Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8976 |
| ensemblid | ENSG00000106299.8 |
| hgncid | 12735 |
| symbol | WASL |
| name | WASP like actin nucleation promoting factor |
| refseq_nuc | NM_003941.4 |
| refseq_prot | NP_003932.3 |
| ensembl_nuc | ENST00000223023.5 |
| ensembl_prot | ENSP00000223023.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 123681943 |
| end | 123749003 |
| strand | - |
| ver | v1.2 |
| region | chr7:123681943-123749003 |
| region5000 | chr7:123676943-123754003 |
| regionname0 | WASL_chr7_123681943_123749003 |
| regionname5000 | WASL_chr7_123676943_123754003 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 505 | 355 | 88 | 60 | 151 | 14 | 40 | 117 | WASL_chr7_123676943_123754003 | WASL | MSSVQ others(500): Show |
chr7 | 123676943 | 123754003 |
| a0002 | 0/0 | 505 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | MSSVQ others(500): Show |
chr7 | 123676943 | 123754003 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1515 | 189 | 59 | 34 | 73 | 7 | 14 | WASL_chr7_123676943_123754003 | WASL | ATGAG others(1510): Show |
chr7 | 123676943 | 123754003 | ||
| a0001c0002 | 0/0 | 1515 | 150 | 29 | 24 | 64 | 7 | 26 | WASL_chr7_123676943_123754003 | WASL | ATGAG others(1510): Show |
chr7 | 123676943 | 123754003 | ||
| a0001c0003 | 0/0 | 1515 | 15 | 0 | 1 | 14 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | ATGAG others(1510): Show |
chr7 | 123676943 | 123754003 | ||
| a0001c0005 | 0/0 | 1515 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | ATGAG others(1510): Show |
chr7 | 123676943 | 123754003 | ||
| a0002c0004 | 0/0 | 1515 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | ATGAG others(1510): Show |
chr7 | 123676943 | 123754003 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4361 | 3 | 3 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4356): Show |
chr7 | 123676943 | 123754003 |
| a0001c0001t0002 | 1/0 | 4363 | 88 | 32 | 13 | 31 | 3 | 8 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4358): Show |
chr7 | 123676943 | 123754003 |
| a0001c0001t0003 | 0/1 | 4363 | 47 | 13 | 11 | 19 | 1 | 2 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4358): Show |
chr7 | 123676943 | 123754003 |
| a0001c0001t0004 | 0/0 | 4363 | 33 | 3 | 4 | 19 | 3 | 4 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4358): Show |
chr7 | 123676943 | 123754003 |
| a0001c0001t0006 | 0/0 | 4361 | 3 | 3 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4356): Show |
chr7 | 123676943 | 123754003 |
| a0001c0001t0007 | 0/0 | 4363 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4358): Show |
chr7 | 123676943 | 123754003 |
| a0001c0001t0008 | 0/0 | 4363 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4358): Show |
chr7 | 123676943 | 123754003 |
| a0001c0001t0009 | 0/0 | 4363 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4358): Show |
chr7 | 123676943 | 123754003 |
| a0001c0001t0010 | 0/0 | 4361 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4356): Show |
chr7 | 123676943 | 123754003 |
| a0001c0001t0011 | 0/0 | 4363 | 2 | 0 | 2 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCCGT others(4358): Show |
chr7 | 123676943 | 123754003 |
| a0001c0001t0012 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4358): Show |
chr7 | 123676943 | 123754003 |
| a0001c0001t0013 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4358): Show |
chr7 | 123676943 | 123754003 |
| a0001c0001t0014 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4358): Show |
chr7 | 123676943 | 123754003 |
| a0001c0001t0015 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4358): Show |
chr7 | 123676943 | 123754003 |
| a0001c0001t0016 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4358): Show |
chr7 | 123676943 | 123754003 |
| a0001c0002t0001 | 0/0 | 4361 | 141 | 26 | 22 | 63 | 6 | 24 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4356): Show |
chr7 | 123676943 | 123754003 |
| a0001c0002t0003 | 0/0 | 4363 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4358): Show |
chr7 | 123676943 | 123754003 |
| a0001c0002t0017 | 0/0 | 4361 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4356): Show |
chr7 | 123676943 | 123754003 |
| a0001c0002t0018 | 0/0 | 4361 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4356): Show |
chr7 | 123676943 | 123754003 |
| a0001c0002t0019 | 0/0 | 4361 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4356): Show |
chr7 | 123676943 | 123754003 |
| a0001c0002t0021 | 0/0 | 4361 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4356): Show |
chr7 | 123676943 | 123754003 |
| a0001c0002t0022 | 0/0 | 4361 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4356): Show |
chr7 | 123676943 | 123754003 |
| a0001c0002t0023 | 0/0 | 4361 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4356): Show |
chr7 | 123676943 | 123754003 |
| a0001c0002t0024 | 0/0 | 4361 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4356): Show |
chr7 | 123676943 | 123754003 |
| a0001c0003t0003 | 0/0 | 4363 | 10 | 0 | 1 | 9 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4358): Show |
chr7 | 123676943 | 123754003 |
| a0001c0003t0005 | 0/0 | 4363 | 4 | 0 | 0 | 4 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4358): Show |
chr7 | 123676943 | 123754003 |
| a0001c0003t0020 | 0/0 | 4361 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4356): Show |
chr7 | 123676943 | 123754003 |
| a0001c0005t0001 | 0/0 | 4361 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4356): Show |
chr7 | 123676943 | 123754003 |
| a0002c0004t0002 | 0/0 | 4363 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | GCAGT others(4358): Show |
chr7 | 123676943 | 123754003 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0005 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0010 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0108 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0006g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0007g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0008g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0008g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0009g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0009g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0010g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0010g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0011g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0012g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0013g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0014g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0015g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0001t0016g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0001 | 0/0 | 8 | 1 | 2 | 4 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0017g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0018g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0019g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0021g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0022g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0023g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0002t0024g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0003t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0003t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0003t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0003t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0003t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0003t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0003t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0003t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0003t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0003t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0003t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0003t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0003t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0003t0020g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0001c0005t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| a0002c0004t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0097 | EUR | GBR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00099 | hp2 | a0001 | c0002 | t0021 | g0250 | EUR | GBR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0230 | EUR | GBR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0213 | EUR | GBR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0149 | EUR | FIN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0282 | EUR | FIN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0148 | EUR | FIN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0220 | EUR | FIN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00408 | hp1 | a0001 | c0001 | t0008 | g0156 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00544 | hp1 | a0001 | c0003 | t0003 | g0122 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0283 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00639 | hp2 | a0001 | c0001 | t0015 | g0064 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0291 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00673 | hp1 | a0001 | c0003 | t0005 | g0127 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0168 | EAS | CHS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0191 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00735 | hp1 | a0001 | c0002 | t0018 | g0202 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0150 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0286 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0266 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0261 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0201 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0154 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01109 | hp2 | a0001 | c0005 | t0001 | g0223 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01167 | hp1 | a0001 | c0001 | t0011 | g0040 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0237 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01169 | hp1 | a0001 | c0001 | t0011 | g0040 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0147 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0280 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0183 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0211 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0289 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0193 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01361 | hp2 | a0001 | c0001 | t0016 | g0135 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0137 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0153 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0151 | EUR | IBS | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0178 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0264 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01943 | hp2 | a0001 | c0003 | t0003 | g0130 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0290 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0300 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01981 | hp2 | a0001 | c0001 | t0012 | g0054 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0292 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0166 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0247 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02071 | hp2 | a0001 | c0003 | t0005 | g0134 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0159 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0242 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02148 | hp1 | a0001 | c0001 | t0013 | g0083 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0179 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | CDX | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | CDX | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0241 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02273 | hp2 | a0001 | c0002 | t0022 | g0288 | AMR | PEL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0129 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0287 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0119 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | KHV | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0245 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0132 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0206 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0038 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0301 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0174 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0007 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0235 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0195 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0041 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02970 | hp1 | a0001 | c0002 | t0003 | g0295 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0252 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03098 | hp1 | a0001 | c0001 | t0014 | g0187 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03130 | hp2 | a0001 | c0002 | t0003 | g0296 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0208 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0042 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | ESN | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0043 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0207 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0279 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0038 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0253 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0293 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0199 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0204 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | GWD | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0118 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0299 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03688 | hp1 | a0001 | c0002 | t0023 | g0215 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0224 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0284 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0196 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0225 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0260 | SAS | PJL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0281 | SAS | BEB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0212 | SAS | BEB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0162 | SAS | BEB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03942 | hp2 | a0001 | c0002 | t0024 | g0236 | SAS | BEB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0275 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0214 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0238 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0089 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0029 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0197 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0198 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0051 | SAS | STU | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0229 | AFR | YRI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0272 | AFR | YRI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18747 | hp1 | a0001 | c0002 | t0019 | g0297 | EAS | CHB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | CHB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0209 | AFR | YRI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | YRI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18941 | hp1 | a0002 | c0004 | t0002 | g0069 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18949 | hp1 | a0001 | c0003 | t0003 | g0186 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18949 | hp2 | a0001 | c0001 | t0008 | g0157 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18964 | hp1 | a0001 | c0003 | t0005 | g0126 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18967 | hp1 | a0001 | c0003 | t0005 | g0138 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18972 | hp1 | a0001 | c0003 | t0003 | g0123 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18986 | hp1 | a0001 | c0003 | t0003 | g0120 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18993 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18998 | hp1 | a0001 | c0003 | t0003 | g0124 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0170 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | LWK | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | LWK | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | LWK | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | LWK | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19063 | hp1 | a0001 | c0003 | t0020 | g0125 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19070 | hp2 | a0001 | c0003 | t0003 | g0140 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19074 | hp2 | a0001 | c0003 | t0003 | g0016 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19084 | hp2 | a0001 | c0003 | t0003 | g0016 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19087 | hp1 | a0001 | c0003 | t0003 | g0121 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19091 | hp2 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0200 | AFR | YRI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA19240 | hp2 | a0001 | c0002 | t0017 | g0294 | AFR | YRI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0192 | AFR | ASW | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ASW | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0103 | EUR | TSI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0094 | EUR | TSI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0203 | EUR | TSI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0078 | EUR | TSI | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0221 | SAS | GIH | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | GIH | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0227 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0205 | AFR | MSL | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0145 | AFR | USA | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | USA | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | USA | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0254 | AFR | USA | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | LWK | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0228 | AFR | LWK | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0108 | REF | REF | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0059 | REF | REF | WASL_chr7_123676943_123754003 | WASL | chr7 | 123676943 | 123754003 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:123692700 | C | T | 1 | a0002 | 1 | NA18941.hp1 | missense_variant | MODERATE | c.994G>A | p.Val332Ile | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/11 | 1263/4363 | 994/1518 | 332/505 | chr7 | 123692700 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:123696668 | G | A | 1 | a0001c0003 | 15 | HG00544.hp1 HG00673.hp1 HG01943.hp2 others(12): Show |
synonymous_variant | LOW | c.540C>T | p.Asn180Asn | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 6/11 | 809/4363 | 540/1518 | 180/505 | chr7 | 123696668 | |||
| chr7:123709197 | T | C | 1 | a0001c0005 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.144A>G | p.Leu48Leu | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/11 | 413/4363 | 144/1518 | 48/505 | chr7 | 123709197 | |||
| chr7:123748678 | G | A | 2 | a0001c0002 a0001c0005 |
151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
synonymous_variant | LOW | c.57C>T | p.Ser19Ser | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/11 | 326/4363 | 57/1518 | 19/505 | chr7 | 123748678 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:123681982 | G | T | 1 | a0001c0002t0021 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2537C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 2537 | chr7 | 123681982 | ||||||
| chr7:123682134 | G | A | 1 | a0001c0001t0006 | 3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2385C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 2385 | chr7 | 123682134 | ||||||
| chr7:123682209 | A | C | 1 | a0001c0001t0014 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2310T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 2310 | chr7 | 123682209 | ||||||
| chr7:123682329 | G | A | 1 | a0001c0002t0022 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2190C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 2190 | chr7 | 123682329 | ||||||
| chr7:123682622 | G | A | 1 | a0001c0003t0005 | 4 | HG00673.hp1 HG02071.hp2 NA18964.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1897C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 1897 | chr7 | 123682622 | ||||||
| chr7:123682662 | T | A | 12 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0010 others(9): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*1857A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 1857 | chr7 | 123682662 | ||||||
| chr7:123682725 | G | C | 2 | a0001c0001t0004 a0001c0001t0008 |
35 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1794C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 1794 | chr7 | 123682725 | ||||||
| chr7:123683030 | C | G | 1 | a0001c0001t0013 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1489G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 1489 | chr7 | 123683030 | ||||||
| chr7:123683197 | T | G | 2 | a0001c0001t0004 a0001c0001t0008 |
35 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1322A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 1322 | chr7 | 123683197 | ||||||
| chr7:123683248 | T | C | 1 | a0001c0002t0023 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1271A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 1271 | chr7 | 123683248 | ||||||
| chr7:123683374 | T | A | 6 | a0001c0001t0003 a0001c0001t0016 a0001c0002t0003 others(3): Show |
64 | HG00544.hp1 HG00673.hp1 HG01099.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1145A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 1145 | chr7 | 123683374 | ||||||
| chr7:123683512 | G | A | 1 | a0001c0001t0008 | 2 | HG00408.hp1 NA18949.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1007C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 1007 | chr7 | 123683512 | ||||||
| chr7:123683610 | C | T | 1 | a0001c0003t0020 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*909G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 909 | chr7 | 123683610 | ||||||
| chr7:123683624 | T | C | 1 | a0001c0001t0010 | 2 | HG02922.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*895A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 895 | chr7 | 123683624 | ||||||
| chr7:123683687 | A | G | 1 | a0001c0001t0012 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*832T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 832 | chr7 | 123683687 | ||||||
| chr7:123683700 | T | C | 1 | a0001c0002t0024 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*819A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 819 | chr7 | 123683700 | ||||||
| chr7:123683771 | T | A | 1 | a0001c0001t0009 | 2 | HG02451.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*748A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 748 | chr7 | 123683771 | ||||||
| chr7:123683928 | C | T | 1 | a0001c0002t0019 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*591G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 591 | chr7 | 123683928 | ||||||
| chr7:123684016 | G | T | 1 | a0001c0001t0007 | 2 | NA18993.hp1 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*503C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 503 | chr7 | 123684016 | ||||||
| chr7:123684019 | C | A | 1 | a0001c0001t0015 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*500G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 500 | chr7 | 123684019 | ||||||
| chr7:123684107 | A | T | 1 | a0001c0002t0018 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*412T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 412 | chr7 | 123684107 | ||||||
| chr7:123684113 | G | T | 1 | a0001c0002t0017 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*406C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 406 | chr7 | 123684113 | ||||||
| chr7:123684332 | T | C | 1 | a0001c0001t0016 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*187A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 187 | chr7 | 123684332 | ||||||
| chr7:123684492 | AAT | A | 13 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0010 others(10): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*25_*26delAT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 11/11 | 25 | chr7 | 123684492 | ||||||
| chr7:123749001 | T | G | 1 | a0001c0001t0011 | 2 | HG01167.hp1 HG01169.hp1 |
5_prime_UTR_variant | MODIFIER | c.-267A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/11 | 267 | chr7 | 123749001 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:123684691 | CCAG | C | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1457-114_1457-112d others(5): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123684691 | |||||||
| chr7:123684770 | T | C | 1 | a0001c0002t0001g0239 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1457-190A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123684770 | |||||||
| chr7:123684809 | A | G | 1 | a0001c0001t0002g0078 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1457-229T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123684809 | |||||||
| chr7:123684903 | T | C | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1457-323A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123684903 | |||||||
| chr7:123685285 | A | G | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1457-705T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685285 | |||||||
| chr7:123685297 | A | T | 3 | a0001c0001t0004g0006 a0001c0001t0004g0147 a0001c0001t0004g0148 |
5 | HG00323.hp1 HG01175.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.1457-717T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685297 | |||||||
| chr7:123685333 | A | G | 1 | a0001c0002t0001g0283 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1457-753T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685333 | |||||||
| chr7:123685337 | C | T | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1457-757G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685337 | |||||||
| chr7:123685405 | C | T | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1457-825G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685405 | |||||||
| chr7:123685611 | T | C | 1 | a0001c0001t0003g0132 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1457-1031A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685611 | |||||||
| chr7:123685642 | A | G | 2 | a0001c0001t0003g0023 a0001c0001t0003g0173 |
3 | NA18941.hp2 NA18984.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1457-1062T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685642 | |||||||
| chr7:123685654 | T | C | 2 | a0001c0002t0001g0263 a0001c0002t0001g0269 |
2 | HG00423.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1457-1074A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685654 | |||||||
| chr7:123685682 | C | G | 1 | a0001c0001t0008g0157 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1457-1102G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685682 | |||||||
| chr7:123685781 | C | T | 1 | a0001c0001t0003g0174 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1457-1201G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685781 | |||||||
| chr7:123685783 | T | A | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1457-1203A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685783 | |||||||
| chr7:123685805 | A | G | 2 | a0001c0001t0006g0008 a0001c0001t0006g0043 |
3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1457-1225T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685805 | |||||||
| chr7:123685859 | TATATATA others(1): Show |
T | 6 | a0001c0002t0001g0227 a0001c0002t0001g0228 a0001c0002t0001g0229 others(3): Show |
6 | HG02109.hp1 HG02258.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1457-1287_1457-128 others(12): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685859 | |||||||
| chr7:123685871 | TATAA | T | 53 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0023 others(50): Show |
60 | HG00544.hp1 HG00673.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.1457-1295_1457-129 others(8): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685871 | |||||||
| chr7:123685905 | T | C | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1457-1325A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685905 | |||||||
| chr7:123685990 | G | T | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1457-1410C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123685990 | |||||||
| chr7:123686001 | T | C | 2 | a0001c0001t0006g0008 a0001c0001t0006g0043 |
3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1457-1421A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123686001 | |||||||
| chr7:123686183 | A | T | 1 | a0001c0002t0001g0265 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1457-1603T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123686183 | |||||||
| chr7:123686281 | T | C | 2 | a0001c0001t0003g0014 a0001c0001t0003g0103 |
3 | HG01168.hp2 HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1457-1701A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123686281 | |||||||
| chr7:123686302 | C | T | 1 | a0001c0002t0001g0284 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1457-1722G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123686302 | |||||||
| chr7:123686926 | A | G | 2 | a0001c0001t0002g0109 a0001c0001t0002g0110 |
2 | NA19001.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1456+2116T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123686926 | |||||||
| chr7:123686939 | A | G | 1 | a0001c0003t0005g0126 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1456+2103T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123686939 | |||||||
| chr7:123686969 | A | G | 1 | a0001c0002t0001g0031 | 2 | NA18945.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1456+2073T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123686969 | |||||||
| chr7:123687109 | T | C | 2 | a0001c0001t0004g0145 a0001c0001t0004g0149 |
2 | HG00280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1456+1933A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123687109 | |||||||
| chr7:123687346 | A | G | 1 | a0001c0002t0001g0301 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1456+1696T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123687346 | |||||||
| chr7:123687426 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1456+1616T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123687426 | |||||||
| chr7:123687618 | C | T | 1 | a0001c0002t0001g0195 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1456+1424G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123687618 | |||||||
| chr7:123687756 | C | CTT | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1456+1284_1456+128 others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123687756 | |||||||
| chr7:123687806 | T | C | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1456+1236A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123687806 | |||||||
| chr7:123687882 | G | C | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1456+1160C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123687882 | |||||||
| chr7:123688256 | A | C | 1 | a0001c0001t0002g0018 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1456+786T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123688256 | |||||||
| chr7:123688321 | T | A | 1 | a0001c0002t0001g0234 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1456+721A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123688321 | |||||||
| chr7:123688371 | T | A | 1 | a0001c0001t0002g0098 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1456+671A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123688371 | |||||||
| chr7:123688382 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1456+660G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123688382 | |||||||
| chr7:123688485 | C | T | 2 | a0001c0001t0009g0118 a0001c0001t0009g0119 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1456+557G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123688485 | |||||||
| chr7:123688992 | C | T | 3 | a0001c0002t0001g0220 a0001c0002t0001g0221 a0001c0002t0001g0230 |
3 | HG00140.hp1 HG00323.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1456+50G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123688992 | |||||||
| chr7:123689006 | G | GTC | 10 | a0001c0001t0002g0045 a0001c0001t0002g0095 a0001c0001t0002g0146 others(7): Show |
10 | HG01256.hp2 HG02258.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.1456+34_1456+35dup others(2): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123689006 | |||||||
| chr7:123689006 | GTC | G | 205 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(202): Show |
247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1456+34_1456+35del others(2): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123689006 | |||||||
| chr7:123689006 | GTCTC | G | 4 | a0001c0001t0002g0063 a0001c0001t0002g0071 a0001c0001t0002g0093 others(1): Show |
4 | HG01243.hp2 HG02970.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.1456+32_1456+35del others(4): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123689006 | |||||||
| chr7:123689006 | GTCTCTCT others(3): Show |
G | 1 | a0001c0001t0015g0064 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1456+26_1456+35del others(10): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123689006 | |||||||
| chr7:123689006 | GTCTCTCT others(9): Show |
G | 2 | a0001c0001t0006g0008 a0001c0001t0006g0043 |
3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1456+20_1456+35del others(16): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123689006 | |||||||
| chr7:123689032 | C | T | 6 | a0001c0002t0001g0227 a0001c0002t0001g0228 a0001c0002t0001g0229 others(3): Show |
6 | HG02109.hp1 HG02258.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1456+10G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 10/10 | chr7 | 123689032 | |||||||
| chr7:123689213 | A | G | 4 | a0001c0001t0004g0150 a0001c0001t0004g0151 a0001c0001t0004g0153 others(1): Show |
4 | HG00738.hp1 HG01099.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348-63T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689213 | |||||||
| chr7:123689313 | C | A | 1 | a0001c0002t0001g0002 | 5 | NA18942.hp1 NA18962.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1348-163G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689313 | |||||||
| chr7:123689427 | T | A | 1 | a0001c0002t0001g0238 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1348-277A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689427 | |||||||
| chr7:123689549 | G | A | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1348-399C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689549 | |||||||
| chr7:123689700 | T | G | 228 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(225): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.1348-550A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689700 | |||||||
| chr7:123689793 | ATT | A | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1348-645_1348-644d others(4): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689793 | |||||||
| chr7:123689798 | A | T | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1348-648T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689798 | |||||||
| chr7:123689799 | AT | A | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1348-650delA | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689799 | |||||||
| chr7:123689825 | T | C | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1348-675A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689825 | |||||||
| chr7:123689900 | A | AATT | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1348-753_1348-751d others(5): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123689900 | |||||||
| chr7:123690071 | T | C | 7 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(4): Show |
8 | HG02145.hp1 HG02559.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1348-921A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690071 | |||||||
| chr7:123690212 | A | C | 1 | a0001c0002t0001g0031 | 2 | NA18945.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1348-1062T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690212 | |||||||
| chr7:123690421 | C | A | 1 | a0001c0001t0002g0066 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1348-1271G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690421 | |||||||
| chr7:123690453 | C | A | 1 | a0001c0001t0002g0066 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1348-1303G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690453 | |||||||
| chr7:123690579 | A | ATCCAACA others(36): Show |
131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1348-1430_1348-142 others(47): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690579 | |||||||
| chr7:123690585 | A | C | 95 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(92): Show |
115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1348-1435T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690585 | |||||||
| chr7:123690612 | T | G | 1 | a0001c0002t0001g0225 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1348-1462A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690612 | |||||||
| chr7:123690613 | C | CT | 8 | a0001c0001t0002g0045 a0001c0001t0002g0074 a0001c0001t0002g0076 others(5): Show |
9 | HG00673.hp2 HG02015.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.1348-1464dupA | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690613 | |||||||
| chr7:123690613 | C | T | 1 | a0001c0001t0002g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1348-1463G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690613 | |||||||
| chr7:123690762 | G | A | 1 | a0001c0001t0002g0018 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1347+1585C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690762 | |||||||
| chr7:123690902 | T | C | 1 | a0001c0003t0003g0123 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1347+1445A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690902 | |||||||
| chr7:123690921 | C | T | 1 | a0001c0002t0001g0289 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1347+1426G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123690921 | |||||||
| chr7:123691108 | T | C | 1 | a0001c0001t0016g0135 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1347+1239A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123691108 | |||||||
| chr7:123691156 | C | G | 3 | a0001c0002t0001g0220 a0001c0002t0001g0221 a0001c0002t0001g0230 |
3 | HG00140.hp1 HG00323.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1347+1191G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123691156 | |||||||
| chr7:123691193 | A | C | 2 | a0001c0002t0003g0295 a0001c0002t0003g0296 |
2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1347+1154T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123691193 | |||||||
| chr7:123691340 | T | C | 2 | a0001c0001t0009g0118 a0001c0001t0009g0119 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1347+1007A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123691340 | |||||||
| chr7:123691359 | G | A | 1 | a0001c0002t0001g0212 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1347+988C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123691359 | |||||||
| chr7:123691399 | A | T | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1347+948T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123691399 | |||||||
| chr7:123691823 | T | C | 1 | a0001c0002t0001g0032 | 2 | HG00642.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1347+524A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123691823 | |||||||
| chr7:123691882 | T | C | 2 | a0001c0001t0003g0128 a0001c0001t0003g0136 |
2 | NA18991.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1347+465A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123691882 | |||||||
| chr7:123691914 | C | G | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1347+433G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123691914 | |||||||
| chr7:123692094 | A | G | 4 | a0001c0001t0003g0024 a0001c0001t0003g0026 a0001c0001t0003g0175 others(1): Show |
6 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1347+253T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123692094 | |||||||
| chr7:123692255 | GAA | G | 4 | a0001c0001t0002g0012 a0001c0001t0002g0082 a0001c0001t0002g0087 others(1): Show |
5 | HG01891.hp2 HG03130.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1347+90_1347+91del others(2): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 9/10 | chr7 | 123692255 | |||||||
| chr7:123692874 | T | C | 1 | a0001c0001t0003g0139 | 1 | HG02886.hp2 | splice_region_variant&intron_variant | LOW | c.827-7A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123692874 | |||||||
| chr7:123693074 | T | C | 2 | a0001c0001t0006g0008 a0001c0001t0006g0043 |
3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.827-207A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123693074 | |||||||
| chr7:123693079 | C | T | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.827-212G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123693079 | |||||||
| chr7:123693235 | A | G | 1 | a0001c0001t0002g0018 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.827-368T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123693235 | |||||||
| chr7:123693336 | T | C | 3 | a0001c0002t0001g0251 a0001c0002t0001g0255 a0001c0002t0001g0273 |
3 | NA18983.hp1 NA19002.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.827-469A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123693336 | |||||||
| chr7:123693676 | A | G | 1 | a0001c0002t0001g0274 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.827-809T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123693676 | |||||||
| chr7:123693753 | G | A | 2 | a0001c0002t0003g0295 a0001c0002t0003g0296 |
2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.827-886C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123693753 | |||||||
| chr7:123694190 | T | A | 2 | a0001c0001t0003g0116 a0001c0001t0003g0117 |
2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.826+525A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123694190 | |||||||
| chr7:123694208 | A | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0144 |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.826+507T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123694208 | |||||||
| chr7:123694209 | C | T | 2 | a0001c0001t0006g0008 a0001c0001t0006g0043 |
3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.826+506G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123694209 | |||||||
| chr7:123694278 | T | G | 31 | a0001c0001t0003g0003 a0001c0001t0004g0006 a0001c0001t0004g0020 others(28): Show |
39 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.826+437A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123694278 | |||||||
| chr7:123694642 | GT | G | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.826+72delA | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123694642 | |||||||
| chr7:123694693 | G | A | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.826+22C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 8/10 | chr7 | 123694693 | |||||||
| chr7:123694911 | T | C | 35 | a0001c0001t0003g0003 a0001c0001t0003g0014 a0001c0001t0003g0015 others(32): Show |
42 | HG00544.hp1 HG00673.hp1 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.673-43A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 7/10 | chr7 | 123694911 | |||||||
| chr7:123695024 | T | G | 95 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(92): Show |
115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.673-156A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 7/10 | chr7 | 123695024 | |||||||
| chr7:123695296 | A | G | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.673-428T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 7/10 | chr7 | 123695296 | |||||||
| chr7:123695429 | T | G | 5 | a0001c0002t0001g0211 a0001c0002t0001g0212 a0001c0002t0001g0238 others(2): Show |
5 | HG01256.hp1 HG02572.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.672+394A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 7/10 | chr7 | 123695429 | |||||||
| chr7:123695544 | G | A | 1 | a0001c0002t0001g0257 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.672+279C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 7/10 | chr7 | 123695544 | |||||||
| chr7:123695630 | C | T | 1 | a0001c0002t0018g0202 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.672+193G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 7/10 | chr7 | 123695630 | |||||||
| chr7:123695879 | T | C | 1 | a0001c0001t0009g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.630-14A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 6/10 | chr7 | 123695879 | |||||||
| chr7:123696115 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.630-250A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 6/10 | chr7 | 123696115 | |||||||
| chr7:123696412 | T | TA | 6 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(3): Show |
6 | HG02071.hp2 HG02886.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.629+166dupT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 6/10 | chr7 | 123696412 | |||||||
| chr7:123696750 | G | A | 95 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(92): Show |
115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
splice_region_variant&intron_variant | LOW | c.461-3C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123696750 | |||||||
| chr7:123696967 | C | T | 1 | a0001c0001t0008g0157 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.461-220G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123696967 | |||||||
| chr7:123697060 | C | A | 38 | a0001c0002t0001g0007 a0001c0002t0001g0036 a0001c0002t0001g0037 others(35): Show |
43 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.461-313G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697060 | |||||||
| chr7:123697067 | T | A | 1 | a0001c0001t0003g0184 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.461-320A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697067 | |||||||
| chr7:123697098 | A | G | 3 | a0001c0001t0004g0006 a0001c0001t0004g0147 a0001c0001t0004g0148 |
5 | HG00323.hp1 HG01175.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.461-351T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697098 | |||||||
| chr7:123697119 | GAAAGT | G | 31 | a0001c0001t0002g0146 a0001c0001t0004g0006 a0001c0001t0004g0020 others(28): Show |
36 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.461-377_461-373del others(5): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697119 | |||||||
| chr7:123697132 | C | T | 1 | a0001c0001t0003g0105 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.461-385G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697132 | |||||||
| chr7:123697348 | T | C | 2 | a0001c0001t0003g0116 a0001c0001t0003g0117 |
2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.461-601A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697348 | |||||||
| chr7:123697680 | G | C | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.461-933C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697680 | |||||||
| chr7:123697772 | A | G | 1 | a0001c0002t0001g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.461-1025T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697772 | |||||||
| chr7:123697809 | T | C | 1 | a0001c0001t0002g0058 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.461-1062A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697809 | |||||||
| chr7:123697819 | C | T | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.461-1072G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123697819 | |||||||
| chr7:123698058 | G | GT | 6 | a0001c0001t0002g0044 a0001c0002t0001g0035 a0001c0002t0001g0192 others(3): Show |
7 | HG02280.hp2 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.461-1312dupA | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123698058 | |||||||
| chr7:123698058 | GT | G | 5 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(2): Show |
6 | HG02145.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.461-1312delA | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123698058 | |||||||
| chr7:123698103 | T | C | 1 | a0001c0002t0001g0214 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.461-1356A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123698103 | |||||||
| chr7:123698234 | A | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.461-1487T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123698234 | |||||||
| chr7:123698351 | G | GA | 13 | a0001c0002t0001g0034 a0001c0002t0001g0205 a0001c0002t0001g0211 others(10): Show |
14 | HG01256.hp1 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.461-1605dupT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123698351 | |||||||
| chr7:123698659 | G | C | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.461-1912C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123698659 | |||||||
| chr7:123698881 | G | A | 1 | a0001c0001t0002g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.461-2134C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123698881 | |||||||
| chr7:123699123 | C | T | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.461-2376G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699123 | |||||||
| chr7:123699223 | C | T | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.461-2476G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699223 | |||||||
| chr7:123699239 | G | A | 1 | a0001c0001t0002g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.461-2492C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699239 | |||||||
| chr7:123699663 | C | G | 1 | a0001c0001t0002g0100 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.461-2916G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699663 | |||||||
| chr7:123699867 | C | T | 95 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(92): Show |
115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.461-3120G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699867 | |||||||
| chr7:123699888 | T | A | 1 | a0001c0002t0001g0220 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.461-3141A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699888 | |||||||
| chr7:123699942 | C | T | 1 | a0001c0001t0002g0094 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.461-3195G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699942 | |||||||
| chr7:123699951 | C | T | 1 | a0001c0002t0001g0210 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.461-3204G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699951 | |||||||
| chr7:123699959 | G | A | 1 | a0001c0001t0003g0183 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.461-3212C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699959 | |||||||
| chr7:123699993 | G | A | 1 | a0001c0002t0001g0284 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.461-3246C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123699993 | |||||||
| chr7:123700133 | G | A | 2 | a0001c0002t0001g0256 a0001c0002t0001g0257 |
2 | NA18948.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.461-3386C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700133 | |||||||
| chr7:123700175 | CA | C | 28 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0012 others(25): Show |
34 | HG00408.hp2 HG00621.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.461-3429delT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700175 | |||||||
| chr7:123700175 | CAA | C | 22 | a0001c0001t0002g0013 a0001c0001t0002g0045 a0001c0001t0002g0048 others(19): Show |
24 | HG00099.hp1 HG00733.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.461-3430_461-3429d others(4): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700175 | |||||||
| chr7:123700175 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0002g0146 a0001c0001t0004g0162 |
2 | HG02258.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.461-3439_461-3429d others(13): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700175 | |||||||
| chr7:123700175 | CAAAAAAA others(5): Show |
C | 37 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0144 others(34): Show |
48 | HG00280.hp1 HG00621.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.461-3440_461-3429d others(14): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700175 | |||||||
| chr7:123700175 | CAAAAAAA others(6): Show |
C | 55 | a0001c0001t0002g0011 a0001c0001t0002g0017 a0001c0001t0002g0046 others(52): Show |
63 | HG00408.hp1 HG00544.hp1 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.461-3441_461-3429d others(15): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700175 | |||||||
| chr7:123700175 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0004g0148 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.461-3442_461-3429d others(16): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700175 | |||||||
| chr7:123700175 | CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0002g0075 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.461-3445_461-3429d others(19): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700175 | |||||||
| chr7:123700183 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0002g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.461-3437_461-3436i others(15): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700183 | |||||||
| chr7:123700198 | AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.461-3461_461-3452d others(12): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700198 | |||||||
| chr7:123700200 | AAAAAAAA others(1): Show |
A | 67 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(64): Show |
79 | HG00099.hp2 HG00738.hp2 HG01071.hp1 others(76): Show |
intron_variant | MODIFIER | c.461-3461_461-3454d others(10): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700200 | |||||||
| chr7:123700201 | AAAAAAAC | A | 50 | a0001c0001t0006g0043 a0001c0002t0001g0001 a0001c0002t0001g0002 others(47): Show |
57 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.461-3461_461-3455d others(9): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700201 | |||||||
| chr7:123700202 | AAAAAAC | A | 13 | a0001c0001t0006g0008 a0001c0002t0001g0031 a0001c0002t0001g0032 others(10): Show |
14 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.461-3461_461-3456d others(8): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700202 | |||||||
| chr7:123700203 | A | AAAAAAAA others(20): Show |
1 | a0001c0001t0002g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.461-3457_461-3456i others(29): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700203 | |||||||
| chr7:123700203 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0002g0005 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.461-3457_461-3456i others(23): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700203 | |||||||
| chr7:123700203 | A | AAAAAAAA others(6): Show |
2 | a0001c0001t0002g0005 a0001c0001t0014g0187 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.461-3457_461-3456i others(15): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700203 | |||||||
| chr7:123700203 | A | C | 1 | a0001c0001t0002g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.461-3456T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700203 | |||||||
| chr7:123700446 | CT | C | 228 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(225): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.461-3700delA | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700446 | |||||||
| chr7:123700533 | G | T | 3 | a0001c0001t0004g0006 a0001c0001t0004g0147 a0001c0001t0004g0148 |
5 | HG00323.hp1 HG01175.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.461-3786C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700533 | |||||||
| chr7:123700795 | C | T | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.460+3839G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123700795 | |||||||
| chr7:123701068 | A | G | 3 | a0001c0002t0001g0229 a0001c0002t0001g0293 a0001c0002t0017g0294 |
3 | HG03486.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.460+3566T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701068 | |||||||
| chr7:123701069 | G | C | 95 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(92): Show |
115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.460+3565C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701069 | |||||||
| chr7:123701129 | T | C | 3 | a0001c0002t0001g0290 a0001c0002t0001g0291 a0001c0002t0001g0292 |
3 | HG00642.hp1 HG01978.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.460+3505A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701129 | |||||||
| chr7:123701162 | G | A | 1 | a0001c0001t0003g0181 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.460+3472C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701162 | |||||||
| chr7:123701270 | A | C | 3 | a0001c0001t0002g0005 a0001c0001t0002g0141 a0001c0001t0014g0187 |
5 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.460+3364T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701270 | |||||||
| chr7:123701456 | A | C | 2 | a0001c0001t0003g0116 a0001c0001t0003g0117 |
2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.460+3178T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701456 | |||||||
| chr7:123701692 | C | A | 2 | a0001c0002t0001g0219 a0001c0002t0001g0226 |
2 | NA18986.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.460+2942G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701692 | |||||||
| chr7:123701884 | T | G | 31 | a0001c0001t0003g0003 a0001c0001t0004g0006 a0001c0001t0004g0020 others(28): Show |
39 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.460+2750A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701884 | |||||||
| chr7:123701892 | T | A | 1 | a0001c0002t0001g0225 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.460+2742A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701892 | |||||||
| chr7:123701945 | T | TA | 220 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(217): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.460+2688dupT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701945 | |||||||
| chr7:123701945 | T | TAA | 6 | a0001c0002t0001g0209 a0001c0002t0001g0237 a0001c0003t0003g0122 others(3): Show |
6 | HG00544.hp1 HG00673.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.460+2687_460+2688d others(4): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123701945 | |||||||
| chr7:123702111 | A | G | 2 | a0001c0001t0004g0166 a0001c0001t0004g0168 |
2 | HG00673.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.460+2523T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123702111 | |||||||
| chr7:123702230 | A | G | 1 | a0001c0001t0002g0055 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.460+2404T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123702230 | |||||||
| chr7:123702231 | C | T | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.460+2403G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123702231 | |||||||
| chr7:123702389 | G | A | 2 | a0001c0002t0001g0301 a0001c0002t0023g0215 |
2 | HG02698.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.460+2245C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123702389 | |||||||
| chr7:123702466 | C | A | 2 | a0001c0002t0001g0293 a0001c0002t0017g0294 |
2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.460+2168G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123702466 | |||||||
| chr7:123702691 | G | A | 1 | a0001c0001t0004g0150 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.460+1943C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123702691 | |||||||
| chr7:123702713 | T | C | 9 | a0001c0002t0001g0036 a0001c0002t0001g0246 a0001c0002t0001g0254 others(6): Show |
10 | HG01081.hp1 HG02080.hp2 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.460+1921A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123702713 | |||||||
| chr7:123702812 | C | A | 2 | a0001c0002t0001g0240 a0001c0002t0001g0244 |
2 | HG02155.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.460+1822G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123702812 | |||||||
| chr7:123703034 | T | C | 2 | a0001c0001t0002g0047 a0001c0001t0002g0079 |
2 | HG01943.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.460+1600A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123703034 | |||||||
| chr7:123703268 | C | T | 1 | a0001c0001t0002g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.460+1366G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123703268 | |||||||
| chr7:123703425 | G | C | 2 | a0001c0001t0002g0005 a0001c0001t0002g0141 |
4 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.460+1209C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123703425 | |||||||
| chr7:123703494 | G | T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.460+1140C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123703494 | |||||||
| chr7:123703665 | A | G | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.460+969T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123703665 | |||||||
| chr7:123703705 | G | T | 2 | a0001c0002t0001g0193 a0001c0002t0001g0194 |
2 | HG01261.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.460+929C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123703705 | |||||||
| chr7:123703893 | A | G | 38 | a0001c0002t0001g0007 a0001c0002t0001g0036 a0001c0002t0001g0037 others(35): Show |
43 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.460+741T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 5/10 | chr7 | 123703893 | |||||||
| chr7:123704760 | G | A | 1 | a0001c0001t0002g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.437-103C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 4/10 | chr7 | 123704760 | |||||||
| chr7:123704975 | A | C | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.437-318T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 4/10 | chr7 | 123704975 | |||||||
| chr7:123705070 | G | T | 2 | a0001c0001t0002g0058 a0001c0001t0002g0115 |
2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.437-413C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 4/10 | chr7 | 123705070 | |||||||
| chr7:123705080 | T | C | 1 | a0001c0001t0010g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.437-423A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 4/10 | chr7 | 123705080 | |||||||
| chr7:123705796 | C | G | 1 | a0001c0001t0002g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.436+481G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 4/10 | chr7 | 123705796 | |||||||
| chr7:123705835 | T | C | 57 | a0001c0001t0002g0017 a0001c0001t0002g0142 a0001c0001t0002g0143 others(54): Show |
68 | HG00544.hp1 HG00673.hp1 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.436+442A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 4/10 | chr7 | 123705835 | |||||||
| chr7:123705843 | T | C | 2 | a0001c0001t0002g0047 a0001c0001t0002g0079 |
2 | HG01943.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.436+434A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 4/10 | chr7 | 123705843 | |||||||
| chr7:123706139 | T | C | 4 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0001g0209 others(1): Show |
4 | HG02886.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+138A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 4/10 | chr7 | 123706139 | |||||||
| chr7:123706244 | C | T | 1 | a0001c0002t0001g0287 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.436+33G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 4/10 | chr7 | 123706244 | |||||||
| chr7:123706539 | A | G | 1 | a0001c0001t0002g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.340-166T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 3/10 | chr7 | 123706539 | |||||||
| chr7:123706595 | T | C | 1 | a0001c0002t0001g0195 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.339+145A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 3/10 | chr7 | 123706595 | |||||||
| chr7:123706708 | T | C | 10 | a0001c0002t0001g0037 a0001c0002t0001g0248 a0001c0002t0001g0249 others(7): Show |
11 | HG00423.hp2 HG01934.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.339+32A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 3/10 | chr7 | 123706708 | |||||||
| chr7:123706943 | C | T | 2 | a0001c0001t0002g0045 a0001c0001t0002g0074 |
2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.253-117G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123706943 | |||||||
| chr7:123706965 | T | C | 1 | a0001c0001t0002g0094 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.253-139A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123706965 | |||||||
| chr7:123707009 | A | C | 226 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(223): Show |
272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.253-183T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123707009 | |||||||
| chr7:123707126 | T | C | 1 | a0001c0001t0003g0180 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.253-300A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123707126 | |||||||
| chr7:123707179 | T | C | 7 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(4): Show |
8 | HG02145.hp1 HG02559.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.253-353A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123707179 | |||||||
| chr7:123707214 | C | T | 6 | a0001c0001t0002g0051 a0001c0001t0002g0065 a0001c0001t0002g0067 others(3): Show |
6 | HG01884.hp1 HG02148.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-388G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123707214 | |||||||
| chr7:123707383 | T | C | 1 | a0001c0001t0003g0179 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.253-557A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123707383 | |||||||
| chr7:123707439 | T | C | 1 | a0001c0001t0014g0187 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.253-613A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123707439 | |||||||
| chr7:123707574 | C | T | 11 | a0001c0001t0003g0025 a0001c0001t0003g0114 a0001c0001t0003g0177 others(8): Show |
12 | HG01192.hp2 HG01346.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.253-748G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123707574 | |||||||
| chr7:123707910 | G | A | 1 | a0001c0002t0001g0247 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.253-1084C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123707910 | |||||||
| chr7:123708152 | T | C | 1 | a0001c0002t0001g0248 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.252+937A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123708152 | |||||||
| chr7:123708181 | AAAC | A | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.252+905_252+907del others(3): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123708181 | |||||||
| chr7:123708261 | C | T | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.252+828G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123708261 | |||||||
| chr7:123708302 | G | T | 42 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0023 others(39): Show |
49 | HG00544.hp1 HG00673.hp1 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.252+787C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123708302 | |||||||
| chr7:123708569 | A | G | 130 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(127): Show |
156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.252+520T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123708569 | |||||||
| chr7:123708690 | C | T | 228 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(225): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.252+399G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123708690 | |||||||
| chr7:123708935 | G | A | 2 | a0001c0002t0001g0286 a0001c0005t0001g0223 |
2 | HG00738.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.252+154C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 2/10 | chr7 | 123708935 | |||||||
| chr7:123709460 | T | G | 4 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0102 others(1): Show |
4 | HG01192.hp1 HG01255.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-237A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709460 | |||||||
| chr7:123709523 | A | T | 13 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0068 others(10): Show |
14 | HG00423.hp1 HG01192.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.118-300T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709523 | |||||||
| chr7:123709572 | G | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(2): Show |
6 | HG02145.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-349C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709572 | |||||||
| chr7:123709573 | T | G | 228 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(225): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.118-350A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709573 | |||||||
| chr7:123709605 | A | G | 1 | a0001c0001t0002g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.118-382T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709605 | |||||||
| chr7:123709732 | T | A | 2 | a0001c0002t0001g0232 a0001c0002t0001g0243 |
2 | HG00544.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.118-509A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709732 | |||||||
| chr7:123709733 | G | C | 2 | a0001c0002t0001g0232 a0001c0002t0001g0243 |
2 | HG00544.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.118-510C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709733 | |||||||
| chr7:123709734 | T | A | 2 | a0001c0002t0001g0232 a0001c0002t0001g0243 |
2 | HG00544.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.118-511A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709734 | |||||||
| chr7:123709784 | G | A | 1 | a0001c0002t0001g0290 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.118-561C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709784 | |||||||
| chr7:123709839 | A | T | 1 | a0001c0001t0002g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.118-616T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709839 | |||||||
| chr7:123709865 | G | T | 1 | a0001c0001t0003g0173 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.118-642C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709865 | |||||||
| chr7:123709870 | G | A | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.118-647C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123709870 | |||||||
| chr7:123710006 | C | T | 130 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(127): Show |
156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.118-783G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123710006 | |||||||
| chr7:123710164 | T | C | 2 | a0001c0002t0001g0263 a0001c0002t0001g0269 |
2 | HG00423.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.118-941A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123710164 | |||||||
| chr7:123710364 | AAGTAATT others(5): Show |
A | 1 | a0001c0002t0001g0216 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.118-1153_118-1142d others(14): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123710364 | |||||||
| chr7:123710481 | T | C | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.118-1258A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123710481 | |||||||
| chr7:123710513 | T | C | 1 | a0001c0001t0003g0132 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.118-1290A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123710513 | |||||||
| chr7:123711005 | A | G | 1 | a0001c0002t0001g0233 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.118-1782T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711005 | |||||||
| chr7:123711141 | C | A | 3 | a0001c0001t0002g0017 a0001c0002t0001g0263 a0001c0002t0001g0269 |
4 | HG00423.hp2 HG02647.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-1918G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711141 | |||||||
| chr7:123711165 | G | C | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.118-1942C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711165 | |||||||
| chr7:123711298 | A | C | 1 | a0001c0001t0002g0052 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.118-2075T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711298 | |||||||
| chr7:123711341 | A | T | 2 | a0001c0002t0001g0256 a0001c0002t0001g0257 |
2 | NA18948.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.118-2118T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711341 | |||||||
| chr7:123711468 | A | G | 3 | a0001c0001t0002g0051 a0001c0001t0002g0065 a0001c0001t0002g0070 |
3 | HG03490.hp2 HG03492.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.118-2245T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711468 | |||||||
| chr7:123711498 | T | C | 1 | a0001c0001t0003g0176 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.118-2275A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711498 | |||||||
| chr7:123711525 | T | C | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.118-2302A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711525 | |||||||
| chr7:123711554 | C | A | 3 | a0001c0001t0002g0005 a0001c0001t0002g0141 a0001c0001t0014g0187 |
5 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-2331G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711554 | |||||||
| chr7:123711766 | C | T | 2 | a0001c0001t0006g0008 a0001c0001t0006g0043 |
3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.118-2543G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711766 | |||||||
| chr7:123711818 | G | A | 7 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(4): Show |
8 | HG02145.hp1 HG02559.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-2595C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711818 | |||||||
| chr7:123711843 | A | G | 1 | a0001c0001t0003g0103 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.118-2620T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123711843 | |||||||
| chr7:123712159 | G | T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.118-2936C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123712159 | |||||||
| chr7:123712253 | T | C | 32 | a0001c0001t0002g0146 a0001c0001t0003g0003 a0001c0001t0004g0006 others(29): Show |
40 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.118-3030A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123712253 | |||||||
| chr7:123712319 | A | G | 1 | a0001c0003t0003g0130 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.118-3096T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123712319 | |||||||
| chr7:123712729 | C | T | 1 | a0001c0001t0003g0116 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.118-3506G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123712729 | |||||||
| chr7:123712802 | T | C | 2 | a0001c0001t0002g0189 a0001c0001t0002g0190 |
2 | NA18952.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.118-3579A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123712802 | |||||||
| chr7:123713093 | CTA | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0144 |
3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.118-3872_118-3871d others(4): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123713093 | |||||||
| chr7:123713360 | G | A | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-4137C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123713360 | |||||||
| chr7:123713432 | T | C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.118-4209A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123713432 | |||||||
| chr7:123713567 | C | T | 1 | a0001c0002t0001g0195 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.118-4344G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123713567 | |||||||
| chr7:123713643 | C | T | 2 | a0001c0001t0003g0014 a0001c0001t0003g0103 |
3 | HG01168.hp2 HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.118-4420G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123713643 | |||||||
| chr7:123713654 | G | C | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.118-4431C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123713654 | |||||||
| chr7:123713780 | G | A | 1 | a0001c0002t0001g0217 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.118-4557C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123713780 | |||||||
| chr7:123713783 | G | A | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.118-4560C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123713783 | |||||||
| chr7:123713964 | T | C | 1 | a0001c0001t0004g0166 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.118-4741A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123713964 | |||||||
| chr7:123714296 | G | A | 4 | a0001c0002t0001g0218 a0001c0002t0001g0219 a0001c0002t0001g0226 others(1): Show |
4 | NA18986.hp2 NA19005.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-5073C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123714296 | |||||||
| chr7:123714482 | A | G | 228 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(225): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.118-5259T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123714482 | |||||||
| chr7:123714746 | G | C | 1 | a0001c0001t0002g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.118-5523C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123714746 | |||||||
| chr7:123714753 | T | C | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-5530A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123714753 | |||||||
| chr7:123714784 | G | C | 1 | a0001c0002t0001g0224 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.118-5561C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123714784 | |||||||
| chr7:123714849 | T | C | 3 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0144 |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-5626A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123714849 | |||||||
| chr7:123715077 | A | G | 1 | a0001c0001t0004g0150 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.118-5854T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715077 | |||||||
| chr7:123715224 | A | C | 1 | a0001c0001t0002g0061 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.118-6001T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715224 | |||||||
| chr7:123715325 | G | T | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.118-6102C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715325 | |||||||
| chr7:123715350 | T | C | 1 | a0001c0002t0001g0281 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.118-6127A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715350 | |||||||
| chr7:123715429 | T | C | 228 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(225): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.118-6206A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715429 | |||||||
| chr7:123715475 | C | A | 1 | a0001c0001t0002g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.118-6252G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715475 | |||||||
| chr7:123715640 | C | G | 2 | a0001c0002t0001g0290 a0001c0002t0001g0291 |
2 | HG00642.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.118-6417G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715640 | |||||||
| chr7:123715665 | A | C | 1 | a0001c0002t0001g0195 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.118-6442T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715665 | |||||||
| chr7:123715709 | A | G | 1 | a0001c0002t0001g0264 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.118-6486T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715709 | |||||||
| chr7:123715723 | G | C | 1 | a0001c0001t0002g0018 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.118-6500C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715723 | |||||||
| chr7:123715920 | A | G | 8 | a0001c0001t0003g0129 a0001c0001t0003g0131 a0001c0001t0003g0132 others(5): Show |
8 | HG01433.hp1 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-6697T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123715920 | |||||||
| chr7:123716008 | C | T | 228 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(225): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.118-6785G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716008 | |||||||
| chr7:123716292 | T | C | 1 | a0001c0002t0001g0224 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.118-7069A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716292 | |||||||
| chr7:123716457 | A | C | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-7234T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716457 | |||||||
| chr7:123716586 | A | G | 2 | a0001c0001t0003g0014 a0001c0001t0003g0103 |
3 | HG01168.hp2 HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.118-7363T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716586 | |||||||
| chr7:123716588 | C | G | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-7365G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716588 | |||||||
| chr7:123716635 | G | GGGAGAGA others(5): Show |
3 | a0001c0002t0001g0251 a0001c0002t0001g0255 a0001c0002t0001g0273 |
3 | NA18983.hp1 NA19002.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.118-7424_118-7413d others(14): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716635 | |||||||
| chr7:123716673 | G | A | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.118-7450C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716673 | |||||||
| chr7:123716841 | A | G | 2 | a0001c0002t0001g0286 a0001c0005t0001g0223 |
2 | HG00738.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.118-7618T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716841 | |||||||
| chr7:123716846 | A | G | 1 | a0001c0003t0003g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.118-7623T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716846 | |||||||
| chr7:123716867 | A | C | 228 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(225): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.118-7644T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123716867 | |||||||
| chr7:123717114 | T | C | 1 | a0001c0002t0001g0193 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.118-7891A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123717114 | |||||||
| chr7:123717224 | C | A | 8 | a0001c0001t0003g0129 a0001c0001t0003g0131 a0001c0001t0003g0132 others(5): Show |
8 | HG01433.hp1 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-8001G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123717224 | |||||||
| chr7:123717456 | G | A | 1 | a0001c0001t0002g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.118-8233C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123717456 | |||||||
| chr7:123717525 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.118-8302G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123717525 | |||||||
| chr7:123717574 | T | C | 1 | a0001c0002t0001g0205 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.118-8351A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123717574 | |||||||
| chr7:123717592 | A | G | 226 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(223): Show |
272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.118-8369T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123717592 | |||||||
| chr7:123717931 | C | T | 1 | a0002c0004t0002g0069 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.118-8708G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123717931 | |||||||
| chr7:123718093 | GTTAA | G | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-8874_118-8871d others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123718093 | |||||||
| chr7:123718295 | G | C | 2 | a0001c0001t0003g0116 a0001c0001t0003g0117 |
2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.118-9072C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123718295 | |||||||
| chr7:123718302 | G | T | 1 | a0001c0001t0002g0092 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.118-9079C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123718302 | |||||||
| chr7:123718331 | T | C | 2 | a0001c0002t0001g0220 a0001c0002t0001g0221 |
2 | HG00323.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.118-9108A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123718331 | |||||||
| chr7:123718393 | C | G | 1 | a0001c0001t0003g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.118-9170G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123718393 | |||||||
| chr7:123718484 | AAGAT | A | 2 | a0001c0001t0006g0008 a0001c0001t0006g0043 |
3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.118-9265_118-9262d others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123718484 | |||||||
| chr7:123718700 | T | C | 31 | a0001c0001t0003g0003 a0001c0001t0004g0006 a0001c0001t0004g0020 others(28): Show |
39 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.118-9477A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123718700 | |||||||
| chr7:123719011 | T | G | 64 | a0001c0002t0001g0007 a0001c0002t0001g0029 a0001c0002t0001g0031 others(61): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.118-9788A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123719011 | |||||||
| chr7:123719144 | C | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0144 |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-9921G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123719144 | |||||||
| chr7:123719218 | A | G | 7 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(4): Show |
8 | HG02145.hp1 HG02559.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-9995T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123719218 | |||||||
| chr7:123719225 | T | C | 1 | a0001c0001t0002g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.118-10002A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123719225 | |||||||
| chr7:123719654 | A | G | 1 | a0001c0001t0003g0172 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.118-10431T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123719654 | |||||||
| chr7:123719953 | A | C | 95 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(92): Show |
115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.118-10730T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123719953 | |||||||
| chr7:123720123 | A | C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.118-10900T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720123 | |||||||
| chr7:123720139 | G | A | 1 | a0001c0002t0001g0225 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.118-10916C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720139 | |||||||
| chr7:123720298 | T | C | 37 | a0001c0001t0002g0005 a0001c0001t0002g0018 a0001c0001t0002g0019 others(34): Show |
46 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.118-11075A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720298 | |||||||
| chr7:123720335 | A | C | 2 | a0001c0002t0001g0254 a0001c0002t0001g0261 |
2 | HG01081.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.118-11112T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720335 | |||||||
| chr7:123720344 | C | CA | 68 | a0001c0001t0002g0017 a0001c0001t0002g0058 a0001c0001t0002g0082 others(65): Show |
80 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.118-11122dupT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720344 | |||||||
| chr7:123720344 | CA | C | 42 | a0001c0001t0002g0050 a0001c0001t0002g0068 a0001c0001t0002g0078 others(39): Show |
47 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.118-11122delT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720344 | |||||||
| chr7:123720344 | CAA | C | 6 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(3): Show |
6 | HG01496.hp1 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-11123_118-1112 others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720344 | |||||||
| chr7:123720369 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.118-11146A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720369 | |||||||
| chr7:123720627 | T | A | 1 | a0001c0001t0003g0133 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.118-11404A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720627 | |||||||
| chr7:123720650 | A | AT | 31 | a0001c0001t0003g0015 a0001c0001t0003g0104 a0001c0001t0003g0105 others(28): Show |
36 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.118-11428dupA | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720650 | |||||||
| chr7:123720650 | A | T | 1 | a0001c0001t0002g0050 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.118-11427T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720650 | |||||||
| chr7:123720650 | AT | A | 9 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(6): Show |
10 | HG02145.hp1 HG02258.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.118-11428delA | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720650 | |||||||
| chr7:123720673 | T | C | 2 | a0001c0001t0009g0118 a0001c0001t0009g0119 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.118-11450A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720673 | |||||||
| chr7:123720681 | C | G | 1 | a0001c0001t0002g0097 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.118-11458G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720681 | |||||||
| chr7:123720689 | C | G | 1 | a0001c0002t0001g0290 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.118-11466G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720689 | |||||||
| chr7:123720793 | G | C | 2 | a0001c0002t0001g0290 a0001c0002t0001g0291 |
2 | HG00642.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.118-11570C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720793 | |||||||
| chr7:123720810 | G | A | 1 | a0001c0001t0002g0050 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.118-11587C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720810 | |||||||
| chr7:123720811 | A | T | 1 | a0001c0001t0002g0050 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.118-11588T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720811 | |||||||
| chr7:123720827 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.118-11604C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720827 | |||||||
| chr7:123720855 | T | A | 1 | a0001c0002t0001g0270 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.118-11632A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720855 | |||||||
| chr7:123720868 | T | C | 2 | a0001c0001t0004g0021 a0001c0001t0004g0160 |
3 | HG02040.hp2 NA18952.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.118-11645A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720868 | |||||||
| chr7:123720872 | C | T | 2 | a0001c0002t0001g0227 a0001c0002t0001g0241 |
2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.118-11649G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123720872 | |||||||
| chr7:123721051 | G | A | 1 | a0001c0002t0001g0285 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.118-11828C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721051 | |||||||
| chr7:123721226 | T | C | 2 | a0001c0001t0009g0118 a0001c0001t0009g0119 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.118-12003A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721226 | |||||||
| chr7:123721231 | A | G | 2 | a0001c0001t0003g0023 a0001c0001t0003g0173 |
3 | NA18941.hp2 NA18984.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.118-12008T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721231 | |||||||
| chr7:123721318 | C | CTT | 292 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(289): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.118-12096_118-1209 others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721318 | |||||||
| chr7:123721337 | T | A | 1 | a0001c0002t0001g0196 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.118-12114A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721337 | |||||||
| chr7:123721366 | C | T | 1 | a0001c0002t0001g0200 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.118-12143G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721366 | |||||||
| chr7:123721391 | T | C | 2 | a0001c0001t0006g0008 a0001c0001t0006g0043 |
3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.118-12168A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721391 | |||||||
| chr7:123721510 | A | T | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.118-12287T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721510 | |||||||
| chr7:123721625 | C | CACAATTT others(26): Show |
1 | a0001c0001t0002g0050 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.118-12435_118-1240 others(37): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721625 | |||||||
| chr7:123721712 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.118-12489C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721712 | |||||||
| chr7:123721717 | A | G | 2 | a0001c0001t0003g0116 a0001c0001t0003g0117 |
2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.118-12494T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721717 | |||||||
| chr7:123721719 | C | T | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-12496G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721719 | |||||||
| chr7:123721856 | C | T | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.118-12633G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721856 | |||||||
| chr7:123721882 | A | ATAACT | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.118-12660_118-1265 others(9): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721882 | |||||||
| chr7:123721942 | C | T | 2 | a0001c0001t0002g0048 a0001c0001t0002g0049 |
2 | NA18968.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.118-12719G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123721942 | |||||||
| chr7:123722016 | G | A | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-12793C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123722016 | |||||||
| chr7:123722092 | T | A | 1 | a0001c0001t0008g0157 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.118-12869A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123722092 | |||||||
| chr7:123722365 | A | T | 3 | a0001c0002t0001g0211 a0001c0002t0001g0212 a0001c0002t0001g0299 |
3 | HG01256.hp1 HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.118-13142T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123722365 | |||||||
| chr7:123722638 | C | T | 2 | a0001c0001t0003g0116 a0001c0001t0003g0117 |
2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.118-13415G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123722638 | |||||||
| chr7:123722818 | A | C | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.118-13595T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123722818 | |||||||
| chr7:123723032 | T | C | 8 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0158 others(5): Show |
10 | HG00408.hp1 HG02040.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.118-13809A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123723032 | |||||||
| chr7:123723058 | T | C | 1 | a0001c0001t0002g0017 | 2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.118-13835A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123723058 | |||||||
| chr7:123723105 | T | C | 1 | a0001c0001t0002g0017 | 2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.118-13882A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123723105 | |||||||
| chr7:123723145 | G | A | 1 | a0001c0002t0001g0198 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.118-13922C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123723145 | |||||||
| chr7:123723194 | T | A | 1 | a0001c0001t0002g0061 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.118-13971A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123723194 | |||||||
| chr7:123723604 | A | G | 228 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(225): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.118-14381T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123723604 | |||||||
| chr7:123723643 | T | C | 3 | a0001c0001t0002g0005 a0001c0001t0002g0141 a0001c0001t0014g0187 |
5 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-14420A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123723643 | |||||||
| chr7:123723920 | T | C | 1 | a0001c0002t0001g0210 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.118-14697A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123723920 | |||||||
| chr7:123724003 | T | C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.118-14780A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123724003 | |||||||
| chr7:123724073 | T | C | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.118-14850A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123724073 | |||||||
| chr7:123724318 | C | T | 9 | a0001c0001t0003g0129 a0001c0001t0003g0131 a0001c0001t0003g0132 others(6): Show |
9 | HG01361.hp2 HG01433.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.118-15095G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123724318 | |||||||
| chr7:123724372 | T | C | 3 | a0001c0001t0002g0017 a0001c0001t0002g0142 a0001c0001t0002g0143 |
4 | HG02647.hp2 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-15149A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123724372 | |||||||
| chr7:123724693 | G | A | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-15470C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123724693 | |||||||
| chr7:123724879 | A | G | 1 | a0001c0001t0003g0128 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.118-15656T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123724879 | |||||||
| chr7:123724936 | G | A | 2 | a0001c0001t0003g0131 a0001c0001t0003g0132 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.118-15713C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123724936 | |||||||
| chr7:123725016 | T | C | 3 | a0001c0001t0002g0095 a0001c0001t0002g0099 a0001c0001t0002g0101 |
3 | HG01074.hp2 HG01256.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.118-15793A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123725016 | |||||||
| chr7:123725068 | G | A | 228 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(225): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.118-15845C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123725068 | |||||||
| chr7:123725417 | A | G | 1 | a0001c0002t0001g0248 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.118-16194T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123725417 | |||||||
| chr7:123725508 | T | TA | 5 | a0001c0001t0002g0049 a0001c0002t0001g0203 a0001c0002t0001g0204 others(2): Show |
5 | HG00280.hp2 HG00735.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-16286dupT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123725508 | |||||||
| chr7:123725652 | C | T | 2 | a0001c0001t0006g0008 a0001c0001t0006g0043 |
3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.118-16429G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123725652 | |||||||
| chr7:123725728 | T | C | 1 | a0001c0002t0001g0246 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.118-16505A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123725728 | |||||||
| chr7:123725734 | C | T | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-16511G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123725734 | |||||||
| chr7:123725747 | G | T | 1 | a0001c0002t0022g0288 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.118-16524C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123725747 | |||||||
| chr7:123726343 | A | G | 1 | a0001c0001t0002g0005 | 3 | HG01243.hp1 HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.118-17120T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123726343 | |||||||
| chr7:123726550 | C | T | 1 | a0001c0003t0005g0126 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.118-17327G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123726550 | |||||||
| chr7:123726787 | A | G | 1 | a0001c0001t0003g0185 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.118-17564T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123726787 | |||||||
| chr7:123726803 | T | C | 3 | a0001c0001t0002g0005 a0001c0001t0002g0141 a0001c0001t0014g0187 |
5 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-17580A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123726803 | |||||||
| chr7:123726866 | A | AAAT | 54 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0013 others(51): Show |
62 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.118-17646_118-1764 others(7): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123726866 | |||||||
| chr7:123726988 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.118-17765C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123726988 | |||||||
| chr7:123727130 | A | G | 2 | a0001c0001t0002g0067 a0001c0001t0002g0078 |
2 | HG01884.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.118-17907T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727130 | |||||||
| chr7:123727349 | T | C | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.118-18126A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727349 | |||||||
| chr7:123727352 | G | GTC | 1 | a0001c0002t0001g0002 | 5 | NA18942.hp1 NA18962.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-18131_118-1813 others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727352 | |||||||
| chr7:123727353 | T | TCA | 46 | a0001c0001t0002g0027 a0001c0001t0002g0056 a0001c0001t0002g0078 others(43): Show |
58 | HG00544.hp2 HG00639.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.118-18132_118-1813 others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | |||||||
| chr7:123727353 | T | TCACA | 21 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(18): Show |
24 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.118-18134_118-1813 others(8): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | |||||||
| chr7:123727353 | T | TCACACA | 58 | a0001c0001t0002g0044 a0001c0002t0001g0007 a0001c0002t0001g0031 others(55): Show |
65 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.118-18136_118-1813 others(10): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | |||||||
| chr7:123727353 | T | TCACACAC others(1): Show |
10 | a0001c0001t0002g0005 a0001c0001t0002g0141 a0001c0001t0009g0118 others(7): Show |
13 | HG01167.hp2 HG01243.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.118-18138_118-1813 others(12): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | |||||||
| chr7:123727353 | T | TCACACAC others(3): Show |
49 | a0001c0001t0002g0142 a0001c0001t0002g0143 a0001c0001t0003g0015 others(46): Show |
57 | HG00544.hp1 HG00673.hp1 HG01192.hp2 others(54): Show |
intron_variant | MODIFIER | c.118-18140_118-1813 others(14): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | |||||||
| chr7:123727353 | T | TCACACAC others(5): Show |
12 | a0001c0001t0003g0014 a0001c0001t0003g0103 a0001c0001t0003g0116 others(9): Show |
15 | HG00280.hp1 HG00621.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.118-18142_118-1813 others(16): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | |||||||
| chr7:123727353 | T | TCACACAC others(7): Show |
7 | a0001c0001t0003g0003 a0001c0001t0004g0150 a0001c0001t0004g0151 others(4): Show |
10 | HG00738.hp1 HG01516.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.118-18144_118-1813 others(18): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | |||||||
| chr7:123727353 | T | TCACACAC others(9): Show |
11 | a0001c0001t0002g0017 a0001c0001t0004g0022 a0001c0001t0004g0145 others(8): Show |
13 | HG00323.hp1 HG00408.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.118-18146_118-1813 others(20): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | |||||||
| chr7:123727353 | T | TCACACAC others(11): Show |
6 | a0001c0001t0004g0155 a0001c0001t0004g0158 a0001c0001t0004g0161 others(3): Show |
6 | HG03942.hp1 NA18945.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-18148_118-1813 others(22): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | |||||||
| chr7:123727353 | T | TCACACAC others(13): Show |
1 | a0001c0001t0004g0168 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.118-18150_118-1813 others(24): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | |||||||
| chr7:123727353 | T | TCGCACAC others(7): Show |
1 | a0001c0001t0002g0018 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.118-18131_118-1813 others(18): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | |||||||
| chr7:123727353 | T | TCGCACAC others(9): Show |
2 | a0001c0001t0002g0019 a0001c0001t0002g0144 |
3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.118-18131_118-1813 others(20): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727353 | |||||||
| chr7:123727383 | A | ACACACAC others(4): Show |
1 | a0001c0003t0003g0124 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.118-18161_118-1816 others(15): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727383 | |||||||
| chr7:123727383 | A | ACACACAC others(6): Show |
1 | a0001c0002t0003g0296 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.118-18161_118-1816 others(17): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727383 | |||||||
| chr7:123727384 | A | C | 1 | a0001c0001t0003g0003 | 4 | NA18960.hp2 NA18970.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-18161T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727384 | |||||||
| chr7:123727429 | G | A | 1 | a0001c0002t0001g0222 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.118-18206C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727429 | |||||||
| chr7:123727639 | C | T | 50 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0023 others(47): Show |
56 | HG00544.hp1 HG00673.hp1 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.118-18416G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727639 | |||||||
| chr7:123727651 | A | C | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.118-18428T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123727651 | |||||||
| chr7:123728023 | G | A | 2 | a0001c0001t0004g0166 a0001c0001t0004g0168 |
2 | HG00673.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.118-18800C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123728023 | |||||||
| chr7:123728227 | T | C | 1 | a0001c0002t0001g0212 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.118-19004A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123728227 | |||||||
| chr7:123728434 | G | A | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.118-19211C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123728434 | |||||||
| chr7:123728567 | C | T | 1 | a0001c0002t0001g0039 | 2 | NA18955.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.118-19344G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123728567 | |||||||
| chr7:123728685 | C | T | 2 | a0001c0001t0009g0118 a0001c0001t0009g0119 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.118-19462G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123728685 | |||||||
| chr7:123728778 | G | A | 60 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0028 others(57): Show |
76 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.118-19555C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123728778 | |||||||
| chr7:123728778 | GTGAGC | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0144 |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-19560_118-1955 others(9): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123728778 | |||||||
| chr7:123728807 | G | C | 2 | a0001c0001t0004g0166 a0001c0001t0004g0168 |
2 | HG00673.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.118-19584C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123728807 | |||||||
| chr7:123728990 | T | C | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.117+19628A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123728990 | |||||||
| chr7:123729106 | G | C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.117+19512C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123729106 | |||||||
| chr7:123729420 | A | G | 7 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(4): Show |
8 | HG02145.hp1 HG02559.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+19198T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123729420 | |||||||
| chr7:123729458 | G | A | 2 | a0001c0002t0001g0286 a0001c0005t0001g0223 |
2 | HG00738.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.117+19160C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123729458 | |||||||
| chr7:123729485 | T | C | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.117+19133A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123729485 | |||||||
| chr7:123729638 | A | G | 1 | a0001c0002t0003g0295 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.117+18980T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123729638 | |||||||
| chr7:123729802 | C | T | 228 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(225): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.117+18816G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123729802 | |||||||
| chr7:123729820 | A | C | 4 | a0001c0003t0005g0126 a0001c0003t0005g0127 a0001c0003t0005g0134 others(1): Show |
4 | HG00673.hp1 HG02071.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+18798T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123729820 | |||||||
| chr7:123730024 | T | C | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.117+18594A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730024 | |||||||
| chr7:123730178 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.117+18440A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730178 | |||||||
| chr7:123730349 | C | T | 53 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0013 others(50): Show |
60 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.117+18269G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730349 | |||||||
| chr7:123730401 | G | C | 2 | a0001c0002t0001g0240 a0001c0002t0001g0244 |
2 | HG02155.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.117+18217C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730401 | |||||||
| chr7:123730468 | A | G | 1 | a0001c0001t0015g0064 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.117+18150T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730468 | |||||||
| chr7:123730496 | T | A | 1 | a0001c0001t0004g0167 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.117+18122A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730496 | |||||||
| chr7:123730656 | A | G | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.117+17962T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730656 | |||||||
| chr7:123730718 | C | G | 2 | a0001c0001t0009g0118 a0001c0001t0009g0119 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.117+17900G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730718 | |||||||
| chr7:123730849 | C | T | 133 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(130): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.117+17769G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730849 | |||||||
| chr7:123730972 | C | A | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.117+17646G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123730972 | |||||||
| chr7:123731387 | A | G | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.117+17231T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123731387 | |||||||
| chr7:123731448 | T | C | 5 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(2): Show |
6 | HG02145.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+17170A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123731448 | |||||||
| chr7:123731524 | G | A | 8 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0158 others(5): Show |
10 | HG00408.hp1 HG02040.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.117+17094C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123731524 | |||||||
| chr7:123731560 | A | G | 1 | a0001c0002t0001g0284 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.117+17058T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123731560 | |||||||
| chr7:123731709 | C | T | 2 | a0001c0001t0002g0048 a0001c0001t0002g0049 |
2 | NA18968.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.117+16909G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123731709 | |||||||
| chr7:123731833 | A | G | 2 | a0001c0001t0009g0118 a0001c0001t0009g0119 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.117+16785T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123731833 | |||||||
| chr7:123732046 | G | A | 1 | a0001c0002t0001g0034 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.117+16572C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123732046 | |||||||
| chr7:123732199 | G | A | 4 | a0001c0002t0001g0032 a0001c0002t0001g0191 a0001c0002t0001g0213 others(1): Show |
5 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+16419C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123732199 | |||||||
| chr7:123732246 | C | T | 1 | a0001c0002t0021g0250 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.117+16372G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123732246 | |||||||
| chr7:123732330 | G | A | 2 | a0001c0001t0009g0118 a0001c0001t0009g0119 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.117+16288C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123732330 | |||||||
| chr7:123732436 | T | G | 1 | a0001c0002t0001g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.117+16182A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123732436 | |||||||
| chr7:123732482 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.117+16136G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123732482 | |||||||
| chr7:123732899 | T | C | 1 | a0001c0001t0009g0119 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.117+15719A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123732899 | |||||||
| chr7:123733008 | C | T | 1 | a0001c0001t0002g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.117+15610G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123733008 | |||||||
| chr7:123733139 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.117+15479G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123733139 | |||||||
| chr7:123733362 | A | T | 3 | a0001c0002t0001g0197 a0001c0002t0001g0198 a0001c0002t0001g0199 |
3 | HG03490.hp1 HG04204.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.117+15256T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123733362 | |||||||
| chr7:123733568 | T | C | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.117+15050A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123733568 | |||||||
| chr7:123733913 | CA | C | 98 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(95): Show |
116 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.117+14704delT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123733913 | |||||||
| chr7:123733913 | CAA | C | 117 | a0001c0001t0002g0044 a0001c0001t0006g0008 a0001c0001t0006g0043 others(114): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.117+14703_117+1470 others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123733913 | |||||||
| chr7:123734070 | G | A | 5 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(2): Show |
6 | HG02145.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+14548C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123734070 | |||||||
| chr7:123734358 | A | G | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.117+14260T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123734358 | |||||||
| chr7:123734591 | T | TA | 121 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0017 others(118): Show |
144 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.117+14026dupT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123734591 | |||||||
| chr7:123734591 | T | TAA | 63 | a0001c0001t0002g0084 a0001c0001t0003g0117 a0001c0001t0003g0136 others(60): Show |
79 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.117+14025_117+1402 others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123734591 | |||||||
| chr7:123734613 | A | T | 3 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0144 |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+14005T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123734613 | |||||||
| chr7:123734666 | G | T | 2 | a0001c0001t0006g0008 a0001c0001t0006g0043 |
3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.117+13952C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123734666 | |||||||
| chr7:123734712 | A | G | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.117+13906T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123734712 | |||||||
| chr7:123734785 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.117+13833G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123734785 | |||||||
| chr7:123734786 | G | A | 95 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(92): Show |
115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.117+13832C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123734786 | |||||||
| chr7:123735019 | C | CAGTCCTT others(29): Show |
1 | a0001c0002t0001g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.117+13563_117+1359 others(40): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735019 | |||||||
| chr7:123735131 | CA | C | 128 | a0001c0001t0002g0109 a0001c0001t0003g0175 a0001c0001t0004g0163 others(125): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.117+13486delT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735131 | |||||||
| chr7:123735162 | A | T | 1 | a0001c0001t0015g0064 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.117+13456T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735162 | |||||||
| chr7:123735337 | T | C | 2 | a0001c0001t0009g0118 a0001c0001t0009g0119 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.117+13281A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735337 | |||||||
| chr7:123735381 | G | GA | 127 | a0001c0001t0002g0063 a0001c0001t0002g0085 a0001c0001t0004g0171 others(124): Show |
153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.117+13236dupT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735381 | |||||||
| chr7:123735451 | G | C | 133 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(130): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.117+13167C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735451 | |||||||
| chr7:123735775 | C | T | 4 | a0001c0001t0003g0024 a0001c0001t0003g0026 a0001c0001t0003g0175 others(1): Show |
6 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+12843G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735775 | |||||||
| chr7:123735853 | G | A | 101 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(98): Show |
121 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.117+12765C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735853 | |||||||
| chr7:123735942 | T | C | 1 | a0001c0002t0001g0242 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.117+12676A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735942 | |||||||
| chr7:123735994 | T | C | 1 | a0001c0002t0001g0230 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.117+12624A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123735994 | |||||||
| chr7:123736006 | G | A | 3 | a0001c0001t0002g0027 a0001c0001t0002g0189 a0001c0001t0002g0190 |
4 | NA18952.hp1 NA18962.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+12612C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123736006 | |||||||
| chr7:123736240 | A | G | 4 | a0001c0001t0002g0011 a0001c0001t0002g0046 a0001c0001t0002g0062 others(1): Show |
5 | HG02922.hp2 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+12378T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123736240 | |||||||
| chr7:123736298 | TCTC | T | 11 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(8): Show |
12 | HG00099.hp1 HG00733.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+12317_117+1231 others(7): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123736298 | |||||||
| chr7:123736393 | T | C | 1 | a0001c0002t0001g0205 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+12225A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123736393 | |||||||
| chr7:123736402 | T | C | 3 | a0001c0002t0001g0231 a0001c0002t0001g0232 a0001c0002t0001g0243 |
3 | HG00544.hp2 NA18970.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.117+12216A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123736402 | |||||||
| chr7:123736436 | C | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0144 |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+12182G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123736436 | |||||||
| chr7:123736506 | G | A | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.117+12112C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123736506 | |||||||
| chr7:123736801 | A | T | 228 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(225): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.117+11817T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123736801 | |||||||
| chr7:123737012 | G | A | 123 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(120): Show |
148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.117+11606C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123737012 | |||||||
| chr7:123737052 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.117+11566T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123737052 | |||||||
| chr7:123737159 | A | G | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.117+11459T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123737159 | |||||||
| chr7:123737466 | C | T | 1 | a0001c0001t0002g0017 | 2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.117+11152G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123737466 | |||||||
| chr7:123737596 | C | CA | 29 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0002g0060 others(26): Show |
30 | HG00621.hp1 HG00621.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.117+11021dupT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123737596 | |||||||
| chr7:123737596 | C | CAAAA | 99 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(96): Show |
122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.117+11018_117+1102 others(8): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123737596 | |||||||
| chr7:123737596 | C | CAAAAA | 22 | a0001c0002t0001g0028 a0001c0002t0001g0033 a0001c0002t0001g0194 others(19): Show |
24 | HG00544.hp2 HG01167.hp2 HG01978.hp2 others(21): Show |
intron_variant | MODIFIER | c.117+11017_117+1102 others(9): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123737596 | |||||||
| chr7:123737990 | A | C | 1 | a0001c0001t0002g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.117+10628T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123737990 | |||||||
| chr7:123738050 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.117+10568A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738050 | |||||||
| chr7:123738158 | C | A | 1 | a0001c0001t0003g0117 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.117+10460G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738158 | |||||||
| chr7:123738170 | G | GTTAA | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.117+10444_117+1044 others(8): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738170 | |||||||
| chr7:123738417 | C | A | 123 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(120): Show |
148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.117+10201G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738417 | |||||||
| chr7:123738424 | T | C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.117+10194A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738424 | |||||||
| chr7:123738640 | T | A | 1 | a0001c0001t0002g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.117+9978A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738640 | |||||||
| chr7:123738723 | G | T | 4 | a0001c0002t0001g0203 a0001c0002t0001g0204 a0001c0002t0001g0282 others(1): Show |
4 | HG00280.hp2 HG00735.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+9895C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738723 | |||||||
| chr7:123738757 | C | CT | 11 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(8): Show |
12 | HG00099.hp1 HG00733.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+9860dupA | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738757 | |||||||
| chr7:123738835 | G | A | 1 | a0001c0002t0001g0244 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.117+9783C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738835 | |||||||
| chr7:123738952 | G | T | 1 | a0001c0001t0002g0102 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.117+9666C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738952 | |||||||
| chr7:123738977 | C | T | 2 | a0001c0002t0001g0290 a0001c0002t0001g0291 |
2 | HG00642.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.117+9641G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738977 | |||||||
| chr7:123738979 | G | A | 1 | a0001c0002t0001g0245 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.117+9639C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123738979 | |||||||
| chr7:123739073 | C | T | 1 | a0001c0002t0001g0246 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.117+9545G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739073 | |||||||
| chr7:123739138 | T | G | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.117+9480A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739138 | |||||||
| chr7:123739463 | A | C | 3 | a0001c0002t0001g0030 a0001c0002t0001g0200 a0001c0002t0001g0201 |
4 | HG01071.hp1 HG01074.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+9155T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739463 | |||||||
| chr7:123739512 | TCAGTA | T | 3 | a0001c0001t0002g0005 a0001c0001t0002g0141 a0001c0001t0014g0187 |
5 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+9101_117+9105d others(7): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739512 | |||||||
| chr7:123739557 | T | C | 96 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(93): Show |
116 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.117+9061A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739557 | |||||||
| chr7:123739603 | T | C | 2 | a0001c0002t0001g0277 a0001c0002t0001g0278 |
2 | NA18955.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.117+9015A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739603 | |||||||
| chr7:123739623 | T | C | 1 | a0001c0002t0001g0034 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.117+8995A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739623 | |||||||
| chr7:123739631 | A | C | 1 | a0001c0001t0002g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.117+8987T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739631 | |||||||
| chr7:123739637 | G | A | 1 | a0001c0002t0001g0198 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.117+8981C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739637 | |||||||
| chr7:123739876 | ATG | A | 42 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(39): Show |
48 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.117+8740_117+8741d others(4): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739876 | |||||||
| chr7:123739876 | ATGTG | A | 3 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0090 |
3 | HG00621.hp1 HG04199.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.117+8738_117+8741d others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739876 | |||||||
| chr7:123739890 | GTGTGTGT others(19): Show |
G | 5 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(2): Show |
6 | HG02145.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+8702_117+8727d others(28): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739890 | |||||||
| chr7:123739894 | GTGTGTGT others(15): Show |
G | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.117+8702_117+8723d others(24): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739894 | |||||||
| chr7:123739896 | GTGTGTGT others(13): Show |
G | 1 | a0001c0002t0001g0028 | 2 | NA19070.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.117+8702_117+8721d others(22): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739896 | |||||||
| chr7:123739902 | GTGTGTGT others(7): Show |
G | 48 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0144 others(45): Show |
64 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.117+8702_117+8715d others(16): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739902 | |||||||
| chr7:123739902 | GTGTGTGT others(9): Show |
G | 1 | a0001c0002t0001g0007 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.117+8700_117+8715d others(18): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739902 | |||||||
| chr7:123739904 | GTGTGTGT others(5): Show |
G | 16 | a0001c0002t0001g0034 a0001c0002t0001g0205 a0001c0002t0001g0211 others(13): Show |
17 | HG01175.hp2 HG01256.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.117+8702_117+8713d others(14): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739904 | |||||||
| chr7:123739904 | GTGTGTGT others(7): Show |
G | 58 | a0001c0002t0001g0007 a0001c0002t0001g0029 a0001c0002t0001g0031 others(55): Show |
66 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.117+8700_117+8713d others(16): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739904 | |||||||
| chr7:123739904 | GTGTGTGT others(9): Show |
G | 1 | a0001c0001t0003g0114 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.117+8698_117+8713d others(18): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739904 | |||||||
| chr7:123739906 | GTGTGTGT others(5): Show |
G | 2 | a0001c0001t0002g0017 a0001c0001t0003g0133 |
2 | HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.117+8700_117+8711d others(14): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739906 | |||||||
| chr7:123739906 | GTGTGTGT others(7): Show |
G | 1 | a0001c0002t0001g0264 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.117+8698_117+8711d others(16): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739906 | |||||||
| chr7:123739906 | GTGTGTGT others(9): Show |
G | 1 | a0001c0002t0001g0204 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.117+8696_117+8711d others(18): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739906 | |||||||
| chr7:123739908 | GTGTGTGT others(3): Show |
G | 9 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0131 others(6): Show |
9 | HG02071.hp2 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+8700_117+8709d others(12): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739908 | |||||||
| chr7:123739910 | GTGTGTAT others(1): Show |
G | 38 | a0001c0001t0002g0044 a0001c0001t0002g0146 a0001c0001t0003g0014 others(35): Show |
45 | HG00323.hp1 HG00544.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.117+8700_117+8707d others(10): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739910 | |||||||
| chr7:123739912 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.117+8706C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739912 | |||||||
| chr7:123739912 | GTGTA | G | 6 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0056 others(3): Show |
7 | HG01167.hp1 HG01169.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+8702_117+8705d others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739912 | |||||||
| chr7:123739912 | GTGTATA | G | 25 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0141 others(22): Show |
29 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.117+8700_117+8705d others(8): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739912 | |||||||
| chr7:123739914 | G | A | 10 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0046 others(7): Show |
11 | HG01255.hp2 HG01943.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.117+8704C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739914 | |||||||
| chr7:123739914 | GTA | G | 5 | a0001c0001t0002g0050 a0001c0001t0002g0092 a0001c0001t0002g0094 others(2): Show |
5 | HG00733.hp1 HG00735.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+8702_117+8703d others(4): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739914 | |||||||
| chr7:123739914 | GTATA | G | 18 | a0001c0001t0002g0005 a0001c0001t0002g0142 a0001c0001t0002g0143 others(15): Show |
19 | HG00673.hp2 HG01192.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.117+8700_117+8703d others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739914 | |||||||
| chr7:123739914 | GTATATA | G | 2 | a0001c0001t0003g0003 a0001c0001t0003g0173 |
5 | NA18960.hp2 NA18970.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+8698_117+8703d others(8): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739914 | |||||||
| chr7:123739916 | A | G | 1 | a0001c0001t0002g0093 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.117+8702T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739916 | |||||||
| chr7:123739918 | A | G | 1 | a0001c0001t0003g0178 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.117+8700T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123739918 | |||||||
| chr7:123740017 | T | C | 1 | a0001c0002t0001g0199 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.117+8601A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740017 | |||||||
| chr7:123740135 | A | C | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.117+8483T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740135 | |||||||
| chr7:123740174 | A | G | 2 | a0001c0001t0006g0008 a0001c0001t0006g0043 |
3 | HG02145.hp1 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.117+8444T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740174 | |||||||
| chr7:123740259 | GC | G | 11 | a0001c0001t0003g0025 a0001c0001t0003g0114 a0001c0001t0003g0177 others(8): Show |
12 | HG01192.hp2 HG01346.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.117+8358delG | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740259 | |||||||
| chr7:123740351 | T | A | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.117+8267A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740351 | |||||||
| chr7:123740454 | GATTT | G | 45 | a0001c0002t0001g0007 a0001c0002t0001g0035 a0001c0002t0001g0036 others(42): Show |
51 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.117+8160_117+8163d others(6): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740454 | |||||||
| chr7:123740490 | T | G | 1 | a0001c0001t0014g0187 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.117+8128A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740490 | |||||||
| chr7:123740627 | C | G | 131 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.117+7991G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740627 | |||||||
| chr7:123740696 | A | G | 3 | a0001c0002t0001g0197 a0001c0002t0001g0198 a0001c0002t0001g0199 |
3 | HG03490.hp1 HG04204.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.117+7922T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740696 | |||||||
| chr7:123740705 | C | A | 1 | a0001c0003t0003g0140 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.117+7913G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740705 | |||||||
| chr7:123740767 | T | C | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.117+7851A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740767 | |||||||
| chr7:123740877 | C | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(2): Show |
6 | HG02145.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+7741G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740877 | |||||||
| chr7:123740949 | T | C | 3 | a0001c0002t0001g0279 a0001c0002t0001g0280 a0001c0002t0001g0281 |
3 | HG01175.hp2 HG03239.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.117+7669A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123740949 | |||||||
| chr7:123741149 | T | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0144 |
3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.117+7469A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123741149 | |||||||
| chr7:123741262 | T | C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG02965.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.117+7356A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123741262 | |||||||
| chr7:123741269 | A | G | 1 | a0001c0001t0002g0045 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.117+7349T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123741269 | |||||||
| chr7:123741333 | T | C | 10 | a0001c0001t0004g0022 a0001c0001t0004g0163 a0001c0001t0004g0164 others(7): Show |
11 | HG00621.hp2 HG00673.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.117+7285A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123741333 | |||||||
| chr7:123741416 | C | T | 1 | a0001c0002t0001g0196 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.117+7202G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123741416 | |||||||
| chr7:123741476 | G | C | 96 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(93): Show |
116 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.117+7142C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123741476 | |||||||
| chr7:123741730 | A | C | 2 | a0001c0001t0003g0014 a0001c0001t0003g0103 |
3 | HG01168.hp2 HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.117+6888T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123741730 | |||||||
| chr7:123741901 | C | T | 1 | a0001c0001t0011g0040 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.117+6717G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123741901 | |||||||
| chr7:123741960 | C | T | 1 | a0001c0003t0003g0186 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.117+6658G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123741960 | |||||||
| chr7:123742075 | T | C | 1 | a0001c0002t0001g0283 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.117+6543A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742075 | |||||||
| chr7:123742098 | A | C | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.117+6520T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742098 | |||||||
| chr7:123742136 | C | T | 1 | a0001c0002t0001g0195 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.117+6482G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742136 | |||||||
| chr7:123742174 | G | T | 1 | a0001c0003t0003g0124 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.117+6444C>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742174 | |||||||
| chr7:123742203 | T | A | 1 | a0001c0001t0003g0174 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.117+6415A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742203 | |||||||
| chr7:123742236 | C | T | 124 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.117+6382G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742236 | |||||||
| chr7:123742264 | A | G | 2 | a0001c0001t0009g0118 a0001c0001t0009g0119 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.117+6354T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742264 | |||||||
| chr7:123742375 | A | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(2): Show |
6 | HG02145.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+6243T>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742375 | |||||||
| chr7:123742387 | C | T | 1 | a0001c0002t0001g0301 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.117+6231G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742387 | |||||||
| chr7:123742455 | C | T | 56 | a0001c0001t0002g0017 a0001c0001t0002g0142 a0001c0001t0002g0143 others(53): Show |
64 | HG00544.hp1 HG00673.hp1 HG01099.hp1 others(61): Show |
intron_variant | MODIFIER | c.117+6163G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742455 | |||||||
| chr7:123742645 | A | G | 1 | a0001c0002t0001g0029 | 2 | HG03017.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.117+5973T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742645 | |||||||
| chr7:123742867 | A | G | 2 | a0001c0001t0009g0118 a0001c0001t0009g0119 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.117+5751T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742867 | |||||||
| chr7:123742878 | G | A | 1 | a0001c0002t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.117+5740C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123742878 | |||||||
| chr7:123743091 | C | T | 2 | a0001c0002t0001g0193 a0001c0002t0001g0194 |
2 | HG01261.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.117+5527G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743091 | |||||||
| chr7:123743336 | C | CA | 97 | a0001c0001t0001g0113 a0001c0001t0002g0005 a0001c0001t0002g0017 others(94): Show |
117 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.117+5281dupT | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743336 | |||||||
| chr7:123743374 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.117+5244T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743374 | |||||||
| chr7:123743407 | G | A | 11 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(8): Show |
12 | HG00099.hp1 HG00733.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+5211C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743407 | |||||||
| chr7:123743427 | C | A | 3 | a0001c0001t0002g0017 a0001c0001t0002g0142 a0001c0001t0002g0143 |
4 | HG02647.hp2 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+5191G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743427 | |||||||
| chr7:123743430 | G | C | 1 | a0001c0001t0002g0102 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.117+5188C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743430 | |||||||
| chr7:123743461 | G | C | 95 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(92): Show |
115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.117+5157C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743461 | |||||||
| chr7:123743487 | C | A | 1 | a0001c0001t0003g0185 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.117+5131G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743487 | |||||||
| chr7:123743835 | T | G | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.117+4783A>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743835 | |||||||
| chr7:123743877 | T | C | 2 | a0001c0001t0009g0118 a0001c0001t0009g0119 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.117+4741A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743877 | |||||||
| chr7:123743922 | G | A | 3 | a0001c0002t0001g0290 a0001c0002t0001g0291 a0001c0002t0001g0292 |
3 | HG00642.hp1 HG01978.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.117+4696C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123743922 | |||||||
| chr7:123744244 | G | A | 1 | a0001c0001t0009g0119 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.117+4374C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123744244 | |||||||
| chr7:123744262 | A | G | 1 | a0001c0001t0004g0145 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.117+4356T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123744262 | |||||||
| chr7:123744282 | A | C | 2 | a0001c0001t0010g0041 a0001c0001t0010g0042 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.117+4336T>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123744282 | |||||||
| chr7:123744290 | C | T | 2 | a0001c0001t0009g0118 a0001c0001t0009g0119 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.117+4328G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123744290 | |||||||
| chr7:123744352 | C | G | 1 | a0001c0002t0001g0192 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.117+4266G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123744352 | |||||||
| chr7:123744392 | T | C | 3 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0144 |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+4226A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123744392 | |||||||
| chr7:123744513 | G | A | 2 | a0001c0002t0001g0293 a0001c0002t0017g0294 |
2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.117+4105C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123744513 | |||||||
| chr7:123744727 | T | C | 95 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(92): Show |
115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.117+3891A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123744727 | |||||||
| chr7:123745111 | G | A | 1 | a0001c0002t0001g0038 | 2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.117+3507C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123745111 | |||||||
| chr7:123745163 | A | G | 1 | a0001c0002t0001g0191 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.117+3455T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123745163 | |||||||
| chr7:123745445 | G | C | 31 | a0001c0001t0002g0146 a0001c0001t0004g0006 a0001c0001t0004g0020 others(28): Show |
36 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.117+3173C>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123745445 | |||||||
| chr7:123745862 | G | A | 4 | a0001c0001t0003g0023 a0001c0001t0003g0172 a0001c0001t0003g0173 others(1): Show |
5 | HG01099.hp1 HG02735.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+2756C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123745862 | |||||||
| chr7:123746177 | T | A | 2 | a0001c0001t0002g0109 a0001c0001t0002g0110 |
2 | NA19001.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.117+2441A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123746177 | |||||||
| chr7:123746184 | T | A | 4 | a0001c0001t0003g0024 a0001c0001t0003g0026 a0001c0001t0003g0175 others(1): Show |
6 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+2434A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123746184 | |||||||
| chr7:123746423 | C | A | 1 | a0001c0002t0019g0297 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.117+2195G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123746423 | |||||||
| chr7:123746428 | T | C | 7 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(4): Show |
8 | HG02145.hp1 HG02559.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+2190A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123746428 | |||||||
| chr7:123746652 | G | A | 2 | a0001c0002t0001g0039 a0001c0002t0001g0298 |
3 | HG02080.hp1 NA18955.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.117+1966C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123746652 | |||||||
| chr7:123746799 | T | C | 11 | a0001c0001t0003g0025 a0001c0001t0003g0114 a0001c0001t0003g0177 others(8): Show |
12 | HG01192.hp2 HG01346.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.117+1819A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123746799 | |||||||
| chr7:123747090 | C | T | 1 | a0001c0002t0001g0028 | 2 | NA19070.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.117+1528G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123747090 | |||||||
| chr7:123747615 | G | A | 1 | a0001c0001t0002g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.117+1003C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123747615 | |||||||
| chr7:123747739 | G | A | 1 | a0001c0003t0003g0186 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.117+879C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123747739 | |||||||
| chr7:123747900 | C | G | 2 | a0001c0001t0003g0116 a0001c0001t0003g0117 |
2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.117+718G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123747900 | |||||||
| chr7:123747982 | G | A | 217 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(214): Show |
261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.117+636C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123747982 | |||||||
| chr7:123748003 | G | A | 1 | a0001c0002t0001g0299 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.117+615C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748003 | |||||||
| chr7:123748123 | T | C | 1 | a0001c0002t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.117+495A>G | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748123 | |||||||
| chr7:123748261 | C | G | 1 | a0001c0001t0002g0045 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.117+357G>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748261 | |||||||
| chr7:123748420 | A | G | 131 | a0001c0001t0002g0044 a0001c0001t0006g0008 a0001c0001t0006g0043 others(128): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.117+198T>C | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748420 | |||||||
| chr7:123748458 | C | T | 4 | a0001c0001t0006g0008 a0001c0001t0006g0043 a0001c0001t0010g0041 others(1): Show |
5 | HG02145.hp1 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+160G>A | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748458 | |||||||
| chr7:123748477 | AGGGGCCG others(5): Show |
A | 2 | a0001c0001t0003g0026 a0001c0001t0014g0187 |
3 | HG02647.hp1 HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.117+129_117+140del others(12): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748477 | |||||||
| chr7:123748478 | GGGGCCGG others(4): Show |
G | 2 | a0001c0001t0002g0005 a0001c0001t0002g0141 |
4 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+129_117+139del others(11): Show |
WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748478 | |||||||
| chr7:123748505 | G | A | 1 | a0001c0002t0001g0301 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.117+113C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748505 | |||||||
| chr7:123748599 | G | A | 1 | a0001c0001t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.117+19C>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748599 | |||||||
| chr7:123748600 | C | A | 1 | a0001c0001t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.117+18G>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748600 | |||||||
| chr7:123748604 | T | A | 3 | a0001c0001t0002g0027 a0001c0001t0002g0189 a0001c0001t0002g0190 |
4 | NA18952.hp1 NA18962.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+14A>T | WASL | ENSG00000106299.8 | transcript | ENST00000223023.5 | protein_coding | 1/10 | chr7 | 123748604 |