Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2273 |
|---|---|
| ensemblid | ENSG00000022267.19 |
| hgncid | 3702 |
| symbol | FHL1 |
| name | four and a half LIM domains 1 |
| refseq_nuc | NM_001159702.3 |
| refseq_prot | NP_001153174.1 |
| ensembl_nuc | ENST00000394155.8 |
| ensembl_prot | ENSP00000377710.2 |
| mane_status | MANE Plus Clinical |
| chr | chrX |
| start | 136147533 |
| end | 136211354 |
| strand | + |
| ver | v1.2 |
| region | chrX:136147533-136211354 |
| region5000 | chrX:136142533-136216354 |
| regionname0 | FHL1_chrX_136147533_136211354 |
| regionname5000 | FHL1_chrX_136142533_136216354 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 323 | 210 | 48 | 32 | 97 | 7 | 24 | 68 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0002 | 0/0 | 129 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0003 | 0/0 | 323 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 972 | 209 | 47 | 32 | 97 | 7 | 24 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| c0002 | 0/0 | 972 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| c0003 | 0/0 | 973 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| c0004 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1597 | 104 | 14 | 13 | 66 | 3 | 7 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| t0002 | 1/0 | 1597 | 90 | 24 | 17 | 29 | 4 | 15 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| t0003 | 0/0 | 1597 | 5 | 5 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| t0004 | 0/0 | 1597 | 2 | 2 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| t0005 | 0/0 | 1606 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| t0006 | 0/0 | 1598 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| t0007 | 0/0 | 1598 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| t0008 | 0/0 | 1597 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| t0009 | 0/0 | 1597 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| t0010 | 0/0 | 1597 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| t0011 | 0/0 | 1597 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| t0012 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| t0013 | 0/0 | 1597 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| t0014 | 0/0 | 1597 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| t0015 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0002 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0003 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0005 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 972 | 209 | 47 | 32 | 97 | 7 | 24 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0001c0004 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0002c0003 | 0/0 | 973 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0003c0002 | 0/0 | 972 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2568 | 103 | 14 | 13 | 65 | 3 | 7 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0001c0001t0002 | 1/0 | 2568 | 89 | 23 | 17 | 29 | 4 | 15 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0001c0001t0003 | 0/0 | 2568 | 5 | 5 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0001c0001t0004 | 0/0 | 2568 | 2 | 2 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0001c0001t0005 | 0/0 | 2577 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0001c0001t0007 | 0/0 | 2569 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0001c0001t0008 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0001c0001t0009 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0001c0001t0010 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0001c0001t0011 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0001c0001t0012 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0001c0001t0013 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0001c0001t0014 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0001c0001t0015 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0001c0004t0002 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0002c0003t0006 | 0/0 | 2570 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| a0003c0002t0001 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | copy fasta | chrX | 136142533 | 136216354 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0003 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0007g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0008g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0009g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0010g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0011g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0012g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0013g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0014g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0015g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0004t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0002c0003t0006g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0003c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | GBR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0052 | EUR | FIN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01109 | hp1 | a0001 | c0001 | t0008 | g0159 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01192 | hp1 | a0001 | c0001 | t0009 | g0177 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | CLM | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0030 | EUR | IBS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0031 | EUR | IBS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | ACB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | ACB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02145 | hp1 | a0001 | c0004 | t0002 | g0168 | AFR | ACB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | CDX | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | CDX | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02165 | hp1 | a0001 | c0001 | t0010 | g0011 | EAS | CDX | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CDX | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0162 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0158 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02970 | hp2 | a0001 | c0001 | t0012 | g0155 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02976 | hp2 | a0001 | c0001 | t0015 | g0163 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0118 | AFR | MSL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | MSL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03490 | hp1 | a0001 | c0001 | t0011 | g0025 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | STU | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03942 | hp1 | a0001 | c0001 | t0014 | g0141 | SAS | BEB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | BEB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | BEB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | STU | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | YRI | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18949 | hp2 | a0001 | c0001 | t0013 | g0040 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18985 | hp1 | a0002 | c0003 | t0006 | g0018 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18990 | hp1 | a0003 | c0002 | t0001 | g0001 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | LWK | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | LWK | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | LWK | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19075 | hp1 | a0001 | c0001 | t0007 | g0182 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | YRI | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | TSI | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0180 | EUR | TSI | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | GIH | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0183 | AFR | ACB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ACB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | MSL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0101 | REF | REF | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0003 | REF | REF | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:136207064
|
G | A | 1 | a0003 | 1 | NA18990.hp1 | missense_variant | MODERATE | c.205G>A | p.Ala69Thr | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 4/8 | 401/2568 | 205/972 | 69/323 | chrX | 136207064 | ||
| chrX:136207837
|
G | GC | 1 | a0002 | 1 | NA18985.hp1 | frameshift_variant | HIGH | c.378dupC | p.Phe127fs | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 5/8 | 575/2568 | 379/972 | 127/323 | INFO_REALIGN_3_PRIME | chrX | 136207837 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:136207910
|
C | T | 1 | a0001c0004 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.450C>T | p.Cys150Cys | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 5/8 | 646/2568 | 450/972 | 150/323 | chrX | 136207910 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:136147535
|
T | TCCGCAGC others(2): Show |
1 | a0001c0001t0005 | 1 | HG02895.hp1 | 5_prime_UTR_variant | MODIFIER | c.-189_-181dupAGCCGC others(3): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/8 | 58884 | INFO_REALIGN_3_PRIME | chrX | 136147535 | ||||
| chrX:136147571
|
C | T | 2 | a0001c0001t0003a0001c0001t0015 | 6 | HG02055.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-158C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/8 | chrX | 136147571 | ||||||
| chrX:136147585
|
G | GC | 1 | a0002c0003t0006 | 1 | NA18985.hp1 | 5_prime_UTR_variant | MODIFIER | c.-142dupC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/8 | 58845 | INFO_REALIGN_3_PRIME | chrX | 136147585 | ||||
| chrX:136147601
|
C | CA | 1 | a0001c0001t0007 | 1 | NA19075.hp1 | 5_prime_UTR_variant | MODIFIER | c.-127dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/8 | 58830 | INFO_REALIGN_3_PRIME | chrX | 136147601 | ||||
| chrX:136169974
|
G | C | 1 | a0001c0001t0008 | 1 | HG01109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-33G>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/8 | 36459 | chrX | 136169974 | |||||
| chrX:136210005
|
G | A | 1 | a0001c0001t0009 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*51G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 8/8 | 51 | chrX | 136210005 | |||||
| chrX:136210042
|
G | A | 1 | a0001c0001t0010 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*88G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 8/8 | 88 | chrX | 136210042 | |||||
| chrX:136210119
|
T | C | 1 | a0001c0001t0011 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*165T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 8/8 | 165 | chrX | 136210119 | |||||
| chrX:136210463
|
C | G | 2 | a0001c0001t0004a0001c0001t0005 | 3 | HG02895.hp1 HG03209.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*509C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 8/8 | 509 | chrX | 136210463 | |||||
| chrX:136210518
|
C | T | 1 | a0001c0001t0008 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*564C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 8/8 | 564 | chrX | 136210518 | |||||
| chrX:136210732
|
C | A | 1 | a0001c0001t0012 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*778C>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 8/8 | 778 | chrX | 136210732 | |||||
| chrX:136210750
|
C | T | 1 | a0001c0001t0015 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*796C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 8/8 | 796 | chrX | 136210750 | |||||
| chrX:136210759
|
G | A | 1 | a0001c0001t0013 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*805G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 8/8 | 805 | chrX | 136210759 | |||||
| chrX:136210923
|
G | A | 13 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(10): Show | 116 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*969G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 8/8 | 969 | chrX | 136210923 | |||||
| chrX:136210930
|
A | G | 1 | a0001c0001t0015 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*976A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 8/8 | 976 | chrX | 136210930 | |||||
| chrX:136210933
|
G | A | 1 | a0001c0001t0014 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*979G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 8/8 | 979 | chrX | 136210933 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:136147630
|
T | TA | 1 | a0001c0001t0002g0017 | 1 | NA18972.hp2 | splice_region_variant&intron_variant | LOW | c.-101+4dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136147630 | |||||
| chrX:136147715
|
GC | G | 1 | a0001c0001t0002g0188 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-101+91delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136147715 | |||||
| chrX:136147722
|
C | G | 2 | a0001c0001t0002g0186a0001c0001t0002g0187 | 2 | HG02080.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-101+94C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136147722 | ||||||
| chrX:136147870
|
T | TC | 2 | a0001c0001t0001g0019a0002c0003t0006g0018 | 2 | NA18985.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.-101+248dupC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136147870 | |||||
| chrX:136147879
|
G | C | 1 | a0001c0001t0002g0020 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-101+251G>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136147879 | ||||||
| chrX:136147926
|
A | AG | 1 | a0001c0001t0001g0019 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-101+300dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136147926 | |||||
| chrX:136147943
|
T | TG | 1 | a0001c0001t0001g0019 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-101+322dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136147943 | |||||
| chrX:136148020
|
A | AG | 1 | a0001c0001t0002g0185 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-101+399dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148020 | |||||
| chrX:136148059
|
T | TG | 1 | a0001c0001t0002g0186 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-101+437dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148059 | |||||
| chrX:136148065
|
G | T | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-101+437G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136148065 | ||||||
| chrX:136148074
|
G | GT | 1 | a0001c0001t0001g0019 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-101+446_-101+447i others(3): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136148074 | ||||||
| chrX:136148076
|
T | G | 1 | a0001c0001t0001g0019 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-101+448T>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136148076 | ||||||
| chrX:136148130
|
C | CG | 1 | a0002c0003t0006g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-101+505dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148130 | |||||
| chrX:136148151
|
G | GT | 1 | a0001c0001t0002g0188 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-101+524dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148151 | |||||
| chrX:136148176
|
A | AG | 1 | a0001c0001t0001g0019 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-101+550dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148176 | |||||
| chrX:136148195
|
A | AG | 1 | a0002c0003t0006g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-101+573dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148195 | |||||
| chrX:136148195
|
AG | A | 1 | a0001c0001t0001g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-101+573delG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148195 | |||||
| chrX:136148240
|
C | CG | 3 | a0001c0001t0001g0022a0001c0001t0002g0023a0001c0001t0002g0024 | 3 | HG01981.hp1 HG02523.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-101+617dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148240 | |||||
| chrX:136148240
|
C | CGG | 1 | a0001c0001t0001g0019 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-101+616_-101+617d others(4): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148240 | |||||
| chrX:136148262
|
ACGTGAG | A | 1 | a0001c0001t0002g0188 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-101+635_-101+640d others(8): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136148262 | ||||||
| chrX:136148276
|
G | GC | 1 | a0001c0001t0001g0019 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-101+650dupC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148276 | |||||
| chrX:136148347
|
AG | A | 1 | a0001c0001t0002g0188 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-101+724delG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148347 | |||||
| chrX:136148404
|
T | TG | 1 | a0001c0001t0001g0019 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-101+781dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148404 | |||||
| chrX:136148415
|
A | AG | 1 | a0001c0001t0001g0019 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-101+792dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148415 | |||||
| chrX:136148471
|
C | CG | 1 | a0001c0001t0001g0019 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-101+848dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148471 | |||||
| chrX:136148500
|
C | CA | 1 | a0001c0001t0002g0017 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-101+876dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148500 | |||||
| chrX:136148524
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-101+896C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136148524 | ||||||
| chrX:136148531
|
G | GA | 1 | a0001c0001t0002g0017 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-101+908dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148531 | |||||
| chrX:136148556
|
GC | G | 1 | a0001c0001t0002g0017 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-101+930delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148556 | |||||
| chrX:136148587
|
TCTG | T | 1 | a0001c0001t0003g0183 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-101+962_-101+964d others(5): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148587 | |||||
| chrX:136148666
|
TA | T | 1 | a0001c0001t0002g0017 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-101+1040delA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148666 | |||||
| chrX:136148716
|
TG | T | 1 | a0001c0001t0002g0188 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-101+1091delG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148716 | |||||
| chrX:136148754
|
T | C | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-101+1126T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136148754 | ||||||
| chrX:136148776
|
T | G | 1 | a0001c0001t0011g0025 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-101+1148T>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136148776 | ||||||
| chrX:136148792
|
GA | G | 1 | a0001c0001t0007g0182 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-101+1168delA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148792 | |||||
| chrX:136148801
|
AG | A | 1 | a0001c0001t0002g0017 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-101+1175delG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148801 | |||||
| chrX:136148866
|
T | TC | 1 | a0001c0001t0002g0188 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-101+1240dupC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148866 | |||||
| chrX:136148978
|
GC | G | 1 | a0001c0001t0002g0017 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-101+1355delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136148978 | |||||
| chrX:136149025
|
GC | G | 1 | a0001c0001t0001g0019 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-101+1399delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136149025 | |||||
| chrX:136149054
|
T | TC | 1 | a0001c0001t0002g0017 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-101+1427dupC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136149054 | |||||
| chrX:136149085
|
T | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(40): Show | 46 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.-101+1457T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136149085 | ||||||
| chrX:136149154
|
C | G | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-101+1526C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136149154 | ||||||
| chrX:136149188
|
A | C | 5 | a0001c0001t0001g0179a0001c0001t0002g0178a0001c0001t0002g0180others(2): Show | 5 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.-101+1560A>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136149188 | ||||||
| chrX:136149228
|
CT | C | 1 | a0001c0001t0001g0019 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-101+1601delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136149228 | ||||||
| chrX:136149229
|
T | C | 109 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(106): Show | 120 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.-101+1601T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136149229 | ||||||
| chrX:136149240
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-101+1612C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136149240 | ||||||
| chrX:136149259
|
G | T | 1 | a0001c0001t0001g0153 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-101+1631G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136149259 | ||||||
| chrX:136149332
|
T | TG | 1 | a0001c0001t0001g0019 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-101+1704_-101+170 others(5): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136149332 | ||||||
| chrX:136149390
|
T | TC | 1 | a0001c0001t0002g0188 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-101+1765dupC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136149390 | |||||
| chrX:136149465
|
AG | A | 1 | a0001c0001t0011g0025 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-101+1840delG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136149465 | |||||
| chrX:136149527
|
A | AC | 1 | a0001c0001t0001g0019 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-101+1901dupC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136149527 | |||||
| chrX:136149560
|
TA | T | 1 | a0001c0001t0001g0019 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-101+1933delA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136149560 | ||||||
| chrX:136149647
|
G | GC | 1 | a0001c0001t0002g0188 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-101+2021dupC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136149647 | |||||
| chrX:136149762
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-101+2134C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136149762 | ||||||
| chrX:136149764
|
A | G | 1 | a0001c0001t0002g0185 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-101+2136A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136149764 | ||||||
| chrX:136150144
|
T | G | 2 | a0001c0001t0002g0156a0001c0001t0012g0155 | 2 | HG01123.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-101+2516T>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136150144 | ||||||
| chrX:136150226
|
T | C | 1 | a0001c0001t0001g0026 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-101+2598T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136150226 | ||||||
| chrX:136150272
|
A | T | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-101+2644A>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136150272 | ||||||
| chrX:136150472
|
TC | T | 1 | a0001c0001t0011g0025 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-101+2848delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136150472 | |||||
| chrX:136150494
|
C | CT | 1 | a0001c0001t0002g0017 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-101+2874dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136150494 | |||||
| chrX:136150763
|
G | C | 3 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0157 | 5 | HG01261.hp1 HG02280.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-101+3135G>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136150763 | ||||||
| chrX:136150841
|
CA | C | 1 | a0001c0001t0011g0025 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-101+3219delA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136150841 | |||||
| chrX:136150982
|
A | C | 1 | a0001c0001t0002g0176 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-101+3354A>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136150982 | ||||||
| chrX:136151287
|
G | A | 6 | a0001c0001t0001g0064a0001c0001t0001g0154a0001c0001t0002g0065others(3): Show | 6 | HG01167.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-101+3659G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136151287 | ||||||
| chrX:136151290
|
G | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0069a0001c0001t0001g0070others(3): Show | 7 | HG02723.hp1 HG02965.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-101+3662G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136151290 | ||||||
| chrX:136151292
|
T | TA | 119 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-101+3665dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136151292 | |||||
| chrX:136151537
|
T | C | 6 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0079others(3): Show | 6 | HG01934.hp1 NA18953.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.-101+3909T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136151537 | ||||||
| chrX:136151556
|
A | T | 2 | a0001c0001t0001g0061a0001c0001t0002g0062 | 2 | HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.-101+3928A>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136151556 | ||||||
| chrX:136151585
|
C | T | 3 | a0001c0001t0002g0004a0001c0001t0002g0023a0001c0001t0002g0185 | 5 | HG01433.hp1 HG01928.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.-101+3957C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136151585 | ||||||
| chrX:136151627
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-101+3999C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136151627 | ||||||
| chrX:136151694
|
C | G | 4 | a0001c0001t0001g0179a0001c0001t0002g0178a0001c0001t0002g0180others(1): Show | 4 | HG01123.hp1 HG01255.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-101+4066C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136151694 | ||||||
| chrX:136151756
|
C | A | 1 | a0001c0001t0001g0027 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-101+4128C>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136151756 | ||||||
| chrX:136151881
|
G | A | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-101+4253G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136151881 | ||||||
| chrX:136151887
|
G | T | 1 | a0001c0001t0001g0152 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-101+4259G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136151887 | ||||||
| chrX:136152126
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-101+4498T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136152126 | ||||||
| chrX:136152668
|
C | T | 7 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-101+5040C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136152668 | ||||||
| chrX:136152719
|
C | CA | 108 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(105): Show | 119 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-101+5113dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136152719 | |||||
| chrX:136152719
|
C | CAA | 12 | a0001c0001t0001g0069a0001c0001t0001g0080a0001c0001t0001g0081others(9): Show | 12 | HG00738.hp1 HG01109.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.-101+5112_-101+511 others(6): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136152719 | |||||
| chrX:136152719
|
CA | C | 1 | a0001c0001t0001g0060 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-101+5113delA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136152719 | |||||
| chrX:136152719
|
CAAAAAA | C | 1 | a0001c0001t0005g0158 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-101+5108_-101+511 others(10): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136152719 | |||||
| chrX:136152918
|
ACC | A | 4 | a0001c0001t0001g0154a0001c0001t0002g0065a0001c0001t0002g0066others(1): Show | 4 | HG01167.hp1 HG03130.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-101+5291_-101+529 others(6): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136152918 | ||||||
| chrX:136152921
|
T | G | 4 | a0001c0001t0001g0154a0001c0001t0002g0065a0001c0001t0002g0066others(1): Show | 4 | HG01167.hp1 HG03130.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-101+5293T>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136152921 | ||||||
| chrX:136152941
|
T | G | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-101+5313T>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136152941 | ||||||
| chrX:136152994
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-101+5366C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136152994 | ||||||
| chrX:136153050
|
G | GT | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-101+5427dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136153050 | |||||
| chrX:136153111
|
A | AT | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-101+5484dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136153111 | |||||
| chrX:136153114
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-101+5486C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136153114 | ||||||
| chrX:136153125
|
A | T | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-101+5497A>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136153125 | ||||||
| chrX:136153183
|
TA | T | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-101+5557delA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136153183 | |||||
| chrX:136153268
|
A | AT | 1 | a0001c0001t0002g0032 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-101+5647dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136153268 | |||||
| chrX:136153284
|
T | TG | 112 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(109): Show | 123 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.-101+5665dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136153284 | |||||
| chrX:136153284
|
T | TGG | 7 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0152others(4): Show | 7 | HG02055.hp1 HG03516.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.-101+5664_-101+566 others(6): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136153284 | |||||
| chrX:136153288
|
G | GC | 1 | a0001c0001t0001g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-101+5660_-101+566 others(5): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136153288 | ||||||
| chrX:136153288
|
G | GT | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-101+5660_-101+566 others(5): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136153288 | ||||||
| chrX:136153354
|
AT | A | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-101+5728delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136153354 | |||||
| chrX:136153361
|
A | AG | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-101+5736dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136153361 | |||||
| chrX:136153401
|
GC | G | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-101+5775delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136153401 | |||||
| chrX:136153422
|
G | GA | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-101+5796dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136153422 | |||||
| chrX:136153466
|
T | G | 1 | a0001c0001t0001g0008 | 2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-101+5838T>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136153466 | ||||||
| chrX:136153495
|
TCAAC | T | 1 | a0001c0001t0001g0146 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-101+5870_-101+587 others(8): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136153495 | |||||
| chrX:136153526
|
T | TA | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-101+5898_-101+589 others(5): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136153526 | ||||||
| chrX:136153530
|
AC | A | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-101+5904delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136153530 | |||||
| chrX:136153768
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-101+6140C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136153768 | ||||||
| chrX:136153805
|
C | G | 1 | a0001c0001t0005g0158 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-101+6177C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136153805 | ||||||
| chrX:136153826
|
A | AT | 1 | a0001c0001t0001g0152 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-101+6207dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136153826 | |||||
| chrX:136153826
|
AT | A | 1 | a0001c0001t0001g0033 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-101+6207delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136153826 | |||||
| chrX:136153846
|
A | AT | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-101+6222dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136153846 | |||||
| chrX:136153986
|
A | G | 1 | a0001c0001t0002g0078 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-101+6358A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136153986 | ||||||
| chrX:136154125
|
C | T | 1 | a0001c0001t0002g0086 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-101+6497C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136154125 | ||||||
| chrX:136154497
|
T | C | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-101+6869T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136154497 | ||||||
| chrX:136154581
|
T | C | 1 | a0001c0001t0008g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-101+6953T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136154581 | ||||||
| chrX:136154710
|
C | CT | 4 | a0001c0001t0001g0145a0001c0001t0001g0152a0001c0001t0002g0184others(1): Show | 4 | HG02148.hp1 HG03453.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.-101+7096dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136154710 | |||||
| chrX:136154710
|
CT | C | 3 | a0001c0001t0001g0034a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | HG01981.hp2 HG01993.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-101+7096delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136154710 | |||||
| chrX:136154788
|
C | T | 117 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 128 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.-101+7160C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136154788 | ||||||
| chrX:136154793
|
G | A | 18 | a0001c0001t0001g0009a0001c0001t0001g0090a0001c0001t0001g0092others(15): Show | 19 | HG00140.hp1 HG01069.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-101+7165G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136154793 | ||||||
| chrX:136154998
|
C | T | 6 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-101+7370C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136154998 | ||||||
| chrX:136155003
|
G | A | 108 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(105): Show | 119 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-101+7375G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136155003 | ||||||
| chrX:136155111
|
A | T | 1 | a0001c0001t0015g0163 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-101+7483A>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136155111 | ||||||
| chrX:136155145
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0002g0068 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-101+7517T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136155145 | ||||||
| chrX:136155571
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-101+7943A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136155571 | ||||||
| chrX:136155575
|
G | C | 6 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-101+7947G>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136155575 | ||||||
| chrX:136155792
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-101+8164G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136155792 | ||||||
| chrX:136155814
|
GA | G | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-101+8197delA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136155814 | |||||
| chrX:136155814
|
GAA | G | 1 | a0001c0001t0001g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-101+8196_-101+819 others(6): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136155814 | |||||
| chrX:136155948
|
G | T | 1 | a0001c0001t0002g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-101+8320G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136155948 | ||||||
| chrX:136155955
|
A | G | 109 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(106): Show | 120 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.-101+8327A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136155955 | ||||||
| chrX:136156195
|
C | A | 1 | a0001c0001t0002g0178 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-101+8567C>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136156195 | ||||||
| chrX:136156283
|
C | CT | 2 | a0001c0001t0001g0056a0001c0001t0002g0017 | 2 | NA18961.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.-101+8671dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136156283 | |||||
| chrX:136156283
|
CT | C | 11 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0080others(8): Show | 11 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-101+8671delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136156283 | |||||
| chrX:136156356
|
C | T | 1 | a0001c0001t0002g0175 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-101+8728C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136156356 | ||||||
| chrX:136156534
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-101+8906G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136156534 | ||||||
| chrX:136156610
|
A | G | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-101+8982A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136156610 | ||||||
| chrX:136156628
|
T | C | 1 | a0001c0001t0004g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-101+9000T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136156628 | ||||||
| chrX:136156645
|
G | A | 1 | a0001c0001t0008g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-101+9017G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136156645 | ||||||
| chrX:136156704
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-101+9076C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136156704 | ||||||
| chrX:136156957
|
TC | T | 1 | a0001c0001t0002g0078 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-101+9335delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136156957 | |||||
| chrX:136156986
|
TACAC | T | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0002g0091others(1): Show | 4 | HG01106.hp1 HG03453.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.-101+9386_-101+938 others(8): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136156986 | |||||
| chrX:136156986
|
TACACAC | T | 115 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 126 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.-101+9384_-101+938 others(10): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136156986 | |||||
| chrX:136157112
|
A | G | 1 | a0001c0001t0002g0055 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-101+9484A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136157112 | ||||||
| chrX:136157183
|
C | T | 118 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(115): Show | 129 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.-101+9555C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136157183 | ||||||
| chrX:136158241
|
C | T | 109 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(106): Show | 120 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.-101+10613C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136158241 | ||||||
| chrX:136158247
|
A | G | 1 | a0001c0001t0005g0158 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-101+10619A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136158247 | ||||||
| chrX:136158366
|
A | G | 109 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(106): Show | 120 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.-101+10738A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136158366 | ||||||
| chrX:136158424
|
G | A | 9 | a0001c0001t0001g0021a0001c0001t0003g0160a0001c0001t0003g0161others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-101+10796G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136158424 | ||||||
| chrX:136158501
|
C | T | 9 | a0001c0001t0001g0021a0001c0001t0003g0160a0001c0001t0003g0161others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-101+10873C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136158501 | ||||||
| chrX:136158546
|
GA | G | 6 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-101+10921delA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136158546 | |||||
| chrX:136158745
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-101+11117G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136158745 | ||||||
| chrX:136158777
|
TA | T | 1 | a0001c0001t0007g0182 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-100-11125delA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136158777 | |||||
| chrX:136158854
|
C | T | 1 | a0001c0001t0005g0158 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-100-11053C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136158854 | ||||||
| chrX:136158970
|
C | T | 109 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(106): Show | 120 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.-100-10937C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136158970 | ||||||
| chrX:136159138
|
T | TA | 13 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0073others(10): Show | 14 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-100-10756dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136159138 | |||||
| chrX:136159138
|
T | TAA | 104 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(101): Show | 114 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.-100-10757_-100-10 others(8): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136159138 | |||||
| chrX:136159138
|
T | TAAA | 2 | a0001c0001t0001g0106a0001c0001t0007g0182 | 2 | NA19007.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.-100-10758_-100-10 others(9): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136159138 | |||||
| chrX:136159288
|
TC | T | 1 | a0001c0001t0007g0182 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-100-10616delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136159288 | |||||
| chrX:136159370
|
T | C | 119 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-100-10537T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136159370 | ||||||
| chrX:136159551
|
CATAA | C | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-100-10341_-100-10 others(10): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136159551 | |||||
| chrX:136159715
|
A | G | 1 | a0001c0001t0002g0176 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-100-10192A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136159715 | ||||||
| chrX:136159774
|
A | G | 1 | a0001c0001t0002g0054 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-100-10133A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136159774 | ||||||
| chrX:136159974
|
G | C | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-100-9933G>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136159974 | ||||||
| chrX:136159977
|
T | C | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-100-9930T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136159977 | ||||||
| chrX:136160442
|
T | G | 2 | a0001c0001t0001g0107a0001c0001t0001g0147 | 2 | HG03516.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-100-9465T>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136160442 | ||||||
| chrX:136160493
|
C | T | 1 | a0001c0001t0002g0005 | 3 | HG03239.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-100-9414C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136160493 | ||||||
| chrX:136160920
|
A | C | 119 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-100-8987A>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136160920 | ||||||
| chrX:136160982
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-100-8925C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136160982 | ||||||
| chrX:136161080
|
TC | T | 1 | a0001c0001t0007g0182 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-100-8824delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136161080 | |||||
| chrX:136161103
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0002g0151 | 2 | HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-100-8804T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136161103 | ||||||
| chrX:136161844
|
C | T | 1 | a0001c0001t0002g0016 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-100-8063C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136161844 | ||||||
| chrX:136161898
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0060 | 2 | NA18994.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-100-8009G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136161898 | ||||||
| chrX:136161952
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-100-7955G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136161952 | ||||||
| chrX:136162122
|
C | CA | 8 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0060others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-100-7764dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136162122 | |||||
| chrX:136162122
|
C | CAA | 9 | a0001c0001t0001g0152a0001c0001t0002g0077a0001c0001t0002g0142others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-100-7765_-100-776 others(6): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136162122 | |||||
| chrX:136162122
|
C | CAAA | 95 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(92): Show | 105 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.-100-7766_-100-776 others(7): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136162122 | |||||
| chrX:136162122
|
C | CAAAA | 13 | a0001c0001t0001g0010a0001c0001t0001g0069a0001c0001t0001g0073others(10): Show | 14 | HG01192.hp1 HG03098.hp1 HG03579.hp1 others(11): Show |
intron_variant | MODIFIER | c.-100-7767_-100-776 others(8): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136162122 | |||||
| chrX:136162122
|
C | CAAAAA | 2 | a0001c0001t0001g0092a0001c0001t0002g0109 | 2 | HG01099.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-100-7768_-100-776 others(9): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136162122 | |||||
| chrX:136162122
|
C | CACAAAA | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-100-7784_-100-778 others(10): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136162122 | |||||
| chrX:136162122
|
CA | C | 2 | a0001c0001t0002g0180a0001c0001t0011g0025 | 2 | HG03490.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-100-7764delA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136162122 | |||||
| chrX:136162612
|
A | T | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-7295A>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136162612 | ||||||
| chrX:136162865
|
A | T | 6 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-100-7042A>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136162865 | ||||||
| chrX:136163262
|
TG | T | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-6643delG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136163262 | |||||
| chrX:136163329
|
A | AG | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-6575dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136163329 | |||||
| chrX:136163620
|
G | T | 1 | a0001c0001t0004g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-100-6287G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136163620 | ||||||
| chrX:136163625
|
T | TG | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-6278dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136163625 | |||||
| chrX:136163659
|
A | AG | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-6246dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136163659 | |||||
| chrX:136163665
|
A | T | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-100-6242A>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136163665 | ||||||
| chrX:136163665
|
AC | A | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-6240delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136163665 | |||||
| chrX:136163667
|
C | G | 6 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-100-6240C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136163667 | ||||||
| chrX:136163958
|
A | AG | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-5948dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136163958 | |||||
| chrX:136164009
|
A | AG | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-5897dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136164009 | |||||
| chrX:136164211
|
A | AT | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-100-5683dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136164211 | |||||
| chrX:136164211
|
A | ATTT | 1 | a0001c0001t0005g0158 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-100-5685_-100-568 others(7): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136164211 | |||||
| chrX:136164211
|
AT | A | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-5683delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136164211 | |||||
| chrX:136164362
|
A | G | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-100-5545A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136164362 | ||||||
| chrX:136164390
|
A | G | 117 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 128 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.-100-5517A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136164390 | ||||||
| chrX:136164483
|
AT | A | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-5420delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136164483 | |||||
| chrX:136164555
|
TC | T | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-5349delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136164555 | |||||
| chrX:136164569
|
T | C | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-5338T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136164569 | ||||||
| chrX:136164770
|
A | AG | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-5134dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136164770 | |||||
| chrX:136164882
|
A | G | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-5025A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136164882 | ||||||
| chrX:136164948
|
TA | T | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-4954delA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136164948 | |||||
| chrX:136164964
|
CT | C | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-4939delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136164964 | |||||
| chrX:136165200
|
G | GT | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-4705dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136165200 | |||||
| chrX:136165217
|
G | GT | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-4688dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136165217 | |||||
| chrX:136165421
|
G | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(119): Show | 133 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.-100-4486G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136165421 | ||||||
| chrX:136165852
|
G | GT | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-4054dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136165852 | |||||
| chrX:136165981
|
GT | G | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-3923delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136165981 | |||||
| chrX:136166003
|
CT | C | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-3901delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136166003 | |||||
| chrX:136166037
|
GT | G | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-3866delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136166037 | |||||
| chrX:136166072
|
CA | C | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-3833delA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136166072 | |||||
| chrX:136166152
|
T | C | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-100-3755T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136166152 | ||||||
| chrX:136166356
|
GC | G | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-3549delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136166356 | |||||
| chrX:136166391
|
CT | C | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-3515delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136166391 | ||||||
| chrX:136166399
|
G | GT | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-3508_-100-350 others(5): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136166399 | ||||||
| chrX:136166482
|
C | G | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-100-3425C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136166482 | ||||||
| chrX:136166660
|
A | AT | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-3246dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136166660 | |||||
| chrX:136166696
|
A | G | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-100-3211A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136166696 | ||||||
| chrX:136166720
|
GT | G | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-3184delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136166720 | |||||
| chrX:136166730
|
TA | T | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-3175delA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136166730 | |||||
| chrX:136166734
|
GTGGATGG others(1183): Show |
G | 1 | a0001c0001t0002g0180 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-100-3167_-100-197 others(4): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136166734 | |||||
| chrX:136166872
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-100-3035G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136166872 | ||||||
| chrX:136166882
|
TG | T | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-3020delG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136166882 | |||||
| chrX:136166908
|
C | G | 1 | a0001c0001t0014g0141 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-100-2999C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136166908 | ||||||
| chrX:136166919
|
C | G | 1 | a0001c0001t0002g0186 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-100-2988C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136166919 | ||||||
| chrX:136166992
|
G | GT | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-2914dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136166992 | |||||
| chrX:136167022
|
G | GC | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-2881dupC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136167022 | |||||
| chrX:136167046
|
C | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(174): Show | 193 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.-100-2861C>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136167046 | ||||||
| chrX:136167097
|
CAGTG | C | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-100-2806_-100-280 others(8): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136167097 | |||||
| chrX:136167109
|
T | TA | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-2797dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136167109 | |||||
| chrX:136167194
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0095 | 2 | NA18979.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-100-2713G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136167194 | ||||||
| chrX:136167280
|
AC | A | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-2625delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136167280 | |||||
| chrX:136167338
|
T | TG | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-2566dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136167338 | |||||
| chrX:136167365
|
CG | C | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-2540delG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136167365 | |||||
| chrX:136167396
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-100-2511G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136167396 | ||||||
| chrX:136167448
|
AC | A | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-2456delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136167448 | |||||
| chrX:136167455
|
G | A | 117 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 128 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.-100-2452G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136167455 | ||||||
| chrX:136167472
|
TG | T | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-2432delG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136167472 | |||||
| chrX:136167515
|
A | G | 1 | a0001c0001t0005g0158 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-100-2392A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136167515 | ||||||
| chrX:136167628
|
GC | G | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-2277delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136167628 | |||||
| chrX:136167662
|
TC | T | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-2242delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136167662 | |||||
| chrX:136167673
|
TC | T | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-2230delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136167673 | |||||
| chrX:136167761
|
CT | C | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-2144delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136167761 | |||||
| chrX:136167794
|
G | C | 6 | a0001c0001t0001g0080a0001c0001t0001g0093a0001c0001t0001g0095others(3): Show | 6 | HG02523.hp2 NA18612.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.-100-2113G>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136167794 | ||||||
| chrX:136167956
|
A | G | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-100-1951A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136167956 | ||||||
| chrX:136168024
|
G | A | 1 | a0001c0001t0002g0176 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-100-1883G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136168024 | ||||||
| chrX:136168156
|
T | C | 117 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 128 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.-100-1751T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136168156 | ||||||
| chrX:136168182
|
G | T | 1 | a0001c0001t0001g0106 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-100-1725G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136168182 | ||||||
| chrX:136168212
|
GC | G | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-1691delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136168212 | |||||
| chrX:136168371
|
A | G | 1 | a0001c0001t0002g0180 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-100-1536A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136168371 | ||||||
| chrX:136168516
|
G | GA | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-1389dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136168516 | |||||
| chrX:136168581
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-100-1326T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136168581 | ||||||
| chrX:136168885
|
AC | A | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-1020delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136168885 | |||||
| chrX:136169053
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-100-854A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136169053 | ||||||
| chrX:136169068
|
CTAAAA | C | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-838_-100-834d others(7): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136169068 | ||||||
| chrX:136169185
|
GGGGA | G | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-100-719_-100-716d others(6): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136169185 | |||||
| chrX:136169188
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-100-719G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136169188 | ||||||
| chrX:136169520
|
G | GA | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-100-378dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136169520 | |||||
| chrX:136169583
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-100-324G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136169583 | ||||||
| chrX:136170075
|
AC | A | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-27+97delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136170075 | |||||
| chrX:136170209
|
A | AT | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-27+232dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136170209 | |||||
| chrX:136170727
|
C | G | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-27+747C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136170727 | ||||||
| chrX:136171702
|
G | A | 1 | a0001c0001t0014g0141 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-27+1722G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136171702 | ||||||
| chrX:136171759
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-27+1779C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136171759 | ||||||
| chrX:136171825
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-27+1845T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136171825 | ||||||
| chrX:136171857
|
T | G | 1 | a0001c0001t0001g0115 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-27+1877T>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136171857 | ||||||
| chrX:136171883
|
G | T | 1 | a0001c0001t0001g0101 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-27+1903G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136171883 | ||||||
| chrX:136171888
|
A | AT | 117 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 128 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.-27+1917dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136171888 | |||||
| chrX:136171976
|
G | A | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-27+1996G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136171976 | ||||||
| chrX:136172021
|
C | G | 1 | a0001c0001t0005g0158 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-27+2041C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136172021 | ||||||
| chrX:136172043
|
A | ATCAACAT others(25): Show |
1 | a0001c0001t0007g0182 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-27+2065_-27+2096d others(34): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136172043 | |||||
| chrX:136172145
|
T | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(119): Show | 133 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.-27+2165T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136172145 | ||||||
| chrX:136172200
|
G | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(44): Show | 50 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.-27+2220G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136172200 | ||||||
| chrX:136172253
|
G | T | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-27+2273G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136172253 | ||||||
| chrX:136172417
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-27+2437T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136172417 | ||||||
| chrX:136172511
|
A | G | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-27+2531A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136172511 | ||||||
| chrX:136172512
|
T | C | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-27+2532T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136172512 | ||||||
| chrX:136172846
|
C | A | 1 | a0001c0001t0001g0145 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-27+2866C>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136172846 | ||||||
| chrX:136173673
|
G | T | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-27+3693G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136173673 | ||||||
| chrX:136173696
|
C | CT | 4 | a0001c0001t0001g0153a0001c0001t0002g0086a0001c0001t0005g0158others(1): Show | 4 | HG00438.hp1 HG02895.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+3733dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136173696 | |||||
| chrX:136173696
|
CT | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0104 | 2 | HG02965.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-27+3733delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136173696 | |||||
| chrX:136174340
|
C | CG | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+4363dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136174340 | |||||
| chrX:136174549
|
A | AG | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+4571dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136174549 | |||||
| chrX:136174632
|
G | GT | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+4654dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136174632 | |||||
| chrX:136174719
|
TG | T | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-27+4742delG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136174719 | |||||
| chrX:136174768
|
G | GC | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+4789dupC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136174768 | |||||
| chrX:136174889
|
A | AT | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+4910dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136174889 | |||||
| chrX:136174956
|
G | GA | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+4979dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136174956 | |||||
| chrX:136175106
|
G | GC | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-27+5127dupC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136175106 | |||||
| chrX:136175142
|
T | C | 1 | a0001c0001t0002g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-27+5162T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136175142 | ||||||
| chrX:136175173
|
TG | T | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-27+5196delG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136175173 | |||||
| chrX:136175226
|
C | T | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-27+5246C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136175226 | ||||||
| chrX:136175241
|
A | G | 4 | a0001c0001t0001g0179a0001c0001t0002g0178a0001c0001t0002g0180others(1): Show | 4 | HG01123.hp1 HG01255.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+5261A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136175241 | ||||||
| chrX:136175279
|
CT | C | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+5303delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136175279 | |||||
| chrX:136175355
|
T | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0069a0001c0001t0001g0070others(3): Show | 7 | HG02723.hp1 HG02965.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-27+5375T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136175355 | ||||||
| chrX:136175549
|
AAAAG | A | 3 | a0001c0001t0001g0053a0001c0001t0002g0032a0001c0001t0002g0052 | 3 | HG00280.hp1 HG02148.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.-27+5576_-27+5579d others(6): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136175549 | |||||
| chrX:136175557
|
G | T | 1 | a0001c0001t0002g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-27+5577G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136175557 | ||||||
| chrX:136175711
|
C | T | 110 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 121 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.-27+5731C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136175711 | ||||||
| chrX:136175908
|
A | T | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-27+5928A>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136175908 | ||||||
| chrX:136176024
|
TAGTTCCT others(27): Show |
T | 1 | a0001c0001t0007g0182 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-27+6047_-27+6080d others(36): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136176024 | |||||
| chrX:136176105
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0085 | 3 | NA18954.hp2 NA18984.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.-27+6125C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136176105 | ||||||
| chrX:136176368
|
T | C | 1 | a0001c0001t0005g0158 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-27+6388T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136176368 | ||||||
| chrX:136176393
|
C | CTT | 1 | a0001c0001t0001g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-27+6416_-27+6417d others(4): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136176393 | |||||
| chrX:136176514
|
A | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0060 | 2 | NA18994.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-27+6534A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136176514 | ||||||
| chrX:136176818
|
G | T | 1 | a0001c0001t0005g0158 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-27+6838G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136176818 | ||||||
| chrX:136177013
|
T | TAC | 46 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(43): Show | 49 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.-27+7065_-27+7066d others(4): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136177013 | |||||
| chrX:136177013
|
T | TACAC | 5 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0002g0037others(2): Show | 6 | HG01069.hp1 HG01081.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27+7063_-27+7066d others(6): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136177013 | |||||
| chrX:136177013
|
T | TACACAC | 3 | a0001c0001t0001g0021a0001c0001t0008g0159a0001c0001t0015g0163 | 3 | HG01109.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-27+7061_-27+7066d others(8): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136177013 | |||||
| chrX:136177013
|
T | TACACACA others(1): Show |
3 | a0001c0001t0001g0107a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG02572.hp1 HG02886.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-27+7059_-27+7066d others(10): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136177013 | |||||
| chrX:136177013
|
T | TACACACA others(3): Show |
7 | a0001c0001t0001g0064a0001c0001t0001g0147a0001c0001t0002g0139others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-27+7057_-27+7066d others(12): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136177013 | |||||
| chrX:136177013
|
T | TACACACA others(5): Show |
8 | a0001c0001t0001g0073a0001c0001t0001g0080a0001c0001t0001g0136others(5): Show | 8 | HG02080.hp2 HG02976.hp1 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.-27+7055_-27+7066d others(14): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136177013 | |||||
| chrX:136177013
|
T | TACACACA others(7): Show |
22 | a0001c0001t0001g0007a0001c0001t0001g0069a0001c0001t0001g0070others(19): Show | 23 | HG00609.hp1 HG00738.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-27+7053_-27+7066d others(16): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136177013 | |||||
| chrX:136177013
|
T | TACACACA others(9): Show |
33 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0022others(30): Show | 40 | HG00140.hp1 HG00642.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.-27+7051_-27+7066d others(18): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136177013 | |||||
| chrX:136177013
|
T | TACACACA others(11): Show |
24 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(21): Show | 26 | HG00438.hp1 HG00544.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.-27+7049_-27+7066d others(20): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136177013 | |||||
| chrX:136177013
|
T | TACACACA others(13): Show |
10 | a0001c0001t0001g0088a0001c0001t0001g0101a0001c0001t0001g0103others(7): Show | 10 | HG01106.hp1 HG01517.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.-27+7047_-27+7066d others(22): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136177013 | |||||
| chrX:136177013
|
T | TACACACA others(15): Show |
4 | a0001c0001t0001g0116a0001c0001t0001g0149a0001c0001t0002g0117others(1): Show | 4 | HG01256.hp1 HG02155.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+7045_-27+7066d others(24): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136177013 | |||||
| chrX:136177013
|
T | TACACACA others(17): Show |
1 | a0001c0001t0014g0141 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-27+7043_-27+7066d others(26): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136177013 | |||||
| chrX:136177013
|
TACACACA others(7): Show |
T | 1 | a0001c0001t0002g0175 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-27+7053_-27+7066d others(16): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136177013 | |||||
| chrX:136177028
|
A | ACACACAC others(9): Show |
1 | a0001c0001t0002g0100 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-27+7063_-27+7064i others(18): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136177028 | |||||
| chrX:136177046
|
A | ACACACAC others(6): Show |
1 | a0001c0001t0001g0097 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-27+7066_-27+7067i others(15): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136177046 | ||||||
| chrX:136177047
|
T | C | 3 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0042 | 3 | HG01515.hp1 HG01517.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-27+7067T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136177047 | ||||||
| chrX:136177129
|
CT | C | 1 | a0001c0001t0002g0178 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-27+7153delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136177129 | |||||
| chrX:136177811
|
T | C | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-27+7831T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136177811 | ||||||
| chrX:136178332
|
G | GA | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+8354dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136178332 | |||||
| chrX:136178351
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(184): Show | 206 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.-27+8371T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136178351 | ||||||
| chrX:136178372
|
C | CT | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+8395dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136178372 | |||||
| chrX:136178597
|
AAAAC | A | 75 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 83 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.-27+8623_-27+8626d others(6): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136178597 | |||||
| chrX:136178598
|
AAAC | A | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+8621_-27+8623d others(5): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136178598 | |||||
| chrX:136178611
|
A | AAAC | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-27+8652_-27+8654d others(5): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136178611 | |||||
| chrX:136178611
|
AAAC | A | 1 | a0001c0001t0001g0153 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-27+8652_-27+8654d others(5): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136178611 | |||||
| chrX:136178746
|
CT | C | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+8771delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136178746 | |||||
| chrX:136178757
|
C | CT | 2 | a0001c0001t0001g0053a0001c0001t0013g0040 | 2 | HG02148.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.-27+8792dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136178757 | |||||
| chrX:136178757
|
CT | C | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-27+8792delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136178757 | |||||
| chrX:136178757
|
CTT | C | 117 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 128 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.-27+8791_-27+8792d others(4): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136178757 | |||||
| chrX:136178776
|
A | AC | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+8797dupC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136178776 | |||||
| chrX:136178821
|
C | CT | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+8843dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136178821 | |||||
| chrX:136178900
|
G | A | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-27+8920G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136178900 | ||||||
| chrX:136178904
|
G | GC | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+8926dupC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136178904 | |||||
| chrX:136179222
|
G | GT | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+9242_-27+9243i others(3): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136179222 | ||||||
| chrX:136179812
|
C | T | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-27+9832C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136179812 | ||||||
| chrX:136179817
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-27+9837C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136179817 | ||||||
| chrX:136179835
|
T | G | 1 | a0001c0001t0001g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-27+9855T>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136179835 | ||||||
| chrX:136179841
|
G | A | 1 | a0001c0001t0008g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-27+9861G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136179841 | ||||||
| chrX:136179895
|
C | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0097 | 2 | HG02523.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.-27+9915C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136179895 | ||||||
| chrX:136179943
|
T | A | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-27+9963T>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136179943 | ||||||
| chrX:136180162
|
CT | C | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+10185delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136180162 | |||||
| chrX:136180319
|
T | TG | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+10343dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136180319 | |||||
| chrX:136180453
|
G | GA | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-27+10474dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136180453 | |||||
| chrX:136180465
|
T | TG | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+10487dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136180465 | |||||
| chrX:136180473
|
C | T | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-27+10493C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136180473 | ||||||
| chrX:136180780
|
C | G | 1 | a0001c0001t0002g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-27+10800C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136180780 | ||||||
| chrX:136180800
|
G | GAC | 1 | a0001c0001t0001g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-27+10820_-27+1082 others(6): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136180800 | ||||||
| chrX:136180802
|
C | CGT | 119 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-27+10824_-27+1082 others(6): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136180802 | |||||
| chrX:136180802
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-27+10822C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136180802 | ||||||
| chrX:136180952
|
G | A | 106 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(103): Show | 117 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.-27+10972G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136180952 | ||||||
| chrX:136181019
|
A | C | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-27+11039A>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136181019 | ||||||
| chrX:136181020
|
G | T | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 131 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-27+11040G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136181020 | ||||||
| chrX:136181075
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0105 | 3 | NA18959.hp1 NA18970.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-27+11095A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136181075 | ||||||
| chrX:136181129
|
G | A | 3 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0005g0158 | 3 | HG02895.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-27+11149G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136181129 | ||||||
| chrX:136181989
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-27+12009T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136181989 | ||||||
| chrX:136181993
|
A | G | 2 | a0001c0001t0001g0064a0001c0001t0002g0068 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-27+12013A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136181993 | ||||||
| chrX:136182144
|
T | A | 89 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 94 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-27+12164T>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136182144 | ||||||
| chrX:136182168
|
A | AG | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+12192dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136182168 | |||||
| chrX:136182282
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0002g0068 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-27+12302C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136182282 | ||||||
| chrX:136182296
|
A | G | 2 | a0001c0001t0001g0064a0001c0001t0002g0068 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-27+12316A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136182296 | ||||||
| chrX:136182390
|
A | C | 1 | a0001c0001t0002g0016 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-27+12410A>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136182390 | ||||||
| chrX:136182390
|
AATT | A | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-27+12423_-27+1242 others(7): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136182390 | |||||
| chrX:136182632
|
CTT | C | 1 | a0001c0001t0001g0120 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-27+12653_-27+1265 others(6): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136182632 | ||||||
| chrX:136182797
|
A | C | 1 | a0001c0001t0001g0051 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-27+12817A>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136182797 | ||||||
| chrX:136183094
|
C | CA | 6 | a0001c0001t0002g0005a0001c0001t0002g0042a0001c0001t0002g0057others(3): Show | 8 | HG01109.hp1 HG02572.hp1 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27+13128dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136183094 | |||||
| chrX:136183102
|
A | C | 1 | a0001c0001t0001g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-27+13122A>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136183102 | ||||||
| chrX:136183107
|
A | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0060 | 2 | NA18994.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-27+13127A>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136183107 | ||||||
| chrX:136183109
|
C | A | 5 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0002g0166others(2): Show | 5 | HG02895.hp1 HG02922.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27+13129C>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136183109 | ||||||
| chrX:136183112
|
A | C | 3 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0005g0158 | 3 | HG02895.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-27+13132A>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136183112 | ||||||
| chrX:136183124
|
C | CA | 32 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0081others(29): Show | 38 | HG00642.hp1 HG00738.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.-27+13154dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136183124 | |||||
| chrX:136183128
|
A | C | 84 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 89 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.-27+13148A>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136183128 | ||||||
| chrX:136183528
|
CAA | C | 1 | a0001c0001t0001g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-27+13549_-27+1355 others(6): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136183528 | ||||||
| chrX:136183888
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0002g0068 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-27+13908G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136183888 | ||||||
| chrX:136183930
|
A | G | 89 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 94 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-27+13950A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136183930 | ||||||
| chrX:136184413
|
G | C | 3 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0005g0158 | 3 | HG02895.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-27+14433G>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136184413 | ||||||
| chrX:136184651
|
A | T | 89 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 94 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-27+14671A>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136184651 | ||||||
| chrX:136184670
|
G | A | 89 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 94 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-27+14690G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136184670 | ||||||
| chrX:136184684
|
A | ATG | 1 | a0001c0001t0008g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-27+14714_-27+1471 others(6): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136184684 | |||||
| chrX:136184709
|
T | G | 1 | a0001c0001t0002g0037 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-27+14729T>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136184709 | ||||||
| chrX:136184892
|
G | GAC | 1 | a0001c0001t0001g0146 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-27+14914_-27+1491 others(6): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136184892 | |||||
| chrX:136185141
|
C | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0145 | 3 | HG01099.hp1 HG01978.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-27+15161C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136185141 | ||||||
| chrX:136185397
|
T | G | 1 | a0001c0001t0002g0185 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-27+15417T>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136185397 | ||||||
| chrX:136185483
|
T | C | 1 | a0001c0001t0002g0176 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-27+15503T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136185483 | ||||||
| chrX:136185488
|
A | C | 1 | a0001c0001t0002g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-27+15508A>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136185488 | ||||||
| chrX:136185493
|
G | A | 83 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(80): Show | 88 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.-27+15513G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136185493 | ||||||
| chrX:136185620
|
A | T | 3 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0005g0158 | 3 | HG02895.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-27+15640A>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136185620 | ||||||
| chrX:136186150
|
A | T | 1 | a0001c0001t0001g0147 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-27+16170A>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186150 | ||||||
| chrX:136186310
|
T | C | 86 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(83): Show | 91 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.-27+16330T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186310 | ||||||
| chrX:136186383
|
T | C | 1 | a0001c0001t0002g0032 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-27+16403T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186383 | ||||||
| chrX:136186863
|
AAAAT | A | 3 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0157 | 5 | HG01261.hp1 HG02280.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27+16885_-27+1688 others(8): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136186863 | |||||
| chrX:136186863
|
AAAATATA others(3): Show |
A | 2 | a0001c0001t0001g0064a0001c0001t0002g0068 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-27+16885_-27+1689 others(14): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136186863 | |||||
| chrX:136186865
|
A | ATAT | 1 | a0001c0001t0002g0016 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-27+16885_-27+1688 others(7): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186865 | ||||||
| chrX:136186865
|
AAT | A | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-27+16901_-27+1690 others(6): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136186865 | |||||
| chrX:136186865
|
AATAT | A | 4 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0004g0165others(1): Show | 4 | HG02895.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+16899_-27+1690 others(8): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136186865 | |||||
| chrX:136186866
|
AT | A | 2 | a0001c0001t0001g0036a0001c0001t0012g0155 | 2 | HG02970.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-27+16887delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186866 | ||||||
| chrX:136186866
|
ATAT | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0022others(66): Show | 78 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-27+16887_-27+1688 others(7): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186866 | ||||||
| chrX:136186866
|
ATATAT | A | 12 | a0001c0001t0001g0046a0001c0001t0001g0051a0001c0001t0001g0060others(9): Show | 14 | HG00408.hp1 HG00544.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.-27+16887_-27+1689 others(9): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186866 | ||||||
| chrX:136186866
|
ATATATAT others(2): Show |
A | 2 | a0001c0001t0002g0129a0001c0001t0003g0162 | 2 | HG02886.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-27+16887_-27+1689 others(13): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186866 | ||||||
| chrX:136186866
|
ATATATAT others(10): Show |
A | 5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0164others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27+16887_-27+1690 others(21): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186866 | ||||||
| chrX:136186866
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+16887_-27+1690 others(23): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186866 | ||||||
| chrX:136186866
|
ATATATAT others(14): Show |
A | 3 | a0001c0001t0001g0098a0001c0001t0001g0128a0001c0001t0002g0134 | 3 | HG01074.hp1 NA18954.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-27+16887_-27+1690 others(25): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186866 | ||||||
| chrX:136186867
|
T | A | 79 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 84 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.-27+16887T>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186867 | ||||||
| chrX:136186869
|
T | A | 3 | a0001c0001t0001g0036a0001c0001t0002g0044a0001c0001t0012g0155 | 3 | HG02015.hp1 HG02970.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-27+16889T>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186869 | ||||||
| chrX:136186871
|
T | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0022others(61): Show | 73 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-27+16891T>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186871 | ||||||
| chrX:136186871
|
TATATATA others(9): Show |
T | 3 | a0001c0001t0001g0106a0001c0001t0001g0136a0001c0001t0002g0151 | 3 | HG02080.hp2 HG04184.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-27+16895_-27+1691 others(20): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136186871 | |||||
| chrX:136186871
|
TATATATA others(13): Show |
T | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(61): Show | 69 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.-27+16895_-27+1691 others(24): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136186871 | |||||
| chrX:136186873
|
T | A | 16 | a0001c0001t0001g0013a0001c0001t0001g0046a0001c0001t0001g0051others(13): Show | 19 | HG00408.hp1 HG00544.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.-27+16893T>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186873 | ||||||
| chrX:136186873
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0008g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-27+16897_-27+1690 others(14): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136186873 | |||||
| chrX:136186875
|
TATATATA others(1): Show |
T | 1 | a0001c0001t0002g0044 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-27+16899_-27+1690 others(12): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136186875 | |||||
| chrX:136186877
|
T | A | 1 | a0001c0001t0002g0129 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-27+16897T>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186877 | ||||||
| chrX:136186877
|
TATATAG | T | 1 | a0001c0001t0002g0023 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-27+16901_-27+1690 others(10): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136186877 | |||||
| chrX:136186877
|
TATATAGA others(3): Show |
T | 4 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0049others(1): Show | 4 | HG02165.hp2 NA18961.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+16901_-27+1691 others(14): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136186877 | |||||
| chrX:136186877
|
TATATAGA others(7): Show |
T | 1 | a0001c0001t0001g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-27+16901_-27+1691 others(18): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136186877 | |||||
| chrX:136186879
|
T | G | 6 | a0001c0001t0002g0016a0001c0001t0002g0065a0001c0001t0002g0067others(3): Show | 7 | HG02109.hp2 HG02895.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.-27+16899T>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186879 | ||||||
| chrX:136186879
|
TATAG | T | 2 | a0001c0001t0002g0169a0001c0001t0002g0174 | 2 | HG01243.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-27+16938_-27+1694 others(8): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136186879 | |||||
| chrX:136186879
|
TATAGATA others(1): Show |
T | 6 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0050others(3): Show | 6 | HG01123.hp2 HG01981.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27+16934_-27+1694 others(12): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136186879 | |||||
| chrX:136186881
|
TAGATAG | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0022others(61): Show | 73 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.-27+16903_-27+1690 others(10): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136186881 | |||||
| chrX:136186881
|
TAGATAGA others(3): Show |
T | 6 | a0001c0001t0001g0053a0001c0001t0001g0081a0001c0001t0002g0032others(3): Show | 6 | HG00280.hp1 HG02148.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-27+16903_-27+1691 others(14): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136186881 | |||||
| chrX:136186883
|
G | T | 16 | a0001c0001t0001g0046a0001c0001t0001g0051a0001c0001t0001g0060others(13): Show | 20 | HG00408.hp1 HG00544.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.-27+16903G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186883 | ||||||
| chrX:136186887
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+16907G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186887 | ||||||
| chrX:136186887
|
G | T | 5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0164others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27+16907G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186887 | ||||||
| chrX:136186891
|
G | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0098a0001c0001t0001g0128others(1): Show | 4 | HG01074.hp1 NA18954.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+16911G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186891 | ||||||
| chrX:136187131
|
G | GT | 2 | a0001c0001t0002g0156a0001c0001t0012g0155 | 2 | HG01123.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-27+17162dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136187131 | |||||
| chrX:136187131
|
GT | G | 7 | a0001c0001t0001g0059a0001c0001t0002g0065a0001c0001t0002g0067others(4): Show | 7 | HG02895.hp1 HG03453.hp1 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.-27+17162delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136187131 | |||||
| chrX:136187142
|
T | A | 2 | a0001c0001t0002g0131a0001c0001t0002g0139 | 2 | NA18960.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-27+17162T>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136187142 | ||||||
| chrX:136187151
|
A | T | 4 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0004g0165others(1): Show | 4 | HG02895.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+17171A>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136187151 | ||||||
| chrX:136187154
|
AAG | A | 76 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 81 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-27+17176_-27+1717 others(6): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136187154 | |||||
| chrX:136187457
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-27+17477A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136187457 | ||||||
| chrX:136187841
|
A | C | 1 | a0001c0001t0001g0148 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-27+17861A>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136187841 | ||||||
| chrX:136188157
|
C | T | 6 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27+18177C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136188157 | ||||||
| chrX:136188206
|
T | C | 1 | a0001c0001t0002g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-26-18201T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136188206 | ||||||
| chrX:136188356
|
G | GC | 1 | a0001c0001t0001g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-26-18048dupC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136188356 | |||||
| chrX:136188663
|
A | G | 6 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26-17744A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136188663 | ||||||
| chrX:136189086
|
T | C | 84 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 89 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.-26-17321T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136189086 | ||||||
| chrX:136189152
|
G | T | 84 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 89 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.-26-17255G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136189152 | ||||||
| chrX:136189214
|
C | G | 1 | a0001c0001t0008g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-26-17193C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136189214 | ||||||
| chrX:136189972
|
G | T | 2 | a0001c0001t0001g0021a0001c0001t0002g0184 | 2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-26-16435G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136189972 | ||||||
| chrX:136189981
|
G | T | 4 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0004g0165others(1): Show | 4 | HG02895.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-16426G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136189981 | ||||||
| chrX:136190197
|
A | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0064a0001c0001t0002g0068others(1): Show | 4 | HG02280.hp2 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-16210A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136190197 | ||||||
| chrX:136190688
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-26-15719G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136190688 | ||||||
| chrX:136191020
|
A | G | 4 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0004g0165others(1): Show | 4 | HG02895.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-15387A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136191020 | ||||||
| chrX:136191236
|
G | T | 85 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 90 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.-26-15171G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136191236 | ||||||
| chrX:136191500
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-26-14907G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136191500 | ||||||
| chrX:136191506
|
C | T | 1 | a0001c0001t0008g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-26-14901C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136191506 | ||||||
| chrX:136192168
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0002g0068 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-26-14239C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136192168 | ||||||
| chrX:136192278
|
G | A | 1 | a0001c0001t0002g0057 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-26-14129G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136192278 | ||||||
| chrX:136192626
|
C | G | 1 | a0001c0001t0001g0036 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-26-13781C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136192626 | ||||||
| chrX:136192738
|
G | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0116a0001c0001t0001g0153 | 3 | HG00438.hp1 NA18944.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-26-13669G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136192738 | ||||||
| chrX:136192897
|
T | C | 81 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 86 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-26-13510T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136192897 | ||||||
| chrX:136193082
|
T | TA | 1 | a0001c0001t0002g0014 | 2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-26-13310dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136193082 | |||||
| chrX:136193082
|
TA | T | 81 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 86 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-26-13310delA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136193082 | |||||
| chrX:136193082
|
TAA | T | 4 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0004g0165others(1): Show | 4 | HG02895.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-13311_-26-1331 others(6): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136193082 | |||||
| chrX:136193094
|
A | C | 5 | a0001c0001t0001g0119a0001c0001t0001g0179a0001c0001t0002g0178others(2): Show | 5 | HG01123.hp1 HG01255.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-13313A>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136193094 | ||||||
| chrX:136193120
|
G | T | 85 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 90 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.-26-13287G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136193120 | ||||||
| chrX:136193212
|
A | G | 1 | a0001c0001t0004g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-26-13195A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136193212 | ||||||
| chrX:136193254
|
G | A | 1 | a0001c0001t0011g0025 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-26-13153G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136193254 | ||||||
| chrX:136193370
|
G | A | 1 | a0001c0001t0001g0012 | 2 | NA18959.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.-26-13037G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136193370 | ||||||
| chrX:136193436
|
A | G | 1 | a0001c0001t0008g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-26-12971A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136193436 | ||||||
| chrX:136193649
|
C | T | 70 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(67): Show | 75 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.-26-12758C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136193649 | ||||||
| chrX:136193764
|
A | G | 70 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(67): Show | 75 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.-26-12643A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136193764 | ||||||
| chrX:136193777
|
G | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0128 | 2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-26-12630G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136193777 | ||||||
| chrX:136193938
|
C | G | 1 | a0001c0001t0004g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-26-12469C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136193938 | ||||||
| chrX:136193961
|
C | A | 2 | a0001c0001t0002g0156a0001c0001t0012g0155 | 2 | HG01123.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-26-12446C>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136193961 | ||||||
| chrX:136194061
|
C | A | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-26-12346C>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136194061 | ||||||
| chrX:136194124
|
C | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(72): Show | 80 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26-12283C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136194124 | ||||||
| chrX:136194667
|
T | A | 4 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0004g0165others(1): Show | 4 | HG02895.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-11740T>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136194667 | ||||||
| chrX:136194941
|
C | G | 70 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(67): Show | 75 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.-26-11466C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136194941 | ||||||
| chrX:136195258
|
G | A | 4 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0004g0165others(1): Show | 4 | HG02895.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-11149G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136195258 | ||||||
| chrX:136195283
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-26-11124C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136195283 | ||||||
| chrX:136195538
|
C | T | 2 | a0001c0001t0002g0017a0001c0001t0002g0045 | 2 | HG02155.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.-26-10869C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136195538 | ||||||
| chrX:136196545
|
C | T | 1 | a0001c0001t0003g0162 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-26-9862C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136196545 | ||||||
| chrX:136196992
|
C | G | 1 | a0001c0001t0001g0103 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-26-9415C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136196992 | ||||||
| chrX:136197245
|
T | A | 1 | a0001c0001t0001g0121 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-26-9162T>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136197245 | ||||||
| chrX:136197519
|
G | A | 2 | a0001c0001t0002g0126a0001c0001t0002g0127 | 2 | NA18945.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.-26-8888G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136197519 | ||||||
| chrX:136197545
|
A | G | 85 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 90 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.-26-8862A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136197545 | ||||||
| chrX:136197802
|
G | T | 4 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0004g0165others(1): Show | 4 | HG02895.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-8605G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136197802 | ||||||
| chrX:136197968
|
G | GT | 12 | a0001c0001t0001g0034a0001c0001t0001g0043a0001c0001t0002g0023others(9): Show | 12 | HG01517.hp2 HG01981.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.-26-8424dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136197968 | |||||
| chrX:136197968
|
G | GTT | 39 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(36): Show | 42 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.-26-8425_-26-8424d others(4): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136197968 | |||||
| chrX:136197968
|
G | GTTT | 1 | a0001c0001t0001g0041 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-26-8426_-26-8424d others(5): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136197968 | |||||
| chrX:136197968
|
GT | G | 83 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(80): Show | 88 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.-26-8424delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136197968 | |||||
| chrX:136197968
|
GTT | G | 1 | a0001c0001t0002g0078 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-26-8425_-26-8424d others(4): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136197968 | |||||
| chrX:136198148
|
GT | G | 81 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 86 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-26-8246delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136198148 | |||||
| chrX:136198148
|
GTT | G | 4 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0004g0165others(1): Show | 4 | HG02895.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-8247_-26-8246d others(4): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136198148 | |||||
| chrX:136198325
|
T | C | 3 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0042 | 3 | HG01515.hp1 HG01517.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-26-8082T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136198325 | ||||||
| chrX:136198377
|
CAG | C | 1 | a0001c0001t0001g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-26-8028_-26-8027d others(4): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136198377 | |||||
| chrX:136199390
|
CT | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0085a0001c0001t0007g0182 | 4 | NA18954.hp2 NA18984.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-7016delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136199390 | ||||||
| chrX:136199413
|
G | GA | 4 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0004g0165others(1): Show | 4 | HG02895.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-6988dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136199413 | |||||
| chrX:136199576
|
T | C | 85 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 90 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.-26-6831T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136199576 | ||||||
| chrX:136199768
|
T | C | 5 | a0001c0001t0001g0021a0001c0001t0001g0064a0001c0001t0002g0068others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-6639T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136199768 | ||||||
| chrX:136199863
|
A | T | 6 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26-6544A>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136199863 | ||||||
| chrX:136199911
|
A | G | 2 | a0001c0001t0002g0076a0001c0001t0002g0134 | 2 | NA18954.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-26-6496A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136199911 | ||||||
| chrX:136199933
|
G | C | 87 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(84): Show | 92 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-26-6474G>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136199933 | ||||||
| chrX:136200826
|
G | T | 2 | a0001c0001t0001g0047a0001c0001t0002g0062 | 2 | HG02040.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.-26-5581G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136200826 | ||||||
| chrX:136200997
|
C | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0079 | 2 | NA18953.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-26-5410C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136200997 | ||||||
| chrX:136201394
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0095 | 2 | NA18979.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-26-5013G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136201394 | ||||||
| chrX:136201486
|
G | A | 4 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0004g0165others(1): Show | 4 | HG02895.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-4921G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136201486 | ||||||
| chrX:136201501
|
AG | A | 71 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(68): Show | 76 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-26-4905delG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136201501 | ||||||
| chrX:136202082
|
T | A | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-26-4325T>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136202082 | ||||||
| chrX:136202185
|
C | T | 2 | a0001c0001t0002g0156a0001c0001t0012g0155 | 2 | HG01123.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-26-4222C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136202185 | ||||||
| chrX:136202402
|
C | T | 1 | a0001c0001t0013g0040 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-26-4005C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136202402 | ||||||
| chrX:136203151
|
TTAAG | T | 2 | a0001c0001t0001g0064a0001c0001t0002g0068 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-26-3253_-26-3250d others(6): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136203151 | |||||
| chrX:136203175
|
T | TA | 4 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0004g0165others(1): Show | 4 | HG02895.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-3231dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136203175 | |||||
| chrX:136203205
|
G | A | 1 | a0001c0001t0002g0126 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-26-3202G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136203205 | ||||||
| chrX:136203329
|
T | C | 4 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0004g0165others(1): Show | 4 | HG02895.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-3078T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136203329 | ||||||
| chrX:136203330
|
TAA | T | 4 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0004g0165others(1): Show | 4 | HG02895.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-3076_-26-3075d others(4): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136203330 | ||||||
| chrX:136203578
|
A | G | 5 | a0001c0001t0002g0017a0001c0001t0002g0065a0001c0001t0002g0067others(2): Show | 5 | HG02895.hp1 HG03540.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-2829A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136203578 | ||||||
| chrX:136203602
|
A | G | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-26-2805A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136203602 | ||||||
| chrX:136203653
|
T | C | 4 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0004g0165others(1): Show | 4 | HG02895.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-2754T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136203653 | ||||||
| chrX:136203709
|
G | A | 4 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0004g0165others(1): Show | 4 | HG02895.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-2698G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136203709 | ||||||
| chrX:136203822
|
T | C | 5 | a0001c0001t0001g0021a0001c0001t0001g0064a0001c0001t0002g0068others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-2585T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136203822 | ||||||
| chrX:136203998
|
G | T | 2 | a0001c0001t0002g0156a0001c0001t0012g0155 | 2 | HG01123.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-26-2409G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136203998 | ||||||
| chrX:136204527
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-26-1880G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136204527 | ||||||
| chrX:136204911
|
T | C | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-26-1496T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136204911 | ||||||
| chrX:136205100
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-26-1307G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136205100 | ||||||
| chrX:136205116
|
CG | C | 1 | a0001c0001t0013g0040 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-26-1286delG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136205116 | |||||
| chrX:136205149
|
GA | G | 5 | a0001c0001t0001g0021a0001c0001t0001g0064a0001c0001t0002g0068others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-1256delA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136205149 | |||||
| chrX:136205244
|
G | A | 4 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0004g0165others(1): Show | 4 | HG02895.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-1163G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136205244 | ||||||
| chrX:136205263
|
G | T | 1 | a0001c0001t0001g0153 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-26-1144G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136205263 | ||||||
| chrX:136205285
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-26-1122C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136205285 | ||||||
| chrX:136205286
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-26-1121G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136205286 | ||||||
| chrX:136205531
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-26-876C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136205531 | ||||||
| chrX:136206125
|
A | G | 4 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0004g0165others(1): Show | 4 | HG02895.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-282A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136206125 | ||||||
| chrX:136206155
|
C | T | 5 | a0001c0001t0001g0179a0001c0001t0002g0175a0001c0001t0002g0178others(2): Show | 5 | HG01123.hp1 HG01255.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-252C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136206155 | ||||||
| chrX:136206593
|
C | T | 2 | a0001c0001t0002g0156a0001c0001t0012g0155 | 2 | HG01123.hp2 HG02970.hp2 |
splice_region_variant&intron_variant | LOW | c.156+5C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 3/7 | chrX | 136206593 | ||||||
| chrX:136206959
|
C | T | 3 | a0001c0001t0001g0064a0001c0001t0002g0068a0001c0001t0008g0159 | 3 | HG01109.hp1 HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.157-57C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 3/7 | chrX | 136206959 | ||||||
| chrX:136207550
|
T | TG | 1 | a0002c0003t0006g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.332-237dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 136207550 | |||||
| chrX:136207600
|
T | TC | 1 | a0002c0003t0006g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.332-188dupC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 136207600 | |||||
| chrX:136207705
|
C | A | 1 | a0002c0003t0006g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.332-87C>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 4/7 | chrX | 136207705 | ||||||
| chrX:136207719
|
G | C | 6 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.332-73G>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 4/7 | chrX | 136207719 | ||||||
| chrX:136207743
|
C | T | 6 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.332-49C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 4/7 | chrX | 136207743 | ||||||
| chrX:136207978
|
G | GT | 1 | a0002c0003t0006g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.501+19dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 136207978 | |||||
| chrX:136208025
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.501+64C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 5/7 | chrX | 136208025 | ||||||
| chrX:136208038
|
A | AT | 1 | a0002c0003t0006g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.501+77_501+78insT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 5/7 | chrX | 136208038 | ||||||
| chrX:136208040
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.501+79T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 5/7 | chrX | 136208040 | ||||||
| chrX:136208091
|
G | A | 68 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(65): Show | 73 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.501+130G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 5/7 | chrX | 136208091 | ||||||
| chrX:136208129
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.501+168C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 5/7 | chrX | 136208129 | ||||||
| chrX:136208239
|
AG | A | 1 | a0002c0003t0006g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.502-212delG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 136208239 | |||||
| chrX:136208259
|
T | G | 1 | a0002c0003t0006g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.502-196T>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 5/7 | chrX | 136208259 | ||||||
| chrX:136208365
|
C | G | 1 | a0001c0001t0001g0112 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.502-90C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 5/7 | chrX | 136208365 | ||||||
| chrX:136208734
|
GC | G | 1 | a0002c0003t0006g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.688+98delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 136208734 | |||||
| chrX:136208790
|
GT | G | 1 | a0002c0003t0006g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.688+152delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 136208790 | |||||
| chrX:136208895
|
A | AC | 1 | a0002c0003t0006g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.688+256dupC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 136208895 | |||||
| chrX:136208971
|
A | AG | 1 | a0002c0003t0006g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.689-269dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 136208971 | |||||
| chrX:136208993
|
G | GGA | 1 | a0002c0003t0006g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.689-249_689-248ins others(2): Show |
FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 136208993 | |||||
| chrX:136209069
|
C | CT | 1 | a0001c0001t0012g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.689-164dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 136209069 | |||||
| chrX:136209128
|
TC | T | 1 | a0002c0003t0006g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.689-113delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 136209128 | |||||
| chrX:136209143
|
C | CG | 1 | a0002c0003t0006g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.689-99dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 136209143 | |||||
| chrX:136209858
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.889-13T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 7/7 | chrX | 136209858 | ||||||
| chrX:136209863
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(109): Show | 120 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
splice_region_variant&intron_variant | LOW | c.889-8C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 7/7 | chrX | 136209863 |