| geneid | 27 |
|---|---|
| ensemblid | ENSG00000143322.22 |
| hgncid | 77 |
| symbol | ABL2 |
| name | ABL proto-oncogene 2, non-receptor tyrosine kinase |
| refseq_nuc | NM_007314.4 |
| refseq_prot | NP_009298.1 |
| ensembl_nuc | ENST00000502732.6 |
| ensembl_prot | ENSP00000427562.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 179099330 |
| end | 179229677 |
| strand | - |
| ver | v1.2 |
| region | chr1:179099330-179229677 |
| region5000 | chr1:179094330-179234677 |
| regionname0 | ABL2_chr1_179099330_179229677 |
| regionname5000 | ABL2_chr1_179094330_179234677 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1182 | 335 | 83 | 55 | 150 | 12 | 33 | 115 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0002 | 0/0 | 1182 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0003 | 0/0 | 1182 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0004 | 0/0 | 1182 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0005 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0006 | 0/0 | 1182 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0007 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0008 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0009 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3549 | 286 | 70 | 45 | 127 | 9 | 33 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| c0002 | 0/0 | 3549 | 19 | 2 | 5 | 10 | 2 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| c0003 | 0/0 | 3549 | 18 | 0 | 5 | 12 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| c0004 | 0/0 | 3549 | 7 | 7 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| c0005 | 0/0 | 3549 | 4 | 2 | 2 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| c0006 | 0/0 | 3549 | 4 | 0 | 0 | 4 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| c0007 | 0/0 | 3549 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| c0008 | 0/0 | 3549 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| c0009 | 0/0 | 3549 | 2 | 0 | 2 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| c0010 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| c0011 | 0/0 | 3549 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| c0012 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| c0013 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| c0014 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| c0015 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 8663 | 44 | 10 | 6 | 20 | 1 | 7 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0002 | 0/0 | 8664 | 26 | 9 | 2 | 11 | 2 | 2 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0003 | 0/0 | 8675 | 18 | 1 | 9 | 6 | 0 | 2 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0004 | 0/0 | 8674 | 17 | 1 | 6 | 6 | 3 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0005 | 0/0 | 8660 | 17 | 0 | 0 | 13 | 1 | 3 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0006 | 0/0 | 8676 | 12 | 0 | 2 | 8 | 0 | 2 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0007 | 0/0 | 8666 | 11 | 0 | 2 | 9 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0008 | 0/1 | 8664 | 11 | 5 | 2 | 2 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0009 | 0/0 | 8663 | 10 | 3 | 2 | 4 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0010 | 0/0 | 8670 | 7 | 0 | 2 | 4 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0011 | 0/0 | 8661 | 7 | 1 | 0 | 5 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0012 | 0/0 | 8675 | 5 | 0 | 1 | 4 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0013 | 0/0 | 8674 | 5 | 0 | 0 | 5 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0014 | 0/0 | 8677 | 5 | 0 | 0 | 3 | 1 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0015 | 0/0 | 8667 | 5 | 1 | 3 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0016 | 0/0 | 8670 | 5 | 4 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0017 | 0/0 | 8678 | 5 | 1 | 2 | 1 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0018 | 0/0 | 8675 | 4 | 0 | 0 | 4 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0019 | 0/0 | 8679 | 4 | 0 | 1 | 3 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0020 | 0/0 | 8663 | 4 | 3 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0021 | 0/0 | 8670 | 4 | 3 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0022 | 0/0 | 8658 | 4 | 2 | 2 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0023 | 0/0 | 8661 | 3 | 0 | 0 | 3 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0024 | 0/0 | 8680 | 3 | 3 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0025 | 0/0 | 8663 | 3 | 0 | 0 | 3 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0026 | 0/0 | 8677 | 3 | 0 | 0 | 0 | 0 | 3 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0027 | 0/0 | 8666 | 3 | 3 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0028 | 0/0 | 8686 | 2 | 0 | 0 | 2 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0029 | 0/0 | 8674 | 2 | 0 | 0 | 2 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0030 | 0/0 | 8661 | 2 | 0 | 0 | 2 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0031 | 0/0 | 8679 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0032 | 0/0 | 8682 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0033 | 0/0 | 8676 | 2 | 0 | 0 | 2 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0034 | 0/0 | 8654 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0035 | 0/0 | 8665 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0036 | 0/0 | 8670 | 2 | 0 | 0 | 0 | 0 | 2 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0037 | 0/0 | 8665 | 2 | 1 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0038 | 0/0 | 8664 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0039 | 0/0 | 8663 | 2 | 0 | 2 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0040 | 0/0 | 8669 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0041 | 0/0 | 8668 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0042 | 0/0 | 8664 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0043 | 0/0 | 8668 | 2 | 0 | 0 | 0 | 0 | 2 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0044 | 0/0 | 8670 | 2 | 0 | 0 | 2 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0045 | 0/0 | 8661 | 2 | 0 | 0 | 2 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0046 | 0/0 | 8690 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0047 | 0/0 | 8689 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0048 | 0/0 | 8687 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0049 | 0/0 | 8686 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0050 | 0/0 | 8682 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0051 | 0/0 | 8680 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0052 | 0/0 | 8665 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0053 | 0/0 | 8669 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0054 | 0/0 | 8665 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0055 | 0/0 | 8654 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0056 | 0/0 | 8676 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0057 | 0/0 | 8689 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0058 | 0/0 | 8677 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0059 | 0/0 | 8669 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0060 | 0/0 | 8677 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0061 | 0/0 | 8676 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0062 | 0/0 | 8674 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0063 | 0/0 | 8676 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0064 | 0/0 | 8674 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0065 | 0/0 | 8662 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0066 | 0/0 | 8673 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0067 | 0/0 | 8669 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0068 | 0/0 | 8678 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0069 | 0/0 | 8675 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0070 | 0/0 | 8674 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0071 | 0/0 | 8675 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0072 | 0/0 | 8676 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0073 | 0/0 | 8676 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0074 | 0/0 | 8674 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0075 | 0/0 | 8667 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0076 | 0/0 | 8673 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0077 | 0/0 | 8669 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0078 | 0/0 | 8668 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0079 | 0/0 | 8672 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0080 | 0/0 | 8671 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0081 | 0/0 | 8655 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0082 | 0/0 | 8682 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0083 | 0/0 | 8664 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0084 | 0/0 | 8663 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0085 | 0/0 | 8664 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0086 | 0/0 | 8662 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0087 | 0/0 | 8664 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0088 | 0/0 | 8664 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0089 | 1/0 | 8669 | 1 | 0 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0090 | 0/0 | 8664 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0091 | 0/0 | 8664 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0092 | 0/0 | 8656 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0093 | 0/0 | 8681 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0094 | 0/0 | 8680 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0095 | 0/0 | 8678 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0096 | 0/0 | 8666 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0097 | 0/0 | 8665 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0098 | 0/0 | 8678 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0099 | 0/0 | 8668 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0100 | 0/0 | 8678 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0101 | 0/0 | 8660 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0102 | 0/0 | 8665 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0103 | 0/0 | 8663 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0104 | 0/0 | 8665 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0105 | 0/0 | 8660 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0106 | 0/0 | 8660 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0107 | 0/0 | 8660 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0108 | 0/0 | 8660 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0109 | 0/0 | 8660 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0110 | 0/0 | 8660 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0111 | 0/0 | 8656 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0112 | 0/0 | 8676 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0113 | 0/0 | 8675 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| t0114 | 0/0 | 8687 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0282 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3549 | 286 | 70 | 45 | 127 | 9 | 33 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0002 | 0/0 | 3549 | 19 | 2 | 5 | 10 | 2 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0003 | 0/0 | 3549 | 18 | 0 | 5 | 12 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0004 | 0/0 | 3549 | 7 | 7 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0007 | 0/0 | 3549 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0008 | 0/0 | 3549 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0013 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0002c0005 | 0/0 | 3549 | 4 | 2 | 2 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0003c0006 | 0/0 | 3549 | 4 | 0 | 0 | 4 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0004c0009 | 0/0 | 3549 | 2 | 0 | 2 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0005c0010 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0006c0011 | 0/0 | 3549 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0007c0015 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0008c0012 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0009c0014 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 12211 | 39 | 9 | 6 | 16 | 1 | 7 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0002 | 0/0 | 12212 | 24 | 8 | 1 | 11 | 2 | 2 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0003 | 0/0 | 12223 | 18 | 1 | 9 | 6 | 0 | 2 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0004 | 0/0 | 12222 | 17 | 1 | 6 | 6 | 3 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0005 | 0/0 | 12208 | 16 | 0 | 0 | 12 | 1 | 3 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0006 | 0/0 | 12224 | 11 | 0 | 2 | 7 | 0 | 2 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0007 | 0/0 | 12214 | 11 | 0 | 2 | 9 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0008 | 0/1 | 12212 | 11 | 5 | 2 | 2 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0009 | 0/0 | 12211 | 10 | 3 | 2 | 4 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0011 | 0/0 | 12209 | 6 | 1 | 0 | 4 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0012 | 0/0 | 12223 | 5 | 0 | 1 | 4 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0013 | 0/0 | 12222 | 5 | 0 | 0 | 5 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0014 | 0/0 | 12225 | 5 | 0 | 0 | 3 | 1 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0015 | 0/0 | 12215 | 5 | 1 | 3 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0016 | 0/0 | 12218 | 5 | 4 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0018 | 0/0 | 12223 | 4 | 0 | 0 | 4 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0019 | 0/0 | 12227 | 4 | 0 | 1 | 3 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0020 | 0/0 | 12211 | 4 | 3 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0021 | 0/0 | 12218 | 4 | 3 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0025 | 0/0 | 12211 | 3 | 0 | 0 | 3 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0026 | 0/0 | 12225 | 3 | 0 | 0 | 0 | 0 | 3 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0027 | 0/0 | 12214 | 3 | 3 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0032 | 0/0 | 12230 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0033 | 0/0 | 12224 | 2 | 0 | 0 | 2 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0034 | 0/0 | 12202 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0035 | 0/0 | 12213 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0036 | 0/0 | 12218 | 2 | 0 | 0 | 0 | 0 | 2 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0037 | 0/0 | 12213 | 2 | 1 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0038 | 0/0 | 12212 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0041 | 0/0 | 12216 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0042 | 0/0 | 12212 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0043 | 0/0 | 12216 | 2 | 0 | 0 | 0 | 0 | 2 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0045 | 0/0 | 12209 | 2 | 0 | 0 | 2 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0055 | 0/0 | 12202 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0056 | 0/0 | 12224 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0057 | 0/0 | 12237 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0059 | 0/0 | 12217 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0060 | 0/0 | 12225 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0061 | 0/0 | 12224 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0062 | 0/0 | 12222 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0063 | 0/0 | 12224 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0064 | 0/0 | 12222 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0065 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0066 | 0/0 | 12221 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0067 | 0/0 | 12217 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0068 | 0/0 | 12226 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0069 | 0/0 | 12223 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0070 | 0/0 | 12222 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0071 | 0/0 | 12223 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0072 | 0/0 | 12224 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0073 | 0/0 | 12224 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0074 | 0/0 | 12222 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0075 | 0/0 | 12215 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0076 | 0/0 | 12221 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0077 | 0/0 | 12217 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0078 | 0/0 | 12216 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0079 | 0/0 | 12220 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0080 | 0/0 | 12219 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0081 | 0/0 | 12203 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0082 | 0/0 | 12230 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0083 | 0/0 | 12212 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0085 | 0/0 | 12212 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0086 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0087 | 0/0 | 12212 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0088 | 0/0 | 12212 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0089 | 1/0 | 12217 | 1 | 0 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0090 | 0/0 | 12212 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0091 | 0/0 | 12212 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0096 | 0/0 | 12214 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0097 | 0/0 | 12213 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0098 | 0/0 | 12226 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0099 | 0/0 | 12216 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0102 | 0/0 | 12213 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0103 | 0/0 | 12211 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0104 | 0/0 | 12213 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0105 | 0/0 | 12208 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0106 | 0/0 | 12208 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0107 | 0/0 | 12208 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0108 | 0/0 | 12208 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0109 | 0/0 | 12208 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0110 | 0/0 | 12208 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0112 | 0/0 | 12224 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0113 | 0/0 | 12223 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0001t0114 | 0/0 | 12235 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0002t0010 | 0/0 | 12218 | 7 | 0 | 2 | 4 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0002t0017 | 0/0 | 12226 | 5 | 1 | 2 | 1 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0002t0044 | 0/0 | 12218 | 2 | 0 | 0 | 2 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0002t0093 | 0/0 | 12229 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0002t0094 | 0/0 | 12228 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0002t0095 | 0/0 | 12226 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0002t0100 | 0/0 | 12226 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0002t0101 | 0/0 | 12208 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0003t0023 | 0/0 | 12209 | 3 | 0 | 0 | 3 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0003t0028 | 0/0 | 12234 | 2 | 0 | 0 | 2 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0003t0029 | 0/0 | 12222 | 2 | 0 | 0 | 2 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0003t0030 | 0/0 | 12209 | 2 | 0 | 0 | 2 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0003t0046 | 0/0 | 12238 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0003t0047 | 0/0 | 12237 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0003t0048 | 0/0 | 12235 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0003t0049 | 0/0 | 12234 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0003t0050 | 0/0 | 12230 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0003t0051 | 0/0 | 12228 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0003t0052 | 0/0 | 12213 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0003t0053 | 0/0 | 12217 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0003t0054 | 0/0 | 12213 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0004t0024 | 0/0 | 12228 | 3 | 3 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0004t0031 | 0/0 | 12227 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0004t0058 | 0/0 | 12225 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0004t0111 | 0/0 | 12204 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0007t0040 | 0/0 | 12217 | 2 | 2 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0008t0001 | 0/0 | 12211 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0008t0002 | 0/0 | 12212 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0001c0013t0011 | 0/0 | 12209 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0002c0005t0022 | 0/0 | 12206 | 4 | 2 | 2 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0003c0006t0001 | 0/0 | 12211 | 4 | 0 | 0 | 4 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0004c0009t0039 | 0/0 | 12211 | 2 | 0 | 2 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0005c0010t0006 | 0/0 | 12224 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0006c0011t0084 | 0/0 | 12211 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0007c0015t0092 | 0/0 | 12204 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0008c0012t0005 | 0/0 | 12208 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| a0009c0014t0002 | 0/0 | 12212 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | copy fasta | chr1 | 179094330 | 179234677 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0005g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0005g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0005g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0005g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0005g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0005g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0005g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0005g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0005g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0005g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0006g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0006g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0007g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0007g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0007g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0007g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0007g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0008g0282 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0008g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0008g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0008g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0008g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0008g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0008g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0008g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0008g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0008g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0008g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0009g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0009g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0009g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0009g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0009g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0009g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0009g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0009g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0009g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0009g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0011g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0011g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0011g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0011g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0011g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0011g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0012g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0012g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0012g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0012g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0012g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0013g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0013g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0013g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0013g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0013g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0014g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0014g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0014g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0014g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0014g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0015g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0015g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0015g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0015g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0015g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0016g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0016g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0016g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0016g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0016g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0018g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0018g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0018g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0018g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0019g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0019g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0019g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0019g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0020g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0020g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0020g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0020g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0021g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0021g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0021g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0021g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0025g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0025g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0025g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0026g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0026g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0026g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0027g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0027g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0027g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0032g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0032g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0033g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0033g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0034g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0034g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0035g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0035g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0036g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0036g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0037g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0037g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0038g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0038g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0041g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0041g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0042g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0042g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0043g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0043g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0045g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0045g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0055g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0056g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0057g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0059g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0060g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0061g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0062g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0063g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0064g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0065g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0066g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0067g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0068g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0069g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0070g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0071g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0072g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0073g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0074g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0075g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0076g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0077g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0078g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0079g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0080g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0081g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0082g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0083g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0085g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0086g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0087g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0088g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0089g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0090g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0091g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0096g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0097g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0098g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0099g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0102g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0103g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0104g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0105g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0106g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0107g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0108g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0109g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0110g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0112g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0113g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0001t0114g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0002t0010g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0002t0010g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0002t0010g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0002t0010g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0002t0010g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0002t0010g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0002t0010g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0002t0017g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0002t0017g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0002t0017g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0002t0017g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0002t0017g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0002t0044g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0002t0044g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0002t0093g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0002t0094g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0002t0095g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0002t0100g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0002t0101g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0003t0023g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0003t0023g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0003t0023g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0003t0028g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0003t0028g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0003t0029g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0003t0029g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0003t0030g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0003t0030g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0003t0046g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0003t0047g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0003t0048g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0003t0049g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0003t0050g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0003t0051g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0003t0052g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0003t0053g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0003t0054g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0004t0024g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0004t0024g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0004t0024g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0004t0031g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0004t0031g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0004t0058g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0004t0111g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0007t0040g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0007t0040g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0008t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0008t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0001c0013t0011g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0002c0005t0022g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0002c0005t0022g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0002c0005t0022g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0002c0005t0022g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0003c0006t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0003c0006t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0003c0006t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0003c0006t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0004c0009t0039g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0004c0009t0039g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0005c0010t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0006c0011t0084g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0007c0015t0092g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0008c0012t0005g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| a0009c0014t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | GBR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0050 | EUR | GBR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00140 | hp1 | a0001 | c0002 | t0010 | g0267 | EUR | GBR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0148 | EUR | GBR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0242 | EUR | FIN | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0073 | EUR | FIN | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00408 | hp1 | a0001 | c0001 | t0033 | g0070 | EAS | CHS | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0345 | EAS | CHS | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | CHS | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00544 | hp1 | a0008 | c0012 | t0005 | g0323 | EAS | CHS | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00544 | hp2 | a0001 | c0002 | t0010 | g0256 | EAS | CHS | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0334 | EAS | CHS | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0090 | EAS | CHS | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00597 | hp1 | a0001 | c0013 | t0011 | g0346 | EAS | CHS | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00597 | hp2 | a0001 | c0003 | t0030 | g0005 | EAS | CHS | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00621 | hp1 | a0001 | c0001 | t0061 | g0031 | EAS | CHS | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00639 | hp1 | a0001 | c0002 | t0017 | g0269 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00673 | hp1 | a0001 | c0001 | t0011 | g0341 | EAS | CHS | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00673 | hp2 | a0001 | c0001 | t0006 | g0075 | EAS | CHS | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00733 | hp2 | a0001 | c0002 | t0010 | g0266 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00735 | hp1 | a0001 | c0001 | t0104 | g0278 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00735 | hp2 | a0001 | c0001 | t0087 | g0239 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0088 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG00741 | hp2 | a0009 | c0014 | t0002 | g0227 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01069 | hp1 | a0001 | c0001 | t0021 | g0311 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01070 | hp1 | a0002 | c0005 | t0022 | g0253 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01070 | hp2 | a0001 | c0002 | t0010 | g0262 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01071 | hp1 | a0002 | c0005 | t0022 | g0275 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0046 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01081 | hp1 | a0001 | c0001 | t0009 | g0285 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01099 | hp1 | a0001 | c0001 | t0016 | g0223 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01106 | hp1 | a0001 | c0003 | t0051 | g0017 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01106 | hp2 | a0001 | c0001 | t0012 | g0039 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01109 | hp1 | a0001 | c0001 | t0020 | g0235 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01109 | hp2 | a0001 | c0001 | t0071 | g0101 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01167 | hp2 | a0001 | c0001 | t0009 | g0314 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01168 | hp1 | a0001 | c0001 | t0007 | g0124 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01168 | hp2 | a0004 | c0009 | t0039 | g0145 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01169 | hp1 | a0004 | c0009 | t0039 | g0147 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0049 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01175 | hp1 | a0001 | c0001 | t0056 | g0020 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01175 | hp2 | a0001 | c0002 | t0093 | g0274 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01243 | hp1 | a0001 | c0001 | t0075 | g0138 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01243 | hp2 | a0001 | c0001 | t0079 | g0212 | AMR | PUR | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | CLM | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01257 | hp1 | a0001 | c0001 | t0015 | g0129 | AMR | CLM | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01257 | hp2 | a0001 | c0001 | t0019 | g0067 | AMR | CLM | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0096 | AMR | CLM | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | CLM | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0110 | AMR | CLM | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01346 | hp2 | a0001 | c0001 | t0008 | g0295 | AMR | CLM | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0038 | AMR | CLM | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0298 | AMR | CLM | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01433 | hp1 | a0001 | c0002 | t0017 | g0273 | AMR | CLM | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01433 | hp2 | a0001 | c0003 | t0049 | g0014 | AMR | CLM | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01496 | hp1 | a0001 | c0003 | t0050 | g0007 | AMR | CLM | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | CLM | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01515 | hp1 | a0001 | c0001 | t0014 | g0079 | EUR | IBS | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01515 | hp2 | a0001 | c0002 | t0017 | g0272 | EUR | IBS | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01516 | hp1 | a0001 | c0001 | t0009 | g0286 | EUR | IBS | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0048 | EUR | IBS | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01884 | hp1 | a0001 | c0001 | t0041 | g0250 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01884 | hp2 | a0001 | c0001 | t0113 | g0349 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01891 | hp1 | a0001 | c0001 | t0077 | g0142 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01891 | hp2 | a0001 | c0001 | t0098 | g0308 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01928 | hp1 | a0001 | c0001 | t0015 | g0141 | AMR | PEL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01928 | hp2 | a0001 | c0001 | t0065 | g0037 | AMR | PEL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01934 | hp1 | a0001 | c0003 | t0048 | g0003 | AMR | PEL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0111 | AMR | PEL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0076 | AMR | PEL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PEL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01952 | hp2 | a0001 | c0003 | t0047 | g0013 | AMR | PEL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01975 | hp1 | a0001 | c0001 | t0007 | g0130 | AMR | PEL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0077 | AMR | PEL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01981 | hp1 | a0001 | c0001 | t0015 | g0127 | AMR | PEL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0074 | AMR | PEL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | PEL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02015 | hp1 | a0001 | c0002 | t0010 | g0254 | EAS | KHV | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02015 | hp2 | a0001 | c0001 | t0013 | g0065 | EAS | KHV | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | KHV | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02040 | hp2 | a0001 | c0001 | t0005 | g0319 | EAS | KHV | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02055 | hp1 | a0001 | c0001 | t0038 | g0216 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0288 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02071 | hp1 | a0001 | c0003 | t0029 | g0018 | EAS | KHV | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | KHV | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0328 | EAS | KHV | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02080 | hp2 | a0001 | c0001 | t0013 | g0108 | EAS | KHV | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02083 | hp2 | a0001 | c0001 | t0072 | g0121 | EAS | KHV | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02132 | hp1 | a0001 | c0001 | t0074 | g0123 | EAS | KHV | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02132 | hp2 | a0001 | c0003 | t0030 | g0006 | EAS | KHV | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02135 | hp1 | a0001 | c0001 | t0006 | g0114 | EAS | KHV | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02135 | hp2 | a0001 | c0002 | t0044 | g0271 | EAS | KHV | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02145 | hp1 | a0001 | c0008 | t0002 | g0157 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02145 | hp2 | a0001 | c0001 | t0016 | g0158 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02165 | hp1 | a0001 | c0001 | t0012 | g0103 | EAS | CDX | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02165 | hp2 | a0001 | c0003 | t0054 | g0004 | EAS | CDX | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0083 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0289 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02258 | hp2 | a0001 | c0001 | t0080 | g0217 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02451 | hp1 | a0001 | c0001 | t0020 | g0196 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02451 | hp2 | a0001 | c0001 | t0097 | g0304 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02523 | hp2 | a0001 | c0001 | t0066 | g0036 | EAS | KHV | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02572 | hp1 | a0001 | c0001 | t0042 | g0252 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02572 | hp2 | a0001 | c0001 | t0032 | g0027 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0104 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02602 | hp2 | a0001 | c0001 | t0090 | g0305 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02615 | hp2 | a0001 | c0004 | t0058 | g0028 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02622 | hp2 | a0001 | c0001 | t0016 | g0188 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02630 | hp1 | a0001 | c0001 | t0096 | g0306 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02630 | hp2 | a0001 | c0001 | t0011 | g0322 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02647 | hp1 | a0001 | c0001 | t0032 | g0026 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02647 | hp2 | a0001 | c0001 | t0034 | g0219 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0094 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0290 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02717 | hp2 | a0001 | c0001 | t0027 | g0226 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02723 | hp1 | a0001 | c0001 | t0021 | g0309 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02723 | hp2 | a0001 | c0001 | t0016 | g0222 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0243 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02738 | hp2 | a0001 | c0001 | t0008 | g0299 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02809 | hp1 | a0001 | c0001 | t0021 | g0307 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02886 | hp1 | a0001 | c0001 | t0034 | g0213 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02895 | hp2 | a0001 | c0007 | t0040 | g0302 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02897 | hp2 | a0001 | c0007 | t0040 | g0303 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02922 | hp1 | a0001 | c0001 | t0035 | g0220 | AFR | ESN | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02965 | hp1 | a0001 | c0004 | t0031 | g0022 | AFR | ESN | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0280 | AFR | ESN | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | ESN | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02970 | hp2 | a0001 | c0001 | t0027 | g0195 | AFR | ESN | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02976 | hp2 | a0001 | c0004 | t0031 | g0021 | AFR | ESN | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0325 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03017 | hp2 | a0001 | c0001 | t0043 | g0260 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03130 | hp1 | a0001 | c0001 | t0042 | g0249 | AFR | ESN | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0287 | AFR | ESN | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | ESN | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03209 | hp1 | a0001 | c0001 | t0020 | g0155 | AFR | MSL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03209 | hp2 | a0001 | c0001 | t0091 | g0312 | AFR | MSL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | MSL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03225 | hp2 | a0001 | c0001 | t0035 | g0225 | AFR | MSL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03239 | hp1 | a0001 | c0001 | t0014 | g0116 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03239 | hp2 | a0001 | c0001 | t0036 | g0229 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03453 | hp1 | a0001 | c0004 | t0111 | g0347 | AFR | MSL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03453 | hp2 | a0001 | c0004 | t0024 | g0025 | AFR | MSL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03486 | hp1 | a0001 | c0001 | t0041 | g0251 | AFR | MSL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03486 | hp2 | a0001 | c0001 | t0081 | g0218 | AFR | MSL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03490 | hp1 | a0001 | c0001 | t0110 | g0324 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03490 | hp2 | a0001 | c0001 | t0026 | g0041 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03491 | hp2 | a0001 | c0001 | t0043 | g0259 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03492 | hp2 | a0001 | c0001 | t0026 | g0044 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03516 | hp1 | a0001 | c0001 | t0021 | g0310 | AFR | ESN | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03516 | hp2 | a0001 | c0001 | t0037 | g0231 | AFR | ESN | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03540 | hp2 | a0001 | c0001 | t0078 | g0143 | AFR | GWD | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03579 | hp1 | a0001 | c0004 | t0024 | g0023 | AFR | MSL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03704 | hp1 | a0001 | c0001 | t0036 | g0207 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0342 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03710 | hp1 | a0001 | c0001 | t0068 | g0093 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0335 | SAS | PJL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0100 | SAS | BEB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03927 | hp1 | a0001 | c0001 | t0026 | g0120 | SAS | BEB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03927 | hp2 | a0001 | c0001 | t0083 | g0194 | SAS | BEB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0118 | SAS | BEB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | BEB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG04115 | hp1 | a0006 | c0011 | t0084 | g0156 | SAS | STU | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG04115 | hp2 | a0001 | c0001 | t0088 | g0236 | SAS | STU | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG04228 | hp1 | a0001 | c0001 | t0063 | g0117 | SAS | STU | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | STU | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18522 | hp1 | a0001 | c0008 | t0001 | g0165 | AFR | YRI | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18522 | hp2 | a0001 | c0001 | t0102 | g0296 | AFR | YRI | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18612 | hp1 | a0001 | c0001 | t0064 | g0053 | EAS | CHB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | CHB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18747 | hp1 | a0001 | c0001 | t0006 | g0084 | EAS | CHB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18747 | hp2 | a0001 | c0001 | t0109 | g0326 | EAS | CHB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18906 | hp1 | a0001 | c0001 | t0016 | g0189 | AFR | YRI | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18906 | hp2 | a0001 | c0001 | t0038 | g0221 | AFR | YRI | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18939 | hp2 | a0001 | c0001 | t0025 | g0032 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18940 | hp1 | a0001 | c0001 | t0015 | g0125 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18940 | hp2 | a0001 | c0001 | t0008 | g0297 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18942 | hp1 | a0001 | c0001 | t0018 | g0069 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18942 | hp2 | a0001 | c0002 | t0101 | g0263 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0317 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18943 | hp2 | a0001 | c0003 | t0046 | g0019 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18945 | hp1 | a0001 | c0001 | t0009 | g0281 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18946 | hp2 | a0001 | c0001 | t0006 | g0092 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18947 | hp2 | a0001 | c0001 | t0057 | g0029 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18948 | hp1 | a0001 | c0001 | t0005 | g0331 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18948 | hp2 | a0005 | c0010 | t0006 | g0055 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18950 | hp1 | a0001 | c0002 | t0100 | g0270 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18951 | hp1 | a0001 | c0002 | t0094 | g0255 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0318 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18952 | hp1 | a0003 | c0006 | t0001 | g0187 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18952 | hp2 | a0001 | c0001 | t0025 | g0060 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18954 | hp1 | a0001 | c0001 | t0107 | g0337 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18961 | hp1 | a0001 | c0001 | t0069 | g0056 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18961 | hp2 | a0001 | c0001 | t0005 | g0336 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18962 | hp2 | a0001 | c0001 | t0013 | g0061 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18963 | hp1 | a0001 | c0001 | t0007 | g0140 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18963 | hp2 | a0001 | c0001 | t0009 | g0279 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18964 | hp1 | a0001 | c0003 | t0023 | g0009 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18965 | hp1 | a0001 | c0001 | t0045 | g0339 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18967 | hp1 | a0001 | c0001 | t0011 | g0321 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18967 | hp2 | a0001 | c0001 | t0018 | g0064 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18969 | hp1 | a0001 | c0001 | t0019 | g0091 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18969 | hp2 | a0001 | c0001 | t0108 | g0340 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18970 | hp1 | a0001 | c0001 | t0007 | g0128 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18970 | hp2 | a0001 | c0001 | t0007 | g0136 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18971 | hp2 | a0001 | c0001 | t0007 | g0133 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18975 | hp2 | a0001 | c0002 | t0044 | g0264 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18979 | hp1 | a0001 | c0003 | t0029 | g0008 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18979 | hp2 | a0001 | c0001 | t0011 | g0344 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18980 | hp2 | a0001 | c0001 | t0037 | g0183 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18981 | hp1 | a0001 | c0001 | t0085 | g0234 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18981 | hp2 | a0001 | c0001 | t0014 | g0087 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18985 | hp1 | a0001 | c0001 | t0012 | g0051 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18985 | hp2 | a0003 | c0006 | t0001 | g0209 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18986 | hp1 | a0001 | c0001 | t0076 | g0135 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18986 | hp2 | a0001 | c0001 | t0062 | g0068 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18990 | hp2 | a0001 | c0001 | t0018 | g0112 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18991 | hp1 | a0001 | c0003 | t0028 | g0016 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18991 | hp2 | a0001 | c0001 | t0014 | g0115 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18992 | hp1 | a0001 | c0001 | t0067 | g0102 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18993 | hp1 | a0003 | c0006 | t0001 | g0151 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18993 | hp2 | a0001 | c0001 | t0060 | g0042 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18995 | hp1 | a0001 | c0001 | t0006 | g0081 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18995 | hp2 | a0001 | c0001 | t0005 | g0320 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18998 | hp1 | a0001 | c0001 | t0086 | g0192 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA18998 | hp2 | a0001 | c0003 | t0023 | g0010 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19000 | hp1 | a0001 | c0002 | t0010 | g0261 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19000 | hp2 | a0001 | c0001 | t0033 | g0062 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0066 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19002 | hp2 | a0001 | c0001 | t0007 | g0137 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19004 | hp1 | a0001 | c0002 | t0017 | g0257 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19004 | hp2 | a0001 | c0001 | t0013 | g0105 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19007 | hp2 | a0001 | c0001 | t0008 | g0283 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19009 | hp1 | a0001 | c0001 | t0045 | g0338 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19009 | hp2 | a0001 | c0001 | t0012 | g0113 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19012 | hp1 | a0001 | c0001 | t0009 | g0300 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19012 | hp2 | a0001 | c0001 | t0007 | g0139 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19043 | hp1 | a0001 | c0002 | t0095 | g0265 | AFR | LWK | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19043 | hp2 | a0007 | c0015 | t0092 | g0313 | AFR | LWK | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19054 | hp1 | a0001 | c0001 | t0005 | g0332 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19054 | hp2 | a0001 | c0001 | t0070 | g0078 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19056 | hp1 | a0001 | c0001 | t0009 | g0284 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19058 | hp1 | a0001 | c0001 | t0007 | g0126 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19058 | hp2 | a0001 | c0001 | t0018 | g0080 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19062 | hp1 | a0001 | c0001 | t0082 | g0210 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19062 | hp2 | a0001 | c0001 | t0014 | g0034 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19064 | hp1 | a0001 | c0001 | t0005 | g0315 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19064 | hp2 | a0001 | c0002 | t0010 | g0258 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19065 | hp1 | a0001 | c0001 | t0007 | g0131 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19065 | hp2 | a0001 | c0003 | t0028 | g0001 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19066 | hp2 | a0001 | c0001 | t0019 | g0098 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19068 | hp1 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19074 | hp1 | a0003 | c0006 | t0001 | g0205 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19074 | hp2 | a0001 | c0001 | t0114 | g0350 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19077 | hp2 | a0001 | c0001 | t0106 | g0329 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19079 | hp2 | a0001 | c0003 | t0052 | g0015 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19082 | hp2 | a0001 | c0001 | t0019 | g0119 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19083 | hp1 | a0001 | c0001 | t0105 | g0333 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19085 | hp1 | a0001 | c0001 | t0005 | g0316 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19085 | hp2 | a0001 | c0001 | t0013 | g0107 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19086 | hp1 | a0001 | c0001 | t0012 | g0063 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19086 | hp2 | a0001 | c0003 | t0023 | g0011 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19087 | hp2 | a0001 | c0001 | t0025 | g0043 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19088 | hp2 | a0001 | c0001 | t0011 | g0330 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19089 | hp1 | a0001 | c0001 | t0055 | g0012 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19089 | hp2 | a0001 | c0001 | t0007 | g0134 | EAS | JPT | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0291 | AFR | YRI | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA19240 | hp2 | a0001 | c0001 | t0020 | g0197 | AFR | YRI | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA20129 | hp1 | a0001 | c0001 | t0009 | g0292 | AFR | ASW | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA20129 | hp2 | a0001 | c0001 | t0073 | g0122 | AFR | ASW | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0327 | EUR | TSI | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA20805 | hp2 | a0001 | c0003 | t0053 | g0002 | EUR | TSI | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA20905 | hp1 | a0001 | c0001 | t0011 | g0343 | SAS | GIH | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | GIH | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02109 | hp1 | a0001 | c0001 | t0099 | g0301 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02109 | hp2 | a0002 | c0005 | t0022 | g0277 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02486 | hp1 | a0001 | c0001 | t0112 | g0348 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02486 | hp2 | a0001 | c0001 | t0027 | g0224 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02559 | hp1 | a0002 | c0005 | t0022 | g0276 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG02559 | hp2 | a0001 | c0001 | t0103 | g0293 | AFR | ACB | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03471 | hp1 | a0001 | c0001 | t0009 | g0294 | AFR | MSL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG06807 | hp1 | a0001 | c0002 | t0017 | g0268 | AFR | USA | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | USA | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | USA | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA20300 | hp2 | a0001 | c0001 | t0015 | g0132 | AFR | USA | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA21309 | hp1 | a0001 | c0004 | t0024 | g0024 | AFR | LWK | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| NA21309 | hp2 | a0001 | c0001 | t0059 | g0030 | AFR | LWK | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0008 | g0282 | REF | REF | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0089 | g0164 | REF | REF | ABL2_chr1_179094330_179234677 | ABL2 | chr1 | 179094330 | 179234677 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:179107777
|
G | C | 1 | a0008 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.3490C>G | p.Pro1164Ala | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 3770/12217 | 3490/3549 | 1164/1182 | chr1 | 179107777 | ||
| chr1:179107974
|
C | T | 1 | a0002 | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
missense_variant | MODERATE | c.3293G>A | p.Ser1098Asn | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 3573/12217 | 3293/3549 | 1098/1182 | chr1 | 179107974 | ||
| chr1:179108280
|
G | C | 1 | a0003 | 4 | NA18952.hp1 NA18985.hp2 NA18993.hp1 others(1): Show |
missense_variant | MODERATE | c.2987C>G | p.Pro996Arg | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 3267/12217 | 2987/3549 | 996/1182 | chr1 | 179108280 | ||
| chr1:179108431
|
C | T | 1 | a0007 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.2836G>A | p.Val946Met | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 3116/12217 | 2836/3549 | 946/1182 | chr1 | 179108431 | ||
| chr1:179108478
|
T | C | 1 | a0009 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.2789A>G | p.Lys930Arg | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 3069/12217 | 2789/3549 | 930/1182 | chr1 | 179108478 | ||
| chr1:179109210
|
G | A | 1 | a0004 | 2 | HG01168.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.2057C>T | p.Thr686Met | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 2337/12217 | 2057/3549 | 686/1182 | chr1 | 179109210 | ||
| chr1:179109393
|
C | T | 1 | a0006 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.1874G>A | p.Arg625Gln | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 2154/12217 | 1874/3549 | 625/1182 | chr1 | 179109393 | ||
| chr1:179131469
|
C | T | 1 | a0005 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.233G>A | p.Arg78His | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/12 | 513/12217 | 233/3549 | 78/1182 | chr1 | 179131469 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:179107976
|
G | A | 1 | a0001c0013 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.3291C>T | p.Ser1097Ser | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 3571/12217 | 3291/3549 | 1097/1182 | chr1 | 179107976 | ||
| chr1:179108423
|
G | A | 1 | a0001c0008 | 2 | HG02145.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.2844C>T | p.Leu948Leu | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 3124/12217 | 2844/3549 | 948/1182 | chr1 | 179108423 | ||
| chr1:179109209
|
C | A | 1 | a0007c0015 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.2058G>T | p.Thr686Thr | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 2338/12217 | 2058/3549 | 686/1182 | chr1 | 179109209 | ||
| chr1:179114945
|
T | G | 1 | a0001c0002 | 19 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(16): Show |
synonymous_variant | LOW | c.1494A>C | p.Leu498Leu | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/12 | 1774/12217 | 1494/3549 | 498/1182 | chr1 | 179114945 | ||
| chr1:179121600
|
A | G | 1 | a0001c0007 | 2 | HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.955T>C | p.Leu319Leu | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/12 | 1235/12217 | 955/3549 | 319/1182 | chr1 | 179121600 | ||
| chr1:179121616
|
T | C | 1 | a0001c0004 | 7 | HG02615.hp2 HG02965.hp1 HG02976.hp2 others(4): Show |
synonymous_variant | LOW | c.939A>G | p.Thr313Thr | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/12 | 1219/12217 | 939/3549 | 313/1182 | chr1 | 179121616 | ||
| chr1:179126413
|
C | T | 1 | a0001c0003 | 18 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(15): Show |
synonymous_variant | LOW | c.651G>A | p.Val217Val | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/12 | 931/12217 | 651/3549 | 217/1182 | chr1 | 179126413 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:179099334
|
C | A | 1 | a0001c0002t0095 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8384G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 8384 | chr1 | 179099334 | |||||
| chr1:179099384
|
C | T | 1 | a0001c0001t0107 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8334G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 8334 | chr1 | 179099384 | |||||
| chr1:179099716
|
A | G | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(35): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*8002T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 8002 | chr1 | 179099716 | |||||
| chr1:179099727
|
C | T | 1 | a0007c0015t0092 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7991G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 7991 | chr1 | 179099727 | |||||
| chr1:179100071
|
G | C | 13 | a0001c0003t0023a0001c0003t0028a0001c0003t0029others(10): Show | 18 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*7647C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 7647 | chr1 | 179100071 | |||||
| chr1:179100294
|
C | T | 79 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(76): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*7424G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 7424 | chr1 | 179100294 | |||||
| chr1:179100430
|
A | G | 2 | a0001c0001t0096a0001c0001t0097 | 2 | HG02451.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7288T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 7288 | chr1 | 179100430 | |||||
| chr1:179100592
|
C | T | 2 | a0001c0001t0020a0001c0001t0038 | 6 | HG01109.hp1 HG02055.hp1 HG02451.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7126G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 7126 | chr1 | 179100592 | |||||
| chr1:179100970
|
G | A | 1 | a0001c0001t0106 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6748C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 6748 | chr1 | 179100970 | |||||
| chr1:179100979
|
A | AGACCTTG others(6): Show |
1 | a0001c0001t0082 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6738_*6739insACCT others(9): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 6738 | chr1 | 179100979 | |||||
| chr1:179100985
|
C | T | 52 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(49): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*6733G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 6733 | chr1 | 179100985 | |||||
| chr1:179101052
|
G | A | 3 | a0001c0001t0016a0001c0001t0027a0001c0001t0035 | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6666C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 6666 | chr1 | 179101052 | |||||
| chr1:179101199
|
C | G | 52 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(49): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*6519G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 6519 | chr1 | 179101199 | |||||
| chr1:179101371
|
G | A | 3 | a0001c0001t0045a0001c0001t0107a0001c0001t0108 | 4 | NA18954.hp1 NA18965.hp1 NA18969.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6347C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 6347 | chr1 | 179101371 | |||||
| chr1:179101377
|
C | CT | 80 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(77): Show | 238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*6340dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 6340 | chr1 | 179101377 | |||||
| chr1:179101377
|
CT | C | 4 | a0001c0001t0041a0001c0001t0042a0001c0001t0066others(1): Show | 6 | HG01884.hp1 HG02109.hp1 HG02523.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6340delA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 6340 | chr1 | 179101377 | |||||
| chr1:179101462
|
C | T | 1 | a0001c0001t0090 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6256G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 6256 | chr1 | 179101462 | |||||
| chr1:179101643
|
T | C | 1 | a0002c0005t0022 | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6075A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 6075 | chr1 | 179101643 | |||||
| chr1:179101780
|
G | C | 1 | a0002c0005t0022 | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5938C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5938 | chr1 | 179101780 | |||||
| chr1:179101802
|
G | C | 12 | a0001c0003t0023a0001c0003t0028a0001c0003t0029others(9): Show | 17 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5916C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5916 | chr1 | 179101802 | |||||
| chr1:179101816
|
A | G | 1 | a0001c0001t0083 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5902T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5902 | chr1 | 179101816 | |||||
| chr1:179101902
|
A | G | 8 | a0001c0002t0010a0001c0002t0017a0001c0002t0044others(5): Show | 19 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*5816T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5816 | chr1 | 179101902 | |||||
| chr1:179101965
|
G | GA | 2 | a0001c0001t0085a0002c0005t0022 | 5 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5752dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5752 | chr1 | 179101965 | |||||
| chr1:179101996
|
C | CT | 8 | a0001c0001t0006a0001c0001t0033a0001c0001t0061others(5): Show | 19 | HG00408.hp1 HG00621.hp1 HG00673.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*5721dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5721 | chr1 | 179101996 | |||||
| chr1:179101996
|
C | CTT | 4 | a0001c0001t0014a0001c0001t0057a0001c0001t0060others(1): Show | 8 | HG01243.hp2 HG01515.hp1 HG03239.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5720_*5721dupAA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5721 | chr1 | 179101996 | |||||
| chr1:179101996
|
C | CTTTT | 3 | a0001c0001t0019a0001c0003t0052a0001c0003t0054 | 6 | HG01257.hp2 HG02165.hp2 NA18969.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5718_*5721dupAAAA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5721 | chr1 | 179101996 | |||||
| chr1:179101996
|
C | CTTTTTTT others(1): Show |
5 | a0001c0001t0098a0001c0002t0017a0001c0002t0095others(2): Show | 9 | HG00639.hp1 HG01433.hp1 HG01515.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5714_*5721dupAAAA others(4): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5721 | chr1 | 179101996 | |||||
| chr1:179101996
|
C | CTTTTTTT others(3): Show |
1 | a0001c0002t0094 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5712_*5721dupAAAA others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5721 | chr1 | 179101996 | |||||
| chr1:179101996
|
C | CTTTTTTT others(4): Show |
1 | a0001c0002t0093 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5711_*5721dupAAAA others(7): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5721 | chr1 | 179101996 | |||||
| chr1:179101996
|
C | CTTTTTTT others(6): Show |
1 | a0001c0003t0029 | 2 | HG02071.hp1 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5709_*5721dupAAAA others(9): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5721 | chr1 | 179101996 | |||||
| chr1:179101996
|
C | CTTTTTTT others(12): Show |
1 | a0001c0003t0051 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5703_*5721dupAAAA others(15): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5721 | chr1 | 179101996 | |||||
| chr1:179101996
|
C | CTTTTTTT others(14): Show |
1 | a0001c0003t0050 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5701_*5721dupAAAA others(17): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5721 | chr1 | 179101996 | |||||
| chr1:179101996
|
C | CTTTTTTT others(18): Show |
2 | a0001c0003t0028a0001c0003t0049 | 3 | HG01433.hp2 NA18991.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5697_*5721dupAAAA others(21): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5721 | chr1 | 179101996 | |||||
| chr1:179101996
|
C | CTTTTTTT others(19): Show |
1 | a0001c0003t0048 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5696_*5721dupAAAA others(22): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5721 | chr1 | 179101996 | |||||
| chr1:179101996
|
C | CTTTTTTT others(21): Show |
1 | a0001c0003t0047 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5694_*5721dupAAAA others(24): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5721 | chr1 | 179101996 | |||||
| chr1:179101996
|
C | CTTTTTTT others(22): Show |
1 | a0001c0003t0046 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5693_*5721dupAAAA others(25): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5721 | chr1 | 179101996 | |||||
| chr1:179101996
|
CT | C | 9 | a0001c0001t0004a0001c0001t0013a0001c0001t0026others(6): Show | 32 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*5721delA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5721 | chr1 | 179101996 | |||||
| chr1:179101996
|
CTTTT | C | 4 | a0001c0001t0027a0001c0001t0042a0001c0001t0077others(1): Show | 7 | HG01891.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5718_*5721delAAAA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5718 | chr1 | 179101996 | |||||
| chr1:179101996
|
CTTTTT | C | 6 | a0001c0001t0035a0001c0001t0037a0001c0001t0078others(3): Show | 8 | HG00735.hp1 HG02451.hp2 HG02922.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5717_*5721delAAAA others(1): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5717 | chr1 | 179101996 | |||||
| chr1:179101996
|
CTTTTTT | C | 22 | a0001c0001t0002a0001c0001t0008a0001c0001t0011others(19): Show | 67 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*5716_*5721delAAAA others(2): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5716 | chr1 | 179101996 | |||||
| chr1:179101996
|
CTTTTTTT | C | 19 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(16): Show | 98 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*5715_*5721delAAAA others(3): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5715 | chr1 | 179101996 | |||||
| chr1:179101996
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0101 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5712_*5721delAAAA others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5712 | chr1 | 179101996 | |||||
| chr1:179101996
|
CTTTTTTT others(4): Show |
C | 4 | a0001c0004t0024a0001c0004t0031a0001c0004t0058others(1): Show | 7 | HG02615.hp2 HG02965.hp1 HG02976.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5711_*5721delAAAA others(7): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5711 | chr1 | 179101996 | |||||
| chr1:179101996
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0025 | 3 | NA18939.hp2 NA18952.hp2 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5710_*5721delAAAA others(8): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5710 | chr1 | 179101996 | |||||
| chr1:179101996
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0065a0002c0005t0022 | 5 | HG01070.hp1 HG01071.hp1 HG01928.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5709_*5721delAAAA others(9): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5709 | chr1 | 179101996 | |||||
| chr1:179101996
|
CTTTTTTT others(7): Show |
C | 1 | a0007c0015t0092 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5708_*5721delAAAA others(10): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5708 | chr1 | 179101996 | |||||
| chr1:179101996
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0081 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5707_*5721delAAAA others(11): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5707 | chr1 | 179101996 | |||||
| chr1:179101996
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0034 | 2 | HG02647.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5706_*5721delAAAA others(12): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5706 | chr1 | 179101996 | |||||
| chr1:179102037
|
G | A | 1 | a0001c0007t0040 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5681C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5681 | chr1 | 179102037 | |||||
| chr1:179102254
|
A | G | 4 | a0001c0001t0012a0001c0001t0013a0001c0001t0033others(1): Show | 13 | HG00408.hp1 HG01106.hp2 HG01928.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5464T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5464 | chr1 | 179102254 | |||||
| chr1:179102301
|
G | A | 1 | a0001c0001t0087 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5417C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5417 | chr1 | 179102301 | |||||
| chr1:179102458
|
G | GCTA | 2 | a0001c0001t0026a0001c0001t0068 | 4 | HG03490.hp2 HG03492.hp2 HG03710.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5257_*5259dupTAG | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5259 | chr1 | 179102458 | |||||
| chr1:179102595
|
G | A | 2 | a0001c0001t0069a0001c0001t0070 | 2 | NA18961.hp1 NA19054.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5123C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5123 | chr1 | 179102595 | |||||
| chr1:179102621
|
G | A | 50 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(47): Show | 183 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*5097C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5097 | chr1 | 179102621 | |||||
| chr1:179102714
|
A | T | 1 | a0001c0001t0091 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5004T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 5004 | chr1 | 179102714 | |||||
| chr1:179102730
|
G | A | 52 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(49): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*4988C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 4988 | chr1 | 179102730 | |||||
| chr1:179102783
|
G | T | 90 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(87): Show | 252 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*4935C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 4935 | chr1 | 179102783 | |||||
| chr1:179102986
|
A | T | 1 | a0001c0001t0064 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4732T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 4732 | chr1 | 179102986 | |||||
| chr1:179103123
|
G | A | 1 | a0001c0001t0032 | 2 | HG02572.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4595C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 4595 | chr1 | 179103123 | |||||
| chr1:179103345
|
T | A | 1 | a0001c0001t0109 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4373A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 4373 | chr1 | 179103345 | |||||
| chr1:179103593
|
T | C | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(35): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*4125A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 4125 | chr1 | 179103593 | |||||
| chr1:179103831
|
C | T | 49 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(46): Show | 181 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*3887G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 3887 | chr1 | 179103831 | |||||
| chr1:179103904
|
C | G | 90 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(87): Show | 252 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*3814G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 3814 | chr1 | 179103904 | |||||
| chr1:179103940
|
C | T | 2 | a0001c0001t0077a0001c0001t0078 | 2 | HG01891.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3778G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 3778 | chr1 | 179103940 | |||||
| chr1:179104505
|
T | C | 2 | a0001c0001t0077a0001c0001t0078 | 2 | HG01891.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3213A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 3213 | chr1 | 179104505 | |||||
| chr1:179104507
|
T | A | 2 | a0001c0001t0077a0001c0001t0078 | 2 | HG01891.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3211A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 3211 | chr1 | 179104507 | |||||
| chr1:179104664
|
T | C | 1 | a0001c0001t0110 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3054A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 3054 | chr1 | 179104664 | |||||
| chr1:179105124
|
A | G | 1 | a0001c0001t0105 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2594T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 2594 | chr1 | 179105124 | |||||
| chr1:179105125
|
T | C | 2 | a0001c0001t0021a0001c0001t0098 | 5 | HG01069.hp1 HG01891.hp2 HG02723.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2593A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 2593 | chr1 | 179105125 | |||||
| chr1:179105139
|
C | T | 1 | a0001c0007t0040 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2579G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 2579 | chr1 | 179105139 | |||||
| chr1:179105464
|
A | C | 8 | a0001c0003t0023a0001c0003t0046a0001c0003t0047others(5): Show | 10 | HG01106.hp1 HG01433.hp2 HG01496.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2254T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 2254 | chr1 | 179105464 | |||||
| chr1:179105636
|
C | T | 2 | a0001c0001t0077a0001c0001t0078 | 2 | HG01891.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2082G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 2082 | chr1 | 179105636 | |||||
| chr1:179105662
|
G | T | 4 | a0001c0001t0034a0001c0001t0079a0001c0001t0080others(1): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2056C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 2056 | chr1 | 179105662 | |||||
| chr1:179105734
|
T | G | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(35): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*1984A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 1984 | chr1 | 179105734 | |||||
| chr1:179105805
|
T | A | 1 | a0001c0001t0088 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1913A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 1913 | chr1 | 179105805 | |||||
| chr1:179105812
|
G | C | 1 | a0001c0001t0088 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1906C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 1906 | chr1 | 179105812 | |||||
| chr1:179105977
|
T | C | 1 | a0001c0001t0099 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1741A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 1741 | chr1 | 179105977 | |||||
| chr1:179106239
|
C | T | 1 | a0001c0001t0075 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1479G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 1479 | chr1 | 179106239 | |||||
| chr1:179106415
|
T | C | 1 | a0002c0005t0022 | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1303A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 1303 | chr1 | 179106415 | |||||
| chr1:179106489
|
G | C | 3 | a0001c0002t0044a0001c0002t0100a0001c0002t0101 | 4 | HG02135.hp2 NA18942.hp2 NA18950.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1229C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 1229 | chr1 | 179106489 | |||||
| chr1:179106620
|
A | G | 113 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(110): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*1098T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 1098 | chr1 | 179106620 | |||||
| chr1:179107313
|
A | T | 1 | a0001c0001t0063 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*405T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 405 | chr1 | 179107313 | |||||
| chr1:179107371
|
G | A | 1 | a0001c0001t0078 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*347C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 347 | chr1 | 179107371 | |||||
| chr1:179107401
|
A | G | 1 | a0001c0001t0090 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*317T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 317 | chr1 | 179107401 | |||||
| chr1:179107537
|
G | A | 2 | a0001c0001t0056a0001c0001t0104 | 2 | HG00735.hp1 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*181C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 181 | chr1 | 179107537 | |||||
| chr1:179107545
|
C | T | 1 | a0001c0007t0040 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*173G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 173 | chr1 | 179107545 | |||||
| chr1:179107686
|
A | G | 5 | a0001c0001t0018a0001c0001t0057a0001c0001t0060others(2): Show | 8 | HG00621.hp1 NA18942.hp1 NA18947.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*32T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 12/12 | 32 | chr1 | 179107686 | |||||
| chr1:179229458
|
G | C | 1 | a0001c0001t0072 | 1 | HG02083.hp2 | 5_prime_UTR_variant | MODIFIER | c.-61C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/12 | 61 | chr1 | 179229458 | |||||
| chr1:179229518
|
T | C | 77 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(74): Show | 192 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(189): Show |
5_prime_UTR_variant | MODIFIER | c.-121A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/12 | 121 | chr1 | 179229518 | |||||
| chr1:179229540
|
G | A | 1 | a0001c0001t0073 | 1 | NA20129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-143C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/12 | 143 | chr1 | 179229540 | |||||
| chr1:179229572
|
G | A | 1 | a0001c0001t0074 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-175C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/12 | 175 | chr1 | 179229572 | |||||
| chr1:179229632
|
A | ACGC | 6 | a0001c0001t0007a0001c0001t0015a0001c0001t0075others(3): Show | 20 | HG01168.hp1 HG01243.hp1 HG01257.hp1 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-238_-236dupGCG | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/12 | 236 | chr1 | 179229632 | |||||
| chr1:179229632
|
A | ACGCCGC | 28 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(25): Show | 94 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
5_prime_UTR_variant | MODIFIER | c.-241_-236dupGCGGCG | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/12 | 236 | chr1 | 179229632 | |||||
| chr1:179229632
|
A | ACGCCGCC others(11): Show |
3 | a0001c0001t0032a0001c0001t0057a0001c0004t0058 | 4 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-253_-236dupGCGGCG others(12): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/12 | 236 | chr1 | 179229632 | |||||
| chr1:179229632
|
A | ACGCCGCC others(14): Show |
2 | a0001c0004t0024a0001c0004t0031 | 5 | HG02965.hp1 HG02976.hp2 HG03453.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-256_-236dupGCGGCG others(15): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/12 | 236 | chr1 | 179229632 | |||||
| chr1:179229632
|
ACGC | A | 12 | a0001c0001t0005a0001c0001t0011a0001c0001t0045others(9): Show | 33 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(30): Show |
5_prime_UTR_variant | MODIFIER | c.-238_-236delGCG | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/12 | 236 | chr1 | 179229632 | |||||
| chr1:179229640
|
G | GCCGCCGC others(5): Show |
2 | a0001c0001t0112a0001c0001t0113 | 2 | HG01884.hp2 HG02486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-244_-243insTGGCGG others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/12 | 244 | chr1 | 179229640 | |||||
| chr1:179229643
|
G | GCCGCCGC others(11): Show |
1 | a0001c0001t0114 | 1 | NA19074.hp2 | 5_prime_UTR_variant | MODIFIER | c.-247_-246insTGGCGG others(12): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/12 | 247 | chr1 | 179229643 | |||||
| chr1:179229646
|
GCCGCCGC others(2): Show |
G | 14 | a0001c0001t0055a0001c0003t0023a0001c0003t0028others(11): Show | 19 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-258_-250delTGGCGG others(3): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/12 | 250 | chr1 | 179229646 | |||||
| chr1:179229652
|
G | GCCGCCGC others(5): Show |
1 | a0001c0001t0056 | 1 | HG01175.hp1 | 5_prime_UTR_variant | MODIFIER | c.-256_-255insTGGCGG others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/12 | 256 | chr1 | 179229652 | |||||
| chr1:179229655
|
A | G | 1 | a0001c0001t0056 | 1 | HG01175.hp1 | 5_prime_UTR_variant | MODIFIER | c.-258T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/12 | 258 | chr1 | 179229655 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:179109456
|
C | T | 7 | a0001c0004t0024g0023a0001c0004t0024g0024a0001c0004t0024g0025others(4): Show | 7 | HG02615.hp2 HG02965.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1826-15G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 11/11 | chr1 | 179109456 | ||||||
| chr1:179109506
|
C | T | 2 | a0001c0001t0077g0142a0001c0001t0078g0143 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1826-65G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 11/11 | chr1 | 179109506 | ||||||
| chr1:179109552
|
T | C | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1826-111A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 11/11 | chr1 | 179109552 | ||||||
| chr1:179109621
|
T | C | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1826-180A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 11/11 | chr1 | 179109621 | ||||||
| chr1:179109797
|
G | A | 1 | a0007c0015t0092g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1826-356C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 11/11 | chr1 | 179109797 | ||||||
| chr1:179109798
|
G | A | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1826-357C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 11/11 | chr1 | 179109798 | ||||||
| chr1:179109927
|
CA | C | 219 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(216): Show | 219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1825+354delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 11/11 | chr1 | 179109927 | ||||||
| chr1:179110055
|
T | C | 250 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(247): Show | 250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.1825+227A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 11/11 | chr1 | 179110055 | ||||||
| chr1:179110221
|
C | G | 1 | a0001c0001t0015g0141 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1825+61G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 11/11 | chr1 | 179110221 | ||||||
| chr1:179110262
|
A | G | 2 | a0001c0001t0077g0142a0001c0001t0078g0143 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1825+20T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 11/11 | chr1 | 179110262 | ||||||
| chr1:179110499
|
G | C | 1 | a0001c0003t0050g0007 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1652-44C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179110499 | ||||||
| chr1:179110515
|
C | A | 3 | a0001c0001t0001g0237a0001c0001t0036g0207a0001c0001t0088g0236 | 3 | HG03704.hp1 HG03831.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1652-60G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179110515 | ||||||
| chr1:179110645
|
C | T | 2 | a0001c0001t0077g0142a0001c0001t0078g0143 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1652-190G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179110645 | ||||||
| chr1:179110646
|
G | A | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1652-191C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179110646 | ||||||
| chr1:179110652
|
G | C | 1 | a0001c0004t0031g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1652-197C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179110652 | ||||||
| chr1:179110744
|
T | C | 3 | a0001c0001t0019g0091a0001c0001t0019g0098a0001c0001t0019g0119 | 3 | NA18969.hp1 NA19066.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1652-289A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179110744 | ||||||
| chr1:179110820
|
C | T | 3 | a0001c0001t0018g0069a0001c0001t0018g0080a0001c0001t0057g0029 | 3 | NA18942.hp1 NA18947.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1652-365G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179110820 | ||||||
| chr1:179110866
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1652-411G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179110866 | ||||||
| chr1:179110980
|
C | CT | 9 | a0001c0001t0004g0085a0001c0001t0004g0100a0001c0001t0006g0081others(6): Show | 9 | HG00544.hp2 HG01928.hp2 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.1652-526dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179110980 | ||||||
| chr1:179110980
|
C | T | 1 | a0001c0001t0018g0080 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1652-525G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179110980 | ||||||
| chr1:179110980
|
CT | C | 47 | a0001c0001t0001g0247a0001c0001t0002g0184a0001c0001t0002g0243others(44): Show | 47 | HG00597.hp2 HG00621.hp2 HG01106.hp1 others(44): Show |
intron_variant | MODIFIER | c.1652-526delA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179110980 | ||||||
| chr1:179110980
|
CTT | C | 160 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(157): Show | 160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1652-527_1652-526d others(4): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179110980 | ||||||
| chr1:179110980
|
CTTT | C | 10 | a0001c0001t0002g0245a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02486.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1652-528_1652-526d others(5): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179110980 | ||||||
| chr1:179111086
|
C | T | 30 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(27): Show | 30 | HG00735.hp1 HG01081.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.1652-631G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179111086 | ||||||
| chr1:179111097
|
T | C | 1 | a0001c0004t0024g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1652-642A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179111097 | ||||||
| chr1:179111220
|
G | T | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.1652-765C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179111220 | ||||||
| chr1:179111281
|
C | CT | 124 | a0001c0001t0002g0243a0001c0001t0003g0054a0001c0001t0003g0058others(121): Show | 124 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1652-827dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179111281 | ||||||
| chr1:179111281
|
C | CTT | 47 | a0001c0001t0003g0052a0001c0001t0004g0073a0001c0001t0004g0088others(44): Show | 47 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.1652-828_1652-827d others(4): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179111281 | ||||||
| chr1:179111281
|
C | CTTT | 6 | a0001c0001t0008g0299a0001c0001t0034g0213a0001c0001t0034g0219others(3): Show | 6 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1652-829_1652-827d others(5): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179111281 | ||||||
| chr1:179111284
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1652-829A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179111284 | ||||||
| chr1:179111308
|
G | A | 5 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(2): Show | 5 | HG01069.hp1 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1652-853C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179111308 | ||||||
| chr1:179111379
|
G | A | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.1652-924C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179111379 | ||||||
| chr1:179111605
|
C | G | 1 | a0001c0001t0011g0343 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1651+704G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179111605 | ||||||
| chr1:179111879
|
A | C | 1 | a0001c0001t0011g0330 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1651+430T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179111879 | ||||||
| chr1:179111912
|
G | A | 8 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0001g0178others(5): Show | 8 | HG00438.hp2 NA18945.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.1651+397C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179111912 | ||||||
| chr1:179111950
|
C | A | 25 | a0001c0003t0023g0009a0001c0003t0023g0010a0001c0003t0023g0011others(22): Show | 25 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1651+359G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179111950 | ||||||
| chr1:179112126
|
TAA | T | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1651+181_1651+182d others(4): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179112126 | ||||||
| chr1:179112173
|
T | C | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1651+136A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 10/11 | chr1 | 179112173 | ||||||
| chr1:179112756
|
A | AT | 12 | a0001c0001t0001g0169a0001c0001t0001g0190a0001c0001t0001g0199others(9): Show | 12 | HG00741.hp1 HG02055.hp1 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.1562-359dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179112756 | ||||||
| chr1:179112778
|
G | A | 1 | a0001c0003t0054g0004 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1562-380C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179112778 | ||||||
| chr1:179112814
|
G | A | 1 | a0001c0001t0007g0128 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1562-416C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179112814 | ||||||
| chr1:179112823
|
C | T | 147 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(144): Show | 147 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1562-425G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179112823 | ||||||
| chr1:179113059
|
G | A | 1 | a0001c0001t0083g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1562-661C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179113059 | ||||||
| chr1:179113116
|
A | G | 5 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(2): Show | 5 | HG01069.hp1 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1562-718T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179113116 | ||||||
| chr1:179113123
|
A | G | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1562-725T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179113123 | ||||||
| chr1:179113242
|
C | T | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1562-844G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179113242 | ||||||
| chr1:179113260
|
T | C | 2 | a0001c0001t0002g0248a0001c0001t0085g0234 | 2 | NA18949.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1562-862A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179113260 | ||||||
| chr1:179113390
|
C | T | 194 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(191): Show | 194 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1562-992G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179113390 | ||||||
| chr1:179113484
|
A | G | 1 | a0001c0008t0001g0165 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1562-1086T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179113484 | ||||||
| chr1:179113591
|
G | A | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1562-1193C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179113591 | ||||||
| chr1:179113625
|
C | T | 7 | a0001c0001t0008g0282a0001c0001t0008g0298a0001c0001t0008g0299others(4): Show | 7 | HG01081.hp1 HG01167.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1562-1227G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179113625 | ||||||
| chr1:179113695
|
G | A | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1561+1183C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179113695 | ||||||
| chr1:179113865
|
T | C | 225 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(222): Show | 225 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1561+1013A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179113865 | ||||||
| chr1:179113866
|
G | A | 6 | a0001c0004t0024g0023a0001c0004t0024g0024a0001c0004t0024g0025others(3): Show | 6 | HG02965.hp1 HG02976.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1561+1012C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179113866 | ||||||
| chr1:179113894
|
A | C | 1 | a0001c0001t0001g0150 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1561+984T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179113894 | ||||||
| chr1:179113939
|
A | AT | 144 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(141): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1561+938dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179113939 | ||||||
| chr1:179114002
|
C | A | 2 | a0001c0001t0077g0142a0001c0001t0078g0143 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1561+876G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179114002 | ||||||
| chr1:179114026
|
G | A | 1 | a0001c0001t0080g0217 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1561+852C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179114026 | ||||||
| chr1:179114030
|
G | A | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1561+848C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179114030 | ||||||
| chr1:179114187
|
G | A | 1 | a0001c0001t0005g0335 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1561+691C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179114187 | ||||||
| chr1:179114201
|
T | C | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1561+677A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179114201 | ||||||
| chr1:179114334
|
T | G | 192 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(189): Show | 192 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1561+544A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179114334 | ||||||
| chr1:179114350
|
GTGAGCCG others(12): Show |
G | 190 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(187): Show | 190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1561+509_1561+527d others(21): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179114350 | ||||||
| chr1:179114364
|
C | T | 5 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1561+514G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179114364 | ||||||
| chr1:179114365
|
G | A | 18 | a0001c0003t0023g0009a0001c0003t0023g0010a0001c0003t0023g0011others(15): Show | 18 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.1561+513C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179114365 | ||||||
| chr1:179114530
|
A | AC | 226 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(223): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1561+347dupG | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179114530 | ||||||
| chr1:179114774
|
G | A | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1561+104C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179114774 | ||||||
| chr1:179114792
|
C | A | 1 | a0001c0002t0095g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1561+86G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179114792 | ||||||
| chr1:179114863
|
T | C | 1 | a0001c0002t0044g0271 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1561+15A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 9/11 | chr1 | 179114863 | ||||||
| chr1:179115036
|
T | C | 1 | a0001c0001t0013g0065 | 1 | HG02015.hp2 | splice_region_variant&intron_variant | LOW | c.1409-6A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179115036 | ||||||
| chr1:179115133
|
G | A | 12 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0241others(9): Show | 12 | HG00280.hp1 HG00621.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1409-103C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179115133 | ||||||
| chr1:179115263
|
A | G | 2 | a0001c0004t0031g0021a0001c0004t0031g0022 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1409-233T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179115263 | ||||||
| chr1:179115273
|
C | A | 19 | a0001c0002t0010g0254a0001c0002t0010g0256a0001c0002t0010g0258others(16): Show | 19 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.1409-243G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179115273 | ||||||
| chr1:179115392
|
C | T | 1 | a0001c0002t0095g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1409-362G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179115392 | ||||||
| chr1:179115481
|
A | T | 18 | a0001c0003t0023g0009a0001c0003t0023g0010a0001c0003t0023g0011others(15): Show | 18 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.1409-451T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179115481 | ||||||
| chr1:179115644
|
A | G | 24 | a0001c0001t0001g0144a0001c0001t0001g0149a0001c0001t0001g0161others(21): Show | 24 | HG00140.hp2 HG01168.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1409-614T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179115644 | ||||||
| chr1:179115649
|
T | C | 5 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1409-619A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179115649 | ||||||
| chr1:179115679
|
G | A | 1 | a0001c0001t0099g0301 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1409-649C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179115679 | ||||||
| chr1:179115852
|
G | C | 5 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1409-822C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179115852 | ||||||
| chr1:179115974
|
C | T | 2 | a0001c0001t0077g0142a0001c0001t0078g0143 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1409-944G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179115974 | ||||||
| chr1:179115981
|
A | C | 1 | a0001c0001t0027g0226 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1409-951T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179115981 | ||||||
| chr1:179115993
|
T | C | 11 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(8): Show | 11 | HG01099.hp1 HG01433.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1409-963A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179115993 | ||||||
| chr1:179115995
|
G | C | 3 | a0001c0001t0001g0162a0001c0008t0001g0165a0001c0008t0002g0157 | 3 | HG02145.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1409-965C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179115995 | ||||||
| chr1:179116032
|
G | GA | 8 | a0001c0001t0018g0080a0001c0001t0020g0155a0001c0001t0020g0196others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1409-1003dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179116032 | ||||||
| chr1:179116150
|
G | A | 1 | a0001c0001t0002g0184 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1409-1120C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179116150 | ||||||
| chr1:179116171
|
C | T | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1409-1141G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179116171 | ||||||
| chr1:179116202
|
CATCTCTA others(5): Show |
C | 145 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(142): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1408+1118_1408+112 others(16): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179116202 | ||||||
| chr1:179116282
|
G | A | 1 | a0001c0001t0107g0337 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1408+1050C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179116282 | ||||||
| chr1:179116565
|
C | CA | 162 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(159): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.1408+766dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179116565 | ||||||
| chr1:179116664
|
C | T | 4 | a0001c0001t0008g0282a0001c0001t0008g0298a0001c0001t0009g0285others(1): Show | 4 | HG01081.hp1 HG01167.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1408+668G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179116664 | ||||||
| chr1:179116829
|
CT | C | 11 | a0001c0001t0002g0184a0001c0001t0003g0095a0001c0001t0021g0311others(8): Show | 11 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1408+502delA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179116829 | ||||||
| chr1:179116829
|
CTT | C | 191 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(188): Show | 191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1408+501_1408+502d others(4): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179116829 | ||||||
| chr1:179116869
|
A | G | 1 | a0001c0001t0063g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1408+463T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179116869 | ||||||
| chr1:179116895
|
C | T | 1 | a0001c0001t0110g0324 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1408+437G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179116895 | ||||||
| chr1:179116984
|
C | T | 4 | a0001c0001t0026g0041a0001c0001t0026g0044a0001c0001t0026g0120others(1): Show | 4 | HG03490.hp2 HG03492.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1408+348G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179116984 | ||||||
| chr1:179116985
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1408+347C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179116985 | ||||||
| chr1:179117069
|
C | T | 1 | a0001c0001t0077g0142 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1408+263G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179117069 | ||||||
| chr1:179117081
|
A | C | 5 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1408+251T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179117081 | ||||||
| chr1:179117284
|
T | TA | 18 | a0001c0002t0010g0254a0001c0002t0010g0256a0001c0002t0010g0258others(15): Show | 18 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.1408+47dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179117284 | ||||||
| chr1:179117284
|
TA | T | 10 | a0001c0001t0008g0287a0001c0001t0008g0288a0001c0001t0008g0289others(7): Show | 10 | HG01346.hp2 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1408+47delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 8/11 | chr1 | 179117284 | ||||||
| chr1:179117600
|
T | C | 1 | a0001c0001t0019g0119 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1224-84A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 7/11 | chr1 | 179117600 | ||||||
| chr1:179117951
|
T | TA | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1224-436dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 7/11 | chr1 | 179117951 | ||||||
| chr1:179117953
|
C | A | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1224-437G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 7/11 | chr1 | 179117953 | ||||||
| chr1:179117990
|
C | A | 24 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(21): Show | 24 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.1224-474G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 7/11 | chr1 | 179117990 | ||||||
| chr1:179118010
|
G | A | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1224-494C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 7/11 | chr1 | 179118010 | ||||||
| chr1:179118045
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1224-529G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 7/11 | chr1 | 179118045 | ||||||
| chr1:179118074
|
G | A | 24 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(21): Show | 24 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.1223+513C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 7/11 | chr1 | 179118074 | ||||||
| chr1:179118254
|
T | C | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1223+333A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 7/11 | chr1 | 179118254 | ||||||
| chr1:179118312
|
A | G | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1223+275T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 7/11 | chr1 | 179118312 | ||||||
| chr1:179118410
|
T | G | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1223+177A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 7/11 | chr1 | 179118410 | ||||||
| chr1:179118498
|
A | G | 1 | a0001c0001t0099g0301 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1223+89T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 7/11 | chr1 | 179118498 | ||||||
| chr1:179118780
|
T | C | 1 | a0001c0013t0011g0346 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1046-16A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179118780 | ||||||
| chr1:179118790
|
T | C | 7 | a0001c0001t0005g0345a0001c0001t0011g0341a0001c0001t0045g0338others(4): Show | 7 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.1046-26A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179118790 | ||||||
| chr1:179118799
|
T | C | 190 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(187): Show | 190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1046-35A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179118799 | ||||||
| chr1:179118968
|
T | C | 1 | a0001c0001t0102g0296 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1046-204A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179118968 | ||||||
| chr1:179118983
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1046-219G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179118983 | ||||||
| chr1:179119086
|
TCTC | T | 145 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(142): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1046-325_1046-323d others(5): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179119086 | ||||||
| chr1:179119265
|
G | C | 1 | a0001c0001t0072g0121 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1046-501C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179119265 | ||||||
| chr1:179119396
|
C | T | 4 | a0001c0001t0001g0169a0001c0001t0001g0190a0001c0001t0001g0199others(1): Show | 4 | HG00741.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1046-632G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179119396 | ||||||
| chr1:179119505
|
T | C | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1045+685A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179119505 | ||||||
| chr1:179119522
|
C | CA | 5 | a0001c0001t0011g0321a0001c0001t0056g0020a0001c0001t0083g0194others(2): Show | 5 | HG00735.hp1 HG01175.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1045+667dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179119522 | ||||||
| chr1:179119522
|
CAAAA | C | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1045+664_1045+667d others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179119522 | ||||||
| chr1:179119534
|
C | A | 1 | a0001c0001t0005g0334 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1045+656G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179119534 | ||||||
| chr1:179119548
|
C | T | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1045+642G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179119548 | ||||||
| chr1:179119558
|
G | GA | 8 | a0001c0001t0003g0052a0001c0001t0003g0094a0001c0001t0006g0104others(5): Show | 8 | HG01243.hp2 HG01952.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1045+631dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179119558 | ||||||
| chr1:179119586
|
A | T | 190 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(187): Show | 190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1045+604T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179119586 | ||||||
| chr1:179119609
|
G | A | 190 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(187): Show | 190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1045+581C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179119609 | ||||||
| chr1:179119743
|
C | G | 1 | a0001c0002t0095g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1045+447G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179119743 | ||||||
| chr1:179119791
|
G | C | 28 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(25): Show | 28 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.1045+399C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179119791 | ||||||
| chr1:179119894
|
G | A | 19 | a0001c0002t0010g0254a0001c0002t0010g0256a0001c0002t0010g0258others(16): Show | 19 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.1045+296C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179119894 | ||||||
| chr1:179120038
|
A | G | 1 | a0001c0001t0004g0085 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1045+152T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179120038 | ||||||
| chr1:179120075
|
G | A | 1 | a0001c0001t0074g0123 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1045+115C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179120075 | ||||||
| chr1:179120078
|
C | T | 190 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(187): Show | 190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1045+112G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 6/11 | chr1 | 179120078 | ||||||
| chr1:179120319
|
A | G | 1 | a0001c0001t0060g0042 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.961-45T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/11 | chr1 | 179120319 | ||||||
| chr1:179120340
|
C | G | 190 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(187): Show | 190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.961-66G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/11 | chr1 | 179120340 | ||||||
| chr1:179120356
|
A | C | 190 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(187): Show | 190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.961-82T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/11 | chr1 | 179120356 | ||||||
| chr1:179120382
|
A | G | 1 | a0001c0001t0002g0168 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.961-108T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/11 | chr1 | 179120382 | ||||||
| chr1:179120383
|
C | G | 189 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(186): Show | 189 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.961-109G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/11 | chr1 | 179120383 | ||||||
| chr1:179120446
|
T | C | 145 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(142): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.961-172A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/11 | chr1 | 179120446 | ||||||
| chr1:179120455
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.961-181C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/11 | chr1 | 179120455 | ||||||
| chr1:179120458
|
C | T | 1 | a0001c0001t0091g0312 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.961-184G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/11 | chr1 | 179120458 | ||||||
| chr1:179120489
|
G | A | 1 | a0001c0001t0041g0250 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.961-215C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/11 | chr1 | 179120489 | ||||||
| chr1:179120831
|
G | A | 6 | a0001c0001t0001g0149a0001c0001t0001g0161a0001c0001t0002g0148others(3): Show | 6 | HG00140.hp2 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.961-557C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/11 | chr1 | 179120831 | ||||||
| chr1:179120945
|
C | T | 1 | a0001c0001t0063g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.960+650G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/11 | chr1 | 179120945 | ||||||
| chr1:179121024
|
TA | T | 252 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(249): Show | 252 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.960+570delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/11 | chr1 | 179121024 | ||||||
| chr1:179121125
|
G | A | 3 | a0001c0001t0005g0315a0001c0001t0005g0316a0001c0001t0005g0317 | 3 | NA18943.hp1 NA19064.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.960+470C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/11 | chr1 | 179121125 | ||||||
| chr1:179121161
|
T | C | 1 | a0006c0011t0084g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.960+434A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/11 | chr1 | 179121161 | ||||||
| chr1:179121190
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.960+405A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/11 | chr1 | 179121190 | ||||||
| chr1:179121239
|
G | T | 18 | a0001c0003t0023g0009a0001c0003t0023g0010a0001c0003t0023g0011others(15): Show | 18 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.960+356C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/11 | chr1 | 179121239 | ||||||
| chr1:179121285
|
C | G | 1 | a0001c0001t0091g0312 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.960+310G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/11 | chr1 | 179121285 | ||||||
| chr1:179121355
|
T | A | 3 | a0001c0001t0019g0091a0001c0001t0019g0098a0001c0001t0019g0119 | 3 | NA18969.hp1 NA19066.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.960+240A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/11 | chr1 | 179121355 | ||||||
| chr1:179121548
|
G | A | 1 | a0001c0001t0088g0236 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.960+47C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 5/11 | chr1 | 179121548 | ||||||
| chr1:179121915
|
A | AT | 26 | a0001c0001t0003g0045a0001c0001t0003g0059a0001c0001t0003g0109others(23): Show | 26 | HG00621.hp1 HG01167.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.688-49dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179121915 | ||||||
| chr1:179121915
|
AT | A | 11 | a0001c0001t0003g0072a0001c0001t0004g0076a0001c0001t0004g0106others(8): Show | 11 | HG01069.hp1 HG01891.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.688-49delA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179121915 | ||||||
| chr1:179121915
|
ATTT | A | 17 | a0001c0001t0002g0153a0001c0001t0005g0315a0001c0001t0008g0288others(14): Show | 17 | HG01243.hp2 HG01516.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.688-51_688-49delAA others(1): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179121915 | ||||||
| chr1:179121915
|
ATTTT | A | 136 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0159others(133): Show | 136 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.688-52_688-49delAA others(2): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179121915 | ||||||
| chr1:179121915
|
ATTTTT | A | 37 | a0001c0001t0001g0144a0001c0001t0001g0149a0001c0001t0001g0160others(34): Show | 37 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.688-53_688-49delAA others(3): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179121915 | ||||||
| chr1:179122026
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.688-159G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179122026 | ||||||
| chr1:179122071
|
C | T | 1 | a0001c0001t0006g0092 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.688-204G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179122071 | ||||||
| chr1:179122276
|
T | TA | 6 | a0001c0001t0003g0109a0001c0001t0033g0062a0001c0001t0056g0020others(3): Show | 6 | HG00735.hp1 HG01175.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.688-410dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179122276 | ||||||
| chr1:179122276
|
TA | T | 111 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0001g0150others(108): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.688-410delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179122276 | ||||||
| chr1:179122276
|
TAA | T | 100 | a0001c0001t0001g0144a0001c0001t0001g0170a0001c0001t0001g0185others(97): Show | 100 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.688-411_688-410del others(2): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179122276 | ||||||
| chr1:179122296
|
A | AG | 6 | a0001c0001t0003g0052a0001c0001t0003g0071a0001c0001t0003g0072others(3): Show | 6 | HG01361.hp1 HG01952.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.688-430_688-429ins others(1): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179122296 | ||||||
| chr1:179122296
|
A | G | 1 | a0001c0001t0019g0067 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.688-429T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179122296 | ||||||
| chr1:179122296
|
A | T | 1 | a0001c0001t0099g0301 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.688-429T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179122296 | ||||||
| chr1:179122298
|
A | T | 1 | a0001c0001t0099g0301 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.688-431T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179122298 | ||||||
| chr1:179122816
|
G | A | 160 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(157): Show | 160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.688-949C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179122816 | ||||||
| chr1:179122822
|
T | C | 1 | a0001c0001t0002g0215 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.688-955A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179122822 | ||||||
| chr1:179122891
|
C | T | 1 | a0001c0001t0011g0341 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.688-1024G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179122891 | ||||||
| chr1:179123180
|
G | A | 3 | a0001c0001t0019g0091a0001c0001t0019g0098a0001c0001t0019g0119 | 3 | NA18969.hp1 NA19066.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.688-1313C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179123180 | ||||||
| chr1:179123477
|
A | C | 196 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(193): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.688-1610T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179123477 | ||||||
| chr1:179123478
|
G | C | 196 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(193): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.688-1611C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179123478 | ||||||
| chr1:179123606
|
A | C | 252 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(249): Show | 252 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.688-1739T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179123606 | ||||||
| chr1:179123713
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0083g0194 | 2 | HG02698.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.688-1846A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179123713 | ||||||
| chr1:179123807
|
T | A | 5 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.688-1940A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179123807 | ||||||
| chr1:179123936
|
T | C | 3 | a0001c0001t0001g0160a0001c0001t0001g0193a0001c0001t0036g0229 | 3 | HG00099.hp1 HG03239.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.688-2069A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179123936 | ||||||
| chr1:179123968
|
G | A | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.688-2101C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179123968 | ||||||
| chr1:179124081
|
A | T | 19 | a0001c0002t0010g0254a0001c0002t0010g0256a0001c0002t0010g0258others(16): Show | 19 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.688-2214T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124081 | ||||||
| chr1:179124102
|
G | A | 2 | a0001c0001t0001g0244a0001c0001t0001g0247 | 2 | HG00621.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.688-2235C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124102 | ||||||
| chr1:179124172
|
C | T | 2 | a0001c0001t0012g0063a0001c0001t0013g0065 | 2 | HG02015.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.687+2205G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124172 | ||||||
| chr1:179124190
|
G | A | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.687+2187C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124190 | ||||||
| chr1:179124196
|
G | T | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.687+2181C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124196 | ||||||
| chr1:179124215
|
G | T | 338 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(335): Show | 338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.687+2162C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124215 | ||||||
| chr1:179124245
|
GA | G | 32 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(29): Show | 32 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.687+2131delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124245 | ||||||
| chr1:179124319
|
A | C | 1 | a0001c0001t0020g0155 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.687+2058T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124319 | ||||||
| chr1:179124323
|
T | G | 2 | a0001c0001t0077g0142a0001c0001t0078g0143 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.687+2054A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124323 | ||||||
| chr1:179124387
|
T | G | 1 | a0001c0001t0001g0150 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.687+1990A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124387 | ||||||
| chr1:179124464
|
C | CTTT | 26 | a0001c0001t0041g0250a0001c0001t0042g0249a0001c0001t0042g0252others(23): Show | 26 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.687+1910_687+1912d others(5): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124464 | ||||||
| chr1:179124464
|
C | CTTTT | 11 | a0001c0001t0001g0146a0001c0001t0009g0286a0001c0001t0009g0314others(8): Show | 11 | HG01167.hp2 HG01516.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.687+1909_687+1912d others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124464 | ||||||
| chr1:179124464
|
C | CTTTTT | 149 | a0001c0001t0001g0144a0001c0001t0001g0150a0001c0001t0001g0159others(146): Show | 149 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.687+1908_687+1912d others(7): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124464 | ||||||
| chr1:179124464
|
C | CTTTTTT | 49 | a0001c0001t0001g0149a0001c0001t0001g0190a0001c0001t0001g0201others(46): Show | 49 | HG00140.hp1 HG00597.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.687+1907_687+1912d others(8): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124464 | ||||||
| chr1:179124464
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0016g0189a0001c0001t0016g0222a0001c0001t0016g0223 | 3 | HG01099.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.687+1902_687+1912d others(13): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124464 | ||||||
| chr1:179124464
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0016g0158a0001c0001t0027g0195 | 2 | HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.687+1901_687+1912d others(14): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124464 | ||||||
| chr1:179124464
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0027g0224 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.687+1900_687+1912d others(15): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124464 | ||||||
| chr1:179124464
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0016g0188a0001c0001t0027g0226 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.687+1899_687+1912d others(16): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124464 | ||||||
| chr1:179124499
|
C | T | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.687+1878G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124499 | ||||||
| chr1:179124510
|
C | T | 1 | a0001c0001t0003g0111 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.687+1867G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124510 | ||||||
| chr1:179124553
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.687+1824G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124553 | ||||||
| chr1:179124603
|
G | A | 160 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(157): Show | 160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.687+1774C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179124603 | ||||||
| chr1:179125002
|
T | C | 3 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0081g0218 | 3 | HG02647.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.687+1375A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179125002 | ||||||
| chr1:179125248
|
C | T | 1 | a0001c0001t0003g0054 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.687+1129G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179125248 | ||||||
| chr1:179125445
|
G | A | 1 | a0001c0001t0002g0153 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.687+932C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179125445 | ||||||
| chr1:179125480
|
C | A | 1 | a0002c0005t0022g0277 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.687+897G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179125480 | ||||||
| chr1:179125691
|
G | C | 5 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.687+686C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179125691 | ||||||
| chr1:179125704
|
T | G | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.687+673A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179125704 | ||||||
| chr1:179125708
|
G | A | 192 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(189): Show | 192 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.687+669C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179125708 | ||||||
| chr1:179125820
|
A | G | 1 | a0001c0001t0002g0184 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.687+557T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179125820 | ||||||
| chr1:179126096
|
A | G | 1 | a0001c0001t0088g0236 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.687+281T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179126096 | ||||||
| chr1:179126265
|
A | G | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+112T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 4/11 | chr1 | 179126265 | ||||||
| chr1:179126775
|
A | T | 1 | a0001c0001t0103g0293 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.392-103T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179126775 | ||||||
| chr1:179126793
|
A | C | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.392-121T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179126793 | ||||||
| chr1:179126805
|
T | A | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.392-133A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179126805 | ||||||
| chr1:179126905
|
T | C | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.392-233A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179126905 | ||||||
| chr1:179126953
|
A | G | 252 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(249): Show | 252 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.392-281T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179126953 | ||||||
| chr1:179127038
|
C | T | 4 | a0001c0004t0024g0023a0001c0004t0024g0024a0001c0004t0058g0028others(1): Show | 4 | HG02615.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.392-366G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179127038 | ||||||
| chr1:179127048
|
T | G | 2 | a0001c0002t0017g0269a0001c0002t0093g0274 | 2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.392-376A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179127048 | ||||||
| chr1:179127450
|
T | C | 7 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-778A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179127450 | ||||||
| chr1:179127652
|
T | C | 1 | a0001c0001t0002g0206 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.392-980A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179127652 | ||||||
| chr1:179127685
|
TCA | T | 4 | a0001c0001t0026g0041a0001c0001t0026g0044a0001c0001t0026g0120others(1): Show | 4 | HG03490.hp2 HG03492.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.392-1015_392-1014d others(4): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179127685 | ||||||
| chr1:179127754
|
G | T | 6 | a0001c0001t0020g0155a0001c0001t0020g0196a0001c0001t0020g0197others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.392-1082C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179127754 | ||||||
| chr1:179127794
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.392-1122C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179127794 | ||||||
| chr1:179127823
|
G | C | 5 | a0001c0001t0003g0052a0001c0001t0003g0072a0001c0001t0006g0038others(2): Show | 5 | HG01257.hp2 HG01361.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.392-1151C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179127823 | ||||||
| chr1:179127913
|
T | C | 4 | a0001c0001t0001g0237a0001c0001t0002g0232a0001c0001t0036g0207others(1): Show | 4 | HG03704.hp1 HG03831.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.392-1241A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179127913 | ||||||
| chr1:179127958
|
C | G | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.392-1286G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179127958 | ||||||
| chr1:179127988
|
T | C | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.392-1316A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179127988 | ||||||
| chr1:179128006
|
G | C | 3 | a0001c0004t0024g0023a0001c0004t0024g0024a0001c0004t0111g0347 | 3 | HG03453.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.392-1334C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179128006 | ||||||
| chr1:179128030
|
T | TA | 117 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0159others(114): Show | 117 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.392-1359dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179128030 | ||||||
| chr1:179128030
|
T | TAA | 27 | a0001c0001t0001g0186a0001c0001t0005g0320a0001c0001t0008g0282others(24): Show | 27 | HG01081.hp1 HG01099.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.392-1360_392-1359d others(4): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179128030 | ||||||
| chr1:179128071
|
A | G | 157 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(154): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.392-1399T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179128071 | ||||||
| chr1:179128160
|
G | C | 204 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.392-1488C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179128160 | ||||||
| chr1:179128439
|
T | G | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.392-1767A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179128439 | ||||||
| chr1:179128672
|
G | A | 18 | a0001c0003t0023g0009a0001c0003t0023g0010a0001c0003t0023g0011others(15): Show | 18 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.392-2000C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179128672 | ||||||
| chr1:179128730
|
C | T | 1 | a0001c0001t0003g0095 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.392-2058G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179128730 | ||||||
| chr1:179128949
|
T | G | 5 | a0001c0001t0001g0160a0001c0001t0001g0193a0001c0001t0002g0214others(2): Show | 5 | HG00099.hp1 HG02622.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.392-2277A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179128949 | ||||||
| chr1:179128996
|
A | T | 7 | a0001c0004t0024g0023a0001c0004t0024g0024a0001c0004t0024g0025others(4): Show | 7 | HG02615.hp2 HG02965.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.391+2315T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179128996 | ||||||
| chr1:179129049
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.391+2262G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179129049 | ||||||
| chr1:179129340
|
C | T | 155 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(152): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.391+1971G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179129340 | ||||||
| chr1:179129423
|
C | T | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.391+1888G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179129423 | ||||||
| chr1:179129498
|
T | C | 349 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(346): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.391+1813A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179129498 | ||||||
| chr1:179129542
|
C | T | 3 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0081g0218 | 3 | HG02647.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.391+1769G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179129542 | ||||||
| chr1:179129549
|
G | A | 2 | a0001c0001t0006g0038a0001c0001t0019g0067 | 2 | HG01257.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.391+1762C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179129549 | ||||||
| chr1:179129635
|
C | T | 155 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(152): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.391+1676G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179129635 | ||||||
| chr1:179129681
|
C | CA | 13 | a0001c0001t0003g0109a0001c0001t0004g0100a0001c0001t0008g0299others(10): Show | 13 | HG00735.hp1 HG01175.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.391+1629dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179129681 | ||||||
| chr1:179129780
|
T | TA | 18 | a0001c0003t0023g0009a0001c0003t0023g0010a0001c0003t0023g0011others(15): Show | 18 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.391+1530dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179129780 | ||||||
| chr1:179129878
|
A | G | 1 | a0001c0001t0027g0226 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.391+1433T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179129878 | ||||||
| chr1:179129886
|
T | C | 159 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(156): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.391+1425A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179129886 | ||||||
| chr1:179129948
|
G | GT | 7 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.391+1362dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179129948 | ||||||
| chr1:179129963
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.391+1348C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179129963 | ||||||
| chr1:179130005
|
T | A | 1 | a0001c0001t0006g0114 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.391+1306A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130005 | ||||||
| chr1:179130035
|
G | A | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391+1276C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130035 | ||||||
| chr1:179130106
|
A | G | 1 | a0001c0001t0005g0318 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.391+1205T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130106 | ||||||
| chr1:179130507
|
T | C | 2 | a0001c0001t0003g0109a0001c0001t0006g0081 | 2 | NA18995.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.391+804A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130507 | ||||||
| chr1:179130651
|
A | C | 6 | a0001c0001t0020g0155a0001c0001t0020g0196a0001c0001t0020g0197others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.391+660T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130651 | ||||||
| chr1:179130661
|
C | T | 10 | a0001c0001t0003g0058a0001c0001t0003g0095a0001c0001t0003g0111others(7): Show | 10 | HG00741.hp1 HG01346.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.391+650G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130661 | ||||||
| chr1:179130662
|
G | A | 4 | a0001c0002t0010g0261a0001c0002t0044g0264a0001c0002t0044g0271others(1): Show | 4 | HG02135.hp2 NA18942.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+649C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130662 | ||||||
| chr1:179130726
|
T | TTG | 40 | a0001c0001t0001g0160a0001c0001t0001g0177a0001c0001t0001g0193others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.391+583_391+584dup others(2): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130726 | ||||||
| chr1:179130726
|
T | TTGTG | 17 | a0001c0001t0001g0175a0001c0001t0008g0298a0001c0001t0016g0222others(14): Show | 17 | HG00140.hp1 HG00741.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.391+581_391+584dup others(4): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130726 | ||||||
| chr1:179130726
|
T | TTGTGTG | 12 | a0001c0001t0008g0283a0001c0001t0008g0290a0001c0001t0008g0297others(9): Show | 12 | HG00733.hp2 HG01167.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.391+579_391+584dup others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130726 | ||||||
| chr1:179130726
|
T | TTGTGTGT others(1): Show |
23 | a0001c0001t0008g0282a0001c0001t0008g0287a0001c0001t0008g0289others(20): Show | 23 | HG01081.hp1 HG01099.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.391+577_391+584dup others(8): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130726 | ||||||
| chr1:179130726
|
T | TTGTGTGT others(3): Show |
4 | a0001c0001t0008g0288a0001c0001t0016g0158a0001c0001t0016g0188others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+575_391+584dup others(10): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130726 | ||||||
| chr1:179130726
|
T | TTGTGTGT others(5): Show |
2 | a0001c0001t0027g0226a0001c0001t0035g0220 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.391+573_391+584dup others(12): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130726 | ||||||
| chr1:179130726
|
T | TTGTGTGT others(7): Show |
1 | a0001c0001t0027g0224 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.391+571_391+584dup others(14): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130726 | ||||||
| chr1:179130726
|
T | TTGTGTGT others(9): Show |
1 | a0001c0001t0035g0225 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.391+569_391+584dup others(16): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130726 | ||||||
| chr1:179130726
|
T | TTTTTTTT others(3): Show |
2 | a0001c0001t0034g0213a0001c0001t0034g0219 | 2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.391+584_391+585ins others(10): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130726 | ||||||
| chr1:179130726
|
TTG | T | 22 | a0001c0001t0001g0149a0001c0001t0001g0161a0001c0001t0001g0162others(19): Show | 22 | HG00140.hp2 HG00735.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.391+583_391+584del others(2): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130726 | ||||||
| chr1:179130726
|
TTGTG | T | 9 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0002g0152others(6): Show | 9 | HG00408.hp2 HG01169.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.391+581_391+584del others(4): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130726 | ||||||
| chr1:179130726
|
TTGTGTG | T | 6 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0001t0056g0020others(3): Show | 6 | HG00735.hp1 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.391+579_391+584del others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130726 | ||||||
| chr1:179130726
|
TTGTGTGT others(3): Show |
T | 18 | a0001c0003t0023g0009a0001c0003t0023g0010a0001c0003t0023g0011others(15): Show | 18 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.391+575_391+584del others(10): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130726 | ||||||
| chr1:179130726
|
TTGTGTGT others(7): Show |
T | 2 | a0001c0001t0001g0144a0001c0004t0058g0028 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.391+571_391+584del others(14): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130726 | ||||||
| chr1:179130863
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.391+448C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130863 | ||||||
| chr1:179130878
|
T | C | 1 | a0001c0001t0002g0184 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.391+433A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130878 | ||||||
| chr1:179130910
|
C | T | 155 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(152): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.391+401G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130910 | ||||||
| chr1:179130936
|
A | AT | 163 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(160): Show | 163 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.391+374dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130936 | ||||||
| chr1:179130986
|
G | A | 123 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(120): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.391+325C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179130986 | ||||||
| chr1:179131066
|
G | C | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.391+245C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179131066 | ||||||
| chr1:179131082
|
AG | A | 6 | a0001c0004t0024g0023a0001c0004t0024g0024a0001c0004t0024g0025others(3): Show | 6 | HG02965.hp1 HG02976.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.391+228delC | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179131082 | ||||||
| chr1:179131156
|
T | C | 204 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.391+155A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179131156 | ||||||
| chr1:179131234
|
G | C | 1 | a0001c0001t0011g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.391+77C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179131234 | ||||||
| chr1:179131240
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0202 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.391+71C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 3/11 | chr1 | 179131240 | ||||||
| chr1:179131575
|
C | T | 19 | a0001c0002t0010g0254a0001c0002t0010g0256a0001c0002t0010g0258others(16): Show | 19 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.221-94G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179131575 | ||||||
| chr1:179131590
|
G | A | 7 | a0001c0004t0024g0023a0001c0004t0024g0024a0001c0004t0024g0025others(4): Show | 7 | HG02615.hp2 HG02965.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.221-109C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179131590 | ||||||
| chr1:179131667
|
T | C | 25 | a0001c0003t0023g0009a0001c0003t0023g0010a0001c0003t0023g0011others(22): Show | 25 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.221-186A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179131667 | ||||||
| chr1:179131734
|
T | C | 18 | a0001c0003t0023g0009a0001c0003t0023g0010a0001c0003t0023g0011others(15): Show | 18 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.221-253A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179131734 | ||||||
| chr1:179131774
|
G | A | 4 | a0001c0001t0026g0041a0001c0001t0026g0044a0001c0001t0026g0120others(1): Show | 4 | HG03490.hp2 HG03492.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-293C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179131774 | ||||||
| chr1:179131799
|
C | A | 1 | a0001c0001t0005g0325 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.221-318G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179131799 | ||||||
| chr1:179131813
|
G | A | 1 | a0007c0015t0092g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.221-332C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179131813 | ||||||
| chr1:179132088
|
C | A | 1 | a0001c0001t0108g0340 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.221-607G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179132088 | ||||||
| chr1:179132274
|
C | T | 1 | a0001c0001t0018g0064 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.221-793G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179132274 | ||||||
| chr1:179132375
|
C | G | 6 | a0001c0001t0011g0341a0001c0001t0045g0338a0001c0001t0045g0339others(3): Show | 6 | HG00597.hp1 HG00673.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-894G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179132375 | ||||||
| chr1:179132382
|
C | T | 1 | a0001c0001t0002g0242 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.221-901G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179132382 | ||||||
| chr1:179132471
|
C | G | 153 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(150): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.220+841G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179132471 | ||||||
| chr1:179132525
|
GATT | G | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+784_220+786del others(3): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179132525 | ||||||
| chr1:179132599
|
G | A | 10 | a0001c0001t0003g0058a0001c0001t0003g0095a0001c0001t0003g0111others(7): Show | 10 | HG00741.hp1 HG01346.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+713C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179132599 | ||||||
| chr1:179132659
|
C | A | 2 | a0001c0002t0010g0267a0001c0002t0017g0268 | 2 | HG00140.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.220+653G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179132659 | ||||||
| chr1:179132691
|
C | T | 1 | a0001c0001t0005g0319 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.220+621G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179132691 | ||||||
| chr1:179132888
|
T | C | 3 | a0001c0001t0001g0162a0001c0008t0001g0165a0001c0008t0002g0157 | 3 | HG02145.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.220+424A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179132888 | ||||||
| chr1:179132980
|
T | G | 1 | a0001c0001t0099g0301 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.220+332A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179132980 | ||||||
| chr1:179133133
|
A | T | 24 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(21): Show | 24 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.220+179T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179133133 | ||||||
| chr1:179133137
|
G | A | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.220+175C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 2/11 | chr1 | 179133137 | ||||||
| chr1:179133630
|
A | C | 11 | a0001c0001t0011g0322a0001c0001t0016g0158a0001c0001t0016g0188others(8): Show | 11 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.158-256T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179133630 | ||||||
| chr1:179133941
|
G | A | 1 | a0001c0001t0066g0036 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.158-567C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179133941 | ||||||
| chr1:179133979
|
G | T | 1 | a0001c0001t0008g0299 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.158-605C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179133979 | ||||||
| chr1:179134143
|
T | C | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-769A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134143 | ||||||
| chr1:179134464
|
C | T | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-1090G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134464 | ||||||
| chr1:179134552
|
C | T | 155 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(152): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.158-1178G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134552 | ||||||
| chr1:179134566
|
C | T | 130 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.158-1192G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134566 | ||||||
| chr1:179134573
|
T | G | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-1199A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134573 | ||||||
| chr1:179134593
|
A | T | 1 | a0001c0001t0002g0184 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.158-1219T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134593 | ||||||
| chr1:179134699
|
T | C | 43 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0159others(40): Show | 43 | HG00438.hp1 HG00438.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.158-1325A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134699 | ||||||
| chr1:179134710
|
GCCTCTC | G | 162 | a0001c0001t0001g0171a0001c0001t0002g0154a0001c0001t0003g0033others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.158-1342_158-1337d others(8): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134710 | ||||||
| chr1:179134738
|
G | A | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-1364C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134738 | ||||||
| chr1:179134741
|
C | T | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.158-1367G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134741 | ||||||
| chr1:179134742
|
G | T | 159 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(156): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.158-1368C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134742 | ||||||
| chr1:179134848
|
G | T | 2 | a0001c0001t0001g0149a0001c0001t0002g0148 | 2 | HG00140.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.158-1474C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134848 | ||||||
| chr1:179134865
|
G | C | 1 | a0001c0001t0063g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.158-1491C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134865 | ||||||
| chr1:179134867
|
G | T | 1 | a0001c0001t0063g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.158-1493C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134867 | ||||||
| chr1:179134875
|
G | A | 1 | a0001c0001t0063g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.158-1501C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134875 | ||||||
| chr1:179134879
|
A | G | 1 | a0001c0001t0063g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.158-1505T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134879 | ||||||
| chr1:179134902
|
G | A | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-1528C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134902 | ||||||
| chr1:179134905
|
T | C | 2 | a0001c0001t0020g0197a0001c0001t0020g0235 | 2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.158-1531A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134905 | ||||||
| chr1:179134943
|
G | A | 25 | a0001c0003t0023g0009a0001c0003t0023g0010a0001c0003t0023g0011others(22): Show | 25 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.158-1569C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134943 | ||||||
| chr1:179134983
|
C | T | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.158-1609G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179134983 | ||||||
| chr1:179135018
|
T | C | 1 | a0001c0001t0091g0312 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.158-1644A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135018 | ||||||
| chr1:179135019
|
C | T | 2 | a0001c0001t0112g0348a0001c0001t0113g0349 | 2 | HG01884.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.158-1645G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135019 | ||||||
| chr1:179135029
|
G | A | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-1655C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135029 | ||||||
| chr1:179135070
|
C | T | 155 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(152): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.158-1696G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135070 | ||||||
| chr1:179135117
|
A | G | 7 | a0001c0004t0024g0023a0001c0004t0024g0024a0001c0004t0024g0025others(4): Show | 7 | HG02615.hp2 HG02965.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.158-1743T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135117 | ||||||
| chr1:179135126
|
G | A | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.158-1752C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135126 | ||||||
| chr1:179135150
|
A | AC | 5 | a0001c0001t0001g0161a0001c0001t0001g0237a0001c0001t0009g0286others(2): Show | 5 | HG01516.hp1 HG02145.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-1777dupG | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135150 | ||||||
| chr1:179135258
|
C | G | 11 | a0001c0001t0008g0287a0001c0001t0008g0288a0001c0001t0008g0289others(8): Show | 11 | HG01346.hp2 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.158-1884G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135258 | ||||||
| chr1:179135276
|
AGGAAGTG others(33): Show |
A | 6 | a0001c0001t0020g0155a0001c0001t0020g0196a0001c0001t0020g0197others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-1942_158-1903d others(42): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135276 | ||||||
| chr1:179135448
|
C | T | 204 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.158-2074G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135448 | ||||||
| chr1:179135452
|
T | C | 2 | a0003c0006t0001g0151a0003c0006t0001g0209 | 2 | NA18985.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.158-2078A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135452 | ||||||
| chr1:179135465
|
G | A | 1 | a0001c0001t0005g0325 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.158-2091C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135465 | ||||||
| chr1:179135569
|
T | G | 204 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.158-2195A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135569 | ||||||
| chr1:179135583
|
TCGTCCGG others(169): Show |
T | 1 | a0001c0001t0036g0207 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.158-2385_158-2210d others(2): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135583 | ||||||
| chr1:179135689
|
G | A | 2 | a0001c0001t0038g0216a0001c0001t0038g0221 | 2 | HG02055.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.158-2315C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135689 | ||||||
| chr1:179135743
|
TGCCCGGC others(42): Show |
T | 1 | a0001c0003t0049g0014 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.158-2418_158-2370d others(51): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135743 | ||||||
| chr1:179135761
|
G | A | 1 | a0001c0001t0002g0184 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.158-2387C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135761 | ||||||
| chr1:179135764
|
CGGGAGGG others(46): Show |
C | 1 | a0001c0001t0003g0097 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.158-2443_158-2391d others(55): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135764 | ||||||
| chr1:179135765
|
G | A | 5 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(2): Show | 5 | HG01069.hp1 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-2391C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135765 | ||||||
| chr1:179135793
|
G | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0170 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.158-2419C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135793 | ||||||
| chr1:179135794
|
C | G | 5 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(2): Show | 5 | HG01069.hp1 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-2420G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135794 | ||||||
| chr1:179135813
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.158-2439G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135813 | ||||||
| chr1:179135833
|
G | C | 1 | a0001c0001t0003g0057 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.158-2459C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135833 | ||||||
| chr1:179135862
|
C | T | 1 | a0001c0001t0004g0110 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.158-2488G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135862 | ||||||
| chr1:179135867
|
A | G | 159 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(156): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.158-2493T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135867 | ||||||
| chr1:179135869
|
G | A | 2 | a0001c0001t0077g0142a0001c0001t0078g0143 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.158-2495C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135869 | ||||||
| chr1:179135955
|
G | GT | 94 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.158-2582dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135955 | ||||||
| chr1:179135956
|
T | TTG | 3 | a0001c0001t0003g0057a0001c0001t0003g0109a0001c0001t0004g0048 | 3 | HG01496.hp2 HG01516.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.158-2583_158-2582i others(4): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135956 | ||||||
| chr1:179135975
|
A | G | 159 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(156): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.158-2601T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179135975 | ||||||
| chr1:179136069
|
C | T | 123 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(120): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.158-2695G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136069 | ||||||
| chr1:179136070
|
G | A | 7 | a0001c0004t0024g0023a0001c0004t0024g0024a0001c0004t0024g0025others(4): Show | 7 | HG02615.hp2 HG02965.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.158-2696C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136070 | ||||||
| chr1:179136084
|
T | G | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.158-2710A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136084 | ||||||
| chr1:179136084
|
T | TG | 31 | a0001c0001t0001g0186a0001c0001t0001g0241a0001c0001t0002g0243others(28): Show | 31 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.158-2711dupC | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136084 | ||||||
| chr1:179136091
|
G | C | 25 | a0001c0003t0023g0009a0001c0003t0023g0010a0001c0003t0023g0011others(22): Show | 25 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.158-2717C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136091 | ||||||
| chr1:179136137
|
C | T | 3 | a0001c0001t0018g0069a0001c0001t0018g0080a0001c0001t0057g0029 | 3 | NA18942.hp1 NA18947.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.158-2763G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136137 | ||||||
| chr1:179136138
|
G | A | 2 | a0001c0001t0020g0155a0001c0001t0020g0196 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.158-2764C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136138 | ||||||
| chr1:179136223
|
T | C | 1 | a0001c0001t0008g0295 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.158-2849A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136223 | ||||||
| chr1:179136230
|
T | C | 49 | a0001c0001t0005g0315a0001c0001t0005g0316a0001c0001t0005g0317others(46): Show | 49 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.158-2856A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136230 | ||||||
| chr1:179136292
|
G | A | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-2918C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136292 | ||||||
| chr1:179136328
|
G | A | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.158-2954C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136328 | ||||||
| chr1:179136340
|
A | G | 2 | a0001c0001t0001g0160a0001c0001t0036g0229 | 2 | HG00099.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.158-2966T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136340 | ||||||
| chr1:179136409
|
C | T | 18 | a0001c0003t0023g0009a0001c0003t0023g0010a0001c0003t0023g0011others(15): Show | 18 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.158-3035G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136409 | ||||||
| chr1:179136418
|
C | T | 25 | a0001c0003t0023g0009a0001c0003t0023g0010a0001c0003t0023g0011others(22): Show | 25 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.158-3044G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136418 | ||||||
| chr1:179136659
|
T | C | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.158-3285A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136659 | ||||||
| chr1:179136709
|
A | AAAAT | 73 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0159others(70): Show | 73 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.158-3339_158-3336d others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136709 | ||||||
| chr1:179136709
|
A | AAAATAAA others(1): Show |
117 | a0001c0001t0001g0166a0001c0001t0001g0170a0001c0001t0001g0174others(114): Show | 117 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.158-3343_158-3336d others(10): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136709 | ||||||
| chr1:179136709
|
A | AAAATAAA others(5): Show |
45 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0086others(42): Show | 45 | HG00099.hp2 HG01106.hp2 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.158-3347_158-3336d others(14): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136709 | ||||||
| chr1:179136709
|
A | AAAATAAA others(9): Show |
6 | a0001c0001t0005g0319a0001c0001t0006g0075a0001c0001t0006g0084others(3): Show | 6 | HG00408.hp1 HG00673.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.158-3351_158-3336d others(18): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136709 | ||||||
| chr1:179136709
|
AAAAT | A | 8 | a0001c0001t0001g0204a0001c0001t0014g0116a0001c0001t0056g0020others(5): Show | 8 | HG00735.hp1 HG01175.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.158-3339_158-3336d others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136709 | ||||||
| chr1:179136709
|
AAAATAAA others(1): Show |
A | 14 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(11): Show | 14 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.158-3343_158-3336d others(10): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136709 | ||||||
| chr1:179136709
|
AAAATAAA others(9): Show |
A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | NA18947.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.158-3351_158-3336d others(18): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136709 | ||||||
| chr1:179136714
|
A | C | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.158-3340T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136714 | ||||||
| chr1:179136718
|
A | C | 1 | a0001c0001t0091g0312 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.158-3344T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136718 | ||||||
| chr1:179136722
|
A | C | 1 | a0001c0001t0091g0312 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.158-3348T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136722 | ||||||
| chr1:179136733
|
TAAATAAA others(3): Show |
T | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-3369_158-3360d others(12): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136733 | ||||||
| chr1:179136741
|
T | TAAATAAA others(1): Show |
17 | a0001c0003t0023g0009a0001c0003t0023g0010a0001c0003t0023g0011others(14): Show | 17 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.158-3368_158-3367i others(10): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136741 | ||||||
| chr1:179136741
|
T | TAAATAAA others(9): Show |
1 | a0001c0003t0053g0002 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.158-3368_158-3367i others(18): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136741 | ||||||
| chr1:179136741
|
TAA | T | 3 | a0001c0001t0077g0142a0001c0001t0078g0143a0001c0001t0098g0308 | 3 | HG01891.hp1 HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.158-3369_158-3368d others(4): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136741 | ||||||
| chr1:179136873
|
C | CG | 9 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.158-3500dupC | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136873 | ||||||
| chr1:179136916
|
C | CA | 74 | a0001c0001t0001g0166a0001c0001t0001g0170a0001c0001t0005g0319others(71): Show | 74 | HG00597.hp2 HG00735.hp1 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.158-3543dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136916 | ||||||
| chr1:179136916
|
C | CAA | 124 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(121): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.158-3544_158-3543d others(4): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136916 | ||||||
| chr1:179136916
|
C | CAAA | 11 | a0001c0001t0003g0089a0001c0001t0004g0048a0001c0001t0006g0092others(8): Show | 11 | HG01109.hp2 HG01516.hp2 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.158-3545_158-3543d others(5): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136916 | ||||||
| chr1:179136959
|
A | G | 1 | a0001c0004t0024g0023 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.158-3585T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179136959 | ||||||
| chr1:179137155
|
T | C | 3 | a0001c0001t0025g0032a0001c0001t0025g0043a0001c0001t0025g0060 | 3 | NA18939.hp2 NA18952.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.158-3781A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179137155 | ||||||
| chr1:179137442
|
T | A | 1 | a0001c0001t0001g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.158-4068A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179137442 | ||||||
| chr1:179137612
|
T | C | 5 | a0001c0001t0001g0169a0001c0001t0001g0190a0001c0001t0001g0199others(2): Show | 5 | HG00741.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-4238A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179137612 | ||||||
| chr1:179137718
|
T | C | 24 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(21): Show | 24 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.158-4344A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179137718 | ||||||
| chr1:179137764
|
A | G | 159 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(156): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.158-4390T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179137764 | ||||||
| chr1:179137838
|
C | T | 24 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(21): Show | 24 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.158-4464G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179137838 | ||||||
| chr1:179137990
|
T | C | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.158-4616A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179137990 | ||||||
| chr1:179138295
|
T | C | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.158-4921A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179138295 | ||||||
| chr1:179138337
|
G | A | 1 | a0001c0001t0060g0042 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.158-4963C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179138337 | ||||||
| chr1:179138348
|
C | T | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-4974G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179138348 | ||||||
| chr1:179138389
|
G | A | 7 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.158-5015C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179138389 | ||||||
| chr1:179138698
|
C | T | 1 | a0001c0001t0072g0121 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.158-5324G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179138698 | ||||||
| chr1:179138744
|
G | C | 1 | a0001c0001t0001g0237 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.158-5370C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179138744 | ||||||
| chr1:179138921
|
C | T | 1 | a0001c0003t0048g0003 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.158-5547G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179138921 | ||||||
| chr1:179138946
|
A | G | 159 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(156): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.158-5572T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179138946 | ||||||
| chr1:179139112
|
A | G | 1 | a0001c0003t0053g0002 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.158-5738T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179139112 | ||||||
| chr1:179139119
|
C | T | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-5745G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179139119 | ||||||
| chr1:179139160
|
T | A | 1 | a0001c0001t0085g0234 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.158-5786A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179139160 | ||||||
| chr1:179139161
|
T | C | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-5787A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179139161 | ||||||
| chr1:179139181
|
G | C | 1 | a0001c0001t0004g0099 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.158-5807C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179139181 | ||||||
| chr1:179139215
|
C | T | 204 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.158-5841G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179139215 | ||||||
| chr1:179139327
|
A | T | 1 | a0001c0001t0085g0234 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.158-5953T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179139327 | ||||||
| chr1:179139340
|
G | A | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.158-5966C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179139340 | ||||||
| chr1:179139356
|
G | A | 2 | a0001c0001t0002g0211a0001c0001t0002g0245 | 2 | NA18946.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.158-5982C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179139356 | ||||||
| chr1:179139431
|
C | T | 25 | a0001c0003t0023g0009a0001c0003t0023g0010a0001c0003t0023g0011others(22): Show | 25 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.158-6057G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179139431 | ||||||
| chr1:179139825
|
A | T | 189 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.158-6451T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179139825 | ||||||
| chr1:179139877
|
T | C | 5 | a0001c0003t0047g0013a0001c0003t0048g0003a0001c0003t0049g0014others(2): Show | 5 | HG01106.hp1 HG01433.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-6503A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179139877 | ||||||
| chr1:179140115
|
C | T | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.158-6741G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179140115 | ||||||
| chr1:179140375
|
T | C | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-7001A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179140375 | ||||||
| chr1:179140452
|
A | G | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-7078T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179140452 | ||||||
| chr1:179140805
|
G | A | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-7431C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179140805 | ||||||
| chr1:179140852
|
C | T | 18 | a0001c0003t0023g0009a0001c0003t0023g0010a0001c0003t0023g0011others(15): Show | 18 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.158-7478G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179140852 | ||||||
| chr1:179140985
|
G | A | 1 | a0008c0012t0005g0323 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.158-7611C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179140985 | ||||||
| chr1:179140985
|
G | C | 24 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(21): Show | 24 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.158-7611C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179140985 | ||||||
| chr1:179141055
|
G | A | 5 | a0001c0001t0001g0160a0001c0001t0001g0193a0001c0001t0002g0214others(2): Show | 5 | HG00099.hp1 HG02622.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-7681C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179141055 | ||||||
| chr1:179141115
|
C | CA | 53 | a0001c0001t0001g0201a0001c0001t0001g0237a0001c0001t0001g0240others(50): Show | 53 | HG00597.hp2 HG00621.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.158-7742dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179141115 | ||||||
| chr1:179141115
|
CA | C | 11 | a0001c0001t0001g0146a0001c0001t0001g0202a0001c0001t0002g0198others(8): Show | 11 | HG00673.hp1 HG01256.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.158-7742delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179141115 | ||||||
| chr1:179141138
|
T | G | 1 | a0001c0001t0001g0203 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.158-7764A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179141138 | ||||||
| chr1:179141294
|
G | GA | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-7921dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179141294 | ||||||
| chr1:179141337
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | NA18947.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.158-7963C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179141337 | ||||||
| chr1:179141476
|
C | T | 1 | a0001c0001t0042g0249 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.158-8102G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179141476 | ||||||
| chr1:179141506
|
T | C | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-8132A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179141506 | ||||||
| chr1:179141868
|
G | A | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-8494C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179141868 | ||||||
| chr1:179141925
|
G | A | 157 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(154): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.158-8551C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179141925 | ||||||
| chr1:179142274
|
A | T | 1 | a0001c0001t0099g0301 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.158-8900T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179142274 | ||||||
| chr1:179142288
|
T | C | 3 | a0001c0001t0002g0153a0001c0001t0002g0179a0001c0001t0002g0208 | 3 | HG00438.hp1 HG02071.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.158-8914A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179142288 | ||||||
| chr1:179142355
|
T | C | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.158-8981A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179142355 | ||||||
| chr1:179142692
|
T | C | 1 | a0001c0001t0064g0053 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.158-9318A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179142692 | ||||||
| chr1:179142975
|
G | T | 4 | a0001c0001t0026g0041a0001c0001t0026g0044a0001c0001t0026g0120others(1): Show | 4 | HG03490.hp2 HG03492.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-9601C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179142975 | ||||||
| chr1:179143010
|
C | G | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.158-9636G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179143010 | ||||||
| chr1:179143300
|
G | A | 157 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(154): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.158-9926C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179143300 | ||||||
| chr1:179143442
|
C | G | 2 | a0001c0001t0001g0149a0001c0001t0002g0148 | 2 | HG00140.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.158-10068G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179143442 | ||||||
| chr1:179143683
|
C | T | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-10309G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179143683 | ||||||
| chr1:179143759
|
C | G | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-10385G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179143759 | ||||||
| chr1:179143788
|
A | C | 205 | a0001c0001t0001g0181a0001c0001t0003g0033a0001c0001t0003g0045others(202): Show | 205 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.158-10414T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179143788 | ||||||
| chr1:179143799
|
T | C | 2 | a0001c0001t0006g0038a0001c0001t0019g0067 | 2 | HG01257.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.158-10425A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179143799 | ||||||
| chr1:179143841
|
C | T | 1 | a0001c0002t0010g0266 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.158-10467G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179143841 | ||||||
| chr1:179143854
|
G | A | 3 | a0001c0001t0018g0069a0001c0001t0018g0080a0001c0001t0057g0029 | 3 | NA18942.hp1 NA18947.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.158-10480C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179143854 | ||||||
| chr1:179143957
|
A | G | 1 | a0001c0001t0005g0327 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.158-10583T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179143957 | ||||||
| chr1:179143988
|
G | T | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-10614C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179143988 | ||||||
| chr1:179144036
|
T | C | 1 | a0001c0001t0071g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.158-10662A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179144036 | ||||||
| chr1:179144172
|
T | C | 24 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(21): Show | 24 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.158-10798A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179144172 | ||||||
| chr1:179144181
|
G | C | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.158-10807C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179144181 | ||||||
| chr1:179144191
|
C | T | 2 | a0001c0001t0016g0188a0001c0001t0027g0226 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.158-10817G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179144191 | ||||||
| chr1:179144205
|
C | G | 36 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(33): Show | 36 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.158-10831G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179144205 | ||||||
| chr1:179144234
|
T | G | 157 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(154): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.158-10860A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179144234 | ||||||
| chr1:179144318
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.158-10944C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179144318 | ||||||
| chr1:179144346
|
G | A | 1 | a0001c0001t0005g0318 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.158-10972C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179144346 | ||||||
| chr1:179144373
|
A | T | 157 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(154): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.158-10999T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179144373 | ||||||
| chr1:179144391
|
T | C | 1 | a0001c0001t0005g0327 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.158-11017A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179144391 | ||||||
| chr1:179144439
|
G | A | 1 | a0001c0001t0004g0110 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.158-11065C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179144439 | ||||||
| chr1:179144683
|
AATT | A | 121 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.158-11312_158-1131 others(7): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179144683 | ||||||
| chr1:179144921
|
T | C | 1 | a0001c0001t0107g0337 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.158-11547A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179144921 | ||||||
| chr1:179144921
|
T | G | 1 | a0001c0001t0011g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.158-11547A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179144921 | ||||||
| chr1:179145093
|
A | C | 24 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(21): Show | 24 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.158-11719T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179145093 | ||||||
| chr1:179145263
|
T | C | 7 | a0001c0004t0024g0023a0001c0004t0024g0024a0001c0004t0024g0025others(4): Show | 7 | HG02615.hp2 HG02965.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.158-11889A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179145263 | ||||||
| chr1:179145430
|
T | A | 2 | a0001c0003t0030g0005a0001c0003t0030g0006 | 2 | HG00597.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.158-12056A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179145430 | ||||||
| chr1:179145521
|
A | G | 2 | a0001c0001t0002g0214a0001c0001t0002g0215 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.158-12147T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179145521 | ||||||
| chr1:179145668
|
C | G | 19 | a0001c0002t0010g0254a0001c0002t0010g0256a0001c0002t0010g0258others(16): Show | 19 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.158-12294G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179145668 | ||||||
| chr1:179145874
|
T | A | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-12500A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179145874 | ||||||
| chr1:179145888
|
G | C | 1 | a0001c0001t0021g0310 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.158-12514C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179145888 | ||||||
| chr1:179145895
|
A | AT | 288 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0167others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.158-12522dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179145895 | ||||||
| chr1:179145895
|
A | ATT | 35 | a0001c0001t0001g0150a0001c0001t0002g0179a0001c0001t0006g0081others(32): Show | 35 | HG00438.hp1 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.158-12523_158-1252 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179145895 | ||||||
| chr1:179145919
|
G | C | 3 | a0001c0001t0001g0162a0001c0008t0001g0165a0001c0008t0002g0157 | 3 | HG02145.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158-12545C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179145919 | ||||||
| chr1:179145920
|
G | T | 2 | a0001c0001t0007g0136a0001c0001t0086g0192 | 2 | NA18970.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.158-12546C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179145920 | ||||||
| chr1:179145990
|
T | C | 1 | a0001c0002t0010g0267 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.158-12616A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179145990 | ||||||
| chr1:179146350
|
C | T | 154 | a0001c0001t0001g0181a0001c0001t0003g0033a0001c0001t0003g0045others(151): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.158-12976G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179146350 | ||||||
| chr1:179146361
|
T | A | 1 | a0001c0001t0009g0279 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.158-12987A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179146361 | ||||||
| chr1:179146543
|
A | C | 1 | a0001c0001t0109g0326 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.158-13169T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179146543 | ||||||
| chr1:179146817
|
A | G | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-13443T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179146817 | ||||||
| chr1:179146829
|
A | G | 1 | a0002c0005t0022g0276 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.158-13455T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179146829 | ||||||
| chr1:179146910
|
A | G | 1 | a0001c0001t0003g0094 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.158-13536T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179146910 | ||||||
| chr1:179146960
|
T | C | 1 | a0001c0001t0061g0031 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.158-13586A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179146960 | ||||||
| chr1:179147054
|
C | T | 1 | a0001c0001t0004g0100 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.158-13680G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147054 | ||||||
| chr1:179147090
|
A | T | 1 | a0001c0001t0091g0312 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.158-13716T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147090 | ||||||
| chr1:179147110
|
T | TCCAAAGA others(14): Show |
2 | a0001c0001t0032g0026a0001c0001t0032g0027 | 2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.158-13757_158-1373 others(25): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147110 | ||||||
| chr1:179147181
|
C | CA | 78 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0001g0161others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.158-13808dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147181 | ||||||
| chr1:179147181
|
C | CAA | 92 | a0001c0001t0001g0144a0001c0001t0001g0160a0001c0001t0001g0162others(89): Show | 92 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.158-13809_158-1380 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147181 | ||||||
| chr1:179147181
|
C | CAAA | 38 | a0001c0001t0001g0193a0001c0001t0001g0241a0001c0001t0003g0096others(35): Show | 38 | HG00408.hp2 HG00544.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.158-13810_158-1380 others(7): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147181 | ||||||
| chr1:179147181
|
C | CAAAA | 20 | a0001c0001t0005g0315a0001c0001t0005g0317a0001c0001t0008g0288others(17): Show | 20 | HG00735.hp1 HG01175.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.158-13811_158-1380 others(8): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147181 | ||||||
| chr1:179147181
|
C | CAAAAA | 9 | a0001c0001t0008g0299a0001c0001t0041g0250a0001c0001t0041g0251others(6): Show | 9 | HG01496.hp1 HG01884.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.158-13812_158-1380 others(9): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147181 | ||||||
| chr1:179147181
|
C | CAAAAAA | 11 | a0001c0003t0023g0009a0001c0003t0028g0001a0001c0003t0028g0016others(8): Show | 11 | HG01071.hp1 HG01106.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.158-13813_158-1380 others(10): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147181 | ||||||
| chr1:179147181
|
C | CAAAAAAA | 10 | a0001c0001t0012g0063a0001c0003t0023g0010a0001c0003t0023g0011others(7): Show | 10 | HG00597.hp2 HG01070.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.158-13814_158-1380 others(11): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147181 | ||||||
| chr1:179147181
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0077g0142a0001c0001t0078g0143a0001c0001t0096g0306 | 3 | HG01891.hp1 HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.158-13818_158-1380 others(15): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147181 | ||||||
| chr1:179147181
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0097g0304 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.158-13821_158-1380 others(18): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147181 | ||||||
| chr1:179147181
|
CAAAAAAA others(4): Show |
C | 24 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(21): Show | 24 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.158-13818_158-1380 others(15): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147181 | ||||||
| chr1:179147301
|
T | C | 1 | a0001c0001t0007g0130 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.158-13927A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147301 | ||||||
| chr1:179147314
|
A | G | 1 | a0001c0001t0018g0080 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.158-13940T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147314 | ||||||
| chr1:179147339
|
C | G | 154 | a0001c0001t0001g0181a0001c0001t0003g0033a0001c0001t0003g0045others(151): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.158-13965G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147339 | ||||||
| chr1:179147419
|
T | G | 7 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0244others(4): Show | 7 | HG00621.hp2 HG03669.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.158-14045A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147419 | ||||||
| chr1:179147649
|
C | T | 205 | a0001c0001t0001g0181a0001c0001t0003g0033a0001c0001t0003g0045others(202): Show | 205 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.158-14275G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147649 | ||||||
| chr1:179147660
|
C | T | 2 | a0004c0009t0039g0145a0004c0009t0039g0147 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.158-14286G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147660 | ||||||
| chr1:179147867
|
A | G | 205 | a0001c0001t0001g0181a0001c0001t0003g0033a0001c0001t0003g0045others(202): Show | 205 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.158-14493T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147867 | ||||||
| chr1:179147966
|
G | A | 205 | a0001c0001t0001g0181a0001c0001t0003g0033a0001c0001t0003g0045others(202): Show | 205 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.158-14592C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179147966 | ||||||
| chr1:179148039
|
C | CT | 178 | a0001c0001t0001g0181a0001c0001t0003g0033a0001c0001t0003g0045others(175): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.158-14666dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179148039 | ||||||
| chr1:179148039
|
C | CTT | 7 | a0001c0001t0008g0288a0001c0001t0013g0065a0001c0001t0033g0062others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.158-14667_158-1466 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179148039 | ||||||
| chr1:179148039
|
CT | C | 7 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0020g0155others(4): Show | 7 | HG02055.hp1 HG02451.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.158-14666delA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179148039 | ||||||
| chr1:179148318
|
G | A | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.158-14944C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179148318 | ||||||
| chr1:179148531
|
T | C | 7 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.158-15157A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179148531 | ||||||
| chr1:179148605
|
C | T | 153 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(150): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.158-15231G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179148605 | ||||||
| chr1:179148849
|
G | T | 2 | a0001c0001t0006g0092a0001c0001t0014g0115 | 2 | NA18946.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.158-15475C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179148849 | ||||||
| chr1:179148900
|
GA | G | 58 | a0001c0001t0004g0048a0001c0001t0012g0063a0001c0001t0021g0307others(55): Show | 58 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.158-15527delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179148900 | ||||||
| chr1:179148912
|
AAG | A | 95 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(92): Show | 95 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.158-15540_158-1553 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179148912 | ||||||
| chr1:179148915
|
GA | G | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-15542delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179148915 | ||||||
| chr1:179148916
|
A | G | 95 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(92): Show | 95 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.158-15542T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179148916 | ||||||
| chr1:179149023
|
G | A | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-15649C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179149023 | ||||||
| chr1:179149088
|
T | C | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-15714A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179149088 | ||||||
| chr1:179149213
|
C | T | 1 | a0001c0002t0095g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.158-15839G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179149213 | ||||||
| chr1:179149327
|
G | A | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.158-15953C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179149327 | ||||||
| chr1:179149621
|
A | C | 1 | a0001c0001t0014g0034 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.158-16247T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179149621 | ||||||
| chr1:179149623
|
C | T | 325 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0159others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.158-16249G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179149623 | ||||||
| chr1:179149667
|
A | G | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-16293T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179149667 | ||||||
| chr1:179149929
|
T | A | 1 | a0001c0001t0025g0043 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.158-16555A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179149929 | ||||||
| chr1:179150013
|
C | T | 1 | a0001c0001t0042g0249 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.158-16639G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179150013 | ||||||
| chr1:179150066
|
T | TA | 7 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.158-16693dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179150066 | ||||||
| chr1:179150109
|
G | A | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.158-16735C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179150109 | ||||||
| chr1:179150227
|
G | A | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-16853C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179150227 | ||||||
| chr1:179150561
|
G | T | 31 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(28): Show | 31 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.158-17187C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179150561 | ||||||
| chr1:179150631
|
G | A | 1 | a0001c0002t0017g0257 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.158-17257C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179150631 | ||||||
| chr1:179150829
|
TTG | T | 5 | a0001c0001t0018g0064a0001c0001t0018g0112a0001c0001t0060g0042others(2): Show | 5 | HG00621.hp1 NA18967.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-17457_158-1745 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179150829 | ||||||
| chr1:179150833
|
CTTATT | C | 24 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(21): Show | 24 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.158-17464_158-1746 others(9): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179150833 | ||||||
| chr1:179150873
|
C | T | 4 | a0001c0001t0001g0237a0001c0001t0002g0232a0001c0001t0036g0207others(1): Show | 4 | HG03704.hp1 HG03831.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-17499G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179150873 | ||||||
| chr1:179151299
|
C | A | 1 | a0001c0004t0024g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.158-17925G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179151299 | ||||||
| chr1:179151421
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0202 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.158-18047G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179151421 | ||||||
| chr1:179151660
|
A | C | 120 | a0001c0001t0001g0181a0001c0001t0003g0033a0001c0001t0003g0045others(117): Show | 120 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.158-18286T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179151660 | ||||||
| chr1:179152065
|
G | A | 4 | a0001c0001t0008g0282a0001c0001t0008g0298a0001c0001t0009g0285others(1): Show | 4 | HG01081.hp1 HG01167.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-18691C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179152065 | ||||||
| chr1:179152111
|
T | G | 2 | a0001c0001t0069g0056a0001c0001t0070g0078 | 2 | NA18961.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.158-18737A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179152111 | ||||||
| chr1:179152145
|
G | A | 56 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(53): Show | 56 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.158-18771C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179152145 | ||||||
| chr1:179152254
|
C | T | 3 | a0001c0001t0002g0153a0001c0001t0002g0179a0001c0001t0002g0208 | 3 | HG00438.hp1 HG02071.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.158-18880G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179152254 | ||||||
| chr1:179152563
|
C | T | 2 | a0001c0001t0008g0297a0001c0001t0009g0284 | 2 | NA18940.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.158-19189G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179152563 | ||||||
| chr1:179152736
|
A | C | 1 | a0001c0001t0006g0074 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.158-19362T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179152736 | ||||||
| chr1:179152995
|
G | A | 1 | a0001c0001t0005g0342 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.158-19621C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179152995 | ||||||
| chr1:179153124
|
G | T | 7 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.158-19750C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179153124 | ||||||
| chr1:179153128
|
G | C | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.158-19754C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179153128 | ||||||
| chr1:179153145
|
C | T | 1 | a0001c0001t0087g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.158-19771G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179153145 | ||||||
| chr1:179153173
|
C | T | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-19799G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179153173 | ||||||
| chr1:179153324
|
G | C | 13 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0297others(10): Show | 13 | HG01081.hp1 HG01167.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.158-19950C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179153324 | ||||||
| chr1:179153590
|
T | C | 186 | a0001c0001t0001g0181a0001c0001t0003g0033a0001c0001t0003g0045others(183): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.158-20216A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179153590 | ||||||
| chr1:179153644
|
T | C | 156 | a0001c0001t0001g0181a0001c0001t0003g0033a0001c0001t0003g0045others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.158-20270A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179153644 | ||||||
| chr1:179153673
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.158-20299A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179153673 | ||||||
| chr1:179153855
|
A | G | 3 | a0001c0001t0004g0083a0001c0001t0004g0100a0001c0001t0073g0122 | 3 | HG02257.hp2 HG03831.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.158-20481T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179153855 | ||||||
| chr1:179153888
|
TTTTGTTC others(10): Show |
T | 18 | a0001c0002t0010g0254a0001c0002t0010g0256a0001c0002t0010g0258others(15): Show | 18 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.158-20531_158-2051 others(21): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179153888 | ||||||
| chr1:179154053
|
A | G | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.158-20679T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179154053 | ||||||
| chr1:179154082
|
C | T | 1 | a0001c0001t0011g0344 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.158-20708G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179154082 | ||||||
| chr1:179154459
|
C | G | 1 | a0001c0002t0095g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.158-21085G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179154459 | ||||||
| chr1:179154890
|
C | T | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.158-21516G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179154890 | ||||||
| chr1:179154902
|
T | C | 1 | a0001c0001t0014g0115 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.158-21528A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179154902 | ||||||
| chr1:179155132
|
C | T | 1 | a0001c0001t0009g0285 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.158-21758G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179155132 | ||||||
| chr1:179155137
|
T | C | 1 | a0001c0004t0058g0028 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.158-21763A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179155137 | ||||||
| chr1:179155155
|
G | A | 5 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(2): Show | 5 | HG01069.hp1 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-21781C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179155155 | ||||||
| chr1:179155255
|
T | A | 1 | a0001c0001t0042g0249 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.158-21881A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179155255 | ||||||
| chr1:179155265
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.158-21891C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179155265 | ||||||
| chr1:179155267
|
T | C | 1 | a0001c0001t0042g0249 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.158-21893A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179155267 | ||||||
| chr1:179155276
|
G | A | 24 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(21): Show | 24 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.158-21902C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179155276 | ||||||
| chr1:179155288
|
A | C | 3 | a0001c0001t0001g0160a0001c0001t0001g0193a0001c0001t0036g0229 | 3 | HG00099.hp1 HG03239.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.158-21914T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179155288 | ||||||
| chr1:179155302
|
G | A | 2 | a0001c0001t0003g0047a0001c0001t0004g0046 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.158-21928C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179155302 | ||||||
| chr1:179155338
|
A | G | 3 | a0001c0001t0001g0169a0001c0001t0001g0190a0001c0001t0001g0199 | 3 | HG02809.hp2 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.158-21964T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179155338 | ||||||
| chr1:179155591
|
C | T | 1 | a0001c0001t0002g0198 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.158-22217G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179155591 | ||||||
| chr1:179155602
|
A | G | 62 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(59): Show | 62 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.158-22228T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179155602 | ||||||
| chr1:179155663
|
A | G | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-22289T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179155663 | ||||||
| chr1:179155720
|
G | C | 6 | a0001c0001t0008g0283a0001c0001t0008g0297a0001c0001t0009g0279others(3): Show | 6 | NA18940.hp2 NA18945.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.158-22346C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179155720 | ||||||
| chr1:179155725
|
C | T | 7 | a0001c0001t0005g0345a0001c0001t0011g0341a0001c0001t0045g0338others(4): Show | 7 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.158-22351G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179155725 | ||||||
| chr1:179155734
|
TA | T | 112 | a0001c0001t0001g0146a0001c0001t0001g0178a0001c0001t0002g0246others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.158-22361delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179155734 | ||||||
| chr1:179155915
|
G | C | 1 | a0001c0001t0001g0170 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.158-22541C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179155915 | ||||||
| chr1:179156030
|
C | A | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-22656G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179156030 | ||||||
| chr1:179156166
|
C | G | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-22792G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179156166 | ||||||
| chr1:179156316
|
C | T | 25 | a0001c0003t0023g0009a0001c0003t0023g0010a0001c0003t0023g0011others(22): Show | 25 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.158-22942G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179156316 | ||||||
| chr1:179156325
|
C | T | 1 | a0001c0001t0091g0312 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.158-22951G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179156325 | ||||||
| chr1:179156406
|
T | C | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-23032A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179156406 | ||||||
| chr1:179156527
|
T | C | 3 | a0001c0001t0005g0315a0001c0001t0005g0316a0001c0001t0005g0317 | 3 | NA18943.hp1 NA19064.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.158-23153A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179156527 | ||||||
| chr1:179156532
|
T | C | 2 | a0001c0001t0043g0259a0001c0001t0043g0260 | 2 | HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.158-23158A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179156532 | ||||||
| chr1:179156696
|
C | G | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.158-23322G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179156696 | ||||||
| chr1:179156835
|
G | A | 1 | a0001c0003t0053g0002 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.158-23461C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179156835 | ||||||
| chr1:179156882
|
A | AAAAT | 3 | a0001c0001t0001g0199a0001c0001t0090g0305a0001c0003t0030g0005 | 3 | HG00597.hp2 HG02602.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.158-23512_158-2350 others(8): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179156882 | ||||||
| chr1:179156882
|
AAAAT | A | 92 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0238others(89): Show | 92 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.158-23512_158-2350 others(8): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179156882 | ||||||
| chr1:179156882
|
AAAATAAA others(1): Show |
A | 106 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.158-23516_158-2350 others(12): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179156882 | ||||||
| chr1:179156882
|
AAAATAAA others(5): Show |
A | 19 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0006g0035others(16): Show | 19 | HG00673.hp2 HG01069.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.158-23520_158-2350 others(16): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179156882 | ||||||
| chr1:179156882
|
AAAATAAA others(9): Show |
A | 94 | a0001c0001t0001g0177a0001c0001t0003g0033a0001c0001t0003g0045others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.158-23524_158-2350 others(20): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179156882 | ||||||
| chr1:179156882
|
AAAATAAA others(13): Show |
A | 5 | a0001c0001t0003g0094a0002c0005t0022g0253a0002c0005t0022g0275others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-23528_158-2350 others(24): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179156882 | ||||||
| chr1:179156972
|
A | G | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.158-23598T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179156972 | ||||||
| chr1:179157017
|
C | T | 1 | a0001c0001t0004g0085 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.158-23643G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179157017 | ||||||
| chr1:179157260
|
T | G | 1 | a0001c0001t0006g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.158-23886A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179157260 | ||||||
| chr1:179157414
|
T | C | 5 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(2): Show | 5 | HG01069.hp1 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-24040A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179157414 | ||||||
| chr1:179157494
|
C | CA | 11 | a0001c0001t0001g0159a0001c0001t0001g0175a0001c0001t0001g0177others(8): Show | 11 | HG00438.hp2 HG02523.hp1 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.158-24121dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179157494 | ||||||
| chr1:179157572
|
C | T | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-24198G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179157572 | ||||||
| chr1:179157602
|
T | C | 1 | a0001c0001t0002g0163 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.158-24228A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179157602 | ||||||
| chr1:179157615
|
A | G | 1 | a0001c0001t0104g0278 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.158-24241T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179157615 | ||||||
| chr1:179157692
|
G | C | 3 | a0001c0001t0001g0160a0001c0001t0001g0193a0001c0001t0036g0229 | 3 | HG00099.hp1 HG03239.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.158-24318C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179157692 | ||||||
| chr1:179157705
|
A | C | 1 | a0001c0001t0002g0163 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.158-24331T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179157705 | ||||||
| chr1:179157707
|
C | CT | 119 | a0001c0001t0001g0181a0001c0001t0003g0033a0001c0001t0003g0045others(116): Show | 119 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.158-24334dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179157707 | ||||||
| chr1:179157707
|
C | CTT | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.158-24335_158-2433 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179157707 | ||||||
| chr1:179157892
|
T | G | 12 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(9): Show | 12 | HG01099.hp1 HG02145.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.158-24518A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179157892 | ||||||
| chr1:179157966
|
C | T | 5 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(2): Show | 5 | HG01069.hp1 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-24592G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179157966 | ||||||
| chr1:179158200
|
A | G | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.158-24826T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179158200 | ||||||
| chr1:179158375
|
G | C | 1 | a0001c0001t0001g0161 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.158-25001C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179158375 | ||||||
| chr1:179158528
|
C | A | 1 | a0001c0001t0056g0020 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.158-25154G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179158528 | ||||||
| chr1:179158557
|
G | A | 1 | a0001c0002t0095g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.158-25183C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179158557 | ||||||
| chr1:179158603
|
G | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0170 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.158-25229C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179158603 | ||||||
| chr1:179158743
|
T | C | 2 | a0001c0001t0077g0142a0001c0001t0078g0143 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.158-25369A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179158743 | ||||||
| chr1:179158809
|
G | A | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.158-25435C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179158809 | ||||||
| chr1:179158887
|
C | T | 1 | a0001c0001t0009g0279 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.158-25513G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179158887 | ||||||
| chr1:179159054
|
T | C | 1 | a0001c0001t0006g0118 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.158-25680A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179159054 | ||||||
| chr1:179159240
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.158-25866A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179159240 | ||||||
| chr1:179159644
|
C | A | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.158-26270G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179159644 | ||||||
| chr1:179159719
|
G | A | 1 | a0001c0001t0021g0310 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.158-26345C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179159719 | ||||||
| chr1:179159760
|
T | C | 1 | a0001c0002t0010g0266 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.158-26386A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179159760 | ||||||
| chr1:179159838
|
G | A | 1 | a0001c0001t0014g0079 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.158-26464C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179159838 | ||||||
| chr1:179159876
|
G | A | 2 | a0001c0003t0028g0001a0001c0003t0028g0016 | 2 | NA18991.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.158-26502C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179159876 | ||||||
| chr1:179159880
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.158-26506T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179159880 | ||||||
| chr1:179159929
|
C | T | 1 | a0001c0008t0002g0157 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.158-26555G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179159929 | ||||||
| chr1:179159969
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.158-26595G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179159969 | ||||||
| chr1:179160274
|
G | A | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.158-26900C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179160274 | ||||||
| chr1:179160338
|
A | AC | 97 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.158-26965dupG | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179160338 | ||||||
| chr1:179160395
|
G | C | 1 | a0001c0004t0058g0028 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.158-27021C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179160395 | ||||||
| chr1:179160485
|
G | A | 1 | a0001c0004t0024g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.158-27111C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179160485 | ||||||
| chr1:179160531
|
G | A | 9 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0004t0024g0023others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.158-27157C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179160531 | ||||||
| chr1:179160546
|
G | C | 1 | a0001c0001t0006g0118 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.158-27172C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179160546 | ||||||
| chr1:179160659
|
AT | A | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.158-27286delA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179160659 | ||||||
| chr1:179160787
|
T | G | 1 | a0001c0001t0002g0163 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.158-27413A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179160787 | ||||||
| chr1:179161224
|
T | C | 50 | a0001c0001t0005g0315a0001c0001t0005g0316a0001c0001t0005g0317others(47): Show | 50 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.158-27850A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179161224 | ||||||
| chr1:179161311
|
A | T | 2 | a0003c0006t0001g0151a0003c0006t0001g0209 | 2 | NA18985.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.158-27937T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179161311 | ||||||
| chr1:179161356
|
G | GA | 180 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(177): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.158-27983dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179161356 | ||||||
| chr1:179161448
|
C | T | 1 | a0001c0001t0002g0163 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.158-28074G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179161448 | ||||||
| chr1:179161534
|
A | T | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.158-28160T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179161534 | ||||||
| chr1:179161734
|
T | C | 1 | a0001c0001t0015g0127 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.158-28360A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179161734 | ||||||
| chr1:179161771
|
G | A | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-28397C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179161771 | ||||||
| chr1:179161813
|
A | C | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.158-28439T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179161813 | ||||||
| chr1:179161822
|
G | A | 1 | a0001c0001t0006g0118 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.158-28448C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179161822 | ||||||
| chr1:179162004
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.158-28630C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179162004 | ||||||
| chr1:179162142
|
C | G | 1 | a0001c0001t0005g0335 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.158-28768G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179162142 | ||||||
| chr1:179162382
|
C | G | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.158-29008G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179162382 | ||||||
| chr1:179162458
|
G | A | 28 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0001t0055g0012others(25): Show | 28 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.158-29084C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179162458 | ||||||
| chr1:179162480
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0036g0229 | 2 | HG00099.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.158-29106C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179162480 | ||||||
| chr1:179162493
|
G | A | 1 | a0001c0001t0021g0309 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.158-29119C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179162493 | ||||||
| chr1:179162500
|
G | A | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.158-29126C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179162500 | ||||||
| chr1:179162511
|
G | C | 28 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0001t0055g0012others(25): Show | 28 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.158-29137C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179162511 | ||||||
| chr1:179162571
|
C | T | 1 | a0001c0001t0006g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.158-29197G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179162571 | ||||||
| chr1:179162575
|
ACT | A | 5 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(2): Show | 5 | HG01069.hp1 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-29203_158-2920 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179162575 | ||||||
| chr1:179162585
|
T | C | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.158-29211A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179162585 | ||||||
| chr1:179162586
|
A | T | 97 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.158-29212T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179162586 | ||||||
| chr1:179162915
|
T | C | 1 | a0001c0001t0002g0232 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.158-29541A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179162915 | ||||||
| chr1:179162962
|
T | C | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.158-29588A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179162962 | ||||||
| chr1:179163416
|
C | A | 1 | a0001c0001t0001g0244 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.158-30042G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179163416 | ||||||
| chr1:179163573
|
C | T | 97 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.158-30199G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179163573 | ||||||
| chr1:179163620
|
A | G | 1 | a0001c0002t0017g0257 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.158-30246T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179163620 | ||||||
| chr1:179163684
|
T | C | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.158-30310A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179163684 | ||||||
| chr1:179163742
|
G | A | 1 | a0001c0001t0006g0118 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.158-30368C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179163742 | ||||||
| chr1:179164086
|
T | A | 162 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.158-30712A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179164086 | ||||||
| chr1:179164218
|
A | G | 24 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(21): Show | 24 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.158-30844T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179164218 | ||||||
| chr1:179164306
|
T | C | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-30932A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179164306 | ||||||
| chr1:179164315
|
T | C | 28 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0001t0055g0012others(25): Show | 28 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.158-30941A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179164315 | ||||||
| chr1:179164593
|
A | G | 1 | a0001c0002t0093g0274 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.158-31219T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179164593 | ||||||
| chr1:179164613
|
T | C | 19 | a0001c0001t0055g0012a0001c0003t0023g0009a0001c0003t0023g0010others(16): Show | 19 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.158-31239A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179164613 | ||||||
| chr1:179164890
|
A | C | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-31516T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179164890 | ||||||
| chr1:179165152
|
T | C | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-31778A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179165152 | ||||||
| chr1:179165372
|
AG | A | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-31999delC | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179165372 | ||||||
| chr1:179165419
|
C | T | 1 | a0001c0002t0017g0269 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.158-32045G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179165419 | ||||||
| chr1:179165640
|
T | C | 1 | a0001c0001t0099g0301 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.158-32266A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179165640 | ||||||
| chr1:179165798
|
TA | T | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-32425delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179165798 | ||||||
| chr1:179165799
|
AT | A | 181 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(178): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.158-32426delA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179165799 | ||||||
| chr1:179165848
|
T | G | 1 | a0001c0001t0012g0051 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.158-32474A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179165848 | ||||||
| chr1:179165849
|
G | A | 1 | a0001c0001t0003g0059 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.158-32475C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179165849 | ||||||
| chr1:179165859
|
G | A | 50 | a0001c0001t0005g0315a0001c0001t0005g0316a0001c0001t0005g0317others(47): Show | 50 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.158-32485C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179165859 | ||||||
| chr1:179165952
|
C | T | 1 | a0001c0003t0052g0015 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.158-32578G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179165952 | ||||||
| chr1:179165985
|
C | T | 24 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(21): Show | 24 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.158-32611G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179165985 | ||||||
| chr1:179166196
|
T | C | 3 | a0001c0001t0005g0332a0001c0001t0011g0344a0001c0001t0105g0333 | 3 | NA18979.hp2 NA19054.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.158-32822A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179166196 | ||||||
| chr1:179166342
|
TCATCTTA others(8): Show |
T | 1 | a0001c0001t0006g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.158-32983_158-3296 others(19): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179166342 | ||||||
| chr1:179166394
|
TA | T | 75 | a0001c0001t0001g0169a0001c0001t0001g0190a0001c0001t0001g0199others(72): Show | 75 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.158-33021delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179166394 | ||||||
| chr1:179166394
|
TAA | T | 45 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(42): Show | 45 | HG00597.hp2 HG01081.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.158-33022_158-3302 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179166394 | ||||||
| chr1:179166395
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.158-33021T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179166395 | ||||||
| chr1:179166505
|
G | A | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-33131C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179166505 | ||||||
| chr1:179166593
|
A | G | 1 | a0001c0001t0020g0155 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.158-33219T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179166593 | ||||||
| chr1:179166700
|
C | T | 11 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(8): Show | 11 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.158-33326G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179166700 | ||||||
| chr1:179166776
|
C | CA | 93 | a0001c0001t0003g0033a0001c0001t0003g0047a0001c0001t0003g0052others(90): Show | 93 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.158-33403dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179166776 | ||||||
| chr1:179166776
|
CA | C | 6 | a0001c0001t0001g0202a0001c0001t0001g0238a0001c0001t0005g0342others(3): Show | 6 | HG01169.hp1 HG01256.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.158-33403delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179166776 | ||||||
| chr1:179167134
|
G | C | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.158-33760C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179167134 | ||||||
| chr1:179167588
|
T | C | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-34214A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179167588 | ||||||
| chr1:179167621
|
C | T | 1 | a0001c0002t0095g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.158-34247G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179167621 | ||||||
| chr1:179167915
|
G | A | 1 | a0001c0001t0005g0327 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.158-34541C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179167915 | ||||||
| chr1:179167945
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.158-34571G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179167945 | ||||||
| chr1:179167949
|
A | T | 1 | a0001c0001t0001g0241 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.158-34575T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179167949 | ||||||
| chr1:179168003
|
A | G | 23 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(20): Show | 23 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.158-34629T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179168003 | ||||||
| chr1:179168329
|
A | G | 1 | a0001c0001t0007g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.158-34955T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179168329 | ||||||
| chr1:179168397
|
G | A | 1 | a0001c0001t0009g0286 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.158-35023C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179168397 | ||||||
| chr1:179168680
|
C | T | 1 | a0001c0003t0051g0017 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.158-35306G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179168680 | ||||||
| chr1:179168714
|
A | C | 207 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(204): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.158-35340T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179168714 | ||||||
| chr1:179168720
|
G | A | 1 | a0001c0001t0020g0155 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.158-35346C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179168720 | ||||||
| chr1:179168884
|
G | A | 1 | a0001c0001t0005g0320 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.158-35510C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179168884 | ||||||
| chr1:179168942
|
G | A | 1 | a0001c0001t0099g0301 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.158-35568C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179168942 | ||||||
| chr1:179169287
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.158-35913C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179169287 | ||||||
| chr1:179169374
|
C | T | 2 | a0001c0001t0091g0312a0007c0015t0092g0313 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.158-36000G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179169374 | ||||||
| chr1:179169413
|
T | C | 1 | a0005c0010t0006g0055 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.158-36039A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179169413 | ||||||
| chr1:179169421
|
A | G | 192 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(189): Show | 192 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.158-36047T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179169421 | ||||||
| chr1:179169473
|
G | A | 97 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.158-36099C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179169473 | ||||||
| chr1:179169501
|
T | C | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-36127A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179169501 | ||||||
| chr1:179169517
|
C | T | 327 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0159others(324): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.158-36143G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179169517 | ||||||
| chr1:179169935
|
G | A | 3 | a0001c0001t0018g0069a0001c0001t0018g0080a0001c0001t0057g0029 | 3 | NA18942.hp1 NA18947.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.158-36561C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179169935 | ||||||
| chr1:179170043
|
C | G | 1 | a0001c0001t0002g0232 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.158-36669G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179170043 | ||||||
| chr1:179170230
|
A | C | 1 | a0001c0001t0005g0327 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.158-36856T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179170230 | ||||||
| chr1:179170421
|
G | A | 207 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(204): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.158-37047C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179170421 | ||||||
| chr1:179170510
|
G | A | 9 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0004t0024g0023others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.158-37136C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179170510 | ||||||
| chr1:179170627
|
G | A | 1 | a0001c0001t0091g0312 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.158-37253C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179170627 | ||||||
| chr1:179170657
|
C | T | 5 | a0001c0001t0005g0331a0001c0001t0041g0250a0001c0001t0041g0251others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-37283G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179170657 | ||||||
| chr1:179170753
|
C | A | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-37379G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179170753 | ||||||
| chr1:179170798
|
T | C | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.158-37424A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179170798 | ||||||
| chr1:179170810
|
G | C | 1 | a0001c0001t0019g0119 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.158-37436C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179170810 | ||||||
| chr1:179170887
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.158-37513C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179170887 | ||||||
| chr1:179171007
|
A | G | 9 | a0001c0001t0003g0086a0001c0001t0003g0089a0001c0001t0006g0092others(6): Show | 9 | NA18946.hp2 NA18954.hp2 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.158-37633T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179171007 | ||||||
| chr1:179171010
|
C | G | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.158-37636G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179171010 | ||||||
| chr1:179171043
|
T | C | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.158-37669A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179171043 | ||||||
| chr1:179171102
|
A | G | 1 | a0001c0001t0067g0102 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.158-37728T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179171102 | ||||||
| chr1:179171137
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.158-37763G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179171137 | ||||||
| chr1:179171362
|
T | G | 1 | a0001c0001t0002g0184 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.158-37988A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179171362 | ||||||
| chr1:179171515
|
C | T | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-38141G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179171515 | ||||||
| chr1:179171563
|
C | T | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.158-38189G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179171563 | ||||||
| chr1:179171594
|
C | T | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-38220G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179171594 | ||||||
| chr1:179171893
|
T | C | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-38519A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179171893 | ||||||
| chr1:179172155
|
T | C | 3 | a0001c0001t0005g0332a0001c0001t0011g0344a0001c0001t0105g0333 | 3 | NA18979.hp2 NA19054.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.158-38781A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179172155 | ||||||
| chr1:179172194
|
G | T | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-38820C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179172194 | ||||||
| chr1:179172353
|
T | C | 7 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.158-38979A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179172353 | ||||||
| chr1:179172594
|
A | C | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-39220T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179172594 | ||||||
| chr1:179172630
|
G | A | 2 | a0003c0006t0001g0187a0003c0006t0001g0205 | 2 | NA18952.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.158-39256C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179172630 | ||||||
| chr1:179172775
|
G | A | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.158-39401C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179172775 | ||||||
| chr1:179173009
|
T | G | 207 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(204): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.158-39635A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179173009 | ||||||
| chr1:179173017
|
C | T | 1 | a0001c0001t0004g0083 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.158-39643G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179173017 | ||||||
| chr1:179173168
|
C | T | 1 | a0001c0001t0091g0312 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.158-39794G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179173168 | ||||||
| chr1:179173190
|
C | CA | 9 | a0001c0001t0001g0193a0001c0001t0003g0094a0001c0001t0008g0297others(6): Show | 9 | HG02135.hp2 HG02258.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.158-39817dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179173190 | ||||||
| chr1:179173190
|
CA | C | 11 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0054others(8): Show | 11 | HG00099.hp2 HG00639.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.158-39817delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179173190 | ||||||
| chr1:179173358
|
A | AT | 33 | a0001c0001t0001g0162a0001c0001t0001g0237a0001c0001t0002g0153others(30): Show | 33 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.158-39985dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179173358 | ||||||
| chr1:179173358
|
A | ATT | 25 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(22): Show | 25 | HG00735.hp1 HG01081.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.158-39986_158-3998 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179173358 | ||||||
| chr1:179173358
|
AT | A | 51 | a0001c0001t0001g0144a0001c0001t0001g0170a0001c0001t0002g0214others(48): Show | 51 | HG00597.hp2 HG00735.hp2 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.158-39985delA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179173358 | ||||||
| chr1:179173358
|
ATT | A | 108 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(105): Show | 108 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.158-39986_158-3998 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179173358 | ||||||
| chr1:179173425
|
C | T | 2 | a0001c0001t0012g0039a0001c0001t0065g0037 | 2 | HG01106.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.158-40051G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179173425 | ||||||
| chr1:179173426
|
G | A | 10 | a0001c0002t0010g0254a0001c0002t0010g0256a0001c0002t0010g0258others(7): Show | 10 | HG00544.hp2 HG02015.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-40052C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179173426 | ||||||
| chr1:179173514
|
C | T | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.158-40140G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179173514 | ||||||
| chr1:179173522
|
C | CCAGCTAA others(4): Show |
51 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(48): Show | 51 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.158-40149_158-4014 others(15): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179173522 | ||||||
| chr1:179173560
|
C | A | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-40186G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179173560 | ||||||
| chr1:179173759
|
G | A | 7 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.158-40385C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179173759 | ||||||
| chr1:179173835
|
T | C | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.158-40461A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179173835 | ||||||
| chr1:179173854
|
C | T | 1 | a0001c0001t0025g0043 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.158-40480G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179173854 | ||||||
| chr1:179173941
|
CACCT | C | 96 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.158-40571_158-4056 others(8): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179173941 | ||||||
| chr1:179173949
|
T | C | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-40575A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179173949 | ||||||
| chr1:179174027
|
C | A | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.158-40653G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174027 | ||||||
| chr1:179174046
|
T | C | 6 | a0001c0001t0096g0306a0001c0001t0097g0304a0002c0005t0022g0253others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.158-40672A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174046 | ||||||
| chr1:179174056
|
G | A | 1 | a0001c0001t0011g0343 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.158-40682C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174056 | ||||||
| chr1:179174143
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.158-40769G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174143 | ||||||
| chr1:179174166
|
T | C | 2 | a0001c0001t0055g0012a0001c0003t0046g0019 | 2 | NA18943.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.158-40792A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174166 | ||||||
| chr1:179174266
|
C | T | 1 | a0001c0001t0027g0195 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.158-40892G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174266 | ||||||
| chr1:179174291
|
T | TA | 7 | a0001c0001t0002g0153a0001c0001t0006g0074a0001c0001t0038g0216others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.158-40918dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174291 | ||||||
| chr1:179174471
|
G | T | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.158-41097C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174471 | ||||||
| chr1:179174532
|
G | GTGTGTGT others(25): Show |
1 | a0001c0001t0002g0242 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.158-41190_158-4115 others(36): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174532 | ||||||
| chr1:179174661
|
C | T | 187 | a0001c0001t0002g0230a0001c0001t0003g0033a0001c0001t0003g0045others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.158-41287G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174661 | ||||||
| chr1:179174700
|
C | A | 3 | a0001c0001t0077g0142a0001c0001t0078g0143a0001c0001t0099g0301 | 3 | HG01891.hp1 HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.158-41326G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174700 | ||||||
| chr1:179174901
|
AAAAAAAA others(6): Show |
A | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.158-41540_158-4152 others(17): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174901 | ||||||
| chr1:179174904
|
AAAAAT | A | 23 | a0001c0001t0002g0230a0001c0001t0003g0052a0001c0001t0003g0072others(20): Show | 23 | HG00408.hp1 HG00735.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.158-41535_158-4153 others(9): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174904 | ||||||
| chr1:179174905
|
A | T | 5 | a0001c0001t0001g0160a0001c0001t0001g0193a0001c0001t0002g0214others(2): Show | 5 | HG00099.hp1 HG02622.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-41531T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174905 | ||||||
| chr1:179174905
|
AAAAT | A | 50 | a0001c0001t0004g0040a0001c0001t0008g0282a0001c0001t0008g0287others(47): Show | 50 | HG00544.hp2 HG00639.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.158-41535_158-4153 others(8): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174905 | ||||||
| chr1:179174906
|
A | T | 6 | a0001c0001t0020g0155a0001c0001t0020g0196a0001c0001t0020g0197others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-41532T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174906 | ||||||
| chr1:179174906
|
AAAT | A | 9 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0002t0010g0258others(6): Show | 9 | HG00140.hp1 HG01496.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.158-41535_158-4153 others(7): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174906 | ||||||
| chr1:179174907
|
A | T | 1 | a0001c0008t0001g0165 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.158-41533T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174907 | ||||||
| chr1:179174907
|
AAT | A | 7 | a0001c0001t0001g0238a0001c0001t0003g0047a0002c0005t0022g0253others(4): Show | 7 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.158-41535_158-4153 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174907 | ||||||
| chr1:179174908
|
A | T | 1 | a0001c0001t0001g0237 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.158-41534T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174908 | ||||||
| chr1:179174908
|
AT | A | 35 | a0001c0001t0001g0178a0001c0001t0001g0240a0001c0001t0001g0241others(32): Show | 35 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.158-41535delA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174908 | ||||||
| chr1:179174908
|
ATAAAAT | A | 88 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0054others(85): Show | 88 | HG00280.hp2 HG00558.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.158-41540_158-4153 others(10): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174908 | ||||||
| chr1:179174909
|
T | A | 130 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(127): Show | 130 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.158-41535A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174909 | ||||||
| chr1:179174910
|
A | T | 2 | a0001c0001t0001g0233a0001c0001t0083g0194 | 2 | HG02922.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.158-41536T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174910 | ||||||
| chr1:179174911
|
A | T | 1 | a0009c0014t0002g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.158-41537T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174911 | ||||||
| chr1:179174914
|
T | A | 175 | a0001c0001t0001g0146a0001c0001t0001g0159a0001c0001t0001g0166others(172): Show | 175 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.158-41540A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174914 | ||||||
| chr1:179174914
|
TAAA | T | 32 | a0001c0001t0003g0047a0001c0001t0008g0283a0001c0001t0008g0299others(29): Show | 32 | HG00597.hp2 HG01069.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.158-41543_158-4154 others(7): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174914 | ||||||
| chr1:179174917
|
A | T | 59 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0159others(56): Show | 59 | HG00621.hp2 HG00673.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.158-41543T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174917 | ||||||
| chr1:179174918
|
A | T | 1 | a0001c0001t0004g0090 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.158-41544T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174918 | ||||||
| chr1:179174920
|
A | T | 235 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0159others(232): Show | 235 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(232): Show |
intron_variant | MODIFIER | c.158-41546T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174920 | ||||||
| chr1:179174923
|
T | A | 5 | a0001c0001t0006g0104a0001c0001t0014g0034a0001c0001t0071g0101others(2): Show | 5 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-41549A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179174923 | ||||||
| chr1:179175000
|
C | T | 2 | a0003c0006t0001g0151a0003c0006t0001g0209 | 2 | NA18985.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.158-41626G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179175000 | ||||||
| chr1:179175062
|
A | G | 2 | a0001c0002t0017g0272a0001c0002t0017g0273 | 2 | HG01433.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.158-41688T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179175062 | ||||||
| chr1:179175211
|
G | A | 2 | a0001c0001t0034g0213a0001c0001t0034g0219 | 2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.158-41837C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179175211 | ||||||
| chr1:179175290
|
G | GATGTCAA others(15): Show |
2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.158-41938_158-4191 others(26): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179175290 | ||||||
| chr1:179175505
|
T | C | 7 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(4): Show | 7 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.158-42131A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179175505 | ||||||
| chr1:179175847
|
C | CT | 93 | a0001c0001t0001g0190a0001c0001t0004g0040a0001c0001t0005g0315others(90): Show | 93 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.158-42474dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179175847 | ||||||
| chr1:179175847
|
C | CTT | 95 | a0001c0001t0002g0230a0001c0001t0003g0033a0001c0001t0003g0045others(92): Show | 95 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.158-42475_158-4247 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179175847 | ||||||
| chr1:179175847
|
C | CTTT | 22 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(19): Show | 22 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.158-42476_158-4247 others(7): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179175847 | ||||||
| chr1:179175848
|
T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01943.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.158-42474A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179175848 | ||||||
| chr1:179175879
|
G | A | 19 | a0001c0002t0010g0254a0001c0002t0010g0256a0001c0002t0010g0258others(16): Show | 19 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.158-42505C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179175879 | ||||||
| chr1:179175934
|
C | T | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.158-42560G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179175934 | ||||||
| chr1:179176013
|
G | A | 2 | a0001c0001t0007g0136a0001c0001t0086g0192 | 2 | NA18970.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.158-42639C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179176013 | ||||||
| chr1:179176090
|
A | G | 2 | a0001c0001t0077g0142a0001c0001t0078g0143 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.158-42716T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179176090 | ||||||
| chr1:179176134
|
T | C | 19 | a0001c0002t0010g0254a0001c0002t0010g0256a0001c0002t0010g0258others(16): Show | 19 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.158-42760A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179176134 | ||||||
| chr1:179176434
|
C | T | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-43060G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179176434 | ||||||
| chr1:179176485
|
C | CA | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.158-43112dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179176485 | ||||||
| chr1:179176682
|
T | A | 2 | a0001c0001t0077g0142a0001c0001t0078g0143 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.158-43308A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179176682 | ||||||
| chr1:179176702
|
C | CTTTTTTT others(4): Show |
24 | a0001c0001t0006g0118a0001c0001t0041g0250a0001c0001t0041g0251others(21): Show | 24 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.158-43329_158-4332 others(15): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179176702 | ||||||
| chr1:179176702
|
C | CTTTTTTT others(5): Show |
93 | a0001c0001t0002g0230a0001c0001t0003g0033a0001c0001t0003g0045others(90): Show | 93 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.158-43329_158-4332 others(16): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179176702 | ||||||
| chr1:179176702
|
C | CTTTTTTT others(6): Show |
58 | a0001c0001t0001g0170a0001c0001t0002g0168a0001c0001t0003g0052others(55): Show | 58 | HG00597.hp2 HG00735.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.158-43329_158-4332 others(17): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179176702 | ||||||
| chr1:179176702
|
C | CTTTTTTT others(7): Show |
138 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0159others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.158-43329_158-4332 others(18): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179176702 | ||||||
| chr1:179176702
|
C | CTTTTTTT others(8): Show |
10 | a0001c0001t0002g0211a0001c0001t0002g0243a0001c0001t0002g0248others(7): Show | 10 | HG01981.hp1 HG02080.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-43329_158-4332 others(19): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179176702 | ||||||
| chr1:179176712
|
T | TTTTTTTT others(5): Show |
2 | a0001c0001t0069g0056a0001c0001t0070g0078 | 2 | NA18961.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.158-43339_158-4333 others(16): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179176712 | ||||||
| chr1:179176838
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.158-43464C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179176838 | ||||||
| chr1:179177192
|
G | T | 19 | a0001c0002t0010g0254a0001c0002t0010g0256a0001c0002t0010g0258others(16): Show | 19 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.158-43818C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179177192 | ||||||
| chr1:179177217
|
C | CA | 5 | a0001c0001t0001g0160a0001c0001t0001g0193a0001c0001t0002g0214others(2): Show | 5 | HG00099.hp1 HG02622.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-43844dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179177217 | ||||||
| chr1:179177910
|
G | A | 1 | a0001c0001t0088g0236 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.158-44536C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179177910 | ||||||
| chr1:179178061
|
A | C | 7 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.158-44687T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178061 | ||||||
| chr1:179178169
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.158-44795C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178169 | ||||||
| chr1:179178401
|
C | CA | 7 | a0001c0001t0001g0193a0001c0001t0001g0204a0001c0001t0002g0176others(4): Show | 7 | HG00673.hp1 HG02717.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.158-45028dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178401 | ||||||
| chr1:179178401
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0012g0103 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.158-45037_158-4502 others(14): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178401 | ||||||
| chr1:179178401
|
C | CAAAAAAA others(4): Show |
7 | a0001c0001t0032g0026a0001c0001t0055g0012a0001c0004t0024g0024others(4): Show | 7 | HG02615.hp2 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.158-45038_158-4502 others(15): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178401 | ||||||
| chr1:179178401
|
C | CAAAAAAA others(5): Show |
17 | a0001c0001t0032g0027a0001c0001t0077g0142a0001c0001t0078g0143others(14): Show | 17 | HG00597.hp2 HG01433.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.158-45039_158-4502 others(16): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178401 | ||||||
| chr1:179178401
|
C | CAAAAAAA others(6): Show |
8 | a0001c0001t0004g0040a0001c0003t0023g0011a0001c0003t0029g0008others(5): Show | 8 | HG01106.hp1 HG01496.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.158-45040_158-4502 others(17): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178401 | ||||||
| chr1:179178401
|
C | CAAAAAAA others(7): Show |
6 | a0001c0001t0009g0284a0001c0001t0021g0307a0001c0001t0021g0309others(3): Show | 6 | HG02723.hp1 HG02809.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.158-45041_158-4502 others(18): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178401 | ||||||
| chr1:179178401
|
C | CAAAAAAA others(8): Show |
21 | a0001c0001t0008g0283a0001c0001t0008g0289a0001c0001t0008g0297others(18): Show | 21 | HG01069.hp1 HG01070.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.158-45042_158-4502 others(19): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178401 | ||||||
| chr1:179178401
|
C | CAAAAAAA others(9): Show |
21 | a0001c0001t0003g0047a0001c0001t0006g0092a0001c0001t0008g0282others(18): Show | 21 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.158-45043_158-4502 others(20): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178401 | ||||||
| chr1:179178401
|
C | CAAAAAAA others(10): Show |
54 | a0001c0001t0002g0230a0001c0001t0003g0033a0001c0001t0003g0052others(51): Show | 54 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.158-45044_158-4502 others(21): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178401 | ||||||
| chr1:179178401
|
C | CAAAAAAA others(11): Show |
34 | a0001c0001t0003g0045a0001c0001t0003g0072a0001c0001t0003g0097others(31): Show | 34 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.158-45045_158-4502 others(22): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178401 | ||||||
| chr1:179178401
|
C | CAAAAAAA others(12): Show |
12 | a0001c0001t0003g0054a0001c0001t0003g0058a0001c0001t0003g0095others(9): Show | 12 | HG00639.hp2 HG01106.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.158-45046_158-4502 others(23): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178401 | ||||||
| chr1:179178401
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0004g0082 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.158-45028_158-4502 others(24): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178401 | ||||||
| chr1:179178401
|
C | CAAAAAAA others(15): Show |
2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.158-45028_158-4502 others(26): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178401 | ||||||
| chr1:179178421
|
T | A | 6 | a0001c0001t0020g0155a0001c0001t0020g0196a0001c0001t0020g0197others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-45047A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178421 | ||||||
| chr1:179178473
|
A | C | 1 | a0001c0001t0042g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.158-45099T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178473 | ||||||
| chr1:179178567
|
G | A | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-45193C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178567 | ||||||
| chr1:179178588
|
C | A | 1 | a0001c0001t0009g0314 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.158-45214G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178588 | ||||||
| chr1:179178598
|
T | G | 10 | a0001c0001t0008g0287a0001c0001t0008g0288a0001c0001t0008g0289others(7): Show | 10 | HG01346.hp2 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.158-45224A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178598 | ||||||
| chr1:179178763
|
G | T | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-45389C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178763 | ||||||
| chr1:179178933
|
C | T | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.158-45559G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179178933 | ||||||
| chr1:179179089
|
A | G | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-45715T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179179089 | ||||||
| chr1:179179101
|
G | A | 1 | a0001c0003t0029g0008 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.158-45727C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179179101 | ||||||
| chr1:179179167
|
T | C | 9 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0004t0024g0023others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.158-45793A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179179167 | ||||||
| chr1:179179460
|
G | GT | 18 | a0001c0001t0004g0082a0001c0001t0006g0114a0001c0001t0007g0124others(15): Show | 18 | HG01168.hp1 HG01168.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.158-46087dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179179460 | ||||||
| chr1:179179560
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.158-46186A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179179560 | ||||||
| chr1:179179604
|
T | C | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.158-46230A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179179604 | ||||||
| chr1:179179622
|
A | T | 1 | a0001c0003t0053g0002 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.158-46248T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179179622 | ||||||
| chr1:179179768
|
C | T | 9 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0004t0024g0023others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.158-46394G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179179768 | ||||||
| chr1:179179866
|
C | T | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-46492G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179179866 | ||||||
| chr1:179179946
|
C | CA | 10 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0008g0298others(7): Show | 10 | HG00735.hp1 HG01070.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.158-46573dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179179946 | ||||||
| chr1:179179977
|
T | C | 1 | a0001c0004t0031g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.158-46603A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179179977 | ||||||
| chr1:179180127
|
C | A | 1 | a0001c0001t0072g0121 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.158-46753G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179180127 | ||||||
| chr1:179180127
|
C | CA | 12 | a0001c0001t0002g0211a0001c0001t0003g0072a0001c0001t0008g0299others(9): Show | 12 | HG01106.hp2 HG01928.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-46754dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179180127 | ||||||
| chr1:179180138
|
A | G | 12 | a0001c0001t0001g0146a0001c0001t0001g0174a0001c0001t0001g0202others(9): Show | 12 | HG01109.hp1 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-46764T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179180138 | ||||||
| chr1:179180139
|
G | A | 207 | a0001c0001t0002g0230a0001c0001t0003g0033a0001c0001t0003g0045others(204): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.158-46765C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179180139 | ||||||
| chr1:179180212
|
T | C | 1 | a0001c0002t0044g0271 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.158-46838A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179180212 | ||||||
| chr1:179180333
|
GT | G | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-46960delA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179180333 | ||||||
| chr1:179180700
|
T | A | 5 | a0001c0002t0010g0261a0001c0002t0044g0264a0001c0002t0044g0271others(2): Show | 5 | HG02135.hp2 NA18942.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-47326A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179180700 | ||||||
| chr1:179180747
|
A | C | 10 | a0001c0001t0001g0167a0001c0001t0001g0180a0001c0001t0001g0181others(7): Show | 10 | HG00438.hp1 HG02071.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.158-47373T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179180747 | ||||||
| chr1:179180867
|
A | G | 1 | a0001c0001t0006g0035 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.158-47493T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179180867 | ||||||
| chr1:179181181
|
T | C | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.158-47807A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179181181 | ||||||
| chr1:179181222
|
AG | A | 9 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0004t0024g0023others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.158-47849delC | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179181222 | ||||||
| chr1:179181421
|
A | T | 6 | a0001c0001t0056g0020a0001c0001t0096g0306a0001c0001t0097g0304others(3): Show | 6 | HG00735.hp1 HG01175.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.157+47820T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179181421 | ||||||
| chr1:179181746
|
G | A | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+47495C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179181746 | ||||||
| chr1:179181790
|
T | C | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+47451A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179181790 | ||||||
| chr1:179181825
|
G | A | 19 | a0001c0001t0055g0012a0001c0003t0023g0009a0001c0003t0023g0010others(16): Show | 19 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.157+47416C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179181825 | ||||||
| chr1:179181913
|
C | T | 2 | a0001c0001t0001g0233a0001c0002t0017g0272 | 2 | HG01515.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.157+47328G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179181913 | ||||||
| chr1:179181921
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.157+47320A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179181921 | ||||||
| chr1:179181946
|
A | AT | 136 | a0001c0001t0001g0237a0001c0001t0002g0152a0001c0001t0002g0230others(133): Show | 136 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.157+47294dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179181946 | ||||||
| chr1:179181946
|
A | ATT | 47 | a0001c0001t0003g0072a0001c0001t0004g0073a0001c0001t0004g0088others(44): Show | 47 | HG00280.hp2 HG00741.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.157+47293_157+4729 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179181946 | ||||||
| chr1:179181946
|
A | ATTT | 8 | a0001c0001t0004g0100a0001c0001t0008g0287a0001c0001t0008g0295others(5): Show | 8 | HG01346.hp2 HG02602.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.157+47292_157+4729 others(7): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179181946 | ||||||
| chr1:179181946
|
A | T | 1 | a0001c0001t0001g0159 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.157+47295T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179181946 | ||||||
| chr1:179181946
|
AT | A | 25 | a0001c0001t0001g0233a0001c0001t0002g0153a0001c0001t0002g0154others(22): Show | 25 | HG00438.hp1 HG00741.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.157+47294delA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179181946 | ||||||
| chr1:179181946
|
ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.157+47284_157+4729 others(15): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179181946 | ||||||
| chr1:179181946
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.157+47283_157+4729 others(16): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179181946 | ||||||
| chr1:179182037
|
C | T | 1 | a0001c0001t0011g0330 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.157+47204G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179182037 | ||||||
| chr1:179182076
|
C | T | 348 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(345): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.157+47165G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179182076 | ||||||
| chr1:179182116
|
C | G | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+47125G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179182116 | ||||||
| chr1:179182314
|
C | T | 1 | a0001c0002t0017g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.157+46927G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179182314 | ||||||
| chr1:179182479
|
TG | T | 24 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(21): Show | 24 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.157+46761delC | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179182479 | ||||||
| chr1:179182877
|
T | C | 1 | a0001c0003t0023g0011 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.157+46364A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179182877 | ||||||
| chr1:179182884
|
TGGAATAT others(12): Show |
T | 1 | a0001c0001t0004g0040 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.157+46338_157+4635 others(23): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179182884 | ||||||
| chr1:179183032
|
T | C | 1 | a0001c0001t0004g0090 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.157+46209A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179183032 | ||||||
| chr1:179183084
|
G | A | 1 | a0001c0001t0091g0312 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.157+46157C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179183084 | ||||||
| chr1:179183342
|
T | C | 2 | a0001c0001t0035g0220a0001c0001t0035g0225 | 2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.157+45899A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179183342 | ||||||
| chr1:179183594
|
A | T | 1 | a0001c0001t0066g0036 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.157+45647T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179183594 | ||||||
| chr1:179184000
|
G | C | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.157+45241C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179184000 | ||||||
| chr1:179184037
|
T | G | 1 | a0001c0001t0009g0300 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.157+45204A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179184037 | ||||||
| chr1:179184127
|
G | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0170 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.157+45114C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179184127 | ||||||
| chr1:179184178
|
C | T | 3 | a0001c0001t0077g0142a0001c0001t0078g0143a0001c0001t0099g0301 | 3 | HG01891.hp1 HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.157+45063G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179184178 | ||||||
| chr1:179184392
|
C | T | 2 | a0001c0001t0003g0047a0001c0001t0004g0046 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.157+44849G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179184392 | ||||||
| chr1:179184420
|
A | C | 1 | a0001c0001t0002g0184 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.157+44821T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179184420 | ||||||
| chr1:179184540
|
C | T | 18 | a0001c0002t0010g0254a0001c0002t0010g0256a0001c0002t0010g0258others(15): Show | 18 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.157+44701G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179184540 | ||||||
| chr1:179184546
|
G | A | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.157+44695C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179184546 | ||||||
| chr1:179184562
|
G | A | 182 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(179): Show | 182 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.157+44679C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179184562 | ||||||
| chr1:179184625
|
G | A | 1 | a0001c0001t0066g0036 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.157+44616C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179184625 | ||||||
| chr1:179184819
|
C | T | 3 | a0001c0004t0024g0023a0001c0004t0024g0024a0001c0004t0111g0347 | 3 | HG03453.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.157+44422G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179184819 | ||||||
| chr1:179184959
|
G | C | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.157+44282C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179184959 | ||||||
| chr1:179184963
|
T | C | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+44278A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179184963 | ||||||
| chr1:179184966
|
C | A | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.157+44275G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179184966 | ||||||
| chr1:179185166
|
G | A | 3 | a0001c0001t0077g0142a0001c0001t0078g0143a0001c0001t0099g0301 | 3 | HG01891.hp1 HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.157+44075C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179185166 | ||||||
| chr1:179185322
|
A | G | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+43919T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179185322 | ||||||
| chr1:179185448
|
A | T | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+43793T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179185448 | ||||||
| chr1:179185455
|
A | T | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.157+43786T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179185455 | ||||||
| chr1:179185561
|
C | T | 2 | a0001c0001t0077g0142a0001c0001t0078g0143 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.157+43680G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179185561 | ||||||
| chr1:179185670
|
G | GT | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+43570dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179185670 | ||||||
| chr1:179185911
|
C | T | 1 | a0001c0001t0036g0207 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.157+43330G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179185911 | ||||||
| chr1:179186065
|
C | T | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+43176G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179186065 | ||||||
| chr1:179186338
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.157+42903G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179186338 | ||||||
| chr1:179186419
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0170 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.157+42822G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179186419 | ||||||
| chr1:179186439
|
C | T | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.157+42802G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179186439 | ||||||
| chr1:179186481
|
C | T | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.157+42760G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179186481 | ||||||
| chr1:179186482
|
G | A | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.157+42759C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179186482 | ||||||
| chr1:179186506
|
A | G | 182 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(179): Show | 182 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.157+42735T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179186506 | ||||||
| chr1:179186628
|
G | A | 1 | a0001c0004t0058g0028 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.157+42613C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179186628 | ||||||
| chr1:179186744
|
C | CTATT | 28 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0001t0055g0012others(25): Show | 28 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.157+42493_157+4249 others(8): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179186744 | ||||||
| chr1:179186880
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.157+42361C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179186880 | ||||||
| chr1:179186946
|
A | C | 28 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0001t0055g0012others(25): Show | 28 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.157+42295T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179186946 | ||||||
| chr1:179187001
|
G | A | 1 | a0001c0001t0003g0054 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.157+42240C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179187001 | ||||||
| chr1:179187010
|
T | C | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+42231A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179187010 | ||||||
| chr1:179187047
|
G | A | 1 | a0001c0001t0004g0085 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.157+42194C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179187047 | ||||||
| chr1:179187240
|
A | C | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.157+42001T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179187240 | ||||||
| chr1:179187486
|
C | A | 10 | a0001c0001t0003g0086a0001c0001t0003g0089a0001c0001t0006g0092others(7): Show | 10 | NA18946.hp2 NA18954.hp2 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.157+41755G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179187486 | ||||||
| chr1:179187828
|
G | C | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG01081.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.157+41413C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179187828 | ||||||
| chr1:179187833
|
C | T | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+41408G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179187833 | ||||||
| chr1:179187870
|
C | T | 1 | a0001c0001t0066g0036 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.157+41371G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179187870 | ||||||
| chr1:179188021
|
A | G | 1 | a0001c0001t0002g0154 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.157+41220T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179188021 | ||||||
| chr1:179188227
|
T | C | 1 | a0001c0003t0053g0002 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.157+41014A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179188227 | ||||||
| chr1:179188323
|
C | T | 1 | a0001c0001t0091g0312 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.157+40918G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179188323 | ||||||
| chr1:179188349
|
C | T | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.157+40892G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179188349 | ||||||
| chr1:179188360
|
G | A | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.157+40881C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179188360 | ||||||
| chr1:179188477
|
G | GT | 9 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0004t0024g0023others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.157+40763dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179188477 | ||||||
| chr1:179188485
|
T | C | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+40756A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179188485 | ||||||
| chr1:179188577
|
C | G | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+40664G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179188577 | ||||||
| chr1:179188681
|
A | G | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+40560T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179188681 | ||||||
| chr1:179188689
|
T | G | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+40552A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179188689 | ||||||
| chr1:179188808
|
A | G | 1 | a0001c0001t0013g0107 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.157+40433T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179188808 | ||||||
| chr1:179188905
|
G | C | 1 | a0001c0001t0011g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.157+40336C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179188905 | ||||||
| chr1:179189098
|
G | T | 9 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0004t0024g0023others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.157+40143C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179189098 | ||||||
| chr1:179189271
|
G | T | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.157+39970C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179189271 | ||||||
| chr1:179189324
|
G | A | 19 | a0001c0001t0055g0012a0001c0003t0023g0009a0001c0003t0023g0010others(16): Show | 19 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.157+39917C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179189324 | ||||||
| chr1:179189334
|
A | T | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+39907T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179189334 | ||||||
| chr1:179189391
|
C | G | 2 | a0001c0001t0007g0136a0001c0001t0086g0192 | 2 | NA18970.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.157+39850G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179189391 | ||||||
| chr1:179189426
|
G | A | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.157+39815C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179189426 | ||||||
| chr1:179189479
|
A | C | 208 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(205): Show | 208 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.157+39762T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179189479 | ||||||
| chr1:179189547
|
G | A | 6 | a0001c0001t0020g0155a0001c0001t0020g0196a0001c0001t0020g0197others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+39694C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179189547 | ||||||
| chr1:179189601
|
A | G | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.157+39640T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179189601 | ||||||
| chr1:179189646
|
A | G | 25 | a0001c0001t0005g0315a0001c0001t0005g0316a0001c0001t0005g0317others(22): Show | 25 | HG00544.hp1 HG00558.hp1 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.157+39595T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179189646 | ||||||
| chr1:179189699
|
C | T | 7 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.157+39542G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179189699 | ||||||
| chr1:179189779
|
C | T | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+39462G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179189779 | ||||||
| chr1:179189797
|
G | A | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.157+39444C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179189797 | ||||||
| chr1:179189987
|
A | C | 7 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.157+39254T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179189987 | ||||||
| chr1:179190082
|
G | C | 1 | a0001c0001t0005g0335 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.157+39159C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179190082 | ||||||
| chr1:179190096
|
C | T | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+39145G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179190096 | ||||||
| chr1:179190234
|
T | C | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.157+39007A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179190234 | ||||||
| chr1:179190264
|
C | A | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.157+38977G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179190264 | ||||||
| chr1:179190329
|
G | A | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.157+38912C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179190329 | ||||||
| chr1:179190459
|
T | C | 1 | a0001c0001t0011g0344 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.157+38782A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179190459 | ||||||
| chr1:179190511
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.157+38730T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179190511 | ||||||
| chr1:179190549
|
A | G | 1 | a0001c0001t0008g0287 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.157+38692T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179190549 | ||||||
| chr1:179190560
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.157+38681C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179190560 | ||||||
| chr1:179190572
|
C | T | 3 | a0001c0001t0077g0142a0001c0001t0078g0143a0001c0001t0099g0301 | 3 | HG01891.hp1 HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.157+38669G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179190572 | ||||||
| chr1:179190724
|
C | G | 1 | a0001c0001t0014g0116 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.157+38517G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179190724 | ||||||
| chr1:179190827
|
T | C | 9 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0004t0024g0023others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.157+38414A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179190827 | ||||||
| chr1:179191119
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.157+38122G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179191119 | ||||||
| chr1:179191147
|
T | A | 1 | a0001c0001t0004g0083 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.157+38094A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179191147 | ||||||
| chr1:179191311
|
T | A | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.157+37930A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179191311 | ||||||
| chr1:179191344
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157+37897T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179191344 | ||||||
| chr1:179191375
|
T | A | 1 | a0001c0001t0006g0118 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.157+37866A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179191375 | ||||||
| chr1:179191412
|
C | G | 1 | a0001c0001t0009g0314 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.157+37829G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179191412 | ||||||
| chr1:179191413
|
C | CT | 111 | a0001c0001t0001g0237a0001c0001t0003g0033a0001c0001t0003g0045others(108): Show | 111 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.157+37827dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179191413 | ||||||
| chr1:179191413
|
C | CTT | 22 | a0001c0001t0003g0052a0001c0001t0003g0094a0001c0001t0004g0040others(19): Show | 22 | HG00621.hp1 HG01106.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.157+37826_157+3782 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179191413 | ||||||
| chr1:179191413
|
CT | C | 160 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0001g0150others(157): Show | 160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.157+37827delA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179191413 | ||||||
| chr1:179191450
|
C | T | 1 | a0002c0005t0022g0277 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.157+37791G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179191450 | ||||||
| chr1:179191482
|
A | G | 182 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(179): Show | 182 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.157+37759T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179191482 | ||||||
| chr1:179191816
|
C | A | 206 | a0001c0001t0003g0045a0001c0001t0003g0047a0001c0001t0003g0052others(203): Show | 206 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.157+37425G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179191816 | ||||||
| chr1:179191822
|
C | A | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+37419G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179191822 | ||||||
| chr1:179191880
|
A | G | 1 | a0001c0001t0003g0072 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.157+37361T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179191880 | ||||||
| chr1:179191896
|
A | C | 1 | a0001c0001t0059g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.157+37345T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179191896 | ||||||
| chr1:179192120
|
C | T | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+37121G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179192120 | ||||||
| chr1:179192475
|
C | A | 1 | a0001c0001t0001g0149 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.157+36766G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179192475 | ||||||
| chr1:179192491
|
T | C | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+36750A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179192491 | ||||||
| chr1:179192530
|
A | T | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+36711T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179192530 | ||||||
| chr1:179192552
|
A | G | 1 | a0001c0003t0030g0005 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.157+36689T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179192552 | ||||||
| chr1:179192714
|
T | C | 1 | a0001c0001t0090g0305 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.157+36527A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179192714 | ||||||
| chr1:179192762
|
T | A | 182 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(179): Show | 182 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.157+36479A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179192762 | ||||||
| chr1:179192920
|
C | G | 1 | a0001c0001t0011g0341 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.157+36321G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179192920 | ||||||
| chr1:179193000
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.157+36241C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179193000 | ||||||
| chr1:179193218
|
G | A | 182 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(179): Show | 182 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.157+36023C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179193218 | ||||||
| chr1:179193269
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0170 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.157+35972G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179193269 | ||||||
| chr1:179193302
|
C | T | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.157+35939G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179193302 | ||||||
| chr1:179193335
|
G | A | 2 | a0001c0001t0011g0341a0001c0013t0011g0346 | 2 | HG00597.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.157+35906C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179193335 | ||||||
| chr1:179193655
|
C | T | 18 | a0001c0001t0055g0012a0001c0003t0023g0009a0001c0003t0023g0010others(15): Show | 18 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.157+35586G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179193655 | ||||||
| chr1:179193701
|
T | C | 28 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0001t0055g0012others(25): Show | 28 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.157+35540A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179193701 | ||||||
| chr1:179193732
|
T | G | 1 | a0009c0014t0002g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.157+35509A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179193732 | ||||||
| chr1:179193751
|
A | T | 1 | a0001c0001t0009g0294 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.157+35490T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179193751 | ||||||
| chr1:179193755
|
G | A | 2 | a0001c0001t0077g0142a0001c0001t0078g0143 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.157+35486C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179193755 | ||||||
| chr1:179193832
|
C | A | 1 | a0001c0001t0004g0090 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.157+35409G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179193832 | ||||||
| chr1:179193832
|
C | T | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.157+35409G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179193832 | ||||||
| chr1:179193881
|
G | A | 2 | a0001c0001t0007g0136a0001c0001t0086g0192 | 2 | NA18970.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.157+35360C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179193881 | ||||||
| chr1:179193963
|
T | C | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+35278A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179193963 | ||||||
| chr1:179193976
|
A | C | 1 | a0007c0015t0092g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.157+35265T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179193976 | ||||||
| chr1:179193994
|
G | A | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.157+35247C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179193994 | ||||||
| chr1:179194070
|
G | A | 6 | a0001c0001t0020g0155a0001c0001t0020g0196a0001c0001t0020g0197others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+35171C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179194070 | ||||||
| chr1:179194160
|
T | C | 2 | a0001c0001t0006g0035a0001c0001t0066g0036 | 2 | HG02523.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.157+35081A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179194160 | ||||||
| chr1:179194202
|
T | C | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.157+35039A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179194202 | ||||||
| chr1:179194241
|
T | C | 1 | a0001c0001t0006g0074 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.157+35000A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179194241 | ||||||
| chr1:179194318
|
C | T | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+34923G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179194318 | ||||||
| chr1:179194625
|
G | A | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+34616C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179194625 | ||||||
| chr1:179194722
|
T | C | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.157+34519A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179194722 | ||||||
| chr1:179194797
|
GA | G | 5 | a0001c0001t0001g0160a0001c0001t0001g0193a0001c0001t0002g0214others(2): Show | 5 | HG00099.hp1 HG02622.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+34443delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179194797 | ||||||
| chr1:179195113
|
C | A | 24 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(21): Show | 24 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.157+34128G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179195113 | ||||||
| chr1:179195410
|
C | T | 12 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0241others(9): Show | 12 | HG00280.hp1 HG00621.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.157+33831G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179195410 | ||||||
| chr1:179195423
|
T | C | 160 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(157): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.157+33818A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179195423 | ||||||
| chr1:179195569
|
A | T | 3 | a0001c0001t0077g0142a0001c0001t0078g0143a0001c0001t0099g0301 | 3 | HG01891.hp1 HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.157+33672T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179195569 | ||||||
| chr1:179195574
|
C | T | 2 | a0004c0009t0039g0145a0004c0009t0039g0147 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.157+33667G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179195574 | ||||||
| chr1:179195739
|
C | G | 1 | a0001c0001t0080g0217 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.157+33502G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179195739 | ||||||
| chr1:179195809
|
T | C | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+33432A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179195809 | ||||||
| chr1:179196014
|
G | A | 1 | a0001c0001t0005g0335 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.157+33227C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179196014 | ||||||
| chr1:179196440
|
T | C | 7 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.157+32801A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179196440 | ||||||
| chr1:179196675
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0082g0210 | 2 | NA18966.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.157+32566C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179196675 | ||||||
| chr1:179196675
|
G | T | 1 | a0001c0003t0053g0002 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.157+32566C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179196675 | ||||||
| chr1:179196776
|
C | A | 25 | a0001c0001t0005g0331a0001c0001t0021g0307a0001c0001t0021g0309others(22): Show | 25 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.157+32465G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179196776 | ||||||
| chr1:179196776
|
C | CA | 31 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(28): Show | 31 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.157+32464dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179196776 | ||||||
| chr1:179196786
|
C | CA | 18 | a0001c0001t0001g0159a0001c0001t0001g0175a0001c0001t0001g0177others(15): Show | 18 | HG00438.hp2 HG00673.hp2 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.157+32454dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179196786 | ||||||
| chr1:179196798
|
C | A | 1 | a0001c0002t0093g0274 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.157+32443G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179196798 | ||||||
| chr1:179196837
|
A | T | 3 | a0001c0001t0011g0322a0001c0001t0112g0348a0001c0001t0113g0349 | 3 | HG01884.hp2 HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.157+32404T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179196837 | ||||||
| chr1:179196873
|
A | G | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.157+32368T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179196873 | ||||||
| chr1:179197028
|
A | G | 1 | a0001c0001t0012g0051 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.157+32213T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179197028 | ||||||
| chr1:179197388
|
G | C | 2 | a0001c0001t0016g0188a0001c0001t0027g0226 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.157+31853C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179197388 | ||||||
| chr1:179197423
|
A | T | 1 | a0001c0001t0035g0225 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.157+31818T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179197423 | ||||||
| chr1:179197556
|
C | CA | 23 | a0001c0001t0001g0173a0001c0001t0001g0201a0001c0001t0001g0244others(20): Show | 23 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.157+31684dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179197556 | ||||||
| chr1:179197576
|
T | A | 1 | a0001c0001t0060g0042 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.157+31665A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179197576 | ||||||
| chr1:179197681
|
C | A | 2 | a0001c0001t0002g0228a0001c0001t0037g0231 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.157+31560G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179197681 | ||||||
| chr1:179197867
|
C | CA | 171 | a0001c0001t0002g0243a0001c0001t0003g0033a0001c0001t0003g0045others(168): Show | 171 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.157+31373dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179197867 | ||||||
| chr1:179197867
|
C | CAA | 29 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(26): Show | 29 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.157+31372_157+3137 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179197867 | ||||||
| chr1:179197867
|
CA | C | 50 | a0001c0001t0001g0240a0001c0001t0005g0315a0001c0001t0005g0316others(47): Show | 50 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.157+31373delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179197867 | ||||||
| chr1:179197991
|
T | C | 1 | a0001c0001t0027g0226 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.157+31250A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179197991 | ||||||
| chr1:179198064
|
T | C | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+31177A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179198064 | ||||||
| chr1:179198168
|
G | C | 8 | a0001c0002t0010g0262a0001c0002t0010g0266a0001c0002t0010g0267others(5): Show | 8 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.157+31073C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179198168 | ||||||
| chr1:179198172
|
C | CA | 30 | a0001c0001t0001g0150a0001c0001t0001g0159a0001c0001t0001g0237others(27): Show | 30 | HG00597.hp1 HG00735.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.157+31068dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179198172 | ||||||
| chr1:179198264
|
G | T | 6 | a0001c0001t0020g0155a0001c0001t0020g0196a0001c0001t0020g0197others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+30977C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179198264 | ||||||
| chr1:179198479
|
G | C | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+30762C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179198479 | ||||||
| chr1:179198565
|
C | T | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+30676G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179198565 | ||||||
| chr1:179198619
|
G | C | 111 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0159others(108): Show | 111 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.157+30622C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179198619 | ||||||
| chr1:179198693
|
C | CA | 156 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0170others(153): Show | 156 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.157+30547dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179198693 | ||||||
| chr1:179198693
|
C | CAA | 72 | a0001c0001t0002g0232a0001c0001t0003g0052a0001c0001t0003g0059others(69): Show | 72 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.157+30546_157+3054 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179198693 | ||||||
| chr1:179198693
|
C | CAAA | 16 | a0001c0001t0003g0111a0001c0001t0026g0120a0001c0001t0032g0026others(13): Show | 16 | HG00140.hp1 HG01175.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.157+30545_157+3054 others(7): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179198693 | ||||||
| chr1:179198717
|
C | A | 1 | a0001c0003t0029g0018 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.157+30524G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179198717 | ||||||
| chr1:179198842
|
C | CT | 12 | a0001c0001t0001g0171a0001c0001t0001g0244a0001c0001t0005g0332others(9): Show | 12 | HG01496.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.157+30398dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179198842 | ||||||
| chr1:179198842
|
CT | C | 22 | a0001c0001t0014g0079a0001c0002t0010g0254a0001c0002t0010g0256others(19): Show | 22 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.157+30398delA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179198842 | ||||||
| chr1:179198991
|
A | G | 1 | a0001c0001t0011g0341 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.157+30250T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179198991 | ||||||
| chr1:179199383
|
C | T | 6 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0002g0211others(3): Show | 6 | HG00621.hp2 NA18946.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+29858G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179199383 | ||||||
| chr1:179199482
|
CTT | C | 18 | a0001c0002t0010g0254a0001c0002t0010g0256a0001c0002t0010g0258others(15): Show | 18 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.157+29757_157+2975 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179199482 | ||||||
| chr1:179199493
|
C | G | 1 | a0001c0001t0006g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.157+29748G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179199493 | ||||||
| chr1:179199670
|
C | G | 121 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.157+29571G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179199670 | ||||||
| chr1:179199731
|
C | CT | 104 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0159others(101): Show | 104 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.157+29509dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179199731 | ||||||
| chr1:179199731
|
CT | C | 16 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(13): Show | 16 | HG01099.hp1 HG01243.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.157+29509delA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179199731 | ||||||
| chr1:179199731
|
CTT | C | 25 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(22): Show | 25 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.157+29508_157+2950 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179199731 | ||||||
| chr1:179199731
|
CTTTTT | C | 119 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.157+29505_157+2950 others(9): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179199731 | ||||||
| chr1:179199731
|
CTTTTTT | C | 36 | a0001c0001t0006g0066a0001c0001t0032g0026a0001c0001t0032g0027others(33): Show | 36 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.157+29504_157+2950 others(10): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179199731 | ||||||
| chr1:179199828
|
G | A | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.157+29413C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179199828 | ||||||
| chr1:179199921
|
G | C | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+29320C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179199921 | ||||||
| chr1:179200038
|
CCTTTTTT | C | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+29196_157+2920 others(11): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179200038 | ||||||
| chr1:179200039
|
CT | C | 92 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0160others(89): Show | 92 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.157+29201delA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179200039 | ||||||
| chr1:179200039
|
CTT | C | 6 | a0001c0001t0016g0158a0001c0001t0056g0020a0001c0001t0076g0135others(3): Show | 6 | HG01175.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.157+29200_157+2920 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179200039 | ||||||
| chr1:179200039
|
CTTT | C | 23 | a0001c0001t0016g0188a0001c0001t0016g0189a0001c0001t0016g0222others(20): Show | 23 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.157+29199_157+2920 others(7): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179200039 | ||||||
| chr1:179200039
|
CTTTT | C | 17 | a0001c0001t0004g0100a0001c0001t0006g0074a0001c0001t0006g0118others(14): Show | 17 | HG01981.hp2 HG02572.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.157+29198_157+2920 others(8): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179200039 | ||||||
| chr1:179200039
|
CTTTTT | C | 131 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.157+29197_157+2920 others(9): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179200039 | ||||||
| chr1:179200070
|
G | A | 5 | a0001c0001t0034g0213a0001c0001t0034g0219a0001c0001t0079g0212others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+29171C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179200070 | ||||||
| chr1:179200111
|
G | A | 207 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(204): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.157+29130C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179200111 | ||||||
| chr1:179200118
|
C | T | 1 | a0001c0001t0063g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.157+29123G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179200118 | ||||||
| chr1:179200261
|
G | A | 1 | a0001c0003t0023g0011 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.157+28980C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179200261 | ||||||
| chr1:179200328
|
T | C | 10 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(7): Show | 10 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.157+28913A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179200328 | ||||||
| chr1:179200343
|
G | A | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+28898C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179200343 | ||||||
| chr1:179200453
|
G | C | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+28788C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179200453 | ||||||
| chr1:179200494
|
A | C | 1 | a0001c0001t0002g0179 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.157+28747T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179200494 | ||||||
| chr1:179200660
|
A | C | 9 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0004t0024g0023others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.157+28581T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179200660 | ||||||
| chr1:179200680
|
T | A | 97 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.157+28561A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179200680 | ||||||
| chr1:179200822
|
T | C | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.157+28419A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179200822 | ||||||
| chr1:179201114
|
T | C | 97 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.157+28127A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179201114 | ||||||
| chr1:179201292
|
C | T | 19 | a0001c0001t0055g0012a0001c0003t0023g0009a0001c0003t0023g0010others(16): Show | 19 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.157+27949G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179201292 | ||||||
| chr1:179201351
|
T | C | 1 | a0001c0001t0099g0301 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.157+27890A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179201351 | ||||||
| chr1:179201428
|
T | A | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+27813A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179201428 | ||||||
| chr1:179201508
|
A | G | 15 | a0001c0001t0055g0012a0001c0003t0023g0009a0001c0003t0023g0010others(12): Show | 15 | HG01106.hp1 HG01433.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.157+27733T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179201508 | ||||||
| chr1:179201623
|
C | T | 1 | a0001c0001t0108g0340 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.157+27618G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179201623 | ||||||
| chr1:179201649
|
G | A | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+27592C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179201649 | ||||||
| chr1:179201994
|
A | G | 207 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(204): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.157+27247T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179201994 | ||||||
| chr1:179202038
|
C | G | 41 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0159others(38): Show | 41 | HG00438.hp1 HG00438.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.157+27203G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179202038 | ||||||
| chr1:179202092
|
TA | T | 203 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(200): Show | 203 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.157+27148delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179202092 | ||||||
| chr1:179202113
|
G | A | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.157+27128C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179202113 | ||||||
| chr1:179202359
|
A | G | 121 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.157+26882T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179202359 | ||||||
| chr1:179202447
|
CTGAG | C | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+26790_157+2679 others(8): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179202447 | ||||||
| chr1:179202578
|
C | T | 97 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.157+26663G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179202578 | ||||||
| chr1:179202596
|
C | G | 19 | a0001c0001t0055g0012a0001c0003t0023g0009a0001c0003t0023g0010others(16): Show | 19 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.157+26645G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179202596 | ||||||
| chr1:179202640
|
C | T | 1 | a0001c0001t0013g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.157+26601G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179202640 | ||||||
| chr1:179202734
|
A | C | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+26507T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179202734 | ||||||
| chr1:179202735
|
G | C | 5 | a0001c0001t0001g0160a0001c0001t0001g0193a0001c0001t0002g0214others(2): Show | 5 | HG00099.hp1 HG02622.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+26506C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179202735 | ||||||
| chr1:179202797
|
A | C | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.157+26444T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179202797 | ||||||
| chr1:179202809
|
T | C | 15 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(12): Show | 15 | HG01099.hp1 HG01243.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.157+26432A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179202809 | ||||||
| chr1:179203092
|
G | A | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+26149C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179203092 | ||||||
| chr1:179203113
|
G | A | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+26128C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179203113 | ||||||
| chr1:179203560
|
A | G | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+25681T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179203560 | ||||||
| chr1:179203721
|
T | A | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.157+25520A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179203721 | ||||||
| chr1:179204017
|
C | CATTT | 3 | a0001c0001t0001g0167a0001c0001t0002g0242a0001c0001t0002g0243 | 3 | HG00280.hp1 HG02083.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.157+25220_157+2522 others(8): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179204017 | ||||||
| chr1:179204079
|
T | C | 1 | a0006c0011t0084g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.157+25162A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179204079 | ||||||
| chr1:179204176
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.157+25065C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179204176 | ||||||
| chr1:179204371
|
T | C | 19 | a0001c0001t0055g0012a0001c0003t0023g0009a0001c0003t0023g0010others(16): Show | 19 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.157+24870A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179204371 | ||||||
| chr1:179204636
|
A | C | 9 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0004t0024g0023others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.157+24605T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179204636 | ||||||
| chr1:179204770
|
C | A | 3 | a0001c0003t0023g0009a0001c0003t0023g0010a0001c0003t0023g0011 | 3 | NA18964.hp1 NA18998.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.157+24471G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179204770 | ||||||
| chr1:179204886
|
A | T | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.157+24355T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179204886 | ||||||
| chr1:179205005
|
A | G | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+24236T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179205005 | ||||||
| chr1:179205029
|
C | CT | 174 | a0001c0001t0003g0033a0001c0001t0003g0047a0001c0001t0003g0052others(171): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.157+24211dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179205029 | ||||||
| chr1:179205029
|
C | CTT | 29 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(26): Show | 29 | HG01071.hp1 HG01081.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.157+24210_157+2421 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179205029 | ||||||
| chr1:179205058
|
A | G | 183 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(180): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.157+24183T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179205058 | ||||||
| chr1:179205066
|
G | A | 11 | a0001c0001t0003g0058a0001c0001t0003g0095a0001c0001t0003g0111others(8): Show | 11 | HG00741.hp1 HG01346.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.157+24175C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179205066 | ||||||
| chr1:179205086
|
G | A | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+24155C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179205086 | ||||||
| chr1:179205219
|
G | T | 50 | a0001c0001t0005g0315a0001c0001t0005g0316a0001c0001t0005g0317others(47): Show | 50 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.157+24022C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179205219 | ||||||
| chr1:179205401
|
G | A | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+23840C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179205401 | ||||||
| chr1:179205423
|
C | A | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.157+23818G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179205423 | ||||||
| chr1:179205683
|
C | T | 28 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0001t0055g0012others(25): Show | 28 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.157+23558G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179205683 | ||||||
| chr1:179205688
|
G | A | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.157+23553C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179205688 | ||||||
| chr1:179205695
|
T | A | 1 | a0001c0001t0003g0071 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.157+23546A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179205695 | ||||||
| chr1:179205728
|
G | A | 1 | a0001c0003t0049g0014 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.157+23513C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179205728 | ||||||
| chr1:179205743
|
A | G | 193 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.157+23498T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179205743 | ||||||
| chr1:179205821
|
G | A | 4 | a0001c0001t0026g0041a0001c0001t0026g0044a0001c0001t0026g0120others(1): Show | 4 | HG03490.hp2 HG03492.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+23420C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179205821 | ||||||
| chr1:179206027
|
A | C | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.157+23214T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179206027 | ||||||
| chr1:179206191
|
C | T | 2 | a0001c0001t0038g0216a0001c0001t0038g0221 | 2 | HG02055.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.157+23050G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179206191 | ||||||
| chr1:179206215
|
C | T | 2 | a0001c0001t0006g0114a0001c0001t0074g0123 | 2 | HG02132.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.157+23026G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179206215 | ||||||
| chr1:179206328
|
C | G | 2 | a0001c0001t0002g0228a0001c0001t0037g0231 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.157+22913G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179206328 | ||||||
| chr1:179206501
|
T | A | 1 | a0001c0002t0094g0255 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.157+22740A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179206501 | ||||||
| chr1:179206501
|
TA | T | 55 | a0001c0001t0005g0315a0001c0001t0005g0316a0001c0001t0005g0317others(52): Show | 55 | HG00558.hp1 HG00735.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.157+22739delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179206501 | ||||||
| chr1:179206501
|
TAA | T | 15 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(12): Show | 15 | HG01099.hp1 HG01243.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.157+22738_157+2273 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179206501 | ||||||
| chr1:179206532
|
T | C | 3 | a0001c0001t0003g0072a0001c0001t0012g0039a0001c0001t0065g0037 | 3 | HG01106.hp2 HG01928.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.157+22709A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179206532 | ||||||
| chr1:179206869
|
G | A | 1 | a0001c0001t0009g0285 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.157+22372C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179206869 | ||||||
| chr1:179206885
|
A | G | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+22356T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179206885 | ||||||
| chr1:179207106
|
T | C | 1 | a0009c0014t0002g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.157+22135A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179207106 | ||||||
| chr1:179207168
|
C | CT | 42 | a0001c0001t0008g0289a0001c0001t0008g0299a0001c0001t0009g0286others(39): Show | 42 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.157+22072dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179207168 | ||||||
| chr1:179207263
|
G | A | 207 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(204): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.157+21978C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179207263 | ||||||
| chr1:179207336
|
A | G | 2 | a0001c0001t0016g0188a0001c0001t0027g0226 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.157+21905T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179207336 | ||||||
| chr1:179207638
|
G | A | 4 | a0001c0001t0003g0058a0001c0001t0003g0095a0001c0001t0004g0082others(1): Show | 4 | HG02040.hp1 NA18965.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+21603C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179207638 | ||||||
| chr1:179207714
|
T | C | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.157+21527A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179207714 | ||||||
| chr1:179207748
|
T | C | 1 | a0001c0001t0042g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.157+21493A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179207748 | ||||||
| chr1:179207932
|
G | A | 1 | a0001c0001t0036g0207 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.157+21309C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179207932 | ||||||
| chr1:179208082
|
C | T | 15 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(12): Show | 15 | HG01099.hp1 HG01243.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.157+21159G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179208082 | ||||||
| chr1:179208315
|
C | T | 1 | a0001c0001t0002g0191 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.157+20926G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179208315 | ||||||
| chr1:179208335
|
T | C | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+20906A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179208335 | ||||||
| chr1:179208373
|
G | A | 6 | a0001c0001t0020g0155a0001c0001t0020g0196a0001c0001t0020g0197others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+20868C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179208373 | ||||||
| chr1:179208431
|
C | T | 1 | a0001c0008t0001g0165 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.157+20810G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179208431 | ||||||
| chr1:179208459
|
A | C | 3 | a0001c0001t0077g0142a0001c0001t0078g0143a0001c0001t0099g0301 | 3 | HG01891.hp1 HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.157+20782T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179208459 | ||||||
| chr1:179208511
|
T | G | 2 | a0001c0001t0002g0206a0001c0001t0007g0134 | 2 | HG00438.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.157+20730A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179208511 | ||||||
| chr1:179208670
|
ATCTC | A | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+20567_157+2057 others(8): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179208670 | ||||||
| chr1:179208761
|
A | G | 28 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0001t0055g0012others(25): Show | 28 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.157+20480T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179208761 | ||||||
| chr1:179209035
|
A | G | 3 | a0001c0001t0077g0142a0001c0001t0078g0143a0001c0001t0099g0301 | 3 | HG01891.hp1 HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.157+20206T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179209035 | ||||||
| chr1:179209248
|
T | C | 2 | a0001c0001t0035g0220a0001c0001t0035g0225 | 2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.157+19993A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179209248 | ||||||
| chr1:179209306
|
A | G | 1 | a0007c0015t0092g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.157+19935T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179209306 | ||||||
| chr1:179209355
|
G | A | 28 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0001t0055g0012others(25): Show | 28 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.157+19886C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179209355 | ||||||
| chr1:179209356
|
C | T | 7 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.157+19885G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179209356 | ||||||
| chr1:179209998
|
C | A | 1 | a0001c0001t0018g0064 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.157+19243G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179209998 | ||||||
| chr1:179210004
|
A | T | 1 | a0001c0001t0018g0064 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.157+19237T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179210004 | ||||||
| chr1:179210145
|
G | A | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.157+19096C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179210145 | ||||||
| chr1:179210176
|
A | G | 6 | a0001c0001t0020g0155a0001c0001t0020g0196a0001c0001t0020g0197others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+19065T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179210176 | ||||||
| chr1:179210323
|
C | T | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.157+18918G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179210323 | ||||||
| chr1:179210367
|
G | A | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+18874C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179210367 | ||||||
| chr1:179210503
|
C | CA | 31 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(28): Show | 31 | HG00597.hp1 HG00735.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.157+18737dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179210503 | ||||||
| chr1:179210503
|
C | CAA | 7 | a0001c0001t0003g0033a0001c0001t0008g0288a0001c0001t0009g0281others(4): Show | 7 | HG01175.hp1 HG01256.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.157+18736_157+1873 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179210503 | ||||||
| chr1:179210503
|
C | CAAA | 103 | a0001c0001t0003g0045a0001c0001t0003g0052a0001c0001t0003g0054others(100): Show | 103 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.157+18735_157+1873 others(7): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179210503 | ||||||
| chr1:179210503
|
C | CAAAA | 38 | a0001c0001t0003g0047a0001c0001t0006g0104a0001c0001t0014g0115others(35): Show | 38 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.157+18734_157+1873 others(8): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179210503 | ||||||
| chr1:179210519
|
G | A | 12 | a0001c0001t0004g0099a0001c0001t0006g0114a0001c0001t0018g0064others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.157+18722C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179210519 | ||||||
| chr1:179210520
|
A | AAG | 5 | a0001c0001t0004g0099a0001c0001t0006g0114a0001c0001t0064g0053others(2): Show | 5 | HG02135.hp1 NA18612.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+18720_157+1872 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179210520 | ||||||
| chr1:179210520
|
A | G | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.157+18721T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179210520 | ||||||
| chr1:179210525
|
A | G | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.157+18716T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179210525 | ||||||
| chr1:179210554
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.157+18687C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179210554 | ||||||
| chr1:179210580
|
C | T | 1 | a0001c0001t0002g0246 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.157+18661G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179210580 | ||||||
| chr1:179210667
|
C | G | 1 | a0001c0001t0009g0300 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.157+18574G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179210667 | ||||||
| chr1:179210858
|
A | T | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.157+18383T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179210858 | ||||||
| chr1:179210867
|
T | TA | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+18373dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179210867 | ||||||
| chr1:179210874
|
T | A | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+18367A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179210874 | ||||||
| chr1:179211069
|
A | T | 1 | a0001c0001t0002g0191 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.157+18172T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211069 | ||||||
| chr1:179211247
|
C | G | 182 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(179): Show | 182 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.157+17994G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211247 | ||||||
| chr1:179211289
|
G | A | 121 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.157+17952C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211289 | ||||||
| chr1:179211305
|
G | C | 1 | a0001c0001t0003g0052 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.157+17936C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211305 | ||||||
| chr1:179211343
|
T | C | 1 | a0001c0001t0035g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.157+17898A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211343 | ||||||
| chr1:179211359
|
A | T | 1 | a0001c0001t0088g0236 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.157+17882T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211359 | ||||||
| chr1:179211360
|
T | A | 6 | a0001c0001t0016g0158a0001c0001t0016g0189a0001c0001t0016g0222others(3): Show | 6 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.157+17881A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211360 | ||||||
| chr1:179211539
|
A | C | 1 | a0001c0001t0018g0064 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.157+17702T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211539 | ||||||
| chr1:179211540
|
T | A | 1 | a0001c0001t0018g0064 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.157+17701A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211540 | ||||||
| chr1:179211541
|
T | C | 1 | a0001c0001t0018g0064 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.157+17700A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211541 | ||||||
| chr1:179211543
|
T | A | 1 | a0001c0001t0018g0064 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.157+17698A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211543 | ||||||
| chr1:179211544
|
T | G | 1 | a0001c0001t0018g0064 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.157+17697A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211544 | ||||||
| chr1:179211547
|
A | G | 1 | a0001c0001t0018g0064 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.157+17694T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211547 | ||||||
| chr1:179211548
|
A | C | 1 | a0001c0001t0018g0064 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.157+17693T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211548 | ||||||
| chr1:179211553
|
A | T | 1 | a0001c0001t0018g0064 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.157+17688T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211553 | ||||||
| chr1:179211554
|
A | T | 1 | a0001c0001t0018g0064 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.157+17687T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211554 | ||||||
| chr1:179211736
|
T | C | 1 | a0001c0004t0031g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.157+17505A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211736 | ||||||
| chr1:179211758
|
C | T | 19 | a0001c0001t0055g0012a0001c0003t0023g0009a0001c0003t0023g0010others(16): Show | 19 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.157+17483G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211758 | ||||||
| chr1:179211791
|
G | GA | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.157+17449dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211791 | ||||||
| chr1:179211791
|
G | GAAA | 15 | a0001c0002t0010g0256a0001c0002t0010g0258a0001c0002t0010g0262others(12): Show | 15 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.157+17447_157+1744 others(7): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211791 | ||||||
| chr1:179211807
|
T | A | 98 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.157+17434A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211807 | ||||||
| chr1:179211918
|
G | C | 1 | a0001c0001t0001g0200 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.157+17323C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211918 | ||||||
| chr1:179211967
|
T | C | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.157+17274A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211967 | ||||||
| chr1:179211995
|
A | C | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.157+17246T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179211995 | ||||||
| chr1:179212411
|
T | C | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.157+16830A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179212411 | ||||||
| chr1:179212559
|
C | T | 3 | a0001c0001t0003g0086a0001c0001t0014g0034a0001c0001t0067g0102 | 3 | NA18954.hp2 NA18992.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.157+16682G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179212559 | ||||||
| chr1:179212657
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.157+16584G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179212657 | ||||||
| chr1:179212820
|
G | A | 28 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0001t0055g0012others(25): Show | 28 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.157+16421C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179212820 | ||||||
| chr1:179212865
|
G | A | 10 | a0001c0001t0008g0287a0001c0001t0008g0288a0001c0001t0008g0289others(7): Show | 10 | HG01346.hp2 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.157+16376C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179212865 | ||||||
| chr1:179212906
|
C | T | 1 | a0001c0001t0102g0296 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.157+16335G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179212906 | ||||||
| chr1:179212961
|
G | A | 1 | a0007c0015t0092g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.157+16280C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179212961 | ||||||
| chr1:179212978
|
G | A | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+16263C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179212978 | ||||||
| chr1:179213046
|
C | CA | 38 | a0001c0001t0001g0160a0001c0001t0002g0214a0001c0001t0002g0215others(35): Show | 38 | HG00099.hp1 HG01099.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.157+16194dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179213046 | ||||||
| chr1:179213046
|
C | CAA | 26 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0001t0055g0012others(23): Show | 26 | HG00597.hp2 HG01433.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.157+16193_157+1619 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179213046 | ||||||
| chr1:179213046
|
CA | C | 31 | a0001c0001t0001g0150a0001c0001t0008g0282a0001c0001t0008g0283others(28): Show | 31 | HG00735.hp1 HG01081.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.157+16194delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179213046 | ||||||
| chr1:179213057
|
A | G | 1 | a0001c0001t0005g0325 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.157+16184T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179213057 | ||||||
| chr1:179213061
|
A | AG | 125 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.157+16179_157+1618 others(5): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179213061 | ||||||
| chr1:179213061
|
A | G | 3 | a0001c0001t0013g0065a0001c0001t0043g0259a0005c0010t0006g0055 | 3 | HG02015.hp2 HG03491.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.157+16180T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179213061 | ||||||
| chr1:179213097
|
C | A | 1 | a0001c0001t0066g0036 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.157+16144G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179213097 | ||||||
| chr1:179213142
|
T | G | 15 | a0001c0001t0003g0059a0001c0001t0003g0109a0001c0001t0004g0040others(12): Show | 15 | HG00280.hp2 HG02132.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.157+16099A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179213142 | ||||||
| chr1:179213311
|
C | T | 1 | a0001c0001t0003g0096 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.157+15930G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179213311 | ||||||
| chr1:179213347
|
C | T | 1 | a0001c0001t0009g0281 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.157+15894G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179213347 | ||||||
| chr1:179213348
|
G | A | 1 | a0001c0001t0025g0060 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.157+15893C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179213348 | ||||||
| chr1:179213392
|
C | T | 3 | a0001c0004t0024g0023a0001c0004t0024g0024a0001c0004t0024g0025 | 3 | HG03453.hp2 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.157+15849G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179213392 | ||||||
| chr1:179213478
|
T | C | 1 | a0001c0001t0018g0064 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.157+15763A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179213478 | ||||||
| chr1:179213613
|
T | A | 1 | a0001c0001t0018g0064 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.157+15628A>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179213613 | ||||||
| chr1:179213790
|
TA | T | 24 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(21): Show | 24 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.157+15450delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179213790 | ||||||
| chr1:179213970
|
C | A | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+15271G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179213970 | ||||||
| chr1:179214067
|
C | A | 1 | a0001c0002t0010g0261 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.157+15174G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214067 | ||||||
| chr1:179214084
|
A | G | 2 | a0001c0001t0091g0312a0007c0015t0092g0313 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.157+15157T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214084 | ||||||
| chr1:179214095
|
GGAAAGAT others(5): Show |
G | 1 | a0001c0001t0080g0217 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.157+15134_157+1514 others(16): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214095 | ||||||
| chr1:179214127
|
A | C | 1 | a0001c0001t0080g0217 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.157+15114T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214127 | ||||||
| chr1:179214473
|
T | C | 4 | a0001c0001t0007g0133a0001c0001t0007g0139a0001c0001t0015g0125others(1): Show | 4 | NA18940.hp1 NA18971.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+14768A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214473 | ||||||
| chr1:179214519
|
C | CAT | 27 | a0001c0001t0001g0144a0001c0001t0001g0149a0001c0001t0001g0233others(24): Show | 27 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.157+14720_157+1472 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214519 | ||||||
| chr1:179214519
|
C | CATAT | 31 | a0001c0001t0002g0232a0001c0001t0003g0052a0001c0001t0003g0071others(28): Show | 31 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(28): Show |
intron_variant | MODIFIER | c.157+14718_157+1472 others(8): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214519 | ||||||
| chr1:179214519
|
C | CATATAT | 26 | a0001c0001t0001g0193a0001c0001t0001g0237a0001c0001t0002g0242others(23): Show | 26 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+14716_157+1472 others(10): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214519 | ||||||
| chr1:179214519
|
C | CATATATA others(1): Show |
23 | a0001c0001t0003g0045a0001c0001t0003g0057a0001c0001t0003g0058others(20): Show | 23 | HG01167.hp1 HG01169.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.157+14714_157+1472 others(12): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214519 | ||||||
| chr1:179214519
|
C | CATATATA others(3): Show |
17 | a0001c0001t0003g0054a0001c0001t0004g0083a0001c0001t0004g0100others(14): Show | 17 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.157+14712_157+1472 others(14): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214519 | ||||||
| chr1:179214519
|
C | CATATATA others(5): Show |
15 | a0001c0001t0004g0082a0001c0001t0004g0099a0001c0001t0019g0098others(12): Show | 15 | HG00621.hp1 HG01496.hp1 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.157+14710_157+1472 others(16): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214519 | ||||||
| chr1:179214519
|
C | CATATATA others(7): Show |
4 | a0001c0001t0006g0092a0001c0001t0073g0122a0001c0003t0023g0009others(1): Show | 4 | NA18946.hp2 NA18964.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+14708_157+1472 others(18): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214519 | ||||||
| chr1:179214519
|
C | CATATATA others(9): Show |
5 | a0001c0001t0012g0039a0001c0001t0019g0091a0001c0001t0026g0041others(2): Show | 5 | HG01106.hp2 HG02071.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+14706_157+1472 others(20): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214519 | ||||||
| chr1:179214519
|
C | CATATATA others(11): Show |
1 | a0001c0001t0014g0115 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.157+14704_157+1472 others(22): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214519 | ||||||
| chr1:179214519
|
C | CATATATA others(15): Show |
1 | a0001c0001t0063g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.157+14700_157+1472 others(26): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214519 | ||||||
| chr1:179214519
|
CAT | C | 41 | a0001c0001t0001g0240a0001c0001t0002g0152a0001c0001t0002g0191others(38): Show | 41 | HG00544.hp1 HG00544.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.157+14720_157+1472 others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214519 | ||||||
| chr1:179214519
|
CATAT | C | 71 | a0001c0001t0001g0169a0001c0001t0001g0171a0001c0001t0001g0190others(68): Show | 71 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.157+14718_157+1472 others(8): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214519 | ||||||
| chr1:179214519
|
CATATAT | C | 20 | a0001c0001t0001g0146a0001c0001t0001g0162a0001c0001t0001g0166others(17): Show | 20 | HG01070.hp1 HG01071.hp1 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.157+14716_157+1472 others(10): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214519 | ||||||
| chr1:179214519
|
CATATATA others(1): Show |
C | 25 | a0001c0001t0001g0150a0001c0001t0001g0167a0001c0001t0001g0170others(22): Show | 25 | HG00438.hp1 HG00733.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.157+14714_157+1472 others(12): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214519 | ||||||
| chr1:179214519
|
CATATATA others(3): Show |
C | 16 | a0001c0001t0001g0159a0001c0001t0001g0175a0001c0001t0001g0177others(13): Show | 16 | HG00438.hp2 HG02523.hp1 NA18945.hp2 others(13): Show |
intron_variant | MODIFIER | c.157+14712_157+1472 others(14): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214519 | ||||||
| chr1:179214611
|
A | G | 2 | a0002c0005t0022g0253a0002c0005t0022g0275 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.157+14630T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214611 | ||||||
| chr1:179214631
|
T | C | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.157+14610A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214631 | ||||||
| chr1:179214642
|
A | G | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.157+14599T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214642 | ||||||
| chr1:179214711
|
G | C | 11 | a0001c0001t0008g0287a0001c0001t0008g0288a0001c0001t0008g0289others(8): Show | 11 | HG01346.hp2 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.157+14530C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214711 | ||||||
| chr1:179214979
|
G | A | 1 | a0007c0015t0092g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.157+14262C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179214979 | ||||||
| chr1:179215005
|
C | T | 121 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.157+14236G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179215005 | ||||||
| chr1:179215006
|
G | A | 1 | a0001c0001t0011g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.157+14235C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179215006 | ||||||
| chr1:179215174
|
T | C | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.157+14067A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179215174 | ||||||
| chr1:179215181
|
G | A | 15 | a0001c0001t0016g0158a0001c0001t0016g0188a0001c0001t0016g0189others(12): Show | 15 | HG01099.hp1 HG01243.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.157+14060C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179215181 | ||||||
| chr1:179215418
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.157+13823G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179215418 | ||||||
| chr1:179215485
|
G | A | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.157+13756C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179215485 | ||||||
| chr1:179215608
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.157+13633A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179215608 | ||||||
| chr1:179215673
|
C | T | 19 | a0001c0002t0010g0254a0001c0002t0010g0256a0001c0002t0010g0258others(16): Show | 19 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.157+13568G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179215673 | ||||||
| chr1:179216037
|
T | C | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.157+13204A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179216037 | ||||||
| chr1:179216105
|
G | A | 2 | a0001c0004t0031g0021a0001c0004t0031g0022 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.157+13136C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179216105 | ||||||
| chr1:179216144
|
A | G | 28 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0001t0055g0012others(25): Show | 28 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.157+13097T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179216144 | ||||||
| chr1:179216154
|
C | T | 4 | a0001c0001t0001g0169a0001c0001t0001g0190a0001c0001t0001g0199others(1): Show | 4 | HG00741.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+13087G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179216154 | ||||||
| chr1:179216345
|
G | T | 1 | a0001c0001t0003g0052 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.157+12896C>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179216345 | ||||||
| chr1:179216718
|
C | CT | 6 | a0001c0001t0001g0149a0001c0001t0001g0178a0001c0001t0001g0185others(3): Show | 6 | HG01081.hp2 HG01261.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+12522dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179216718 | ||||||
| chr1:179216718
|
CT | C | 6 | a0001c0001t0001g0169a0001c0001t0001g0190a0001c0001t0001g0199others(3): Show | 6 | HG00741.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+12522delA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179216718 | ||||||
| chr1:179216828
|
C | T | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG01081.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.157+12413G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179216828 | ||||||
| chr1:179216857
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.157+12384A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179216857 | ||||||
| chr1:179216932
|
C | T | 207 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(204): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.157+12309G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179216932 | ||||||
| chr1:179217112
|
G | A | 5 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(2): Show | 5 | HG01069.hp1 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+12129C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179217112 | ||||||
| chr1:179217122
|
C | T | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.157+12119G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179217122 | ||||||
| chr1:179217216
|
C | T | 3 | a0001c0003t0023g0009a0001c0003t0023g0010a0001c0003t0023g0011 | 3 | NA18964.hp1 NA18998.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.157+12025G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179217216 | ||||||
| chr1:179217226
|
C | A | 1 | a0009c0014t0002g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.157+12015G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179217226 | ||||||
| chr1:179217332
|
G | A | 7 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.157+11909C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179217332 | ||||||
| chr1:179217412
|
G | A | 5 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0002g0245others(2): Show | 5 | HG00621.hp2 NA18946.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+11829C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179217412 | ||||||
| chr1:179217424
|
A | G | 206 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(203): Show | 206 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.157+11817T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179217424 | ||||||
| chr1:179217540
|
C | T | 1 | a0001c0001t0009g0314 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.157+11701G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179217540 | ||||||
| chr1:179217570
|
G | A | 5 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(2): Show | 5 | HG01069.hp1 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+11671C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179217570 | ||||||
| chr1:179217625
|
C | CA | 6 | a0001c0001t0001g0160a0001c0001t0018g0112a0001c0001t0026g0120others(3): Show | 6 | HG00099.hp1 HG03239.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+11615dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179217625 | ||||||
| chr1:179217722
|
G | A | 9 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0004t0024g0023others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.157+11519C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179217722 | ||||||
| chr1:179217773
|
T | C | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.157+11468A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179217773 | ||||||
| chr1:179217991
|
T | C | 2 | a0001c0001t0002g0228a0001c0001t0037g0231 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.157+11250A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179217991 | ||||||
| chr1:179218109
|
T | G | 4 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+11132A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179218109 | ||||||
| chr1:179218133
|
C | A | 1 | a0001c0001t0108g0340 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.157+11108G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179218133 | ||||||
| chr1:179218192
|
AT | A | 182 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(179): Show | 182 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.157+11048delA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179218192 | ||||||
| chr1:179218229
|
T | C | 1 | a0007c0015t0092g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.157+11012A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179218229 | ||||||
| chr1:179218342
|
G | A | 2 | a0001c0001t0043g0259a0001c0001t0043g0260 | 2 | HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.157+10899C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179218342 | ||||||
| chr1:179218409
|
C | CT | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.157+10831dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179218409 | ||||||
| chr1:179218442
|
G | C | 1 | a0001c0001t0001g0178 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.157+10799C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179218442 | ||||||
| chr1:179218443
|
C | G | 1 | a0001c0001t0001g0178 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.157+10798G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179218443 | ||||||
| chr1:179218459
|
C | T | 1 | a0001c0001t0032g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.157+10782G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179218459 | ||||||
| chr1:179218807
|
T | C | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.157+10434A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179218807 | ||||||
| chr1:179218871
|
C | T | 97 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.157+10370G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179218871 | ||||||
| chr1:179218894
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.157+10347T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179218894 | ||||||
| chr1:179219050
|
G | GCTTT | 207 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(204): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.157+10190_157+1019 others(8): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179219050 | ||||||
| chr1:179219194
|
T | C | 5 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(2): Show | 5 | HG01069.hp1 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+10047A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179219194 | ||||||
| chr1:179219402
|
G | GA | 5 | a0002c0005t0022g0253a0002c0005t0022g0275a0002c0005t0022g0276others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+9838dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179219402 | ||||||
| chr1:179219558
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.157+9683G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179219558 | ||||||
| chr1:179219559
|
T | C | 1 | a0001c0001t0001g0178 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.157+9682A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179219559 | ||||||
| chr1:179219597
|
T | C | 1 | a0009c0014t0002g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.157+9644A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179219597 | ||||||
| chr1:179219690
|
A | C | 1 | a0001c0004t0111g0347 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.157+9551T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179219690 | ||||||
| chr1:179220127
|
C | A | 1 | a0001c0001t0072g0121 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.157+9114G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179220127 | ||||||
| chr1:179220193
|
A | C | 26 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(23): Show | 26 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.157+9048T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179220193 | ||||||
| chr1:179220491
|
G | A | 2 | a0001c0001t0077g0142a0001c0001t0078g0143 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.157+8750C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179220491 | ||||||
| chr1:179220533
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.157+8708A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179220533 | ||||||
| chr1:179220710
|
C | G | 96 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.157+8531G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179220710 | ||||||
| chr1:179220872
|
A | T | 1 | a0001c0001t0001g0161 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.157+8369T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179220872 | ||||||
| chr1:179220987
|
T | G | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.157+8254A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179220987 | ||||||
| chr1:179220990
|
A | C | 1 | a0001c0001t0001g0238 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.157+8251T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179220990 | ||||||
| chr1:179221426
|
A | C | 1 | a0001c0001t0001g0161 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.157+7815T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179221426 | ||||||
| chr1:179221523
|
G | A | 28 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0159others(25): Show | 28 | HG00438.hp2 HG00733.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.157+7718C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179221523 | ||||||
| chr1:179221546
|
G | A | 2 | a0001c0001t0035g0220a0001c0001t0035g0225 | 2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.157+7695C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179221546 | ||||||
| chr1:179221635
|
C | G | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.157+7606G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179221635 | ||||||
| chr1:179221639
|
G | A | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.157+7602C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179221639 | ||||||
| chr1:179221756
|
T | C | 28 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0001t0055g0012others(25): Show | 28 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.157+7485A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179221756 | ||||||
| chr1:179221793
|
C | CA | 40 | a0001c0001t0001g0149a0001c0001t0001g0237a0001c0001t0001g0241others(37): Show | 40 | HG00438.hp2 HG00558.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.157+7447dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179221793 | ||||||
| chr1:179221793
|
CA | C | 46 | a0001c0001t0001g0162a0001c0001t0008g0282a0001c0001t0008g0283others(43): Show | 46 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.157+7447delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179221793 | ||||||
| chr1:179221793
|
CAA | C | 144 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(141): Show | 144 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.157+7446_157+7447d others(4): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179221793 | ||||||
| chr1:179221912
|
T | C | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+7329A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179221912 | ||||||
| chr1:179222095
|
G | C | 1 | a0001c0001t0102g0296 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.157+7146C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179222095 | ||||||
| chr1:179222260
|
C | T | 1 | a0001c0001t0025g0043 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.157+6981G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179222260 | ||||||
| chr1:179222330
|
A | G | 2 | a0001c0001t0038g0216a0001c0001t0038g0221 | 2 | HG02055.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.157+6911T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179222330 | ||||||
| chr1:179222396
|
A | AT | 11 | a0001c0001t0009g0279a0001c0001t0012g0051a0001c0001t0032g0026others(8): Show | 11 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.157+6844dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179222396 | ||||||
| chr1:179222425
|
C | T | 192 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(189): Show | 192 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.157+6816G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179222425 | ||||||
| chr1:179222455
|
A | G | 1 | a0001c0002t0093g0274 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.157+6786T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179222455 | ||||||
| chr1:179222494
|
G | A | 2 | a0001c0001t0096g0306a0001c0001t0097g0304 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.157+6747C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179222494 | ||||||
| chr1:179222510
|
C | T | 15 | a0001c0001t0001g0149a0001c0001t0001g0161a0001c0001t0001g0237others(12): Show | 15 | HG00140.hp2 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.157+6731G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179222510 | ||||||
| chr1:179222816
|
C | A | 1 | a0001c0001t0011g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.157+6425G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179222816 | ||||||
| chr1:179222823
|
A | C | 2 | a0001c0001t0001g0160a0001c0001t0036g0229 | 2 | HG00099.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.157+6418T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179222823 | ||||||
| chr1:179223050
|
C | T | 1 | a0001c0001t0005g0345 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.157+6191G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179223050 | ||||||
| chr1:179223103
|
C | T | 156 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.157+6138G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179223103 | ||||||
| chr1:179223109
|
C | CA | 66 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(63): Show | 66 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.157+6131dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179223109 | ||||||
| chr1:179223109
|
CA | C | 127 | a0001c0001t0002g0154a0001c0001t0003g0033a0001c0001t0003g0045others(124): Show | 127 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.157+6131delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179223109 | ||||||
| chr1:179223293
|
A | G | 1 | a0001c0001t0009g0280 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.157+5948T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179223293 | ||||||
| chr1:179223412
|
C | CA | 189 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.157+5828dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179223412 | ||||||
| chr1:179223412
|
C | CAA | 8 | a0001c0001t0004g0082a0001c0001t0006g0092a0001c0001t0008g0297others(5): Show | 8 | HG02738.hp2 NA18940.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.157+5827_157+5828d others(4): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179223412 | ||||||
| chr1:179223473
|
C | T | 1 | a0001c0001t0009g0279 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.157+5768G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179223473 | ||||||
| chr1:179223481
|
G | C | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.157+5760C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179223481 | ||||||
| chr1:179223855
|
C | T | 1 | a0001c0001t0004g0050 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.157+5386G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179223855 | ||||||
| chr1:179223867
|
C | T | 7 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.157+5374G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179223867 | ||||||
| chr1:179223964
|
C | CA | 122 | a0001c0001t0003g0033a0001c0001t0003g0047a0001c0001t0003g0052others(119): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.157+5276dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179223964 | ||||||
| chr1:179223964
|
CA | C | 24 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0003t0028g0001others(21): Show | 24 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.157+5276delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179223964 | ||||||
| chr1:179224123
|
C | T | 1 | a0001c0001t0068g0093 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.157+5118G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179224123 | ||||||
| chr1:179224134
|
C | CA | 63 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0244others(60): Show | 63 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.157+5106dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179224134 | ||||||
| chr1:179224134
|
C | CAA | 35 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(32): Show | 35 | HG01069.hp1 HG01081.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.157+5105_157+5106d others(4): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179224134 | ||||||
| chr1:179224134
|
C | CAAA | 69 | a0001c0001t0003g0052a0001c0001t0003g0054a0001c0001t0003g0057others(66): Show | 69 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.157+5104_157+5106d others(5): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179224134 | ||||||
| chr1:179224134
|
C | CAAAA | 26 | a0001c0001t0003g0086a0001c0001t0003g0089a0001c0001t0003g0095others(23): Show | 26 | HG00558.hp2 HG00621.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.157+5103_157+5106d others(6): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179224134 | ||||||
| chr1:179224134
|
CAAAAAAA others(2): Show |
C | 8 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.157+5098_157+5106d others(11): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179224134 | ||||||
| chr1:179224148
|
A | C | 2 | a0004c0009t0039g0145a0004c0009t0039g0147 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.157+5093T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179224148 | ||||||
| chr1:179224267
|
T | C | 1 | a0009c0014t0002g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.157+4974A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179224267 | ||||||
| chr1:179224352
|
C | T | 1 | a0001c0001t0011g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.157+4889G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179224352 | ||||||
| chr1:179224359
|
G | A | 2 | a0001c0001t0056g0020a0001c0001t0104g0278 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.157+4882C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179224359 | ||||||
| chr1:179224430
|
C | A | 1 | a0001c0001t0002g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.157+4811G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179224430 | ||||||
| chr1:179224542
|
T | G | 2 | a0001c0001t0077g0142a0001c0001t0078g0143 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.157+4699A>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179224542 | ||||||
| chr1:179224795
|
A | T | 1 | a0001c0001t0001g0146 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.157+4446T>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179224795 | ||||||
| chr1:179224797
|
C | T | 121 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.157+4444G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179224797 | ||||||
| chr1:179224852
|
C | CA | 27 | a0001c0001t0001g0149a0001c0001t0001g0190a0001c0001t0001g0237others(24): Show | 27 | HG01884.hp2 HG02055.hp1 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.157+4388dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179224852 | ||||||
| chr1:179224852
|
CA | C | 23 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(20): Show | 23 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.157+4388delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179224852 | ||||||
| chr1:179224895
|
G | A | 1 | a0001c0004t0058g0028 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.157+4346C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179224895 | ||||||
| chr1:179225736
|
G | A | 2 | a0001c0001t0043g0259a0001c0001t0043g0260 | 2 | HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.157+3505C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179225736 | ||||||
| chr1:179225900
|
C | T | 4 | a0001c0001t0001g0160a0001c0001t0001g0193a0001c0001t0036g0229others(1): Show | 4 | HG00099.hp1 HG02602.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+3341G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179225900 | ||||||
| chr1:179225957
|
T | C | 7 | a0001c0001t0005g0345a0001c0001t0011g0341a0001c0001t0045g0338others(4): Show | 7 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.157+3284A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179225957 | ||||||
| chr1:179226000
|
C | T | 1 | a0007c0015t0092g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.157+3241G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179226000 | ||||||
| chr1:179226043
|
C | CA | 55 | a0001c0001t0001g0146a0001c0001t0001g0193a0001c0001t0001g0199others(52): Show | 55 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.157+3197dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179226043 | ||||||
| chr1:179226043
|
C | CAA | 14 | a0001c0001t0001g0237a0001c0001t0002g0214a0001c0001t0002g0215others(11): Show | 14 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.157+3196_157+3197d others(4): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179226043 | ||||||
| chr1:179226043
|
C | CAAA | 11 | a0001c0001t0016g0158a0001c0001t0016g0222a0001c0001t0016g0223others(8): Show | 11 | HG01099.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.157+3195_157+3197d others(5): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179226043 | ||||||
| chr1:179226043
|
CA | C | 83 | a0001c0001t0001g0159a0001c0001t0003g0033a0001c0001t0003g0045others(80): Show | 83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.157+3197delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179226043 | ||||||
| chr1:179226043
|
CAA | C | 26 | a0001c0001t0001g0149a0001c0001t0002g0148a0001c0001t0025g0032others(23): Show | 26 | HG00140.hp2 HG00597.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.157+3196_157+3197d others(4): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179226043 | ||||||
| chr1:179226043
|
CAAAAAAA others(2): Show |
C | 23 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(20): Show | 23 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.157+3189_157+3197d others(11): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179226043 | ||||||
| chr1:179226105
|
C | A | 25 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(22): Show | 25 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.157+3136G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179226105 | ||||||
| chr1:179226310
|
C | CT | 27 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0244others(24): Show | 27 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.157+2930dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179226310 | ||||||
| chr1:179226310
|
CTTTTTT | C | 25 | a0001c0001t0008g0282a0001c0001t0008g0283a0001c0001t0008g0287others(22): Show | 25 | HG01081.hp1 HG01167.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.157+2925_157+2930d others(8): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179226310 | ||||||
| chr1:179226372
|
G | A | 2 | a0001c0001t0112g0348a0001c0001t0113g0349 | 2 | HG01884.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.157+2869C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179226372 | ||||||
| chr1:179226558
|
C | T | 24 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(21): Show | 24 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.157+2683G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179226558 | ||||||
| chr1:179226626
|
T | C | 28 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0001t0055g0012others(25): Show | 28 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.157+2615A>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179226626 | ||||||
| chr1:179226642
|
A | G | 97 | a0001c0001t0003g0033a0001c0001t0003g0045a0001c0001t0003g0047others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.157+2599T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179226642 | ||||||
| chr1:179226733
|
A | C | 2 | a0001c0007t0040g0302a0001c0007t0040g0303 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.157+2508T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179226733 | ||||||
| chr1:179227584
|
A | C | 5 | a0001c0002t0010g0254a0001c0002t0010g0256a0001c0002t0010g0258others(2): Show | 5 | HG00544.hp2 HG02015.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+1657T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179227584 | ||||||
| chr1:179227600
|
C | T | 1 | a0001c0001t0009g0314 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.157+1641G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179227600 | ||||||
| chr1:179227742
|
C | T | 1 | a0001c0001t0005g0318 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.157+1499G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179227742 | ||||||
| chr1:179227790
|
C | T | 2 | a0001c0001t0006g0035a0001c0001t0066g0036 | 2 | HG02523.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.157+1451G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179227790 | ||||||
| chr1:179227861
|
G | A | 5 | a0001c0001t0021g0307a0001c0001t0021g0309a0001c0001t0021g0310others(2): Show | 5 | HG01069.hp1 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+1380C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179227861 | ||||||
| chr1:179227890
|
A | C | 1 | a0001c0001t0001g0146 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.157+1351T>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179227890 | ||||||
| chr1:179228027
|
G | A | 7 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.157+1214C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179228027 | ||||||
| chr1:179228050
|
C | CA | 15 | a0001c0001t0001g0233a0001c0001t0001g0237a0001c0001t0002g0228others(12): Show | 15 | HG00597.hp1 HG00741.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.157+1190dupT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179228050 | ||||||
| chr1:179228050
|
CA | C | 169 | a0001c0001t0001g0238a0001c0001t0003g0045a0001c0001t0003g0047others(166): Show | 169 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.157+1190delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179228050 | ||||||
| chr1:179228050
|
CAA | C | 6 | a0001c0001t0003g0033a0001c0001t0014g0034a0001c0001t0025g0032others(3): Show | 6 | HG01070.hp1 HG01256.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.157+1189_157+1190d others(4): Show |
ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179228050 | ||||||
| chr1:179228203
|
C | T | 3 | a0001c0001t0005g0315a0001c0001t0005g0316a0001c0001t0005g0317 | 3 | NA18943.hp1 NA19064.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.157+1038G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179228203 | ||||||
| chr1:179228204
|
G | A | 11 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0241others(8): Show | 11 | HG00280.hp1 HG00621.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.157+1037C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179228204 | ||||||
| chr1:179228333
|
C | T | 1 | a0001c0001t0091g0312 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.157+908G>A | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179228333 | ||||||
| chr1:179228340
|
C | CT | 19 | a0001c0001t0055g0012a0001c0003t0023g0009a0001c0003t0023g0010others(16): Show | 19 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.157+900dupA | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179228340 | ||||||
| chr1:179228346
|
CA | C | 9 | a0001c0001t0032g0026a0001c0001t0032g0027a0001c0004t0024g0023others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.157+894delT | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179228346 | ||||||
| chr1:179228488
|
G | C | 2 | a0001c0001t0091g0312a0007c0015t0092g0313 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.157+753C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179228488 | ||||||
| chr1:179228692
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.157+549T>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179228692 | ||||||
| chr1:179228794
|
G | A | 1 | a0001c0001t0009g0314 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.157+447C>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179228794 | ||||||
| chr1:179228871
|
C | G | 1 | a0001c0001t0061g0031 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.157+370G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179228871 | ||||||
| chr1:179229069
|
G | C | 5 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0002g0245others(2): Show | 5 | HG00621.hp2 NA18946.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+172C>G | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179229069 | ||||||
| chr1:179229140
|
C | A | 1 | a0001c0001t0042g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.157+101G>T | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179229140 | ||||||
| chr1:179229165
|
C | G | 4 | a0001c0001t0041g0250a0001c0001t0041g0251a0001c0001t0042g0249others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+76G>C | ABL2 | ENSG00000143322.22 | transcript | ENST00000502732.6 | protein_coding | 1/11 | chr1 | 179229165 |