c0001t0001g0175 |
2 | NA18939.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.3647+867G>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43201701 | |||||||
| chr6:43201733 | C | T | 3 | a0007c0013t0001g0093 a0007c0013t0001g0095 a0016c0021t0002g0094 |
3 | HG02809.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3647+899C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43201733 | |||||||
| chr6:43201754 | C | G | 1 | a0002c0009t0001g0135 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3647+920C>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43201754 | |||||||
| chr6:43201771 | G | A | 1 | a0002c0001t0001g0120 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3647+937G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43201771 | |||||||
| chr6:43201914 | G | A | 1 | a0013c0028t0001g0087 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3648-802G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43201914 | |||||||
| chr6:43201953 | C | T | 1 | a0001c0003t0001g0081 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3648-763C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43201953 | |||||||
| chr6:43202139 | C | A | 3 | a0001c0002t0001g0079 a0001c0003t0001g0092 a0001c0042t0001g0091 |
3 | HG02145.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3648-577C>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43202139 | |||||||
| chr6:43202149 | A | G | 20 | a0001c0003t0001g0081 a0001c0003t0001g0084 a0001c0003t0001g0085 others(17): Show |
25 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.3648-567A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43202149 | |||||||
| chr6:43202209 | C | T | 3 | a0001c0002t0001g0047 a0001c0002t0001g0048 a0001c0002t0001g0050 |
3 | NA18952.hp2 NA19055.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.3648-507C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43202209 | |||||||
| chr6:43202545 | C | G | 3 | a0007c0013t0001g0093 a0007c0013t0001g0095 a0016c0021t0002g0094 |
3 | HG02809.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3648-171C>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 16/40 | chr6 | 43202545 | |||||||
| chr6:43203028 | C | T | 1 | a0002c0001t0001g0178 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3754-81C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 17/40 | chr6 | 43203028 | |||||||
| chr6:43203673 | G | A | 18 | a0001c0004t0001g0126 a0001c0004t0001g0136 a0001c0004t0001g0139 others(15): Show |
19 | HG00558.hp2 HG01123.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.4025+81G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 19/40 | chr6 | 43203673 | |||||||
| chr6:43203736 | A | T | 3 | a0007c0013t0001g0093 a0007c0013t0001g0095 a0016c0021t0002g0094 |
3 | HG02809.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4026-118A>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 19/40 | chr6 | 43203736 | |||||||
| chr6:43204692 | G | A | 23 | a0001c0002t0001g0079 a0001c0003t0001g0081 a0001c0003t0001g0084 others(20): Show |
23 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.4340-56G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 21/40 | chr6 | 43204692 | |||||||
| chr6:43205151 | T | C | 1 | a0003c0005t0001g0148 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4632+36T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 23/40 | chr6 | 43205151 | |||||||
| chr6:43205493 | T | A | 1 | a0001c0004t0002g0141 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.4793+70T>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 24/40 | chr6 | 43205493 | |||||||
| chr6:43205689 | C | T | 3 | a0001c0007t0001g0004 a0001c0007t0001g0020 a0001c0042t0001g0091 |
8 | HG02109.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.4793+266C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 24/40 | chr6 | 43205689 | |||||||
| chr6:43205777 | C | G | 2 | a0001c0002t0001g0079 a0001c0003t0001g0092 |
2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.4794-230C>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 24/40 | chr6 | 43205777 | |||||||
| chr6:43205829 | C | CA | 12 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0100 others(9): Show |
12 | HG00741.hp1 HG01255.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.4794-161dupA | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 24/40 | INFO_REALIGN_3_PRIME | chr6 | 43205829 | ||||||
| chr6:43205934 | T | C | 1 | a0012c0035t0001g0083 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4794-73T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 24/40 | chr6 | 43205934 | |||||||
| chr6:43206965 | C | T | 9 | a0001c0011t0002g0183 a0001c0011t0002g0191 a0001c0011t0002g0193 others(6): Show |
9 | HG00741.hp2 HG01243.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.5212+455C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43206965 | |||||||
| chr6:43207047 | T | C | 10 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0100 others(7): Show |
10 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.5212+537T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43207047 | |||||||
| chr6:43207056 | C | G | 22 | a0001c0003t0001g0043 a0001c0004t0001g0126 a0001c0004t0001g0136 others(19): Show |
25 | HG00558.hp2 HG01123.hp2 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.5212+546C>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43207056 | |||||||
| chr6:43207418 | C | T | 2 | a0002c0031t0002g0117 a0002c0033t0002g0110 |
2 | HG01070.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.5212+908C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43207418 | |||||||
| chr6:43207804 | A | C | 3 | a0007c0013t0001g0093 a0007c0013t0001g0095 a0016c0021t0002g0094 |
3 | HG02809.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.5212+1294A>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43207804 | |||||||
| chr6:43208083 | A | G | 1 | a0001c0003t0001g0096 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5212+1573A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43208083 | |||||||
| chr6:43208331 | G | A | 1 | a0001c0003t0001g0092 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5212+1821G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43208331 | |||||||
| chr6:43208433 | T | C | 1 | a0001c0007t0001g0020 | 2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.5212+1923T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43208433 | |||||||
| chr6:43208791 | T | A | 2 | a0003c0005t0001g0013 a0003c0005t0001g0152 |
4 | HG02486.hp1 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.5212+2281T>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43208791 | |||||||
| chr6:43208817 | A | G | 3 | a0001c0010t0002g0009 a0001c0010t0002g0072 a0001c0010t0002g0080 |
5 | HG02258.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.5212+2307A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43208817 | |||||||
| chr6:43208897 | G | A | 1 | a0001c0002t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.5212+2387G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43208897 | |||||||
| chr6:43208903 | C | T | 1 | a0002c0001t0001g0033 | 2 | HG00558.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.5212+2393C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43208903 | |||||||
| chr6:43209147 | C | CT | 19 | a0001c0002t0001g0042 a0001c0003t0001g0081 a0001c0003t0001g0084 others(16): Show |
19 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.5212+2652dupT | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | INFO_REALIGN_3_PRIME | chr6 | 43209147 | ||||||
| chr6:43209206 | C | T | 1 | a0001c0004t0002g0027 | 2 | HG00558.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.5212+2696C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43209206 | |||||||
| chr6:43209218 | T | C | 8 | a0001c0011t0002g0183 a0001c0011t0002g0191 a0001c0011t0002g0193 others(5): Show |
8 | HG00741.hp2 HG01243.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.5212+2708T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43209218 | |||||||
| chr6:43209237 | C | G | 19 | a0001c0003t0001g0043 a0001c0004t0001g0126 a0001c0004t0001g0136 others(16): Show |
20 | HG00558.hp2 HG01123.hp2 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.5212+2727C>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43209237 | |||||||
| chr6:43209428 | C | T | 2 | a0002c0001t0001g0171 a0002c0001t0001g0188 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5212+2918C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43209428 | |||||||
| chr6:43209444 | C | T | 8 | a0001c0003t0001g0081 a0001c0003t0001g0084 a0001c0003t0001g0085 others(5): Show |
8 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.5212+2934C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43209444 | |||||||
| chr6:43209615 | G | A | 18 | a0001c0003t0001g0081 a0001c0003t0001g0084 a0001c0003t0001g0085 others(15): Show |
18 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.5212+3105G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43209615 | |||||||
| chr6:43209687 | C | T | 3 | a0001c0010t0002g0009 a0001c0010t0002g0072 a0001c0010t0002g0080 |
5 | HG02258.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.5212+3177C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43209687 | |||||||
| chr6:43210255 | C | T | 1 | a0002c0006t0001g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5213-2894C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43210255 | |||||||
| chr6:43210299 | T | C | 2 | a0018c0024t0001g0026 a0021c0023t0001g0026 |
2 | NA18947.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.5213-2850T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43210299 | |||||||
| chr6:43210427 | CCTT | C | 45 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0006 others(42): Show |
71 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.5213-2718_5213-271 others(7): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | INFO_REALIGN_3_PRIME | chr6 | 43210427 | ||||||
| chr6:43210431 | CTT | C | 2 | a0002c0001t0001g0007 a0002c0014t0001g0165 |
5 | NA18970.hp1 NA18999.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.5213-2716_5213-271 others(6): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | INFO_REALIGN_3_PRIME | chr6 | 43210431 | ||||||
| chr6:43210496 | A | G | 10 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0100 others(7): Show |
10 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.5213-2653A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43210496 | |||||||
| chr6:43210532 | C | T | 1 | a0001c0003t0002g0041 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.5213-2617C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43210532 | |||||||
| chr6:43210683 | C | T | 1 | a0002c0001t0001g0143 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.5213-2466C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43210683 | |||||||
| chr6:43210683 | CTT | C | 1 | a0001c0002t0001g0008 | 3 | HG00423.hp1 NA18975.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.5213-2462_5213-246 others(6): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | INFO_REALIGN_3_PRIME | chr6 | 43210683 | ||||||
| chr6:43210686 | T | A | 1 | a0001c0002t0001g0008 | 3 | HG00423.hp1 NA18975.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.5213-2463T>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43210686 | |||||||
| chr6:43210687 | T | A | 1 | a0001c0002t0001g0008 | 3 | HG00423.hp1 NA18975.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.5213-2462T>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43210687 | |||||||
| chr6:43210783 | G | A | 4 | a0002c0001t0001g0030 a0002c0006t0001g0049 a0002c0006t0001g0051 others(1): Show |
5 | HG01192.hp1 HG01934.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.5213-2366G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43210783 | |||||||
| chr6:43211198 | G | A | 1 | a0001c0003t0001g0105 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5213-1951G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43211198 | |||||||
| chr6:43211352 | G | A | 1 | a0001c0002t0001g0057 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.5213-1797G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43211352 | |||||||
| chr6:43211447 | A | T | 1 | a0002c0001t0001g0012 | 3 | HG02630.hp1 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.5213-1702A>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43211447 | |||||||
| chr6:43211474 | C | A | 1 | a0002c0001t0001g0150 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.5213-1675C>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43211474 | |||||||
| chr6:43211516 | C | T | 1 | a0012c0035t0001g0083 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5213-1633C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43211516 | |||||||
| chr6:43211565 | A | C | 2 | a0001c0002t0001g0079 a0001c0003t0001g0092 |
2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.5213-1584A>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43211565 | |||||||
| chr6:43211651 | CAT | C | 3 | a0001c0010t0002g0009 a0001c0010t0002g0072 a0001c0010t0002g0080 |
5 | HG02258.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.5213-1497_5213-149 others(6): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43211651 | |||||||
| chr6:43211656 | A | T | 3 | a0001c0010t0002g0009 a0001c0010t0002g0072 a0001c0010t0002g0080 |
5 | HG02258.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.5213-1493A>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43211656 | |||||||
| chr6:43211810 | A | T | 1 | a0002c0006t0001g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5213-1339A>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43211810 | |||||||
| chr6:43211917 | T | C | 10 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0100 others(7): Show |
10 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.5213-1232T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43211917 | |||||||
| chr6:43212001 | C | T | 3 | a0001c0007t0001g0004 a0001c0007t0001g0020 a0001c0042t0001g0091 |
8 | HG02109.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.5213-1148C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43212001 | |||||||
| chr6:43212184 | A | G | 1 | a0017c0037t0001g0088 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5213-965A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43212184 | |||||||
| chr6:43212295 | C | T | 8 | a0001c0003t0001g0081 a0001c0003t0001g0084 a0001c0003t0001g0085 others(5): Show |
8 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.5213-854C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43212295 | |||||||
| chr6:43212448 | CACTA | C | 2 | a0002c0001t0001g0011 a0006c0016t0001g0011 |
3 | HG01258.hp1 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.5213-697_5213-694d others(6): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | INFO_REALIGN_3_PRIME | chr6 | 43212448 | ||||||
| chr6:43212656 | A | AT | 9 | a0001c0011t0002g0183 a0001c0011t0002g0191 a0001c0011t0002g0193 others(6): Show |
9 | HG00741.hp2 HG01243.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.5213-480dupT | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | INFO_REALIGN_3_PRIME | chr6 | 43212656 | ||||||
| chr6:43212813 | G | T | 1 | a0001c0003t0001g0096 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5213-336G>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43212813 | |||||||
| chr6:43213097 | C | T | 1 | a0001c0002t0001g0035 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.5213-52C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 26/40 | chr6 | 43213097 | |||||||
| chr6:43213316 | C | G | 1 | a0002c0009t0001g0025 | 2 | HG01891.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.5358+22C>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 27/40 | chr6 | 43213316 | |||||||
| chr6:43213641 | A | C | 10 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0100 others(7): Show |
10 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.5489-72A>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 28/40 | chr6 | 43213641 | |||||||
| chr6:43213697 | C | T | 1 | a0002c0022t0001g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5489-16C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 28/40 | chr6 | 43213697 | |||||||
| chr6:43213703 | C | T | 3 | a0001c0007t0001g0004 a0001c0007t0001g0020 a0001c0042t0001g0091 |
8 | HG02109.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.5489-10C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 28/40 | chr6 | 43213703 | |||||||
| chr6:43213928 | AC | A | 3 | a0007c0013t0001g0093 a0007c0013t0001g0095 a0016c0021t0002g0094 |
3 | HG02809.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.5688+18delC | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 29/40 | INFO_REALIGN_3_PRIME | chr6 | 43213928 | ||||||
| chr6:43214052 | A | T | 3 | a0001c0010t0002g0009 a0001c0010t0002g0072 a0001c0010t0002g0080 |
5 | HG02258.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.5688+140A>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 29/40 | chr6 | 43214052 | |||||||
| chr6:43214249 | G | A | 3 | a0001c0007t0001g0004 a0001c0007t0001g0020 a0001c0042t0001g0091 |
8 | HG02109.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.5688+337G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 29/40 | chr6 | 43214249 | |||||||
| chr6:43214631 | T | C | 1 | a0001c0003t0001g0092 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5689-448T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 29/40 | chr6 | 43214631 | |||||||
| chr6:43214706 | C | T | 3 | a0007c0013t0001g0093 a0007c0013t0001g0095 a0016c0021t0002g0094 |
3 | HG02809.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.5689-373C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 29/40 | chr6 | 43214706 | |||||||
| chr6:43214759 | C | T | 10 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0100 others(7): Show |
10 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.5689-320C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 29/40 | chr6 | 43214759 | |||||||
| chr6:43214796 | GA | G | 8 | a0001c0002t0001g0079 a0001c0003t0001g0092 a0001c0007t0001g0004 others(5): Show |
13 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.5689-271delA | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 29/40 | INFO_REALIGN_3_PRIME | chr6 | 43214796 | ||||||
| chr6:43214797 | A | G | 1 | a0001c0004t0002g0027 | 2 | HG00558.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.5689-282A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 29/40 | chr6 | 43214797 | |||||||
| chr6:43214976 | TA | T | 8 | a0001c0002t0001g0073 a0001c0003t0001g0074 a0001c0003t0001g0075 others(5): Show |
8 | HG02922.hp1 HG03098.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.5689-94delA | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 29/40 | INFO_REALIGN_3_PRIME | chr6 | 43214976 | ||||||
| chr6:43214993 | A | G | 1 | a0002c0006t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5689-86A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 29/40 | chr6 | 43214993 | |||||||
| chr6:43215428 | C | T | 1 | a0002c0009t0001g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5936+102C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 30/40 | chr6 | 43215428 | |||||||
| chr6:43215715 | C | T | 11 | a0001c0002t0001g0003 a0001c0002t0001g0006 a0001c0002t0001g0054 others(8): Show |
20 | HG02027.hp2 HG02056.hp2 NA18747.hp1 others(17): Show |
intron_variant | MODIFIER | c.5936+389C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 30/40 | chr6 | 43215715 | |||||||
| chr6:43215718 | G | A | 1 | a0003c0005t0001g0148 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5936+392G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 30/40 | chr6 | 43215718 | |||||||
| chr6:43215891 | T | C | 2 | a0007c0013t0001g0093 a0007c0013t0001g0095 |
2 | HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.5937-267T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 30/40 | chr6 | 43215891 | |||||||
| chr6:43216006 | G | A | 1 | a0001c0002t0001g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.5937-152G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 30/40 | chr6 | 43216006 | |||||||
| chr6:43216537 | C | A | 9 | a0001c0003t0001g0099 a0001c0003t0001g0100 a0001c0003t0001g0101 others(6): Show |
9 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.6282+34C>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43216537 | |||||||
| chr6:43216652 | T | A | 1 | a0010c0025t0001g0151 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.6282+149T>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43216652 | |||||||
| chr6:43216835 | C | T | 1 | a0001c0011t0002g0194 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.6282+332C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43216835 | |||||||
| chr6:43216881 | A | C | 1 | a0001c0020t0002g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.6282+378A>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43216881 | |||||||
| chr6:43216903 | G | T | 25 | a0001c0002t0001g0079 a0001c0003t0001g0043 a0001c0004t0001g0126 others(22): Show |
28 | HG00558.hp2 HG01123.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.6282+400G>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43216903 | |||||||
| chr6:43216928 | T | C | 1 | a0001c0002t0001g0058 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.6282+425T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43216928 | |||||||
| chr6:43216970 | T | C | 1 | a0001c0012t0001g0137 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.6282+467T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43216970 | |||||||
| chr6:43217064 | T | A | 1 | a0002c0001t0001g0023 | 2 | HG01433.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.6282+561T>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43217064 | |||||||
| chr6:43217098 | A | G | 3 | a0001c0007t0001g0004 a0001c0007t0001g0020 a0001c0042t0001g0091 |
8 | HG02109.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.6282+595A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43217098 | |||||||
| chr6:43217616 | C | T | 8 | a0001c0003t0001g0099 a0001c0003t0001g0100 a0001c0003t0001g0101 others(5): Show |
8 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.6282+1113C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43217616 | |||||||
| chr6:43217785 | C | G | 1 | a0002c0006t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6282+1282C>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43217785 | |||||||
| chr6:43217825 | T | C | 10 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0100 others(7): Show |
10 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.6282+1322T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43217825 | |||||||
| chr6:43217995 | A | G | 104 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0006 others(101): Show |
139 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.6282+1492A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43217995 | |||||||
| chr6:43218224 | T | C | 1 | a0001c0002t0001g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6282+1721T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43218224 | |||||||
| chr6:43218278 | G | T | 1 | a0002c0009t0001g0025 | 2 | HG01891.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.6282+1775G>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43218278 | |||||||
| chr6:43218279 | C | T | 1 | a0002c0009t0001g0025 | 2 | HG01891.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.6282+1776C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43218279 | |||||||
| chr6:43218400 | T | C | 18 | a0001c0003t0001g0081 a0001c0003t0001g0084 a0001c0003t0001g0085 others(15): Show |
18 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.6282+1897T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43218400 | |||||||
| chr6:43218544 | G | A | 8 | a0001c0011t0002g0183 a0001c0011t0002g0191 a0001c0011t0002g0193 others(5): Show |
8 | HG00741.hp2 HG01243.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.6283-1915G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43218544 | |||||||
| chr6:43218927 | G | A | 8 | a0001c0003t0001g0081 a0001c0003t0001g0084 a0001c0003t0001g0085 others(5): Show |
8 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.6283-1532G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43218927 | |||||||
| chr6:43219037 | A | T | 10 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0100 others(7): Show |
10 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.6283-1422A>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43219037 | |||||||
| chr6:43219056 | G | T | 18 | a0001c0003t0001g0081 a0001c0003t0001g0084 a0001c0003t0001g0085 others(15): Show |
18 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.6283-1403G>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43219056 | |||||||
| chr6:43219063 | C | T | 49 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0006 others(46): Show |
76 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.6283-1396C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43219063 | |||||||
| chr6:43219190 | A | AAG | 13 | a0001c0002t0001g0079 a0001c0003t0001g0098 a0001c0003t0001g0099 others(10): Show |
13 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.6283-1249_6283-124 others(6): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | INFO_REALIGN_3_PRIME | chr6 | 43219190 | ||||||
| chr6:43219327 | C | T | 3 | a0002c0001t0001g0153 a0002c0014t0001g0165 a0002c0014t0001g0168 |
3 | HG00733.hp2 NA18975.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.6283-1132C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43219327 | |||||||
| chr6:43219479 | C | G | 1 | a0001c0003t0001g0077 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.6283-980C>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43219479 | |||||||
| chr6:43219525 | T | TTGTC | 154 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0006 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.6283-932_6283-931i others(6): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | INFO_REALIGN_3_PRIME | chr6 | 43219525 | ||||||
| chr6:43219745 | C | T | 3 | a0001c0003t0001g0092 a0007c0013t0001g0093 a0007c0013t0001g0095 |
3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.6283-714C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43219745 | |||||||
| chr6:43219788 | C | T | 17 | a0001c0003t0001g0081 a0001c0003t0001g0084 a0001c0003t0001g0085 others(14): Show |
17 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.6283-671C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43219788 | |||||||
| chr6:43219885 | C | T | 1 | a0002c0001t0001g0157 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.6283-574C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43219885 | |||||||
| chr6:43219912 | G | C | 1 | a0002c0001t0001g0166 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.6283-547G>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43219912 | |||||||
| chr6:43219913 | A | G | 1 | a0002c0001t0001g0166 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.6283-546A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43219913 | |||||||
| chr6:43219914 | G | A | 1 | a0002c0001t0001g0166 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.6283-545G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43219914 | |||||||
| chr6:43219953 | C | A | 2 | a0001c0002t0001g0035 a0001c0002t0001g0073 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.6283-506C>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43219953 | |||||||
| chr6:43220028 | G | A | 33 | a0001c0003t0001g0077 a0001c0003t0001g0092 a0001c0003t0002g0021 others(30): Show |
40 | HG00099.hp2 HG00741.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.6283-431G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43220028 | |||||||
| chr6:43220175 | T | C | 1 | a0002c0001t0001g0161 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.6283-284T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43220175 | |||||||
| chr6:43220227 | T | A | 1 | a0002c0001t0001g0166 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.6283-232T>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43220227 | |||||||
| chr6:43220313 | G | A | 1 | a0001c0004t0001g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.6283-146G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43220313 | |||||||
| chr6:43220435 | A | G | 10 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0100 others(7): Show |
10 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.6283-24A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 31/40 | chr6 | 43220435 | |||||||
| chr6:43220946 | G | C | 1 | a0001c0011t0002g0183 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.6588+35G>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 33/40 | chr6 | 43220946 | |||||||
| chr6:43220978 | A | T | 150 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0006 others(147): Show |
195 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.6588+67A>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 33/40 | chr6 | 43220978 | |||||||
| chr6:43220999 | G | A | 2 | a0001c0003t0001g0084 a0001c0003t0001g0085 |
2 | HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.6588+88G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 33/40 | chr6 | 43220999 | |||||||
| chr6:43221092 | C | T | 9 | a0001c0004t0002g0027 a0001c0004t0002g0124 a0001c0004t0002g0140 others(6): Show |
12 | HG00558.hp2 HG02135.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.6589-66C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 33/40 | chr6 | 43221092 | |||||||
| chr6:43221093 | C | G | 14 | a0001c0003t0002g0021 a0001c0003t0002g0038 a0001c0003t0002g0041 others(11): Show |
18 | HG00558.hp2 HG02135.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.6589-65C>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 33/40 | chr6 | 43221093 | |||||||
| chr6:43221339 | G | C | 1 | a0001c0004t0002g0124 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.6752+18G>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 34/40 | chr6 | 43221339 | |||||||
| chr6:43221362 | G | C | 3 | a0001c0010t0002g0009 a0001c0010t0002g0072 a0001c0010t0002g0080 |
5 | HG02258.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.6752+41G>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 34/40 | chr6 | 43221362 | |||||||
| chr6:43221637 | A | G | 61 | a0001c0002t0001g0079 a0001c0003t0001g0043 a0001c0003t0001g0074 others(58): Show |
70 | HG00558.hp2 HG00741.hp1 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.6753-48A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 34/40 | chr6 | 43221637 | |||||||
| chr6:43221867 | G | T | 9 | a0001c0011t0002g0183 a0001c0011t0002g0191 a0001c0011t0002g0193 others(6): Show |
9 | HG00741.hp2 HG01070.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.6846+89G>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 35/40 | chr6 | 43221867 | |||||||
| chr6:43221907 | G | A | 10 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0100 others(7): Show |
10 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.6846+129G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 35/40 | chr6 | 43221907 | |||||||
| chr6:43222184 | C | T | 5 | a0001c0003t0002g0021 a0001c0003t0002g0038 a0001c0003t0002g0041 others(2): Show |
6 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.6847-132C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 35/40 | chr6 | 43222184 | |||||||
| chr6:43222302 | C | T | 1 | a0003c0005t0001g0152 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.6847-14C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 35/40 | chr6 | 43222302 | |||||||
| chr6:43222397 | C | T | 5 | a0002c0001t0001g0133 a0002c0001t0001g0150 a0002c0001t0001g0171 others(2): Show |
5 | HG00099.hp1 HG00323.hp1 HG01884.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.6921+7C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 36/40 | chr6 | 43222397 | |||||||
| chr6:43222492 | G | A | 11 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0100 others(8): Show |
12 | HG00741.hp1 HG01255.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.6922-39G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 36/40 | chr6 | 43222492 | |||||||
| chr6:43222752 | C | T | 7 | a0001c0003t0001g0043 a0001c0004t0001g0126 a0001c0004t0001g0136 others(4): Show |
7 | HG01123.hp2 HG01928.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.7033-27C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 37/40 | chr6 | 43222752 | |||||||
| chr6:43222956 | G | A | 1 | a0001c0042t0001g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.7150+60G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 38/40 | chr6 | 43222956 | |||||||
| chr6:43223185 | C | T | 8 | a0001c0003t0001g0081 a0001c0003t0001g0084 a0001c0003t0001g0085 others(5): Show |
8 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.7151-79C>T | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 38/40 | chr6 | 43223185 | |||||||
| chr6:43223489 | A | AGGGCATG others(41): Show |
2 | a0001c0003t0001g0118 a0001c0003t0001g0119 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.7284+93_7284+94ins others(48): Show |
CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 39/40 | INFO_REALIGN_3_PRIME | chr6 | 43223489 | ||||||
| chr6:43223680 | T | C | 8 | a0001c0003t0001g0081 a0001c0003t0001g0084 a0001c0003t0001g0085 others(5): Show |
8 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.7284+283T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 39/40 | chr6 | 43223680 | |||||||
| chr6:43223738 | G | A | 1 | a0014c0026t0001g0167 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.7284+341G>A | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 39/40 | chr6 | 43223738 | |||||||
| chr6:43223782 | A | G | 1 | a0001c0042t0001g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.7285-313A>G | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 39/40 | chr6 | 43223782 | |||||||
| chr6:43224003 | T | C | 1 | a0002c0001t0001g0169 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.7285-92T>C | CUL9 | ENSG00000112659.14 | transcript | ENST00000252050.9 | protein_coding | 39/40 | chr6 | 43224003 |