Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 211 | 48 | 32 | 98 | 7 | 24 | 69 | FHL1_chrX_136142533_136216354 | FHL1 | MAEKF others(318): Show |
chrX | 136142533 | 136216354 |
| a0002 | 0/0 | 323 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | MAEKF others(318): Show |
chrX | 136142533 | 136216354 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 969 | 210 | 47 | 32 | 98 | 7 | 24 | FHL1_chrX_136142533_136216354 | FHL1 | ATGGC others(964): Show |
chrX | 136142533 | 136216354 | ||
| a0001c0003 | 0/0 | 969 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | ATGGC others(964): Show |
chrX | 136142533 | 136216354 | ||
| a0002c0002 | 0/0 | 969 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | ATGGC others(964): Show |
chrX | 136142533 | 136216354 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2568 | 105 | 14 | 13 | 67 | 3 | 7 | FHL1_chrX_136142533_136216354 | FHL1 | AGTCC others(2563): Show |
chrX | 136142533 | 136216354 |
| a0001c0001t0002 | 1/0 | 2568 | 89 | 23 | 17 | 29 | 4 | 15 | FHL1_chrX_136142533_136216354 | FHL1 | AGTCC others(2563): Show |
chrX | 136142533 | 136216354 |
| a0001c0001t0003 | 0/0 | 2568 | 5 | 5 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | AGTCC others(2563): Show |
chrX | 136142533 | 136216354 |
| a0001c0001t0004 | 0/0 | 2568 | 3 | 3 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | AGTCC others(2563): Show |
chrX | 136142533 | 136216354 |
| a0001c0001t0005 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | AGTCC others(2563): Show |
chrX | 136142533 | 136216354 |
| a0001c0001t0006 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | AGTCC others(2563): Show |
chrX | 136142533 | 136216354 |
| a0001c0001t0007 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | AGTCC others(2563): Show |
chrX | 136142533 | 136216354 |
| a0001c0001t0008 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | AGTCC others(2563): Show |
chrX | 136142533 | 136216354 |
| a0001c0001t0009 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | AGTCC others(2563): Show |
chrX | 136142533 | 136216354 |
| a0001c0001t0010 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | AGTCC others(2563): Show |
chrX | 136142533 | 136216354 |
| a0001c0001t0011 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | AGTCC others(2563): Show |
chrX | 136142533 | 136216354 |
| a0001c0001t0012 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | AGTCC others(2563): Show |
chrX | 136142533 | 136216354 |
| a0001c0003t0002 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | AGTCC others(2563): Show |
chrX | 136142533 | 136216354 |
| a0002c0002t0001 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | AGTCC others(2563): Show |
chrX | 136142533 | 136216354 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0025 | 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 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0051 | 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 |
| a0001c0001t0001g0057 | 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 | 0/1 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0088 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0114 | 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 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0144 | 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 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0002 | 1/0 | 5 | 4 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0003 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| 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 |
| a0001c0001t0002g0089 | 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 |
| a0001c0001t0002g0108 | 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 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0122 | 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 |
| a0001c0001t0002g0125 | 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 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0006g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0007g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0008g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0010g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0011g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0001t0012g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0001c0003t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| a0002c0002t0001g0001 | 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 | g0098 | EUR | GBR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0050 | EUR | FIN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0121 | 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 | g0018 | EAS | CHS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0045 | 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 | g0014 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0101 | 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 | t0005 | g0147 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0169 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0029 | EUR | IBS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | IBS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0030 | EUR | IBS | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | ACB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0008 | 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 | g0008 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | 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 | g0008 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | ACB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0057 | 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 | g0175 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0114 | 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 | g0131 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02145 | hp1 | a0001 | c0003 | t0002 | g0157 | AFR | ACB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | CDX | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | CDX | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02165 | hp1 | a0001 | c0001 | t0007 | g0006 | EAS | CDX | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0003 | 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 | g0007 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0061 | 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 | t0012 | g0151 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0089 | 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 | g0168 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0117 | AFR | MSL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | MSL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03490 | hp1 | a0001 | c0001 | t0008 | g0024 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | ESN | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | GWD | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0161 | 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 | g0052 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | STU | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03942 | hp1 | a0001 | c0001 | t0011 | g0112 | SAS | BEB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0145 | 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 | g0040 | SAS | STU | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0066 | 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 | g0032 | EAS | CHB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0002 | 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 | g0006 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0044 | 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 | t0010 | g0038 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0128 | 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 | g0130 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0005 | 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 | g0110 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0138 | 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 | g0037 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0054 | 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 | g0039 | 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 | g0097 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0088 | 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 | g0019 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0096 | 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 | g0142 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | LWK | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | LWK | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | LWK | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0141 | 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 | g0109 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | YRI | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0172 | EUR | TSI | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | GIH | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | ACB | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | MSL | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0060 | REF | REF | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0002 | REF | REF | FHL1_chrX_136142533_136216354 | FHL1 | chrX | 136142533 | 136216354 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:136207064 | G | A | 1 | a0002 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:136207910 | C | T | 1 | a0001c0003 | 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:136147571 | C | T | 2 | a0001c0001t0003 a0001c0001t0012 |
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:136169974 | G | C | 1 | a0001c0001t0005 | 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 | a0001c0001t0006 | 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 | a0001c0001t0007 | 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 | a0001c0001t0008 | 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 | 1 | a0001c0001t0004 | 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 | a0001c0001t0005 | 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 | a0001c0001t0009 | 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 | a0001c0001t0012 | 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 | a0001c0001t0010 | 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 | 10 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(7): Show |
115 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(112): 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 | a0001c0001t0012 | 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 | a0001c0001t0011 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*979G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 8/8 | 979 | chrX | 136210933 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:136147722 | C | G | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
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:136147879 | G | C | 1 | a0001c0001t0002g0022 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-101+251G>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136147879 | |||||||
| chrX:136148065 | G | T | 1 | a0001c0001t0002g0174 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-101+437G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136148065 | |||||||
| chrX:136148076 | T | G | 1 | a0001c0001t0001g0023 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-101+448T>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136148076 | |||||||
| chrX:136148524 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-101+896C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136148524 | |||||||
| chrX:136148754 | T | C | 1 | a0001c0001t0002g0174 | 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 | a0001c0001t0008g0024 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-101+1148T>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136148776 | |||||||
| chrX:136149085 | T | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0025 others(37): 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 | a0001c0001t0002g0174 | 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 | a0001c0001t0001g0171 a0001c0001t0002g0170 a0001c0001t0002g0172 others(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:136149229 | T | C | 103 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(100): Show |
119 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(116): 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 | a0001c0001t0001g0168 | 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 | a0001c0001t0001g0167 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-101+1631G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136149259 | |||||||
| chrX:136149762 | C | T | 1 | a0001c0001t0001g0059 | 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 | a0001c0001t0002g0166 | 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 | a0001c0001t0002g0062 a0001c0001t0009g0061 |
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 | a0001c0001t0001g0025 | 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 | a0001c0001t0002g0174 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-101+2644A>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136150272 | |||||||
| chrX:136150763 | G | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0063 |
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:136150982 | A | C | 1 | a0001c0001t0002g0165 | 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 | a0001c0001t0001g0064 a0001c0001t0001g0168 a0001c0001t0002g0065 others(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 | 5 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0069 others(2): 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 | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(109): Show |
129 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(126): 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 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0057 a0001c0001t0002g0058 |
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 | a0001c0001t0002g0008 a0001c0001t0002g0153 a0001c0001t0002g0166 |
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 | a0001c0001t0002g0174 | 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 | a0001c0001t0001g0171 a0001c0001t0002g0170 a0001c0001t0002g0172 others(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 | a0001c0001t0001g0026 | 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 | a0001c0001t0002g0174 | 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 | a0001c0001t0001g0078 | 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 | 6 | a0001c0001t0003g0020 a0001c0001t0003g0148 a0001c0001t0003g0149 others(3): 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 | 101 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(98): Show |
118 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(115): 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 | a0001c0001t0001g0069 a0001c0001t0001g0079 a0001c0001t0001g0080 others(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:136152918 | ACC | A | 4 | a0001c0001t0001g0168 a0001c0001t0002g0065 a0001c0001t0002g0066 others(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 | a0001c0001t0001g0168 a0001c0001t0002g0065 a0001c0001t0002g0066 others(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 | a0001c0001t0002g0174 | 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 | a0001c0001t0001g0056 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-101+5366C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136152994 | |||||||
| chrX:136153114 | C | T | 1 | a0001c0001t0001g0143 | 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 | a0001c0001t0002g0055 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-101+5497A>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136153125 | |||||||
| chrX:136153284 | T | TG | 105 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(102): Show |
122 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.-101+5665dupG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136153284 | ||||||
| chrX:136153466 | T | G | 1 | a0001c0001t0001g0013 | 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:136153768 | C | T | 1 | a0001c0001t0002g0174 | 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 | a0001c0001t0004g0146 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-101+6177C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136153805 | |||||||
| chrX:136153986 | A | G | 1 | a0001c0001t0002g0073 | 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 | a0001c0001t0002g0174 | 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 | a0001c0001t0005g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-101+6953T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136154581 | |||||||
| chrX:136154788 | C | T | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(107): Show |
127 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.-101+7160C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136154788 | |||||||
| chrX:136154793 | G | A | 17 | a0001c0001t0001g0014 a0001c0001t0001g0090 a0001c0001t0001g0092 others(14): Show |
18 | HG00140.hp1 HG01069.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.-101+7165G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136154793 | |||||||
| chrX:136154998 | C | T | 5 | a0001c0001t0003g0020 a0001c0001t0003g0148 a0001c0001t0003g0149 others(2): 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 | 102 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(99): Show |
118 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(115): 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 | a0001c0001t0012g0151 | 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 | a0001c0001t0001g0064 a0001c0001t0002g0068 |
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 | 5 | a0001c0001t0003g0020 a0001c0001t0003g0148 a0001c0001t0003g0149 others(2): 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 | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-101+8197delA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136155814 | ||||||
| chrX:136155948 | G | T | 1 | a0001c0001t0002g0173 | 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 | 103 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(100): Show |
119 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(116): 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 | a0001c0001t0002g0170 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-101+8567C>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136156195 | |||||||
| chrX:136156283 | CT | C | 10 | a0001c0001t0001g0032 a0001c0001t0001g0078 a0001c0001t0001g0080 others(7): 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 | a0001c0001t0002g0163 | 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0002g0174 | 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 | a0001c0001t0004g0154 | 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 | a0001c0001t0005g0147 | 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 | a0001c0001t0001g0078 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-101+9076C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136156704 | |||||||
| chrX:136156986 | TACAC | T | 4 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0002g0091 others(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 | 108 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(105): Show |
125 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(122): 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 | a0001c0001t0002g0053 | 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 | 111 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(108): Show |
128 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.-101+9555C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136157183 | |||||||
| chrX:136158241 | C | T | 103 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(100): Show |
119 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(116): 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 | a0001c0001t0004g0146 | 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 | 103 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(100): Show |
119 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-101+10738A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136158366 | |||||||
| chrX:136158424 | G | A | 8 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0003g0148 others(5): 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 | 8 | a0001c0001t0001g0078 a0001c0001t0003g0020 a0001c0001t0003g0148 others(5): 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 | 5 | a0001c0001t0003g0020 a0001c0001t0003g0148 a0001c0001t0003g0149 others(2): 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:136158854 | C | T | 1 | a0001c0001t0004g0146 | 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 | 103 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(100): Show |
119 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-100-10937C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136158970 | |||||||
| chrX:136159138 | T | TA | 12 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0071 others(9): 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 | 98 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(95): Show |
113 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(110): 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:136159370 | T | C | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(109): Show |
129 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.-100-10537T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136159370 | |||||||
| chrX:136159715 | A | G | 1 | a0001c0001t0002g0165 | 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 | a0001c0001t0002g0052 | 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 | a0001c0001t0002g0174 | 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 | a0001c0001t0002g0155 a0001c0001t0002g0156 |
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 | a0001c0001t0001g0087 a0001c0001t0001g0106 |
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 | a0001c0001t0002g0009 | 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 | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(109): Show |
129 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(126): 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 | a0001c0001t0001g0140 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-100-8925C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136160982 | |||||||
| chrX:136161103 | T | C | 2 | a0001c0001t0001g0107 a0001c0001t0002g0145 |
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 | a0001c0001t0002g0021 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0078 others(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 | 8 | a0001c0001t0001g0152 a0001c0001t0002g0077 a0001c0001t0002g0137 others(5): 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 | 89 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(86): Show |
104 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(101): 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 | a0001c0001t0001g0015 a0001c0001t0001g0069 a0001c0001t0001g0071 others(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:136162612 | A | T | 1 | a0001c0001t0002g0055 | 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 | 5 | a0001c0001t0003g0020 a0001c0001t0003g0148 a0001c0001t0003g0149 others(2): 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:136163620 | G | T | 1 | a0001c0001t0004g0154 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-100-6287G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136163620 | |||||||
| chrX:136163665 | A | T | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-100-6242A>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136163665 | |||||||
| chrX:136163667 | C | G | 5 | a0001c0001t0003g0020 a0001c0001t0003g0148 a0001c0001t0003g0149 others(2): 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:136164211 | A | AT | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-100-5683dupT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 136164211 | ||||||
| chrX:136164362 | A | G | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-100-5545A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136164362 | |||||||
| chrX:136164390 | A | G | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(107): Show |
127 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.-100-5517A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136164390 | |||||||
| chrX:136164569 | T | C | 1 | a0001c0001t0002g0055 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-5338T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136164569 | |||||||
| chrX:136164882 | A | G | 1 | a0001c0001t0002g0055 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-100-5025A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136164882 | |||||||
| chrX:136165421 | G | A | 115 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(112): Show |
132 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.-100-4486G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136165421 | |||||||
| chrX:136166152 | T | C | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-100-3755T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136166152 | |||||||
| 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:136166696 | A | G | 1 | a0001c0001t0002g0174 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-100-3211A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136166696 | |||||||
| chrX:136166734 | GTGGATGG others(1183): Show |
G | 1 | a0001c0001t0002g0172 | 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 | a0001c0001t0001g0105 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-100-3035G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136166872 | |||||||
| chrX:136166908 | C | G | 1 | a0001c0001t0011g0112 | 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 | a0001c0001t0002g0176 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-100-2988C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136166919 | |||||||
| chrX:136167046 | C | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(164): Show |
192 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.-100-2861C>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136167046 | |||||||
| chrX:136167097 | CAGTG | C | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): 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:136167194 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0096 |
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:136167396 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-100-2511G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136167396 | |||||||
| chrX:136167455 | G | A | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(107): Show |
127 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.-100-2452G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136167455 | |||||||
| chrX:136167515 | A | G | 1 | a0001c0001t0004g0146 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-100-2392A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136167515 | |||||||
| chrX:136167794 | G | C | 6 | a0001c0001t0001g0080 a0001c0001t0001g0093 a0001c0001t0001g0096 others(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 | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): 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 | a0001c0001t0002g0165 | 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 | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(107): Show |
127 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(124): 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 | a0001c0001t0001g0142 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-100-1725G>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136168182 | |||||||
| chrX:136168371 | A | G | 1 | a0001c0001t0002g0172 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-100-1536A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136168371 | |||||||
| chrX:136168581 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-100-1326T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136168581 | |||||||
| chrX:136169053 | A | G | 1 | a0001c0001t0002g0067 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-100-854A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 1/7 | chrX | 136169053 | |||||||
| chrX:136169188 | G | A | 1 | a0001c0001t0001g0007 | 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 | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): 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 | a0001c0001t0002g0159 | 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 | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-27+97delC | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136170075 | ||||||
| chrX:136170727 | C | G | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): 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 | a0001c0001t0011g0112 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0002g0113 | 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 | a0001c0001t0001g0114 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-27+1877T>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136171857 | |||||||
| chrX:136171888 | A | AT | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(107): Show |
127 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(124): 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 | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): 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 | a0001c0001t0004g0146 | 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 | a0001c0001t0001g0141 | 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 | 115 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(112): Show |
132 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.-27+2165T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136172145 | |||||||
| chrX:136172200 | G | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0025 others(41): 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 | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): 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 | a0001c0001t0001g0040 | 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 | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-27+2531A>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136172511 | |||||||
| chrX:136172512 | T | C | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0002g0155 a0001c0001t0002g0156 |
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:136175142 | T | C | 1 | a0001c0001t0002g0066 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-27+5162T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136175142 | |||||||
| chrX:136175226 | C | T | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): 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 | a0001c0001t0001g0171 a0001c0001t0002g0170 a0001c0001t0002g0172 others(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:136175355 | T | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0069 others(2): 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 | a0001c0001t0001g0051 a0001c0001t0002g0031 a0001c0001t0002g0050 |
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 | a0001c0001t0002g0159 | 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 | 104 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(101): Show |
120 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(117): 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 | a0001c0001t0002g0174 | 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 | a0001c0001t0001g0141 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0085 |
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 | a0001c0001t0004g0146 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-27+6388T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136176368 | |||||||
| chrX:136176514 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
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 | a0001c0001t0004g0146 | 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 | 43 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0025 others(40): 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 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0002g0035 others(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 | a0001c0001t0001g0078 a0001c0001t0005g0147 a0001c0001t0012g0151 |
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 | a0001c0001t0001g0106 a0001c0001t0003g0149 a0001c0001t0003g0150 |
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 |
6 | a0001c0001t0001g0064 a0001c0001t0001g0087 a0001c0001t0002g0135 others(3): 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 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0132 others(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 |
20 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0018 others(17): 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 |
31 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0017 others(28): 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 |
23 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(20): 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 |
9 | a0001c0001t0001g0094 a0001c0001t0001g0103 a0001c0001t0001g0118 others(6): Show |
9 | HG01106.hp1 HG01517.hp1 HG01993.hp2 others(6): 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 | a0001c0001t0001g0115 a0001c0001t0001g0141 a0001c0001t0001g0143 others(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 | a0001c0001t0011g0112 | 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 | a0001c0001t0002g0163 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0041 |
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:136177811 | T | C | 1 | a0001c0001t0002g0174 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-27+7831T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136177811 | |||||||
| chrX:136178351 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(173): Show |
205 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.-27+8371T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136178351 | |||||||
| chrX:136178597 | AAAAC | A | 71 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(68): 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:136178757 | CTT | C | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(107): Show |
127 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(124): 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:136178900 | G | A | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-27+8920G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136178900 | |||||||
| chrX:136179812 | C | T | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0005g0147 | 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 | a0001c0001t0001g0080 a0001c0001t0001g0099 |
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 | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-27+9963T>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136179943 | |||||||
| chrX:136180453 | G | GA | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-27+10474dupA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136180453 | ||||||
| chrX:136180473 | C | T | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): 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 | a0001c0001t0002g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-27+10800C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136180780 | |||||||
| chrX:136180802 | C | CGT | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(109): Show |
129 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(126): 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 | a0001c0001t0001g0078 | 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 | 100 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(97): Show |
116 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.-27+10972G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136180952 | |||||||
| chrX:136181019 | A | C | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-27+11039A>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136181019 | |||||||
| chrX:136181020 | G | T | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
130 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(127): 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 | a0001c0001t0001g0016 a0001c0001t0001g0104 |
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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0146 |
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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0064 a0001c0001t0002g0068 |
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 | 83 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(80): Show |
93 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.-27+12164T>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136182144 | |||||||
| chrX:136182282 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0002g0068 |
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 | a0001c0001t0001g0064 a0001c0001t0002g0068 |
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 | a0001c0001t0002g0021 | 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:136182797 | A | C | 1 | a0001c0001t0001g0049 | 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 | a0001c0001t0002g0009 a0001c0001t0002g0041 a0001c0001t0002g0054 others(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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0155 others(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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0146 |
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 | 31 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0079 others(28): 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 | 78 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(75): Show |
88 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.-27+13148A>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136183128 | |||||||
| chrX:136183888 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0002g0068 |
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 | 83 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(80): Show |
93 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(90): 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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0146 |
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 | 83 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(80): Show |
93 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.-27+14671A>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136184651 | |||||||
| chrX:136184670 | G | A | 83 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(80): Show |
93 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.-27+14690G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136184670 | |||||||
| chrX:136184709 | T | G | 1 | a0001c0001t0002g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-27+14729T>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136184709 | |||||||
| chrX:136185141 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0094 a0001c0001t0001g0101 |
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 | a0001c0001t0002g0166 | 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 | a0001c0001t0002g0165 | 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 | a0001c0001t0002g0173 | 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 | 77 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(74): Show |
87 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(84): 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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0146 |
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 | a0001c0001t0001g0087 | 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 | 80 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(77): Show |
90 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(87): 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 | a0001c0001t0002g0031 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-27+16403T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186383 | |||||||
| chrX:136186863 | AAAATATA others(3): Show |
A | 2 | a0001c0001t0001g0064 a0001c0001t0002g0068 |
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 | a0001c0001t0002g0021 | 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:136186866 | AT | A | 2 | a0001c0001t0001g0034 a0001c0001t0009g0061 |
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 | 67 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0019 others(64): 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 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0049 others(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 | a0001c0001t0002g0128 a0001c0001t0003g0150 |
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 | 4 | a0001c0001t0003g0020 a0001c0001t0003g0148 a0001c0001t0003g0149 others(1): 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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0095 a0001c0001t0001g0126 a0001c0001t0002g0130 |
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 | 72 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(69): Show |
83 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(80): 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 | a0001c0001t0001g0034 a0001c0001t0002g0043 a0001c0001t0009g0061 |
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 | 62 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0019 others(59): 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 | a0001c0001t0001g0132 a0001c0001t0001g0142 a0001c0001t0002g0145 |
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 | 59 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(56): Show |
68 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(65): 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 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0001g0046 others(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 | a0001c0001t0005g0147 | 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:136186877 | T | A | 1 | a0001c0001t0002g0128 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-27+16897T>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136186877 | |||||||
| chrX:136186877 | TATATAGA others(3): Show |
T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 |
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 | a0001c0001t0001g0078 | 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 | a0001c0001t0002g0021 a0001c0001t0002g0065 a0001c0001t0002g0066 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0158 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0040 a0001c0001t0001g0048 others(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 | 62 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0019 others(59): 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 | a0001c0001t0001g0051 a0001c0001t0001g0081 a0001c0001t0002g0031 others(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 | 15 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0049 others(12): 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 | a0001c0001t0001g0072 | 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 | 4 | a0001c0001t0003g0020 a0001c0001t0003g0148 a0001c0001t0003g0149 others(1): 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 | a0001c0001t0001g0072 a0001c0001t0001g0095 a0001c0001t0001g0126 others(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 | GT | G | 7 | a0001c0001t0001g0056 a0001c0001t0002g0065 a0001c0001t0002g0066 others(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 | a0001c0001t0002g0127 a0001c0001t0002g0135 |
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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0146 others(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 | 70 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(67): Show |
80 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(77): 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0088 | 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 | 5 | a0001c0001t0003g0020 a0001c0001t0003g0148 a0001c0001t0003g0149 others(2): 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 | a0001c0001t0002g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-26-18201T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136188206 | |||||||
| chrX:136188663 | A | G | 5 | a0001c0001t0003g0020 a0001c0001t0003g0148 a0001c0001t0003g0149 others(2): 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 | 78 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(75): Show |
88 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.-26-17321T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136189086 | |||||||
| chrX:136189152 | G | T | 78 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(75): Show |
88 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(85): 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 | a0001c0001t0005g0147 | 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 | a0001c0001t0001g0078 a0001c0001t0002g0174 |
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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0146 others(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 | a0001c0001t0001g0064 a0001c0001t0001g0078 a0001c0001t0002g0068 others(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 | a0001c0001t0001g0045 | 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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0146 others(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 | 79 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(76): Show |
89 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(86): 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 | a0001c0001t0002g0133 | 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 | a0001c0001t0005g0147 | 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 | a0001c0001t0001g0064 a0001c0001t0002g0068 |
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 | a0001c0001t0002g0054 | 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0115 a0001c0001t0001g0167 |
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 | 75 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
85 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-26-13510T>C | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136192897 | |||||||
| chrX:136193082 | TA | T | 75 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
85 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-26-13310delA | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136193082 | ||||||
| chrX:136193094 | A | C | 5 | a0001c0001t0001g0119 a0001c0001t0001g0171 a0001c0001t0002g0170 others(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 | 79 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(76): Show |
89 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(86): 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 | a0001c0001t0004g0154 | 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 | a0001c0001t0008g0024 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0005g0147 | 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 | 65 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(62): Show |
74 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.-26-12758C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136193649 | |||||||
| chrX:136193764 | A | G | 65 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(62): Show |
74 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(71): 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 | a0001c0001t0001g0095 a0001c0001t0001g0126 |
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 | a0001c0001t0004g0117 | 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 | a0001c0001t0002g0062 a0001c0001t0009g0061 |
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 | a0001c0001t0002g0174 | 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 | 70 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(67): Show |
79 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(76): 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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0146 others(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 | 65 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(62): Show |
74 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(71): 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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0146 others(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 | a0001c0001t0002g0123 | 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 | a0001c0001t0002g0039 a0001c0001t0002g0047 |
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 | a0001c0001t0003g0150 | 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 | a0001c0001t0001g0120 | 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 | a0001c0001t0002g0124 a0001c0001t0002g0125 |
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 | 79 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(76): Show |
89 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(86): 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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0146 others(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 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0002g0030 others(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 | 36 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0025 others(33): 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 | GT | G | 77 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(74): Show |
87 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.-26-8424delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136197968 | ||||||
| chrX:136198148 | GT | G | 75 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
85 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-26-8246delT | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 136198148 | ||||||
| chrX:136198325 | T | C | 3 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0041 |
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:136199390 | CT | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0085 a0001c0001t0001g0141 |
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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0146 others(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 | 79 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(76): Show |
89 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(86): 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 | a0001c0001t0001g0064 a0001c0001t0001g0078 a0001c0001t0002g0068 others(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 | 5 | a0001c0001t0003g0020 a0001c0001t0003g0148 a0001c0001t0003g0149 others(2): 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 | a0001c0001t0002g0076 a0001c0001t0002g0130 |
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 | 81 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(78): Show |
91 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(88): 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 | a0001c0001t0001g0044 a0001c0001t0002g0058 |
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 | a0001c0001t0001g0072 a0001c0001t0001g0075 |
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 | a0001c0001t0001g0093 a0001c0001t0001g0096 |
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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0146 others(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 | 66 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(63): Show |
75 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.-26-4905delG | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136201501 | |||||||
| chrX:136202082 | T | A | 1 | a0001c0001t0002g0174 | 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 | a0001c0001t0002g0062 a0001c0001t0009g0061 |
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 | a0001c0001t0010g0038 | 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 | a0001c0001t0001g0064 a0001c0001t0002g0068 |
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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0146 others(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 | a0001c0001t0002g0124 | 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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0146 others(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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0146 others(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 | a0001c0001t0002g0039 a0001c0001t0002g0065 a0001c0001t0002g0066 others(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 | a0001c0001t0002g0174 | 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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0146 others(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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0146 others(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 | a0001c0001t0001g0064 a0001c0001t0001g0078 a0001c0001t0002g0068 others(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 | a0001c0001t0002g0062 a0001c0001t0009g0061 |
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 | a0001c0001t0001g0121 | 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 | a0001c0001t0002g0174 | 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 | a0001c0001t0001g0140 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-26-1307G>A | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 2/7 | chrX | 136205100 | |||||||
| chrX:136205149 | GA | G | 5 | a0001c0001t0001g0064 a0001c0001t0001g0078 a0001c0001t0002g0068 others(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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0146 others(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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0146 others(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 | a0001c0001t0001g0171 a0001c0001t0002g0163 a0001c0001t0002g0170 others(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 | a0001c0001t0002g0062 a0001c0001t0009g0061 |
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 | a0001c0001t0001g0064 a0001c0001t0002g0068 a0001c0001t0005g0147 |
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:136207705 | C | A | 1 | a0001c0001t0001g0079 | 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 | 5 | a0001c0001t0003g0020 a0001c0001t0003g0148 a0001c0001t0003g0149 others(2): 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 | 5 | a0001c0001t0003g0020 a0001c0001t0003g0148 a0001c0001t0003g0149 others(2): 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: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:136208040 | T | C | 1 | a0001c0001t0001g0096 | 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 | 63 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(60): Show |
72 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(69): 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 | a0001c0001t0001g0042 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.501+168C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 5/7 | chrX | 136208129 | |||||||
| chrX:136208259 | T | G | 1 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0111 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.502-90C>G | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 5/7 | chrX | 136208365 | |||||||
| chrX:136209858 | T | C | 1 | a0001c0001t0001g0143 | 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 | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
119 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
splice_region_variant&intron_variant | LOW | c.889-8C>T | FHL1 | ENSG00000022267.19 | transcript | ENST00000394155.8 | protein_coding | 7/7 | chrX | 136209863 |