Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 285753 |
|---|---|
| ensemblid | ENSG00000183137.16 |
| hgncid | 21561 |
| symbol | CEP57L1 |
| name | centrosomal protein 57 like 1 |
| refseq_nuc | NM_001271852.3 |
| refseq_prot | NP_001258781.1 |
| ensembl_nuc | ENST00000517392.6 |
| ensembl_prot | ENSP00000427844.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 109095507 |
| end | 109174418 |
| strand | + |
| ver | v1.2 |
| region | chr6:109095507-109174418 |
| region5000 | chr6:109090507-109179418 |
| regionname0 | CEP57L1_chr6_109095507_109174418 |
| regionname5000 | CEP57L1_chr6_109090507_109179418 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 460 | 180 | 69 | 29 | 55 | 3 | 22 | 39 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002 | 0/0 | 460 | 37 | 11 | 9 | 7 | 3 | 7 | 5 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0003 | 0/0 | 460 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0004 | 0/0 | 460 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0005 | 0/0 | 460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0006 | 0/0 | 153 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0007 | 0/0 | 460 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1383 | 174 | 67 | 26 | 55 | 3 | 21 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| c0002 | 0/0 | 1383 | 37 | 11 | 9 | 7 | 3 | 7 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| c0003 | 0/0 | 1383 | 5 | 1 | 3 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| c0004 | 0/0 | 1383 | 4 | 4 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| c0005 | 0/0 | 1383 | 4 | 4 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| c0006 | 0/0 | 1383 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| c0007 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| c0008 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| c0009 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 11520 | 48 | 17 | 5 | 17 | 1 | 8 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0002 | 0/0 | 11520 | 25 | 1 | 7 | 16 | 1 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0003 | 0/0 | 11510 | 15 | 1 | 4 | 5 | 1 | 4 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0004 | 0/0 | 11520 | 8 | 0 | 1 | 7 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0005 | 0/1 | 11520 | 8 | 1 | 5 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0006 | 0/0 | 11519 | 8 | 4 | 1 | 0 | 0 | 3 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0007 | 0/0 | 11521 | 5 | 3 | 1 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0008 | 0/0 | 11519 | 5 | 5 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0009 | 0/0 | 11520 | 4 | 4 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0010 | 0/0 | 11520 | 4 | 0 | 3 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0011 | 0/0 | 11520 | 4 | 4 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0012 | 0/0 | 11526 | 3 | 3 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0013 | 0/0 | 11519 | 2 | 0 | 0 | 0 | 1 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0014 | 0/0 | 11520 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0015 | 0/0 | 11520 | 2 | 1 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0016 | 0/0 | 11521 | 2 | 0 | 0 | 1 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0017 | 0/0 | 11519 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0018 | 0/0 | 11521 | 2 | 1 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0019 | 0/0 | 11523 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0020 | 0/0 | 11522 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0021 | 0/0 | 11521 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0022 | 0/0 | 11521 | 2 | 1 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0023 | 1/0 | 11521 | 2 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0024 | 0/0 | 11524 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0025 | 0/0 | 11511 | 2 | 0 | 1 | 0 | 1 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0026 | 0/0 | 11509 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0027 | 0/0 | 11526 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0028 | 0/0 | 11527 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0029 | 0/0 | 11534 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0030 | 0/0 | 11499 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0031 | 0/0 | 11520 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0032 | 0/0 | 11512 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0033 | 0/0 | 11514 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0034 | 0/0 | 11509 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0035 | 0/0 | 11509 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0036 | 0/0 | 11520 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0037 | 0/0 | 11521 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0038 | 0/0 | 11522 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0039 | 0/0 | 11520 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0040 | 0/0 | 11520 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0041 | 0/0 | 11523 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0042 | 0/0 | 11520 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0043 | 0/0 | 11521 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0044 | 0/0 | 11521 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0045 | 0/0 | 11519 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0046 | 0/0 | 11520 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0047 | 0/0 | 11524 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0048 | 0/0 | 11521 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0049 | 0/0 | 11523 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0050 | 0/0 | 11523 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0051 | 0/0 | 11520 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0052 | 0/0 | 11520 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0053 | 0/0 | 11520 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0054 | 0/0 | 11520 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0055 | 0/0 | 11520 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0056 | 0/0 | 11522 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0057 | 0/0 | 11521 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0058 | 0/0 | 11520 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0059 | 0/0 | 11519 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0060 | 0/0 | 11520 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0061 | 0/0 | 11521 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0062 | 0/0 | 11521 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0063 | 0/0 | 11522 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0064 | 0/0 | 11520 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0065 | 0/0 | 11520 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0066 | 0/0 | 11504 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0067 | 0/0 | 11523 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0068 | 0/0 | 11506 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0069 | 0/0 | 11518 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0070 | 0/0 | 11510 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0071 | 0/0 | 11512 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0072 | 0/0 | 11511 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0073 | 0/0 | 11511 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0074 | 0/0 | 11507 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0075 | 0/0 | 11507 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0076 | 0/0 | 11506 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0077 | 0/0 | 11493 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0078 | 0/0 | 11494 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0079 | 0/0 | 11493 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0080 | 0/0 | 11493 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0081 | 0/0 | 11497 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0082 | 0/0 | 11510 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0083 | 0/0 | 11520 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0084 | 0/0 | 11504 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0085 | 0/0 | 11492 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0086 | 0/0 | 11505 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0087 | 0/0 | 11519 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0088 | 0/0 | 11520 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| t0089 | 0/0 | 11521 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 5 | 1 | 2 | 0 | 0 | 2 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0092 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1383 | 174 | 67 | 26 | 55 | 3 | 21 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0003 | 0/0 | 1383 | 5 | 1 | 3 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0007 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002 | 0/0 | 1383 | 37 | 11 | 9 | 7 | 3 | 7 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0003c0005 | 0/0 | 1383 | 4 | 4 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0004c0004 | 0/0 | 1383 | 4 | 4 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0005c0009 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0006c0008 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0007c0006 | 0/0 | 1383 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 12902 | 44 | 13 | 5 | 17 | 1 | 8 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0002 | 0/0 | 12902 | 24 | 1 | 6 | 16 | 1 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0004 | 0/0 | 12902 | 8 | 0 | 1 | 7 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0005 | 0/1 | 12902 | 4 | 0 | 3 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0006 | 0/0 | 12901 | 8 | 4 | 1 | 0 | 0 | 3 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0007 | 0/0 | 12903 | 5 | 3 | 1 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0008 | 0/0 | 12901 | 4 | 4 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0009 | 0/0 | 12902 | 4 | 4 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0010 | 0/0 | 12902 | 4 | 0 | 3 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0011 | 0/0 | 12902 | 4 | 4 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0012 | 0/0 | 12908 | 3 | 3 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0013 | 0/0 | 12901 | 2 | 0 | 0 | 0 | 1 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0014 | 0/0 | 12902 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0015 | 0/0 | 12902 | 2 | 1 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0016 | 0/0 | 12903 | 2 | 0 | 0 | 1 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0017 | 0/0 | 12901 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0018 | 0/0 | 12903 | 2 | 1 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0019 | 0/0 | 12905 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0020 | 0/0 | 12904 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0021 | 0/0 | 12903 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0022 | 0/0 | 12903 | 2 | 1 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0023 | 1/0 | 12903 | 2 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0024 | 0/0 | 12906 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0027 | 0/0 | 12908 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0028 | 0/0 | 12909 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0031 | 0/0 | 12902 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0036 | 0/0 | 12902 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0037 | 0/0 | 12903 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0038 | 0/0 | 12904 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0039 | 0/0 | 12902 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0040 | 0/0 | 12902 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0041 | 0/0 | 12905 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0042 | 0/0 | 12902 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0043 | 0/0 | 12903 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0044 | 0/0 | 12903 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0045 | 0/0 | 12901 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0046 | 0/0 | 12902 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0047 | 0/0 | 12906 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0048 | 0/0 | 12903 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0049 | 0/0 | 12905 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0050 | 0/0 | 12905 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0051 | 0/0 | 12902 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0052 | 0/0 | 12902 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0053 | 0/0 | 12902 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0054 | 0/0 | 12902 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0055 | 0/0 | 12902 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0056 | 0/0 | 12904 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0057 | 0/0 | 12903 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0058 | 0/0 | 12902 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0059 | 0/0 | 12901 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0060 | 0/0 | 12902 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0061 | 0/0 | 12903 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0062 | 0/0 | 12903 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0063 | 0/0 | 12904 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0064 | 0/0 | 12902 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0065 | 0/0 | 12902 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0067 | 0/0 | 12905 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0069 | 0/0 | 12900 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0083 | 0/0 | 12902 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0087 | 0/0 | 12901 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0001t0088 | 0/0 | 12902 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0003t0002 | 0/0 | 12902 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0003t0005 | 0/0 | 12902 | 4 | 1 | 2 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0001c0007t0029 | 0/0 | 12916 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0003 | 0/0 | 12892 | 15 | 1 | 4 | 5 | 1 | 4 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0025 | 0/0 | 12893 | 2 | 0 | 1 | 0 | 1 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0026 | 0/0 | 12891 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0030 | 0/0 | 12881 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0066 | 0/0 | 12886 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0068 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0070 | 0/0 | 12892 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0071 | 0/0 | 12894 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0072 | 0/0 | 12893 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0073 | 0/0 | 12893 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0074 | 0/0 | 12889 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0075 | 0/0 | 12889 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0076 | 0/0 | 12888 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0078 | 0/0 | 12876 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0079 | 0/0 | 12875 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0080 | 0/0 | 12875 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0081 | 0/0 | 12879 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0082 | 0/0 | 12892 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0084 | 0/0 | 12886 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0085 | 0/0 | 12874 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0002c0002t0086 | 0/0 | 12887 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0003c0005t0032 | 0/0 | 12894 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0003c0005t0033 | 0/0 | 12896 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0003c0005t0034 | 0/0 | 12891 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0003c0005t0035 | 0/0 | 12891 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0004c0004t0001 | 0/0 | 12902 | 3 | 3 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0004c0004t0008 | 0/0 | 12901 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0005c0009t0001 | 0/0 | 12902 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0006c0008t0077 | 0/0 | 12875 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| a0007c0006t0089 | 0/0 | 12903 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | copy fasta | chr6 | 109090507 | 109179418 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0005g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0007g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0007g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0007g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0007g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0008g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0008g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0008g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0009g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0009g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0009g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0009g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0010g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0010g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0010g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0011g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0011g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0011g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0011g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0012g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0012g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0012g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0013g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0013g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0014g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0014g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0015g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0015g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0016g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0016g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0017g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0017g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0018g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0018g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0019g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0019g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0020g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0020g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0021g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0021g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0022g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0022g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0023g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0023g0092 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0024g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0024g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0027g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0028g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0031g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0036g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0037g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0038g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0039g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0040g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0041g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0042g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0043g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0044g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0045g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0046g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0047g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0048g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0049g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0050g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0051g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0052g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0053g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0054g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0055g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0056g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0057g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0058g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0059g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0060g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0061g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0062g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0063g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0064g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0065g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0067g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0069g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0083g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0087g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0001t0088g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0003t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0003t0005g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0003t0005g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0003t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0001c0007t0029g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0003g0001 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0003g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0025g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0025g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0026g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0026g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0030g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0066g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0068g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0070g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0071g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0072g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0073g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0074g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0075g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0076g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0078g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0079g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0080g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0081g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0082g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0084g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0085g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0002c0002t0086g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0003c0005t0032g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0003c0005t0033g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0003c0005t0034g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0003c0005t0035g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0004c0004t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0004c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0004c0004t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0004c0004t0008g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0005c0009t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0006c0008t0077g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| a0007c0006t0089g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0013 | g0190 | EUR | GBR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG00099 | hp2 | a0002 | c0002 | t0072 | g0016 | EUR | GBR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG00280 | hp1 | a0002 | c0002 | t0003 | g0013 | EUR | FIN | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0047 | EUR | FIN | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG00323 | hp2 | a0002 | c0002 | t0025 | g0025 | EUR | FIN | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | CHS | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG00438 | hp2 | a0002 | c0002 | t0003 | g0014 | EAS | CHS | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG00558 | hp2 | a0001 | c0001 | t0058 | g0076 | EAS | CHS | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0106 | EAS | CHS | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG00639 | hp1 | a0002 | c0002 | t0003 | g0030 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG00639 | hp2 | a0001 | c0001 | t0057 | g0073 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0187 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG00738 | hp2 | a0002 | c0002 | t0025 | g0020 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01081 | hp1 | a0001 | c0001 | t0007 | g0207 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01109 | hp1 | a0001 | c0001 | t0054 | g0169 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01109 | hp2 | a0001 | c0001 | t0036 | g0100 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01168 | hp1 | a0001 | c0003 | t0005 | g0003 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01168 | hp2 | a0002 | c0002 | t0086 | g0007 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01169 | hp1 | a0002 | c0002 | t0075 | g0008 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0184 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01175 | hp1 | a0002 | c0002 | t0076 | g0010 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01175 | hp2 | a0001 | c0001 | t0023 | g0063 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01192 | hp1 | a0001 | c0001 | t0010 | g0002 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01192 | hp2 | a0001 | c0003 | t0005 | g0003 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01243 | hp2 | a0001 | c0001 | t0038 | g0089 | AMR | PUR | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01255 | hp2 | a0001 | c0003 | t0002 | g0191 | AMR | CLM | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01257 | hp1 | a0002 | c0002 | t0003 | g0015 | AMR | CLM | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01257 | hp2 | a0001 | c0001 | t0010 | g0002 | AMR | CLM | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0178 | AMR | CLM | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01261 | hp2 | a0001 | c0001 | t0040 | g0043 | AMR | CLM | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | CLM | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01433 | hp2 | a0002 | c0002 | t0003 | g0029 | AMR | CLM | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01884 | hp1 | a0001 | c0001 | t0018 | g0153 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01884 | hp2 | a0005 | c0009 | t0001 | g0133 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01891 | hp1 | a0003 | c0005 | t0034 | g0208 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0112 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01952 | hp2 | a0002 | c0002 | t0003 | g0001 | AMR | PEL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0101 | AMR | PEL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0168 | AMR | PEL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02004 | hp2 | a0001 | c0001 | t0010 | g0094 | AMR | PEL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02027 | hp1 | a0001 | c0001 | t0055 | g0157 | EAS | KHV | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02027 | hp2 | a0001 | c0001 | t0015 | g0175 | EAS | KHV | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02055 | hp1 | a0001 | c0001 | t0024 | g0180 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02055 | hp2 | a0001 | c0001 | t0024 | g0093 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02083 | hp1 | a0002 | c0002 | t0003 | g0023 | EAS | KHV | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02129 | hp1 | a0001 | c0001 | t0062 | g0096 | EAS | KHV | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02129 | hp2 | a0001 | c0001 | t0022 | g0196 | EAS | KHV | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02145 | hp1 | a0001 | c0001 | t0049 | g0185 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0140 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02257 | hp2 | a0001 | c0001 | t0020 | g0181 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02258 | hp1 | a0001 | c0001 | t0017 | g0130 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02451 | hp1 | a0001 | c0001 | t0019 | g0206 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02451 | hp2 | a0002 | c0002 | t0074 | g0006 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02572 | hp1 | a0001 | c0001 | t0012 | g0219 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02572 | hp2 | a0001 | c0001 | t0060 | g0174 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02615 | hp2 | a0001 | c0001 | t0065 | g0147 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0161 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02630 | hp1 | a0006 | c0008 | t0077 | g0212 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02630 | hp2 | a0001 | c0001 | t0061 | g0203 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02647 | hp1 | a0001 | c0001 | t0083 | g0110 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02647 | hp2 | a0001 | c0001 | t0088 | g0160 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02683 | hp1 | a0001 | c0001 | t0044 | g0120 | SAS | PJL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02683 | hp2 | a0001 | c0001 | t0052 | g0189 | SAS | PJL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0167 | SAS | PJL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02735 | hp1 | a0002 | c0002 | t0003 | g0027 | SAS | PJL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02735 | hp2 | a0001 | c0001 | t0013 | g0197 | SAS | PJL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02738 | hp1 | a0002 | c0002 | t0071 | g0012 | SAS | PJL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02738 | hp2 | a0001 | c0001 | t0067 | g0186 | SAS | PJL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02818 | hp2 | a0002 | c0002 | t0082 | g0204 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02886 | hp1 | a0002 | c0002 | t0068 | g0009 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02886 | hp2 | a0001 | c0001 | t0015 | g0162 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02895 | hp1 | a0001 | c0001 | t0014 | g0135 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02895 | hp2 | a0001 | c0001 | t0059 | g0165 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02896 | hp1 | a0004 | c0004 | t0008 | g0132 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0111 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0116 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02897 | hp2 | a0001 | c0001 | t0014 | g0154 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0148 | AFR | ESN | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02965 | hp1 | a0001 | c0001 | t0037 | g0090 | AFR | ESN | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02976 | hp1 | a0001 | c0001 | t0051 | g0134 | AFR | ESN | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02976 | hp2 | a0001 | c0001 | t0020 | g0194 | AFR | ESN | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0113 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03041 | hp2 | a0002 | c0002 | t0081 | g0143 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03130 | hp1 | a0002 | c0002 | t0084 | g0011 | AFR | ESN | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03130 | hp2 | a0001 | c0001 | t0050 | g0182 | AFR | ESN | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03195 | hp1 | a0001 | c0001 | t0022 | g0155 | AFR | ESN | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03195 | hp2 | a0001 | c0001 | t0017 | g0129 | AFR | ESN | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0177 | AFR | MSL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0144 | AFR | MSL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03225 | hp1 | a0001 | c0001 | t0012 | g0220 | AFR | MSL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03225 | hp2 | a0001 | c0001 | t0063 | g0151 | AFR | MSL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03239 | hp1 | a0001 | c0001 | t0045 | g0088 | SAS | PJL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03239 | hp2 | a0001 | c0001 | t0006 | g0173 | SAS | PJL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03453 | hp1 | a0003 | c0005 | t0032 | g0004 | AFR | MSL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0183 | AFR | MSL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03486 | hp1 | a0004 | c0004 | t0001 | g0136 | AFR | MSL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03486 | hp2 | a0001 | c0001 | t0011 | g0138 | AFR | MSL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03490 | hp1 | a0001 | c0001 | t0006 | g0172 | SAS | PJL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03516 | hp1 | a0001 | c0001 | t0009 | g0150 | AFR | ESN | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0131 | AFR | ESN | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03540 | hp1 | a0002 | c0002 | t0030 | g0211 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03540 | hp2 | a0001 | c0001 | t0012 | g0218 | AFR | GWD | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03579 | hp1 | a0001 | c0001 | t0027 | g0217 | AFR | MSL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03579 | hp2 | a0002 | c0002 | t0085 | g0213 | AFR | MSL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03654 | hp1 | a0001 | c0003 | t0005 | g0193 | SAS | PJL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03669 | hp2 | a0002 | c0002 | t0070 | g0021 | SAS | PJL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03688 | hp2 | a0002 | c0002 | t0003 | g0028 | SAS | STU | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03704 | hp2 | a0002 | c0002 | t0003 | g0001 | SAS | PJL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03831 | hp1 | a0001 | c0001 | t0018 | g0102 | SAS | BEB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03831 | hp2 | a0001 | c0001 | t0043 | g0067 | SAS | BEB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03834 | hp1 | a0002 | c0002 | t0066 | g0022 | SAS | BEB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03834 | hp2 | a0001 | c0001 | t0016 | g0056 | SAS | BEB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG04115 | hp1 | a0001 | c0001 | t0007 | g0033 | SAS | STU | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG04115 | hp2 | a0007 | c0006 | t0089 | g0062 | SAS | STU | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG04184 | hp1 | a0001 | c0001 | t0056 | g0202 | SAS | BEB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0142 | AFR | YRI | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18906 | hp1 | a0003 | c0005 | t0033 | g0004 | AFR | YRI | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18906 | hp2 | a0001 | c0001 | t0028 | g0221 | AFR | YRI | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18948 | hp1 | a0001 | c0001 | t0064 | g0126 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18951 | hp1 | a0001 | c0001 | t0010 | g0119 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18951 | hp2 | a0002 | c0002 | t0003 | g0019 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18977 | hp1 | a0001 | c0001 | t0046 | g0041 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18977 | hp2 | a0001 | c0001 | t0047 | g0171 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18981 | hp2 | a0001 | c0001 | t0041 | g0070 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA18998 | hp2 | a0002 | c0002 | t0026 | g0026 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19007 | hp1 | a0002 | c0002 | t0003 | g0018 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19010 | hp2 | a0001 | c0001 | t0042 | g0072 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19030 | hp1 | a0001 | c0007 | t0029 | g0005 | AFR | LWK | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19030 | hp2 | a0001 | c0001 | t0069 | g0163 | AFR | LWK | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19043 | hp1 | a0004 | c0004 | t0001 | g0152 | AFR | LWK | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19062 | hp1 | a0001 | c0001 | t0048 | g0170 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19063 | hp1 | a0001 | c0001 | t0039 | g0054 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19063 | hp2 | a0002 | c0002 | t0026 | g0024 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19074 | hp1 | a0001 | c0001 | t0031 | g0046 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19074 | hp2 | a0001 | c0001 | t0016 | g0115 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19088 | hp2 | a0002 | c0002 | t0003 | g0017 | EAS | JPT | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19240 | hp1 | a0001 | c0001 | t0087 | g0159 | AFR | YRI | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0166 | AFR | YRI | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA20129 | hp1 | a0002 | c0002 | t0003 | g0001 | AFR | ASW | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0164 | AFR | ASW | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | GIH | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA20905 | hp2 | a0002 | c0002 | t0003 | g0001 | SAS | GIH | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG01123 | hp2 | a0002 | c0002 | t0073 | g0001 | AMR | CLM | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02109 | hp1 | a0002 | c0002 | t0080 | g0210 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02109 | hp2 | a0001 | c0001 | t0053 | g0141 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02486 | hp1 | a0001 | c0003 | t0005 | g0201 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02486 | hp2 | a0002 | c0002 | t0078 | g0205 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02559 | hp1 | a0002 | c0002 | t0079 | g0209 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG02559 | hp2 | a0001 | c0001 | t0019 | g0179 | AFR | ACB | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0176 | AFR | MSL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0139 | AFR | MSL | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG06807 | hp1 | a0001 | c0001 | t0021 | g0216 | AFR | USA | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| HG06807 | hp2 | a0001 | c0001 | t0021 | g0104 | AFR | USA | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA20300 | hp1 | a0003 | c0005 | t0035 | g0215 | AFR | USA | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0145 | AFR | USA | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA21309 | hp1 | a0004 | c0004 | t0001 | g0137 | AFR | LWK | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0192 | REF | REF | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0023 | g0092 | REF | REF | CEP57L1_chr6_109090507_109179418 | CEP57L1 | chr6 | 109090507 | 109179418 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:109145249
|
G | T | 1 | a0003 | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
missense_variant | MODERATE | c.28G>T | p.Val10Leu | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 2/11 | 100/12903 | 28/1383 | 10/460 | chr6 | 109145249 | ||
| chr6:109150148
|
C | G | 1 | a0005 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.371C>G | p.Ser124Cys | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/11 | 443/12903 | 371/1383 | 124/460 | chr6 | 109150148 | ||
| chr6:109150237
|
C | T | 1 | a0006 | 1 | HG02630.hp1 | stop_gained&splice_region_variant | HIGH | c.460C>T | p.Gln154* | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/11 | 532/12903 | 460/1383 | 154/460 | chr6 | 109150237 | ||
| chr6:109155232
|
C | A | 1 | a0004 | 4 | HG02896.hp1 HG03486.hp1 NA19043.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.582C>A | p.Asp194Glu | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 6/11 | 654/12903 | 582/1383 | 194/460 | chr6 | 109155232 | ||
| chr6:109159339
|
A | T | 1 | a0007 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.893A>T | p.Lys298Met | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 9/11 | 965/12903 | 893/1383 | 298/460 | chr6 | 109159339 | ||
| chr6:109159359
|
T | C | 3 | a0002a0003a0006 | 42 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(39): Show |
missense_variant | MODERATE | c.913T>C | p.Trp305Arg | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 9/11 | 985/12903 | 913/1383 | 305/460 | chr6 | 109159359 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:109146933
|
A | G | 1 | a0001c0003 | 5 | HG01168.hp1 HG01192.hp2 HG01255.hp2 others(2): Show |
synonymous_variant | LOW | c.336A>G | p.Lys112Lys | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/11 | 408/12903 | 336/1383 | 112/460 | chr6 | 109146933 | ||
| chr6:109155850
|
C | T | 1 | a0001c0007 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.717C>T | p.His239His | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/11 | 789/12903 | 717/1383 | 239/460 | chr6 | 109155850 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:109163070
|
T | C | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*100T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 100 | chr6 | 109163070 | |||||
| chr6:109163359
|
A | C | 1 | a0007c0006t0089 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*389A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 389 | chr6 | 109163359 | |||||
| chr6:109163523
|
T | G | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*553T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 553 | chr6 | 109163523 | |||||
| chr6:109163598
|
GT | G | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*636delT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 636 | INFO_REALIGN_3_PRIME | chr6 | 109163598 | ||||
| chr6:109163606
|
T | A | 2 | a0001c0007t0029a0002c0002t0030 | 2 | HG03540.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*636T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 636 | chr6 | 109163606 | |||||
| chr6:109163688
|
A | G | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*718A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 718 | chr6 | 109163688 | |||||
| chr6:109164056
|
AG | A | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1089delG | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 1089 | INFO_REALIGN_3_PRIME | chr6 | 109164056 | ||||
| chr6:109164687
|
G | C | 1 | a0001c0001t0031 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1717G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 1717 | chr6 | 109164687 | |||||
| chr6:109164810
|
G | A | 1 | a0001c0007t0029 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1840G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 1840 | chr6 | 109164810 | |||||
| chr6:109164935
|
G | A | 4 | a0003c0005t0032a0003c0005t0033a0003c0005t0034others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1965G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 1965 | chr6 | 109164935 | |||||
| chr6:109164946
|
C | T | 2 | a0001c0001t0087a0001c0001t0088 | 2 | HG02647.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1976C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 1976 | chr6 | 109164946 | |||||
| chr6:109165058
|
C | A | 1 | a0001c0001t0036 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2088C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 2088 | chr6 | 109165058 | |||||
| chr6:109165076
|
CA | C | 6 | a0001c0001t0008a0001c0001t0083a0002c0002t0084others(3): Show | 9 | HG01168.hp2 HG01891.hp2 HG02647.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2123delA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 2123 | INFO_REALIGN_3_PRIME | chr6 | 109165076 | ||||
| chr6:109165076
|
CAA | C | 4 | a0001c0001t0012a0001c0001t0027a0001c0001t0028others(1): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2122_*2123delAA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 2122 | INFO_REALIGN_3_PRIME | chr6 | 109165076 | ||||
| chr6:109165377
|
A | G | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2407A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 2407 | chr6 | 109165377 | |||||
| chr6:109165414
|
CA | C | 21 | a0001c0001t0069a0002c0002t0003a0002c0002t0025others(18): Show | 37 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2460delA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 2460 | INFO_REALIGN_3_PRIME | chr6 | 109165414 | ||||
| chr6:109165414
|
CAA | C | 4 | a0001c0001t0012a0001c0001t0027a0001c0001t0028others(1): Show | 6 | HG01168.hp2 HG02572.hp1 HG03225.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2459_*2460delAA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 2459 | INFO_REALIGN_3_PRIME | chr6 | 109165414 | ||||
| chr6:109166172
|
T | C | 2 | a0001c0001t0037a0001c0001t0038 | 2 | HG01243.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3202T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 3202 | chr6 | 109166172 | |||||
| chr6:109166332
|
G | A | 3 | a0003c0005t0032a0003c0005t0033a0003c0005t0034 | 3 | HG01891.hp1 HG03453.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3362G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 3362 | chr6 | 109166332 | |||||
| chr6:109166381
|
C | CT | 30 | a0001c0001t0012a0001c0001t0027a0001c0001t0028others(27): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*3427dupT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 3428 | INFO_REALIGN_3_PRIME | chr6 | 109166381 | ||||
| chr6:109166405
|
A | G | 1 | a0002c0002t0082 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3435A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 3435 | chr6 | 109166405 | |||||
| chr6:109166582
|
T | C | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3612T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 3612 | chr6 | 109166582 | |||||
| chr6:109166907
|
C | G | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3937C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 3937 | chr6 | 109166907 | |||||
| chr6:109167063
|
TAAATAA | T | 7 | a0002c0002t0030a0002c0002t0078a0002c0002t0079others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4100_*4105delAAAT others(2): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4100 | INFO_REALIGN_3_PRIME | chr6 | 109167063 | ||||
| chr6:109167155
|
C | G | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4185C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4185 | chr6 | 109167155 | |||||
| chr6:109167199
|
G | A | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4229G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4229 | chr6 | 109167199 | |||||
| chr6:109167205
|
GT | G | 90 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(87): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*4245delT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4245 | INFO_REALIGN_3_PRIME | chr6 | 109167205 | ||||
| chr6:109167207
|
T | G | 4 | a0003c0005t0032a0003c0005t0033a0003c0005t0034others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4237T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4237 | chr6 | 109167207 | |||||
| chr6:109167329
|
AT | A | 23 | a0001c0001t0012a0001c0001t0027a0001c0001t0028others(20): Show | 41 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*4369delT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4369 | INFO_REALIGN_3_PRIME | chr6 | 109167329 | ||||
| chr6:109167329
|
ATT | A | 7 | a0002c0002t0030a0002c0002t0078a0002c0002t0079others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4368_*4369delTT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4368 | INFO_REALIGN_3_PRIME | chr6 | 109167329 | ||||
| chr6:109167341
|
C | G | 1 | a0001c0001t0065 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4371C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4371 | chr6 | 109167341 | |||||
| chr6:109167468
|
A | G | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4498A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4498 | chr6 | 109167468 | |||||
| chr6:109167563
|
G | C | 6 | a0001c0001t0004a0001c0001t0036a0001c0001t0039others(3): Show | 13 | HG00609.hp1 HG01109.hp2 HG01261.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4593G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4593 | chr6 | 109167563 | |||||
| chr6:109167564
|
C | G | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4594C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4594 | chr6 | 109167564 | |||||
| chr6:109167585
|
G | A | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4615G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4615 | chr6 | 109167585 | |||||
| chr6:109167610
|
G | A | 1 | a0001c0001t0043 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4640G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4640 | chr6 | 109167610 | |||||
| chr6:109167617
|
C | T | 1 | a0001c0001t0042 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4647C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4647 | chr6 | 109167617 | |||||
| chr6:109167619
|
G | T | 1 | a0002c0002t0084 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4649G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4649 | chr6 | 109167619 | |||||
| chr6:109167681
|
C | CA | 11 | a0001c0001t0012a0001c0001t0027a0001c0007t0029others(8): Show | 14 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4722dupA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4723 | INFO_REALIGN_3_PRIME | chr6 | 109167681 | ||||
| chr6:109167693
|
G | A | 30 | a0001c0001t0012a0001c0001t0027a0001c0001t0028others(27): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*4723G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4723 | chr6 | 109167693 | |||||
| chr6:109167698
|
G | A | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4728G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4728 | chr6 | 109167698 | |||||
| chr6:109167735
|
G | A | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4765G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4765 | chr6 | 109167735 | |||||
| chr6:109167756
|
C | T | 1 | a0001c0001t0064 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4786C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 4786 | chr6 | 109167756 | |||||
| chr6:109168480
|
A | G | 3 | a0001c0007t0029a0002c0002t0030a0002c0002t0081 | 3 | HG03041.hp2 HG03540.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5510A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 5510 | chr6 | 109168480 | |||||
| chr6:109168590
|
A | AT | 31 | a0001c0001t0012a0001c0001t0022a0001c0001t0024others(28): Show | 50 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*5642dupT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 5643 | INFO_REALIGN_3_PRIME | chr6 | 109168590 | ||||
| chr6:109168590
|
AT | A | 7 | a0001c0001t0005a0001c0001t0013a0001c0001t0044others(4): Show | 14 | HG00099.hp1 HG00738.hp1 HG01168.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5642delT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 5642 | INFO_REALIGN_3_PRIME | chr6 | 109168590 | ||||
| chr6:109168665
|
G | A | 1 | a0001c0001t0009 | 4 | HG02922.hp2 HG03516.hp1 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5695G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 5695 | chr6 | 109168665 | |||||
| chr6:109168724
|
T | G | 22 | a0002c0002t0003a0002c0002t0025a0002c0002t0026others(19): Show | 38 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*5754T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 5754 | chr6 | 109168724 | |||||
| chr6:109168798
|
A | G | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5828A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 5828 | chr6 | 109168798 | |||||
| chr6:109168842
|
C | T | 4 | a0001c0001t0040a0003c0005t0032a0003c0005t0033others(1): Show | 4 | HG01261.hp2 HG01891.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5872C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 5872 | chr6 | 109168842 | |||||
| chr6:109168872
|
A | G | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5902A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 5902 | chr6 | 109168872 | |||||
| chr6:109168905
|
T | A | 2 | a0002c0002t0030a0002c0002t0081 | 2 | HG03041.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5935T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 5935 | chr6 | 109168905 | |||||
| chr6:109169039
|
G | A | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6069G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 6069 | chr6 | 109169039 | |||||
| chr6:109169083
|
G | A | 1 | a0001c0001t0010 | 4 | HG01192.hp1 HG01257.hp2 HG02004.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6113G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 6113 | chr6 | 109169083 | |||||
| chr6:109169096
|
T | C | 1 | a0006c0008t0077 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6126T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 6126 | chr6 | 109169096 | |||||
| chr6:109169111
|
G | A | 1 | a0001c0001t0046 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6141G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 6141 | chr6 | 109169111 | |||||
| chr6:109169158
|
G | A | 1 | a0001c0001t0014 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6188G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 6188 | chr6 | 109169158 | |||||
| chr6:109169190
|
C | T | 3 | a0001c0007t0029a0002c0002t0030a0002c0002t0081 | 3 | HG03041.hp2 HG03540.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6220C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 6220 | chr6 | 109169190 | |||||
| chr6:109169226
|
C | CA | 10 | a0001c0001t0005a0001c0001t0007a0001c0001t0015others(7): Show | 22 | HG00738.hp1 HG01081.hp1 HG01168.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*6277dupA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 6278 | INFO_REALIGN_3_PRIME | chr6 | 109169226 | ||||
| chr6:109169226
|
C | CAA | 7 | a0001c0001t0012a0001c0001t0027a0001c0001t0044others(4): Show | 9 | HG02572.hp1 HG02683.hp1 HG02738.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6276_*6277dupAA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 6278 | INFO_REALIGN_3_PRIME | chr6 | 109169226 | ||||
| chr6:109169226
|
C | CAAA | 6 | a0001c0001t0028a0002c0002t0068a0002c0002t0074others(3): Show | 6 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6275_*6277dupAAA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 6278 | INFO_REALIGN_3_PRIME | chr6 | 109169226 | ||||
| chr6:109169226
|
C | CAAAA | 11 | a0002c0002t0003a0002c0002t0025a0002c0002t0026others(8): Show | 27 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*6274_*6277dupAAAA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 6278 | INFO_REALIGN_3_PRIME | chr6 | 109169226 | ||||
| chr6:109169226
|
CAAA | C | 5 | a0002c0002t0078a0002c0002t0079a0002c0002t0080others(2): Show | 5 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6275_*6277delAAA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 6275 | INFO_REALIGN_3_PRIME | chr6 | 109169226 | ||||
| chr6:109169733
|
T | A | 1 | a0001c0001t0051 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6763T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 6763 | chr6 | 109169733 | |||||
| chr6:109169802
|
T | C | 1 | a0001c0001t0027 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6832T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 6832 | chr6 | 109169802 | |||||
| chr6:109169844
|
C | T | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6874C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 6874 | chr6 | 109169844 | |||||
| chr6:109170081
|
G | A | 1 | a0001c0001t0017 | 2 | HG02258.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7111G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 7111 | chr6 | 109170081 | |||||
| chr6:109170167
|
T | C | 1 | a0001c0001t0052 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7197T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 7197 | chr6 | 109170167 | |||||
| chr6:109170384
|
C | G | 1 | a0001c0001t0045 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7414C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 7414 | chr6 | 109170384 | |||||
| chr6:109170393
|
G | T | 3 | a0002c0002t0070a0002c0002t0071a0002c0002t0072 | 3 | HG00099.hp2 HG02738.hp1 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7423G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 7423 | chr6 | 109170393 | |||||
| chr6:109170673
|
T | G | 1 | a0001c0001t0039 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7703T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 7703 | chr6 | 109170673 | |||||
| chr6:109170690
|
G | T | 4 | a0001c0001t0012a0001c0001t0027a0001c0001t0028others(1): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7720G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 7720 | chr6 | 109170690 | |||||
| chr6:109170744
|
A | G | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7774A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 7774 | chr6 | 109170744 | |||||
| chr6:109170867
|
AC | A | 27 | a0001c0007t0029a0002c0002t0003a0002c0002t0025others(24): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*7899delC | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 7899 | INFO_REALIGN_3_PRIME | chr6 | 109170867 | ||||
| chr6:109170954
|
A | G | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7984A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 7984 | chr6 | 109170954 | |||||
| chr6:109170999
|
A | G | 1 | a0001c0001t0059 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8029A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 8029 | chr6 | 109170999 | |||||
| chr6:109171100
|
A | AG | 30 | a0001c0001t0012a0001c0001t0027a0001c0001t0028others(27): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*8132dupG | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 8133 | INFO_REALIGN_3_PRIME | chr6 | 109171100 | ||||
| chr6:109171111
|
T | C | 27 | a0001c0007t0029a0002c0002t0003a0002c0002t0025others(24): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*8141T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 8141 | chr6 | 109171111 | |||||
| chr6:109171242
|
A | ATTTTTT | 14 | a0001c0001t0012a0001c0001t0027a0002c0002t0068others(11): Show | 16 | HG01168.hp2 HG01169.hp1 HG02109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*8280_*8285dupTTTT others(2): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 8286 | INFO_REALIGN_3_PRIME | chr6 | 109171242 | ||||
| chr6:109171242
|
A | ATTTTTTT | 15 | a0001c0001t0028a0001c0007t0029a0002c0002t0003others(12): Show | 31 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*8279_*8285dupTTTT others(3): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 8286 | INFO_REALIGN_3_PRIME | chr6 | 109171242 | ||||
| chr6:109171278
|
G | C | 1 | a0001c0001t0053 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8308G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 8308 | chr6 | 109171278 | |||||
| chr6:109171325
|
G | T | 1 | a0001c0001t0058 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8355G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 8355 | chr6 | 109171325 | |||||
| chr6:109171403
|
T | TG | 13 | a0001c0007t0029a0002c0002t0003a0002c0002t0025others(10): Show | 29 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*8434dupG | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 8435 | INFO_REALIGN_3_PRIME | chr6 | 109171403 | ||||
| chr6:109171404
|
G | GT | 5 | a0001c0001t0019a0001c0001t0020a0001c0001t0021others(2): Show | 9 | HG02055.hp1 HG02055.hp2 HG02257.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8445dupT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 8446 | INFO_REALIGN_3_PRIME | chr6 | 109171404 | ||||
| chr6:109171404
|
GT | G | 10 | a0001c0001t0006a0001c0001t0015a0001c0001t0017others(7): Show | 19 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*8445delT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 8445 | INFO_REALIGN_3_PRIME | chr6 | 109171404 | ||||
| chr6:109171405
|
T | G | 14 | a0002c0002t0068a0002c0002t0074a0002c0002t0075others(11): Show | 14 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*8435T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 8435 | chr6 | 109171405 | |||||
| chr6:109171537
|
G | A | 27 | a0001c0007t0029a0002c0002t0003a0002c0002t0025others(24): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*8567G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 8567 | chr6 | 109171537 | |||||
| chr6:109171567
|
G | A | 4 | a0002c0002t0068a0002c0002t0074a0002c0002t0075others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8597G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 8597 | chr6 | 109171567 | |||||
| chr6:109171634
|
T | C | 27 | a0001c0007t0029a0002c0002t0003a0002c0002t0025others(24): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*8664T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 8664 | chr6 | 109171634 | |||||
| chr6:109172165
|
TAGACAGA others(16): Show |
T | 27 | a0001c0007t0029a0002c0002t0003a0002c0002t0025others(24): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*9220_*9242delGACA others(19): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 9220 | INFO_REALIGN_3_PRIME | chr6 | 109172165 | ||||
| chr6:109172196
|
C | T | 27 | a0001c0007t0029a0002c0002t0003a0002c0002t0025others(24): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*9226C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 9226 | chr6 | 109172196 | |||||
| chr6:109172301
|
C | T | 1 | a0002c0002t0084 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9331C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 9331 | chr6 | 109172301 | |||||
| chr6:109172609
|
A | G | 27 | a0001c0007t0029a0002c0002t0003a0002c0002t0025others(24): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*9639A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 9639 | chr6 | 109172609 | |||||
| chr6:109172696
|
C | T | 3 | a0001c0001t0009a0001c0001t0011a0001c0001t0065 | 9 | HG02615.hp2 HG02922.hp2 HG03209.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*9726C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 9726 | chr6 | 109172696 | |||||
| chr6:109172947
|
C | A | 1 | a0001c0001t0055 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9977C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 9977 | chr6 | 109172947 | |||||
| chr6:109173034
|
G | A | 4 | a0003c0005t0032a0003c0005t0033a0003c0005t0034others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10064G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10064 | chr6 | 109173034 | |||||
| chr6:109173133
|
A | C | 2 | a0002c0002t0075a0002c0002t0086 | 2 | HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10163A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10163 | chr6 | 109173133 | |||||
| chr6:109173251
|
A | G | 1 | a0003c0005t0035 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10281A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10281 | chr6 | 109173251 | |||||
| chr6:109173270
|
T | G | 27 | a0001c0007t0029a0002c0002t0003a0002c0002t0025others(24): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*10300T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10300 | chr6 | 109173270 | |||||
| chr6:109173377
|
G | T | 2 | a0002c0002t0030a0002c0002t0081 | 2 | HG03041.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10407G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10407 | chr6 | 109173377 | |||||
| chr6:109173410
|
C | T | 1 | a0002c0002t0080 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10440C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10440 | chr6 | 109173410 | |||||
| chr6:109173424
|
CT | C | 17 | a0001c0007t0029a0002c0002t0003a0002c0002t0025others(14): Show | 33 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*10470delT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10470 | INFO_REALIGN_3_PRIME | chr6 | 109173424 | ||||
| chr6:109173424
|
CTT | C | 6 | a0002c0002t0078a0002c0002t0079a0002c0002t0080others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*10469_*10470delTT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10469 | INFO_REALIGN_3_PRIME | chr6 | 109173424 | ||||
| chr6:109173464
|
C | T | 3 | a0001c0007t0029a0002c0002t0030a0002c0002t0081 | 3 | HG03041.hp2 HG03540.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10494C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10494 | chr6 | 109173464 | |||||
| chr6:109173486
|
G | A | 27 | a0001c0007t0029a0002c0002t0003a0002c0002t0025others(24): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*10516G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10516 | chr6 | 109173486 | |||||
| chr6:109173520
|
G | A | 1 | a0001c0001t0061 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10550G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10550 | chr6 | 109173520 | |||||
| chr6:109173593
|
T | TA | 6 | a0001c0001t0047a0001c0001t0049a0001c0001t0054others(3): Show | 6 | HG00639.hp2 HG01109.hp1 HG02145.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*10638dupA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10639 | INFO_REALIGN_3_PRIME | chr6 | 109173593 | ||||
| chr6:109173593
|
TA | T | 26 | a0001c0007t0029a0002c0002t0003a0002c0002t0025others(23): Show | 42 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*10638delA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10638 | INFO_REALIGN_3_PRIME | chr6 | 109173593 | ||||
| chr6:109173609
|
T | A | 9 | a0001c0001t0002a0001c0001t0016a0001c0001t0031others(6): Show | 33 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*10639T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10639 | chr6 | 109173609 | |||||
| chr6:109173630
|
G | C | 27 | a0001c0007t0029a0002c0002t0003a0002c0002t0025others(24): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*10660G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10660 | chr6 | 109173630 | |||||
| chr6:109173748
|
G | A | 27 | a0001c0007t0029a0002c0002t0003a0002c0002t0025others(24): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*10778G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10778 | chr6 | 109173748 | |||||
| chr6:109173825
|
G | A | 27 | a0001c0007t0029a0002c0002t0003a0002c0002t0025others(24): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*10855G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10855 | chr6 | 109173825 | |||||
| chr6:109173869
|
A | C | 30 | a0001c0001t0012a0001c0001t0027a0001c0001t0028others(27): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*10899A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10899 | chr6 | 109173869 | |||||
| chr6:109173934
|
T | TA | 9 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(6): Show | 14 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*10980dupA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10981 | INFO_REALIGN_3_PRIME | chr6 | 109173934 | ||||
| chr6:109173934
|
TAAAAAAA | T | 27 | a0001c0007t0029a0002c0002t0003a0002c0002t0025others(24): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*10974_*10980delAA others(5): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10974 | INFO_REALIGN_3_PRIME | chr6 | 109173934 | ||||
| chr6:109173948
|
A | C | 4 | a0002c0002t0068a0002c0002t0074a0002c0002t0075others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10978A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 10978 | chr6 | 109173948 | |||||
| chr6:109173982
|
C | T | 1 | a0002c0002t0084 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11012C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 11012 | chr6 | 109173982 | |||||
| chr6:109174015
|
G | A | 27 | a0001c0007t0029a0002c0002t0003a0002c0002t0025others(24): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*11045G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 11045 | chr6 | 109174015 | |||||
| chr6:109174099
|
C | CA | 8 | a0001c0001t0018a0001c0001t0019a0001c0001t0041others(5): Show | 10 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*11144dupA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 11145 | INFO_REALIGN_3_PRIME | chr6 | 109174099 | ||||
| chr6:109174099
|
C | CAAAAAAA others(31): Show |
1 | a0001c0007t0029 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11144_*11145insAA others(36): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 11145 | INFO_REALIGN_3_PRIME | chr6 | 109174099 | ||||
| chr6:109174109
|
A | AAAAAAAA others(5): Show |
1 | a0003c0005t0033 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11144_*11145insAA others(10): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 11145 | INFO_REALIGN_3_PRIME | chr6 | 109174109 | ||||
| chr6:109174109
|
A | AAAAAAAA others(4): Show |
6 | a0002c0002t0071a0002c0002t0073a0002c0002t0078others(3): Show | 6 | HG01123.hp2 HG01891.hp1 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*11144_*11145insAA others(9): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 11145 | INFO_REALIGN_3_PRIME | chr6 | 109174109 | ||||
| chr6:109174109
|
A | AAAAAAAA others(3): Show |
19 | a0002c0002t0003a0002c0002t0025a0002c0002t0026others(16): Show | 35 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*11144_*11145insAA others(8): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 11145 | INFO_REALIGN_3_PRIME | chr6 | 109174109 | ||||
| chr6:109174130
|
C | A | 27 | a0001c0007t0029a0002c0002t0003a0002c0002t0025others(24): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*11160C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 11160 | chr6 | 109174130 | |||||
| chr6:109174381
|
T | G | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0028 | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*11411T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 11/11 | 11411 | chr6 | 109174381 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:109095584
|
T | C | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4+9T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109095584 | ||||||
| chr6:109095863
|
G | A | 4 | a0002c0002t0068g0009a0002c0002t0074g0006a0002c0002t0075g0008others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+288G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109095863 | ||||||
| chr6:109096014
|
G | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+439G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109096014 | ||||||
| chr6:109096063
|
G | T | 1 | a0001c0001t0021g0216 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-4+488G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109096063 | ||||||
| chr6:109096278
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+703G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109096278 | ||||||
| chr6:109096303
|
C | A | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4+728C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109096303 | ||||||
| chr6:109096622
|
A | G | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4+1047A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109096622 | ||||||
| chr6:109096768
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+1193A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109096768 | ||||||
| chr6:109096872
|
T | C | 23 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(20): Show | 26 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.-4+1297T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109096872 | ||||||
| chr6:109097112
|
G | T | 1 | a0002c0002t0068g0009 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-4+1537G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109097112 | ||||||
| chr6:109097386
|
C | T | 1 | a0002c0002t0003g0030 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-4+1811C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109097386 | ||||||
| chr6:109097394
|
T | G | 1 | a0001c0001t0001g0031 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-4+1819T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109097394 | ||||||
| chr6:109097396
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-4+1821C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109097396 | ||||||
| chr6:109097546
|
A | C | 1 | a0003c0005t0035g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-4+1971A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109097546 | ||||||
| chr6:109097573
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-4+1998A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109097573 | ||||||
| chr6:109097781
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-4+2206G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109097781 | ||||||
| chr6:109097815
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+2240T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109097815 | ||||||
| chr6:109097867
|
A | G | 95 | a0001c0001t0001g0032a0001c0001t0001g0158a0001c0001t0001g0188others(92): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-4+2292A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109097867 | ||||||
| chr6:109097891
|
C | T | 1 | a0001c0001t0055g0157 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-4+2316C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109097891 | ||||||
| chr6:109097965
|
G | A | 1 | a0002c0002t0076g0010 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-4+2390G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109097965 | ||||||
| chr6:109098287
|
A | G | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4+2712A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109098287 | ||||||
| chr6:109098442
|
G | A | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4+2867G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109098442 | ||||||
| chr6:109098784
|
C | T | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4+3209C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109098784 | ||||||
| chr6:109098856
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+3281G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109098856 | ||||||
| chr6:109098944
|
A | G | 4 | a0002c0002t0030g0211a0002c0002t0080g0210a0002c0002t0085g0213others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+3369A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109098944 | ||||||
| chr6:109099022
|
A | G | 123 | a0001c0001t0001g0032a0001c0001t0001g0146a0001c0001t0001g0149others(120): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.-4+3447A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109099022 | ||||||
| chr6:109099078
|
A | G | 1 | a0002c0002t0085g0213 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-4+3503A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109099078 | ||||||
| chr6:109099088
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-4+3513C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109099088 | ||||||
| chr6:109099146
|
G | A | 3 | a0001c0001t0001g0158a0001c0001t0087g0159a0001c0001t0088g0160 | 3 | HG02647.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-4+3571G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109099146 | ||||||
| chr6:109099226
|
G | C | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4+3651G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109099226 | ||||||
| chr6:109099296
|
C | CTG | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+3722_-4+3723dup others(2): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109099296 | |||||
| chr6:109099321
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+3746A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109099321 | ||||||
| chr6:109099457
|
C | T | 1 | a0002c0002t0079g0209 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-4+3882C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109099457 | ||||||
| chr6:109099525
|
CTTTTATT others(11): Show |
C | 3 | a0001c0001t0001g0158a0001c0001t0087g0159a0001c0001t0088g0160 | 3 | HG02647.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-4+3973_-4+3990del others(18): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109099525 | |||||
| chr6:109099546
|
T | A | 1 | a0001c0001t0007g0033 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-4+3971T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109099546 | ||||||
| chr6:109099548
|
A | T | 1 | a0001c0001t0007g0033 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-4+3973A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109099548 | ||||||
| chr6:109099693
|
A | G | 1 | a0001c0001t0002g0127 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-4+4118A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109099693 | ||||||
| chr6:109099698
|
C | T | 1 | a0001c0001t0064g0126 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-4+4123C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109099698 | ||||||
| chr6:109099710
|
C | T | 2 | a0002c0002t0075g0008a0002c0002t0086g0007 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-4+4135C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109099710 | ||||||
| chr6:109099790
|
C | T | 4 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124others(1): Show | 4 | HG00423.hp1 NA18946.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+4215C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109099790 | ||||||
| chr6:109099794
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+4219C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109099794 | ||||||
| chr6:109099799
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-4+4224C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109099799 | ||||||
| chr6:109099869
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-4+4294A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109099869 | ||||||
| chr6:109099967
|
G | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+4392G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109099967 | ||||||
| chr6:109100033
|
A | G | 4 | a0002c0002t0068g0009a0002c0002t0074g0006a0002c0002t0075g0008others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+4458A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109100033 | ||||||
| chr6:109100070
|
A | G | 1 | a0001c0001t0022g0155 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-4+4495A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109100070 | ||||||
| chr6:109100313
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+4738A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109100313 | ||||||
| chr6:109100397
|
G | A | 19 | a0001c0001t0006g0161a0001c0001t0006g0164a0001c0001t0006g0166others(16): Show | 19 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.-4+4822G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109100397 | ||||||
| chr6:109100484
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+4909G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109100484 | ||||||
| chr6:109100547
|
C | T | 4 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+4972C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109100547 | ||||||
| chr6:109100628
|
T | C | 1 | a0002c0002t0003g0030 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-4+5053T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109100628 | ||||||
| chr6:109100672
|
C | CA | 91 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(88): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.-4+5117dupA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109100672 | |||||
| chr6:109100672
|
CA | C | 6 | a0001c0001t0001g0117a0001c0001t0002g0118a0001c0001t0004g0125others(3): Show | 6 | HG02683.hp1 HG02897.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4+5117delA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109100672 | |||||
| chr6:109100903
|
T | C | 4 | a0002c0002t0068g0009a0002c0002t0074g0006a0002c0002t0075g0008others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+5328T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109100903 | ||||||
| chr6:109100957
|
A | C | 3 | a0001c0001t0001g0158a0001c0001t0087g0159a0001c0001t0088g0160 | 3 | HG02647.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-4+5382A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109100957 | ||||||
| chr6:109101167
|
G | A | 1 | a0001c0001t0006g0161 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-4+5592G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109101167 | ||||||
| chr6:109101359
|
G | T | 1 | a0001c0001t0016g0115 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-4+5784G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109101359 | ||||||
| chr6:109101362
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-4+5787T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109101362 | ||||||
| chr6:109101476
|
T | G | 2 | a0001c0001t0011g0138a0001c0001t0011g0139 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-4+5901T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109101476 | ||||||
| chr6:109101522
|
CA | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+5953delA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109101522 | |||||
| chr6:109101525
|
A | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+5950A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109101525 | ||||||
| chr6:109101616
|
C | CT | 8 | a0001c0001t0015g0175a0001c0001t0060g0174a0002c0002t0068g0009others(5): Show | 8 | HG01168.hp2 HG01169.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4+6047dupT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109101616 | |||||
| chr6:109101622
|
T | C | 23 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(20): Show | 26 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.-4+6047T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109101622 | ||||||
| chr6:109101623
|
C | CT | 18 | a0001c0001t0001g0032a0001c0001t0001g0114a0001c0001t0001g0195others(15): Show | 18 | HG01106.hp2 HG01361.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-4+6063dupT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109101623 | |||||
| chr6:109101623
|
C | T | 63 | a0001c0001t0001g0158a0001c0001t0006g0164a0001c0001t0006g0166others(60): Show | 66 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.-4+6048C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109101623 | ||||||
| chr6:109101626
|
T | TTC | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+6052_-4+6053ins others(2): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109101626 | |||||
| chr6:109101736
|
C | T | 1 | a0001c0001t0044g0120 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-4+6161C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109101736 | ||||||
| chr6:109101788
|
G | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+6213G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109101788 | ||||||
| chr6:109101915
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+6340A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109101915 | ||||||
| chr6:109102118
|
G | T | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4+6543G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109102118 | ||||||
| chr6:109102191
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+6616T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109102191 | ||||||
| chr6:109102228
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+6653C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109102228 | ||||||
| chr6:109102229
|
C | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+6654C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109102229 | ||||||
| chr6:109102431
|
A | T | 1 | a0001c0001t0004g0108 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-4+6856A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109102431 | ||||||
| chr6:109102514
|
C | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+6939C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109102514 | ||||||
| chr6:109102650
|
G | GT | 6 | a0001c0001t0001g0107a0001c0001t0012g0218a0001c0001t0012g0219others(3): Show | 6 | HG00280.hp2 HG02572.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+7085dupT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109102650 | |||||
| chr6:109102689
|
T | C | 2 | a0002c0002t0075g0008a0002c0002t0086g0007 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-4+7114T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109102689 | ||||||
| chr6:109102802
|
A | G | 2 | a0002c0002t0030g0211a0006c0008t0077g0212 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-4+7227A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109102802 | ||||||
| chr6:109102803
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+7228T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109102803 | ||||||
| chr6:109102989
|
A | C | 1 | a0001c0001t0004g0106 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-4+7414A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109102989 | ||||||
| chr6:109103198
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+7623A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109103198 | ||||||
| chr6:109103353
|
GT | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+7779delT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109103353 | ||||||
| chr6:109103363
|
A | G | 2 | a0004c0004t0001g0136a0004c0004t0001g0137 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-4+7788A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109103363 | ||||||
| chr6:109103773
|
C | T | 1 | a0001c0001t0004g0105 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-4+8198C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109103773 | ||||||
| chr6:109103833
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+8258T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109103833 | ||||||
| chr6:109103893
|
A | G | 1 | a0001c0001t0021g0104 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-4+8318A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109103893 | ||||||
| chr6:109104040
|
G | GT | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4+8478dupT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109104040 | |||||
| chr6:109104118
|
C | T | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4+8543C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109104118 | ||||||
| chr6:109104145
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-4+8570A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109104145 | ||||||
| chr6:109104159
|
AACTT | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+8589_-4+8592del others(4): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109104159 | |||||
| chr6:109104183
|
A | G | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4+8608A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109104183 | ||||||
| chr6:109104197
|
G | A | 1 | a0001c0001t0011g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-4+8622G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109104197 | ||||||
| chr6:109104313
|
TA | T | 40 | a0001c0001t0010g0119a0001c0001t0021g0104a0002c0002t0003g0001others(37): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.-4+8748delA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109104313 | |||||
| chr6:109104314
|
A | T | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4+8739A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109104314 | ||||||
| chr6:109104323
|
A | T | 18 | a0001c0001t0006g0164a0001c0001t0006g0166a0001c0001t0006g0167others(15): Show | 18 | HG01109.hp1 HG01884.hp2 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.-4+8748A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109104323 | ||||||
| chr6:109104324
|
T | A | 1 | a0001c0001t0001g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-4+8749T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109104324 | ||||||
| chr6:109104757
|
A | T | 3 | a0001c0001t0001g0099a0001c0001t0004g0101a0001c0001t0036g0100 | 3 | HG01109.hp2 HG01981.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-4+9182A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109104757 | ||||||
| chr6:109104758
|
T | A | 10 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(7): Show | 10 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-4+9183T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109104758 | ||||||
| chr6:109104867
|
A | G | 1 | a0001c0001t0061g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-4+9292A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109104867 | ||||||
| chr6:109104874
|
A | G | 1 | a0001c0001t0002g0098 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-4+9299A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109104874 | ||||||
| chr6:109104982
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+9407C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109104982 | ||||||
| chr6:109105017
|
C | G | 1 | a0001c0001t0001g0097 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-4+9442C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109105017 | ||||||
| chr6:109105085
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+9510G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109105085 | ||||||
| chr6:109105161
|
G | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+9586G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109105161 | ||||||
| chr6:109105273
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+9698G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109105273 | ||||||
| chr6:109105387
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+9812C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109105387 | ||||||
| chr6:109105388
|
G | A | 1 | a0001c0001t0004g0040 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-4+9813G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109105388 | ||||||
| chr6:109105436
|
G | A | 2 | a0002c0002t0068g0009a0002c0002t0074g0006 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-4+9861G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109105436 | ||||||
| chr6:109105490
|
A | G | 1 | a0001c0001t0018g0153 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-4+9915A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109105490 | ||||||
| chr6:109105634
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+10059G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109105634 | ||||||
| chr6:109105736
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+10161A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109105736 | ||||||
| chr6:109105779
|
G | C | 65 | a0001c0001t0001g0158a0001c0001t0006g0161a0001c0001t0006g0164others(62): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.-4+10204G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109105779 | ||||||
| chr6:109105785
|
G | C | 1 | a0001c0001t0006g0164 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-4+10210G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109105785 | ||||||
| chr6:109105886
|
C | T | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4+10311C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109105886 | ||||||
| chr6:109105895
|
C | T | 1 | a0002c0002t0003g0027 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-4+10320C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109105895 | ||||||
| chr6:109105962
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+10387A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109105962 | ||||||
| chr6:109106020
|
T | G | 1 | a0001c0001t0005g0178 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-4+10445T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109106020 | ||||||
| chr6:109106319
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+10744C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109106319 | ||||||
| chr6:109106649
|
C | A | 21 | a0001c0001t0001g0158a0001c0001t0006g0161a0001c0001t0006g0164others(18): Show | 21 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.-4+11074C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109106649 | ||||||
| chr6:109106755
|
C | G | 1 | a0001c0003t0005g0193 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-4+11180C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109106755 | ||||||
| chr6:109106761
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+11186T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109106761 | ||||||
| chr6:109106981
|
C | A | 44 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(41): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.-4+11406C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109106981 | ||||||
| chr6:109106981
|
C | T | 2 | a0004c0004t0001g0136a0004c0004t0001g0137 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-4+11406C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109106981 | ||||||
| chr6:109107054
|
A | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+11479A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109107054 | ||||||
| chr6:109107105
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+11530C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109107105 | ||||||
| chr6:109107173
|
T | A | 16 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0001g0156others(13): Show | 16 | HG02109.hp2 HG02145.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.-4+11598T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109107173 | ||||||
| chr6:109107264
|
CTG | C | 38 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(35): Show | 41 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.-4+11691_-4+11692d others(4): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109107264 | |||||
| chr6:109107322
|
T | A | 1 | a0001c0001t0061g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-4+11747T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109107322 | ||||||
| chr6:109107368
|
G | C | 2 | a0001c0001t0001g0042a0001c0001t0046g0041 | 2 | HG00438.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.-4+11793G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109107368 | ||||||
| chr6:109107370
|
TTTCTC | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+11798_-4+11802d others(7): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109107370 | |||||
| chr6:109107466
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+11891T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109107466 | ||||||
| chr6:109107469
|
G | A | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4+11894G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109107469 | ||||||
| chr6:109107536
|
G | T | 4 | a0002c0002t0030g0211a0002c0002t0080g0210a0002c0002t0085g0213others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+11961G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109107536 | ||||||
| chr6:109107545
|
A | G | 1 | a0001c0001t0062g0096 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-4+11970A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109107545 | ||||||
| chr6:109107769
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+12194T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109107769 | ||||||
| chr6:109107815
|
G | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+12240G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109107815 | ||||||
| chr6:109107872
|
C | T | 3 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208 | 3 | HG01891.hp1 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-4+12297C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109107872 | ||||||
| chr6:109107890
|
G | A | 3 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208 | 3 | HG01891.hp1 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-4+12315G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109107890 | ||||||
| chr6:109107920
|
G | A | 1 | a0004c0004t0001g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-4+12345G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109107920 | ||||||
| chr6:109107940
|
C | CA | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+12373dupA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109107940 | |||||
| chr6:109108010
|
G | A | 1 | a0001c0001t0021g0216 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-4+12435G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109108010 | ||||||
| chr6:109108011
|
T | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+12436T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109108011 | ||||||
| chr6:109108178
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+12603C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109108178 | ||||||
| chr6:109108237
|
T | C | 7 | a0001c0001t0019g0179a0001c0001t0019g0206a0001c0001t0020g0181others(4): Show | 7 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+12662T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109108237 | ||||||
| chr6:109108303
|
C | T | 4 | a0001c0001t0014g0135a0001c0001t0014g0154a0001c0001t0051g0134others(1): Show | 4 | HG01884.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+12728C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109108303 | ||||||
| chr6:109108364
|
C | T | 1 | a0001c0001t0022g0155 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-4+12789C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109108364 | ||||||
| chr6:109108476
|
T | C | 2 | a0002c0002t0075g0008a0002c0002t0086g0007 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-4+12901T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109108476 | ||||||
| chr6:109108509
|
C | T | 1 | a0001c0001t0002g0095 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-4+12934C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109108509 | ||||||
| chr6:109108572
|
A | C | 18 | a0001c0001t0006g0161a0001c0001t0006g0164a0001c0001t0006g0166others(15): Show | 18 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.-4+12997A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109108572 | ||||||
| chr6:109108726
|
C | T | 1 | a0001c0001t0010g0094 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-4+13151C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109108726 | ||||||
| chr6:109109076
|
G | A | 1 | a0001c0001t0002g0127 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-4+13501G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109109076 | ||||||
| chr6:109109182
|
A | G | 1 | a0003c0005t0035g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-4+13607A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109109182 | ||||||
| chr6:109109234
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+13659A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109109234 | ||||||
| chr6:109109602
|
A | G | 4 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+14027A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109109602 | ||||||
| chr6:109109701
|
C | T | 1 | a0001c0001t0006g0164 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-4+14126C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109109701 | ||||||
| chr6:109109712
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+14137C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109109712 | ||||||
| chr6:109109713
|
G | A | 1 | a0002c0002t0084g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-4+14138G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109109713 | ||||||
| chr6:109110035
|
A | G | 1 | a0001c0001t0002g0124 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-4+14460A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109110035 | ||||||
| chr6:109110314
|
T | C | 217 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(214): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-4+14739T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109110314 | ||||||
| chr6:109110318
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+14743T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109110318 | ||||||
| chr6:109110369
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+14794C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109110369 | ||||||
| chr6:109110387
|
T | G | 1 | a0001c0001t0040g0043 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-4+14812T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109110387 | ||||||
| chr6:109110534
|
T | A | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4+14959T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109110534 | ||||||
| chr6:109110536
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+14961C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109110536 | ||||||
| chr6:109110607
|
A | G | 1 | a0001c0001t0028g0221 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-4+15032A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109110607 | ||||||
| chr6:109110665
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+15090T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109110665 | ||||||
| chr6:109110674
|
C | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+15099C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109110674 | ||||||
| chr6:109110702
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+15127G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109110702 | ||||||
| chr6:109110772
|
T | C | 21 | a0001c0001t0001g0158a0001c0001t0006g0161a0001c0001t0006g0164others(18): Show | 21 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.-4+15197T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109110772 | ||||||
| chr6:109110844
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+15269G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109110844 | ||||||
| chr6:109110941
|
G | A | 4 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0027g0217others(1): Show | 4 | HG02572.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+15366G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109110941 | ||||||
| chr6:109111000
|
G | C | 3 | a0001c0001t0001g0034a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | NA19060.hp2 NA19065.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-4+15425G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109111000 | ||||||
| chr6:109111045
|
T | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+15470T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109111045 | ||||||
| chr6:109111056
|
C | T | 1 | a0001c0001t0006g0173 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-4+15481C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109111056 | ||||||
| chr6:109111057
|
A | G | 1 | a0001c0001t0006g0173 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-4+15482A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109111057 | ||||||
| chr6:109111120
|
A | G | 1 | a0002c0002t0082g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-4+15545A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109111120 | ||||||
| chr6:109111133
|
C | T | 1 | a0001c0001t0002g0118 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-4+15558C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109111133 | ||||||
| chr6:109111476
|
A | G | 1 | a0001c0001t0056g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-4+15901A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109111476 | ||||||
| chr6:109111573
|
A | G | 5 | a0002c0002t0068g0009a0002c0002t0074g0006a0002c0002t0075g0008others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+15998A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109111573 | ||||||
| chr6:109111600
|
C | T | 1 | a0003c0005t0034g0208 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-4+16025C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109111600 | ||||||
| chr6:109111692
|
G | A | 4 | a0002c0002t0068g0009a0002c0002t0074g0006a0002c0002t0075g0008others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+16117G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109111692 | ||||||
| chr6:109111766
|
G | A | 1 | a0006c0008t0077g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-4+16191G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109111766 | ||||||
| chr6:109111784
|
G | C | 1 | a0002c0002t0071g0012 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-4+16209G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109111784 | ||||||
| chr6:109111793
|
T | G | 22 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(19): Show | 25 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.-4+16218T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109111793 | ||||||
| chr6:109111861
|
A | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+16286A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109111861 | ||||||
| chr6:109111947
|
C | T | 1 | a0002c0002t0076g0010 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-4+16372C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109111947 | ||||||
| chr6:109111993
|
G | A | 3 | a0001c0001t0002g0047a0001c0001t0002g0109a0001c0001t0031g0046 | 3 | HG00323.hp1 NA19062.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-4+16418G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109111993 | ||||||
| chr6:109112041
|
A | G | 8 | a0001c0001t0006g0167a0001c0001t0006g0168a0001c0001t0006g0172others(5): Show | 8 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4+16466A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109112041 | ||||||
| chr6:109112043
|
G | A | 18 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0001g0156others(15): Show | 18 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-4+16468G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109112043 | ||||||
| chr6:109112044
|
A | C | 4 | a0002c0002t0068g0009a0002c0002t0074g0006a0002c0002t0075g0008others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+16469A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109112044 | ||||||
| chr6:109112220
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+16645C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109112220 | ||||||
| chr6:109112271
|
A | C | 2 | a0002c0002t0078g0205a0002c0002t0079g0209 | 2 | HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-4+16696A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109112271 | ||||||
| chr6:109112280
|
A | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+16705A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109112280 | ||||||
| chr6:109112307
|
A | G | 44 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(41): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.-4+16732A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109112307 | ||||||
| chr6:109112374
|
T | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+16799T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109112374 | ||||||
| chr6:109112412
|
C | A | 1 | a0001c0001t0027g0217 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-4+16837C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109112412 | ||||||
| chr6:109112694
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-4+17119G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109112694 | ||||||
| chr6:109112799
|
T | A | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4+17224T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109112799 | ||||||
| chr6:109112989
|
G | T | 1 | a0001c0001t0045g0088 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-4+17414G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109112989 | ||||||
| chr6:109113116
|
G | A | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4+17541G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109113116 | ||||||
| chr6:109113147
|
T | C | 1 | a0002c0002t0003g0013 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-4+17572T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109113147 | ||||||
| chr6:109113357
|
G | A | 6 | a0002c0002t0030g0211a0002c0002t0078g0205a0002c0002t0079g0209others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+17782G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109113357 | ||||||
| chr6:109113393
|
C | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+17818C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109113393 | ||||||
| chr6:109113492
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+17917T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109113492 | ||||||
| chr6:109113588
|
T | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+18013T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109113588 | ||||||
| chr6:109113611
|
A | G | 3 | a0001c0001t0001g0087a0001c0001t0002g0086a0001c0001t0002g0095 | 3 | NA18981.hp1 NA18983.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-4+18036A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109113611 | ||||||
| chr6:109113644
|
T | C | 34 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(31): Show | 37 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.-4+18069T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109113644 | ||||||
| chr6:109113652
|
A | G | 1 | a0002c0002t0082g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-4+18077A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109113652 | ||||||
| chr6:109114398
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-4+18823A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109114398 | ||||||
| chr6:109114475
|
C | A | 1 | a0001c0001t0002g0048 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-4+18900C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109114475 | ||||||
| chr6:109114569
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+18994A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109114569 | ||||||
| chr6:109114716
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+19141C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109114716 | ||||||
| chr6:109114756
|
A | G | 1 | a0002c0002t0026g0026 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-4+19181A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109114756 | ||||||
| chr6:109114828
|
ATAGC | A | 4 | a0002c0002t0068g0009a0002c0002t0074g0006a0002c0002t0075g0008others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+19256_-4+19259d others(6): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109114828 | |||||
| chr6:109115111
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+19536G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109115111 | ||||||
| chr6:109115142
|
C | A | 23 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(20): Show | 26 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.-4+19567C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109115142 | ||||||
| chr6:109115280
|
C | T | 1 | a0001c0001t0017g0130 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-4+19705C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109115280 | ||||||
| chr6:109115586
|
AAAAT | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+20016_-4+20019d others(6): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109115586 | |||||
| chr6:109115608
|
T | A | 9 | a0001c0001t0001g0195a0001c0001t0011g0138a0001c0001t0011g0139others(6): Show | 9 | HG00639.hp1 HG02083.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4+20033T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109115608 | ||||||
| chr6:109115684
|
G | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+20109G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109115684 | ||||||
| chr6:109115731
|
A | G | 6 | a0002c0002t0030g0211a0002c0002t0078g0205a0002c0002t0079g0209others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+20156A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109115731 | ||||||
| chr6:109115741
|
T | C | 4 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+20166T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109115741 | ||||||
| chr6:109115808
|
G | C | 4 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124others(1): Show | 4 | HG00423.hp1 NA18946.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+20233G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109115808 | ||||||
| chr6:109115894
|
A | G | 4 | a0002c0002t0068g0009a0002c0002t0074g0006a0002c0002t0075g0008others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+20319A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109115894 | ||||||
| chr6:109115903
|
T | C | 1 | a0001c0001t0006g0167 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-4+20328T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109115903 | ||||||
| chr6:109116084
|
C | CATTTT | 7 | a0002c0002t0003g0023a0002c0002t0025g0025a0002c0002t0026g0024others(4): Show | 7 | HG00323.hp2 HG02083.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4+20537_-4+20541d others(7): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109116084 | |||||
| chr6:109116084
|
C | CATTTTAT others(3): Show |
1 | a0002c0002t0068g0009 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-4+20532_-4+20541d others(12): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109116084 | |||||
| chr6:109116084
|
CATTTT | C | 2 | a0001c0001t0045g0088a0001c0001t0053g0141 | 2 | HG02109.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-4+20537_-4+20541d others(7): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109116084 | |||||
| chr6:109116084
|
CATTTTAT others(3): Show |
C | 1 | a0001c0001t0007g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-4+20532_-4+20541d others(12): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109116084 | |||||
| chr6:109116112
|
T | G | 1 | a0001c0001t0053g0141 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-4+20537T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116112 | ||||||
| chr6:109116117
|
G | T | 38 | a0001c0001t0009g0150a0001c0001t0012g0218a0001c0001t0012g0219others(35): Show | 41 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.-4+20542G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116117 | ||||||
| chr6:109116119
|
T | G | 1 | a0001c0001t0053g0141 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-4+20544T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116119 | ||||||
| chr6:109116120
|
A | ATTTTATT others(6): Show |
1 | a0003c0005t0035g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-4+20546_-4+20547i others(15): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109116120 | |||||
| chr6:109116120
|
A | ATTTTATT others(11): Show |
1 | a0003c0005t0034g0208 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-4+20546_-4+20547i others(20): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109116120 | |||||
| chr6:109116120
|
A | ATTTTATT others(16): Show |
2 | a0003c0005t0032g0004a0003c0005t0033g0004 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-4+20546_-4+20547i others(25): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109116120 | |||||
| chr6:109116120
|
A | T | 1 | a0001c0001t0053g0141 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-4+20545A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116120 | ||||||
| chr6:109116120
|
ATG | A | 4 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0027g0217others(1): Show | 4 | HG02572.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+20549_-4+20550d others(4): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109116120 | |||||
| chr6:109116122
|
G | A | 4 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+20547G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116122 | ||||||
| chr6:109116122
|
G | T | 2 | a0001c0001t0012g0220a0006c0008t0077g0212 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-4+20547G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116122 | ||||||
| chr6:109116122
|
GTGTTGTG others(8): Show |
G | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4+20552_-4+20566d others(17): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109116122 | |||||
| chr6:109116124
|
G | T | 38 | a0001c0001t0009g0150a0001c0001t0012g0218a0001c0001t0012g0219others(35): Show | 41 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.-4+20549G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116124 | ||||||
| chr6:109116125
|
T | A | 30 | a0001c0001t0009g0150a0001c0001t0012g0220a0002c0002t0003g0001others(27): Show | 33 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.-4+20550T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116125 | ||||||
| chr6:109116127
|
G | A | 9 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0027g0217others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4+20552G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116127 | ||||||
| chr6:109116127
|
G | GTGTTA | 23 | a0001c0001t0001g0082a0001c0001t0001g0146a0001c0001t0001g0149others(20): Show | 24 | HG00099.hp1 HG01168.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.-4+20608_-4+20612d others(7): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109116127 | |||||
| chr6:109116127
|
G | GTGTTATG others(3): Show |
3 | a0001c0001t0002g0085a0001c0001t0004g0040a0001c0001t0011g0131 | 3 | HG03516.hp2 NA18994.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.-4+20603_-4+20612d others(12): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109116127 | |||||
| chr6:109116127
|
G | T | 1 | a0001c0001t0012g0220 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-4+20552G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116127 | ||||||
| chr6:109116127
|
GTGTTA | G | 74 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0044others(71): Show | 78 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.-4+20608_-4+20612d others(7): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109116127 | |||||
| chr6:109116127
|
GTGTTATG others(3): Show |
G | 17 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0049others(14): Show | 17 | HG01081.hp1 HG01123.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.-4+20603_-4+20612d others(12): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109116127 | |||||
| chr6:109116127
|
GTGTTATG others(8): Show |
G | 15 | a0001c0001t0001g0103a0001c0001t0001g0158a0001c0001t0006g0167others(12): Show | 15 | HG01109.hp1 HG01884.hp1 HG02004.hp1 others(12): Show |
intron_variant | MODIFIER | c.-4+20598_-4+20612d others(17): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109116127 | |||||
| chr6:109116129
|
G | T | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+20554G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116129 | ||||||
| chr6:109116130
|
T | A | 2 | a0001c0001t0012g0220a0006c0008t0077g0212 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-4+20555T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116130 | ||||||
| chr6:109116132
|
A | ATG | 4 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+20559_-4+20560d others(4): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109116132 | |||||
| chr6:109116132
|
A | G | 15 | a0001c0001t0009g0150a0001c0001t0012g0220a0002c0002t0003g0015others(12): Show | 15 | HG00099.hp2 HG00738.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-4+20557A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116132 | ||||||
| chr6:109116134
|
GTTA | G | 4 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0027g0217others(1): Show | 4 | HG02572.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+20561_-4+20563d others(5): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109116134 | |||||
| chr6:109116137
|
A | G | 20 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(17): Show | 23 | HG00280.hp1 HG00438.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.-4+20562A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116137 | ||||||
| chr6:109116188
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+20613C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116188 | ||||||
| chr6:109116419
|
T | C | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4+20844T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116419 | ||||||
| chr6:109116514
|
G | A | 4 | a0002c0002t0068g0009a0002c0002t0074g0006a0002c0002t0075g0008others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+20939G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116514 | ||||||
| chr6:109116517
|
G | A | 1 | a0001c0001t0012g0220 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-4+20942G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116517 | ||||||
| chr6:109116573
|
A | G | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4+20998A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116573 | ||||||
| chr6:109116611
|
C | G | 1 | a0001c0001t0020g0194 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-4+21036C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116611 | ||||||
| chr6:109116691
|
G | A | 1 | a0001c0001t0024g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-4+21116G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116691 | ||||||
| chr6:109116825
|
G | A | 1 | a0001c0001t0027g0217 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-4+21250G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116825 | ||||||
| chr6:109116982
|
G | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0117 | 3 | HG02717.hp1 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-4+21407G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109116982 | ||||||
| chr6:109117014
|
A | T | 21 | a0001c0001t0001g0158a0001c0001t0006g0161a0001c0001t0006g0164others(18): Show | 21 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.-4+21439A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109117014 | ||||||
| chr6:109117021
|
G | T | 1 | a0001c0001t0018g0102 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-4+21446G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109117021 | ||||||
| chr6:109117064
|
C | T | 1 | a0001c0001t0017g0130 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-4+21489C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109117064 | ||||||
| chr6:109117084
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+21509A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109117084 | ||||||
| chr6:109117440
|
T | C | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4+21865T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109117440 | ||||||
| chr6:109117586
|
G | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+22011G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109117586 | ||||||
| chr6:109117644
|
T | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+22069T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109117644 | ||||||
| chr6:109117692
|
A | G | 1 | a0002c0002t0084g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-4+22117A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109117692 | ||||||
| chr6:109117773
|
A | T | 1 | a0001c0001t0001g0128 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-4+22198A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109117773 | ||||||
| chr6:109117789
|
C | T | 3 | a0001c0001t0004g0101a0001c0001t0036g0100a0001c0001t0040g0043 | 3 | HG01109.hp2 HG01261.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.-4+22214C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109117789 | ||||||
| chr6:109117816
|
A | G | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4+22241A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109117816 | ||||||
| chr6:109117891
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+22316G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109117891 | ||||||
| chr6:109117935
|
A | C | 44 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(41): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.-4+22360A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109117935 | ||||||
| chr6:109118031
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+22456A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109118031 | ||||||
| chr6:109118038
|
T | A | 2 | a0002c0002t0075g0008a0002c0002t0086g0007 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-4+22463T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109118038 | ||||||
| chr6:109118202
|
A | C | 1 | a0002c0002t0079g0209 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-4+22627A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109118202 | ||||||
| chr6:109118419
|
G | A | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4+22844G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109118419 | ||||||
| chr6:109118587
|
C | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+23012C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109118587 | ||||||
| chr6:109118622
|
C | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+23047C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109118622 | ||||||
| chr6:109118647
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+23072C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109118647 | ||||||
| chr6:109118725
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+23150C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109118725 | ||||||
| chr6:109118803
|
C | T | 6 | a0002c0002t0030g0211a0002c0002t0078g0205a0002c0002t0079g0209others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+23228C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109118803 | ||||||
| chr6:109118967
|
A | G | 9 | a0001c0001t0001g0032a0001c0001t0001g0195a0001c0001t0001g0198others(6): Show | 9 | HG01106.hp2 HG01361.hp1 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4+23392A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109118967 | ||||||
| chr6:109119335
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+23760A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109119335 | ||||||
| chr6:109119391
|
A | C | 3 | a0001c0001t0006g0166a0001c0001t0059g0165a0001c0001t0060g0174 | 3 | HG02572.hp2 HG02895.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-4+23816A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109119391 | ||||||
| chr6:109119483
|
T | A | 1 | a0001c0001t0007g0144 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-4+23908T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109119483 | ||||||
| chr6:109119496
|
G | C | 18 | a0001c0001t0006g0161a0001c0001t0006g0164a0001c0001t0006g0166others(15): Show | 18 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.-4+23921G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109119496 | ||||||
| chr6:109119847
|
A | C | 1 | a0001c0001t0006g0172 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-4+24272A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109119847 | ||||||
| chr6:109120119
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+24544A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109120119 | ||||||
| chr6:109120224
|
A | G | 1 | a0001c0001t0088g0160 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-4+24649A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109120224 | ||||||
| chr6:109120387
|
G | A | 1 | a0002c0002t0085g0213 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-4+24812G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109120387 | ||||||
| chr6:109120446
|
CT | C | 4 | a0002c0002t0068g0009a0002c0002t0074g0006a0002c0002t0075g0008others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-24772delT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109120446 | ||||||
| chr6:109120611
|
G | C | 1 | a0003c0005t0035g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-3-24608G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109120611 | ||||||
| chr6:109120650
|
T | TTAAATTA others(329): Show |
1 | a0007c0006t0089g0062 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-3-24555_-3-24554i others(338): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109120650 | |||||
| chr6:109120760
|
C | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-24459C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109120760 | ||||||
| chr6:109120905
|
GACACACG others(1): Show |
G | 24 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(21): Show | 27 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.-3-24307_-3-24300d others(10): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109120905 | |||||
| chr6:109120905
|
GACACACG others(3): Show |
G | 4 | a0002c0002t0068g0009a0002c0002t0074g0006a0002c0002t0075g0008others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-24307_-3-24298d others(12): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109120905 | |||||
| chr6:109120905
|
GACACACG others(7): Show |
G | 4 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-24307_-3-24294d others(16): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109120905 | |||||
| chr6:109120905
|
GACACACG others(13): Show |
G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-24307_-3-24288d others(22): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109120905 | |||||
| chr6:109120908
|
ACACG | A | 4 | a0001c0007t0029g0005a0002c0002t0082g0204a0002c0002t0084g0011others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-24307_-3-24304d others(6): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109120908 | |||||
| chr6:109120912
|
G | A | 1 | a0002c0002t0078g0205 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-3-24307G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109120912 | ||||||
| chr6:109120912
|
G | GCA | 3 | a0001c0001t0001g0039a0001c0001t0023g0063a0005c0009t0001g0133 | 3 | HG01175.hp2 HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-3-24262_-3-24261d others(4): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109120912 | |||||
| chr6:109120912
|
GCA | G | 33 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0053others(30): Show | 33 | HG00438.hp1 HG01884.hp1 HG01981.hp2 others(30): Show |
intron_variant | MODIFIER | c.-3-24262_-3-24261d others(4): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109120912 | |||||
| chr6:109120912
|
GCACA | G | 16 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0082others(13): Show | 17 | HG00609.hp1 HG01192.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-3-24264_-3-24261d others(6): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109120912 | |||||
| chr6:109120912
|
GCACACA | G | 25 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0050others(22): Show | 25 | HG00323.hp1 HG00621.hp2 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.-3-24266_-3-24261d others(8): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109120912 | |||||
| chr6:109120912
|
GCACACAC others(1): Show |
G | 27 | a0001c0001t0001g0037a0001c0001t0001g0058a0001c0001t0001g0060others(24): Show | 27 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.-3-24268_-3-24261d others(10): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109120912 | |||||
| chr6:109120912
|
GCACACAC others(3): Show |
G | 3 | a0001c0001t0002g0061a0001c0001t0002g0084a0001c0001t0052g0189 | 3 | HG01433.hp1 HG01952.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-3-24270_-3-24261d others(12): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109120912 | |||||
| chr6:109120912
|
GCACACAC others(5): Show |
G | 2 | a0001c0001t0011g0138a0001c0001t0011g0139 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-3-24272_-3-24261d others(14): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109120912 | |||||
| chr6:109120912
|
GCACACAC others(7): Show |
G | 5 | a0001c0001t0020g0181a0001c0001t0020g0194a0001c0001t0021g0216others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-24274_-3-24261d others(16): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109120912 | |||||
| chr6:109120912
|
GCACACAC others(11): Show |
G | 2 | a0001c0001t0019g0179a0001c0001t0019g0206 | 2 | HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-3-24278_-3-24261d others(20): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109120912 | |||||
| chr6:109120912
|
GCACACAC others(15): Show |
G | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0013g0197 | 3 | HG01106.hp2 HG01361.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-3-24282_-3-24261d others(24): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109120912 | |||||
| chr6:109120912
|
GCACACAC others(17): Show |
G | 21 | a0001c0001t0001g0032a0001c0001t0001g0195a0001c0001t0001g0200others(18): Show | 22 | HG00099.hp1 HG00738.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.-3-24284_-3-24261d others(26): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109120912 | |||||
| chr6:109120914
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-3-24305A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109120914 | ||||||
| chr6:109120916
|
A | G | 10 | a0001c0001t0007g0144a0001c0001t0009g0142a0001c0001t0009g0145others(7): Show | 10 | HG01884.hp1 HG02615.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3-24303A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109120916 | ||||||
| chr6:109120918
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0156 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-3-24301A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109120918 | ||||||
| chr6:109120920
|
A | G | 3 | a0001c0001t0007g0140a0001c0001t0053g0141a0002c0002t0081g0143 | 3 | HG02109.hp2 HG02145.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-3-24299A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109120920 | ||||||
| chr6:109120926
|
A | G | 2 | a0001c0001t0011g0138a0001c0001t0011g0139 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-3-24293A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109120926 | ||||||
| chr6:109120929
|
C | G | 2 | a0001c0001t0010g0002a0001c0001t0010g0094 | 3 | HG01192.hp1 HG01257.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.-3-24290C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109120929 | ||||||
| chr6:109120957
|
C | CACAG | 3 | a0001c0001t0001g0158a0001c0001t0006g0161a0001c0001t0006g0173 | 3 | HG02622.hp1 HG03239.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-3-24261_-3-24260i others(6): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109120957 | |||||
| chr6:109120957
|
C | CAG | 11 | a0001c0001t0006g0164a0001c0001t0006g0167a0001c0001t0006g0168others(8): Show | 11 | HG01109.hp1 HG02004.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-3-24261_-3-24260d others(4): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109120957 | |||||
| chr6:109120957
|
C | G | 44 | a0001c0001t0006g0166a0001c0001t0015g0175a0001c0001t0047g0171others(41): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.-3-24262C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109120957 | ||||||
| chr6:109121180
|
T | C | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-24039T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109121180 | ||||||
| chr6:109121237
|
G | A | 44 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(41): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.-3-23982G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109121237 | ||||||
| chr6:109121651
|
A | G | 22 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(19): Show | 25 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.-3-23568A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109121651 | ||||||
| chr6:109121664
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-3-23555A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109121664 | ||||||
| chr6:109121691
|
AT | A | 4 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-23525delT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109121691 | |||||
| chr6:109121918
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-3-23301A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109121918 | ||||||
| chr6:109122143
|
GA | G | 4 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-23075delA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109122143 | ||||||
| chr6:109122401
|
T | C | 1 | a0002c0002t0084g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-3-22818T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109122401 | ||||||
| chr6:109122402
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-22817G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109122402 | ||||||
| chr6:109122641
|
A | T | 22 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(19): Show | 25 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.-3-22578A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109122641 | ||||||
| chr6:109122739
|
G | A | 1 | a0001c0001t0004g0040 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-3-22480G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109122739 | ||||||
| chr6:109122934
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-22285T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109122934 | ||||||
| chr6:109123136
|
A | G | 2 | a0002c0002t0078g0205a0002c0002t0079g0209 | 2 | HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-3-22083A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109123136 | ||||||
| chr6:109123552
|
A | T | 6 | a0002c0002t0030g0211a0002c0002t0078g0205a0002c0002t0079g0209others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-21667A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109123552 | ||||||
| chr6:109123604
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-3-21615C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109123604 | ||||||
| chr6:109123660
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-21559C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109123660 | ||||||
| chr6:109123834
|
C | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-21385C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109123834 | ||||||
| chr6:109124075
|
C | CA | 12 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(9): Show | 12 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3-21132dupA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109124075 | |||||
| chr6:109124156
|
C | G | 4 | a0002c0002t0068g0009a0002c0002t0074g0006a0002c0002t0075g0008others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-21063C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109124156 | ||||||
| chr6:109124283
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-20936C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109124283 | ||||||
| chr6:109124384
|
A | G | 38 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(35): Show | 41 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.-3-20835A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109124384 | ||||||
| chr6:109124403
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-3-20816T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109124403 | ||||||
| chr6:109124426
|
A | G | 1 | a0002c0002t0082g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-3-20793A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109124426 | ||||||
| chr6:109124498
|
T | C | 1 | a0001c0001t0012g0218 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-3-20721T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109124498 | ||||||
| chr6:109124607
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-20612A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109124607 | ||||||
| chr6:109124615
|
T | A | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-3-20604T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109124615 | ||||||
| chr6:109124648
|
T | G | 1 | a0001c0001t0001g0042 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-3-20571T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109124648 | ||||||
| chr6:109124703
|
C | T | 1 | a0001c0001t0055g0157 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-3-20516C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109124703 | ||||||
| chr6:109124770
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-20449G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109124770 | ||||||
| chr6:109124917
|
T | G | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-3-20302T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109124917 | ||||||
| chr6:109124948
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-20271A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109124948 | ||||||
| chr6:109125116
|
G | A | 1 | a0001c0001t0012g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-3-20103G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109125116 | ||||||
| chr6:109125139
|
C | T | 4 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-20080C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109125139 | ||||||
| chr6:109125492
|
CTA | C | 34 | a0001c0007t0029g0005a0002c0002t0003g0001a0002c0002t0003g0013others(31): Show | 37 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.-3-19712_-3-19711d others(4): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109125492 | |||||
| chr6:109125507
|
T | C | 5 | a0002c0002t0080g0210a0002c0002t0082g0204a0003c0005t0032g0004others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-19712T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109125507 | ||||||
| chr6:109125507
|
T | TATATATA others(27): Show |
1 | a0001c0001t0012g0218 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-3-19711_-3-19710i others(36): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109125507 | |||||
| chr6:109125509
|
C | T | 9 | a0001c0001t0012g0219a0001c0001t0012g0220a0001c0001t0027g0217others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3-19710C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109125509 | ||||||
| chr6:109125521
|
TA | T | 4 | a0001c0001t0055g0157a0002c0002t0075g0008a0002c0002t0086g0007others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-19697delA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109125521 | ||||||
| chr6:109125522
|
A | AT | 3 | a0001c0001t0002g0059a0001c0001t0002g0069a0001c0001t0004g0105 | 3 | NA19065.hp2 NA19084.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-3-19696dupT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109125522 | |||||
| chr6:109125522
|
A | T | 10 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0109others(7): Show | 10 | HG00323.hp1 HG00609.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.-3-19697A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109125522 | ||||||
| chr6:109125523
|
TA | T | 9 | a0001c0001t0012g0218a0001c0003t0002g0191a0002c0002t0025g0020others(6): Show | 9 | HG00323.hp2 HG00738.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3-19695delA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109125523 | ||||||
| chr6:109125524
|
A | ACATATAT others(30): Show |
2 | a0001c0001t0012g0220a0001c0001t0027g0217 | 2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-3-19695_-3-19694i others(39): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109125524 | ||||||
| chr6:109125524
|
A | AT | 5 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0002g0086others(2): Show | 5 | HG02015.hp2 HG04184.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-19685dupT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109125524 | |||||
| chr6:109125524
|
A | ATACATAT others(32): Show |
1 | a0001c0001t0012g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-3-19694_-3-19693i others(41): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109125524 | |||||
| chr6:109125524
|
A | T | 115 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(112): Show | 116 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-3-19695A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109125524 | ||||||
| chr6:109125524
|
AT | A | 23 | a0001c0001t0024g0093a0002c0002t0003g0001a0002c0002t0003g0013others(20): Show | 26 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.-3-19685delT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109125524 | |||||
| chr6:109125525
|
T | A | 1 | a0001c0001t0012g0220 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-3-19694T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109125525 | ||||||
| chr6:109125525
|
T | TA | 6 | a0001c0001t0001g0055a0001c0001t0001g0087a0001c0001t0001g0103others(3): Show | 6 | HG03490.hp1 HG03704.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-19694_-3-19693i others(3): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109125525 | ||||||
| chr6:109125525
|
T | TACATATA others(34): Show |
1 | a0001c0001t0028g0221 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-3-19694_-3-19693i others(43): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109125525 | ||||||
| chr6:109125526
|
T | A | 2 | a0001c0001t0002g0057a0002c0002t0074g0006 | 2 | HG02451.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-3-19693T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109125526 | ||||||
| chr6:109125600
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-19619T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109125600 | ||||||
| chr6:109125705
|
C | CTGAT | 5 | a0001c0001t0001g0158a0001c0001t0012g0218a0001c0001t0023g0063others(2): Show | 5 | HG01175.hp2 HG02647.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-19489_-3-19486d others(6): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109125705 | |||||
| chr6:109125705
|
CTGAT | C | 6 | a0001c0001t0005g0184a0001c0001t0005g0187a0001c0001t0005g0192others(3): Show | 6 | HG00099.hp1 HG00738.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-19489_-3-19486d others(6): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109125705 | |||||
| chr6:109125975
|
T | C | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-3-19244T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109125975 | ||||||
| chr6:109125986
|
T | G | 1 | a0002c0002t0082g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-3-19233T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109125986 | ||||||
| chr6:109126187
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-19032G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109126187 | ||||||
| chr6:109126232
|
C | T | 1 | a0002c0002t0030g0211 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-3-18987C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109126232 | ||||||
| chr6:109126297
|
C | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-18922C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109126297 | ||||||
| chr6:109126376
|
A | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-18843A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109126376 | ||||||
| chr6:109126509
|
A | G | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-18710A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109126509 | ||||||
| chr6:109127024
|
G | A | 1 | a0001c0001t0058g0076 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-3-18195G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109127024 | ||||||
| chr6:109127035
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-18184G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109127035 | ||||||
| chr6:109127049
|
T | G | 4 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-18170T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109127049 | ||||||
| chr6:109127090
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-3-18129C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109127090 | ||||||
| chr6:109127144
|
G | A | 1 | a0002c0002t0003g0030 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-3-18075G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109127144 | ||||||
| chr6:109127187
|
C | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-18032C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109127187 | ||||||
| chr6:109127198
|
C | G | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-3-18021C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109127198 | ||||||
| chr6:109127491
|
T | G | 1 | a0001c0001t0018g0102 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-3-17728T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109127491 | ||||||
| chr6:109127545
|
T | A | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-17674T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109127545 | ||||||
| chr6:109127685
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-17534G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109127685 | ||||||
| chr6:109127854
|
T | A | 3 | a0001c0001t0001g0158a0001c0001t0087g0159a0001c0001t0088g0160 | 3 | HG02647.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-3-17365T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109127854 | ||||||
| chr6:109127864
|
G | T | 1 | a0002c0002t0003g0019 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-3-17355G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109127864 | ||||||
| chr6:109127870
|
C | T | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-17349C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109127870 | ||||||
| chr6:109127888
|
A | G | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-17331A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109127888 | ||||||
| chr6:109127906
|
A | G | 129 | a0001c0001t0001g0032a0001c0001t0001g0049a0001c0001t0001g0050others(126): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-3-17313A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109127906 | ||||||
| chr6:109127921
|
G | T | 1 | a0002c0002t0080g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-3-17298G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109127921 | ||||||
| chr6:109128017
|
G | A | 1 | a0002c0002t0082g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-3-17202G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109128017 | ||||||
| chr6:109128067
|
T | G | 5 | a0002c0002t0068g0009a0002c0002t0074g0006a0002c0002t0075g0008others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-17152T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109128067 | ||||||
| chr6:109128203
|
T | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-17016T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109128203 | ||||||
| chr6:109128455
|
G | A | 18 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0001g0156others(15): Show | 18 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-3-16764G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109128455 | ||||||
| chr6:109128487
|
G | T | 22 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(19): Show | 25 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.-3-16732G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109128487 | ||||||
| chr6:109128713
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-16506C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109128713 | ||||||
| chr6:109128715
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-16504A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109128715 | ||||||
| chr6:109128934
|
C | T | 1 | a0001c0001t0005g0187 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-3-16285C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109128934 | ||||||
| chr6:109128968
|
G | A | 2 | a0004c0004t0001g0136a0004c0004t0001g0137 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-3-16251G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109128968 | ||||||
| chr6:109129236
|
A | C | 1 | a0002c0002t0082g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-3-15983A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109129236 | ||||||
| chr6:109129261
|
G | A | 23 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(20): Show | 26 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.-3-15958G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109129261 | ||||||
| chr6:109129331
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-15888A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109129331 | ||||||
| chr6:109129350
|
C | T | 1 | a0001c0001t0020g0194 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-3-15869C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109129350 | ||||||
| chr6:109129812
|
AT | A | 6 | a0001c0001t0002g0057a0001c0001t0012g0218a0001c0001t0012g0219others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-15397delT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109129812 | |||||
| chr6:109129813
|
T | A | 1 | a0001c0001t0002g0069 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-3-15406T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109129813 | ||||||
| chr6:109129822
|
TAATTTAA | T | 39 | a0001c0001t0008g0113a0002c0002t0003g0001a0002c0002t0003g0013others(36): Show | 42 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.-3-15377_-3-15371d others(9): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109129822 | |||||
| chr6:109130057
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-15162G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109130057 | ||||||
| chr6:109130187
|
G | A | 1 | a0002c0002t0030g0211 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-3-15032G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109130187 | ||||||
| chr6:109130222
|
C | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-14997C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109130222 | ||||||
| chr6:109130293
|
A | G | 1 | a0002c0002t0078g0205 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-3-14926A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109130293 | ||||||
| chr6:109130364
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-14855G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109130364 | ||||||
| chr6:109130397
|
CCT | C | 34 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(31): Show | 37 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.-3-14819_-3-14818d others(4): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109130397 | |||||
| chr6:109130578
|
A | C | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-14641A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109130578 | ||||||
| chr6:109130616
|
G | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-14603G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109130616 | ||||||
| chr6:109130646
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-14573C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109130646 | ||||||
| chr6:109130663
|
GT | G | 37 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(34): Show | 40 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.-3-14539delT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109130663 | |||||
| chr6:109130670
|
T | G | 1 | a0003c0005t0035g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-3-14549T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109130670 | ||||||
| chr6:109130723
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-14496C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109130723 | ||||||
| chr6:109130958
|
C | A | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-3-14261C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109130958 | ||||||
| chr6:109131057
|
A | T | 1 | a0001c0001t0027g0217 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-3-14162A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109131057 | ||||||
| chr6:109131224
|
G | GA | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-13994dupA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109131224 | |||||
| chr6:109131278
|
A | G | 3 | a0001c0001t0001g0158a0001c0001t0087g0159a0001c0001t0088g0160 | 3 | HG02647.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-3-13941A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109131278 | ||||||
| chr6:109131445
|
C | T | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-13774C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109131445 | ||||||
| chr6:109131517
|
A | G | 3 | a0001c0001t0007g0183a0001c0001t0007g0207a0001c0001t0011g0177 | 3 | HG01081.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-3-13702A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109131517 | ||||||
| chr6:109131683
|
T | TA | 16 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0001g0156others(13): Show | 16 | HG02109.hp2 HG02145.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.-3-13528dupA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109131683 | |||||
| chr6:109131683
|
TA | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-13528delA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109131683 | |||||
| chr6:109131691
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-3-13528A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109131691 | ||||||
| chr6:109131692
|
T | A | 2 | a0002c0002t0078g0205a0002c0002t0079g0209 | 2 | HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-3-13527T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109131692 | ||||||
| chr6:109131693
|
T | A | 1 | a0002c0002t0079g0209 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-3-13526T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109131693 | ||||||
| chr6:109131741
|
C | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-13478C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109131741 | ||||||
| chr6:109131793
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-13426C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109131793 | ||||||
| chr6:109132027
|
T | C | 1 | a0001c0001t0007g0207 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-3-13192T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109132027 | ||||||
| chr6:109132261
|
T | C | 1 | a0001c0001t0040g0043 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-3-12958T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109132261 | ||||||
| chr6:109132262
|
G | A | 4 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-12957G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109132262 | ||||||
| chr6:109132368
|
G | T | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-3-12851G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109132368 | ||||||
| chr6:109133037
|
C | T | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-12182C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109133037 | ||||||
| chr6:109133052
|
C | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-12167C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109133052 | ||||||
| chr6:109133067
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-12152C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109133067 | ||||||
| chr6:109133179
|
TTA | T | 4 | a0001c0003t0002g0191a0001c0003t0005g0003a0001c0003t0005g0193others(1): Show | 5 | HG01168.hp1 HG01192.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-12036_-3-12035d others(4): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109133179 | |||||
| chr6:109133358
|
A | G | 2 | a0002c0002t0078g0205a0002c0002t0079g0209 | 2 | HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-3-11861A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109133358 | ||||||
| chr6:109133436
|
G | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-11783G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109133436 | ||||||
| chr6:109133612
|
CTG | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-11604_-3-11603d others(4): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109133612 | |||||
| chr6:109133661
|
C | A | 1 | a0006c0008t0077g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3-11558C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109133661 | ||||||
| chr6:109133778
|
A | C | 1 | a0001c0001t0001g0091 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-3-11441A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109133778 | ||||||
| chr6:109133966
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-3-11253C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109133966 | ||||||
| chr6:109134017
|
A | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-11202A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109134017 | ||||||
| chr6:109134163
|
A | G | 25 | a0001c0001t0001g0032a0001c0001t0001g0188a0001c0001t0001g0195others(22): Show | 26 | HG00099.hp1 HG00738.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.-3-11056A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109134163 | ||||||
| chr6:109134180
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-11039T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109134180 | ||||||
| chr6:109134261
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-10958C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109134261 | ||||||
| chr6:109134262
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-10957A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109134262 | ||||||
| chr6:109134341
|
G | T | 1 | a0002c0002t0080g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-3-10878G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109134341 | ||||||
| chr6:109134458
|
A | G | 1 | a0001c0001t0016g0056 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-3-10761A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109134458 | ||||||
| chr6:109134484
|
G | T | 38 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0060others(35): Show | 38 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.-3-10735G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109134484 | ||||||
| chr6:109134992
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-10227A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109134992 | ||||||
| chr6:109135137
|
G | A | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-3-10082G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109135137 | ||||||
| chr6:109135265
|
C | T | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-3-9954C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109135265 | ||||||
| chr6:109135295
|
CA | C | 4 | a0002c0002t0068g0009a0002c0002t0074g0006a0002c0002t0075g0008others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-9919delA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109135295 | |||||
| chr6:109135305
|
A | C | 2 | a0001c0001t0014g0135a0001c0001t0014g0154 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-3-9914A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109135305 | ||||||
| chr6:109135308
|
T | C | 2 | a0001c0001t0014g0135a0001c0001t0014g0154 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-3-9911T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109135308 | ||||||
| chr6:109135438
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-9781T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109135438 | ||||||
| chr6:109135516
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-3-9703T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109135516 | ||||||
| chr6:109135571
|
A | G | 39 | a0001c0001t0024g0180a0002c0002t0003g0001a0002c0002t0003g0013others(36): Show | 42 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.-3-9648A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109135571 | ||||||
| chr6:109135574
|
T | G | 1 | a0001c0001t0002g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-3-9645T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109135574 | ||||||
| chr6:109135593
|
C | A | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-9626C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109135593 | ||||||
| chr6:109135597
|
C | G | 1 | a0001c0001t0001g0199 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-3-9622C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109135597 | ||||||
| chr6:109135734
|
C | T | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-3-9485C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109135734 | ||||||
| chr6:109135735
|
G | A | 1 | a0001c0001t0059g0165 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-3-9484G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109135735 | ||||||
| chr6:109135735
|
G | C | 6 | a0001c0001t0001g0103a0001c0001t0012g0218a0001c0001t0012g0219others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-9484G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109135735 | ||||||
| chr6:109135784
|
CAT | C | 35 | a0001c0001t0024g0180a0002c0002t0003g0001a0002c0002t0003g0013others(32): Show | 38 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.-3-9434_-3-9433del others(2): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109135784 | ||||||
| chr6:109135843
|
T | C | 2 | a0002c0002t0078g0205a0002c0002t0079g0209 | 2 | HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-3-9376T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109135843 | ||||||
| chr6:109135884
|
A | T | 1 | a0001c0001t0048g0170 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-3-9335A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109135884 | ||||||
| chr6:109135998
|
A | T | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG01891.hp1 HG02572.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-9221A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109135998 | ||||||
| chr6:109136007
|
G | C | 221 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(218): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.-3-9212G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136007 | ||||||
| chr6:109136037
|
C | G | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-3-9182C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136037 | ||||||
| chr6:109136092
|
T | G | 4 | a0001c0001t0015g0175a0001c0001t0047g0171a0001c0001t0048g0170others(1): Show | 4 | HG02027.hp2 HG02559.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-9127T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136092 | ||||||
| chr6:109136128
|
C | T | 6 | a0001c0001t0006g0173a0001c0001t0012g0218a0001c0001t0012g0219others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-9091C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136128 | ||||||
| chr6:109136155
|
A | G | 39 | a0001c0001t0024g0180a0002c0002t0003g0001a0002c0002t0003g0013others(36): Show | 42 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.-3-9064A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136155 | ||||||
| chr6:109136159
|
C | T | 39 | a0001c0001t0024g0180a0002c0002t0003g0001a0002c0002t0003g0013others(36): Show | 42 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.-3-9060C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136159 | ||||||
| chr6:109136174
|
C | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-9045C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136174 | ||||||
| chr6:109136271
|
T | C | 1 | a0001c0001t0008g0113 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-3-8948T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136271 | ||||||
| chr6:109136279
|
G | A | 1 | a0001c0001t0062g0096 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-3-8940G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136279 | ||||||
| chr6:109136280
|
C | T | 1 | a0001c0001t0062g0096 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-3-8939C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136280 | ||||||
| chr6:109136281
|
T | C | 1 | a0001c0001t0062g0096 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-3-8938T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136281 | ||||||
| chr6:109136282
|
G | A | 1 | a0001c0001t0062g0096 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-3-8937G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136282 | ||||||
| chr6:109136287
|
C | T | 1 | a0001c0001t0062g0096 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-3-8932C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136287 | ||||||
| chr6:109136295
|
C | T | 4 | a0002c0002t0068g0009a0002c0002t0074g0006a0002c0002t0075g0008others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-8924C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136295 | ||||||
| chr6:109136308
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-8911C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136308 | ||||||
| chr6:109136374
|
T | C | 1 | a0002c0002t0079g0209 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-3-8845T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136374 | ||||||
| chr6:109136437
|
G | A | 3 | a0001c0001t0001g0158a0001c0001t0087g0159a0001c0001t0088g0160 | 3 | HG02647.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-3-8782G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136437 | ||||||
| chr6:109136492
|
G | A | 2 | a0001c0001t0011g0138a0001c0001t0011g0139 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-3-8727G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136492 | ||||||
| chr6:109136530
|
G | A | 2 | a0001c0001t0011g0138a0001c0001t0011g0139 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-3-8689G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136530 | ||||||
| chr6:109136561
|
T | TA | 167 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(164): Show | 169 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.-3-8642dupA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109136561 | |||||
| chr6:109136561
|
T | TAATTTA | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-8656_-3-8655ins others(6): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109136561 | |||||
| chr6:109136570
|
A | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-8649A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136570 | ||||||
| chr6:109136576
|
A | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-8643A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136576 | ||||||
| chr6:109136617
|
A | C | 2 | a0002c0002t0068g0009a0002c0002t0074g0006 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-3-8602A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136617 | ||||||
| chr6:109136697
|
GTATTTT | G | 23 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(20): Show | 26 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.-3-8515_-3-8510del others(6): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109136697 | |||||
| chr6:109136697
|
GTATTTTT others(4): Show |
G | 7 | a0001c0001t0024g0180a0001c0007t0029g0005a0002c0002t0030g0211others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3-8515_-3-8505del others(11): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109136697 | |||||
| chr6:109136697
|
GTATTTTT others(9): Show |
G | 2 | a0002c0002t0075g0008a0002c0002t0086g0007 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-3-8515_-3-8500del others(16): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109136697 | |||||
| chr6:109136697
|
GTATTTTT others(14): Show |
G | 2 | a0002c0002t0082g0204a0002c0002t0084g0011 | 2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-3-8515_-3-8495del others(21): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109136697 | |||||
| chr6:109136697
|
GTATTTTT others(19): Show |
G | 4 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-8515_-3-8490del others(26): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109136697 | |||||
| chr6:109136697
|
GTATTTTT others(24): Show |
G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-8515_-3-8485del others(31): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109136697 | |||||
| chr6:109136700
|
T | TTTTTA | 24 | a0001c0001t0001g0038a0001c0001t0001g0097a0001c0001t0001g0195others(21): Show | 25 | HG00558.hp1 HG00558.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.-3-8460_-3-8456dup others(5): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109136700 | |||||
| chr6:109136700
|
T | TTTTTATT others(3): Show |
11 | a0001c0001t0001g0031a0001c0001t0001g0146a0001c0001t0001g0156others(8): Show | 11 | HG02145.hp2 HG02615.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-8465_-3-8456dup others(10): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109136700 | |||||
| chr6:109136700
|
T | TTTTTATT others(8): Show |
3 | a0001c0001t0001g0149a0001c0001t0011g0139a0001c0001t0053g0141 | 3 | HG02109.hp2 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-3-8470_-3-8456dup others(15): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109136700 | |||||
| chr6:109136700
|
TTTTTA | T | 17 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0082others(14): Show | 17 | HG00099.hp1 HG00621.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-3-8460_-3-8456del others(5): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109136700 | |||||
| chr6:109136700
|
TTTTTATT others(3): Show |
T | 4 | a0001c0001t0001g0103a0001c0001t0002g0057a0001c0001t0042g0072others(1): Show | 4 | HG03704.hp1 HG04115.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-8465_-3-8456del others(10): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109136700 | |||||
| chr6:109136700
|
TTTTTATT others(8): Show |
T | 17 | a0001c0001t0001g0065a0001c0001t0001g0214a0001c0001t0005g0192others(14): Show | 17 | HG01109.hp1 HG01123.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.-3-8470_-3-8456del others(15): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109136700 | |||||
| chr6:109136700
|
TTTTTATT others(13): Show |
T | 1 | a0001c0001t0006g0164 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-3-8475_-3-8456del others(20): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109136700 | |||||
| chr6:109136700
|
TTTTTATT others(18): Show |
T | 1 | a0001c0001t0017g0130 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-3-8480_-3-8456del others(25): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109136700 | |||||
| chr6:109136700
|
TTTTTATT others(23): Show |
T | 1 | a0001c0001t0006g0173 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-3-8485_-3-8456del others(30): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109136700 | |||||
| chr6:109136756
|
TTTTA | T | 7 | a0001c0001t0024g0180a0002c0002t0030g0211a0002c0002t0078g0205others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3-8455_-3-8452del others(4): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109136756 | |||||
| chr6:109136786
|
T | C | 45 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(42): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.-3-8433T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136786 | ||||||
| chr6:109136799
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-8420A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136799 | ||||||
| chr6:109136843
|
C | T | 1 | a0001c0001t0043g0067 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-3-8376C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136843 | ||||||
| chr6:109136909
|
C | T | 1 | a0001c0003t0005g0003 | 2 | HG01168.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-3-8310C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136909 | ||||||
| chr6:109136939
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-8280T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109136939 | ||||||
| chr6:109137005
|
C | T | 1 | a0001c0001t0002g0085 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-3-8214C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109137005 | ||||||
| chr6:109137082
|
C | T | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-8137C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109137082 | ||||||
| chr6:109137208
|
A | G | 3 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208 | 3 | HG01891.hp1 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-3-8011A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109137208 | ||||||
| chr6:109137260
|
C | T | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-3-7959C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109137260 | ||||||
| chr6:109137312
|
T | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-7907T>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109137312 | ||||||
| chr6:109137341
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-3-7878G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109137341 | ||||||
| chr6:109137357
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-7862G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109137357 | ||||||
| chr6:109137408
|
TCTC | T | 4 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0116others(1): Show | 4 | HG01891.hp2 HG02647.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-7808_-3-7806del others(3): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109137408 | |||||
| chr6:109137508
|
G | A | 1 | a0002c0002t0085g0213 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-3-7711G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109137508 | ||||||
| chr6:109137550
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-7669C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109137550 | ||||||
| chr6:109137574
|
A | G | 4 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-7645A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109137574 | ||||||
| chr6:109137589
|
C | T | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-3-7630C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109137589 | ||||||
| chr6:109138084
|
A | G | 44 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(41): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.-3-7135A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109138084 | ||||||
| chr6:109138202
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0053 | 2 | NA18954.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-3-7017G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109138202 | ||||||
| chr6:109138576
|
A | T | 1 | a0002c0002t0084g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-3-6643A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109138576 | ||||||
| chr6:109138727
|
A | G | 1 | a0002c0002t0080g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-3-6492A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109138727 | ||||||
| chr6:109138740
|
C | T | 1 | a0001c0001t0012g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-3-6479C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109138740 | ||||||
| chr6:109139026
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-3-6193A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109139026 | ||||||
| chr6:109139176
|
A | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-6043A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109139176 | ||||||
| chr6:109139249
|
A | G | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-5970A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109139249 | ||||||
| chr6:109139308
|
G | GTTTA | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-5910_-3-5907dup others(4): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109139308 | |||||
| chr6:109139345
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-5874T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109139345 | ||||||
| chr6:109139417
|
G | A | 18 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0001g0156others(15): Show | 18 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-3-5802G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109139417 | ||||||
| chr6:109139455
|
C | T | 4 | a0002c0002t0068g0009a0002c0002t0074g0006a0002c0002t0075g0008others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-5764C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109139455 | ||||||
| chr6:109139482
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-5737T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109139482 | ||||||
| chr6:109139483
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-5736C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109139483 | ||||||
| chr6:109139631
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-5588G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109139631 | ||||||
| chr6:109139644
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-3-5575C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109139644 | ||||||
| chr6:109139739
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-5480T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109139739 | ||||||
| chr6:109139770
|
G | A | 6 | a0002c0002t0030g0211a0002c0002t0078g0205a0002c0002t0079g0209others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-5449G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109139770 | ||||||
| chr6:109139852
|
G | A | 3 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208 | 3 | HG01891.hp1 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-3-5367G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109139852 | ||||||
| chr6:109139962
|
T | A | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-5257T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109139962 | ||||||
| chr6:109140161
|
C | G | 5 | a0002c0002t0068g0009a0002c0002t0074g0006a0002c0002t0075g0008others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-5058C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109140161 | ||||||
| chr6:109140185
|
C | T | 2 | a0001c0001t0015g0162a0001c0001t0069g0163 | 2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-3-5034C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109140185 | ||||||
| chr6:109140235
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-4984A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109140235 | ||||||
| chr6:109140295
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-3-4924A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109140295 | ||||||
| chr6:109140297
|
C | G | 3 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208 | 3 | HG01891.hp1 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-3-4922C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109140297 | ||||||
| chr6:109140303
|
A | C | 44 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(41): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.-3-4916A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109140303 | ||||||
| chr6:109140362
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-4857T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109140362 | ||||||
| chr6:109140400
|
A | AT | 80 | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0044others(77): Show | 83 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-3-4801dupT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109140400 | |||||
| chr6:109140400
|
A | ATT | 7 | a0001c0001t0001g0031a0001c0001t0012g0218a0001c0001t0012g0219others(4): Show | 7 | HG02572.hp1 HG02717.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3-4802_-3-4801dup others(2): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109140400 | |||||
| chr6:109140462
|
C | T | 1 | a0002c0002t0084g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-3-4757C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109140462 | ||||||
| chr6:109140509
|
C | G | 1 | a0001c0001t0001g0051 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-3-4710C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109140509 | ||||||
| chr6:109140521
|
A | C | 2 | a0001c0001t0001g0068a0001c0001t0007g0033 | 2 | HG03654.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-3-4698A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109140521 | ||||||
| chr6:109140548
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | NA19060.hp2 NA19065.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-3-4671C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109140548 | ||||||
| chr6:109140686
|
G | A | 2 | a0002c0002t0075g0008a0002c0002t0086g0007 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-3-4533G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109140686 | ||||||
| chr6:109140830
|
T | A | 3 | a0001c0001t0017g0129a0001c0007t0029g0005a0002c0002t0082g0204 | 3 | HG02818.hp2 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-3-4389T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109140830 | ||||||
| chr6:109140960
|
A | G | 6 | a0002c0002t0030g0211a0002c0002t0078g0205a0002c0002t0079g0209others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-4259A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109140960 | ||||||
| chr6:109140967
|
A | T | 1 | a0002c0002t0084g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-3-4252A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109140967 | ||||||
| chr6:109141043
|
G | A | 1 | a0001c0001t0041g0070 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-3-4176G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109141043 | ||||||
| chr6:109141073
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-4146G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109141073 | ||||||
| chr6:109141118
|
C | G | 1 | a0002c0002t0082g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-3-4101C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109141118 | ||||||
| chr6:109141189
|
T | A | 2 | a0001c0001t0014g0135a0001c0001t0014g0154 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-3-4030T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109141189 | ||||||
| chr6:109141259
|
G | C | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-3-3960G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109141259 | ||||||
| chr6:109141309
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-3910A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109141309 | ||||||
| chr6:109141744
|
C | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-3475C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109141744 | ||||||
| chr6:109141809
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-3410A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109141809 | ||||||
| chr6:109141983
|
G | A | 7 | a0002c0002t0003g0015a0002c0002t0003g0027a0002c0002t0025g0020others(4): Show | 7 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3-3236G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109141983 | ||||||
| chr6:109142129
|
T | C | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-3-3090T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109142129 | ||||||
| chr6:109142151
|
C | G | 1 | a0002c0002t0030g0211 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-3-3068C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109142151 | ||||||
| chr6:109142315
|
C | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-2904C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109142315 | ||||||
| chr6:109142511
|
A | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-2708A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109142511 | ||||||
| chr6:109142621
|
GA | G | 34 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(31): Show | 37 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.-3-2586delA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109142621 | |||||
| chr6:109142632
|
A | AAAGAAGA others(8): Show |
5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-2586_-3-2585ins others(15): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109142632 | |||||
| chr6:109142642
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-2577T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109142642 | ||||||
| chr6:109142786
|
G | A | 44 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(41): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.-3-2433G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109142786 | ||||||
| chr6:109142888
|
G | GCT | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-2324_-3-2323dup others(2): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109142888 | |||||
| chr6:109142946
|
G | GCT | 9 | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0001g0075others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3-2215_-3-2214dup others(2): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109142946 | |||||
| chr6:109142946
|
G | GCTCT | 8 | a0001c0001t0001g0121a0001c0001t0001g0214a0001c0001t0002g0080others(5): Show | 8 | HG01123.hp1 HG01255.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3-2217_-3-2214dup others(4): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109142946 | |||||
| chr6:109142946
|
GCT | G | 15 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0049others(12): Show | 15 | HG00438.hp1 HG01081.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3-2215_-3-2214del others(2): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109142946 | |||||
| chr6:109142946
|
GCTCT | G | 26 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0051others(23): Show | 27 | HG00280.hp2 HG00621.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.-3-2217_-3-2214del others(4): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109142946 | |||||
| chr6:109142946
|
GCTCTCT | G | 29 | a0001c0001t0001g0039a0001c0001t0001g0064a0001c0001t0001g0065others(26): Show | 29 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.-3-2219_-3-2214del others(6): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109142946 | |||||
| chr6:109142946
|
GCTCTCTC others(1): Show |
G | 25 | a0001c0001t0001g0031a0001c0001t0001g0050a0001c0001t0001g0055others(22): Show | 25 | HG01261.hp2 HG01361.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.-3-2221_-3-2214del others(8): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109142946 | |||||
| chr6:109142946
|
GCTCTCTC others(3): Show |
G | 19 | a0001c0001t0001g0037a0001c0001t0001g0060a0001c0001t0001g0082others(16): Show | 19 | HG00558.hp1 HG00609.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.-3-2223_-3-2214del others(10): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109142946 | |||||
| chr6:109142946
|
GCTCTCTC others(5): Show |
G | 11 | a0001c0001t0006g0164a0001c0001t0006g0166a0001c0001t0010g0119others(8): Show | 11 | HG01109.hp1 HG02027.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-2225_-3-2214del others(12): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109142946 | |||||
| chr6:109142946
|
GCTCTCTC others(7): Show |
G | 10 | a0001c0001t0001g0038a0001c0001t0001g0188a0001c0001t0005g0184others(7): Show | 10 | HG00099.hp1 HG00738.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3-2227_-3-2214del others(14): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109142946 | |||||
| chr6:109142946
|
GCTCTCTC others(9): Show |
G | 4 | a0001c0001t0021g0216a0001c0001t0087g0159a0001c0003t0005g0193others(1): Show | 4 | HG03654.hp1 HG06807.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-2229_-3-2214del others(16): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109142946 | |||||
| chr6:109142946
|
GCTCTCTC others(11): Show |
G | 7 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0001g0158others(4): Show | 7 | HG02258.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3-2231_-3-2214del others(18): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109142946 | |||||
| chr6:109142946
|
GCTCTCTC others(13): Show |
G | 8 | a0001c0001t0006g0167a0001c0001t0010g0002a0001c0001t0010g0094others(5): Show | 9 | HG01168.hp2 HG01169.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3-2233_-3-2214del others(20): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109142946 | |||||
| chr6:109142946
|
GCTCTCTC others(15): Show |
G | 3 | a0001c0001t0088g0160a0002c0002t0079g0209a0002c0002t0084g0011 | 3 | HG02559.hp1 HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-3-2235_-3-2214del others(22): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109142946 | |||||
| chr6:109142946
|
GCTCTCTC others(17): Show |
G | 3 | a0002c0002t0085g0213a0003c0005t0035g0215a0006c0008t0077g0212 | 3 | HG02630.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-3-2237_-3-2214del others(24): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109142946 | |||||
| chr6:109142946
|
GCTCTCTC others(19): Show |
G | 32 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(29): Show | 35 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.-3-2239_-3-2214del others(26): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109142946 | |||||
| chr6:109142946
|
GCTCTCTC others(25): Show |
G | 1 | a0002c0002t0080g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-3-2245_-3-2214del others(32): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109142946 | |||||
| chr6:109143081
|
G | A | 44 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(41): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.-3-2138G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109143081 | ||||||
| chr6:109143164
|
ACTCT | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-2048_-3-2045del others(4): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109143164 | |||||
| chr6:109143182
|
A | T | 1 | a0001c0001t0001g0091 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-3-2037A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109143182 | ||||||
| chr6:109143254
|
ACTC | A | 3 | a0001c0001t0006g0166a0001c0001t0059g0165a0001c0001t0060g0174 | 3 | HG02572.hp2 HG02895.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-3-1959_-3-1957del others(3): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109143254 | |||||
| chr6:109143301
|
T | C | 2 | a0002c0002t0075g0008a0002c0002t0086g0007 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-3-1918T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109143301 | ||||||
| chr6:109143421
|
A | G | 44 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(41): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.-3-1798A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109143421 | ||||||
| chr6:109143445
|
A | G | 5 | a0002c0002t0068g0009a0002c0002t0074g0006a0002c0002t0075g0008others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-1774A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109143445 | ||||||
| chr6:109143598
|
T | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0053others(1): Show | 4 | HG00558.hp1 HG00621.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-1621T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109143598 | ||||||
| chr6:109143721
|
A | G | 1 | a0004c0004t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-3-1498A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109143721 | ||||||
| chr6:109143867
|
A | G | 1 | a0001c0001t0018g0102 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-3-1352A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109143867 | ||||||
| chr6:109143972
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-1247G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109143972 | ||||||
| chr6:109144020
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-1199C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109144020 | ||||||
| chr6:109144240
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-979C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109144240 | ||||||
| chr6:109144336
|
A | G | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0013g0197 | 3 | HG01106.hp2 HG01361.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-3-883A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109144336 | ||||||
| chr6:109144461
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-758G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109144461 | ||||||
| chr6:109144660
|
T | C | 6 | a0001c0001t0005g0184a0001c0001t0005g0187a0001c0001t0005g0192others(3): Show | 6 | HG00099.hp1 HG00738.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-559T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109144660 | ||||||
| chr6:109144748
|
C | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-471C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109144748 | ||||||
| chr6:109144843
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-376A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109144843 | ||||||
| chr6:109145016
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-3-203G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | chr6 | 109145016 | ||||||
| chr6:109145193
|
C | CTATAT | 124 | a0001c0001t0001g0032a0001c0001t0001g0146a0001c0001t0001g0149others(121): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.-3-25_-3-21dupTATA others(1): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 109145193 | |||||
| chr6:109145454
|
A | G | 1 | a0001c0001t0018g0102 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.160+73A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 2/10 | chr6 | 109145454 | ||||||
| chr6:109145683
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+302C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 2/10 | chr6 | 109145683 | ||||||
| chr6:109145687
|
A | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+306A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 2/10 | chr6 | 109145687 | ||||||
| chr6:109145688
|
T | A | 1 | a0001c0001t0016g0115 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.160+307T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 2/10 | chr6 | 109145688 | ||||||
| chr6:109145868
|
A | T | 18 | a0001c0001t0006g0161a0001c0001t0006g0164a0001c0001t0006g0166others(15): Show | 18 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.160+487A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 2/10 | chr6 | 109145868 | ||||||
| chr6:109145921
|
G | A | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+540G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 2/10 | chr6 | 109145921 | ||||||
| chr6:109145932
|
A | G | 1 | a0002c0002t0003g0028 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.160+551A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 2/10 | chr6 | 109145932 | ||||||
| chr6:109145958
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.160+577A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 2/10 | chr6 | 109145958 | ||||||
| chr6:109146026
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+645A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 2/10 | chr6 | 109146026 | ||||||
| chr6:109146360
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-398A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 2/10 | chr6 | 109146360 | ||||||
| chr6:109146477
|
T | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-281T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 2/10 | chr6 | 109146477 | ||||||
| chr6:109146970
|
G | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.340+33G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109146970 | ||||||
| chr6:109147129
|
T | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+192T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109147129 | ||||||
| chr6:109147169
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+232A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109147169 | ||||||
| chr6:109147207
|
A | G | 4 | a0001c0001t0014g0135a0001c0001t0014g0154a0001c0001t0051g0134others(1): Show | 4 | HG01884.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.340+270A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109147207 | ||||||
| chr6:109147233
|
A | G | 1 | a0001c0001t0018g0102 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.340+296A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109147233 | ||||||
| chr6:109147328
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+391T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109147328 | ||||||
| chr6:109147367
|
G | T | 38 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(35): Show | 41 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.340+430G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109147367 | ||||||
| chr6:109147521
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+584C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109147521 | ||||||
| chr6:109147567
|
TAGA | T | 5 | a0002c0002t0025g0020a0002c0002t0025g0025a0002c0002t0070g0021others(2): Show | 5 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+633_340+635del others(3): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 109147567 | |||||
| chr6:109147639
|
G | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0013g0197 | 3 | HG01106.hp2 HG01361.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.340+702G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109147639 | ||||||
| chr6:109147700
|
G | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+763G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109147700 | ||||||
| chr6:109147704
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0053 | 2 | NA18954.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.340+767G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109147704 | ||||||
| chr6:109147945
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+1008G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109147945 | ||||||
| chr6:109148105
|
T | TTTTTA | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+1186_340+1190d others(7): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 109148105 | |||||
| chr6:109148244
|
G | A | 1 | a0002c0002t0084g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.340+1307G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148244 | ||||||
| chr6:109148275
|
C | G | 2 | a0001c0001t0010g0002a0001c0001t0010g0094 | 3 | HG01192.hp1 HG01257.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.340+1338C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148275 | ||||||
| chr6:109148299
|
C | T | 1 | a0001c0001t0064g0126 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.340+1362C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148299 | ||||||
| chr6:109148387
|
C | T | 1 | a0002c0002t0082g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.340+1450C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148387 | ||||||
| chr6:109148414
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+1477T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148414 | ||||||
| chr6:109148454
|
T | A | 1 | a0001c0001t0009g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.340+1517T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148454 | ||||||
| chr6:109148576
|
C | T | 6 | a0001c0001t0001g0051a0001c0001t0001g0064a0001c0001t0001g0065others(3): Show | 6 | HG00280.hp2 HG01106.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-1542C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148576 | ||||||
| chr6:109148583
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-1535G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148583 | ||||||
| chr6:109148597
|
G | A | 44 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(41): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.341-1521G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148597 | ||||||
| chr6:109148604
|
C | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | NA19060.hp2 NA19065.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.341-1514C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148604 | ||||||
| chr6:109148653
|
C | G | 4 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-1465C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148653 | ||||||
| chr6:109148689
|
G | A | 1 | a0001c0001t0011g0131 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.341-1429G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148689 | ||||||
| chr6:109148738
|
A | G | 3 | a0001c0001t0004g0101a0001c0001t0036g0100a0001c0001t0040g0043 | 3 | HG01109.hp2 HG01261.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.341-1380A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148738 | ||||||
| chr6:109148751
|
C | T | 3 | a0001c0001t0004g0101a0001c0001t0036g0100a0001c0001t0040g0043 | 3 | HG01109.hp2 HG01261.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.341-1367C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148751 | ||||||
| chr6:109148752
|
C | G | 1 | a0001c0001t0046g0041 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.341-1366C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148752 | ||||||
| chr6:109148755
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-1363T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148755 | ||||||
| chr6:109148889
|
A | C | 4 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-1229A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148889 | ||||||
| chr6:109148916
|
T | A | 1 | a0002c0002t0082g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.341-1202T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148916 | ||||||
| chr6:109148961
|
G | A | 15 | a0001c0001t0005g0178a0001c0001t0005g0184a0001c0001t0005g0187others(12): Show | 16 | HG00099.hp1 HG00738.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.341-1157G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148961 | ||||||
| chr6:109148999
|
A | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-1119A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109148999 | ||||||
| chr6:109149039
|
G | A | 4 | a0001c0001t0001g0032a0001c0001t0001g0195a0001c0001t0001g0200others(1): Show | 4 | HG02083.hp2 HG02129.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-1079G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109149039 | ||||||
| chr6:109149163
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-955C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109149163 | ||||||
| chr6:109149174
|
G | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-944G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109149174 | ||||||
| chr6:109149176
|
A | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-942A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109149176 | ||||||
| chr6:109149276
|
C | G | 1 | a0001c0001t0009g0142 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.341-842C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109149276 | ||||||
| chr6:109149283
|
A | G | 5 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0001g0156others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-835A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109149283 | ||||||
| chr6:109149307
|
G | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-811G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109149307 | ||||||
| chr6:109149504
|
C | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-614C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109149504 | ||||||
| chr6:109149551
|
G | A | 6 | a0002c0002t0030g0211a0002c0002t0078g0205a0002c0002t0079g0209others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.341-567G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109149551 | ||||||
| chr6:109149555
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-563T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109149555 | ||||||
| chr6:109149576
|
G | T | 23 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(20): Show | 26 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.341-542G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109149576 | ||||||
| chr6:109149582
|
G | T | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-536G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109149582 | ||||||
| chr6:109149596
|
A | G | 2 | a0001c0001t0037g0090a0001c0001t0038g0089 | 2 | HG01243.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.341-522A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109149596 | ||||||
| chr6:109149948
|
G | A | 1 | a0001c0001t0015g0162 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.341-170G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109149948 | ||||||
| chr6:109150019
|
G | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-99G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109150019 | ||||||
| chr6:109150042
|
A | G | 2 | a0002c0002t0078g0205a0002c0002t0079g0209 | 2 | HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.341-76A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 3/10 | chr6 | 109150042 | ||||||
| chr6:109150307
|
C | T | 1 | a0001c0001t0008g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.462+68C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109150307 | ||||||
| chr6:109150329
|
T | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.462+90T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109150329 | ||||||
| chr6:109150476
|
A | G | 22 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(19): Show | 25 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.462+237A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109150476 | ||||||
| chr6:109150524
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.462+285T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109150524 | ||||||
| chr6:109150661
|
CAA | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.462+437_462+438del others(2): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 109150661 | |||||
| chr6:109150839
|
C | T | 7 | a0001c0001t0002g0095a0001c0001t0012g0218a0001c0001t0012g0219others(4): Show | 7 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.462+600C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109150839 | ||||||
| chr6:109150894
|
T | C | 1 | a0001c0001t0004g0125 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.462+655T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109150894 | ||||||
| chr6:109151202
|
A | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.462+963A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109151202 | ||||||
| chr6:109151219
|
A | G | 1 | a0001c0001t0055g0157 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.462+980A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109151219 | ||||||
| chr6:109151412
|
G | T | 7 | a0002c0002t0003g0014a0002c0002t0003g0017a0002c0002t0003g0018others(4): Show | 7 | HG00438.hp2 HG02083.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.462+1173G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109151412 | ||||||
| chr6:109151571
|
T | C | 1 | a0004c0004t0001g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.462+1332T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109151571 | ||||||
| chr6:109151613
|
C | G | 1 | a0001c0001t0001g0082 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.462+1374C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109151613 | ||||||
| chr6:109151649
|
T | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0060 | 2 | HG00609.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.462+1410T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109151649 | ||||||
| chr6:109151790
|
C | T | 2 | a0001c0001t0015g0162a0001c0001t0069g0163 | 2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.462+1551C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109151790 | ||||||
| chr6:109152272
|
C | G | 2 | a0001c0001t0051g0134a0005c0009t0001g0133 | 2 | HG01884.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.463-1561C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109152272 | ||||||
| chr6:109152329
|
C | T | 1 | a0001c0001t0067g0186 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.463-1504C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109152329 | ||||||
| chr6:109152347
|
A | T | 2 | a0004c0004t0001g0152a0004c0004t0008g0132 | 2 | HG02896.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.463-1486A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109152347 | ||||||
| chr6:109152362
|
A | G | 2 | a0001c0001t0018g0153a0001c0001t0063g0151 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.463-1471A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109152362 | ||||||
| chr6:109152434
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.463-1399T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109152434 | ||||||
| chr6:109152636
|
CGTGT | C | 4 | a0001c0001t0004g0106a0001c0001t0024g0093a0001c0001t0037g0090others(1): Show | 4 | HG00609.hp1 HG01243.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.463-1156_463-1153d others(6): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 109152636 | |||||
| chr6:109152636
|
CGTGTGT | C | 16 | a0001c0001t0001g0038a0001c0001t0001g0068a0001c0001t0001g0121others(13): Show | 16 | HG00558.hp2 HG01255.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.463-1158_463-1153d others(8): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 109152636 | |||||
| chr6:109152636
|
CGTGTGTG others(1): Show |
C | 126 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0036others(123): Show | 130 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.463-1160_463-1153d others(10): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 109152636 | |||||
| chr6:109152636
|
CGTGTGTG others(3): Show |
C | 25 | a0001c0001t0001g0035a0001c0001t0006g0164a0001c0001t0006g0166others(22): Show | 25 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.463-1162_463-1153d others(12): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 109152636 | |||||
| chr6:109152636
|
CGTGTGTG others(5): Show |
C | 11 | a0001c0001t0001g0097a0001c0001t0001g0114a0001c0001t0009g0148others(8): Show | 11 | HG00558.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.463-1164_463-1153d others(14): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 109152636 | |||||
| chr6:109152636
|
CGTGTGTG others(7): Show |
C | 29 | a0001c0001t0001g0032a0001c0001t0001g0103a0001c0001t0001g0188others(26): Show | 30 | HG00099.hp1 HG00738.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.463-1166_463-1153d others(16): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 109152636 | |||||
| chr6:109152636
|
CGTGTGTG others(9): Show |
C | 9 | a0001c0001t0005g0178a0001c0001t0006g0167a0001c0001t0006g0168others(6): Show | 9 | HG01109.hp1 HG01261.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.463-1168_463-1153d others(18): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 109152636 | |||||
| chr6:109152636
|
CGTGTGTG others(13): Show |
C | 1 | a0002c0002t0030g0211 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.463-1172_463-1153d others(22): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 109152636 | |||||
| chr6:109152652
|
T | C | 1 | a0001c0001t0064g0126 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.463-1181T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109152652 | ||||||
| chr6:109152679
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.463-1154G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109152679 | ||||||
| chr6:109152689
|
C | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.463-1144C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109152689 | ||||||
| chr6:109152698
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.463-1135T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109152698 | ||||||
| chr6:109152983
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.463-850C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109152983 | ||||||
| chr6:109153000
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.463-833A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109153000 | ||||||
| chr6:109153008
|
A | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.463-825A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109153008 | ||||||
| chr6:109153122
|
AAAAG | A | 3 | a0001c0001t0001g0087a0001c0001t0002g0086a0001c0001t0002g0095 | 3 | NA18981.hp1 NA18983.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.463-707_463-704del others(4): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 109153122 | |||||
| chr6:109153178
|
G | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.463-655G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109153178 | ||||||
| chr6:109153186
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.463-647G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109153186 | ||||||
| chr6:109153189
|
G | A | 1 | a0001c0001t0040g0043 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.463-644G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109153189 | ||||||
| chr6:109153211
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.463-622T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109153211 | ||||||
| chr6:109153231
|
C | CT | 42 | a0001c0001t0001g0068a0001c0001t0001g0114a0001c0001t0001g0121others(39): Show | 42 | HG00438.hp2 HG00738.hp1 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.463-574dupT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 109153231 | |||||
| chr6:109153231
|
CT | C | 29 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0042others(26): Show | 29 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.463-574delT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 109153231 | |||||
| chr6:109153231
|
CTTTTTTT others(4): Show |
C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.463-584_463-574del others(11): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 109153231 | |||||
| chr6:109153263
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.463-570A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109153263 | ||||||
| chr6:109153323
|
C | T | 1 | a0002c0002t0082g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.463-510C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109153323 | ||||||
| chr6:109153332
|
G | C | 7 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(4): Show | 7 | HG02572.hp1 HG03225.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.463-501G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109153332 | ||||||
| chr6:109153443
|
G | A | 44 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(41): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.463-390G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109153443 | ||||||
| chr6:109153458
|
C | G | 2 | a0001c0001t0008g0111a0001c0001t0008g0116 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.463-375C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109153458 | ||||||
| chr6:109153601
|
T | A | 1 | a0002c0002t0082g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.463-232T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109153601 | ||||||
| chr6:109153603
|
A | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.463-230A>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109153603 | ||||||
| chr6:109153615
|
T | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.463-218T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 4/10 | chr6 | 109153615 | ||||||
| chr6:109154213
|
G | A | 29 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0042others(26): Show | 29 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.579+264G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 5/10 | chr6 | 109154213 | ||||||
| chr6:109154295
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+346T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 5/10 | chr6 | 109154295 | ||||||
| chr6:109154307
|
T | C | 1 | a0001c0001t0002g0122 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.579+358T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 5/10 | chr6 | 109154307 | ||||||
| chr6:109154331
|
C | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+382C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 5/10 | chr6 | 109154331 | ||||||
| chr6:109154558
|
A | C | 1 | a0001c0001t0022g0196 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.579+609A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 5/10 | chr6 | 109154558 | ||||||
| chr6:109154672
|
G | A | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.580-558G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 5/10 | chr6 | 109154672 | ||||||
| chr6:109154768
|
A | G | 5 | a0002c0002t0068g0009a0002c0002t0074g0006a0002c0002t0075g0008others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-462A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 5/10 | chr6 | 109154768 | ||||||
| chr6:109155037
|
A | G | 2 | a0001c0001t0006g0167a0001c0001t0006g0172 | 2 | HG02698.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.580-193A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 5/10 | chr6 | 109155037 | ||||||
| chr6:109155626
|
A | G | 1 | a0002c0002t0082g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.658-165A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 6/10 | chr6 | 109155626 | ||||||
| chr6:109155659
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.658-132G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 6/10 | chr6 | 109155659 | ||||||
| chr6:109155748
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.658-43A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 6/10 | chr6 | 109155748 | ||||||
| chr6:109155760
|
AAT | A | 2 | a0002c0002t0075g0008a0002c0002t0086g0007 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.658-30_658-29delAT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 6/10 | chr6 | 109155760 | ||||||
| chr6:109156342
|
A | AG | 7 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(4): Show | 7 | HG02572.hp1 HG03225.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.744+467dupG | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 109156342 | |||||
| chr6:109156769
|
A | G | 3 | a0001c0001t0020g0181a0001c0001t0024g0180a0001c0001t0050g0182 | 3 | HG02055.hp1 HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.744+892A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | chr6 | 109156769 | ||||||
| chr6:109156854
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+977C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | chr6 | 109156854 | ||||||
| chr6:109156980
|
G | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+1103G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | chr6 | 109156980 | ||||||
| chr6:109157182
|
G | A | 23 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(20): Show | 26 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.744+1305G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | chr6 | 109157182 | ||||||
| chr6:109157587
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-1438T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | chr6 | 109157587 | ||||||
| chr6:109157769
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-1256T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | chr6 | 109157769 | ||||||
| chr6:109157943
|
CCTT | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-1080_745-1078d others(5): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 109157943 | |||||
| chr6:109157961
|
A | G | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-1064A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | chr6 | 109157961 | ||||||
| chr6:109158058
|
G | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-967G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | chr6 | 109158058 | ||||||
| chr6:109158058
|
G | T | 1 | a0001c0001t0001g0097 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.745-967G>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | chr6 | 109158058 | ||||||
| chr6:109158210
|
G | A | 2 | a0001c0001t0018g0153a0001c0001t0063g0151 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.745-815G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | chr6 | 109158210 | ||||||
| chr6:109158242
|
G | A | 1 | a0001c0001t0042g0072 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.745-783G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | chr6 | 109158242 | ||||||
| chr6:109158258
|
C | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-767C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | chr6 | 109158258 | ||||||
| chr6:109158456
|
C | T | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.745-569C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | chr6 | 109158456 | ||||||
| chr6:109158488
|
C | CA | 6 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(3): Show | 6 | HG01175.hp2 HG02572.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.745-527dupA | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 109158488 | |||||
| chr6:109158558
|
G | C | 1 | a0001c0001t0015g0175 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.745-467G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | chr6 | 109158558 | ||||||
| chr6:109158609
|
G | A | 2 | a0001c0001t0018g0153a0001c0001t0063g0151 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.745-416G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | chr6 | 109158609 | ||||||
| chr6:109158741
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-284T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | chr6 | 109158741 | ||||||
| chr6:109158967
|
A | G | 3 | a0001c0001t0001g0158a0001c0001t0087g0159a0001c0001t0088g0160 | 3 | HG02647.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.745-58A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | chr6 | 109158967 | ||||||
| chr6:109159001
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.745-24C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | chr6 | 109159001 | ||||||
| chr6:109159015
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0149 | 2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.745-10C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 7/10 | chr6 | 109159015 | ||||||
| chr6:109159127
|
G | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+25G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 8/10 | chr6 | 109159127 | ||||||
| chr6:109159129
|
C | T | 1 | a0001c0001t0002g0127 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.822+27C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 8/10 | chr6 | 109159129 | ||||||
| chr6:109159222
|
C | A | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-47C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 8/10 | chr6 | 109159222 | ||||||
| chr6:109159478
|
C | CT | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1016+27dupT | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 109159478 | |||||
| chr6:109159490
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1016+28C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 9/10 | chr6 | 109159490 | ||||||
| chr6:109159864
|
C | A | 1 | a0001c0001t0001g0103 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1016+402C>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 9/10 | chr6 | 109159864 | ||||||
| chr6:109159939
|
A | G | 1 | a0002c0002t0068g0009 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1016+477A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 9/10 | chr6 | 109159939 | ||||||
| chr6:109160044
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1017-528T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 9/10 | chr6 | 109160044 | ||||||
| chr6:109160046
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0087g0159a0001c0001t0088g0160 | 3 | HG02647.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1017-526C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 9/10 | chr6 | 109160046 | ||||||
| chr6:109160254
|
C | T | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017-318C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 9/10 | chr6 | 109160254 | ||||||
| chr6:109160475
|
A | G | 30 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(27): Show | 33 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.1017-97A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 9/10 | chr6 | 109160475 | ||||||
| chr6:109160514
|
G | A | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1017-58G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 9/10 | chr6 | 109160514 | ||||||
| chr6:109160804
|
G | A | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1161+88G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 10/10 | chr6 | 109160804 | ||||||
| chr6:109160983
|
G | A | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1161+267G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 10/10 | chr6 | 109160983 | ||||||
| chr6:109161067
|
A | G | 35 | a0002c0002t0003g0001a0002c0002t0003g0013a0002c0002t0003g0014others(32): Show | 38 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.1161+351A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 10/10 | chr6 | 109161067 | ||||||
| chr6:109161190
|
C | G | 1 | a0002c0002t0080g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1161+474C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 10/10 | chr6 | 109161190 | ||||||
| chr6:109161258
|
T | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1161+542T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 10/10 | chr6 | 109161258 | ||||||
| chr6:109161444
|
G | C | 66 | a0001c0001t0001g0158a0001c0001t0006g0161a0001c0001t0006g0164others(63): Show | 69 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1161+728G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 10/10 | chr6 | 109161444 | ||||||
| chr6:109161467
|
T | C | 1 | a0002c0002t0068g0009 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1161+751T>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 10/10 | chr6 | 109161467 | ||||||
| chr6:109161509
|
C | T | 1 | a0001c0007t0029g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1161+793C>T | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 10/10 | chr6 | 109161509 | ||||||
| chr6:109161510
|
G | C | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1161+794G>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 10/10 | chr6 | 109161510 | ||||||
| chr6:109161534
|
T | A | 4 | a0003c0005t0032g0004a0003c0005t0033g0004a0003c0005t0034g0208others(1): Show | 4 | HG01891.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1161+818T>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 10/10 | chr6 | 109161534 | ||||||
| chr6:109161763
|
G | A | 1 | a0001c0001t0002g0085 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1162-986G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 10/10 | chr6 | 109161763 | ||||||
| chr6:109161814
|
C | G | 2 | a0002c0002t0030g0211a0002c0002t0081g0143 | 2 | HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1162-935C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 10/10 | chr6 | 109161814 | ||||||
| chr6:109161995
|
G | A | 6 | a0001c0001t0005g0184a0001c0001t0005g0187a0001c0001t0005g0192others(3): Show | 6 | HG00099.hp1 HG00738.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-754G>A | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 10/10 | chr6 | 109161995 | ||||||
| chr6:109162111
|
C | G | 3 | a0001c0007t0029g0005a0002c0002t0030g0211a0002c0002t0081g0143 | 3 | HG03041.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1162-638C>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 10/10 | chr6 | 109162111 | ||||||
| chr6:109162371
|
T | TTA | 5 | a0001c0001t0012g0218a0001c0001t0012g0219a0001c0001t0012g0220others(2): Show | 5 | HG02572.hp1 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1162-373_1162-372d others(4): Show |
CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 109162371 | |||||
| chr6:109162623
|
A | C | 66 | a0001c0001t0001g0158a0001c0001t0006g0161a0001c0001t0006g0164others(63): Show | 69 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1162-126A>C | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 10/10 | chr6 | 109162623 | ||||||
| chr6:109162647
|
A | G | 3 | a0001c0007t0029g0005a0002c0002t0030g0211a0002c0002t0081g0143 | 3 | HG03041.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1162-102A>G | CEP57L1 | ENSG00000183137.16 | transcript | ENST00000517392.6 | protein_coding | 10/10 | chr6 | 109162647 |