Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84188 |
| ensemblid | ENSG00000197601.14 |
| hgncid | 26222 |
| symbol | FAR1 |
| name | fatty acyl-CoA reductase 1 |
| refseq_nuc | NM_032228.6 |
| refseq_prot | NP_115604.1 |
| ensembl_nuc | ENST00000354817.8 |
| ensembl_prot | ENSP00000346874.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 13668668 |
| end | 13732346 |
| strand | + |
| ver | v1.2 |
| region | chr11:13668668-13732346 |
| region5000 | chr11:13663668-13737346 |
| regionname0 | FAR1_chr11_13668668_13732346 |
| regionname5000 | FAR1_chr11_13663668_13737346 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 515 | 351 | 90 | 59 | 140 | 16 | 44 | 108 | FAR1_chr11_13663668_13737346 | FAR1 | MVSIP others(510): Show |
chr11 | 13663668 | 13737346 |
| a0002 | 0/0 | 515 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | MVSIP others(510): Show |
chr11 | 13663668 | 13737346 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1545 | 345 | 90 | 59 | 137 | 16 | 41 | FAR1_chr11_13663668_13737346 | FAR1 | ATGGT others(1540): Show |
chr11 | 13663668 | 13737346 | ||
| a0001c0002 | 0/0 | 1545 | 2 | 0 | 0 | 0 | 0 | 2 | FAR1_chr11_13663668_13737346 | FAR1 | ATGGT others(1540): Show |
chr11 | 13663668 | 13737346 | ||
| a0001c0004 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | ATGGT others(1540): Show |
chr11 | 13663668 | 13737346 | ||
| a0001c0005 | 0/0 | 1545 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | ATGGT others(1540): Show |
chr11 | 13663668 | 13737346 | ||
| a0001c0006 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | ATGGT others(1540): Show |
chr11 | 13663668 | 13737346 | ||
| a0001c0007 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | ATGGT others(1540): Show |
chr11 | 13663668 | 13737346 | ||
| a0002c0003 | 0/0 | 1545 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | ATGGT others(1540): Show |
chr11 | 13663668 | 13737346 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5266 | 95 | 14 | 16 | 50 | 4 | 10 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5261): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0002 | 0/1 | 5266 | 84 | 12 | 10 | 47 | 4 | 10 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5261): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0003 | 0/0 | 5265 | 83 | 28 | 16 | 26 | 5 | 8 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5260): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0004 | 0/0 | 5261 | 31 | 4 | 7 | 8 | 2 | 10 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5256): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0005 | 0/0 | 5260 | 9 | 8 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5255): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0006 | 0/0 | 5264 | 5 | 5 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5259): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0007 | 0/0 | 5265 | 4 | 4 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5260): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0008 | 0/0 | 5260 | 4 | 2 | 2 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5255): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0009 | 0/0 | 5268 | 3 | 2 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5263): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0011 | 0/0 | 5260 | 3 | 3 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5255): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0012 | 0/0 | 5265 | 3 | 0 | 0 | 3 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5260): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0013 | 0/0 | 5265 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5260): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0014 | 0/0 | 5266 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5261): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0015 | 0/0 | 5265 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5260): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0016 | 0/0 | 5266 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5261): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0017 | 0/0 | 5265 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5260): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0018 | 0/0 | 5261 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5256): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0019 | 0/0 | 5266 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5261): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0020 | 0/0 | 5266 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5261): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0021 | 0/0 | 5266 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5261): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0022 | 0/0 | 5264 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5259): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0023 | 0/0 | 5266 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5261): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0024 | 0/0 | 5265 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5260): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0025 | 0/0 | 5265 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5260): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0026 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5260): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0027 | 0/0 | 5265 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5260): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0028 | 0/0 | 5264 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5259): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0029 | 0/0 | 5266 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5261): Show |
chr11 | 13663668 | 13737346 |
| a0001c0001t0030 | 0/0 | 5266 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5261): Show |
chr11 | 13663668 | 13737346 |
| a0001c0002t0010 | 0/0 | 5261 | 2 | 0 | 0 | 0 | 0 | 2 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5256): Show |
chr11 | 13663668 | 13737346 |
| a0001c0004t0001 | 0/0 | 5266 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5261): Show |
chr11 | 13663668 | 13737346 |
| a0001c0005t0003 | 0/0 | 5265 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5260): Show |
chr11 | 13663668 | 13737346 |
| a0001c0006t0002 | 0/0 | 5266 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5261): Show |
chr11 | 13663668 | 13737346 |
| a0001c0007t0002 | 0/0 | 5266 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5261): Show |
chr11 | 13663668 | 13737346 |
| a0002c0003t0010 | 0/0 | 5261 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | GCCAC others(5256): Show |
chr11 | 13663668 | 13737346 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 4 | 1 | 0 | 2 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0005 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0008 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0005g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0006g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0007g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0008g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0008g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0008g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0008g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0009g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0009g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0011g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0011g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0011g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0012g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0012g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0012g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0013g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0013g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0014g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0014g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0015g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0015g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0016g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0017g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0018g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0019g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0020g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0021g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0022g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0023g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0024g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0025g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0026g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0027g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0028g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0029g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0001t0030g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0002t0010g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0002t0010g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0004t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0005t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0006t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0001c0007t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| a0002c0003t0010g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0196 | EUR | GBR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00280 | hp1 | a0001 | c0001 | t0009 | g0235 | EUR | FIN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0174 | EUR | FIN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | FIN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00558 | hp2 | a0001 | c0006 | t0002 | g0010 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00639 | hp1 | a0001 | c0001 | t0027 | g0051 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00642 | hp1 | a0002 | c0003 | t0010 | g0035 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0266 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00735 | hp1 | a0001 | c0001 | t0008 | g0203 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01069 | hp1 | a0001 | c0001 | t0021 | g0011 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01069 | hp2 | a0001 | c0001 | t0029 | g0158 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0261 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0282 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01106 | hp1 | a0001 | c0001 | t0016 | g0010 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0273 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0243 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0280 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0263 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0275 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0201 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0229 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01255 | hp1 | a0001 | c0001 | t0024 | g0194 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0193 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01261 | hp1 | a0001 | c0001 | t0019 | g0007 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01261 | hp2 | a0001 | c0001 | t0018 | g0278 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01358 | hp1 | a0001 | c0001 | t0023 | g0075 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0269 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0033 | EUR | IBS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0028 | EUR | IBS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0008 | EUR | IBS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0028 | EUR | IBS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0033 | EUR | IBS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0287 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0253 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0244 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02055 | hp2 | a0001 | c0001 | t0014 | g0149 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0179 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CDX | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CDX | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02257 | hp1 | a0001 | c0001 | t0013 | g0184 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0284 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0248 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0192 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0180 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0032 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0177 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0239 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0246 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02630 | hp2 | a0001 | c0001 | t0009 | g0240 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0198 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0262 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02717 | hp1 | a0001 | c0001 | t0011 | g0260 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0285 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02738 | hp1 | a0001 | c0002 | t0010 | g0183 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0276 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0039 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02818 | hp2 | a0001 | c0001 | t0014 | g0090 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02886 | hp1 | a0001 | c0001 | t0015 | g0233 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0277 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0040 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0249 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0259 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0274 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02897 | hp2 | a0001 | c0001 | t0011 | g0257 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0202 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0181 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0250 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0242 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0085 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0254 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0270 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0286 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0245 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0238 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03540 | hp2 | a0001 | c0001 | t0015 | g0234 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0236 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0283 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0222 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03834 | hp1 | a0001 | c0002 | t0010 | g0035 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0197 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0264 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0237 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03942 | hp2 | a0001 | c0001 | t0030 | g0084 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0258 | SAS | STU | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0272 | SAS | STU | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG04184 | hp1 | a0001 | c0001 | t0025 | g0199 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0020 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0255 | SAS | STU | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0112 | SAS | STU | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0032 | SAS | STU | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0268 | SAS | STU | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | STU | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | YRI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | YRI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | CHB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0252 | AFR | YRI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18946 | hp2 | a0001 | c0001 | t0017 | g0210 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0279 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18967 | hp1 | a0001 | c0007 | t0002 | g0148 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18969 | hp1 | a0001 | c0001 | t0022 | g0208 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18974 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18982 | hp2 | a0001 | c0001 | t0012 | g0067 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18984 | hp2 | a0001 | c0001 | t0012 | g0120 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19002 | hp2 | a0001 | c0001 | t0020 | g0048 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0217 | AFR | LWK | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | LWK | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0251 | AFR | LWK | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | LWK | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | YRI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA20129 | hp1 | a0001 | c0001 | t0028 | g0050 | AFR | ASW | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0228 | AFR | ASW | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0111 | EUR | TSI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0191 | EUR | TSI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | TSI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | GIH | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA20905 | hp2 | a0001 | c0005 | t0003 | g0247 | SAS | GIH | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02109 | hp1 | a0001 | c0001 | t0026 | g0186 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0182 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0204 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18955 | hp1 | a0001 | c0001 | t0012 | g0125 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | USA | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | USA | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA21309 | hp1 | a0001 | c0001 | t0013 | g0185 | AFR | LWK | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | LWK | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0071 | REF | REF | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0049 | REF | REF | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:13700413 | G | A | 1 | a0002 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.286G>A | p.Glu96Lys | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/12 | 432/5266 | 286/1548 | 96/515 | chr11 | 13700413 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:13710702 | T | C | 1 | a0001c0004 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.555T>C | p.Asp185Asp | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 5/12 | 701/5266 | 555/1548 | 185/515 | chr11 | 13710702 | |||
| chr11:13712020 | G | A | 1 | a0001c0005 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.861G>A | p.Ala287Ala | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 7/12 | 1007/5266 | 861/1548 | 287/515 | chr11 | 13712020 | |||
| chr11:13712987 | T | C | 1 | a0001c0006 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.909T>C | p.Tyr303Tyr | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/12 | 1055/5266 | 909/1548 | 303/515 | chr11 | 13712987 | |||
| chr11:13713008 | T | C | 2 | a0001c0002 a0002c0003 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
synonymous_variant | LOW | c.930T>C | p.Thr310Thr | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/12 | 1076/5266 | 930/1548 | 310/515 | chr11 | 13713008 | |||
| chr11:13728708 | C | T | 1 | a0001c0007 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.1482C>T | p.Tyr494Tyr | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 1628/5266 | 1482/1548 | 494/515 | chr11 | 13728708 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:13668733 | A | G | 1 | a0001c0001t0030 | 1 | HG03942.hp2 | 5_prime_UTR_variant | MODIFIER | c.-81A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/12 | 26033 | chr11 | 13668733 | ||||||
| chr11:13668752 | C | CGCA | 1 | a0001c0001t0009 | 3 | HG00280.hp1 HG02622.hp2 HG02630.hp2 |
5_prime_UTR_variant | MODIFIER | c.-59_-57dupAGC | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/12 | 26008 | INFO_REALIGN_3_PRIME | chr11 | 13668752 | |||||
| chr11:13668773 | A | T | 1 | a0001c0001t0029 | 1 | HG01069.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-41A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/12 | chr11 | 13668773 | |||||||
| chr11:13728803 | A | G | 1 | a0001c0001t0015 | 2 | HG02886.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*29A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 29 | chr11 | 13728803 | ||||||
| chr11:13729044 | A | G | 2 | a0001c0001t0027 a0001c0001t0028 |
2 | HG00639.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*270A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 270 | chr11 | 13729044 | ||||||
| chr11:13729074 | G | A | 1 | a0001c0001t0016 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*300G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 300 | chr11 | 13729074 | ||||||
| chr11:13729328 | TCTC | T | 2 | a0001c0002t0010 a0002c0003t0010 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*555_*557delCTC | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 555 | chr11 | 13729328 | ||||||
| chr11:13729334 | TTTTC | T | 1 | a0001c0001t0008 | 4 | HG00735.hp1 HG01243.hp1 HG02486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*564_*567delCTTT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 564 | INFO_REALIGN_3_PRIME | chr11 | 13729334 | |||||
| chr11:13729354 | G | A | 2 | a0001c0001t0006 a0001c0001t0007 |
9 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*580G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 580 | chr11 | 13729354 | ||||||
| chr11:13729399 | A | C | 1 | a0001c0001t0026 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*625A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 625 | chr11 | 13729399 | ||||||
| chr11:13729414 | T | C | 1 | a0001c0001t0013 | 2 | HG02257.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*640T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 640 | chr11 | 13729414 | ||||||
| chr11:13729433 | G | A | 1 | a0001c0001t0017 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*659G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 659 | chr11 | 13729433 | ||||||
| chr11:13729841 | T | C | 1 | a0001c0001t0011 | 3 | HG02717.hp1 HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1067T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 1067 | chr11 | 13729841 | ||||||
| chr11:13729919 | G | A | 1 | a0001c0001t0018 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1145G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 1145 | chr11 | 13729919 | ||||||
| chr11:13729958 | A | G | 28 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(25): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
3_prime_UTR_variant | MODIFIER | c.*1184A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 1184 | chr11 | 13729958 | ||||||
| chr11:13730228 | ACTTT | A | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0011 others(1): Show |
44 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1459_*1462delCTTT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 1459 | INFO_REALIGN_3_PRIME | chr11 | 13730228 | |||||
| chr11:13730459 | G | A | 1 | a0001c0001t0019 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1685G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 1685 | chr11 | 13730459 | ||||||
| chr11:13730555 | C | T | 1 | a0001c0001t0021 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1781C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 1781 | chr11 | 13730555 | ||||||
| chr11:13730812 | A | T | 1 | a0001c0001t0025 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2038A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 2038 | chr11 | 13730812 | ||||||
| chr11:13731010 | G | C | 1 | a0001c0001t0015 | 2 | HG02886.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2236G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 2236 | chr11 | 13731010 | ||||||
| chr11:13731059 | T | G | 1 | a0001c0001t0008 | 4 | HG00735.hp1 HG01243.hp1 HG02486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2285T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 2285 | chr11 | 13731059 | ||||||
| chr11:13731550 | T | C | 1 | a0001c0001t0014 | 2 | HG02055.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2776T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 2776 | chr11 | 13731550 | ||||||
| chr11:13731830 | A | G | 1 | a0001c0001t0024 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3056A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 3056 | chr11 | 13731830 | ||||||
| chr11:13731939 | G | A | 1 | a0001c0001t0020 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3165G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 3165 | chr11 | 13731939 | ||||||
| chr11:13731988 | C | G | 1 | a0001c0001t0023 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3214C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 3214 | chr11 | 13731988 | ||||||
| chr11:13732070 | A | G | 1 | a0001c0001t0008 | 4 | HG00735.hp1 HG01243.hp1 HG02486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3296A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 3296 | chr11 | 13732070 | ||||||
| chr11:13732125 | TA | T | 14 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(11): Show |
135 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*3363delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 3363 | INFO_REALIGN_3_PRIME | chr11 | 13732125 | |||||
| chr11:13732125 | TAA | T | 8 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(5): Show |
26 | HG00642.hp1 HG00735.hp1 HG01243.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3362_*3363delAA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 3362 | INFO_REALIGN_3_PRIME | chr11 | 13732125 | |||||
| chr11:13732329 | A | C | 1 | a0001c0001t0013 | 2 | HG02257.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3555A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 3555 | chr11 | 13732329 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:13668887 | G | C | 1 | a0001c0001t0004g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8+81G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13668887 | |||||||
| chr11:13668901 | G | C | 1 | a0001c0001t0003g0038 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8+95G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13668901 | |||||||
| chr11:13668938 | C | A | 1 | a0001c0001t0001g0013 | 2 | HG00438.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.-8+132C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13668938 | |||||||
| chr11:13668943 | G | T | 1 | a0001c0001t0001g0288 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-8+137G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13668943 | |||||||
| chr11:13668983 | G | A | 3 | a0001c0001t0006g0009 a0001c0001t0006g0039 a0001c0001t0006g0040 |
5 | HG02809.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+177G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13668983 | |||||||
| chr11:13668992 | C | T | 4 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0003g0286 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+186C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13668992 | |||||||
| chr11:13669091 | C | T | 1 | a0001c0001t0002g0036 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-8+285C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13669091 | |||||||
| chr11:13669250 | C | T | 2 | a0001c0002t0010g0035 a0002c0003t0010g0035 |
2 | HG00642.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-8+444C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13669250 | |||||||
| chr11:13669251 | A | G | 1 | a0001c0001t0002g0283 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-8+445A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13669251 | |||||||
| chr11:13669884 | TA | T | 151 | a0001c0001t0002g0036 a0001c0001t0002g0157 a0001c0001t0002g0159 others(148): Show |
168 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-8+1088delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13669884 | ||||||
| chr11:13669912 | A | G | 1 | a0001c0001t0003g0282 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-8+1106A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13669912 | |||||||
| chr11:13669963 | G | A | 20 | a0001c0001t0002g0157 a0001c0001t0002g0159 a0001c0001t0002g0160 others(17): Show |
20 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8+1157G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13669963 | |||||||
| chr11:13670307 | G | T | 1 | a0001c0001t0003g0281 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-8+1501G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13670307 | |||||||
| chr11:13670363 | G | T | 1 | a0001c0001t0003g0280 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-8+1557G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13670363 | |||||||
| chr11:13670415 | C | G | 39 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(36): Show |
43 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.-8+1609C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13670415 | |||||||
| chr11:13670522 | C | G | 2 | a0001c0001t0004g0034 a0001c0001t0004g0279 |
3 | NA18953.hp2 NA18989.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-8+1716C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13670522 | |||||||
| chr11:13670543 | C | T | 2 | a0001c0001t0002g0155 a0001c0001t0002g0156 |
2 | NA18943.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.-8+1737C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13670543 | |||||||
| chr11:13670549 | C | T | 2 | a0001c0001t0002g0153 a0001c0001t0003g0154 |
2 | NA18940.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-8+1743C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13670549 | |||||||
| chr11:13670647 | T | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | NA18946.hp1 NA18951.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-8+1841T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13670647 | |||||||
| chr11:13670714 | G | GT | 26 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0002g0151 others(23): Show |
31 | HG00280.hp1 HG00423.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-8+1923dupT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13670714 | ||||||
| chr11:13670714 | G | GTT | 20 | a0001c0001t0002g0036 a0001c0001t0002g0159 a0001c0001t0002g0160 others(17): Show |
21 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8+1922_-8+1923dup others(2): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13670714 | ||||||
| chr11:13670724 | T | A | 1 | a0001c0001t0001g0044 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-8+1918T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13670724 | |||||||
| chr11:13670945 | T | C | 40 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(37): Show |
44 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-8+2139T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13670945 | |||||||
| chr11:13671045 | A | T | 1 | a0001c0001t0003g0038 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8+2239A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13671045 | |||||||
| chr11:13671289 | A | G | 1 | a0001c0005t0003g0247 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-8+2483A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13671289 | |||||||
| chr11:13671374 | A | G | 1 | a0001c0001t0003g0281 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-8+2568A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13671374 | |||||||
| chr11:13671424 | G | T | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-8+2618G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13671424 | |||||||
| chr11:13671976 | T | A | 1 | a0001c0001t0003g0178 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-8+3170T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13671976 | |||||||
| chr11:13672388 | C | CA | 16 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0002g0045 others(13): Show |
18 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8+3598dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13672388 | ||||||
| chr11:13672388 | C | CAA | 20 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(17): Show |
25 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8+3597_-8+3598dup others(2): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13672388 | ||||||
| chr11:13672393 | A | AT | 40 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(37): Show |
44 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-8+3587_-8+3588ins others(1): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13672393 | |||||||
| chr11:13672399 | A | T | 40 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(37): Show |
44 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-8+3593A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13672399 | |||||||
| chr11:13672404 | A | G | 1 | a0001c0001t0002g0176 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-8+3598A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13672404 | |||||||
| chr11:13672504 | C | T | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8+3698C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13672504 | |||||||
| chr11:13672544 | C | CA | 56 | a0001c0001t0001g0288 a0001c0001t0003g0038 a0001c0001t0003g0188 others(53): Show |
62 | HG00544.hp2 HG00642.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.-8+3754dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13672544 | ||||||
| chr11:13672544 | C | CAA | 17 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(14): Show |
22 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-8+3753_-8+3754dup others(2): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13672544 | ||||||
| chr11:13672560 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-8+3754A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13672560 | |||||||
| chr11:13672663 | AG | A | 15 | a0001c0001t0002g0195 a0001c0001t0003g0012 a0001c0001t0003g0025 others(12): Show |
18 | HG00140.hp1 HG01081.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8+3858delG | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13672663 | |||||||
| chr11:13672681 | C | T | 47 | a0001c0001t0002g0195 a0001c0001t0002g0219 a0001c0001t0002g0224 others(44): Show |
52 | HG00140.hp1 HG00621.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.-8+3875C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13672681 | |||||||
| chr11:13672830 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-8+4024A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13672830 | |||||||
| chr11:13672861 | T | G | 4 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0003g0286 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+4055T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13672861 | |||||||
| chr11:13673033 | C | T | 1 | a0001c0001t0003g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-8+4227C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13673033 | |||||||
| chr11:13673056 | A | G | 286 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(283): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.-8+4250A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13673056 | |||||||
| chr11:13673239 | G | C | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-8+4433G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13673239 | |||||||
| chr11:13673241 | G | A | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8+4435G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13673241 | |||||||
| chr11:13673377 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-8+4571T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13673377 | |||||||
| chr11:13673435 | T | A | 1 | a0001c0001t0003g0038 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8+4629T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13673435 | |||||||
| chr11:13674047 | C | T | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8+5241C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674047 | |||||||
| chr11:13674087 | G | A | 1 | a0001c0001t0004g0248 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-8+5281G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674087 | |||||||
| chr11:13674115 | G | A | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8+5309G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674115 | |||||||
| chr11:13674165 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0022 others(44): Show |
57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.-8+5359C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674165 | |||||||
| chr11:13674266 | G | A | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8+5460G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674266 | |||||||
| chr11:13674294 | G | C | 1 | a0001c0001t0001g0114 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-8+5488G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674294 | |||||||
| chr11:13674303 | C | T | 3 | a0001c0001t0003g0038 a0001c0001t0013g0184 a0001c0001t0013g0185 |
3 | HG01884.hp1 HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-8+5497C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674303 | |||||||
| chr11:13674308 | CA | C | 6 | a0001c0001t0001g0147 a0001c0001t0002g0021 a0001c0001t0002g0113 others(3): Show |
7 | HG00323.hp2 HG02897.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+5518delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13674308 | ||||||
| chr11:13674320 | A | G | 1 | a0001c0001t0004g0248 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-8+5514A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674320 | |||||||
| chr11:13674342 | A | G | 2 | a0001c0001t0013g0184 a0001c0001t0013g0185 |
2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-8+5536A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674342 | |||||||
| chr11:13674349 | C | T | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-8+5543C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674349 | |||||||
| chr11:13674362 | G | T | 1 | a0001c0001t0003g0020 | 2 | HG00408.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-8+5556G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674362 | |||||||
| chr11:13674500 | A | G | 2 | a0001c0001t0013g0184 a0001c0001t0013g0185 |
2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-8+5694A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674500 | |||||||
| chr11:13674810 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | NA18944.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.-8+6004T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674810 | |||||||
| chr11:13674826 | A | G | 4 | a0001c0001t0007g0179 a0001c0001t0007g0180 a0001c0001t0007g0181 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+6020A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674826 | |||||||
| chr11:13674929 | A | G | 7 | a0001c0001t0006g0009 a0001c0001t0006g0039 a0001c0001t0006g0040 others(4): Show |
9 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+6123A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674929 | |||||||
| chr11:13675053 | C | CT | 229 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(226): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.-8+6262dupT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13675053 | ||||||
| chr11:13675053 | C | CTT | 40 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0003g0286 others(37): Show |
43 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.-8+6261_-8+6262dup others(2): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13675053 | ||||||
| chr11:13675103 | TA | T | 50 | a0001c0001t0002g0195 a0001c0001t0002g0219 a0001c0001t0002g0224 others(47): Show |
55 | HG00140.hp1 HG00621.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.-8+6299delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13675103 | ||||||
| chr11:13675317 | C | G | 33 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(30): Show |
36 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-8+6511C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13675317 | |||||||
| chr11:13675396 | A | G | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-8+6590A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13675396 | |||||||
| chr11:13675439 | G | T | 71 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(68): Show |
82 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.-8+6633G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13675439 | |||||||
| chr11:13675440 | C | T | 71 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(68): Show |
82 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.-8+6634C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13675440 | |||||||
| chr11:13675441 | T | C | 71 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(68): Show |
82 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.-8+6635T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13675441 | |||||||
| chr11:13675574 | C | T | 3 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0151 |
3 | HG03669.hp2 HG04199.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-8+6768C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13675574 | |||||||
| chr11:13675666 | T | C | 2 | a0001c0001t0004g0037 a0001c0001t0004g0253 |
2 | HG02027.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-8+6860T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13675666 | |||||||
| chr11:13675930 | A | G | 1 | a0001c0001t0003g0178 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-8+7124A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13675930 | |||||||
| chr11:13676159 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-8+7353G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13676159 | |||||||
| chr11:13676422 | G | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-8+7616G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13676422 | |||||||
| chr11:13676569 | A | C | 3 | a0001c0001t0002g0174 a0001c0001t0002g0176 a0001c0001t0029g0158 |
3 | HG00323.hp1 HG01069.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.-8+7763A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13676569 | |||||||
| chr11:13676598 | G | A | 4 | a0001c0001t0007g0179 a0001c0001t0007g0180 a0001c0001t0007g0181 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+7792G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13676598 | |||||||
| chr11:13676701 | C | T | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8+7895C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13676701 | |||||||
| chr11:13677037 | C | T | 2 | a0001c0002t0010g0035 a0002c0003t0010g0035 |
2 | HG00642.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-8+8231C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677037 | |||||||
| chr11:13677056 | A | G | 1 | a0001c0001t0002g0110 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-8+8250A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677056 | |||||||
| chr11:13677117 | A | G | 4 | a0001c0001t0003g0211 a0001c0001t0003g0230 a0001c0001t0003g0231 others(1): Show |
4 | HG02074.hp2 HG02523.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+8311A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677117 | |||||||
| chr11:13677136 | A | G | 1 | a0001c0001t0003g0200 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-8+8330A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677136 | |||||||
| chr11:13677286 | A | G | 55 | a0001c0001t0002g0153 a0001c0001t0002g0195 a0001c0001t0002g0219 others(52): Show |
60 | HG00140.hp1 HG00621.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.-8+8480A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677286 | |||||||
| chr11:13677582 | C | T | 4 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0003g0286 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+8776C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677582 | |||||||
| chr11:13677656 | C | T | 7 | a0001c0001t0003g0008 a0001c0001t0003g0029 a0001c0001t0003g0241 others(4): Show |
11 | HG00738.hp2 HG00741.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8+8850C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677656 | |||||||
| chr11:13677678 | A | C | 1 | a0001c0001t0007g0182 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-8+8872A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677678 | |||||||
| chr11:13677826 | A | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | NA18954.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.-8+9020A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677826 | |||||||
| chr11:13677994 | G | T | 1 | a0001c0001t0001g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-8+9188G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677994 | |||||||
| chr11:13678266 | A | G | 1 | a0001c0001t0004g0276 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-8+9460A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13678266 | |||||||
| chr11:13678288 | T | TGAGTCTC others(234): Show |
1 | a0001c0001t0001g0143 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-8+9584_-8+9585ins others(241): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13678288 | ||||||
| chr11:13678486 | G | A | 1 | a0001c0001t0005g0177 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-8+9680G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13678486 | |||||||
| chr11:13678621 | T | C | 1 | a0001c0001t0003g0038 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8+9815T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13678621 | |||||||
| chr11:13678703 | C | T | 1 | a0001c0001t0003g0038 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8+9897C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13678703 | |||||||
| chr11:13678722 | G | GT | 57 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0003g0008 others(54): Show |
66 | HG00280.hp1 HG00544.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.-8+9917dupT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13678722 | ||||||
| chr11:13678724 | C | T | 151 | a0001c0001t0002g0036 a0001c0001t0002g0157 a0001c0001t0002g0159 others(148): Show |
168 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-8+9918C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13678724 | |||||||
| chr11:13679010 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0119 |
2 | NA19006.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-8+10204G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679010 | |||||||
| chr11:13679062 | ATATTT | A | 3 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0161 |
3 | HG02647.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-8+10260_-8+10264d others(7): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13679062 | ||||||
| chr11:13679092 | G | A | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8+10286G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679092 | |||||||
| chr11:13679178 | A | T | 2 | a0001c0001t0013g0184 a0001c0001t0013g0185 |
2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-8+10372A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679178 | |||||||
| chr11:13679213 | A | AC | 153 | a0001c0001t0002g0036 a0001c0001t0002g0153 a0001c0001t0002g0157 others(150): Show |
170 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.-8+10407_-8+10408i others(3): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679213 | |||||||
| chr11:13679383 | A | C | 1 | a0001c0001t0004g0273 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-8+10577A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679383 | |||||||
| chr11:13679466 | C | T | 4 | a0001c0001t0002g0171 a0001c0001t0002g0174 a0001c0001t0002g0176 others(1): Show |
4 | HG00323.hp1 HG01069.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+10660C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679466 | |||||||
| chr11:13679568 | A | G | 1 | a0001c0001t0008g0204 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-8+10762A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679568 | |||||||
| chr11:13679726 | G | A | 1 | a0001c0002t0010g0183 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-8+10920G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679726 | |||||||
| chr11:13679734 | A | G | 4 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0003g0286 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+10928A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679734 | |||||||
| chr11:13679927 | G | A | 1 | a0001c0001t0003g0212 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-8+11121G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679927 | |||||||
| chr11:13679940 | G | C | 2 | a0001c0001t0002g0066 a0001c0001t0002g0110 |
2 | HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-8+11134G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679940 | |||||||
| chr11:13679940 | G | T | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-8+11134G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679940 | |||||||
| chr11:13680034 | A | G | 1 | a0001c0001t0025g0199 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-8+11228A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13680034 | |||||||
| chr11:13680098 | T | C | 4 | a0001c0001t0008g0201 a0001c0001t0008g0202 a0001c0001t0008g0203 others(1): Show |
4 | HG00735.hp1 HG01243.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+11292T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13680098 | |||||||
| chr11:13680110 | T | C | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-8+11304T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13680110 | |||||||
| chr11:13680228 | CTCTT | C | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-8+11424_-8+11427d others(6): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13680228 | ||||||
| chr11:13680315 | A | G | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-8+11509A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13680315 | |||||||
| chr11:13680320 | T | C | 1 | a0001c0001t0003g0190 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-8+11514T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13680320 | |||||||
| chr11:13680787 | T | C | 1 | a0001c0001t0012g0067 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-8+11981T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13680787 | |||||||
| chr11:13680808 | G | A | 1 | a0001c0001t0003g0038 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8+12002G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13680808 | |||||||
| chr11:13680813 | T | C | 6 | a0001c0001t0001g0068 a0001c0001t0002g0003 a0001c0001t0002g0014 others(3): Show |
12 | NA18939.hp2 NA18954.hp2 NA18955.hp2 others(9): Show |
intron_variant | MODIFIER | c.-8+12007T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13680813 | |||||||
| chr11:13680837 | G | C | 91 | a0001c0001t0002g0036 a0001c0001t0002g0157 a0001c0001t0002g0159 others(88): Show |
102 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.-8+12031G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13680837 | |||||||
| chr11:13681184 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-8+12378G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681184 | |||||||
| chr11:13681270 | G | A | 1 | a0001c0001t0003g0038 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8+12464G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681270 | |||||||
| chr11:13681475 | G | A | 7 | a0001c0001t0005g0031 a0001c0001t0005g0177 a0001c0001t0005g0249 others(4): Show |
8 | HG02559.hp2 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+12669G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681475 | |||||||
| chr11:13681524 | A | G | 1 | a0001c0001t0003g0286 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-8+12718A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681524 | |||||||
| chr11:13681559 | A | G | 1 | a0001c0001t0002g0112 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-8+12753A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681559 | |||||||
| chr11:13681682 | A | G | 1 | a0001c0001t0003g0229 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-8+12876A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681682 | |||||||
| chr11:13681894 | T | A | 21 | a0001c0001t0002g0036 a0001c0001t0002g0157 a0001c0001t0002g0159 others(18): Show |
22 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-7-12865T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681894 | |||||||
| chr11:13681904 | T | C | 2 | a0001c0001t0027g0051 a0001c0001t0028g0050 |
2 | HG00639.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-7-12855T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681904 | |||||||
| chr11:13681973 | T | A | 1 | a0001c0001t0003g0191 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-7-12786T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681973 | |||||||
| chr11:13681979 | C | G | 1 | a0001c0001t0004g0253 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-7-12780C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681979 | |||||||
| chr11:13682108 | T | C | 20 | a0001c0001t0002g0157 a0001c0001t0002g0159 a0001c0001t0002g0160 others(17): Show |
20 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.-7-12651T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13682108 | |||||||
| chr11:13682140 | G | A | 35 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0038 others(32): Show |
40 | HG00280.hp1 HG00642.hp1 HG01516.hp1 others(37): Show |
intron_variant | MODIFIER | c.-7-12619G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13682140 | |||||||
| chr11:13682327 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0012g0120 |
2 | NA18984.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-7-12432T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13682327 | |||||||
| chr11:13682374 | C | G | 2 | a0001c0001t0003g0227 a0001c0001t0003g0228 |
2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-7-12385C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13682374 | |||||||
| chr11:13682644 | TGTCACCC others(8540): Show |
T | 1 | a0001c0001t0004g0276 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-7-12113_-7-3567de others(1): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13682644 | ||||||
| chr11:13682875 | G | A | 3 | a0001c0001t0002g0224 a0001c0001t0003g0207 a0001c0001t0003g0218 |
3 | NA18940.hp1 NA18962.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-7-11884G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13682875 | |||||||
| chr11:13683187 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-7-11572G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13683187 | |||||||
| chr11:13683253 | C | T | 1 | a0001c0001t0002g0219 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-7-11506C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13683253 | |||||||
| chr11:13683306 | T | C | 1 | a0001c0001t0025g0199 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-7-11453T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13683306 | |||||||
| chr11:13683322 | G | A | 8 | a0001c0001t0002g0004 a0001c0001t0003g0004 a0001c0001t0003g0052 others(5): Show |
10 | HG00639.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-11437G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13683322 | |||||||
| chr11:13683329 | G | A | 1 | a0001c0001t0007g0180 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-7-11430G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13683329 | |||||||
| chr11:13683350 | A | G | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7-11409A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13683350 | |||||||
| chr11:13683468 | A | T | 3 | a0001c0001t0003g0029 a0001c0001t0003g0241 a0001c0001t0003g0242 |
4 | HG01884.hp2 HG02145.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-11291A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13683468 | |||||||
| chr11:13683518 | G | A | 1 | a0001c0001t0004g0262 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-7-11241G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13683518 | |||||||
| chr11:13683541 | GT | G | 13 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0236 others(10): Show |
15 | HG00280.hp1 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.-7-11209delT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13683541 | ||||||
| chr11:13683745 | G | GA | 3 | a0001c0001t0006g0009 a0001c0001t0006g0039 a0001c0001t0006g0040 |
5 | HG02809.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-11008dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13683745 | ||||||
| chr11:13683761 | G | A | 13 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0236 others(10): Show |
15 | HG00280.hp1 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.-7-10998G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13683761 | |||||||
| chr11:13684196 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-7-10563G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13684196 | |||||||
| chr11:13684283 | TA | T | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-7-10473delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13684283 | ||||||
| chr11:13684364 | G | C | 1 | a0001c0001t0004g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-7-10395G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13684364 | |||||||
| chr11:13684414 | G | C | 4 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0003g0286 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-10345G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13684414 | |||||||
| chr11:13684513 | T | C | 1 | a0001c0001t0002g0010 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-7-10246T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13684513 | |||||||
| chr11:13684733 | T | C | 1 | a0001c0001t0015g0234 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-7-10026T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13684733 | |||||||
| chr11:13685042 | A | T | 1 | a0001c0001t0001g0007 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-7-9717A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685042 | |||||||
| chr11:13685219 | C | T | 3 | a0001c0001t0006g0009 a0001c0001t0006g0039 a0001c0001t0006g0040 |
5 | HG02809.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-9540C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685219 | |||||||
| chr11:13685283 | A | AT | 6 | a0001c0001t0001g0138 a0001c0001t0003g0038 a0001c0001t0003g0214 others(3): Show |
6 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-9463dupT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13685283 | ||||||
| chr11:13685291 | T | G | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7-9468T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685291 | |||||||
| chr11:13685292 | T | G | 7 | a0001c0001t0007g0179 a0001c0001t0007g0180 a0001c0001t0007g0181 others(4): Show |
7 | HG00642.hp1 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-9467T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685292 | |||||||
| chr11:13685293 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-7-9466T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685293 | |||||||
| chr11:13685294 | T | G | 3 | a0001c0001t0001g0006 a0001c0001t0015g0233 a0001c0001t0015g0234 |
3 | HG02886.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-7-9465T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685294 | |||||||
| chr11:13685395 | C | T | 1 | a0001c0001t0003g0237 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-7-9364C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685395 | |||||||
| chr11:13685482 | A | G | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-7-9277A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685482 | |||||||
| chr11:13685769 | A | C | 3 | a0001c0001t0006g0009 a0001c0001t0006g0039 a0001c0001t0006g0040 |
5 | HG02809.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-8990A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685769 | |||||||
| chr11:13685932 | A | G | 52 | a0001c0001t0001g0068 a0001c0001t0001g0086 a0001c0001t0002g0002 others(49): Show |
70 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.-7-8827A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685932 | |||||||
| chr11:13686368 | T | C | 1 | a0001c0001t0003g0284 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-7-8391T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13686368 | |||||||
| chr11:13686449 | T | C | 1 | a0001c0001t0013g0185 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-7-8310T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13686449 | |||||||
| chr11:13686495 | C | T | 2 | a0001c0001t0003g0211 a0001c0001t0005g0177 |
2 | HG02622.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.-7-8264C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13686495 | |||||||
| chr11:13686615 | CTG | C | 7 | a0001c0001t0006g0009 a0001c0001t0006g0039 a0001c0001t0006g0040 others(4): Show |
9 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-8141_-7-8140del others(2): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13686615 | ||||||
| chr11:13686685 | T | C | 1 | a0001c0001t0003g0285 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-7-8074T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13686685 | |||||||
| chr11:13686717 | TA | T | 288 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(285): Show |
341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.-7-8034delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13686717 | ||||||
| chr11:13686948 | C | T | 21 | a0001c0001t0002g0036 a0001c0001t0002g0157 a0001c0001t0002g0159 others(18): Show |
22 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-7-7811C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13686948 | |||||||
| chr11:13687336 | T | C | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-7-7423T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13687336 | |||||||
| chr11:13687383 | G | A | 1 | a0001c0001t0003g0027 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-7-7376G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13687383 | |||||||
| chr11:13687591 | C | T | 2 | a0001c0001t0003g0026 a0001c0001t0003g0217 |
2 | HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-7-7168C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13687591 | |||||||
| chr11:13687605 | C | G | 3 | a0001c0001t0006g0009 a0001c0001t0006g0039 a0001c0001t0006g0040 |
5 | HG02809.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-7154C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13687605 | |||||||
| chr11:13687767 | G | A | 1 | a0001c0001t0026g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-7-6992G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13687767 | |||||||
| chr11:13687829 | C | T | 3 | a0001c0001t0006g0009 a0001c0001t0006g0039 a0001c0001t0006g0040 |
5 | HG02809.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-6930C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13687829 | |||||||
| chr11:13687869 | C | T | 1 | a0001c0001t0004g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-7-6890C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13687869 | |||||||
| chr11:13687961 | A | G | 1 | a0001c0001t0002g0005 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-7-6798A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13687961 | |||||||
| chr11:13688041 | T | C | 1 | a0001c0001t0001g0288 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-7-6718T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688041 | |||||||
| chr11:13688177 | C | CA | 14 | a0001c0001t0005g0031 a0001c0001t0005g0177 a0001c0001t0005g0249 others(11): Show |
17 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.-7-6573dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13688177 | ||||||
| chr11:13688185 | A | T | 6 | a0001c0001t0002g0074 a0001c0001t0002g0091 a0001c0001t0002g0113 others(3): Show |
6 | HG00558.hp2 HG02027.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-6574A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688185 | |||||||
| chr11:13688187 | T | A | 39 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(36): Show |
45 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.-7-6572T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688187 | |||||||
| chr11:13688243 | T | G | 1 | a0001c0001t0003g0178 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-7-6516T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688243 | |||||||
| chr11:13688251 | TC | T | 128 | a0001c0001t0001g0043 a0001c0001t0002g0195 a0001c0001t0002g0219 others(125): Show |
143 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.-7-6504delC | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13688251 | ||||||
| chr11:13688252 | C | T | 1 | a0001c0001t0003g0012 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-7-6507C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688252 | |||||||
| chr11:13688307 | A | C | 2 | a0001c0001t0002g0172 a0001c0001t0002g0173 |
2 | NA18964.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-7-6452A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688307 | |||||||
| chr11:13688333 | A | G | 1 | a0001c0001t0003g0286 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-7-6426A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688333 | |||||||
| chr11:13688368 | G | C | 1 | a0001c0001t0001g0019 | 2 | HG02083.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.-7-6391G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688368 | |||||||
| chr11:13688530 | A | G | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-7-6229A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688530 | |||||||
| chr11:13688564 | T | C | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7-6195T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688564 | |||||||
| chr11:13688620 | G | A | 7 | a0001c0001t0005g0031 a0001c0001t0005g0177 a0001c0001t0005g0249 others(4): Show |
8 | HG02559.hp2 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7-6139G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688620 | |||||||
| chr11:13688655 | A | G | 1 | a0001c0001t0003g0215 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-7-6104A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688655 | |||||||
| chr11:13688821 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-7-5938G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688821 | |||||||
| chr11:13689144 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-7-5615T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13689144 | |||||||
| chr11:13689193 | T | A | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7-5566T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13689193 | |||||||
| chr11:13689263 | A | G | 1 | a0001c0001t0002g0015 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-7-5496A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13689263 | |||||||
| chr11:13689682 | G | A | 1 | a0001c0001t0026g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-7-5077G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13689682 | |||||||
| chr11:13689796 | G | T | 26 | a0001c0001t0004g0032 a0001c0001t0004g0033 a0001c0001t0004g0034 others(23): Show |
28 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.-7-4963G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13689796 | |||||||
| chr11:13689869 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-7-4890C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13689869 | |||||||
| chr11:13689873 | C | CT | 71 | a0001c0001t0001g0007 a0001c0001t0001g0063 a0001c0001t0001g0115 others(68): Show |
79 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.-7-4866dupT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13689873 | ||||||
| chr11:13689873 | CT | C | 49 | a0001c0001t0002g0002 a0001c0001t0004g0030 a0001c0001t0004g0032 others(46): Show |
52 | HG00544.hp2 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.-7-4866delT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13689873 | ||||||
| chr11:13690303 | G | A | 1 | a0001c0001t0003g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-7-4456G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13690303 | |||||||
| chr11:13690465 | G | A | 32 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(29): Show |
35 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-7-4294G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13690465 | |||||||
| chr11:13690611 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-7-4148C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13690611 | |||||||
| chr11:13690769 | G | A | 1 | a0001c0001t0002g0195 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-7-3990G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13690769 | |||||||
| chr11:13690866 | G | A | 1 | a0001c0001t0003g0187 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-7-3893G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13690866 | |||||||
| chr11:13691001 | C | A | 1 | a0001c0001t0001g0006 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-7-3758C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13691001 | |||||||
| chr11:13691685 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-7-3074G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13691685 | |||||||
| chr11:13691836 | C | A | 2 | a0001c0001t0013g0184 a0001c0001t0013g0185 |
2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-7-2923C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13691836 | |||||||
| chr11:13691874 | T | G | 15 | a0001c0001t0002g0195 a0001c0001t0003g0012 a0001c0001t0003g0025 others(12): Show |
18 | HG00140.hp1 HG01081.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-7-2885T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13691874 | |||||||
| chr11:13692247 | A | G | 1 | a0001c0001t0003g0226 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-7-2512A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692247 | |||||||
| chr11:13692300 | A | G | 9 | a0001c0001t0003g0028 a0001c0001t0003g0236 a0001c0001t0003g0237 others(6): Show |
10 | HG00280.hp1 HG01516.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-2459A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692300 | |||||||
| chr11:13692316 | G | A | 1 | a0001c0001t0003g0178 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-7-2443G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692316 | |||||||
| chr11:13692322 | C | T | 1 | a0001c0001t0002g0171 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-7-2437C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692322 | |||||||
| chr11:13692544 | TA | T | 20 | a0001c0001t0002g0157 a0001c0001t0002g0159 a0001c0001t0002g0160 others(17): Show |
20 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.-7-2214delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692544 | |||||||
| chr11:13692596 | G | C | 1 | a0001c0001t0004g0276 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-7-2163G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692596 | |||||||
| chr11:13692641 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | NA18944.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.-7-2118T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692641 | |||||||
| chr11:13692695 | A | G | 25 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0017 others(22): Show |
31 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.-7-2064A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692695 | |||||||
| chr11:13692820 | A | G | 8 | a0001c0001t0001g0024 a0001c0001t0001g0047 a0001c0001t0001g0117 others(5): Show |
9 | HG02027.hp1 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-1939A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692820 | |||||||
| chr11:13692824 | A | C | 1 | a0001c0001t0005g0177 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-7-1935A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692824 | |||||||
| chr11:13692902 | G | C | 2 | a0001c0001t0003g0286 a0001c0001t0003g0287 |
2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-7-1857G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692902 | |||||||
| chr11:13693099 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-7-1660A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13693099 | |||||||
| chr11:13693262 | A | C | 2 | a0001c0001t0003g0243 a0001c0001t0003g0244 |
2 | HG01109.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-7-1497A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13693262 | |||||||
| chr11:13693295 | C | T | 21 | a0001c0001t0002g0036 a0001c0001t0002g0157 a0001c0001t0002g0159 others(18): Show |
22 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-7-1464C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13693295 | |||||||
| chr11:13693359 | CTTTTGTT others(3): Show |
C | 8 | a0001c0001t0002g0004 a0001c0001t0003g0004 a0001c0001t0003g0052 others(5): Show |
10 | HG00639.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-1390_-7-1381del others(10): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13693359 | ||||||
| chr11:13693403 | C | T | 2 | a0001c0001t0002g0169 a0001c0001t0002g0170 |
2 | NA18990.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-7-1356C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13693403 | |||||||
| chr11:13693432 | C | T | 1 | a0001c0001t0007g0181 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-7-1327C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13693432 | |||||||
| chr11:13693532 | A | G | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-7-1227A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13693532 | |||||||
| chr11:13693577 | CT | C | 44 | a0001c0001t0001g0068 a0001c0001t0002g0002 a0001c0001t0002g0003 others(41): Show |
62 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.-7-1178delT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13693577 | ||||||
| chr11:13693742 | A | G | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7-1017A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13693742 | |||||||
| chr11:13693834 | T | A | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-7-925T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13693834 | |||||||
| chr11:13693892 | A | C | 4 | a0001c0001t0007g0179 a0001c0001t0007g0180 a0001c0001t0007g0181 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-867A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13693892 | |||||||
| chr11:13694102 | T | C | 75 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(72): Show |
86 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.-7-657T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13694102 | |||||||
| chr11:13694291 | A | G | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-7-468A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13694291 | |||||||
| chr11:13694525 | G | A | 3 | a0001c0001t0003g0038 a0001c0001t0013g0184 a0001c0001t0013g0185 |
3 | HG01884.hp1 HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-7-234G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13694525 | |||||||
| chr11:13694635 | G | A | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-7-124G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13694635 | |||||||
| chr11:13694696 | T | C | 1 | a0001c0001t0001g0017 | 2 | HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-7-63T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13694696 | |||||||
| chr11:13694732 | A | G | 2 | a0001c0001t0005g0249 a0001c0001t0005g0274 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-7-27A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13694732 | |||||||
| chr11:13694983 | A | G | 153 | a0001c0001t0002g0036 a0001c0001t0002g0153 a0001c0001t0002g0157 others(150): Show |
170 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.189+29A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13694983 | |||||||
| chr11:13695067 | T | TA | 43 | a0001c0001t0003g0008 a0001c0001t0003g0243 a0001c0001t0003g0244 others(40): Show |
50 | HG00544.hp2 HG00733.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.189+117dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 13695067 | ||||||
| chr11:13695072 | C | A | 71 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(68): Show |
82 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.189+118C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13695072 | |||||||
| chr11:13695235 | GTTGT | G | 4 | a0001c0001t0008g0201 a0001c0001t0008g0202 a0001c0001t0008g0203 others(1): Show |
4 | HG00735.hp1 HG01243.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+286_189+289del others(4): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 13695235 | ||||||
| chr11:13695330 | T | A | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.189+376T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13695330 | |||||||
| chr11:13695737 | G | A | 2 | a0001c0001t0001g0086 a0001c0005t0003g0247 |
2 | NA18906.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.189+783G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13695737 | |||||||
| chr11:13695990 | C | T | 1 | a0001c0001t0007g0182 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.189+1036C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13695990 | |||||||
| chr11:13696144 | A | G | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.189+1190A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13696144 | |||||||
| chr11:13696347 | T | G | 1 | a0001c0001t0003g0284 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.189+1393T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13696347 | |||||||
| chr11:13696353 | A | G | 1 | a0001c0001t0006g0040 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.189+1399A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13696353 | |||||||
| chr11:13696641 | GACTTA | G | 47 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(44): Show |
53 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.189+1692_189+1696d others(7): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 13696641 | ||||||
| chr11:13696743 | TATGTATA others(3): Show |
T | 1 | a0001c0001t0003g0085 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.189+1790_189+1799d others(12): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13696743 | |||||||
| chr11:13696830 | T | G | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.189+1876T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13696830 | |||||||
| chr11:13696834 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.189+1880G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13696834 | |||||||
| chr11:13697282 | G | T | 1 | a0001c0001t0026g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.189+2328G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13697282 | |||||||
| chr11:13697321 | G | A | 3 | a0001c0001t0007g0179 a0001c0001t0007g0180 a0001c0001t0007g0181 |
3 | HG02145.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.189+2367G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13697321 | |||||||
| chr11:13697401 | G | T | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.189+2447G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13697401 | |||||||
| chr11:13697423 | C | G | 4 | a0001c0001t0007g0179 a0001c0001t0007g0180 a0001c0001t0007g0181 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+2469C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13697423 | |||||||
| chr11:13697553 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.189+2599G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13697553 | |||||||
| chr11:13697865 | T | A | 153 | a0001c0001t0002g0036 a0001c0001t0002g0153 a0001c0001t0002g0157 others(150): Show |
170 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.190-2452T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13697865 | |||||||
| chr11:13697975 | T | G | 289 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(286): Show |
342 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.190-2342T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13697975 | |||||||
| chr11:13697995 | C | G | 2 | a0001c0001t0003g0286 a0001c0001t0003g0287 |
2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.190-2322C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13697995 | |||||||
| chr11:13698059 | A | G | 4 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0003g0286 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-2258A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698059 | |||||||
| chr11:13698319 | C | T | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.190-1998C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698319 | |||||||
| chr11:13698357 | T | C | 1 | a0001c0001t0004g0254 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.190-1960T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698357 | |||||||
| chr11:13698408 | A | G | 1 | a0001c0001t0002g0036 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.190-1909A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698408 | |||||||
| chr11:13698435 | A | G | 1 | a0001c0001t0007g0181 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.190-1882A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698435 | |||||||
| chr11:13698553 | C | T | 1 | a0001c0001t0003g0225 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.190-1764C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698553 | |||||||
| chr11:13698602 | G | T | 1 | a0001c0001t0003g0020 | 2 | HG00408.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.190-1715G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698602 | |||||||
| chr11:13698626 | C | T | 1 | a0001c0001t0003g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.190-1691C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698626 | |||||||
| chr11:13698691 | C | T | 1 | a0001c0001t0004g0276 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.190-1626C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698691 | |||||||
| chr11:13698780 | G | A | 1 | a0001c0001t0003g0285 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.190-1537G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698780 | |||||||
| chr11:13698785 | C | T | 39 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(36): Show |
43 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.190-1532C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698785 | |||||||
| chr11:13698806 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.190-1511G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698806 | |||||||
| chr11:13698830 | C | CA | 9 | a0001c0001t0001g0046 a0001c0001t0001g0121 a0001c0001t0001g0122 others(6): Show |
9 | HG00408.hp1 HG01255.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.190-1472dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 13698830 | ||||||
| chr11:13698845 | A | G | 8 | a0001c0001t0002g0004 a0001c0001t0003g0004 a0001c0001t0003g0052 others(5): Show |
10 | HG00639.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.190-1472A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698845 | |||||||
| chr11:13698847 | C | A | 4 | a0001c0001t0003g0206 a0001c0001t0003g0213 a0001c0001t0003g0214 others(1): Show |
4 | NA18965.hp1 NA19009.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.190-1470C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698847 | |||||||
| chr11:13698905 | A | G | 8 | a0001c0001t0003g0038 a0001c0001t0006g0009 a0001c0001t0006g0039 others(5): Show |
10 | HG01884.hp1 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.190-1412A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698905 | |||||||
| chr11:13698921 | G | T | 1 | a0001c0001t0003g0215 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.190-1396G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698921 | |||||||
| chr11:13699071 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0012g0120 |
2 | NA18984.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-1246T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13699071 | |||||||
| chr11:13699121 | A | G | 4 | a0001c0001t0003g0028 a0001c0001t0009g0235 a0001c0001t0009g0239 others(1): Show |
5 | HG00280.hp1 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-1196A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13699121 | |||||||
| chr11:13699512 | A | T | 1 | a0001c0001t0001g0043 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.190-805A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13699512 | |||||||
| chr11:13699930 | A | G | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.190-387A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13699930 | |||||||
| chr11:13700312 | G | T | 4 | a0001c0001t0007g0179 a0001c0001t0007g0180 a0001c0001t0007g0181 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.190-5G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13700312 | |||||||
| chr11:13700651 | C | CTCT | 152 | a0001c0001t0001g0108 a0001c0001t0002g0036 a0001c0001t0002g0153 others(149): Show |
169 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.365+169_365+171dup others(3): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13700651 | ||||||
| chr11:13700692 | A | G | 2 | a0001c0001t0003g0198 a0001c0001t0003g0282 |
2 | HG01081.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.365+200A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13700692 | |||||||
| chr11:13700842 | T | G | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.365+350T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13700842 | |||||||
| chr11:13700937 | CAA | C | 13 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0236 others(10): Show |
15 | HG00280.hp1 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.365+447_365+448del others(2): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13700937 | ||||||
| chr11:13700989 | T | G | 5 | a0001c0001t0003g0026 a0001c0001t0003g0216 a0001c0001t0003g0217 others(2): Show |
6 | HG01891.hp2 HG02258.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.365+497T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13700989 | |||||||
| chr11:13701019 | C | G | 1 | a0001c0001t0003g0197 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.365+527C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13701019 | |||||||
| chr11:13701133 | A | T | 75 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(72): Show |
86 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.365+641A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13701133 | |||||||
| chr11:13701285 | TGCTC | T | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.365+794_365+797del others(4): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13701285 | |||||||
| chr11:13701378 | A | G | 2 | a0001c0001t0004g0272 a0001c0001t0018g0278 |
2 | HG01261.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.365+886A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13701378 | |||||||
| chr11:13701496 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.365+1004C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13701496 | |||||||
| chr11:13701605 | G | A | 1 | a0001c0001t0004g0256 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.365+1113G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13701605 | |||||||
| chr11:13701919 | T | C | 2 | a0001c0001t0013g0184 a0001c0001t0013g0185 |
2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.365+1427T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13701919 | |||||||
| chr11:13701950 | G | T | 71 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(68): Show |
82 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.365+1458G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13701950 | |||||||
| chr11:13701959 | C | T | 4 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0003g0286 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+1467C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13701959 | |||||||
| chr11:13702198 | C | G | 47 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(44): Show |
53 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.365+1706C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13702198 | |||||||
| chr11:13702561 | A | G | 4 | a0001c0001t0004g0034 a0001c0001t0004g0256 a0001c0001t0004g0271 others(1): Show |
5 | HG00544.hp2 NA18953.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.365+2069A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13702561 | |||||||
| chr11:13702565 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.365+2073A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13702565 | |||||||
| chr11:13702682 | A | G | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.365+2190A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13702682 | |||||||
| chr11:13702735 | G | A | 1 | a0001c0001t0002g0155 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.365+2243G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13702735 | |||||||
| chr11:13703025 | C | T | 56 | a0001c0001t0001g0068 a0001c0001t0001g0104 a0001c0001t0001g0105 others(53): Show |
74 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.365+2533C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703025 | |||||||
| chr11:13703044 | A | G | 1 | a0001c0001t0030g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.365+2552A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703044 | |||||||
| chr11:13703111 | C | T | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.365+2619C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703111 | |||||||
| chr11:13703168 | G | GTTTGTT | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.365+2702_365+2707d others(8): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13703168 | ||||||
| chr11:13703168 | GTTTGTT | G | 8 | a0001c0001t0002g0036 a0001c0001t0002g0219 a0001c0001t0003g0209 others(5): Show |
9 | HG00621.hp2 HG02080.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.365+2702_365+2707d others(8): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13703168 | ||||||
| chr11:13703168 | GTTTGTTT others(5): Show |
G | 3 | a0001c0001t0003g0154 a0001c0001t0003g0207 a0001c0001t0003g0218 |
3 | NA18940.hp2 NA18962.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.365+2696_365+2707d others(14): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13703168 | ||||||
| chr11:13703205 | A | G | 2 | a0001c0001t0003g0187 a0001c0001t0003g0205 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.365+2713A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703205 | |||||||
| chr11:13703242 | G | A | 1 | a0001c0001t0003g0038 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.365+2750G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703242 | |||||||
| chr11:13703269 | G | A | 5 | a0001c0001t0003g0012 a0001c0001t0003g0025 a0001c0001t0003g0192 others(2): Show |
8 | HG01257.hp1 HG01258.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.365+2777G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703269 | |||||||
| chr11:13703386 | C | G | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.365+2894C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703386 | |||||||
| chr11:13703394 | C | G | 4 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0060 others(1): Show |
6 | HG02258.hp1 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.365+2902C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703394 | |||||||
| chr11:13703397 | T | C | 1 | a0001c0001t0003g0038 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.365+2905T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703397 | |||||||
| chr11:13703405 | CTTG | C | 49 | a0001c0001t0002g0195 a0001c0001t0002g0219 a0001c0001t0003g0012 others(46): Show |
54 | HG00140.hp1 HG00621.hp2 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.365+2916_365+2918d others(5): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13703405 | ||||||
| chr11:13703452 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.365+2960T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703452 | |||||||
| chr11:13703611 | A | G | 1 | a0001c0001t0002g0072 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.365+3119A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703611 | |||||||
| chr11:13703669 | G | C | 1 | a0001c0001t0003g0038 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.365+3177G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703669 | |||||||
| chr11:13703740 | TACTG | T | 4 | a0001c0001t0002g0157 a0001c0001t0002g0163 a0001c0001t0002g0164 others(1): Show |
4 | NA18942.hp2 NA18966.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.365+3251_365+3254d others(6): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13703740 | ||||||
| chr11:13703781 | C | A | 1 | a0001c0001t0001g0147 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.365+3289C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703781 | |||||||
| chr11:13703888 | A | G | 2 | a0001c0001t0009g0239 a0001c0001t0009g0240 |
2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.365+3396A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703888 | |||||||
| chr11:13703940 | A | G | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.365+3448A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703940 | |||||||
| chr11:13703993 | A | C | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.365+3501A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703993 | |||||||
| chr11:13703993 | A | G | 43 | a0001c0001t0003g0008 a0001c0001t0003g0243 a0001c0001t0003g0244 others(40): Show |
50 | HG00544.hp2 HG00733.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.365+3501A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703993 | |||||||
| chr11:13704044 | C | CA | 9 | a0001c0001t0001g0094 a0001c0001t0001g0123 a0001c0001t0003g0038 others(6): Show |
11 | HG01884.hp1 HG01981.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.365+3572dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13704044 | ||||||
| chr11:13704044 | CA | C | 87 | a0001c0001t0001g0137 a0001c0001t0002g0175 a0001c0001t0002g0195 others(84): Show |
96 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.365+3572delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13704044 | ||||||
| chr11:13704288 | C | T | 1 | a0001c0001t0002g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.366-3612C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13704288 | |||||||
| chr11:13704465 | CTTAAGAA others(2): Show |
C | 4 | a0001c0001t0007g0179 a0001c0001t0007g0180 a0001c0001t0007g0181 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-3434_366-3426d others(11): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13704465 | |||||||
| chr11:13704542 | G | A | 4 | a0001c0001t0003g0188 a0001c0001t0003g0189 a0001c0001t0003g0212 others(1): Show |
4 | NA18942.hp1 NA18982.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-3358G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13704542 | |||||||
| chr11:13704735 | TA | T | 33 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(30): Show |
36 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.366-3157delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13704735 | ||||||
| chr11:13704765 | C | G | 3 | a0001c0001t0007g0179 a0001c0001t0007g0180 a0001c0001t0007g0181 |
3 | HG02145.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.366-3135C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13704765 | |||||||
| chr11:13704944 | G | A | 1 | a0001c0001t0004g0276 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.366-2956G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13704944 | |||||||
| chr11:13705146 | C | T | 1 | a0001c0001t0004g0270 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.366-2754C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13705146 | |||||||
| chr11:13705274 | AGTCTGAA others(1): Show |
A | 4 | a0001c0001t0008g0201 a0001c0001t0008g0202 a0001c0001t0008g0203 others(1): Show |
4 | HG00735.hp1 HG01243.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-2622_366-2615d others(10): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13705274 | ||||||
| chr11:13705287 | A | G | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.366-2613A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13705287 | |||||||
| chr11:13705362 | C | G | 52 | a0001c0001t0003g0008 a0001c0001t0003g0243 a0001c0001t0003g0244 others(49): Show |
61 | HG00544.hp2 HG00733.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.366-2538C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13705362 | |||||||
| chr11:13705363 | T | G | 151 | a0001c0001t0002g0036 a0001c0001t0002g0157 a0001c0001t0002g0159 others(148): Show |
168 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.366-2537T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13705363 | |||||||
| chr11:13705533 | C | T | 4 | a0001c0001t0007g0179 a0001c0001t0007g0180 a0001c0001t0007g0181 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-2367C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13705533 | |||||||
| chr11:13705659 | C | G | 1 | a0001c0001t0002g0168 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.366-2241C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13705659 | |||||||
| chr11:13705726 | A | T | 1 | a0001c0001t0001g0136 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.366-2174A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13705726 | |||||||
| chr11:13705759 | C | G | 47 | a0001c0001t0002g0195 a0001c0001t0002g0219 a0001c0001t0003g0012 others(44): Show |
52 | HG00140.hp1 HG00621.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.366-2141C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13705759 | |||||||
| chr11:13705936 | G | A | 1 | a0001c0001t0002g0036 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.366-1964G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13705936 | |||||||
| chr11:13706074 | CT | C | 5 | a0001c0001t0003g0211 a0001c0001t0008g0201 a0001c0001t0008g0202 others(2): Show |
5 | HG00735.hp1 HG01243.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.366-1819delT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13706074 | ||||||
| chr11:13706183 | CAT | C | 5 | a0001c0001t0008g0201 a0001c0001t0008g0202 a0001c0001t0008g0203 others(2): Show |
5 | HG00735.hp1 HG01243.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.366-1715_366-1714d others(4): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13706183 | ||||||
| chr11:13706253 | T | A | 4 | a0001c0001t0007g0179 a0001c0001t0007g0180 a0001c0001t0007g0181 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-1647T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13706253 | |||||||
| chr11:13706464 | A | G | 153 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0036 others(150): Show |
172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.366-1436A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13706464 | |||||||
| chr11:13706465 | T | A | 2 | a0001c0001t0013g0184 a0001c0001t0013g0185 |
2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.366-1435T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13706465 | |||||||
| chr11:13706469 | G | A | 2 | a0001c0001t0013g0184 a0001c0001t0013g0185 |
2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.366-1431G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13706469 | |||||||
| chr11:13706689 | C | G | 1 | a0001c0001t0002g0082 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.366-1211C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13706689 | |||||||
| chr11:13706849 | T | G | 4 | a0001c0001t0002g0074 a0001c0001t0002g0091 a0001c0001t0002g0113 others(1): Show |
4 | NA18952.hp2 NA18980.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-1051T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13706849 | |||||||
| chr11:13707007 | C | G | 1 | a0001c0001t0001g0108 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.366-893C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13707007 | |||||||
| chr11:13707102 | T | G | 1 | a0001c0005t0003g0247 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.366-798T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13707102 | |||||||
| chr11:13707287 | T | A | 5 | a0001c0001t0015g0233 a0001c0001t0015g0234 a0001c0002t0010g0035 others(2): Show |
5 | HG00642.hp1 HG02738.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.366-613T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13707287 | |||||||
| chr11:13707494 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.366-406A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13707494 | |||||||
| chr11:13707669 | T | G | 3 | a0001c0001t0011g0257 a0001c0001t0011g0259 a0001c0001t0011g0260 |
3 | HG02717.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.366-231T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13707669 | |||||||
| chr11:13707670 | A | G | 1 | a0001c0001t0002g0081 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.366-230A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13707670 | |||||||
| chr11:13707757 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.366-143T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13707757 | |||||||
| chr11:13708092 | G | A | 40 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(37): Show |
44 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.545+13G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708092 | |||||||
| chr11:13708093 | A | T | 40 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(37): Show |
44 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.545+14A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708093 | |||||||
| chr11:13708259 | G | A | 1 | a0001c0001t0005g0177 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.545+180G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708259 | |||||||
| chr11:13708315 | G | A | 2 | a0001c0001t0002g0060 a0001c0001t0003g0190 |
2 | HG01361.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.545+236G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708315 | |||||||
| chr11:13708372 | C | CA | 12 | a0001c0001t0001g0087 a0001c0001t0001g0124 a0001c0001t0002g0097 others(9): Show |
13 | HG00741.hp1 HG01109.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.545+303dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708372 | ||||||
| chr11:13708432 | T | C | 71 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(68): Show |
82 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.545+353T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708432 | |||||||
| chr11:13708434 | T | TGC | 28 | a0001c0001t0001g0087 a0001c0001t0002g0157 a0001c0001t0002g0160 others(25): Show |
29 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(26): Show |
intron_variant | MODIFIER | c.545+368_545+369dup others(2): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708434 | ||||||
| chr11:13708434 | T | TGCGC | 6 | a0001c0001t0001g0094 a0001c0001t0002g0173 a0001c0001t0003g0209 others(3): Show |
6 | HG00735.hp1 HG01243.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.545+366_545+369dup others(4): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708434 | ||||||
| chr11:13708434 | T | TGCGCGC | 3 | a0001c0001t0003g0055 a0001c0001t0006g0009 a0001c0001t0008g0202 |
5 | HG02280.hp1 HG02970.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.545+364_545+369dup others(6): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708434 | ||||||
| chr11:13708445 | G | A | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.545+366G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708445 | |||||||
| chr11:13708446 | C | T | 1 | a0001c0001t0004g0253 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.545+367C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708446 | |||||||
| chr11:13708447 | G | A | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.545+368G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708447 | |||||||
| chr11:13708447 | G | GCA | 30 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0019 others(27): Show |
34 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.545+397_545+398dup others(2): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708447 | G | GCACA | 10 | a0001c0001t0001g0018 a0001c0001t0001g0064 a0001c0001t0001g0098 others(7): Show |
12 | HG01891.hp1 HG02080.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.545+395_545+398dup others(4): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708447 | G | GCACACA | 2 | a0001c0001t0001g0017 a0001c0001t0013g0185 |
3 | HG03017.hp2 HG03491.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.545+393_545+398dup others(6): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708447 | G | GCACACAC others(1): Show |
3 | a0001c0001t0007g0179 a0001c0001t0007g0180 a0001c0001t0013g0184 |
3 | HG02145.hp2 HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.545+391_545+398dup others(8): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708447 | G | GCACACAC others(5): Show |
1 | a0001c0001t0005g0177 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.545+387_545+398dup others(12): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708447 | G | GCGCA | 29 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0121 others(26): Show |
32 | HG01069.hp1 HG01243.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.545+369_545+370ins others(4): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708447 | G | GCGCACA | 11 | a0001c0001t0001g0124 a0001c0001t0001g0131 a0001c0001t0001g0132 others(8): Show |
11 | HG01081.hp2 HG01978.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.545+369_545+370ins others(6): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708447 | G | GCGCACAC others(1): Show |
16 | a0001c0001t0003g0012 a0001c0001t0003g0191 a0001c0001t0003g0192 others(13): Show |
20 | HG00733.hp2 HG01167.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.545+369_545+370ins others(8): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708447 | G | GCGCACAC others(3): Show |
7 | a0001c0001t0004g0030 a0001c0001t0004g0264 a0001c0001t0004g0271 others(4): Show |
8 | HG01106.hp2 HG03927.hp2 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.545+369_545+370ins others(10): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708447 | G | GCGCACAC others(5): Show |
8 | a0001c0001t0004g0032 a0001c0001t0004g0033 a0001c0001t0004g0255 others(5): Show |
9 | HG01167.hp2 HG01515.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.545+369_545+370ins others(12): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708447 | G | GCGCACAC others(7): Show |
4 | a0001c0001t0004g0261 a0001c0001t0004g0270 a0001c0001t0004g0276 others(1): Show |
4 | HG01070.hp2 HG02738.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+369_545+370ins others(14): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708447 | G | GCGCACAC others(9): Show |
1 | a0001c0001t0015g0233 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.545+369_545+370ins others(16): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708447 | G | GCGCACAC others(11): Show |
3 | a0001c0001t0004g0275 a0001c0001t0011g0257 a0001c0001t0011g0260 |
3 | HG01168.hp2 HG02717.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.545+369_545+370ins others(18): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708447 | G | GCGCACAC others(13): Show |
2 | a0001c0001t0003g0178 a0001c0001t0011g0259 |
2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.545+369_545+370ins others(20): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708447 | G | GCGCGCAC others(1): Show |
4 | a0001c0001t0001g0134 a0001c0001t0003g0223 a0001c0001t0006g0040 others(1): Show |
4 | HG01934.hp2 HG02895.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+369_545+370ins others(8): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708447 | G | GCGCGCAC others(3): Show |
4 | a0001c0001t0003g0038 a0001c0001t0003g0154 a0001c0001t0003g0207 others(1): Show |
4 | HG00544.hp2 HG01884.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+369_545+370ins others(10): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708447 | G | GCGCGCAC others(7): Show |
1 | a0001c0001t0004g0248 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.545+369_545+370ins others(14): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708447 | G | GCGCGCGC others(5): Show |
1 | a0001c0001t0003g0218 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.545+369_545+370ins others(12): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708447 | GCA | G | 9 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0047 others(6): Show |
11 | HG00642.hp2 HG01515.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.545+397_545+398del others(2): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708447 | GCACA | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0042 others(24): Show |
34 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.545+395_545+398del others(4): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | ||||||
| chr11:13708449 | A | G | 16 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0002g0004 others(13): Show |
18 | HG00639.hp1 HG00735.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.545+370A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708449 | |||||||
| chr11:13708451 | A | G | 11 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0142 others(8): Show |
13 | HG00639.hp1 HG02083.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.545+372A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708451 | |||||||
| chr11:13708453 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.545+374A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708453 | |||||||
| chr11:13708468 | CACACACA others(7): Show |
C | 2 | a0001c0001t0003g0238 a0001c0001t0003g0245 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.545+390_545+403del others(14): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708468 | |||||||
| chr11:13708470 | CACACACA others(5): Show |
C | 1 | a0001c0001t0003g0237 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.545+392_545+403del others(12): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708470 | |||||||
| chr11:13708472 | CACACATA others(3): Show |
C | 10 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(7): Show |
15 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.545+394_545+403del others(10): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708472 | |||||||
| chr11:13708474 | CACAT | C | 2 | a0001c0001t0002g0015 a0001c0001t0002g0016 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.545+400_545+403del others(4): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708474 | ||||||
| chr11:13708478 | T | C | 42 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(39): Show |
46 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.545+399T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708478 | |||||||
| chr11:13708728 | C | G | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.545+649C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708728 | |||||||
| chr11:13708911 | G | T | 5 | a0001c0001t0001g0114 a0001c0001t0001g0119 a0001c0001t0001g0122 others(2): Show |
5 | NA18964.hp2 NA18980.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.545+832G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708911 | |||||||
| chr11:13709057 | A | G | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.545+978A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709057 | |||||||
| chr11:13709134 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02165.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.545+1055T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709134 | |||||||
| chr11:13709252 | T | TA | 4 | a0001c0001t0005g0031 a0001c0001t0005g0251 a0001c0001t0005g0252 others(1): Show |
5 | HG02486.hp1 HG02559.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.545+1181dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13709252 | ||||||
| chr11:13709328 | G | T | 1 | a0001c0001t0001g0107 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.545+1249G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709328 | |||||||
| chr11:13709331 | C | G | 2 | a0001c0001t0004g0258 a0001c0001t0004g0263 |
2 | HG01167.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.545+1252C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709331 | |||||||
| chr11:13709351 | TC | T | 5 | a0001c0001t0002g0005 a0001c0001t0002g0066 a0001c0001t0002g0080 others(2): Show |
8 | HG00140.hp2 HG00735.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.545+1273delC | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709351 | |||||||
| chr11:13709388 | C | T | 153 | a0001c0001t0001g0094 a0001c0001t0002g0036 a0001c0001t0002g0093 others(150): Show |
170 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.546-1305C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709388 | |||||||
| chr11:13709415 | G | A | 2 | a0001c0001t0013g0184 a0001c0001t0013g0185 |
2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.546-1278G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709415 | |||||||
| chr11:13709524 | G | T | 1 | a0001c0001t0002g0079 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546-1169G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709524 | |||||||
| chr11:13709702 | A | G | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.546-991A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709702 | |||||||
| chr11:13709790 | T | C | 71 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(68): Show |
82 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.546-903T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709790 | |||||||
| chr11:13709839 | A | C | 1 | a0001c0001t0004g0276 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.546-854A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709839 | |||||||
| chr11:13709899 | T | C | 71 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(68): Show |
82 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.546-794T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709899 | |||||||
| chr11:13709928 | C | A | 13 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0236 others(10): Show |
15 | HG00280.hp1 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.546-765C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709928 | |||||||
| chr11:13709969 | A | G | 1 | a0001c0001t0003g0227 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.546-724A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709969 | |||||||
| chr11:13710069 | T | C | 20 | a0001c0001t0002g0157 a0001c0001t0002g0159 a0001c0001t0002g0160 others(17): Show |
20 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.546-624T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13710069 | |||||||
| chr11:13710081 | C | T | 4 | a0001c0001t0003g0028 a0001c0001t0009g0235 a0001c0001t0009g0239 others(1): Show |
5 | HG00280.hp1 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.546-612C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13710081 | |||||||
| chr11:13710095 | A | G | 52 | a0001c0001t0001g0094 a0001c0001t0002g0093 a0001c0001t0002g0195 others(49): Show |
57 | HG00140.hp1 HG00621.hp2 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.546-598A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13710095 | |||||||
| chr11:13710383 | A | G | 2 | a0001c0001t0003g0211 a0001c0001t0003g0232 |
2 | NA18939.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.546-310A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13710383 | |||||||
| chr11:13710464 | G | T | 2 | a0001c0001t0004g0258 a0001c0001t0004g0263 |
2 | HG01167.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.546-229G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13710464 | |||||||
| chr11:13710466 | A | G | 4 | a0001c0001t0008g0201 a0001c0001t0008g0202 a0001c0001t0008g0203 others(1): Show |
4 | HG00735.hp1 HG01243.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.546-227A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13710466 | |||||||
| chr11:13710987 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.723+117C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 5/11 | chr11 | 13710987 | |||||||
| chr11:13711010 | A | C | 1 | a0001c0001t0002g0036 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.723+140A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 5/11 | chr11 | 13711010 | |||||||
| chr11:13711854 | C | T | 40 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(37): Show |
44 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.768+46C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 6/11 | chr11 | 13711854 | |||||||
| chr11:13711904 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.769-24G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 6/11 | chr11 | 13711904 | |||||||
| chr11:13712134 | A | G | 1 | a0001c0001t0003g0054 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.887+88A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 7/11 | chr11 | 13712134 | |||||||
| chr11:13712150 | A | G | 1 | a0001c0001t0003g0178 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.887+104A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 7/11 | chr11 | 13712150 | |||||||
| chr11:13712291 | G | GA | 18 | a0001c0001t0002g0036 a0001c0001t0003g0038 a0001c0001t0003g0284 others(15): Show |
21 | HG00642.hp1 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.887+258dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 13712291 | ||||||
| chr11:13712525 | A | G | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.888-441A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 7/11 | chr11 | 13712525 | |||||||
| chr11:13712535 | TTGATAAT others(10): Show |
T | 4 | a0001c0001t0003g0038 a0001c0001t0006g0009 a0001c0001t0006g0039 others(1): Show |
6 | HG01884.hp1 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.888-428_888-412del others(17): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 13712535 | ||||||
| chr11:13712542 | T | C | 4 | a0001c0001t0007g0179 a0001c0001t0007g0180 a0001c0001t0007g0181 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.888-424T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 7/11 | chr11 | 13712542 | |||||||
| chr11:13712703 | A | T | 1 | a0001c0001t0004g0276 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.888-263A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 7/11 | chr11 | 13712703 | |||||||
| chr11:13712763 | GTTA | G | 4 | a0001c0001t0003g0008 a0001c0001t0003g0053 a0001c0001t0003g0243 others(1): Show |
7 | HG00738.hp2 HG00741.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.888-197_888-195del others(3): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 13712763 | ||||||
| chr11:13713131 | A | T | 1 | a0001c0001t0003g0280 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.955+98A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713131 | |||||||
| chr11:13713132 | C | A | 1 | a0001c0001t0003g0280 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.955+99C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713132 | |||||||
| chr11:13713293 | C | T | 1 | a0001c0001t0003g0191 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.955+260C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713293 | |||||||
| chr11:13713323 | T | A | 8 | a0001c0001t0003g0038 a0001c0001t0006g0009 a0001c0001t0006g0039 others(5): Show |
10 | HG01884.hp1 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.955+290T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713323 | |||||||
| chr11:13713520 | C | T | 1 | a0001c0001t0007g0182 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.955+487C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713520 | |||||||
| chr11:13713794 | G | C | 1 | a0001c0001t0002g0036 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.956-715G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713794 | |||||||
| chr11:13713831 | A | G | 17 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0047 others(14): Show |
19 | HG00280.hp2 HG00621.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.956-678A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713831 | |||||||
| chr11:13713920 | T | C | 1 | a0001c0001t0003g0198 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.956-589T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713920 | |||||||
| chr11:13713927 | T | C | 1 | a0001c0001t0004g0264 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.956-582T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713927 | |||||||
| chr11:13713948 | G | A | 3 | a0001c0001t0006g0009 a0001c0001t0006g0039 a0001c0001t0006g0040 |
5 | HG02809.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.956-561G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713948 | |||||||
| chr11:13714154 | TA | T | 8 | a0001c0001t0002g0004 a0001c0001t0003g0004 a0001c0001t0003g0052 others(5): Show |
10 | HG00639.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.956-353delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 13714154 | ||||||
| chr11:13714187 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.956-322G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13714187 | |||||||
| chr11:13714195 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.956-314C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13714195 | |||||||
| chr11:13714371 | T | G | 1 | a0001c0001t0001g0127 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.956-138T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13714371 | |||||||
| chr11:13714410 | T | A | 1 | a0001c0001t0003g0055 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.956-99T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13714410 | |||||||
| chr11:13714843 | G | A | 2 | a0001c0001t0013g0184 a0001c0001t0013g0185 |
2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1127+163G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13714843 | |||||||
| chr11:13714906 | C | A | 4 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0003g0286 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1127+226C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13714906 | |||||||
| chr11:13714997 | T | G | 1 | a0001c0001t0003g0188 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1127+317T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13714997 | |||||||
| chr11:13715124 | T | C | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1127+444T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13715124 | |||||||
| chr11:13715746 | C | T | 6 | a0001c0001t0005g0031 a0001c0001t0005g0249 a0001c0001t0005g0251 others(3): Show |
7 | HG02559.hp2 HG02886.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1127+1066C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13715746 | |||||||
| chr11:13715957 | T | C | 20 | a0001c0001t0002g0157 a0001c0001t0002g0159 a0001c0001t0002g0160 others(17): Show |
20 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.1127+1277T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13715957 | |||||||
| chr11:13716061 | A | G | 1 | a0001c0001t0003g0028 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1127+1381A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716061 | |||||||
| chr11:13716168 | A | G | 1 | a0001c0001t0003g0038 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1127+1488A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716168 | |||||||
| chr11:13716227 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1127+1547T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716227 | |||||||
| chr11:13716304 | T | C | 50 | a0001c0001t0003g0008 a0001c0001t0003g0243 a0001c0001t0003g0244 others(47): Show |
59 | HG00544.hp2 HG00733.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.1127+1624T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716304 | |||||||
| chr11:13716485 | T | C | 1 | a0001c0001t0004g0265 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1127+1805T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716485 | |||||||
| chr11:13716533 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1127+1853C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716533 | |||||||
| chr11:13716684 | G | A | 289 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(286): Show |
342 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.1127+2004G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716684 | |||||||
| chr11:13716803 | T | A | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1127+2123T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716803 | |||||||
| chr11:13716900 | T | G | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1127+2220T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716900 | |||||||
| chr11:13716941 | C | G | 2 | a0001c0001t0003g0187 a0001c0001t0003g0205 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1127+2261C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716941 | |||||||
| chr11:13717059 | A | G | 1 | a0001c0001t0003g0217 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1127+2379A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13717059 | |||||||
| chr11:13717063 | T | G | 1 | a0001c0001t0003g0154 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1127+2383T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13717063 | |||||||
| chr11:13717074 | AC | A | 4 | a0001c0001t0007g0179 a0001c0001t0007g0180 a0001c0001t0007g0181 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1127+2396delC | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 13717074 | ||||||
| chr11:13717119 | A | G | 3 | a0001c0001t0003g0029 a0001c0001t0003g0241 a0001c0001t0003g0242 |
4 | HG01884.hp2 HG02145.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1127+2439A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13717119 | |||||||
| chr11:13717201 | T | C | 2 | a0001c0001t0013g0184 a0001c0001t0013g0185 |
2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1127+2521T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13717201 | |||||||
| chr11:13717367 | A | G | 1 | a0001c0001t0004g0248 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1127+2687A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13717367 | |||||||
| chr11:13717614 | C | T | 3 | a0001c0001t0003g0213 a0001c0001t0003g0214 a0001c0001t0003g0215 |
3 | NA18965.hp1 NA19009.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1127+2934C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13717614 | |||||||
| chr11:13718009 | T | C | 75 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(72): Show |
86 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.1127+3329T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13718009 | |||||||
| chr11:13718032 | A | G | 1 | a0001c0001t0004g0255 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1127+3352A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13718032 | |||||||
| chr11:13718286 | A | G | 19 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(16): Show |
24 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1128-3444A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13718286 | |||||||
| chr11:13718359 | A | G | 1 | a0001c0001t0003g0225 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1128-3371A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13718359 | |||||||
| chr11:13718510 | C | T | 1 | a0001c0001t0002g0016 | 2 | HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1128-3220C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13718510 | |||||||
| chr11:13718827 | G | C | 4 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0003g0286 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128-2903G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13718827 | |||||||
| chr11:13719248 | T | G | 40 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(37): Show |
44 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.1128-2482T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13719248 | |||||||
| chr11:13719714 | A | C | 1 | a0001c0007t0002g0148 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1128-2016A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13719714 | |||||||
| chr11:13719728 | G | A | 5 | a0001c0001t0008g0201 a0001c0001t0008g0202 a0001c0001t0008g0203 others(2): Show |
5 | HG00735.hp1 HG01243.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1128-2002G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13719728 | |||||||
| chr11:13719923 | A | C | 26 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(23): Show |
33 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.1128-1807A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13719923 | |||||||
| chr11:13719939 | A | G | 2 | a0001c0001t0002g0172 a0001c0001t0002g0173 |
2 | NA18964.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1128-1791A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13719939 | |||||||
| chr11:13720035 | C | G | 1 | a0001c0001t0003g0020 | 2 | HG00408.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1128-1695C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13720035 | |||||||
| chr11:13720073 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1128-1657A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13720073 | |||||||
| chr11:13720346 | C | G | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1128-1384C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13720346 | |||||||
| chr11:13720536 | T | C | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1128-1194T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13720536 | |||||||
| chr11:13720553 | T | C | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1128-1177T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13720553 | |||||||
| chr11:13720650 | A | AT | 27 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0017 others(24): Show |
33 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1128-1073dupT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 13720650 | ||||||
| chr11:13720660 | CCTT | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0124 a0001c0001t0001g0131 others(2): Show |
6 | HG01069.hp1 HG01943.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1128-1069_1128-106 others(7): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13720660 | |||||||
| chr11:13720703 | A | G | 1 | a0001c0001t0007g0182 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1128-1027A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13720703 | |||||||
| chr11:13720754 | T | C | 1 | a0001c0001t0003g0189 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1128-976T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13720754 | |||||||
| chr11:13721016 | A | G | 4 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0060 others(1): Show |
6 | HG02258.hp1 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1128-714A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13721016 | |||||||
| chr11:13721030 | G | A | 1 | a0001c0001t0004g0267 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1128-700G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13721030 | |||||||
| chr11:13721257 | G | C | 71 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(68): Show |
82 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.1128-473G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13721257 | |||||||
| chr11:13721284 | G | A | 1 | a0001c0001t0003g0038 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1128-446G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13721284 | |||||||
| chr11:13721287 | TTATAAA | T | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1128-437_1128-432d others(8): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 13721287 | ||||||
| chr11:13721638 | A | G | 6 | a0001c0001t0005g0031 a0001c0001t0005g0249 a0001c0001t0005g0251 others(3): Show |
7 | HG02559.hp2 HG02886.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1128-92A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13721638 | |||||||
| chr11:13721957 | A | G | 1 | a0001c0001t0026g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1257+98A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13721957 | |||||||
| chr11:13722005 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0109 |
2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1257+146G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13722005 | |||||||
| chr11:13722010 | T | C | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1257+151T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13722010 | |||||||
| chr11:13722261 | C | G | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1257+402C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13722261 | |||||||
| chr11:13722574 | A | G | 1 | a0001c0001t0004g0253 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1257+715A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13722574 | |||||||
| chr11:13722576 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1257+717C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13722576 | |||||||
| chr11:13722662 | C | T | 2 | a0001c0001t0004g0248 a0001c0001t0004g0275 |
2 | HG01168.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1257+803C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13722662 | |||||||
| chr11:13722843 | C | CCT | 48 | a0001c0001t0001g0145 a0001c0001t0002g0002 a0001c0001t0002g0003 others(45): Show |
63 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.1257+999_1257+1000 others(5): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722843 | ||||||
| chr11:13722843 | C | CCTCT | 12 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0236 others(9): Show |
16 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1257+997_1257+1000 others(7): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722843 | ||||||
| chr11:13722843 | C | CCTCTCT | 2 | a0001c0001t0003g0029 a0001c0001t0003g0242 |
3 | HG02145.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1257+995_1257+1000 others(9): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722843 | ||||||
| chr11:13722843 | C | CCTCTCTC others(3): Show |
27 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(24): Show |
31 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1257+991_1257+1000 others(13): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722843 | ||||||
| chr11:13722843 | C | CCTCTCTC others(5): Show |
5 | a0001c0001t0004g0255 a0001c0001t0004g0258 a0001c0001t0004g0263 others(2): Show |
5 | HG01167.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1257+989_1257+1000 others(15): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722843 | ||||||
| chr11:13722858 | C | CTCTCTCT others(3): Show |
1 | a0001c0001t0011g0260 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1257+1000_1257+100 others(14): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722858 | ||||||
| chr11:13722858 | C | CTCTCTCT others(3): Show |
4 | a0001c0001t0004g0253 a0001c0001t0004g0265 a0001c0001t0011g0257 others(1): Show |
4 | HG02027.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1257+1000_1257+100 others(14): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722858 | ||||||
| chr11:13722858 | C | CTCTCTCT others(5): Show |
1 | a0001c0001t0005g0277 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1257+1000_1257+100 others(16): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722858 | ||||||
| chr11:13722858 | C | CTCTCTCT others(5): Show |
2 | a0001c0001t0004g0262 a0001c0001t0005g0177 |
2 | HG02622.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1257+1000_1257+100 others(16): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722858 | ||||||
| chr11:13722858 | CTATA | C | 42 | a0001c0001t0002g0219 a0001c0001t0003g0012 a0001c0001t0003g0025 others(39): Show |
47 | HG00140.hp1 HG00621.hp2 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.1257+1016_1257+101 others(8): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722858 | ||||||
| chr11:13722860 | A | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.1257+1001A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13722860 | |||||||
| chr11:13722862 | A | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0023 others(55): Show |
68 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.1257+1003A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13722862 | |||||||
| chr11:13722864 | A | C | 5 | a0001c0001t0001g0152 a0001c0001t0002g0166 a0001c0001t0003g0226 others(2): Show |
5 | HG00423.hp1 HG02080.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257+1005A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13722864 | |||||||
| chr11:13723006 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0063 |
3 | HG00597.hp2 HG02083.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1257+1147T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723006 | |||||||
| chr11:13723186 | G | A | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1257+1327G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723186 | |||||||
| chr11:13723256 | T | C | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1257+1397T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723256 | |||||||
| chr11:13723290 | G | A | 1 | a0001c0001t0002g0077 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1257+1431G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723290 | |||||||
| chr11:13723351 | T | G | 1 | a0001c0001t0001g0136 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1257+1492T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723351 | |||||||
| chr11:13723362 | C | CA | 101 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0022 others(98): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.1257+1524dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13723362 | ||||||
| chr11:13723362 | C | CAA | 22 | a0001c0001t0001g0024 a0001c0001t0001g0043 a0001c0001t0001g0044 others(19): Show |
23 | HG00621.hp1 HG00621.hp2 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1257+1523_1257+152 others(6): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13723362 | ||||||
| chr11:13723362 | CA | C | 35 | a0001c0001t0001g0096 a0001c0001t0002g0110 a0001c0001t0002g0172 others(32): Show |
38 | HG00544.hp2 HG00642.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1257+1524delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13723362 | ||||||
| chr11:13723380 | A | C | 1 | a0001c0001t0007g0180 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1257+1521A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723380 | |||||||
| chr11:13723384 | C | A | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1257+1525C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723384 | |||||||
| chr11:13723388 | A | C | 39 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(36): Show |
43 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1257+1529A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723388 | |||||||
| chr11:13723389 | A | C | 2 | a0001c0001t0004g0270 a0001c0001t0004g0276 |
2 | HG02738.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1257+1530A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723389 | |||||||
| chr11:13723411 | T | G | 40 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(37): Show |
44 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.1257+1552T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723411 | |||||||
| chr11:13723739 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1257+1880G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723739 | |||||||
| chr11:13724226 | G | A | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1257+2367G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724226 | |||||||
| chr11:13724274 | G | GTACTAC | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1257+2416_1257+241 others(10): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13724274 | ||||||
| chr11:13724276 | G | T | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1257+2417G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724276 | |||||||
| chr11:13724277 | G | T | 16 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1257+2418G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724277 | |||||||
| chr11:13724335 | C | T | 2 | a0001c0001t0002g0005 a0001c0001t0023g0075 |
5 | HG00140.hp2 HG01358.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257+2476C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724335 | |||||||
| chr11:13724371 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1257+2512C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724371 | |||||||
| chr11:13724398 | A | G | 1 | a0001c0001t0006g0039 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1257+2539A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724398 | |||||||
| chr11:13724549 | CA | C | 10 | a0001c0001t0001g0115 a0001c0001t0001g0145 a0001c0001t0001g0147 others(7): Show |
10 | HG00323.hp2 HG00741.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1257+2710delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13724549 | ||||||
| chr11:13724549 | CAA | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(235): Show |
289 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.1257+2709_1257+271 others(6): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13724549 | ||||||
| chr11:13724549 | CAAA | C | 45 | a0001c0001t0003g0012 a0001c0001t0003g0025 a0001c0001t0003g0026 others(42): Show |
50 | HG00140.hp1 HG00621.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.1257+2708_1257+271 others(7): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13724549 | ||||||
| chr11:13724645 | C | G | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1257+2786C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724645 | |||||||
| chr11:13724776 | C | T | 3 | a0001c0001t0002g0174 a0001c0001t0002g0176 a0001c0001t0029g0158 |
3 | HG00323.hp1 HG01069.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.1258-2780C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724776 | |||||||
| chr11:13724781 | A | C | 1 | a0001c0001t0003g0192 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1258-2775A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724781 | |||||||
| chr11:13724833 | G | T | 1 | a0001c0001t0007g0182 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1258-2723G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724833 | |||||||
| chr11:13725175 | A | T | 1 | a0001c0001t0003g0198 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1258-2381A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13725175 | |||||||
| chr11:13725294 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0109 |
2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1258-2262T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13725294 | |||||||
| chr11:13725349 | T | A | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1258-2207T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13725349 | |||||||
| chr11:13725443 | TA | T | 100 | a0001c0001t0003g0008 a0001c0001t0003g0012 a0001c0001t0003g0025 others(97): Show |
113 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.1258-2097delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13725443 | ||||||
| chr11:13725443 | TAA | T | 16 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0198 others(13): Show |
18 | HG00280.hp1 HG01081.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.1258-2098_1258-209 others(6): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13725443 | ||||||
| chr11:13725617 | G | A | 1 | a0001c0001t0002g0113 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1258-1939G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13725617 | |||||||
| chr11:13725853 | C | A | 2 | a0001c0001t0015g0233 a0001c0001t0015g0234 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1258-1703C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13725853 | |||||||
| chr11:13725867 | T | G | 1 | a0001c0001t0002g0036 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1258-1689T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13725867 | |||||||
| chr11:13726114 | C | A | 4 | a0001c0001t0001g0118 a0001c0002t0010g0035 a0001c0002t0010g0183 others(1): Show |
4 | HG00642.hp1 HG01993.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1258-1442C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13726114 | |||||||
| chr11:13726116 | G | A | 3 | a0001c0001t0006g0009 a0001c0001t0006g0039 a0001c0001t0006g0040 |
5 | HG02809.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1258-1440G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13726116 | |||||||
| chr11:13726121 | T | C | 1 | a0001c0001t0003g0285 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1258-1435T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13726121 | |||||||
| chr11:13726245 | C | T | 2 | a0001c0001t0014g0090 a0001c0001t0014g0149 |
2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1258-1311C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13726245 | |||||||
| chr11:13726257 | C | T | 1 | a0001c0001t0002g0169 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1258-1299C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13726257 | |||||||
| chr11:13726639 | G | A | 2 | a0001c0001t0013g0184 a0001c0001t0013g0185 |
2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1258-917G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13726639 | |||||||
| chr11:13726662 | G | C | 211 | a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0003 others(208): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1258-894G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13726662 | |||||||
| chr11:13726741 | T | A | 66 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0029 others(63): Show |
77 | HG00280.hp1 HG00544.hp2 HG00733.hp2 others(74): Show |
intron_variant | MODIFIER | c.1258-815T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13726741 | |||||||
| chr11:13726741 | T | TA | 3 | a0001c0001t0004g0268 a0001c0001t0015g0233 a0001c0001t0015g0234 |
3 | HG02886.hp1 HG03540.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1258-812dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13726741 | ||||||
| chr11:13726992 | G | A | 2 | a0001c0001t0004g0034 a0001c0001t0004g0279 |
3 | NA18953.hp2 NA18989.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1258-564G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13726992 | |||||||
| chr11:13727340 | G | C | 3 | a0001c0002t0010g0035 a0001c0002t0010g0183 a0002c0003t0010g0035 |
3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1258-216G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13727340 | |||||||
| chr11:13727900 | C | A | 3 | a0001c0001t0006g0009 a0001c0001t0006g0039 a0001c0001t0006g0040 |
5 | HG02809.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1385+217C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 11/11 | chr11 | 13727900 | |||||||
| chr11:13728044 | A | C | 1 | a0001c0001t0003g0178 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1385+361A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 11/11 | chr11 | 13728044 | |||||||
| chr11:13728369 | A | T | 13 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0236 others(10): Show |
15 | HG00280.hp1 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.1386-243A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 11/11 | chr11 | 13728369 | |||||||
| chr11:13728499 | C | A | 49 | a0001c0001t0003g0012 a0001c0001t0003g0025 a0001c0001t0003g0026 others(46): Show |
54 | HG00140.hp1 HG00621.hp2 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.1386-113C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 11/11 | chr11 | 13728499 |