Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8087 |
| ensemblid | ENSG00000114416.19 |
| hgncid | 4023 |
| symbol | FXR1 |
| name | FMR1 autosomal homolog 1 |
| refseq_nuc | NM_005087.4 |
| refseq_prot | NP_005078.2 |
| ensembl_nuc | ENST00000357559.9 |
| ensembl_prot | ENSP00000350170.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 180912670 |
| end | 180982753 |
| strand | + |
| ver | v1.2 |
| region | chr3:180912670-180982753 |
| region5000 | chr3:180907670-180987753 |
| regionname0 | FXR1_chr3_180912670_180982753 |
| regionname5000 | FXR1_chr3_180907670_180987753 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 621 | 318 | 73 | 64 | 125 | 18 | 36 | 96 | FXR1_chr3_180907670_180987753 | FXR1 | MAELT others(616): Show |
chr3 | 180907670 | 180987753 |
| a0002 | 0/0 | 621 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | MAELT others(616): Show |
chr3 | 180907670 | 180987753 |
| a0003 | 0/0 | 621 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | MAELT others(616): Show |
chr3 | 180907670 | 180987753 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1863 | 296 | 59 | 60 | 123 | 18 | 34 | FXR1_chr3_180907670_180987753 | FXR1 | ATGGC others(1858): Show |
chr3 | 180907670 | 180987753 | ||
| a0001c0002 | 0/0 | 1863 | 15 | 11 | 4 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | ATGGC others(1858): Show |
chr3 | 180907670 | 180987753 | ||
| a0001c0003 | 0/0 | 1863 | 3 | 3 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | ATGGC others(1858): Show |
chr3 | 180907670 | 180987753 | ||
| a0001c0004 | 0/0 | 1863 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | ATGGC others(1858): Show |
chr3 | 180907670 | 180987753 | ||
| a0001c0007 | 0/0 | 1863 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | ATGGC others(1858): Show |
chr3 | 180907670 | 180987753 | ||
| a0001c0008 | 0/0 | 1863 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | ATGGC others(1858): Show |
chr3 | 180907670 | 180987753 | ||
| a0001c0009 | 0/0 | 1863 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | ATGGC others(1858): Show |
chr3 | 180907670 | 180987753 | ||
| a0002c0006 | 0/0 | 1863 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | ATGGC others(1858): Show |
chr3 | 180907670 | 180987753 | ||
| a0003c0005 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | ATGGC others(1858): Show |
chr3 | 180907670 | 180987753 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8344 | 78 | 16 | 12 | 37 | 5 | 8 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8339): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0002 | 0/1 | 8343 | 48 | 1 | 9 | 26 | 5 | 6 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8338): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0003 | 0/0 | 8342 | 37 | 7 | 9 | 16 | 2 | 3 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8337): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0004 | 1/0 | 8343 | 36 | 0 | 11 | 13 | 3 | 8 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8338): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0006 | 0/0 | 8343 | 8 | 0 | 0 | 8 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8338): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0007 | 0/0 | 8344 | 7 | 0 | 0 | 7 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8339): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0008 | 0/0 | 8343 | 7 | 0 | 2 | 5 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8338): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0009 | 0/0 | 8346 | 6 | 5 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8341): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0010 | 0/0 | 8343 | 6 | 6 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8338): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0011 | 0/0 | 8344 | 5 | 3 | 2 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8339): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0012 | 0/0 | 8342 | 5 | 4 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8337): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0013 | 0/0 | 8343 | 4 | 1 | 2 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8338): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0014 | 0/0 | 8343 | 3 | 2 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8338): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0015 | 0/0 | 8345 | 3 | 2 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8340): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0016 | 0/0 | 8341 | 3 | 0 | 0 | 0 | 0 | 3 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8336): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0017 | 0/0 | 8344 | 3 | 0 | 2 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8339): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0018 | 0/0 | 8344 | 2 | 2 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8339): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0019 | 0/0 | 8344 | 2 | 0 | 2 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8339): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0020 | 0/0 | 8343 | 2 | 0 | 0 | 2 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8338): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0021 | 0/0 | 8342 | 2 | 0 | 1 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8337): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0022 | 0/0 | 8342 | 2 | 0 | 0 | 0 | 0 | 2 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8337): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0023 | 0/0 | 8343 | 2 | 0 | 0 | 0 | 1 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8338): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0024 | 0/0 | 8344 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8339): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0025 | 0/0 | 8342 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8337): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0026 | 0/0 | 8342 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8337): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0027 | 0/0 | 8343 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8338): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0028 | 0/0 | 8341 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8336): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0029 | 0/0 | 8343 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8338): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0030 | 0/0 | 8343 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8338): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0031 | 0/0 | 8343 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8338): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0032 | 0/0 | 8344 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8339): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0033 | 0/0 | 8344 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8339): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0034 | 0/0 | 8344 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8339): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0035 | 0/0 | 8344 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8339): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0036 | 0/0 | 8344 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8339): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0037 | 0/0 | 8343 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8338): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0038 | 0/0 | 8344 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8339): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0039 | 0/0 | 8343 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8338): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0040 | 0/0 | 8343 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8338): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0041 | 0/0 | 8342 | 1 | 0 | 0 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8337): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0042 | 0/0 | 8342 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8337): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0043 | 0/0 | 8342 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8337): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0045 | 0/0 | 8344 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8339): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0046 | 0/0 | 8343 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8338): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0047 | 0/0 | 8342 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8337): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0048 | 0/0 | 8345 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8340): Show |
chr3 | 180907670 | 180987753 |
| a0001c0001t0049 | 0/0 | 8345 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8340): Show |
chr3 | 180907670 | 180987753 |
| a0001c0002t0005 | 0/0 | 8345 | 14 | 10 | 4 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8340): Show |
chr3 | 180907670 | 180987753 |
| a0001c0002t0044 | 0/0 | 8344 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8339): Show |
chr3 | 180907670 | 180987753 |
| a0001c0003t0001 | 0/0 | 8344 | 3 | 3 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8339): Show |
chr3 | 180907670 | 180987753 |
| a0001c0004t0001 | 0/0 | 8344 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8339): Show |
chr3 | 180907670 | 180987753 |
| a0001c0007t0001 | 0/0 | 8344 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8339): Show |
chr3 | 180907670 | 180987753 |
| a0001c0008t0002 | 0/0 | 8343 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8338): Show |
chr3 | 180907670 | 180987753 |
| a0001c0009t0003 | 0/0 | 8342 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8337): Show |
chr3 | 180907670 | 180987753 |
| a0002c0006t0002 | 0/0 | 8343 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8338): Show |
chr3 | 180907670 | 180987753 |
| a0003c0005t0011 | 0/0 | 8344 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | CCTTT others(8339): Show |
chr3 | 180907670 | 180987753 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0207 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0200 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0006g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0006g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0006g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0007g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0007g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0007g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0007g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0007g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0007g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0008g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0008g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0008g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0008g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0008g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0008g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0008g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0009g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0009g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0009g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0009g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0009g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0009g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0010g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0010g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0010g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0010g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0010g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0010g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0011g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0011g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0011g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0011g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0011g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0012g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0012g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0012g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0012g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0012g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0013g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0013g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0013g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0013g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0014g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0014g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0014g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0015g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0015g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0015g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0016g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0016g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0016g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0017g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0017g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0017g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0018g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0018g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0019g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0020g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0020g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0021g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0021g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0022g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0022g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0023g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0023g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0024g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0025g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0026g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0027g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0028g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0029g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0030g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0031g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0032g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0033g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0034g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0035g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0036g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0037g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0038g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0039g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0040g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0041g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0042g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0043g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0045g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0046g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0047g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0048g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0001t0049g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0002t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0002t0005g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0002t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0002t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0002t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0002t0005g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0002t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0002t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0002t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0002t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0002t0005g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0002t0005g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0002t0005g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0002t0005g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0002t0044g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0007t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0008t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0001c0009t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0002c0006t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| a0003c0005t0011g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0269 | EUR | GBR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00099 | hp2 | a0001 | c0001 | t0023 | g0288 | EUR | GBR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0199 | EUR | GBR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0088 | EUR | GBR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0198 | EUR | FIN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0086 | EUR | FIN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00323 | hp1 | a0001 | c0001 | t0041 | g0047 | EUR | FIN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00323 | hp2 | a0001 | c0001 | t0017 | g0314 | EUR | FIN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | CHS | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | CHS | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00423 | hp2 | a0001 | c0001 | t0008 | g0277 | EAS | CHS | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | CHS | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | CHS | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00639 | hp1 | a0001 | c0001 | t0015 | g0292 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | CHS | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00673 | hp2 | a0001 | c0001 | t0031 | g0194 | EAS | CHS | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0226 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0272 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0258 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00741 | hp1 | a0001 | c0001 | t0046 | g0197 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01069 | hp1 | a0001 | c0002 | t0005 | g0301 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01069 | hp2 | a0001 | c0001 | t0011 | g0105 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01070 | hp1 | a0001 | c0001 | t0042 | g0021 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01070 | hp2 | a0001 | c0001 | t0019 | g0004 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01071 | hp1 | a0001 | c0001 | t0019 | g0004 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01071 | hp2 | a0001 | c0001 | t0011 | g0106 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0268 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01081 | hp1 | a0001 | c0001 | t0014 | g0074 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01109 | hp2 | a0001 | c0001 | t0033 | g0140 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01167 | hp1 | a0001 | c0002 | t0005 | g0309 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01167 | hp2 | a0001 | c0001 | t0028 | g0040 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01169 | hp2 | a0001 | c0002 | t0005 | g0310 | AMR | PUR | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01255 | hp1 | a0001 | c0001 | t0012 | g0059 | AMR | CLM | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | CLM | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | CLM | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01256 | hp2 | a0001 | c0001 | t0017 | g0313 | AMR | CLM | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0260 | AMR | CLM | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | CLM | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | CLM | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01261 | hp2 | a0001 | c0001 | t0009 | g0067 | AMR | CLM | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0274 | AMR | CLM | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01361 | hp1 | a0001 | c0001 | t0017 | g0315 | AMR | CLM | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0273 | AMR | CLM | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01433 | hp2 | a0001 | c0002 | t0005 | g0296 | AMR | CLM | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0120 | AMR | CLM | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0082 | AMR | CLM | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0022 | EUR | IBS | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0109 | EUR | IBS | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | IBS | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0110 | EUR | IBS | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0108 | EUR | IBS | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01934 | hp1 | a0001 | c0001 | t0013 | g0240 | AMR | PEL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01943 | hp2 | a0001 | c0001 | t0008 | g0247 | AMR | PEL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01952 | hp2 | a0001 | c0001 | t0013 | g0245 | AMR | PEL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0266 | AMR | PEL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01993 | hp1 | a0001 | c0001 | t0008 | g0249 | AMR | PEL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02015 | hp2 | a0001 | c0001 | t0034 | g0152 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02040 | hp1 | a0001 | c0001 | t0035 | g0153 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | ACB | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02055 | hp2 | a0001 | c0001 | t0018 | g0089 | AFR | ACB | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02071 | hp1 | a0002 | c0006 | t0002 | g0265 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0202 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02145 | hp2 | a0001 | c0001 | t0011 | g0085 | AFR | ACB | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02148 | hp1 | a0001 | c0001 | t0021 | g0039 | AMR | PEL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PEL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02155 | hp1 | a0001 | c0001 | t0008 | g0263 | EAS | CDX | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | CDX | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02258 | hp1 | a0001 | c0001 | t0018 | g0112 | AFR | ACB | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0078 | AFR | ACB | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02451 | hp1 | a0001 | c0002 | t0005 | g0295 | AFR | ACB | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02451 | hp2 | a0001 | c0002 | t0005 | g0298 | AFR | ACB | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0201 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02572 | hp2 | a0001 | c0001 | t0014 | g0072 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0257 | SAS | PJL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0077 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02622 | hp1 | a0001 | c0001 | t0011 | g0102 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02622 | hp2 | a0001 | c0002 | t0005 | g0305 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02630 | hp1 | a0003 | c0005 | t0011 | g0103 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02647 | hp1 | a0001 | c0001 | t0012 | g0069 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02647 | hp2 | a0001 | c0001 | t0036 | g0312 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02683 | hp2 | a0001 | c0001 | t0016 | g0037 | SAS | PJL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0079 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0080 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02895 | hp1 | a0001 | c0002 | t0005 | g0303 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02895 | hp2 | a0001 | c0001 | t0012 | g0061 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02896 | hp1 | a0001 | c0002 | t0005 | g0308 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02896 | hp2 | a0001 | c0001 | t0010 | g0262 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0261 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02897 | hp2 | a0001 | c0002 | t0005 | g0302 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0071 | AFR | ESN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ESN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0062 | AFR | ESN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02970 | hp1 | a0001 | c0002 | t0005 | g0304 | AFR | ESN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0066 | AFR | ESN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02976 | hp1 | a0001 | c0001 | t0048 | g0306 | AFR | ESN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02976 | hp2 | a0001 | c0001 | t0026 | g0065 | AFR | ESN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03017 | hp1 | a0001 | c0001 | t0043 | g0006 | SAS | PJL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0068 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0284 | AFR | ESN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | ESN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03139 | hp2 | a0001 | c0002 | t0005 | g0300 | AFR | ESN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0283 | AFR | ESN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | MSL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03209 | hp2 | a0001 | c0002 | t0005 | g0299 | AFR | MSL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0237 | SAS | PJL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03486 | hp1 | a0001 | c0002 | t0044 | g0297 | AFR | MSL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03486 | hp2 | a0001 | c0001 | t0012 | g0060 | AFR | MSL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0227 | SAS | PJL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | PJL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03516 | hp2 | a0001 | c0001 | t0027 | g0090 | AFR | ESN | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03540 | hp1 | a0001 | c0001 | t0047 | g0052 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03540 | hp2 | a0001 | c0001 | t0010 | g0124 | AFR | GWD | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0104 | AFR | MSL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03579 | hp2 | a0001 | c0002 | t0005 | g0307 | AFR | MSL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0275 | SAS | PJL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03669 | hp2 | a0001 | c0008 | t0002 | g0206 | SAS | PJL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03688 | hp1 | a0001 | c0001 | t0016 | g0038 | SAS | STU | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0122 | SAS | STU | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03704 | hp1 | a0001 | c0001 | t0023 | g0221 | SAS | PJL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0228 | SAS | PJL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03710 | hp2 | a0001 | c0001 | t0016 | g0015 | SAS | PJL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | BEB | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03831 | hp2 | a0001 | c0001 | t0030 | g0196 | SAS | BEB | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0121 | SAS | BEB | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03927 | hp2 | a0001 | c0001 | t0022 | g0043 | SAS | BEB | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | STU | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG04115 | hp2 | a0001 | c0004 | t0001 | g0137 | SAS | STU | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0020 | SAS | BEB | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0118 | SAS | BEB | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0055 | SAS | STU | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0256 | SAS | STU | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | STU | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG04228 | hp1 | a0001 | c0001 | t0022 | g0008 | SAS | STU | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | STU | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0070 | AFR | YRI | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | YRI | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18946 | hp2 | a0001 | c0001 | t0008 | g0271 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18947 | hp1 | a0001 | c0001 | t0006 | g0223 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18947 | hp2 | a0001 | c0009 | t0003 | g0016 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18962 | hp2 | a0001 | c0001 | t0007 | g0184 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18963 | hp1 | a0001 | c0001 | t0008 | g0243 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18963 | hp2 | a0001 | c0001 | t0021 | g0012 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18964 | hp1 | a0001 | c0001 | t0006 | g0213 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18967 | hp2 | a0001 | c0001 | t0020 | g0126 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18968 | hp1 | a0001 | c0001 | t0007 | g0081 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18972 | hp1 | a0001 | c0001 | t0007 | g0101 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18972 | hp2 | a0001 | c0001 | t0006 | g0279 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18973 | hp1 | a0001 | c0001 | t0013 | g0250 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18975 | hp1 | a0001 | c0001 | t0020 | g0267 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18980 | hp1 | a0001 | c0001 | t0006 | g0252 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18983 | hp2 | a0001 | c0001 | t0007 | g0154 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18986 | hp1 | a0001 | c0001 | t0006 | g0278 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18991 | hp1 | a0001 | c0001 | t0025 | g0264 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18993 | hp1 | a0001 | c0001 | t0024 | g0220 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18994 | hp2 | a0001 | c0001 | t0038 | g0212 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19009 | hp2 | a0001 | c0001 | t0032 | g0096 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19030 | hp2 | a0001 | c0001 | t0040 | g0125 | AFR | LWK | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19054 | hp1 | a0001 | c0001 | t0007 | g0182 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19054 | hp2 | a0001 | c0001 | t0007 | g0204 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19058 | hp2 | a0001 | c0001 | t0006 | g0254 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19060 | hp2 | a0001 | c0001 | t0006 | g0280 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19066 | hp2 | a0001 | c0001 | t0008 | g0251 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19079 | hp2 | a0001 | c0001 | t0006 | g0230 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19085 | hp2 | a0001 | c0007 | t0001 | g0148 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19089 | hp2 | a0001 | c0001 | t0007 | g0158 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | YRI | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA19240 | hp2 | a0001 | c0001 | t0029 | g0064 | AFR | YRI | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ASW | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA20129 | hp2 | a0001 | c0001 | t0014 | g0073 | AFR | ASW | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | TSI | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0236 | EUR | TSI | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0025 | EUR | TSI | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA20905 | hp1 | a0001 | c0001 | t0037 | g0032 | SAS | GIH | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | GIH | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0259 | AMR | CLM | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | CLM | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02109 | hp2 | a0001 | c0001 | t0049 | g0058 | AFR | ACB | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02559 | hp1 | a0001 | c0001 | t0045 | g0057 | AFR | ACB | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG02559 | hp2 | a0001 | c0001 | t0039 | g0131 | AFR | ACB | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | MSL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG03471 | hp2 | a0001 | c0001 | t0012 | g0063 | AFR | MSL | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG06807 | hp1 | a0001 | c0001 | t0015 | g0293 | AFR | USA | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA20300 | hp1 | a0001 | c0001 | t0013 | g0244 | AFR | USA | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | USA | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA21309 | hp1 | a0001 | c0001 | t0015 | g0294 | AFR | LWK | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | LWK | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0207 | REF | REF | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0200 | REF | REF | FXR1_chr3_180907670_180987753 | FXR1 | chr3 | 180907670 | 180987753 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:180961522 | G | T | 1 | a0002 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.1045G>T | p.Val349Phe | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 11/17 | 1061/8343 | 1045/1866 | 349/621 | chr3 | 180961522 | |||
| chr3:180976213 | G | A | 1 | a0003 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.1787G>A | p.Arg596His | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 1803/8343 | 1787/1866 | 596/621 | chr3 | 180976213 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:180912712 | C | T | 1 | a0001c0002 | 15 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
synonymous_variant | LOW | c.27C>T | p.Arg9Arg | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/17 | 43/8343 | 27/1866 | 9/621 | chr3 | 180912712 | |||
| chr3:180948769 | A | T | 1 | a0001c0009 | 1 | NA18947.hp2 | synonymous_variant | LOW | c.468A>T | p.Ala156Ala | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 6/17 | 484/8343 | 468/1866 | 156/621 | chr3 | 180948769 | |||
| chr3:180951420 | C | T | 1 | a0001c0008 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.753C>T | p.Thr251Thr | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/17 | 769/8343 | 753/1866 | 251/621 | chr3 | 180951420 | |||
| chr3:180951454 | A | C | 1 | a0001c0007 | 1 | NA19085.hp2 | synonymous_variant | LOW | c.787A>C | p.Arg263Arg | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/17 | 803/8343 | 787/1866 | 263/621 | chr3 | 180951454 | |||
| chr3:180961515 | T | C | 1 | a0001c0004 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.1038T>C | p.Asn346Asn | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 11/17 | 1054/8343 | 1038/1866 | 346/621 | chr3 | 180961515 | |||
| chr3:180961539 | T | C | 1 | a0001c0003 | 3 | HG02258.hp2 HG02615.hp1 HG02717.hp1 |
synonymous_variant | LOW | c.1062T>C | p.His354His | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 11/17 | 1078/8343 | 1062/1866 | 354/621 | chr3 | 180961539 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:180977075 | C | CT | 4 | a0001c0001t0017 a0001c0001t0048 a0001c0001t0049 others(1): Show |
19 | HG00323.hp2 HG01069.hp1 HG01167.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*797dupT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 798 | INFO_REALIGN_3_PRIME | chr3 | 180977075 | |||||
| chr3:180977075 | CT | C | 5 | a0001c0001t0012 a0001c0001t0014 a0001c0001t0027 others(2): Show |
11 | HG01081.hp1 HG01167.hp2 HG01255.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*797delT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 797 | INFO_REALIGN_3_PRIME | chr3 | 180977075 | |||||
| chr3:180977075 | CTT | C | 2 | a0001c0001t0009 a0001c0001t0026 |
7 | HG01261.hp2 HG02922.hp1 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*796_*797delTT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 796 | INFO_REALIGN_3_PRIME | chr3 | 180977075 | |||||
| chr3:180977078 | T | A | 3 | a0001c0001t0006 a0001c0001t0024 a0001c0001t0025 |
10 | NA18947.hp1 NA18964.hp1 NA18972.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*786T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 786 | chr3 | 180977078 | ||||||
| chr3:180977121 | G | T | 1 | a0001c0001t0047 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*829G>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 829 | chr3 | 180977121 | ||||||
| chr3:180977396 | C | A | 1 | a0001c0001t0030 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1104C>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 1104 | chr3 | 180977396 | ||||||
| chr3:180977507 | T | C | 1 | a0001c0001t0031 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1215T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 1215 | chr3 | 180977507 | ||||||
| chr3:180977510 | T | G | 1 | a0001c0001t0032 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1218T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 1218 | chr3 | 180977510 | ||||||
| chr3:180977832 | T | A | 1 | a0001c0001t0018 | 2 | HG02055.hp2 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1540T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 1540 | chr3 | 180977832 | ||||||
| chr3:180977843 | C | T | 1 | a0001c0001t0046 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1551C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 1551 | chr3 | 180977843 | ||||||
| chr3:180978181 | T | TA | 15 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0018 others(12): Show |
102 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1904dupA | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 1905 | INFO_REALIGN_3_PRIME | chr3 | 180978181 | |||||
| chr3:180978181 | TA | T | 12 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0014 others(9): Show |
38 | HG01069.hp1 HG01081.hp1 HG01167.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1904delA | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 1904 | INFO_REALIGN_3_PRIME | chr3 | 180978181 | |||||
| chr3:180978203 | T | C | 11 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0014 others(8): Show |
37 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1911T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 1911 | chr3 | 180978203 | ||||||
| chr3:180978217 | A | G | 1 | a0001c0001t0023 | 2 | HG00099.hp2 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1925A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 1925 | chr3 | 180978217 | ||||||
| chr3:180978291 | TAA | T | 11 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0021 others(8): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*2002_*2003delAA | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 2002 | INFO_REALIGN_3_PRIME | chr3 | 180978291 | |||||
| chr3:180978444 | C | T | 1 | a0001c0001t0022 | 2 | HG03927.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2152C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 2152 | chr3 | 180978444 | ||||||
| chr3:180978506 | G | A | 1 | a0001c0001t0048 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2214G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 2214 | chr3 | 180978506 | ||||||
| chr3:180978643 | A | G | 1 | a0001c0001t0036 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2351A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 2351 | chr3 | 180978643 | ||||||
| chr3:180978682 | G | A | 1 | a0001c0001t0007 | 7 | NA18962.hp2 NA18968.hp1 NA18972.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2390G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 2390 | chr3 | 180978682 | ||||||
| chr3:180978762 | A | G | 11 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0021 others(8): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*2470A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 2470 | chr3 | 180978762 | ||||||
| chr3:180978820 | T | C | 1 | a0001c0001t0041 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2528T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 2528 | chr3 | 180978820 | ||||||
| chr3:180979101 | G | A | 1 | a0001c0001t0033 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2809G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 2809 | chr3 | 180979101 | ||||||
| chr3:180979234 | A | G | 1 | a0001c0001t0040 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2942A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 2942 | chr3 | 180979234 | ||||||
| chr3:180979292 | A | C | 1 | a0001c0001t0043 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3000A>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 3000 | chr3 | 180979292 | ||||||
| chr3:180979468 | T | C | 3 | a0001c0001t0048 a0001c0002t0005 a0001c0002t0044 |
16 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3176T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 3176 | chr3 | 180979468 | ||||||
| chr3:180979508 | C | T | 1 | a0001c0001t0019 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3216C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 3216 | chr3 | 180979508 | ||||||
| chr3:180979584 | C | A | 1 | a0001c0001t0021 | 2 | HG02148.hp1 NA18963.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3292C>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 3292 | chr3 | 180979584 | ||||||
| chr3:180979617 | C | T | 2 | a0001c0001t0028 a0001c0001t0042 |
2 | HG01070.hp1 HG01167.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3325C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 3325 | chr3 | 180979617 | ||||||
| chr3:180979639 | T | G | 1 | a0001c0001t0019 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3347T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 3347 | chr3 | 180979639 | ||||||
| chr3:180980340 | A | T | 46 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(43): Show |
254 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*4048A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 4048 | chr3 | 180980340 | ||||||
| chr3:180980342 | T | C | 13 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0019 others(10): Show |
99 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*4050T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 4050 | chr3 | 180980342 | ||||||
| chr3:180980384 | C | CT | 2 | a0001c0001t0011 a0003c0005t0011 |
6 | HG01069.hp2 HG01071.hp2 HG02145.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4101dupT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 4102 | INFO_REALIGN_3_PRIME | chr3 | 180980384 | |||||
| chr3:180980393 | T | G | 11 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0014 others(8): Show |
37 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*4101T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 4101 | chr3 | 180980393 | ||||||
| chr3:180980650 | G | A | 1 | a0001c0001t0013 | 4 | HG01934.hp1 HG01952.hp2 NA18973.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4358G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 4358 | chr3 | 180980650 | ||||||
| chr3:180980878 | T | G | 1 | a0001c0001t0045 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4586T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 4586 | chr3 | 180980878 | ||||||
| chr3:180980928 | A | AT | 11 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0015 others(8): Show |
33 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*4646dupT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 4647 | INFO_REALIGN_3_PRIME | chr3 | 180980928 | |||||
| chr3:180981133 | T | TAGAA | 1 | a0001c0001t0009 | 6 | HG01261.hp2 HG02922.hp1 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4842_*4845dupAGAA | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 4846 | INFO_REALIGN_3_PRIME | chr3 | 180981133 | |||||
| chr3:180981211 | T | A | 1 | a0001c0001t0015 | 3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4919T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 4919 | chr3 | 180981211 | ||||||
| chr3:180981386 | T | C | 5 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0014 others(2): Show |
16 | HG01081.hp1 HG01255.hp1 HG01261.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5094T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 5094 | chr3 | 180981386 | ||||||
| chr3:180981533 | A | G | 5 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0024 others(2): Show |
18 | HG00423.hp2 HG01943.hp2 HG01993.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5241A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 5241 | chr3 | 180981533 | ||||||
| chr3:180981578 | C | T | 1 | a0001c0001t0035 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5286C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 5286 | chr3 | 180981578 | ||||||
| chr3:180981706 | C | T | 1 | a0001c0001t0029 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5414C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 5414 | chr3 | 180981706 | ||||||
| chr3:180981813 | A | G | 1 | a0001c0001t0034 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5521A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 5521 | chr3 | 180981813 | ||||||
| chr3:180981927 | G | A | 2 | a0001c0001t0010 a0001c0001t0040 |
7 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5635G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 5635 | chr3 | 180981927 | ||||||
| chr3:180982166 | C | T | 1 | a0001c0001t0015 | 3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5874C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 5874 | chr3 | 180982166 | ||||||
| chr3:180982295 | G | C | 1 | a0001c0001t0020 | 2 | NA18967.hp2 NA18975.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6003G>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 6003 | chr3 | 180982295 | ||||||
| chr3:180982336 | A | AC | 22 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0012 others(19): Show |
88 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*6045dupC | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 6046 | INFO_REALIGN_3_PRIME | chr3 | 180982336 | |||||
| chr3:180982350 | C | T | 1 | a0001c0001t0040 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6058C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 6058 | chr3 | 180982350 | ||||||
| chr3:180982362 | A | G | 22 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0012 others(19): Show |
88 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*6070A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 6070 | chr3 | 180982362 | ||||||
| chr3:180982413 | T | A | 1 | a0001c0001t0020 | 2 | NA18967.hp2 NA18975.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6121T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 17/17 | 6121 | chr3 | 180982413 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:180912777 | T | C | 51 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(48): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.51+41T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180912777 | |||||||
| chr3:180912861 | T | C | 18 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(15): Show |
18 | HG01081.hp1 HG01255.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.51+125T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180912861 | |||||||
| chr3:180912873 | T | G | 2 | a0001c0001t0003g0007 a0001c0001t0043g0006 |
2 | HG00733.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.51+137T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180912873 | |||||||
| chr3:180912884 | C | T | 3 | a0001c0001t0017g0313 a0001c0001t0017g0314 a0001c0001t0017g0315 |
3 | HG00323.hp2 HG01256.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.51+148C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180912884 | |||||||
| chr3:180912917 | C | G | 16 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(13): Show |
16 | HG01081.hp1 HG01255.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.51+181C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180912917 | |||||||
| chr3:180912974 | C | T | 1 | a0001c0001t0036g0312 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.51+238C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180912974 | |||||||
| chr3:180913169 | C | T | 1 | a0001c0001t0002g0311 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.51+433C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180913169 | |||||||
| chr3:180913201 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.51+465G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180913201 | |||||||
| chr3:180913472 | A | T | 37 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(34): Show |
37 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.51+736A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180913472 | |||||||
| chr3:180913508 | G | GGTTTT | 4 | a0001c0001t0010g0080 a0001c0003t0001g0077 a0001c0003t0001g0078 others(1): Show |
4 | HG02258.hp2 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+788_51+792dupGT others(3): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180913508 | ||||||
| chr3:180913667 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.51+931C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180913667 | |||||||
| chr3:180913748 | C | T | 2 | a0001c0001t0003g0007 a0001c0001t0043g0006 |
2 | HG00733.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.51+1012C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180913748 | |||||||
| chr3:180913821 | A | G | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.51+1085A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180913821 | |||||||
| chr3:180913902 | C | T | 37 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(34): Show |
37 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.51+1166C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180913902 | |||||||
| chr3:180913946 | A | G | 1 | a0001c0001t0049g0058 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.51+1210A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180913946 | |||||||
| chr3:180914186 | T | G | 16 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(13): Show |
16 | HG01081.hp1 HG01255.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.51+1450T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180914186 | |||||||
| chr3:180914242 | T | C | 51 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(48): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.51+1506T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180914242 | |||||||
| chr3:180914319 | T | A | 2 | a0001c0001t0003g0007 a0001c0001t0043g0006 |
2 | HG00733.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.51+1583T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180914319 | |||||||
| chr3:180914323 | T | C | 1 | a0001c0001t0007g0081 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.51+1587T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180914323 | |||||||
| chr3:180914338 | T | G | 88 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(85): Show |
88 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.51+1602T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180914338 | |||||||
| chr3:180914406 | C | T | 1 | a0001c0001t0023g0288 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.51+1670C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180914406 | |||||||
| chr3:180914503 | A | G | 1 | a0001c0001t0001g0287 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.51+1767A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180914503 | |||||||
| chr3:180914527 | A | G | 8 | a0001c0001t0004g0082 a0001c0001t0004g0122 a0001c0001t0004g0227 others(5): Show |
8 | HG01074.hp2 HG01258.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+1791A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180914527 | |||||||
| chr3:180914732 | C | A | 1 | a0001c0001t0022g0008 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.51+1996C>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180914732 | |||||||
| chr3:180914845 | A | G | 2 | a0001c0001t0001g0285 a0001c0001t0001g0286 |
2 | NA18946.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.51+2109A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180914845 | |||||||
| chr3:180915008 | C | G | 1 | a0001c0001t0003g0056 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.51+2272C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180915008 | |||||||
| chr3:180915369 | G | T | 2 | a0001c0001t0010g0283 a0001c0001t0010g0284 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.51+2633G>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180915369 | |||||||
| chr3:180915452 | G | A | 1 | a0001c0001t0045g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.51+2716G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180915452 | |||||||
| chr3:180915485 | A | C | 1 | a0001c0001t0002g0282 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.51+2749A>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180915485 | |||||||
| chr3:180915604 | T | G | 1 | a0001c0001t0004g0082 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.51+2868T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180915604 | |||||||
| chr3:180915697 | G | A | 51 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(48): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.51+2961G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180915697 | |||||||
| chr3:180915983 | A | G | 1 | a0001c0001t0003g0055 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.51+3247A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180915983 | |||||||
| chr3:180916639 | G | A | 2 | a0001c0001t0010g0283 a0001c0001t0010g0284 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.51+3903G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180916639 | |||||||
| chr3:180916871 | T | C | 1 | a0001c0001t0045g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.51+4135T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180916871 | |||||||
| chr3:180916991 | C | T | 15 | a0001c0001t0048g0306 a0001c0002t0005g0296 a0001c0002t0005g0298 others(12): Show |
15 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.51+4255C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180916991 | |||||||
| chr3:180917045 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.51+4309A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180917045 | |||||||
| chr3:180917197 | A | G | 3 | a0001c0001t0006g0278 a0001c0001t0006g0279 a0001c0001t0006g0280 |
3 | NA18972.hp2 NA18986.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.51+4461A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180917197 | |||||||
| chr3:180917274 | A | AG | 87 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(84): Show |
87 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.51+4538_51+4539ins others(1): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180917274 | |||||||
| chr3:180917345 | C | A | 1 | a0001c0001t0045g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.51+4609C>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180917345 | |||||||
| chr3:180917520 | T | C | 2 | a0001c0001t0002g0083 a0001c0001t0002g0084 |
2 | HG00408.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.51+4784T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180917520 | |||||||
| chr3:180917686 | T | C | 88 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(85): Show |
88 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.51+4950T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180917686 | |||||||
| chr3:180917787 | A | G | 1 | a0001c0001t0008g0277 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.51+5051A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180917787 | |||||||
| chr3:180917873 | G | A | 1 | a0001c0001t0003g0009 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.51+5137G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180917873 | |||||||
| chr3:180917913 | C | T | 7 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(4): Show |
7 | HG02055.hp1 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.51+5177C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180917913 | |||||||
| chr3:180917947 | C | CA | 40 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(37): Show |
40 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.51+5233dupA | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180917947 | ||||||
| chr3:180917947 | C | CAA | 48 | a0001c0001t0002g0086 a0001c0001t0002g0087 a0001c0001t0002g0088 others(45): Show |
48 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.51+5232_51+5233dup others(2): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180917947 | ||||||
| chr3:180917947 | C | CAAA | 7 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0013 others(4): Show |
7 | HG00673.hp1 HG01978.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+5231_51+5233dup others(3): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180917947 | ||||||
| chr3:180917947 | CAAAA | C | 35 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(32): Show |
35 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.51+5230_51+5233del others(4): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180917947 | ||||||
| chr3:180917948 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.51+5212A>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180917948 | |||||||
| chr3:180918148 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(88): Show |
96 | HG00408.hp1 HG00642.hp2 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.51+5412G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180918148 | |||||||
| chr3:180918151 | C | A | 1 | a0001c0003t0001g0077 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.51+5415C>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180918151 | |||||||
| chr3:180918363 | C | G | 1 | a0001c0001t0027g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.51+5627C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180918363 | |||||||
| chr3:180918375 | C | CAAT | 50 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(47): Show |
50 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.51+5641_51+5643dup others(3): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180918375 | ||||||
| chr3:180918375 | C | CAATAATA others(18): Show |
1 | a0001c0001t0003g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.51+5643_51+5644ins others(25): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180918375 | ||||||
| chr3:180918458 | G | A | 14 | a0001c0001t0002g0086 a0001c0001t0002g0087 a0001c0001t0002g0088 others(11): Show |
14 | HG00140.hp2 HG00280.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.51+5722G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180918458 | |||||||
| chr3:180918530 | T | C | 2 | a0001c0001t0018g0089 a0001c0001t0018g0112 |
2 | HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.51+5794T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180918530 | |||||||
| chr3:180918549 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.51+5813A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180918549 | |||||||
| chr3:180918956 | A | G | 87 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(84): Show |
87 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.51+6220A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180918956 | |||||||
| chr3:180919150 | A | G | 1 | a0001c0001t0016g0015 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.51+6414A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180919150 | |||||||
| chr3:180919179 | A | G | 4 | a0001c0001t0004g0272 a0001c0001t0004g0273 a0001c0001t0004g0274 others(1): Show |
4 | HG00735.hp1 HG01358.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+6443A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180919179 | |||||||
| chr3:180919208 | G | A | 1 | a0001c0001t0003g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.51+6472G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180919208 | |||||||
| chr3:180919242 | T | TA | 6 | a0001c0001t0011g0085 a0001c0001t0011g0102 a0001c0001t0011g0104 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.51+6515dupA | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180919242 | ||||||
| chr3:180919259 | C | A | 2 | a0001c0001t0002g0113 a0001c0001t0002g0186 |
2 | NA19000.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.51+6523C>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180919259 | |||||||
| chr3:180919270 | TA | T | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.51+6535delA | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180919270 | |||||||
| chr3:180919271 | A | T | 1 | a0001c0001t0048g0306 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.51+6535A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180919271 | |||||||
| chr3:180919276 | T | A | 1 | a0001c0001t0002g0187 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.51+6540T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180919276 | |||||||
| chr3:180919282 | A | T | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.51+6546A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180919282 | |||||||
| chr3:180919288 | G | GT | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(88): Show |
96 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.51+6566dupT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180919288 | ||||||
| chr3:180919288 | GT | G | 83 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(80): Show |
83 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.51+6566delT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180919288 | ||||||
| chr3:180919371 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.51+6635G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180919371 | |||||||
| chr3:180919473 | C | T | 36 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(33): Show |
36 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.51+6737C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180919473 | |||||||
| chr3:180919485 | A | G | 1 | a0001c0001t0003g0044 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.51+6749A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180919485 | |||||||
| chr3:180919493 | C | T | 1 | a0001c0001t0004g0268 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.51+6757C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180919493 | |||||||
| chr3:180919503 | C | T | 3 | a0001c0002t0005g0308 a0001c0002t0005g0309 a0001c0002t0005g0310 |
3 | HG01167.hp1 HG01169.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.51+6767C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180919503 | |||||||
| chr3:180919515 | C | A | 16 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(13): Show |
16 | HG01081.hp1 HG01255.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.51+6779C>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180919515 | |||||||
| chr3:180919535 | C | G | 34 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(31): Show |
34 | HG01069.hp1 HG01081.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.51+6799C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180919535 | |||||||
| chr3:180919660 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
187 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.51+6924T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180919660 | |||||||
| chr3:180919877 | A | G | 51 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(48): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.51+7141A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180919877 | |||||||
| chr3:180920116 | G | A | 1 | a0001c0009t0003g0016 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.51+7380G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180920116 | |||||||
| chr3:180920121 | C | T | 1 | a0001c0001t0014g0073 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.51+7385C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180920121 | |||||||
| chr3:180920182 | A | G | 2 | a0001c0001t0018g0089 a0001c0001t0018g0112 |
2 | HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.51+7446A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180920182 | |||||||
| chr3:180920329 | G | A | 2 | a0001c0001t0011g0102 a0003c0005t0011g0103 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.51+7593G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180920329 | |||||||
| chr3:180920508 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.51+7772A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180920508 | |||||||
| chr3:180920517 | C | CT | 14 | a0001c0001t0001g0100 a0001c0001t0001g0183 a0001c0001t0003g0014 others(11): Show |
14 | HG01981.hp2 HG02071.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.51+7799dupT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180920517 | ||||||
| chr3:180920517 | CT | C | 40 | a0001c0001t0001g0091 a0001c0001t0001g0289 a0001c0001t0001g0290 others(37): Show |
40 | HG01069.hp1 HG01081.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.51+7799delT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180920517 | ||||||
| chr3:180920665 | C | A | 1 | a0001c0001t0012g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.51+7929C>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180920665 | |||||||
| chr3:180920703 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(89): Show |
97 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.51+7967G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180920703 | |||||||
| chr3:180920710 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG01081.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.51+7974C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180920710 | |||||||
| chr3:180920757 | T | C | 37 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(34): Show |
37 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.51+8021T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180920757 | |||||||
| chr3:180920860 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(89): Show |
97 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.51+8124A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180920860 | |||||||
| chr3:180920881 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.51+8145A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180920881 | |||||||
| chr3:180921097 | T | C | 88 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(85): Show |
88 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.51+8361T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180921097 | |||||||
| chr3:180921178 | C | T | 1 | a0001c0001t0048g0306 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.51+8442C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180921178 | |||||||
| chr3:180921362 | A | G | 1 | a0001c0001t0003g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.51+8626A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180921362 | |||||||
| chr3:180921372 | T | TA | 73 | a0001c0001t0001g0092 a0001c0001t0001g0127 a0001c0001t0001g0130 others(70): Show |
73 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.51+8653dupA | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180921372 | ||||||
| chr3:180921390 | C | A | 8 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0001c0001t0002g0189 others(5): Show |
8 | HG02135.hp1 HG02148.hp2 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+8654C>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180921390 | |||||||
| chr3:180921392 | T | A | 1 | a0001c0001t0001g0093 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.51+8656T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180921392 | |||||||
| chr3:180921464 | A | G | 51 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(48): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.51+8728A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180921464 | |||||||
| chr3:180921502 | G | A | 2 | a0001c0001t0003g0049 a0001c0001t0003g0050 |
2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.51+8766G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180921502 | |||||||
| chr3:180921549 | G | T | 1 | a0001c0001t0003g0042 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.51+8813G>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180921549 | |||||||
| chr3:180921630 | A | G | 3 | a0001c0001t0003g0041 a0001c0001t0014g0072 a0001c0001t0014g0073 |
3 | HG02572.hp2 NA19077.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.51+8894A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180921630 | |||||||
| chr3:180921631 | T | C | 1 | a0001c0001t0012g0061 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.51+8895T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180921631 | |||||||
| chr3:180921703 | C | G | 2 | a0001c0001t0045g0057 a0001c0001t0049g0058 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.51+8967C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180921703 | |||||||
| chr3:180921703 | C | T | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.51+8967C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180921703 | |||||||
| chr3:180921775 | C | G | 1 | a0001c0001t0003g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.51+9039C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180921775 | |||||||
| chr3:180921813 | A | G | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.51+9077A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180921813 | |||||||
| chr3:180921845 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.51+9109G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180921845 | |||||||
| chr3:180921941 | C | T | 1 | a0001c0001t0012g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.51+9205C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180921941 | |||||||
| chr3:180922031 | T | C | 1 | a0001c0001t0039g0131 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.51+9295T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180922031 | |||||||
| chr3:180922140 | G | A | 16 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(13): Show |
16 | HG01081.hp1 HG01255.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.51+9404G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180922140 | |||||||
| chr3:180922374 | A | G | 1 | a0001c0001t0048g0306 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.51+9638A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180922374 | |||||||
| chr3:180922561 | C | T | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.51+9825C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180922561 | |||||||
| chr3:180922677 | A | G | 1 | a0001c0001t0008g0263 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.51+9941A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180922677 | |||||||
| chr3:180922763 | C | G | 16 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(13): Show |
16 | HG01081.hp1 HG01255.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.51+10027C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180922763 | |||||||
| chr3:180922889 | C | T | 3 | a0001c0001t0010g0080 a0001c0001t0010g0261 a0001c0001t0010g0262 |
3 | HG02717.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.51+10153C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180922889 | |||||||
| chr3:180922993 | A | G | 1 | a0001c0001t0004g0260 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.51+10257A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180922993 | |||||||
| chr3:180923394 | G | A | 1 | a0001c0001t0002g0115 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.52-9940G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180923394 | |||||||
| chr3:180923599 | ATTACT | A | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.52-9728_52-9724del others(5): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180923599 | ||||||
| chr3:180923816 | A | G | 2 | a0001c0001t0009g0070 a0001c0001t0009g0071 |
2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.52-9518A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180923816 | |||||||
| chr3:180923876 | A | G | 87 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(84): Show |
87 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.52-9458A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180923876 | |||||||
| chr3:180924019 | C | T | 51 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(48): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.52-9315C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180924019 | |||||||
| chr3:180924073 | C | T | 4 | a0001c0001t0004g0256 a0001c0001t0004g0257 a0001c0001t0004g0258 others(1): Show |
4 | HG00738.hp2 HG01123.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-9261C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180924073 | |||||||
| chr3:180924106 | G | A | 1 | a0001c0001t0004g0256 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.52-9228G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180924106 | |||||||
| chr3:180924391 | C | T | 16 | a0001c0001t0048g0306 a0001c0002t0005g0295 a0001c0002t0005g0296 others(13): Show |
16 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.52-8943C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180924391 | |||||||
| chr3:180924412 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.52-8922C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180924412 | |||||||
| chr3:180924601 | A | T | 2 | a0001c0001t0018g0089 a0001c0001t0018g0112 |
2 | HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.52-8733A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180924601 | |||||||
| chr3:180924691 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.52-8643C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180924691 | |||||||
| chr3:180924744 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.52-8590G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180924744 | |||||||
| chr3:180925032 | G | A | 5 | a0001c0001t0002g0187 a0001c0001t0002g0195 a0001c0001t0002g0270 others(2): Show |
5 | HG00673.hp2 HG03831.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.52-8302G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180925032 | |||||||
| chr3:180925240 | A | G | 1 | a0001c0001t0002g0255 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.52-8094A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180925240 | |||||||
| chr3:180925276 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(73): Show |
81 | HG00408.hp1 HG00642.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.52-8058G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180925276 | |||||||
| chr3:180925359 | C | CA | 54 | a0001c0001t0002g0083 a0001c0001t0002g0186 a0001c0001t0002g0188 others(51): Show |
54 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.52-7960dupA | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180925359 | ||||||
| chr3:180925377 | A | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
208 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.52-7957A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180925377 | |||||||
| chr3:180925600 | A | G | 1 | a0001c0002t0005g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.52-7734A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180925600 | |||||||
| chr3:180925731 | G | A | 3 | a0001c0001t0014g0072 a0001c0001t0014g0073 a0001c0001t0014g0074 |
3 | HG01081.hp1 HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.52-7603G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180925731 | |||||||
| chr3:180925788 | A | G | 1 | a0001c0001t0045g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.52-7546A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180925788 | |||||||
| chr3:180925799 | C | T | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.52-7535C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180925799 | |||||||
| chr3:180925879 | A | G | 1 | a0001c0003t0001g0077 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.52-7455A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180925879 | |||||||
| chr3:180926116 | T | G | 2 | a0001c0001t0004g0201 a0001c0001t0004g0202 |
2 | HG02132.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.52-7218T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180926116 | |||||||
| chr3:180926194 | C | T | 2 | a0001c0001t0045g0057 a0001c0001t0049g0058 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.52-7140C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180926194 | |||||||
| chr3:180926322 | C | G | 1 | a0001c0001t0006g0254 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.52-7012C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180926322 | |||||||
| chr3:180926460 | A | C | 1 | a0001c0001t0030g0196 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.52-6874A>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180926460 | |||||||
| chr3:180926477 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.52-6857T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180926477 | |||||||
| chr3:180926478 | G | GTA | 16 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0115 others(13): Show |
16 | HG00408.hp2 HG00741.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.52-6828_52-6827dup others(2): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180926478 | ||||||
| chr3:180926478 | G | GTATA | 9 | a0001c0001t0002g0113 a0001c0001t0002g0186 a0001c0001t0002g0208 others(6): Show |
9 | HG00673.hp2 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.52-6830_52-6827dup others(4): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180926478 | ||||||
| chr3:180926478 | GTA | G | 29 | a0001c0001t0001g0269 a0001c0001t0002g0107 a0001c0001t0003g0022 others(26): Show |
29 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.52-6828_52-6827del others(2): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180926478 | ||||||
| chr3:180926478 | GTATA | G | 63 | a0001c0001t0001g0003 a0001c0001t0001g0093 a0001c0001t0001g0097 others(60): Show |
65 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.52-6830_52-6827del others(4): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180926478 | ||||||
| chr3:180926478 | GTATATA | G | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0007g0184 |
3 | HG03669.hp1 NA18962.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.52-6832_52-6827del others(6): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180926478 | ||||||
| chr3:180926495 | TATATA | T | 11 | a0001c0001t0001g0147 a0001c0001t0001g0149 a0001c0001t0001g0174 others(8): Show |
11 | HG02109.hp1 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.52-6838_52-6834del others(5): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180926495 | |||||||
| chr3:180926497 | TATATA | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0091 others(33): Show |
38 | HG00642.hp2 HG00738.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.52-6836_52-6832del others(5): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180926497 | |||||||
| chr3:180926498 | A | T | 1 | a0001c0001t0014g0072 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.52-6836A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180926498 | |||||||
| chr3:180926499 | TATA | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0161 others(10): Show |
14 | HG01934.hp2 HG01952.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.52-6834_52-6832del others(3): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180926499 | |||||||
| chr3:180926499 | TATATA | T | 13 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0099 others(10): Show |
13 | HG02145.hp1 HG02148.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.52-6834_52-6830del others(5): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180926499 | |||||||
| chr3:180926500 | A | T | 6 | a0001c0001t0001g0095 a0001c0001t0001g0185 a0001c0001t0007g0158 others(3): Show |
6 | HG00408.hp1 HG02572.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-6834A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180926500 | |||||||
| chr3:180926501 | TATA | T | 3 | a0001c0001t0001g0177 a0001c0001t0028g0040 a0001c0001t0042g0021 |
3 | HG01070.hp1 HG01167.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.52-6832_52-6830del others(3): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180926501 | |||||||
| chr3:180926502 | A | ATTT | 7 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0070 others(4): Show |
7 | HG01255.hp1 HG01261.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-6831_52-6830ins others(3): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180926502 | ||||||
| chr3:180926502 | A | T | 41 | a0001c0001t0001g0095 a0001c0001t0001g0143 a0001c0001t0001g0147 others(38): Show |
41 | HG00408.hp1 HG00733.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.52-6832A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180926502 | |||||||
| chr3:180926504 | A | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
159 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.52-6830A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180926504 | |||||||
| chr3:180926506 | A | ATATATAT others(8): Show |
1 | a0001c0001t0004g0273 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.52-6827_52-6826ins others(15): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180926506 | ||||||
| chr3:180926506 | A | ATATATAT others(22): Show |
1 | a0001c0001t0004g0272 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.52-6827_52-6826ins others(29): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180926506 | ||||||
| chr3:180926506 | A | ATATATAT others(17): Show |
1 | a0001c0001t0015g0292 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.52-6827_52-6826ins others(24): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180926506 | ||||||
| chr3:180926506 | A | ATATATAT others(3): Show |
2 | a0001c0001t0001g0203 a0001c0001t0007g0204 |
2 | NA19054.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.52-6827_52-6826ins others(10): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180926506 | ||||||
| chr3:180926506 | A | ATATATAT others(15): Show |
2 | a0001c0001t0015g0293 a0001c0001t0015g0294 |
2 | HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.52-6827_52-6826ins others(22): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180926506 | ||||||
| chr3:180926506 | A | ATATATTT others(3): Show |
2 | a0001c0001t0038g0212 a0001c0002t0005g0296 |
2 | HG01433.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.52-6827_52-6826ins others(10): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180926506 | ||||||
| chr3:180926506 | A | ATATT | 5 | a0001c0001t0002g0219 a0001c0001t0010g0261 a0001c0001t0010g0262 others(2): Show |
5 | HG02896.hp2 HG02897.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.52-6827_52-6826ins others(4): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180926506 | ||||||
| chr3:180926506 | A | ATT | 9 | a0001c0001t0002g0116 a0001c0001t0002g0187 a0001c0001t0002g0189 others(6): Show |
9 | HG02148.hp2 NA18962.hp1 NA18983.hp1 others(6): Show |
intron_variant | MODIFIER | c.52-6820_52-6819dup others(2): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180926506 | ||||||
| chr3:180926506 | A | ATTTTT | 6 | a0001c0002t0005g0295 a0001c0002t0005g0300 a0001c0002t0005g0301 others(3): Show |
6 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.52-6823_52-6819dup others(5): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180926506 | ||||||
| chr3:180926506 | A | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
209 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.52-6828A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180926506 | |||||||
| chr3:180926508 | T | A | 5 | a0001c0001t0004g0205 a0001c0001t0006g0213 a0001c0001t0006g0254 others(2): Show |
5 | HG03669.hp2 NA18964.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.52-6826T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180926508 | |||||||
| chr3:180926513 | T | A | 1 | a0001c0001t0006g0279 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.52-6821T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180926513 | |||||||
| chr3:180927196 | A | T | 37 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(34): Show |
37 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.52-6138A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180927196 | |||||||
| chr3:180927249 | A | G | 1 | a0001c0001t0002g0114 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.52-6085A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180927249 | |||||||
| chr3:180927305 | G | A | 1 | a0001c0001t0004g0258 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.52-6029G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180927305 | |||||||
| chr3:180927425 | T | G | 1 | a0001c0001t0023g0221 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.52-5909T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180927425 | |||||||
| chr3:180927442 | C | T | 1 | a0001c0001t0002g0235 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.52-5892C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180927442 | |||||||
| chr3:180927491 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.52-5843A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180927491 | |||||||
| chr3:180928125 | A | AT | 92 | a0001c0001t0002g0107 a0001c0001t0003g0007 a0001c0001t0003g0009 others(89): Show |
92 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.52-5196dupT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180928125 | ||||||
| chr3:180928239 | C | T | 88 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(85): Show |
88 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.52-5095C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180928239 | |||||||
| chr3:180928472 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(89): Show |
97 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.52-4862A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180928472 | |||||||
| chr3:180928479 | G | C | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.52-4855G>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180928479 | |||||||
| chr3:180928604 | A | AT | 15 | a0001c0002t0005g0295 a0001c0002t0005g0296 a0001c0002t0005g0298 others(12): Show |
15 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.52-4724dupT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180928604 | ||||||
| chr3:180928678 | G | T | 1 | a0001c0001t0001g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.52-4656G>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180928678 | |||||||
| chr3:180928681 | A | C | 1 | a0001c0001t0001g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.52-4653A>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180928681 | |||||||
| chr3:180928843 | G | A | 51 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(48): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.52-4491G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180928843 | |||||||
| chr3:180928931 | G | GT | 51 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(48): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.52-4394dupT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180928931 | ||||||
| chr3:180928990 | C | T | 2 | a0001c0001t0045g0057 a0001c0001t0049g0058 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.52-4344C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180928990 | |||||||
| chr3:180929082 | C | A | 1 | a0001c0001t0007g0081 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.52-4252C>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180929082 | |||||||
| chr3:180929180 | C | T | 1 | a0001c0001t0003g0036 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.52-4154C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180929180 | |||||||
| chr3:180929201 | G | A | 1 | a0001c0001t0023g0288 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.52-4133G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180929201 | |||||||
| chr3:180929288 | T | C | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
2 | HG02071.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.52-4046T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180929288 | |||||||
| chr3:180929388 | A | G | 1 | a0001c0001t0034g0152 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.52-3946A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180929388 | |||||||
| chr3:180929475 | T | C | 88 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(85): Show |
88 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.52-3859T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180929475 | |||||||
| chr3:180929573 | C | T | 1 | a0001c0001t0036g0312 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.52-3761C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180929573 | |||||||
| chr3:180929622 | C | T | 51 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(48): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.52-3712C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180929622 | |||||||
| chr3:180929843 | A | G | 5 | a0001c0001t0001g0269 a0001c0001t0004g0121 a0001c0001t0017g0313 others(2): Show |
5 | HG00099.hp1 HG00323.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.52-3491A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180929843 | |||||||
| chr3:180929910 | G | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG01081.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.52-3424G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180929910 | |||||||
| chr3:180929910 | G | C | 1 | a0001c0001t0035g0153 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.52-3424G>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180929910 | |||||||
| chr3:180929974 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(89): Show |
97 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.52-3360A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180929974 | |||||||
| chr3:180930003 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.52-3331C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180930003 | |||||||
| chr3:180930013 | C | T | 1 | a0001c0001t0027g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.52-3321C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180930013 | |||||||
| chr3:180930132 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(88): Show |
96 | HG00408.hp1 HG00642.hp2 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.52-3202G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180930132 | |||||||
| chr3:180930166 | G | A | 1 | a0001c0001t0015g0293 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.52-3168G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180930166 | |||||||
| chr3:180930331 | G | C | 1 | a0001c0001t0001g0127 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.52-3003G>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180930331 | |||||||
| chr3:180930419 | T | A | 1 | a0001c0001t0002g0270 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.52-2915T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180930419 | |||||||
| chr3:180930557 | TGAA | T | 18 | a0001c0001t0001g0001 a0001c0001t0001g0091 a0001c0001t0001g0100 others(15): Show |
19 | HG00738.hp1 HG01081.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.52-2773_52-2771del others(3): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180930557 | ||||||
| chr3:180930582 | G | A | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.52-2752G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180930582 | |||||||
| chr3:180930688 | A | G | 1 | a0001c0001t0004g0120 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.52-2646A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180930688 | |||||||
| chr3:180930894 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(88): Show |
96 | HG00408.hp1 HG00642.hp2 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.52-2440G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180930894 | |||||||
| chr3:180931026 | C | CA | 33 | a0001c0001t0001g0099 a0001c0001t0001g0203 a0001c0001t0002g0083 others(30): Show |
33 | HG00408.hp2 HG00639.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.52-2287dupA | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180931026 | ||||||
| chr3:180931026 | C | CAAAAA | 36 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0013 others(33): Show |
36 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.52-2291_52-2287dup others(5): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180931026 | ||||||
| chr3:180931026 | C | CAAAAAA | 12 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0020 others(9): Show |
12 | HG00673.hp1 HG01261.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.52-2292_52-2287dup others(6): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180931026 | ||||||
| chr3:180931026 | C | CAAAAAAA others(3): Show |
2 | a0001c0003t0001g0077 a0001c0003t0001g0079 |
2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.52-2296_52-2287dup others(10): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180931026 | ||||||
| chr3:180931026 | C | CAAAAAAA others(4): Show |
9 | a0001c0001t0001g0139 a0001c0001t0001g0150 a0001c0001t0001g0159 others(6): Show |
9 | HG01516.hp1 HG02083.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.52-2297_52-2287dup others(11): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180931026 | ||||||
| chr3:180931026 | C | CAAAAAAA others(5): Show |
31 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0092 others(28): Show |
33 | HG00099.hp1 HG00738.hp1 HG01358.hp2 others(30): Show |
intron_variant | MODIFIER | c.52-2298_52-2287dup others(12): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180931026 | ||||||
| chr3:180931026 | C | CAAAAAAA others(6): Show |
22 | a0001c0001t0001g0076 a0001c0001t0001g0129 a0001c0001t0001g0132 others(19): Show |
23 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.52-2299_52-2287dup others(13): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180931026 | ||||||
| chr3:180931026 | C | CAAAAAAA others(7): Show |
12 | a0001c0001t0001g0091 a0001c0001t0001g0097 a0001c0001t0001g0128 others(9): Show |
12 | HG00642.hp2 HG01081.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.52-2300_52-2287dup others(14): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180931026 | ||||||
| chr3:180931026 | C | CAAAAAAA others(8): Show |
10 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0075 others(7): Show |
12 | HG01099.hp2 HG06807.hp2 NA18966.hp2 others(9): Show |
intron_variant | MODIFIER | c.52-2301_52-2287dup others(15): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180931026 | ||||||
| chr3:180931026 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0133 a0001c0001t0002g0114 |
2 | HG00735.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.52-2302_52-2287dup others(16): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180931026 | ||||||
| chr3:180931026 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0039g0131 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.52-2303_52-2287dup others(17): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180931026 | ||||||
| chr3:180931026 | C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0173 a0001c0001t0033g0140 |
2 | HG01109.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.52-2304_52-2287dup others(18): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180931026 | ||||||
| chr3:180931026 | CAAAAAAA others(1): Show |
C | 33 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(30): Show |
33 | HG01069.hp1 HG01081.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.52-2294_52-2287del others(8): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180931026 | ||||||
| chr3:180931048 | G | A | 3 | a0001c0003t0001g0077 a0001c0003t0001g0078 a0001c0003t0001g0079 |
3 | HG02258.hp2 HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.52-2286G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180931048 | |||||||
| chr3:180931257 | C | T | 1 | a0001c0001t0014g0074 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.52-2077C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180931257 | |||||||
| chr3:180931346 | G | C | 1 | a0001c0001t0004g0224 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.52-1988G>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180931346 | |||||||
| chr3:180931438 | C | T | 1 | a0001c0001t0006g0223 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.52-1896C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180931438 | |||||||
| chr3:180931739 | G | GT | 56 | a0001c0001t0001g0185 a0001c0001t0002g0113 a0001c0001t0002g0118 others(53): Show |
56 | HG00408.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.52-1575dupT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180931739 | ||||||
| chr3:180931739 | GT | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.52-1575delT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180931739 | ||||||
| chr3:180931740 | T | G | 2 | a0001c0001t0045g0057 a0001c0001t0049g0058 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.52-1594T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180931740 | |||||||
| chr3:180931741 | T | G | 2 | a0001c0001t0045g0057 a0001c0001t0049g0058 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.52-1593T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180931741 | |||||||
| chr3:180931780 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(89): Show |
97 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.52-1554A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180931780 | |||||||
| chr3:180931807 | T | C | 88 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(85): Show |
88 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.52-1527T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180931807 | |||||||
| chr3:180931808 | A | G | 51 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(48): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.52-1526A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180931808 | |||||||
| chr3:180931854 | C | G | 16 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(13): Show |
16 | HG01081.hp1 HG01255.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.52-1480C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180931854 | |||||||
| chr3:180931931 | G | A | 2 | a0001c0001t0002g0208 a0001c0001t0002g0209 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.52-1403G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180931931 | |||||||
| chr3:180932075 | C | CAAAAAA | 6 | a0001c0001t0001g0160 a0001c0001t0010g0283 a0001c0001t0010g0284 others(3): Show |
6 | HG00639.hp1 HG02080.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-1249_52-1244dup others(6): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180932075 | ||||||
| chr3:180932075 | C | CAAAAAAA | 50 | a0001c0001t0001g0005 a0001c0001t0001g0093 a0001c0001t0001g0098 others(47): Show |
51 | HG00323.hp2 HG00408.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.52-1250_52-1244dup others(7): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180932075 | ||||||
| chr3:180932075 | C | CAAAAAAA others(1): Show |
84 | a0001c0001t0001g0002 a0001c0001t0001g0076 a0001c0001t0001g0092 others(81): Show |
85 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.52-1251_52-1244dup others(8): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180932075 | ||||||
| chr3:180932075 | C | CAAAAAAA others(2): Show |
79 | a0001c0001t0001g0075 a0001c0001t0001g0099 a0001c0001t0001g0144 others(76): Show |
79 | HG00323.hp1 HG00423.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.52-1252_52-1244dup others(9): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180932075 | ||||||
| chr3:180932075 | C | CAAAAAAA others(3): Show |
51 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0091 others(48): Show |
54 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.52-1253_52-1244dup others(10): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180932075 | ||||||
| chr3:180932075 | C | CAAAAAAA others(4): Show |
11 | a0001c0001t0001g0100 a0001c0001t0002g0186 a0001c0001t0002g0192 others(8): Show |
11 | HG00642.hp1 HG02129.hp1 HG03669.hp2 others(8): Show |
intron_variant | MODIFIER | c.52-1254_52-1244dup others(11): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180932075 | ||||||
| chr3:180932075 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0219 |
3 | HG01256.hp1 HG01258.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.52-1255_52-1244dup others(12): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180932075 | ||||||
| chr3:180932075 | CA | C | 14 | a0001c0002t0005g0296 a0001c0002t0005g0298 a0001c0002t0005g0299 others(11): Show |
14 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.52-1244delA | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180932075 | ||||||
| chr3:180932075 | CAAAA | C | 7 | a0001c0001t0002g0111 a0001c0001t0011g0085 a0001c0001t0011g0102 others(4): Show |
7 | HG01069.hp2 HG01071.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.52-1247_52-1244del others(4): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 180932075 | ||||||
| chr3:180932109 | A | G | 1 | a0001c0001t0001g0286 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.52-1225A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180932109 | |||||||
| chr3:180932454 | A | G | 2 | a0001c0001t0006g0213 a0001c0001t0006g0223 |
2 | NA18947.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.52-880A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180932454 | |||||||
| chr3:180932591 | T | C | 1 | a0001c0001t0002g0235 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.52-743T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180932591 | |||||||
| chr3:180932628 | A | G | 1 | a0002c0006t0002g0265 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.52-706A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180932628 | |||||||
| chr3:180932639 | G | A | 2 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.52-695G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180932639 | |||||||
| chr3:180932674 | G | A | 5 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.52-660G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180932674 | |||||||
| chr3:180932878 | T | G | 1 | a0001c0001t0003g0020 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.52-456T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180932878 | |||||||
| chr3:180933085 | G | A | 1 | a0001c0001t0014g0074 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.52-249G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180933085 | |||||||
| chr3:180933174 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
199 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.52-160G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180933174 | |||||||
| chr3:180933269 | A | G | 1 | a0001c0001t0006g0254 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.52-65A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 1/16 | chr3 | 180933269 | |||||||
| chr3:180933881 | C | T | 1 | a0001c0001t0006g0280 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.104+495C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 2/16 | chr3 | 180933881 | |||||||
| chr3:180933935 | C | A | 51 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(48): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.104+549C>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 2/16 | chr3 | 180933935 | |||||||
| chr3:180933961 | A | G | 1 | a0001c0001t0002g0229 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.104+575A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 2/16 | chr3 | 180933961 | |||||||
| chr3:180933978 | T | TG | 10 | a0001c0001t0001g0291 a0001c0001t0002g0118 a0001c0001t0002g0186 others(7): Show |
10 | HG01109.hp2 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.104+599dupG | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 180933978 | ||||||
| chr3:180933978 | TG | T | 86 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(83): Show |
86 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.104+599delG | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 180933978 | ||||||
| chr3:180934067 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.104+681C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 2/16 | chr3 | 180934067 | |||||||
| chr3:180934081 | T | G | 1 | a0001c0001t0003g0031 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.104+695T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 2/16 | chr3 | 180934081 | |||||||
| chr3:180934082 | C | G | 50 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(47): Show |
50 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.104+696C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 2/16 | chr3 | 180934082 | |||||||
| chr3:180934134 | A | G | 1 | a0001c0001t0004g0237 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.104+748A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 2/16 | chr3 | 180934134 | |||||||
| chr3:180934276 | T | A | 1 | a0001c0002t0005g0295 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.105-862T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 2/16 | chr3 | 180934276 | |||||||
| chr3:180934367 | A | T | 2 | a0001c0001t0004g0227 a0001c0001t0004g0268 |
2 | HG01074.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.105-771A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 2/16 | chr3 | 180934367 | |||||||
| chr3:180934545 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.105-593A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 2/16 | chr3 | 180934545 | |||||||
| chr3:180934660 | T | A | 1 | a0001c0001t0045g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.105-478T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 2/16 | chr3 | 180934660 | |||||||
| chr3:180935453 | T | C | 1 | a0001c0001t0004g0225 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.198+222T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180935453 | |||||||
| chr3:180935842 | G | A | 2 | a0001c0001t0003g0017 a0001c0001t0003g0031 |
2 | HG00621.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.198+611G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180935842 | |||||||
| chr3:180935862 | C | T | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
2 | HG02071.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.198+631C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180935862 | |||||||
| chr3:180936306 | C | T | 16 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(13): Show |
16 | HG01081.hp1 HG01255.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.198+1075C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180936306 | |||||||
| chr3:180936355 | CT | C | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.198+1126delT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180936355 | ||||||
| chr3:180936356 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0291 |
2 | HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.198+1125T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180936356 | |||||||
| chr3:180936507 | ATCCGCCC others(3): Show |
A | 2 | a0001c0001t0002g0218 a0001c0001t0002g0311 |
2 | NA18960.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.198+1278_198+1287d others(12): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180936507 | ||||||
| chr3:180936509 | C | G | 1 | a0001c0001t0004g0120 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.198+1278C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180936509 | |||||||
| chr3:180936660 | C | T | 1 | a0001c0001t0004g0228 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.198+1429C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180936660 | |||||||
| chr3:180936668 | A | G | 1 | a0001c0001t0003g0018 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.198+1437A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180936668 | |||||||
| chr3:180936801 | A | G | 1 | a0001c0001t0002g0114 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.198+1570A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180936801 | |||||||
| chr3:180936812 | T | G | 2 | a0001c0001t0002g0083 a0001c0001t0002g0084 |
2 | HG00408.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.198+1581T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180936812 | |||||||
| chr3:180937019 | A | G | 51 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(48): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.198+1788A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180937019 | |||||||
| chr3:180937128 | T | C | 51 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(48): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.198+1897T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180937128 | |||||||
| chr3:180937230 | G | A | 1 | a0001c0001t0003g0018 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.198+1999G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180937230 | |||||||
| chr3:180937349 | T | C | 1 | a0001c0001t0010g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.198+2118T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180937349 | |||||||
| chr3:180938417 | A | G | 14 | a0001c0001t0048g0306 a0001c0002t0005g0296 a0001c0002t0005g0298 others(11): Show |
14 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+3186A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180938417 | |||||||
| chr3:180938484 | A | G | 2 | a0001c0001t0018g0089 a0001c0001t0018g0112 |
2 | HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.198+3253A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180938484 | |||||||
| chr3:180938572 | G | T | 1 | a0001c0001t0048g0306 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.198+3341G>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180938572 | |||||||
| chr3:180938605 | A | G | 33 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(30): Show |
33 | HG01069.hp1 HG01081.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.198+3374A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180938605 | |||||||
| chr3:180938609 | T | C | 7 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(4): Show |
7 | HG01261.hp2 HG02922.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+3378T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180938609 | |||||||
| chr3:180938611 | C | T | 1 | a0001c0001t0010g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.198+3380C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180938611 | |||||||
| chr3:180938676 | G | A | 1 | a0001c0001t0002g0114 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.198+3445G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180938676 | |||||||
| chr3:180938733 | C | T | 1 | a0001c0001t0012g0063 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.198+3502C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180938733 | |||||||
| chr3:180939026 | C | T | 1 | a0001c0001t0003g0018 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.198+3795C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180939026 | |||||||
| chr3:180939049 | A | C | 36 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(33): Show |
36 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.198+3818A>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180939049 | |||||||
| chr3:180939186 | G | T | 15 | a0001c0001t0048g0306 a0001c0002t0005g0296 a0001c0002t0005g0298 others(12): Show |
15 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.198+3955G>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180939186 | |||||||
| chr3:180939219 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.198+3988T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180939219 | |||||||
| chr3:180939265 | G | A | 15 | a0001c0001t0048g0306 a0001c0002t0005g0296 a0001c0002t0005g0298 others(12): Show |
15 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.198+4034G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180939265 | |||||||
| chr3:180939272 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.198+4041G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180939272 | |||||||
| chr3:180939396 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.198+4165A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180939396 | |||||||
| chr3:180939414 | G | C | 1 | a0001c0003t0001g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.198+4183G>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180939414 | |||||||
| chr3:180939429 | G | A | 7 | a0001c0001t0001g0091 a0001c0001t0001g0100 a0001c0001t0001g0133 others(4): Show |
7 | NA18939.hp1 NA18966.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+4198G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180939429 | |||||||
| chr3:180939534 | T | C | 1 | a0001c0001t0001g0285 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.198+4303T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180939534 | |||||||
| chr3:180939559 | A | T | 3 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0239 |
3 | HG00408.hp2 NA18952.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.198+4328A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180939559 | |||||||
| chr3:180939919 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0003g0041 |
2 | NA18980.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.198+4688A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180939919 | |||||||
| chr3:180940045 | C | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(91): Show |
99 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.198+4814C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180940045 | |||||||
| chr3:180940060 | A | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0136 |
2 | NA18966.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.198+4829A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180940060 | |||||||
| chr3:180940092 | C | T | 50 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(47): Show |
50 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.198+4861C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180940092 | |||||||
| chr3:180940388 | T | C | 50 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(47): Show |
50 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.198+5157T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180940388 | |||||||
| chr3:180940514 | C | G | 1 | a0001c0001t0003g0055 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.198+5283C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180940514 | |||||||
| chr3:180940580 | G | GTTTTGTT | 42 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(39): Show |
42 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.198+5353_198+5354i others(9): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180940580 | ||||||
| chr3:180940580 | G | GTTTTGTT others(1): Show |
6 | a0001c0001t0003g0014 a0001c0001t0003g0030 a0001c0001t0003g0055 others(3): Show |
6 | HG01081.hp1 HG02572.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+5353_198+5354i others(10): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180940580 | ||||||
| chr3:180940580 | G | GTTTTGTT others(2): Show |
10 | a0001c0001t0009g0066 a0001c0001t0009g0070 a0001c0001t0009g0071 others(7): Show |
10 | HG01255.hp1 HG02647.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.198+5353_198+5354i others(11): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180940580 | ||||||
| chr3:180940580 | G | GTTTTGTT others(3): Show |
3 | a0001c0001t0009g0062 a0001c0001t0009g0067 a0001c0001t0009g0068 |
3 | HG01261.hp2 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.198+5353_198+5354i others(12): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180940580 | ||||||
| chr3:180940585 | C | CTTTTTTT others(1): Show |
13 | a0001c0001t0048g0306 a0001c0002t0005g0296 a0001c0002t0005g0299 others(10): Show |
13 | HG01069.hp1 HG01169.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.198+5357_198+5364d others(10): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180940585 | ||||||
| chr3:180940585 | C | T | 68 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(65): Show |
68 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.198+5354C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180940585 | |||||||
| chr3:180940662 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.198+5431C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180940662 | |||||||
| chr3:180940756 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
187 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.198+5525G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180940756 | |||||||
| chr3:180940764 | C | T | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.198+5533C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180940764 | |||||||
| chr3:180940951 | G | T | 1 | a0001c0001t0002g0191 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.198+5720G>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180940951 | |||||||
| chr3:180940983 | T | C | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.198+5752T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180940983 | |||||||
| chr3:180941060 | G | A | 2 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.198+5829G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180941060 | |||||||
| chr3:180941098 | G | A | 1 | a0001c0001t0008g0263 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.198+5867G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180941098 | |||||||
| chr3:180941178 | AT | A | 35 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(32): Show |
35 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.198+5960delT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180941178 | ||||||
| chr3:180941441 | C | A | 14 | a0001c0002t0005g0296 a0001c0002t0005g0298 a0001c0002t0005g0299 others(11): Show |
14 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+6210C>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180941441 | |||||||
| chr3:180941609 | A | T | 15 | a0001c0001t0048g0306 a0001c0002t0005g0296 a0001c0002t0005g0298 others(12): Show |
15 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.199-6256A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180941609 | |||||||
| chr3:180941755 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.199-6110A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180941755 | |||||||
| chr3:180942117 | A | G | 85 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(82): Show |
85 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.199-5748A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180942117 | |||||||
| chr3:180942221 | A | T | 2 | a0001c0001t0002g0214 a0001c0001t0002g0216 |
2 | HG02129.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.199-5644A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180942221 | |||||||
| chr3:180942303 | C | T | 5 | a0001c0001t0012g0059 a0001c0001t0012g0060 a0001c0001t0012g0061 others(2): Show |
5 | HG01255.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-5562C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180942303 | |||||||
| chr3:180942367 | G | A | 50 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(47): Show |
50 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.199-5498G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180942367 | |||||||
| chr3:180942377 | C | CA | 96 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0095 others(93): Show |
96 | HG00408.hp1 HG00408.hp2 HG00735.hp2 others(93): Show |
intron_variant | MODIFIER | c.199-5460dupA | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180942377 | ||||||
| chr3:180942377 | C | CAA | 55 | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0001t0001g0100 others(52): Show |
56 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.199-5461_199-5460d others(4): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180942377 | ||||||
| chr3:180942377 | C | CAAA | 23 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0002g0229 others(20): Show |
23 | HG00423.hp1 HG00621.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-5462_199-5460d others(5): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180942377 | ||||||
| chr3:180942377 | C | CAAAA | 7 | a0001c0001t0002g0219 a0001c0001t0002g0222 a0001c0001t0003g0007 others(4): Show |
7 | HG00639.hp2 HG00733.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-5463_199-5460d others(6): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180942377 | ||||||
| chr3:180942377 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0009g0067 a0001c0001t0009g0068 |
2 | HG01261.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.199-5470_199-5460d others(13): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180942377 | ||||||
| chr3:180942377 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0026g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.199-5471_199-5460d others(14): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180942377 | ||||||
| chr3:180942377 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0012g0060 a0001c0001t0012g0063 a0001c0001t0012g0069 |
3 | HG02647.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.199-5472_199-5460d others(15): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180942377 | ||||||
| chr3:180942377 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0009g0066 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.199-5479_199-5460d others(22): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180942377 | ||||||
| chr3:180942377 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0012g0059 a0001c0001t0012g0061 |
2 | HG01255.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.199-5469_199-5460d others(12): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180942377 | ||||||
| chr3:180942377 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0014g0072 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.199-5475_199-5460d others(18): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180942377 | ||||||
| chr3:180942640 | A | G | 1 | a0001c0001t0004g0274 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.199-5225A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180942640 | |||||||
| chr3:180942658 | T | C | 1 | a0001c0001t0036g0312 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.199-5207T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180942658 | |||||||
| chr3:180942787 | G | A | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 |
3 | HG02109.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.199-5078G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180942787 | |||||||
| chr3:180942815 | C | G | 1 | a0001c0001t0004g0226 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.199-5050C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180942815 | |||||||
| chr3:180942990 | T | C | 87 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(84): Show |
87 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.199-4875T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180942990 | |||||||
| chr3:180943018 | G | A | 1 | a0001c0001t0014g0074 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.199-4847G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180943018 | |||||||
| chr3:180943076 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.199-4789C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180943076 | |||||||
| chr3:180943156 | G | A | 1 | a0001c0001t0009g0067 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.199-4709G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180943156 | |||||||
| chr3:180943262 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.199-4603C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180943262 | |||||||
| chr3:180943265 | C | CT | 43 | a0001c0001t0001g0100 a0001c0001t0001g0135 a0001c0001t0001g0136 others(40): Show |
43 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.199-4573dupT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180943265 | ||||||
| chr3:180943265 | C | CTT | 11 | a0001c0001t0001g0138 a0001c0001t0003g0009 a0001c0001t0003g0011 others(8): Show |
11 | HG00673.hp1 HG00741.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.199-4574_199-4573d others(4): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180943265 | ||||||
| chr3:180943265 | CT | C | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(185): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.199-4573delT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180943265 | ||||||
| chr3:180943265 | CTT | C | 10 | a0001c0001t0001g0151 a0001c0001t0004g0201 a0001c0001t0004g0258 others(7): Show |
10 | HG00738.hp2 HG01943.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.199-4574_199-4573d others(4): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180943265 | ||||||
| chr3:180943267 | T | C | 1 | a0001c0001t0004g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.199-4598T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180943267 | |||||||
| chr3:180943432 | A | G | 1 | a0001c0002t0005g0307 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.199-4433A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180943432 | |||||||
| chr3:180943439 | G | C | 37 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(34): Show |
37 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.199-4426G>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180943439 | |||||||
| chr3:180943792 | G | T | 1 | a0001c0001t0001g0127 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.199-4073G>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180943792 | |||||||
| chr3:180943905 | T | C | 1 | a0001c0001t0004g0228 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.199-3960T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180943905 | |||||||
| chr3:180943977 | C | G | 1 | a0001c0001t0006g0279 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.199-3888C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180943977 | |||||||
| chr3:180943978 | G | C | 1 | a0001c0001t0006g0279 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.199-3887G>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180943978 | |||||||
| chr3:180943985 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0145 |
2 | NA18982.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.199-3880C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180943985 | |||||||
| chr3:180944048 | C | A | 4 | a0001c0001t0002g0214 a0001c0001t0002g0216 a0001c0001t0002g0233 others(1): Show |
4 | HG02129.hp1 HG02523.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-3817C>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180944048 | |||||||
| chr3:180944096 | A | G | 1 | a0001c0001t0004g0202 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.199-3769A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180944096 | |||||||
| chr3:180944204 | C | T | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.199-3661C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180944204 | |||||||
| chr3:180944230 | A | T | 2 | a0001c0001t0045g0057 a0001c0001t0049g0058 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.199-3635A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180944230 | |||||||
| chr3:180944326 | CT | C | 86 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(83): Show |
86 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.199-3527delT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180944326 | ||||||
| chr3:180944351 | C | T | 37 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(34): Show |
37 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.199-3514C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180944351 | |||||||
| chr3:180944368 | T | G | 1 | a0001c0001t0002g0215 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.199-3497T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180944368 | |||||||
| chr3:180944499 | A | T | 49 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(46): Show |
49 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.199-3366A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180944499 | |||||||
| chr3:180944521 | C | T | 1 | a0001c0001t0006g0279 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.199-3344C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180944521 | |||||||
| chr3:180944522 | T | C | 1 | a0001c0001t0006g0279 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.199-3343T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180944522 | |||||||
| chr3:180944682 | A | C | 3 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0042 |
3 | HG02071.hp2 HG02083.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.199-3183A>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180944682 | |||||||
| chr3:180944804 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0291 |
2 | HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.199-3061A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180944804 | |||||||
| chr3:180944834 | G | A | 1 | a0001c0001t0010g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.199-3031G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180944834 | |||||||
| chr3:180944843 | G | A | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.199-3022G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180944843 | |||||||
| chr3:180944902 | C | T | 16 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(13): Show |
16 | HG01081.hp1 HG01255.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.199-2963C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180944902 | |||||||
| chr3:180944984 | G | C | 2 | a0001c0001t0045g0057 a0001c0001t0049g0058 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.199-2881G>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180944984 | |||||||
| chr3:180945340 | T | C | 2 | a0001c0001t0001g0285 a0001c0001t0001g0286 |
2 | NA18946.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.199-2525T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180945340 | |||||||
| chr3:180945415 | T | C | 2 | a0001c0001t0004g0274 a0001c0001t0004g0275 |
2 | HG01358.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.199-2450T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180945415 | |||||||
| chr3:180945417 | T | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0091 others(50): Show |
55 | HG00099.hp1 HG00408.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.199-2448T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180945417 | |||||||
| chr3:180945620 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.199-2245G>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180945620 | |||||||
| chr3:180945646 | G | A | 1 | a0001c0001t0010g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.199-2219G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180945646 | |||||||
| chr3:180945651 | C | T | 2 | a0001c0001t0045g0057 a0001c0001t0049g0058 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.199-2214C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180945651 | |||||||
| chr3:180945788 | A | T | 1 | a0001c0001t0002g0311 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.199-2077A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180945788 | |||||||
| chr3:180945883 | TGTTTGAG others(9): Show |
T | 87 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(84): Show |
87 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.199-1950_199-1935d others(18): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 180945883 | ||||||
| chr3:180946254 | A | G | 87 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(84): Show |
87 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.199-1611A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180946254 | |||||||
| chr3:180946307 | C | G | 2 | a0001c0001t0020g0126 a0001c0001t0020g0267 |
2 | NA18967.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.199-1558C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180946307 | |||||||
| chr3:180946374 | A | G | 50 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(47): Show |
50 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.199-1491A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180946374 | |||||||
| chr3:180946495 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.199-1370C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180946495 | |||||||
| chr3:180946543 | G | A | 3 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 |
3 | HG00423.hp1 NA18964.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.199-1322G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180946543 | |||||||
| chr3:180946882 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
5 | HG00738.hp1 HG01358.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-983C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180946882 | |||||||
| chr3:180947020 | T | C | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 |
3 | HG02109.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.199-845T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180947020 | |||||||
| chr3:180947062 | T | C | 1 | a0001c0001t0006g0230 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.199-803T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180947062 | |||||||
| chr3:180947191 | G | A | 1 | a0001c0001t0003g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.199-674G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180947191 | |||||||
| chr3:180947311 | T | C | 2 | a0001c0001t0002g0187 a0001c0001t0030g0196 |
2 | HG03831.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.199-554T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180947311 | |||||||
| chr3:180947343 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.199-522G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180947343 | |||||||
| chr3:180947397 | T | C | 5 | a0001c0001t0012g0059 a0001c0001t0012g0060 a0001c0001t0012g0061 others(2): Show |
5 | HG01255.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-468T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180947397 | |||||||
| chr3:180947457 | A | G | 16 | a0001c0001t0048g0306 a0001c0002t0005g0295 a0001c0002t0005g0296 others(13): Show |
16 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.199-408A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180947457 | |||||||
| chr3:180947623 | G | A | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.199-242G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180947623 | |||||||
| chr3:180947798 | A | G | 1 | a0001c0001t0004g0242 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.199-67A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180947798 | |||||||
| chr3:180947826 | T | C | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.199-39T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 3/16 | chr3 | 180947826 | |||||||
| chr3:180948154 | G | A | 87 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(84): Show |
87 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.271-193G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 4/16 | chr3 | 180948154 | |||||||
| chr3:180948252 | T | G | 1 | a0001c0001t0001g0164 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.271-95T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 4/16 | chr3 | 180948252 | |||||||
| chr3:180948279 | T | G | 2 | a0001c0001t0003g0007 a0001c0001t0043g0006 |
2 | HG00733.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.271-68T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 4/16 | chr3 | 180948279 | |||||||
| chr3:180948702 | TAA | T | 18 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(15): Show |
18 | HG01081.hp1 HG01255.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.420-17_420-16delAA | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 180948702 | ||||||
| chr3:180949173 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.514-54G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 6/16 | chr3 | 180949173 | |||||||
| chr3:180949373 | C | T | 6 | a0001c0001t0001g0203 a0001c0001t0007g0081 a0001c0001t0007g0101 others(3): Show |
6 | NA18962.hp2 NA18968.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.630+30C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 7/16 | chr3 | 180949373 | |||||||
| chr3:180949510 | C | T | 3 | a0001c0001t0009g0066 a0001c0001t0009g0070 a0001c0001t0009g0071 |
3 | HG02922.hp1 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.630+167C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 7/16 | chr3 | 180949510 | |||||||
| chr3:180949633 | C | T | 1 | a0001c0001t0002g0189 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.630+290C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 7/16 | chr3 | 180949633 | |||||||
| chr3:180949698 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.630+355T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 7/16 | chr3 | 180949698 | |||||||
| chr3:180949770 | C | T | 37 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(34): Show |
37 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.630+427C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 7/16 | chr3 | 180949770 | |||||||
| chr3:180949771 | G | A | 1 | a0001c0001t0004g0257 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.630+428G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 7/16 | chr3 | 180949771 | |||||||
| chr3:180949777 | C | G | 87 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(84): Show |
87 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.630+434C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 7/16 | chr3 | 180949777 | |||||||
| chr3:180949857 | A | G | 1 | a0001c0001t0012g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.630+514A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 7/16 | chr3 | 180949857 | |||||||
| chr3:180949885 | A | G | 15 | a0001c0002t0005g0295 a0001c0002t0005g0296 a0001c0002t0005g0298 others(12): Show |
15 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.630+542A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 7/16 | chr3 | 180949885 | |||||||
| chr3:180950090 | C | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.630+747C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 7/16 | chr3 | 180950090 | |||||||
| chr3:180950323 | C | G | 49 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(46): Show |
49 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.631-975C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 7/16 | chr3 | 180950323 | |||||||
| chr3:180950586 | A | G | 1 | a0001c0001t0004g0225 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.631-712A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 7/16 | chr3 | 180950586 | |||||||
| chr3:180950644 | C | G | 1 | a0001c0001t0023g0288 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.631-654C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 7/16 | chr3 | 180950644 | |||||||
| chr3:180950934 | C | T | 35 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(32): Show |
35 | HG01069.hp1 HG01081.hp1 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.631-364C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 7/16 | chr3 | 180950934 | |||||||
| chr3:180950935 | G | A | 1 | a0001c0001t0003g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.631-363G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 7/16 | chr3 | 180950935 | |||||||
| chr3:180950937 | G | A | 1 | a0001c0001t0048g0306 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.631-361G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 7/16 | chr3 | 180950937 | |||||||
| chr3:180950990 | A | G | 34 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(31): Show |
34 | HG01069.hp1 HG01081.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.631-308A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 7/16 | chr3 | 180950990 | |||||||
| chr3:180951231 | C | A | 1 | a0001c0001t0001g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.631-67C>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 7/16 | chr3 | 180951231 | |||||||
| chr3:180951584 | A | G | 1 | a0001c0001t0012g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.801+116A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/16 | chr3 | 180951584 | |||||||
| chr3:180951741 | A | C | 1 | a0001c0001t0004g0238 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.801+273A>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/16 | chr3 | 180951741 | |||||||
| chr3:180951760 | A | AT | 16 | a0001c0001t0048g0306 a0001c0002t0005g0295 a0001c0002t0005g0296 others(13): Show |
16 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.801+299dupT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 180951760 | ||||||
| chr3:180951791 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.801+323C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/16 | chr3 | 180951791 | |||||||
| chr3:180951837 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.801+369G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/16 | chr3 | 180951837 | |||||||
| chr3:180951950 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.801+482C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/16 | chr3 | 180951950 | |||||||
| chr3:180951953 | G | C | 8 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0001c0001t0002g0189 others(5): Show |
8 | HG02135.hp1 HG02148.hp2 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.801+485G>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/16 | chr3 | 180951953 | |||||||
| chr3:180952047 | T | A | 37 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(34): Show |
37 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.801+579T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/16 | chr3 | 180952047 | |||||||
| chr3:180952447 | G | T | 87 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(84): Show |
87 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.801+979G>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/16 | chr3 | 180952447 | |||||||
| chr3:180952575 | GA | G | 35 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(32): Show |
35 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.801+1119delA | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 180952575 | ||||||
| chr3:180952576 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.801+1108A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/16 | chr3 | 180952576 | |||||||
| chr3:180952810 | T | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
183 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.802-952T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/16 | chr3 | 180952810 | |||||||
| chr3:180952828 | C | CT | 8 | a0001c0001t0001g0133 a0001c0001t0002g0211 a0001c0001t0003g0054 others(5): Show |
8 | HG02717.hp2 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.802-914dupT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 180952828 | ||||||
| chr3:180952828 | CT | C | 13 | a0001c0001t0001g0176 a0001c0001t0001g0285 a0001c0001t0002g0231 others(10): Show |
13 | HG00639.hp1 HG00733.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.802-914delT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 180952828 | ||||||
| chr3:180952828 | CTT | C | 72 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0011 others(69): Show |
72 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.802-915_802-914del others(2): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 180952828 | ||||||
| chr3:180952931 | C | T | 37 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(34): Show |
37 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.802-831C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/16 | chr3 | 180952931 | |||||||
| chr3:180953097 | C | T | 1 | a0001c0001t0045g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.802-665C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/16 | chr3 | 180953097 | |||||||
| chr3:180953531 | T | C | 1 | a0001c0001t0003g0019 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.802-231T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/16 | chr3 | 180953531 | |||||||
| chr3:180953569 | T | C | 1 | a0001c0001t0037g0032 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.802-193T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 8/16 | chr3 | 180953569 | |||||||
| chr3:180953892 | A | T | 2 | a0001c0001t0002g0218 a0001c0001t0002g0311 |
2 | NA18960.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.880+52A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180953892 | |||||||
| chr3:180953971 | T | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0130 |
3 | NA18991.hp2 NA19064.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.880+131T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180953971 | |||||||
| chr3:180954185 | C | T | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.880+345C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180954185 | |||||||
| chr3:180954215 | G | C | 1 | a0001c0001t0002g0216 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.880+375G>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180954215 | |||||||
| chr3:180954331 | T | G | 1 | a0001c0001t0002g0115 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.880+491T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180954331 | |||||||
| chr3:180954334 | T | G | 1 | a0001c0001t0002g0114 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.880+494T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180954334 | |||||||
| chr3:180954696 | G | T | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.880+856G>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180954696 | |||||||
| chr3:180954872 | A | AT | 55 | a0001c0001t0001g0162 a0001c0001t0002g0190 a0001c0001t0002g0282 others(52): Show |
55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.880+1054dupT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 180954872 | ||||||
| chr3:180954872 | A | ATT | 21 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0027 others(18): Show |
21 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.880+1053_880+1054d others(4): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 180954872 | ||||||
| chr3:180954872 | AT | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0076 others(97): Show |
103 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.880+1054delT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 180954872 | ||||||
| chr3:180954926 | T | C | 1 | a0001c0001t0003g0045 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.880+1086T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180954926 | |||||||
| chr3:180954987 | A | AT | 7 | a0001c0001t0001g0098 a0001c0001t0001g0165 a0001c0001t0002g0215 others(4): Show |
7 | HG01167.hp2 HG01981.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.880+1165dupT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 180954987 | ||||||
| chr3:180954987 | A | ATT | 43 | a0001c0001t0003g0007 a0001c0001t0003g0011 a0001c0001t0003g0013 others(40): Show |
43 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.880+1164_880+1165d others(4): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 180954987 | ||||||
| chr3:180955042 | G | C | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.880+1202G>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180955042 | |||||||
| chr3:180955139 | C | T | 50 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(47): Show |
50 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.880+1299C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180955139 | |||||||
| chr3:180955201 | G | A | 1 | a0001c0001t0003g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.880+1361G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180955201 | |||||||
| chr3:180955237 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.880+1397G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180955237 | |||||||
| chr3:180955289 | G | A | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.880+1449G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180955289 | |||||||
| chr3:180955368 | A | G | 1 | a0001c0001t0004g0120 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.880+1528A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180955368 | |||||||
| chr3:180955405 | A | G | 4 | a0001c0001t0002g0087 a0001c0001t0002g0088 a0001c0001t0002g0107 others(1): Show |
4 | HG00140.hp2 HG01255.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.880+1565A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180955405 | |||||||
| chr3:180955427 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.880+1587A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180955427 | |||||||
| chr3:180955566 | T | C | 87 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(84): Show |
87 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.880+1726T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180955566 | |||||||
| chr3:180955633 | T | C | 7 | a0001c0001t0002g0086 a0001c0001t0002g0087 a0001c0001t0002g0088 others(4): Show |
7 | HG00140.hp2 HG00280.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.880+1793T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180955633 | |||||||
| chr3:180955680 | A | C | 16 | a0001c0001t0048g0306 a0001c0002t0005g0295 a0001c0002t0005g0296 others(13): Show |
16 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.880+1840A>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180955680 | |||||||
| chr3:180955725 | G | A | 2 | a0001c0001t0045g0057 a0001c0001t0049g0058 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.880+1885G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180955725 | |||||||
| chr3:180955989 | A | G | 1 | a0001c0001t0013g0245 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.881-1830A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180955989 | |||||||
| chr3:180956148 | C | T | 50 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(47): Show |
50 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.881-1671C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180956148 | |||||||
| chr3:180956167 | G | C | 1 | a0001c0001t0048g0306 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.881-1652G>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180956167 | |||||||
| chr3:180956174 | C | G | 50 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(47): Show |
50 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.881-1645C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180956174 | |||||||
| chr3:180956345 | C | G | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.881-1474C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180956345 | |||||||
| chr3:180956512 | G | T | 2 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.881-1307G>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180956512 | |||||||
| chr3:180956671 | G | A | 1 | a0001c0001t0004g0121 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.881-1148G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180956671 | |||||||
| chr3:180956803 | T | A | 1 | a0001c0001t0008g0263 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.881-1016T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180956803 | |||||||
| chr3:180956870 | G | A | 5 | a0001c0002t0005g0295 a0001c0002t0005g0301 a0001c0002t0005g0302 others(2): Show |
5 | HG01069.hp1 HG02451.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.881-949G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180956870 | |||||||
| chr3:180957036 | A | T | 1 | a0001c0001t0001g0147 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.881-783A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180957036 | |||||||
| chr3:180957191 | G | GA | 87 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(84): Show |
87 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.881-625dupA | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 180957191 | ||||||
| chr3:180957281 | T | C | 1 | a0001c0001t0026g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.881-538T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180957281 | |||||||
| chr3:180957426 | T | C | 8 | a0001c0001t0001g0091 a0001c0001t0001g0100 a0001c0001t0001g0133 others(5): Show |
8 | HG02647.hp2 NA18939.hp1 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.881-393T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180957426 | |||||||
| chr3:180957602 | A | G | 1 | a0001c0001t0014g0073 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.881-217A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 9/16 | chr3 | 180957602 | |||||||
| chr3:180957964 | G | T | 1 | a0001c0001t0013g0250 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.990+36G>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180957964 | |||||||
| chr3:180958017 | T | A | 1 | a0001c0001t0046g0197 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.990+89T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180958017 | |||||||
| chr3:180958031 | C | G | 2 | a0001c0001t0045g0057 a0001c0001t0049g0058 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.990+103C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180958031 | |||||||
| chr3:180958359 | A | G | 3 | a0001c0002t0005g0298 a0001c0002t0005g0300 a0001c0002t0005g0304 |
3 | HG02451.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.990+431A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180958359 | |||||||
| chr3:180958367 | T | G | 3 | a0001c0001t0004g0119 a0001c0001t0004g0123 a0001c0001t0004g0253 |
3 | NA18966.hp1 NA18982.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.990+439T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180958367 | |||||||
| chr3:180958637 | G | A | 1 | a0001c0001t0003g0022 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.990+709G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180958637 | |||||||
| chr3:180958725 | T | C | 1 | a0002c0006t0002g0265 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.990+797T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180958725 | |||||||
| chr3:180958804 | C | CT | 16 | a0001c0001t0001g0075 a0001c0001t0002g0087 a0001c0001t0002g0113 others(13): Show |
16 | HG00423.hp1 HG01361.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.990+894dupT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr3 | 180958804 | ||||||
| chr3:180958831 | C | T | 16 | a0001c0001t0048g0306 a0001c0002t0005g0295 a0001c0002t0005g0296 others(13): Show |
16 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.990+903C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180958831 | |||||||
| chr3:180958841 | C | G | 1 | a0001c0001t0002g0231 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.990+913C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180958841 | |||||||
| chr3:180958853 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.990+925G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180958853 | |||||||
| chr3:180958973 | A | G | 1 | a0001c0001t0003g0034 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.990+1045A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180958973 | |||||||
| chr3:180959046 | T | C | 16 | a0001c0001t0048g0306 a0001c0002t0005g0295 a0001c0002t0005g0296 others(13): Show |
16 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.990+1118T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180959046 | |||||||
| chr3:180959136 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.990+1208C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180959136 | |||||||
| chr3:180959350 | G | GT | 50 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(47): Show |
50 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.990+1433dupT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr3 | 180959350 | ||||||
| chr3:180959576 | C | T | 1 | a0001c0001t0002g0255 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.990+1648C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180959576 | |||||||
| chr3:180959692 | T | A | 1 | a0001c0001t0001g0151 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.990+1764T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180959692 | |||||||
| chr3:180959763 | A | G | 1 | a0001c0001t0003g0007 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.991-1705A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180959763 | |||||||
| chr3:180960276 | C | T | 1 | a0001c0001t0006g0213 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.991-1192C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180960276 | |||||||
| chr3:180960733 | A | G | 1 | a0001c0001t0014g0074 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.991-735A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180960733 | |||||||
| chr3:180960818 | A | G | 1 | a0001c0001t0026g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.991-650A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180960818 | |||||||
| chr3:180960919 | A | G | 1 | a0001c0001t0002g0113 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.991-549A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180960919 | |||||||
| chr3:180960933 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.991-535A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180960933 | |||||||
| chr3:180961104 | G | A | 2 | a0001c0001t0045g0057 a0001c0001t0049g0058 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.991-364G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180961104 | |||||||
| chr3:180961177 | A | G | 49 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(46): Show |
49 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.991-291A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180961177 | |||||||
| chr3:180961339 | C | CA | 23 | a0001c0001t0001g0169 a0001c0001t0002g0113 a0001c0001t0002g0115 others(20): Show |
23 | HG00621.hp1 HG00673.hp2 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.991-101dupA | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr3 | 180961339 | ||||||
| chr3:180961355 | AAAAAAAA others(6): Show |
A | 31 | a0001c0001t0002g0255 a0001c0001t0009g0062 a0001c0001t0009g0066 others(28): Show |
31 | HG01069.hp1 HG01081.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.991-112_991-100del others(13): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180961355 | |||||||
| chr3:180961355 | AAAAAAAA others(8): Show |
A | 2 | a0001c0001t0015g0292 a0001c0001t0015g0293 |
2 | HG00639.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.991-112_991-98delA others(14): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180961355 | |||||||
| chr3:180961356 | AAAAAAAA others(5): Show |
A | 4 | a0001c0001t0012g0059 a0001c0001t0012g0060 a0001c0001t0012g0061 others(1): Show |
4 | HG01255.hp1 HG02647.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-111_991-100del others(12): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180961356 | |||||||
| chr3:180961357 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0012g0063 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.991-110_991-100del others(11): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180961357 | |||||||
| chr3:180961366 | AAG | A | 6 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0180 others(3): Show |
6 | HG01081.hp2 HG02818.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.991-101_991-100del others(2): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180961366 | |||||||
| chr3:180961367 | AG | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
121 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.991-99delG | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr3 | 180961367 | ||||||
| chr3:180961368 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0075 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.991-100G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180961368 | |||||||
| chr3:180961383 | GCC | G | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.991-84_991-83delCC | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 10/16 | chr3 | 180961383 | |||||||
| chr3:180961586 | T | C | 1 | a0001c0001t0004g0274 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1077+32T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 11/16 | chr3 | 180961586 | |||||||
| chr3:180961865 | A | C | 10 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(7): Show |
10 | HG02109.hp1 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1077+311A>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 11/16 | chr3 | 180961865 | |||||||
| chr3:180962148 | C | T | 2 | a0001c0001t0045g0057 a0001c0001t0049g0058 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1077+594C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 11/16 | chr3 | 180962148 | |||||||
| chr3:180962188 | G | A | 2 | a0001c0001t0018g0089 a0001c0001t0018g0112 |
2 | HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1077+634G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 11/16 | chr3 | 180962188 | |||||||
| chr3:180962225 | G | C | 8 | a0001c0001t0004g0082 a0001c0001t0004g0122 a0001c0001t0004g0227 others(5): Show |
8 | HG01074.hp2 HG01258.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1078-658G>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 11/16 | chr3 | 180962225 | |||||||
| chr3:180962351 | G | A | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1078-532G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 11/16 | chr3 | 180962351 | |||||||
| chr3:180962354 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1078-529C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 11/16 | chr3 | 180962354 | |||||||
| chr3:180962599 | T | C | 3 | a0001c0003t0001g0077 a0001c0003t0001g0078 a0001c0003t0001g0079 |
3 | HG02258.hp2 HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1078-284T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 11/16 | chr3 | 180962599 | |||||||
| chr3:180962755 | C | A | 1 | a0001c0001t0004g0225 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1078-128C>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 11/16 | chr3 | 180962755 | |||||||
| chr3:180962855 | G | A | 1 | a0001c0001t0002g0195 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1078-28G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 11/16 | chr3 | 180962855 | |||||||
| chr3:180963101 | A | AT | 11 | a0001c0001t0001g0092 a0001c0001t0001g0164 a0001c0001t0001g0276 others(8): Show |
11 | HG00639.hp1 HG01081.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1198+29dupT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180963101 | ||||||
| chr3:180963101 | AT | A | 20 | a0001c0001t0002g0115 a0001c0001t0003g0049 a0001c0001t0004g0082 others(17): Show |
20 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.1198+29delT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180963101 | ||||||
| chr3:180963315 | C | A | 1 | a0001c0001t0048g0306 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1198+225C>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180963315 | |||||||
| chr3:180963523 | C | T | 7 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(4): Show |
7 | HG01261.hp2 HG02922.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1198+433C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180963523 | |||||||
| chr3:180963681 | A | G | 1 | a0001c0001t0004g0275 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1198+591A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180963681 | |||||||
| chr3:180963882 | CTCTT | C | 51 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(48): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1198+794_1198+797d others(6): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180963882 | ||||||
| chr3:180963951 | C | T | 1 | a0001c0001t0004g0236 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1198+861C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180963951 | |||||||
| chr3:180964060 | T | C | 1 | a0001c0002t0005g0296 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1198+970T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180964060 | |||||||
| chr3:180964133 | T | C | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1198+1043T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180964133 | |||||||
| chr3:180964597 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(75): Show |
83 | HG00408.hp1 HG00642.hp2 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.1198+1507G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180964597 | |||||||
| chr3:180964673 | T | TTA | 18 | a0001c0001t0001g0075 a0001c0001t0001g0127 a0001c0001t0001g0149 others(15): Show |
18 | HG00733.hp1 HG00735.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1198+1610_1198+161 others(6): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180964673 | ||||||
| chr3:180964673 | T | TTATA | 6 | a0001c0001t0001g0076 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
6 | HG01981.hp1 HG02071.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.1198+1608_1198+161 others(8): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180964673 | ||||||
| chr3:180964673 | T | TTATATAT others(1): Show |
7 | a0001c0002t0005g0300 a0001c0002t0005g0304 a0001c0002t0005g0305 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1198+1604_1198+161 others(12): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180964673 | ||||||
| chr3:180964673 | T | TTATATAT others(3): Show |
1 | a0001c0002t0005g0298 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1198+1602_1198+161 others(14): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180964673 | ||||||
| chr3:180964673 | T | TTATATAT others(5): Show |
1 | a0001c0001t0048g0306 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1198+1600_1198+161 others(16): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180964673 | ||||||
| chr3:180964673 | T | TTATATAT others(7): Show |
2 | a0001c0002t0005g0299 a0001c0002t0005g0301 |
2 | HG01069.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1198+1598_1198+161 others(18): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180964673 | ||||||
| chr3:180964673 | T | TTATATAT others(9): Show |
7 | a0001c0001t0012g0059 a0001c0001t0012g0061 a0001c0001t0012g0069 others(4): Show |
7 | HG01255.hp1 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1198+1596_1198+161 others(20): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180964673 | ||||||
| chr3:180964673 | T | TTATATAT others(11): Show |
1 | a0001c0001t0003g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1198+1594_1198+161 others(22): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180964673 | ||||||
| chr3:180964673 | T | TTATATAT others(13): Show |
4 | a0001c0001t0014g0073 a0001c0001t0014g0074 a0001c0001t0029g0064 others(1): Show |
4 | HG01081.hp1 HG01433.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198+1592_1198+161 others(24): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180964673 | ||||||
| chr3:180964673 | T | TTATATAT others(17): Show |
1 | a0001c0001t0014g0072 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1198+1588_1198+161 others(28): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180964673 | ||||||
| chr3:180964673 | T | TTATATAT others(19): Show |
2 | a0001c0001t0009g0070 a0001c0001t0049g0058 |
2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1198+1586_1198+161 others(30): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180964673 | ||||||
| chr3:180964673 | T | TTATATAT others(21): Show |
2 | a0001c0001t0009g0071 a0001c0001t0012g0063 |
2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1198+1584_1198+161 others(32): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180964673 | ||||||
| chr3:180964673 | T | TTATATAT others(23): Show |
1 | a0001c0001t0012g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1198+1611_1198+161 others(34): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180964673 | ||||||
| chr3:180964673 | T | TTTTATAT others(17): Show |
1 | a0001c0001t0026g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1198+1584_1198+158 others(28): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180964673 | ||||||
| chr3:180964673 | T | TTTTATAT others(21): Show |
4 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(1): Show |
4 | HG01261.hp2 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198+1584_1198+158 others(32): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180964673 | ||||||
| chr3:180964673 | TTA | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0091 others(113): Show |
119 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1198+1610_1198+161 others(6): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180964673 | ||||||
| chr3:180964673 | TTATATA | T | 49 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(46): Show |
49 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1198+1606_1198+161 others(10): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180964673 | ||||||
| chr3:180964829 | G | A | 1 | a0001c0001t0002g0188 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1198+1739G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180964829 | |||||||
| chr3:180964871 | G | A | 1 | a0001c0001t0010g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1198+1781G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180964871 | |||||||
| chr3:180964918 | T | C | 1 | a0001c0001t0002g0114 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1198+1828T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180964918 | |||||||
| chr3:180965031 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1198+1941T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180965031 | |||||||
| chr3:180965097 | A | G | 37 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(34): Show |
37 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.1198+2007A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180965097 | |||||||
| chr3:180965264 | C | G | 1 | a0001c0002t0005g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1198+2174C>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180965264 | |||||||
| chr3:180965310 | G | A | 3 | a0001c0001t0015g0292 a0001c0001t0015g0293 a0001c0001t0015g0294 |
3 | HG00639.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1198+2220G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180965310 | |||||||
| chr3:180965341 | A | T | 1 | a0001c0001t0048g0306 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1198+2251A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180965341 | |||||||
| chr3:180965473 | A | G | 2 | a0001c0001t0001g0142 a0001c0001t0033g0140 |
2 | HG01109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1198+2383A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180965473 | |||||||
| chr3:180965480 | TTTA | T | 51 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(48): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1198+2395_1198+239 others(7): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 180965480 | ||||||
| chr3:180965577 | C | T | 4 | a0001c0001t0004g0121 a0001c0001t0017g0313 a0001c0001t0017g0314 others(1): Show |
4 | HG00323.hp2 HG01256.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.1199-2474C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180965577 | |||||||
| chr3:180965780 | A | G | 1 | a0001c0001t0002g0117 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1199-2271A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180965780 | |||||||
| chr3:180965803 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1199-2248G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180965803 | |||||||
| chr3:180965811 | C | T | 2 | a0001c0001t0003g0017 a0001c0001t0003g0031 |
2 | HG00621.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1199-2240C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180965811 | |||||||
| chr3:180966095 | T | G | 2 | a0001c0001t0020g0126 a0001c0001t0020g0267 |
2 | NA18967.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1199-1956T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180966095 | |||||||
| chr3:180966097 | T | C | 1 | a0001c0001t0002g0211 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1199-1954T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180966097 | |||||||
| chr3:180966308 | T | A | 2 | a0001c0001t0003g0049 a0001c0001t0003g0050 |
2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1199-1743T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180966308 | |||||||
| chr3:180966368 | C | T | 15 | a0001c0002t0005g0295 a0001c0002t0005g0296 a0001c0002t0005g0298 others(12): Show |
15 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1199-1683C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180966368 | |||||||
| chr3:180966547 | G | A | 1 | a0001c0001t0003g0022 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1199-1504G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180966547 | |||||||
| chr3:180966730 | C | T | 2 | a0001c0001t0002g0218 a0001c0001t0002g0311 |
2 | NA18960.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1199-1321C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180966730 | |||||||
| chr3:180966826 | C | T | 1 | a0001c0002t0005g0295 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1199-1225C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180966826 | |||||||
| chr3:180966903 | A | T | 1 | a0001c0001t0023g0288 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1199-1148A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180966903 | |||||||
| chr3:180967269 | T | G | 1 | a0001c0001t0040g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1199-782T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180967269 | |||||||
| chr3:180967318 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1199-733C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180967318 | |||||||
| chr3:180967376 | T | C | 2 | a0001c0001t0045g0057 a0001c0001t0049g0058 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1199-675T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180967376 | |||||||
| chr3:180967588 | A | G | 1 | a0001c0001t0021g0012 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1199-463A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180967588 | |||||||
| chr3:180967601 | T | C | 2 | a0001c0001t0018g0089 a0001c0001t0018g0112 |
2 | HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1199-450T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180967601 | |||||||
| chr3:180967665 | T | A | 1 | a0001c0001t0003g0019 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1199-386T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180967665 | |||||||
| chr3:180968028 | T | C | 1 | a0001c0001t0002g0114 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1199-23T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 13/16 | chr3 | 180968028 | |||||||
| chr3:180968577 | T | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
254 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1402+323T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 14/16 | chr3 | 180968577 | |||||||
| chr3:180968583 | G | A | 2 | a0001c0001t0045g0057 a0001c0001t0049g0058 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1402+329G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 14/16 | chr3 | 180968583 | |||||||
| chr3:180968601 | G | C | 34 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(31): Show |
34 | HG01069.hp1 HG01081.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.1402+347G>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 14/16 | chr3 | 180968601 | |||||||
| chr3:180968679 | A | G | 1 | a0001c0001t0035g0153 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1402+425A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 14/16 | chr3 | 180968679 | |||||||
| chr3:180968700 | AC | A | 3 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0042 |
3 | HG02071.hp2 HG02083.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1402+447delC | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 14/16 | chr3 | 180968700 | |||||||
| chr3:180968984 | G | A | 1 | a0001c0001t0002g0210 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1402+730G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 14/16 | chr3 | 180968984 | |||||||
| chr3:180969131 | CTTTG | C | 51 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(48): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1402+885_1402+888d others(6): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 180969131 | ||||||
| chr3:180969495 | C | T | 1 | a0001c0001t0045g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1403-663C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 14/16 | chr3 | 180969495 | |||||||
| chr3:180969747 | G | A | 2 | a0001c0001t0045g0057 a0001c0001t0049g0058 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1403-411G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 14/16 | chr3 | 180969747 | |||||||
| chr3:180969748 | A | T | 2 | a0001c0001t0045g0057 a0001c0001t0049g0058 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1403-410A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 14/16 | chr3 | 180969748 | |||||||
| chr3:180969809 | T | A | 50 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(47): Show |
50 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.1403-349T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 14/16 | chr3 | 180969809 | |||||||
| chr3:180969810 | T | A | 51 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(48): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1403-348T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 14/16 | chr3 | 180969810 | |||||||
| chr3:180969850 | C | T | 1 | a0001c0001t0049g0058 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1403-308C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 14/16 | chr3 | 180969850 | |||||||
| chr3:180969873 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1403-285A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 14/16 | chr3 | 180969873 | |||||||
| chr3:180969902 | C | T | 1 | a0001c0001t0003g0014 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1403-256C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 14/16 | chr3 | 180969902 | |||||||
| chr3:180970383 | A | AAT | 32 | a0001c0001t0001g0144 a0001c0001t0001g0169 a0001c0001t0001g0177 others(29): Show |
32 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1603+63_1603+64dup others(2): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180970383 | ||||||
| chr3:180970383 | A | AATAT | 11 | a0001c0001t0001g0203 a0001c0001t0001g0281 a0001c0001t0002g0108 others(8): Show |
11 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1603+61_1603+64dup others(4): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180970383 | ||||||
| chr3:180970383 | A | AATATAT | 9 | a0001c0001t0001g0151 a0001c0001t0002g0113 a0001c0001t0002g0270 others(6): Show |
9 | HG00741.hp2 HG01943.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.1603+59_1603+64dup others(6): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180970383 | ||||||
| chr3:180970383 | A | AATATATA others(1): Show |
3 | a0001c0001t0001g0127 a0001c0001t0001g0171 a0001c0001t0003g0007 |
3 | HG00733.hp2 HG03669.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1603+57_1603+64dup others(8): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180970383 | ||||||
| chr3:180970383 | A | AATATATA others(3): Show |
8 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0141 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1603+55_1603+64dup others(10): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180970383 | ||||||
| chr3:180970383 | A | AATATATA others(5): Show |
2 | a0001c0001t0009g0062 a0001c0001t0010g0080 |
2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1603+53_1603+64dup others(12): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180970383 | ||||||
| chr3:180970383 | A | AATATATA others(7): Show |
3 | a0001c0001t0001g0132 a0001c0001t0001g0146 a0001c0001t0001g0173 |
3 | HG01109.hp1 HG02027.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1603+51_1603+64dup others(14): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180970383 | ||||||
| chr3:180970383 | A | AATATATA others(9): Show |
2 | a0001c0001t0003g0034 a0001c0001t0018g0089 |
2 | HG01074.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1603+49_1603+64dup others(16): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180970383 | ||||||
| chr3:180970383 | A | AATATATA others(11): Show |
1 | a0001c0001t0004g0121 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1603+47_1603+64dup others(18): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180970383 | ||||||
| chr3:180970383 | A | AATATATA others(13): Show |
1 | a0001c0001t0002g0186 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1603+45_1603+64dup others(20): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180970383 | ||||||
| chr3:180970383 | AAT | A | 70 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0001t0001g0097 others(67): Show |
71 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1603+63_1603+64del others(2): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180970383 | ||||||
| chr3:180970383 | AATAT | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(98): Show |
103 | HG00408.hp2 HG00423.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.1603+61_1603+64del others(4): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180970383 | ||||||
| chr3:180970383 | AATATAT | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0172 a0001c0001t0002g0117 others(8): Show |
11 | HG01069.hp1 HG01099.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.1603+59_1603+64del others(6): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180970383 | ||||||
| chr3:180970383 | AATATATA others(1): Show |
A | 3 | a0001c0001t0008g0243 a0001c0001t0008g0271 a0001c0001t0010g0283 |
3 | HG03195.hp2 NA18946.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1603+57_1603+64del others(8): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180970383 | ||||||
| chr3:180970383 | AATATATA others(3): Show |
A | 3 | a0001c0001t0001g0269 a0001c0001t0010g0284 a0001c0003t0001g0077 |
3 | HG00099.hp1 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1603+55_1603+64del others(10): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180970383 | ||||||
| chr3:180970383 | AATATATA others(9): Show |
A | 1 | a0001c0001t0048g0306 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1603+49_1603+64del others(16): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180970383 | ||||||
| chr3:180970602 | A | T | 1 | a0001c0001t0001g0097 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1603+244A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180970602 | |||||||
| chr3:180970659 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1603+301C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180970659 | |||||||
| chr3:180970727 | A | T | 1 | a0001c0001t0037g0032 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1603+369A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180970727 | |||||||
| chr3:180971083 | G | GA | 5 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0171 others(2): Show |
5 | HG01261.hp2 HG02080.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1603+733dupA | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180971083 | ||||||
| chr3:180971209 | C | CA | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
184 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.1603+851_1603+852i others(3): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180971209 | |||||||
| chr3:180971260 | T | A | 16 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(13): Show |
16 | HG01081.hp1 HG01255.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.1603+902T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180971260 | |||||||
| chr3:180971364 | T | A | 1 | a0001c0001t0001g0129 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1603+1006T>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180971364 | |||||||
| chr3:180971721 | ATACT | A | 44 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0113 others(41): Show |
44 | HG00408.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1603+1370_1603+137 others(8): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180971721 | ||||||
| chr3:180971970 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1603+1612G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180971970 | |||||||
| chr3:180972040 | A | T | 8 | a0001c0002t0005g0298 a0001c0002t0005g0300 a0001c0002t0005g0304 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1603+1682A>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180972040 | |||||||
| chr3:180972394 | C | T | 16 | a0001c0001t0048g0306 a0001c0002t0005g0295 a0001c0002t0005g0296 others(13): Show |
16 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1603+2036C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180972394 | |||||||
| chr3:180972433 | G | A | 1 | a0001c0001t0034g0152 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1603+2075G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180972433 | |||||||
| chr3:180972449 | G | C | 1 | a0001c0001t0023g0288 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1603+2091G>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180972449 | |||||||
| chr3:180972464 | G | A | 1 | a0001c0009t0003g0016 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1603+2106G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180972464 | |||||||
| chr3:180972467 | T | C | 13 | a0001c0001t0004g0201 a0001c0001t0004g0202 a0001c0001t0004g0224 others(10): Show |
13 | HG00423.hp2 HG00621.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.1603+2109T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180972467 | |||||||
| chr3:180972585 | A | G | 1 | a0001c0001t0002g0219 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1603+2227A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180972585 | |||||||
| chr3:180972675 | T | C | 1 | a0001c0001t0004g0082 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1603+2317T>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180972675 | |||||||
| chr3:180973214 | G | A | 2 | a0001c0001t0022g0008 a0001c0001t0022g0043 |
2 | HG03927.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1604-2099G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180973214 | |||||||
| chr3:180973304 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
188 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1604-2009G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180973304 | |||||||
| chr3:180973333 | A | AG | 85 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(82): Show |
85 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.1604-1979dupG | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180973333 | ||||||
| chr3:180973542 | C | T | 16 | a0001c0001t0048g0306 a0001c0002t0005g0295 a0001c0002t0005g0296 others(13): Show |
16 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1604-1771C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180973542 | |||||||
| chr3:180973628 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1604-1685A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180973628 | |||||||
| chr3:180973873 | G | A | 34 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(31): Show |
34 | HG01069.hp1 HG01081.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.1604-1440G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180973873 | |||||||
| chr3:180974053 | T | G | 1 | a0001c0001t0001g0147 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1604-1260T>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180974053 | |||||||
| chr3:180974064 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1604-1249G>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180974064 | |||||||
| chr3:180974160 | C | CT | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1604-1138dupT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180974160 | ||||||
| chr3:180974160 | C | CTT | 10 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0210 others(7): Show |
10 | HG00408.hp2 HG02135.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1604-1139_1604-113 others(6): Show |
FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 180974160 | ||||||
| chr3:180974316 | C | T | 2 | a0001c0001t0010g0261 a0001c0001t0010g0262 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1604-997C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180974316 | |||||||
| chr3:180974438 | C | T | 1 | a0001c0001t0048g0306 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1604-875C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180974438 | |||||||
| chr3:180974548 | G | C | 16 | a0001c0001t0009g0062 a0001c0001t0009g0066 a0001c0001t0009g0067 others(13): Show |
16 | HG01081.hp1 HG01255.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.1604-765G>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180974548 | |||||||
| chr3:180974948 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1604-365C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 15/16 | chr3 | 180974948 | |||||||
| chr3:180975427 | G | GT | 81 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(78): Show |
81 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.1695+37dupT | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 180975427 | ||||||
| chr3:180975519 | A | G | 1 | a0001c0001t0002g0270 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1695+115A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 16/16 | chr3 | 180975519 | |||||||
| chr3:180975716 | C | T | 51 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(48): Show |
51 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1695+312C>T | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 16/16 | chr3 | 180975716 | |||||||
| chr3:180975952 | G | C | 3 | a0001c0001t0003g0009 a0001c0001t0003g0013 a0001c0001t0003g0034 |
3 | HG00741.hp2 HG01074.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1696-170G>C | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 16/16 | chr3 | 180975952 | |||||||
| chr3:180975986 | G | A | 1 | a0001c0001t0014g0074 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1696-136G>A | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 16/16 | chr3 | 180975986 | |||||||
| chr3:180976025 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1696-97A>G | FXR1 | ENSG00000114416.19 | transcript | ENST00000357559.9 | protein_coding | 16/16 | chr3 | 180976025 |