Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 85302 |
| ensemblid | ENSG00000188878.20 |
| hgncid | 24674 |
| symbol | FBF1 |
| name | Fas binding factor 1 |
| refseq_nuc | NM_001319193.2 |
| refseq_prot | NP_001306122.1 |
| ensembl_nuc | ENST00000636174.2 |
| ensembl_prot | ENSP00000490726.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 75909574 |
| end | 75941042 |
| strand | - |
| ver | v1.2 |
| region | chr17:75909574-75941042 |
| region5000 | chr17:75904574-75946042 |
| regionname0 | FBF1_chr17_75909574_75941042 |
| regionname5000 | FBF1_chr17_75904574_75946042 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1148 | 128 | 18 | 29 | 59 | 5 | 15 | 45 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0002 | 0/0 | 1148 | 76 | 16 | 9 | 40 | 5 | 6 | 34 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0003 | 0/0 | 1148 | 50 | 24 | 9 | 11 | 0 | 6 | 9 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0004 | 0/0 | 1148 | 33 | 27 | 4 | 1 | 0 | 1 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0005 | 0/0 | 1148 | 7 | 0 | 2 | 4 | 0 | 1 | 4 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0006 | 0/0 | 1148 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0007 | 0/0 | 1148 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0008 | 0/0 | 1148 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0009 | 0/0 | 1148 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0010 | 0/0 | 1148 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0011 | 0/0 | 1148 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0012 | 0/0 | 1148 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0013 | 0/0 | 1148 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0014 | 0/0 | 1148 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0015 | 0/0 | 1148 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0016 | 0/0 | 1148 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0017 | 0/0 | 1148 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0018 | 0/0 | 1148 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0019 | 0/0 | 1148 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0020 | 0/0 | 1148 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| a0021 | 0/0 | 1148 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | MAPKT others(1143): Show |
chr17 | 75904574 | 75946042 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3444 | 121 | 18 | 29 | 52 | 5 | 15 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0001c0007 | 0/0 | 3444 | 5 | 0 | 0 | 5 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0001c0021 | 0/0 | 3444 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0001c0023 | 0/0 | 3444 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0002c0002 | 0/0 | 3444 | 74 | 16 | 9 | 40 | 5 | 4 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0002c0016 | 0/0 | 3444 | 2 | 0 | 0 | 0 | 0 | 2 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0003c0003 | 0/0 | 3444 | 28 | 11 | 3 | 10 | 0 | 4 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0003c0005 | 0/0 | 3444 | 9 | 3 | 4 | 0 | 0 | 2 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0003c0008 | 0/0 | 3444 | 5 | 4 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0003c0009 | 0/0 | 3444 | 5 | 5 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0003c0013 | 0/0 | 3444 | 2 | 1 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0003c0030 | 0/0 | 3444 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0004c0004 | 0/0 | 3444 | 27 | 23 | 3 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0004c0010 | 0/0 | 3444 | 4 | 2 | 1 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0004c0027 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0004c0028 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0005c0006 | 0/0 | 3444 | 7 | 0 | 2 | 4 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0006c0012 | 0/0 | 3444 | 3 | 3 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0007c0011 | 0/0 | 3444 | 3 | 3 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0008c0017 | 0/0 | 3444 | 2 | 0 | 0 | 0 | 2 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0009c0018 | 0/0 | 3444 | 2 | 2 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0010c0014 | 0/0 | 3444 | 2 | 0 | 0 | 0 | 0 | 2 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0011c0015 | 0/0 | 3444 | 2 | 0 | 0 | 2 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0012c0022 | 0/0 | 3444 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0013c0032 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0014c0031 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0015c0029 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0016c0025 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0017c0026 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0018c0033 | 0/0 | 3444 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0019c0019 | 0/0 | 3444 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0020c0020 | 0/0 | 3444 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 | ||
| a0021c0024 | 0/0 | 3444 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | ATGGC others(3439): Show |
chr17 | 75904574 | 75946042 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4874 | 118 | 17 | 28 | 51 | 5 | 15 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0001c0001t0004 | 0/0 | 4874 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0001c0001t0006 | 0/0 | 4874 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0001c0001t0007 | 0/0 | 4874 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0001c0007t0001 | 0/0 | 4874 | 5 | 0 | 0 | 5 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0001c0021t0001 | 0/0 | 4874 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0001c0023t0001 | 0/0 | 4874 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0002c0002t0001 | 0/0 | 4874 | 52 | 16 | 6 | 25 | 2 | 3 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0002c0002t0003 | 0/0 | 4874 | 21 | 0 | 3 | 14 | 3 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0002c0002t0010 | 0/0 | 4874 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0002c0016t0003 | 0/0 | 4874 | 2 | 0 | 0 | 0 | 0 | 2 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0003c0003t0002 | 0/0 | 4874 | 27 | 11 | 2 | 10 | 0 | 4 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0003c0003t0009 | 0/0 | 4874 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0003c0005t0002 | 0/0 | 4874 | 9 | 3 | 4 | 0 | 0 | 2 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0003c0008t0002 | 0/0 | 4874 | 5 | 4 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0003c0009t0002 | 0/0 | 4874 | 5 | 5 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0003c0013t0002 | 0/0 | 4874 | 2 | 1 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0003c0030t0002 | 0/0 | 4874 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0004c0004t0001 | 0/0 | 4874 | 27 | 23 | 3 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0004c0010t0004 | 0/0 | 4874 | 4 | 2 | 1 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0004c0027t0001 | 0/0 | 4874 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0004c0028t0008 | 0/0 | 4874 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0005c0006t0001 | 0/0 | 4874 | 7 | 0 | 2 | 4 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0006c0012t0001 | 0/0 | 4874 | 3 | 3 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0007c0011t0005 | 0/0 | 4874 | 3 | 3 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0008c0017t0001 | 0/0 | 4874 | 2 | 0 | 0 | 0 | 2 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0009c0018t0001 | 0/0 | 4874 | 2 | 2 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0010c0014t0001 | 0/0 | 4874 | 2 | 0 | 0 | 0 | 0 | 2 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0011c0015t0001 | 0/0 | 4874 | 2 | 0 | 0 | 2 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0012c0022t0001 | 0/0 | 4874 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0013c0032t0004 | 0/0 | 4874 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0014c0031t0002 | 0/0 | 4874 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0015c0029t0002 | 0/0 | 4874 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0016c0025t0011 | 0/0 | 4874 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0017c0026t0012 | 0/0 | 4874 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0018c0033t0001 | 0/0 | 4874 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0019c0019t0001 | 0/0 | 4874 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0020c0020t0001 | 0/0 | 4874 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| a0021c0024t0002 | 0/0 | 4874 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | AGACG others(4869): Show |
chr17 | 75904574 | 75946042 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 18 | 3 | 5 | 6 | 1 | 2 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0004 | 0/0 | 7 | 1 | 1 | 5 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0005 | 0/0 | 6 | 1 | 2 | 2 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0012 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0096 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0006g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0001t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0007t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0007t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0007t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0007t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0007t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0021t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0001c0023t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0002 | 0/0 | 10 | 6 | 1 | 3 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0003g0003 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0003g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0002t0010g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0016t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0002c0016t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0002g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0003t0009g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0005t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0005t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0005t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0005t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0005t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0005t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0005t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0005t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0008t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0008t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0008t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0008t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0009t0002g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0009t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0009t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0013t0002g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0003c0030t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0004t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0010t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0010t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0010t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0010t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0027t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0004c0028t0008g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0005c0006t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0005c0006t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0005c0006t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0005c0006t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0005c0006t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0005c0006t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0005c0006t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0006c0012t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0006c0012t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0006c0012t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0007c0011t0005g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0007c0011t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0008c0017t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0008c0017t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0009c0018t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0009c0018t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0010c0014t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0010c0014t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0011c0015t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0012c0022t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0013c0032t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0014c0031t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0015c0029t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0016c0025t0011g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0017c0026t0012g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0018c0033t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0019c0019t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0020c0020t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| a0021c0024t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0204 | EUR | GBR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00140 | hp2 | a0002 | c0002 | t0003 | g0018 | EUR | GBR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | FIN | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00423 | hp2 | a0002 | c0002 | t0003 | g0197 | EAS | CHS | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | CHS | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | CHS | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | CHS | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00639 | hp1 | a0004 | c0004 | t0001 | g0030 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00639 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00735 | hp1 | a0003 | c0003 | t0002 | g0024 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00738 | hp1 | a0003 | c0008 | t0002 | g0235 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01069 | hp1 | a0003 | c0005 | t0002 | g0028 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01069 | hp2 | a0004 | c0004 | t0001 | g0007 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01071 | hp1 | a0003 | c0005 | t0002 | g0028 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0021 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01074 | hp2 | a0004 | c0010 | t0004 | g0163 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01106 | hp1 | a0012 | c0022 | t0001 | g0076 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01109 | hp1 | a0003 | c0005 | t0002 | g0214 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0166 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0181 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01175 | hp2 | a0005 | c0006 | t0001 | g0060 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01243 | hp2 | a0003 | c0013 | t0002 | g0026 | AMR | PUR | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01255 | hp2 | a0002 | c0002 | t0003 | g0154 | AMR | CLM | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0165 | AMR | CLM | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01358 | hp2 | a0002 | c0002 | t0003 | g0018 | AMR | CLM | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01361 | hp1 | a0003 | c0005 | t0002 | g0215 | AMR | CLM | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0174 | AMR | CLM | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01433 | hp2 | a0003 | c0003 | t0002 | g0024 | AMR | CLM | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01515 | hp1 | a0002 | c0002 | t0003 | g0156 | EUR | IBS | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01515 | hp2 | a0008 | c0017 | t0001 | g0170 | EUR | IBS | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01517 | hp2 | a0008 | c0017 | t0001 | g0185 | EUR | IBS | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01884 | hp1 | a0004 | c0004 | t0001 | g0034 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01891 | hp1 | a0004 | c0004 | t0001 | g0033 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01891 | hp2 | a0003 | c0003 | t0002 | g0211 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01934 | hp1 | a0004 | c0004 | t0001 | g0035 | AMR | PEL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01952 | hp2 | a0005 | c0006 | t0001 | g0051 | AMR | PEL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02015 | hp1 | a0003 | c0030 | t0002 | g0219 | EAS | KHV | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02027 | hp1 | a0001 | c0007 | t0001 | g0126 | EAS | KHV | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02071 | hp1 | a0001 | c0021 | t0001 | g0111 | EAS | KHV | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02132 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | KHV | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02145 | hp1 | a0009 | c0018 | t0001 | g0119 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02145 | hp2 | a0013 | c0032 | t0004 | g0209 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CDX | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02258 | hp1 | a0004 | c0004 | t0001 | g0052 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02258 | hp2 | a0006 | c0012 | t0001 | g0057 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02280 | hp1 | a0004 | c0004 | t0001 | g0151 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0184 | AMR | PEL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02451 | hp2 | a0014 | c0031 | t0002 | g0228 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02523 | hp2 | a0003 | c0003 | t0002 | g0223 | EAS | KHV | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0206 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02572 | hp2 | a0004 | c0004 | t0001 | g0152 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02615 | hp1 | a0003 | c0003 | t0002 | g0008 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02615 | hp2 | a0004 | c0004 | t0001 | g0007 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02622 | hp2 | a0004 | c0004 | t0001 | g0010 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02630 | hp2 | a0003 | c0005 | t0002 | g0233 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02647 | hp1 | a0003 | c0003 | t0002 | g0241 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02717 | hp1 | a0015 | c0029 | t0002 | g0230 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02717 | hp2 | a0004 | c0004 | t0001 | g0043 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02723 | hp2 | a0004 | c0004 | t0001 | g0037 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02735 | hp2 | a0010 | c0014 | t0001 | g0121 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0189 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02809 | hp2 | a0003 | c0005 | t0002 | g0232 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0176 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02818 | hp2 | a0003 | c0008 | t0002 | g0234 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02886 | hp1 | a0003 | c0009 | t0002 | g0240 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02886 | hp2 | a0004 | c0028 | t0008 | g0236 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02895 | hp1 | a0003 | c0008 | t0002 | g0027 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0178 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02896 | hp2 | a0003 | c0008 | t0002 | g0027 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ESN | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02922 | hp2 | a0016 | c0025 | t0011 | g0244 | AFR | ESN | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02965 | hp1 | a0007 | c0011 | t0005 | g0011 | AFR | ESN | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02965 | hp2 | a0003 | c0003 | t0002 | g0216 | AFR | ESN | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02970 | hp1 | a0003 | c0009 | t0002 | g0237 | AFR | ESN | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02970 | hp2 | a0004 | c0004 | t0001 | g0150 | AFR | ESN | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02976 | hp1 | a0004 | c0004 | t0001 | g0148 | AFR | ESN | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03041 | hp1 | a0003 | c0003 | t0002 | g0023 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03041 | hp2 | a0004 | c0027 | t0001 | g0036 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0188 | AFR | MSL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03098 | hp2 | a0004 | c0004 | t0001 | g0045 | AFR | MSL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03130 | hp1 | a0004 | c0010 | t0004 | g0162 | AFR | ESN | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ESN | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03139 | hp1 | a0003 | c0013 | t0002 | g0026 | AFR | ESN | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03139 | hp2 | a0007 | c0011 | t0005 | g0011 | AFR | ESN | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03195 | hp1 | a0004 | c0004 | t0001 | g0039 | AFR | ESN | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03195 | hp2 | a0003 | c0003 | t0002 | g0008 | AFR | ESN | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03209 | hp1 | a0003 | c0008 | t0002 | g0239 | AFR | MSL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03209 | hp2 | a0004 | c0004 | t0001 | g0038 | AFR | MSL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03225 | hp2 | a0009 | c0018 | t0001 | g0056 | AFR | MSL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0169 | AFR | MSL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03453 | hp2 | a0003 | c0003 | t0002 | g0226 | AFR | MSL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03486 | hp1 | a0017 | c0026 | t0012 | g0245 | AFR | MSL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03490 | hp1 | a0002 | c0016 | t0003 | g0195 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03490 | hp2 | a0003 | c0005 | t0002 | g0213 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03491 | hp1 | a0003 | c0003 | t0002 | g0025 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03492 | hp1 | a0002 | c0016 | t0003 | g0196 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03492 | hp2 | a0003 | c0003 | t0002 | g0025 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0190 | AFR | ESN | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03516 | hp2 | a0007 | c0011 | t0005 | g0054 | AFR | ESN | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03540 | hp1 | a0003 | c0003 | t0002 | g0023 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03540 | hp2 | a0004 | c0004 | t0001 | g0046 | AFR | GWD | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0158 | AFR | MSL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03579 | hp2 | a0003 | c0005 | t0002 | g0238 | AFR | MSL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03654 | hp1 | a0002 | c0002 | t0003 | g0155 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03654 | hp2 | a0003 | c0003 | t0002 | g0242 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03669 | hp1 | a0004 | c0010 | t0004 | g0164 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03704 | hp1 | a0018 | c0033 | t0001 | g0201 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0186 | SAS | PJL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0202 | SAS | BEB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0200 | SAS | BEB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG04115 | hp1 | a0003 | c0003 | t0002 | g0227 | SAS | STU | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG04115 | hp2 | a0010 | c0014 | t0001 | g0144 | SAS | STU | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG04204 | hp1 | a0003 | c0005 | t0002 | g0212 | SAS | STU | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG04228 | hp2 | a0005 | c0006 | t0001 | g0047 | SAS | STU | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18522 | hp1 | a0003 | c0009 | t0002 | g0009 | AFR | YRI | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18522 | hp2 | a0004 | c0004 | t0001 | g0041 | AFR | YRI | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | CHB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18906 | hp1 | a0004 | c0004 | t0001 | g0149 | AFR | YRI | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18939 | hp1 | a0003 | c0003 | t0002 | g0229 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18944 | hp1 | a0002 | c0002 | t0003 | g0160 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18949 | hp2 | a0001 | c0007 | t0001 | g0147 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18952 | hp2 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18953 | hp2 | a0005 | c0006 | t0001 | g0050 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18954 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18964 | hp1 | a0003 | c0003 | t0002 | g0217 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18966 | hp1 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18968 | hp1 | a0003 | c0003 | t0002 | g0218 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18971 | hp1 | a0001 | c0007 | t0001 | g0066 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18971 | hp2 | a0001 | c0023 | t0001 | g0062 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18973 | hp2 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18978 | hp1 | a0003 | c0003 | t0002 | g0224 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18980 | hp2 | a0002 | c0002 | t0003 | g0020 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18982 | hp2 | a0002 | c0002 | t0003 | g0020 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18985 | hp1 | a0005 | c0006 | t0001 | g0049 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18985 | hp2 | a0002 | c0002 | t0010 | g0243 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18994 | hp2 | a0005 | c0006 | t0001 | g0059 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19002 | hp1 | a0003 | c0003 | t0002 | g0222 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19002 | hp2 | a0001 | c0007 | t0001 | g0135 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19007 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19010 | hp1 | a0002 | c0002 | t0003 | g0161 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19011 | hp1 | a0004 | c0004 | t0001 | g0053 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19012 | hp1 | a0019 | c0019 | t0001 | g0089 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19030 | hp1 | a0004 | c0004 | t0001 | g0153 | AFR | LWK | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0198 | AFR | LWK | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19043 | hp1 | a0004 | c0004 | t0001 | g0032 | AFR | LWK | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19043 | hp2 | a0004 | c0004 | t0001 | g0044 | AFR | LWK | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19056 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19057 | hp1 | a0011 | c0015 | t0001 | g0019 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19057 | hp2 | a0005 | c0006 | t0001 | g0048 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19058 | hp1 | a0001 | c0007 | t0001 | g0095 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19065 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19067 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19080 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19080 | hp2 | a0011 | c0015 | t0001 | g0019 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19083 | hp1 | a0020 | c0020 | t0001 | g0031 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19084 | hp2 | a0021 | c0024 | t0002 | g0221 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19085 | hp1 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19087 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19090 | hp1 | a0002 | c0002 | t0003 | g0159 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19090 | hp2 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19240 | hp1 | a0006 | c0012 | t0001 | g0040 | AFR | YRI | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | YRI | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ASW | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA20129 | hp2 | a0003 | c0003 | t0002 | g0220 | AFR | ASW | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | TSI | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA20752 | hp2 | a0002 | c0002 | t0003 | g0157 | EUR | TSI | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0021 | EUR | TSI | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | TSI | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01123 | hp1 | a0003 | c0003 | t0009 | g0231 | AMR | CLM | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02109 | hp2 | a0006 | c0012 | t0001 | g0042 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02486 | hp1 | a0004 | c0004 | t0001 | g0007 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02559 | hp1 | a0003 | c0003 | t0002 | g0225 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG02559 | hp2 | a0004 | c0004 | t0001 | g0058 | AFR | ACB | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03471 | hp1 | a0003 | c0009 | t0002 | g0009 | AFR | MSL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG03471 | hp2 | a0004 | c0004 | t0001 | g0010 | AFR | MSL | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | USA | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| HG06807 | hp2 | a0003 | c0003 | t0002 | g0008 | AFR | USA | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0193 | AFR | USA | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA20300 | hp2 | a0003 | c0009 | t0002 | g0009 | AFR | USA | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA21309 | hp1 | a0004 | c0010 | t0004 | g0199 | AFR | LWK | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0055 | AFR | LWK | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0096 | REF | REF | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | FBF1_chr17_75904574_75946042 | FBF1 | chr17 | 75904574 | 75946042 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:75914865 | G | A | 1 | a0014 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.2696C>T | p.Ala899Val | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 25/30 | 2974/4874 | 2696/3447 | 899/1148 | chr17 | 75914865 | |||
| chr17:75917943 | C | T | 1 | a0018 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.2374G>A | p.Glu792Lys | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 22/30 | 2652/4874 | 2374/3447 | 792/1148 | chr17 | 75917943 | |||
| chr17:75917948 | C | T | 1 | a0015 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.2369G>A | p.Arg790His | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 22/30 | 2647/4874 | 2369/3447 | 790/1148 | chr17 | 75917948 | |||
| chr17:75919722 | G | A | 1 | a0008 | 2 | HG01515.hp2 HG01517.hp2 |
missense_variant | MODERATE | c.2084C>T | p.Ala695Val | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 20/30 | 2362/4874 | 2084/3447 | 695/1148 | chr17 | 75919722 | |||
| chr17:75920318 | C | T | 1 | a0012 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.1786G>A | p.Glu596Lys | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 18/30 | 2064/4874 | 1786/3447 | 596/1148 | chr17 | 75920318 | |||
| chr17:75920342 | A | T | 5 | a0003 a0014 a0015 others(2): Show |
54 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(51): Show |
missense_variant | MODERATE | c.1762T>A | p.Cys588Ser | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 18/30 | 2040/4874 | 1762/3447 | 588/1148 | chr17 | 75920342 | |||
| chr17:75921255 | C | T | 1 | a0011 | 2 | NA19057.hp1 NA19080.hp2 |
missense_variant | MODERATE | c.1663G>A | p.Val555Met | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 17/30 | 1941/4874 | 1663/3447 | 555/1148 | chr17 | 75921255 | |||
| chr17:75921291 | A | G | 1 | a0005 | 7 | HG01175.hp2 HG01952.hp2 HG04228.hp2 others(4): Show |
missense_variant | MODERATE | c.1627T>C | p.Cys543Arg | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 17/30 | 1905/4874 | 1627/3447 | 543/1148 | chr17 | 75921291 | |||
| chr17:75921991 | C | T | 1 | a0007 | 3 | HG02965.hp1 HG03139.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.1480G>A | p.Gly494Arg | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 15/30 | 1758/4874 | 1480/3447 | 494/1148 | chr17 | 75921991 | |||
| chr17:75923204 | C | A | 1 | a0006 | 3 | HG02109.hp2 HG02258.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.1406G>T | p.Gly469Val | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 14/30 | 1684/4874 | 1406/3447 | 469/1148 | chr17 | 75923204 | |||
| chr17:75923364 | C | T | 1 | a0020 | 1 | NA19083.hp1 | missense_variant | MODERATE | c.1246G>A | p.Gly416Arg | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 14/30 | 1524/4874 | 1246/3447 | 416/1148 | chr17 | 75923364 | |||
| chr17:75923450 | G | A | 1 | a0017 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.1160C>T | p.Thr387Met | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 14/30 | 1438/4874 | 1160/3447 | 387/1148 | chr17 | 75923450 | |||
| chr17:75923457 | G | A | 5 | a0003 a0010 a0014 others(2): Show |
55 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(52): Show |
missense_variant | MODERATE | c.1153C>T | p.Pro385Ser | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 14/30 | 1431/4874 | 1153/3447 | 385/1148 | chr17 | 75923457 | |||
| chr17:75923464 | A | T | 1 | a0017 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.1146T>A | p.Ser382Arg | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 14/30 | 1424/4874 | 1146/3447 | 382/1148 | chr17 | 75923464 | |||
| chr17:75923471 | C | T | 1 | a0017 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.1139G>A | p.Arg380Gln | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 14/30 | 1417/4874 | 1139/3447 | 380/1148 | chr17 | 75923471 | |||
| chr17:75926116 | C | T | 1 | a0016 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.782G>A | p.Arg261Gln | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 12/30 | 1060/4874 | 782/3447 | 261/1148 | chr17 | 75926116 | |||
| chr17:75926137 | G | A | 1 | a0013 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.761C>T | p.Thr254Met | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 12/30 | 1039/4874 | 761/3447 | 254/1148 | chr17 | 75926137 | |||
| chr17:75926848 | A | G | 1 | a0021 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.505T>C | p.Ser169Pro | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 10/30 | 783/4874 | 505/3447 | 169/1148 | chr17 | 75926848 | |||
| chr17:75926860 | T | C | 17 | a0002 a0003 a0004 others(14): Show |
187 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(184): Show |
missense_variant | MODERATE | c.493A>G | p.Arg165Gly | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 10/30 | 771/4874 | 493/3447 | 165/1148 | chr17 | 75926860 | |||
| chr17:75930040 | C | A | 4 | a0002 a0008 a0011 others(1): Show |
81 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(78): Show |
missense_variant | MODERATE | c.236G>T | p.Gly79Val | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 7/30 | 514/4874 | 236/3447 | 79/1148 | chr17 | 75930040 | |||
| chr17:75931279 | C | G | 1 | a0019 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.178G>C | p.Gly60Arg | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 6/30 | 456/4874 | 178/3447 | 60/1148 | chr17 | 75931279 | |||
| chr17:75933037 | G | A | 1 | a0009 | 2 | HG02145.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.125C>T | p.Thr42Ile | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/30 | 403/4874 | 125/3447 | 42/1148 | chr17 | 75933037 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:75913946 | C | T | 2 | a0004c0010 a0013c0032 |
5 | HG01074.hp2 HG02145.hp2 HG03130.hp1 others(2): Show |
synonymous_variant | LOW | c.3096G>A | p.Glu1032Glu | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 27/30 | 3374/4874 | 3096/3447 | 1032/1148 | chr17 | 75913946 | |||
| chr17:75913961 | C | T | 1 | a0017c0026 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.3081G>A | p.Val1027Val | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 27/30 | 3359/4874 | 3081/3447 | 1027/1148 | chr17 | 75913961 | |||
| chr17:75914747 | C | T | 1 | a0004c0028 | 1 | HG02886.hp2 | splice_region_variant&synonymous_variant | LOW | c.2814G>A | p.Lys938Lys | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 25/30 | 3092/4874 | 2814/3447 | 938/1148 | chr17 | 75914747 | |||
| chr17:75915026 | T | C | 1 | a0017c0026 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.2619A>G | p.Glu873Glu | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 24/30 | 2897/4874 | 2619/3447 | 873/1148 | chr17 | 75915026 | |||
| chr17:75915062 | C | T | 1 | a0003c0030 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.2583G>A | p.Thr861Thr | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 24/30 | 2861/4874 | 2583/3447 | 861/1148 | chr17 | 75915062 | |||
| chr17:75915071 | C | T | 1 | a0002c0016 | 2 | HG03490.hp1 HG03492.hp1 |
synonymous_variant | LOW | c.2574G>A | p.Arg858Arg | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 24/30 | 2852/4874 | 2574/3447 | 858/1148 | chr17 | 75915071 | |||
| chr17:75917746 | G | T | 1 | a0009c0018 | 2 | HG02145.hp1 HG03225.hp2 |
synonymous_variant | LOW | c.2491C>A | p.Arg831Arg | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/30 | 2769/4874 | 2491/3447 | 831/1148 | chr17 | 75917746 | |||
| chr17:75918188 | C | T | 1 | a0003c0013 | 2 | HG01243.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.2220G>A | p.Ala740Ala | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 21/30 | 2498/4874 | 2220/3447 | 740/1148 | chr17 | 75918188 | |||
| chr17:75920015 | A | G | 1 | a0001c0007 | 5 | HG02027.hp1 NA18949.hp2 NA18971.hp1 others(2): Show |
synonymous_variant | LOW | c.1923T>C | p.Ser641Ser | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 19/30 | 2201/4874 | 1923/3447 | 641/1148 | chr17 | 75920015 | |||
| chr17:75920391 | C | T | 1 | a0001c0021 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.1713G>A | p.Pro571Pro | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 18/30 | 1991/4874 | 1713/3447 | 571/1148 | chr17 | 75920391 | |||
| chr17:75921536 | G | A | 1 | a0001c0023 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.1551C>T | p.Ala517Ala | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 16/30 | 1829/4874 | 1551/3447 | 517/1148 | chr17 | 75921536 | |||
| chr17:75923413 | C | T | 1 | a0003c0008 | 5 | HG00738.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
synonymous_variant | LOW | c.1197G>A | p.Thr399Thr | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 14/30 | 1475/4874 | 1197/3447 | 399/1148 | chr17 | 75923413 | |||
| chr17:75923440 | C | T | 6 | a0003c0003 a0003c0013 a0003c0030 others(3): Show |
34 | HG00735.hp1 HG01123.hp1 HG01243.hp2 others(31): Show |
synonymous_variant | LOW | c.1170G>A | p.Val390Val | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 14/30 | 1448/4874 | 1170/3447 | 390/1148 | chr17 | 75923440 | |||
| chr17:75923449 | C | T | 1 | a0004c0027 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.1161G>A | p.Thr387Thr | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 14/30 | 1439/4874 | 1161/3447 | 387/1148 | chr17 | 75923449 | |||
| chr17:75923542 | T | A | 1 | a0003c0009 | 5 | HG02886.hp1 HG02970.hp1 HG03471.hp1 others(2): Show |
synonymous_variant | LOW | c.1068A>T | p.Gly356Gly | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 14/30 | 1346/4874 | 1068/3447 | 356/1148 | chr17 | 75923542 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:75909703 | G | A | 1 | a0017c0026t0012 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1020C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 30/30 | 1020 | chr17 | 75909703 | ||||||
| chr17:75909713 | C | T | 10 | a0003c0003t0002 a0003c0003t0009 a0003c0005t0002 others(7): Show |
53 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1010G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 30/30 | 1010 | chr17 | 75909713 | ||||||
| chr17:75910039 | T | C | 1 | a0001c0001t0007 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*684A>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 30/30 | 684 | chr17 | 75910039 | ||||||
| chr17:75910116 | C | T | 1 | a0007c0011t0005 | 3 | HG02965.hp1 HG03139.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*607G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 30/30 | 607 | chr17 | 75910116 | ||||||
| chr17:75910141 | G | T | 2 | a0002c0002t0003 a0002c0016t0003 |
23 | HG00140.hp2 HG00423.hp2 HG00639.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*582C>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 30/30 | 582 | chr17 | 75910141 | ||||||
| chr17:75910575 | T | G | 1 | a0003c0003t0009 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*148A>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 30/30 | 148 | chr17 | 75910575 | ||||||
| chr17:75938154 | C | T | 3 | a0001c0001t0004 a0004c0010t0004 a0013c0032t0004 |
6 | HG01074.hp2 HG01261.hp1 HG02145.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-5G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 2/30 | chr17 | 75938154 | |||||||
| chr17:75940916 | T | C | 12 | a0003c0003t0002 a0003c0003t0009 a0003c0005t0002 others(9): Show |
55 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(52): Show |
5_prime_UTR_variant | MODIFIER | c.-152A>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/30 | 2767 | chr17 | 75940916 | ||||||
| chr17:75940930 | C | T | 1 | a0002c0002t0010 | 1 | NA18985.hp2 | 5_prime_UTR_variant | MODIFIER | c.-166G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/30 | 2781 | chr17 | 75940930 | ||||||
| chr17:75940935 | G | C | 1 | a0002c0002t0010 | 1 | NA18985.hp2 | 5_prime_UTR_variant | MODIFIER | c.-171C>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/30 | 2786 | chr17 | 75940935 | ||||||
| chr17:75940938 | G | A | 1 | a0016c0025t0011 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-174C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/30 | 2789 | chr17 | 75940938 | ||||||
| chr17:75940991 | C | G | 1 | a0001c0001t0006 | 1 | NA18973.hp2 | 5_prime_UTR_variant | MODIFIER | c.-227G>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/30 | 2842 | chr17 | 75940991 | ||||||
| chr17:75940998 | G | C | 1 | a0017c0026t0012 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-234C>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/30 | 2849 | chr17 | 75940998 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:75910853 | G | A | 152 | a0001c0001t0001g0061 a0001c0001t0001g0071 a0001c0001t0001g0072 others(149): Show |
191 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.3364-47C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 29/29 | chr17 | 75910853 | |||||||
| chr17:75910910 | C | T | 1 | a0003c0003t0002g0226 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3364-104G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 29/29 | chr17 | 75910910 | |||||||
| chr17:75910948 | C | T | 2 | a0001c0001t0001g0118 a0020c0020t0001g0031 |
2 | NA18975.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.3364-142G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 29/29 | chr17 | 75910948 | |||||||
| chr17:75910971 | G | A | 1 | a0020c0020t0001g0031 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.3364-165C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 29/29 | chr17 | 75910971 | |||||||
| chr17:75910987 | TCTCAATC others(4): Show |
T | 1 | a0004c0010t0004g0163 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3364-192_3364-182d others(13): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 29/29 | chr17 | 75910987 | |||||||
| chr17:75911150 | G | A | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3364-344C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 29/29 | chr17 | 75911150 | |||||||
| chr17:75911248 | C | A | 2 | a0009c0018t0001g0056 a0009c0018t0001g0119 |
2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3364-442G>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 29/29 | chr17 | 75911248 | |||||||
| chr17:75911381 | T | C | 42 | a0003c0003t0002g0006 a0003c0003t0002g0008 a0003c0003t0002g0023 others(39): Show |
55 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.3364-575A>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 29/29 | chr17 | 75911381 | |||||||
| chr17:75911489 | G | T | 1 | a0019c0019t0001g0089 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3364-683C>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 29/29 | chr17 | 75911489 | |||||||
| chr17:75911494 | G | A | 3 | a0003c0009t0002g0009 a0003c0009t0002g0237 a0003c0009t0002g0240 |
5 | HG02886.hp1 HG02970.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.3364-688C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 29/29 | chr17 | 75911494 | |||||||
| chr17:75911528 | A | G | 3 | a0003c0005t0002g0232 a0003c0005t0002g0233 a0003c0005t0002g0238 |
3 | HG02630.hp2 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3363+664T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 29/29 | chr17 | 75911528 | |||||||
| chr17:75911534 | A | T | 1 | a0003c0008t0002g0239 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3363+658T>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 29/29 | chr17 | 75911534 | |||||||
| chr17:75911555 | G | A | 1 | a0003c0003t0002g0024 | 2 | HG00735.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.3363+637C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 29/29 | chr17 | 75911555 | |||||||
| chr17:75911742 | C | T | 7 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.3363+450G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 29/29 | chr17 | 75911742 | |||||||
| chr17:75911843 | T | G | 4 | a0003c0009t0002g0009 a0003c0009t0002g0237 a0003c0009t0002g0240 others(1): Show |
6 | HG02886.hp1 HG02970.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.3363+349A>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 29/29 | chr17 | 75911843 | |||||||
| chr17:75911862 | G | A | 1 | a0004c0010t0004g0162 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3363+330C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 29/29 | chr17 | 75911862 | |||||||
| chr17:75912342 | T | C | 1 | a0002c0002t0001g0177 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3248-35A>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75912342 | |||||||
| chr17:75912394 | C | G | 37 | a0003c0003t0002g0006 a0003c0003t0002g0008 a0003c0003t0002g0023 others(34): Show |
48 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.3248-87G>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75912394 | |||||||
| chr17:75912485 | A | C | 147 | a0001c0001t0004g0165 a0002c0002t0001g0002 a0002c0002t0001g0021 others(144): Show |
186 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.3248-178T>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75912485 | |||||||
| chr17:75912525 | G | A | 2 | a0002c0002t0001g0158 a0002c0002t0001g0198 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3248-218C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75912525 | |||||||
| chr17:75912622 | A | T | 1 | a0001c0001t0001g0130 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3248-315T>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75912622 | |||||||
| chr17:75912856 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0138 |
3 | HG00642.hp2 HG01099.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.3248-549G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75912856 | |||||||
| chr17:75912923 | G | T | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3248-616C>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75912923 | |||||||
| chr17:75912988 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.3248-681G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75912988 | |||||||
| chr17:75913049 | A | G | 1 | a0004c0004t0001g0030 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3247+653T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75913049 | |||||||
| chr17:75913061 | AG | A | 16 | a0004c0004t0001g0010 a0004c0004t0001g0043 a0004c0004t0001g0044 others(13): Show |
18 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.3247+640delC | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75913061 | |||||||
| chr17:75913095 | A | G | 16 | a0004c0004t0001g0010 a0004c0004t0001g0043 a0004c0004t0001g0044 others(13): Show |
18 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.3247+607T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75913095 | |||||||
| chr17:75913120 | A | G | 1 | a0013c0032t0004g0209 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3247+582T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75913120 | |||||||
| chr17:75913139 | G | A | 6 | a0004c0004t0001g0148 a0004c0004t0001g0149 a0004c0004t0001g0150 others(3): Show |
6 | HG02280.hp1 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3247+563C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75913139 | |||||||
| chr17:75913144 | C | CT | 45 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0073 others(42): Show |
54 | HG00621.hp1 HG00639.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.3247+557dupA | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75913144 | |||||||
| chr17:75913144 | CT | C | 14 | a0001c0001t0001g0061 a0001c0001t0001g0082 a0002c0002t0001g0175 others(11): Show |
14 | HG00323.hp2 HG01074.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.3247+557delA | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75913144 | |||||||
| chr17:75913190 | C | T | 6 | a0004c0004t0001g0148 a0004c0004t0001g0149 a0004c0004t0001g0150 others(3): Show |
6 | HG02280.hp1 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3247+512G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75913190 | |||||||
| chr17:75913290 | G | A | 1 | a0003c0005t0002g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3247+412C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75913290 | |||||||
| chr17:75913396 | C | T | 10 | a0004c0004t0001g0007 a0004c0004t0001g0030 a0004c0004t0001g0037 others(7): Show |
12 | HG00639.hp1 HG01069.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.3247+306G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75913396 | |||||||
| chr17:75913400 | G | A | 1 | a0002c0002t0003g0156 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3247+302C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75913400 | |||||||
| chr17:75913478 | T | TTC | 16 | a0004c0004t0001g0010 a0004c0004t0001g0043 a0004c0004t0001g0044 others(13): Show |
18 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.3247+222_3247+223d others(4): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75913478 | |||||||
| chr17:75913526 | C | CCTCT | 66 | a0003c0003t0002g0006 a0003c0003t0002g0008 a0003c0003t0002g0023 others(63): Show |
81 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.3247+172_3247+175d others(6): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75913526 | |||||||
| chr17:75913586 | G | A | 4 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(1): Show |
4 | HG00323.hp2 HG02486.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.3247+116C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75913586 | |||||||
| chr17:75913620 | CGG | C | 42 | a0003c0003t0002g0006 a0003c0003t0002g0008 a0003c0003t0002g0023 others(39): Show |
55 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.3247+80_3247+81del others(2): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75913620 | |||||||
| chr17:75913672 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3247+30G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 28/29 | chr17 | 75913672 | |||||||
| chr17:75913867 | C | T | 59 | a0002c0002t0001g0002 a0002c0002t0001g0021 a0002c0002t0001g0022 others(56): Show |
81 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.3129+46G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 27/29 | chr17 | 75913867 | |||||||
| chr17:75913890 | G | A | 17 | a0004c0004t0001g0010 a0004c0004t0001g0043 a0004c0004t0001g0044 others(14): Show |
19 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.3129+23C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 27/29 | chr17 | 75913890 | |||||||
| chr17:75914310 | G | A | 1 | a0002c0002t0001g0175 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2815-12C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 25/29 | chr17 | 75914310 | |||||||
| chr17:75914314 | G | A | 44 | a0002c0002t0001g0002 a0002c0002t0001g0021 a0002c0002t0001g0022 others(41): Show |
56 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2815-16C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 25/29 | chr17 | 75914314 | |||||||
| chr17:75914349 | A | G | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2815-51T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 25/29 | chr17 | 75914349 | |||||||
| chr17:75914460 | T | C | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2815-162A>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 25/29 | chr17 | 75914460 | |||||||
| chr17:75914573 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2814+174G>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 25/29 | chr17 | 75914573 | |||||||
| chr17:75914586 | G | C | 1 | a0003c0009t0002g0237 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2814+161C>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 25/29 | chr17 | 75914586 | |||||||
| chr17:75914660 | C | T | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2814+87G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 25/29 | chr17 | 75914660 | |||||||
| chr17:75914933 | C | G | 1 | a0003c0003t0002g0217 | 1 | NA18964.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.2629-1G>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 24/29 | chr17 | 75914933 | |||||||
| chr17:75915002 | G | A | 1 | a0002c0002t0003g0154 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2628+15C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 24/29 | chr17 | 75915002 | |||||||
| chr17:75915191 | G | A | 2 | a0007c0011t0005g0011 a0007c0011t0005g0054 |
3 | HG02965.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2506-52C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75915191 | |||||||
| chr17:75915225 | C | T | 1 | a0002c0002t0003g0155 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2506-86G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75915225 | |||||||
| chr17:75915271 | C | T | 14 | a0004c0004t0001g0010 a0004c0004t0001g0043 a0004c0004t0001g0044 others(11): Show |
15 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2506-132G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75915271 | |||||||
| chr17:75915443 | G | A | 5 | a0003c0003t0002g0008 a0003c0003t0002g0220 a0003c0003t0002g0226 others(2): Show |
7 | HG02451.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2506-304C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75915443 | |||||||
| chr17:75915488 | G | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0103 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2506-349C>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75915488 | |||||||
| chr17:75915493 | C | G | 1 | a0003c0008t0002g0234 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2506-354G>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75915493 | |||||||
| chr17:75915598 | T | TCAAAATG others(10): Show |
1 | a0001c0001t0001g0134 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2506-476_2506-460d others(19): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75915598 | |||||||
| chr17:75915609 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0136 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2506-470G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75915609 | |||||||
| chr17:75915634 | C | T | 146 | a0001c0001t0004g0165 a0002c0002t0001g0002 a0002c0002t0001g0021 others(143): Show |
185 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.2506-495G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75915634 | |||||||
| chr17:75915717 | CATT | C | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG01884.hp2 HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2506-581_2506-579d others(5): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75915717 | |||||||
| chr17:75915779 | C | T | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2506-640G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75915779 | |||||||
| chr17:75915858 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2506-719T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75915858 | |||||||
| chr17:75915917 | A | C | 3 | a0006c0012t0001g0040 a0006c0012t0001g0042 a0006c0012t0001g0057 |
3 | HG02109.hp2 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2506-778T>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75915917 | |||||||
| chr17:75915980 | C | G | 1 | a0001c0001t0001g0109 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2506-841G>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75915980 | |||||||
| chr17:75916007 | C | CA | 19 | a0001c0001t0001g0061 a0001c0001t0001g0065 a0001c0001t0001g0069 others(16): Show |
19 | HG00642.hp1 HG00741.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.2506-869dupT | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75916007 | |||||||
| chr17:75916007 | CA | C | 61 | a0001c0001t0001g0063 a0001c0001t0001g0098 a0002c0002t0001g0158 others(58): Show |
75 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.2506-869delT | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75916007 | |||||||
| chr17:75916007 | CAA | C | 59 | a0001c0001t0004g0165 a0002c0002t0001g0002 a0002c0002t0001g0021 others(56): Show |
81 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2506-870_2506-869d others(4): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75916007 | |||||||
| chr17:75916030 | A | T | 1 | a0004c0010t0004g0162 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2506-891T>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75916030 | |||||||
| chr17:75916057 | C | T | 23 | a0004c0004t0001g0007 a0004c0004t0001g0030 a0004c0004t0001g0032 others(20): Show |
25 | HG00639.hp1 HG01069.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.2506-918G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75916057 | |||||||
| chr17:75916309 | C | A | 3 | a0001c0001t0001g0080 a0001c0001t0001g0097 a0001c0001t0001g0105 |
3 | HG01167.hp1 HG02602.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2506-1170G>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75916309 | |||||||
| chr17:75916325 | A | G | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG01884.hp2 HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2506-1186T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75916325 | |||||||
| chr17:75916326 | A | AT | 68 | a0001c0001t0001g0097 a0001c0001t0001g0143 a0001c0001t0004g0165 others(65): Show |
90 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.2506-1188dupA | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75916326 | |||||||
| chr17:75916392 | G | A | 1 | a0002c0002t0001g0189 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2506-1253C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75916392 | |||||||
| chr17:75916441 | A | G | 147 | a0001c0001t0004g0165 a0002c0002t0001g0002 a0002c0002t0001g0021 others(144): Show |
186 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.2505+1291T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75916441 | |||||||
| chr17:75916639 | T | TAAAACCT others(4376): Show |
1 | a0001c0001t0001g0093 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2505+1092_2505+109 others(4387): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75916639 | |||||||
| chr17:75916836 | C | T | 1 | a0004c0028t0008g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2505+896G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75916836 | |||||||
| chr17:75916862 | T | A | 2 | a0003c0005t0002g0212 a0003c0005t0002g0213 |
2 | HG03490.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2505+870A>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75916862 | |||||||
| chr17:75917054 | C | G | 1 | a0002c0002t0003g0159 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2505+678G>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75917054 | |||||||
| chr17:75917170 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2505+562C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75917170 | |||||||
| chr17:75917219 | C | T | 1 | a0002c0002t0003g0197 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2505+513G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75917219 | |||||||
| chr17:75917254 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2505+478C>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75917254 | |||||||
| chr17:75917319 | A | G | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2505+413T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75917319 | |||||||
| chr17:75917415 | C | T | 9 | a0004c0004t0001g0007 a0004c0004t0001g0030 a0004c0004t0001g0037 others(6): Show |
11 | HG00639.hp1 HG01069.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2505+317G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75917415 | |||||||
| chr17:75917485 | C | T | 3 | a0002c0016t0003g0195 a0002c0016t0003g0196 a0017c0026t0012g0245 |
3 | HG03486.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2505+247G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75917485 | |||||||
| chr17:75917645 | T | A | 1 | a0001c0001t0001g0134 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2505+87A>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75917645 | |||||||
| chr17:75917649 | G | A | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2505+83C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75917649 | |||||||
| chr17:75917660 | T | C | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2505+72A>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 23/29 | chr17 | 75917660 | |||||||
| chr17:75918294 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2139-25G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 20/29 | chr17 | 75918294 | |||||||
| chr17:75918344 | T | C | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2139-75A>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 20/29 | chr17 | 75918344 | |||||||
| chr17:75918382 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2139-113G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 20/29 | chr17 | 75918382 | |||||||
| chr17:75918386 | G | A | 1 | a0002c0002t0003g0003 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2139-117C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 20/29 | chr17 | 75918386 | |||||||
| chr17:75918623 | G | A | 1 | a0003c0009t0002g0240 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2139-354C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 20/29 | chr17 | 75918623 | |||||||
| chr17:75918652 | G | A | 10 | a0004c0004t0001g0007 a0004c0004t0001g0030 a0004c0004t0001g0037 others(7): Show |
12 | HG00639.hp1 HG01069.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2139-383C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 20/29 | chr17 | 75918652 | |||||||
| chr17:75918782 | A | G | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2139-513T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 20/29 | chr17 | 75918782 | |||||||
| chr17:75918805 | CT | C | 24 | a0001c0001t0001g0064 a0001c0001t0001g0082 a0001c0001t0001g0086 others(21): Show |
26 | HG00323.hp2 HG01175.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.2139-537delA | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 20/29 | chr17 | 75918805 | |||||||
| chr17:75918843 | A | G | 1 | a0002c0002t0001g0187 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2139-574T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 20/29 | chr17 | 75918843 | |||||||
| chr17:75919072 | T | A | 146 | a0001c0001t0004g0165 a0002c0002t0001g0002 a0002c0002t0001g0021 others(143): Show |
185 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.2138+596A>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 20/29 | chr17 | 75919072 | |||||||
| chr17:75919115 | C | G | 5 | a0004c0004t0001g0007 a0004c0004t0001g0037 a0004c0004t0001g0038 others(2): Show |
7 | HG01069.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2138+553G>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 20/29 | chr17 | 75919115 | |||||||
| chr17:75919167 | A | G | 40 | a0003c0003t0002g0006 a0003c0003t0002g0008 a0003c0003t0002g0023 others(37): Show |
53 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.2138+501T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 20/29 | chr17 | 75919167 | |||||||
| chr17:75919293 | G | A | 1 | a0002c0002t0001g0204 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2138+375C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 20/29 | chr17 | 75919293 | |||||||
| chr17:75919325 | G | A | 1 | a0004c0010t0004g0163 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2138+343C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 20/29 | chr17 | 75919325 | |||||||
| chr17:75919987 | T | G | 1 | a0004c0028t0008g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1931+20A>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 19/29 | chr17 | 75919987 | |||||||
| chr17:75920463 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1675-34C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 17/29 | chr17 | 75920463 | |||||||
| chr17:75920581 | C | A | 1 | a0004c0004t0001g0052 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1675-152G>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 17/29 | chr17 | 75920581 | |||||||
| chr17:75920648 | C | T | 1 | a0002c0002t0001g0188 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1675-219G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 17/29 | chr17 | 75920648 | |||||||
| chr17:75920830 | T | TG | 16 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0065 others(13): Show |
18 | HG01243.hp1 HG01255.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.1675-402dupC | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 17/29 | chr17 | 75920830 | |||||||
| chr17:75920830 | TG | T | 37 | a0001c0001t0001g0017 a0001c0001t0001g0071 a0001c0001t0001g0078 others(34): Show |
42 | HG00423.hp1 HG00544.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.1675-402delC | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 17/29 | chr17 | 75920830 | |||||||
| chr17:75920830 | TGG | T | 55 | a0002c0002t0001g0167 a0002c0002t0001g0168 a0002c0002t0001g0179 others(52): Show |
65 | HG00735.hp1 HG00738.hp1 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.1675-403_1675-402d others(4): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 17/29 | chr17 | 75920830 | |||||||
| chr17:75920830 | TGGG | T | 67 | a0002c0002t0001g0002 a0002c0002t0001g0021 a0002c0002t0001g0022 others(64): Show |
92 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1675-404_1675-402d others(5): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 17/29 | chr17 | 75920830 | |||||||
| chr17:75920831 | G | C | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1675-402C>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 17/29 | chr17 | 75920831 | |||||||
| chr17:75921119 | G | A | 1 | a0004c0004t0001g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1674+125C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 17/29 | chr17 | 75921119 | |||||||
| chr17:75921215 | G | A | 1 | a0004c0004t0001g0030 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1674+29C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 17/29 | chr17 | 75921215 | |||||||
| chr17:75921223 | C | T | 1 | a0004c0004t0001g0046 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1674+21G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 17/29 | chr17 | 75921223 | |||||||
| chr17:75921329 | A | G | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1616-27T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 16/29 | chr17 | 75921329 | |||||||
| chr17:75921345 | A | T | 41 | a0003c0003t0002g0006 a0003c0003t0002g0008 a0003c0003t0002g0023 others(38): Show |
54 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.1616-43T>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 16/29 | chr17 | 75921345 | |||||||
| chr17:75921383 | C | T | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1616-81G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 16/29 | chr17 | 75921383 | |||||||
| chr17:75921618 | G | T | 1 | a0004c0028t0008g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1527-58C>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 15/29 | chr17 | 75921618 | |||||||
| chr17:75921699 | G | A | 1 | a0004c0028t0008g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1527-139C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 15/29 | chr17 | 75921699 | |||||||
| chr17:75921721 | C | T | 16 | a0004c0004t0001g0010 a0004c0004t0001g0043 a0004c0004t0001g0044 others(13): Show |
18 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1527-161G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 15/29 | chr17 | 75921721 | |||||||
| chr17:75921750 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1527-190C>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 15/29 | chr17 | 75921750 | |||||||
| chr17:75921760 | G | A | 4 | a0001c0001t0004g0165 a0004c0010t0004g0163 a0004c0010t0004g0164 others(1): Show |
4 | HG01074.hp2 HG01261.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1526+185C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 15/29 | chr17 | 75921760 | |||||||
| chr17:75921803 | C | T | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1526+142G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 15/29 | chr17 | 75921803 | |||||||
| chr17:75921833 | C | CACGGGG | 7 | a0002c0002t0003g0018 a0002c0002t0003g0154 a0002c0002t0003g0155 others(4): Show |
8 | HG00140.hp2 HG01255.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.1526+106_1526+111d others(8): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 15/29 | chr17 | 75921833 | |||||||
| chr17:75921836 | G | A | 1 | a0004c0004t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1526+109C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 15/29 | chr17 | 75921836 | |||||||
| chr17:75922070 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1425-24A>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 14/29 | chr17 | 75922070 | |||||||
| chr17:75922183 | A | G | 43 | a0003c0003t0002g0006 a0003c0003t0002g0008 a0003c0003t0002g0023 others(40): Show |
56 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.1425-137T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 14/29 | chr17 | 75922183 | |||||||
| chr17:75922570 | T | G | 16 | a0004c0004t0001g0010 a0004c0004t0001g0043 a0004c0004t0001g0044 others(13): Show |
18 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1425-524A>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 14/29 | chr17 | 75922570 | |||||||
| chr17:75922646 | G | T | 5 | a0005c0006t0001g0048 a0005c0006t0001g0049 a0005c0006t0001g0051 others(2): Show |
5 | HG01175.hp2 HG01952.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.1424+540C>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 14/29 | chr17 | 75922646 | |||||||
| chr17:75922822 | G | A | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1424+364C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 14/29 | chr17 | 75922822 | |||||||
| chr17:75923107 | A | G | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1424+79T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 14/29 | chr17 | 75923107 | |||||||
| chr17:75923687 | C | A | 1 | a0003c0013t0002g0026 | 2 | HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.969-46G>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75923687 | |||||||
| chr17:75923723 | G | A | 1 | a0001c0007t0001g0066 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.969-82C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75923723 | |||||||
| chr17:75923732 | G | A | 1 | a0004c0028t0008g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.969-91C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75923732 | |||||||
| chr17:75923798 | C | T | 1 | a0005c0006t0001g0047 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.969-157G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75923798 | |||||||
| chr17:75923857 | G | A | 4 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(1): Show |
4 | NA18943.hp2 NA18945.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.969-216C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75923857 | |||||||
| chr17:75923906 | G | A | 1 | a0003c0005t0002g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.969-265C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75923906 | |||||||
| chr17:75923962 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.969-321G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75923962 | |||||||
| chr17:75924057 | C | CA | 43 | a0003c0003t0002g0006 a0003c0003t0002g0008 a0003c0003t0002g0023 others(40): Show |
56 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.969-417dupT | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75924057 | |||||||
| chr17:75924138 | C | T | 13 | a0002c0002t0003g0003 a0002c0002t0003g0018 a0002c0002t0003g0020 others(10): Show |
23 | HG00140.hp2 HG00423.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.969-497G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75924138 | |||||||
| chr17:75924204 | ACT | A | 14 | a0004c0004t0001g0010 a0004c0004t0001g0043 a0004c0004t0001g0044 others(11): Show |
15 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.969-565_969-564del others(2): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75924204 | |||||||
| chr17:75924251 | G | T | 2 | a0007c0011t0005g0011 a0007c0011t0005g0054 |
3 | HG02965.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.969-610C>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75924251 | |||||||
| chr17:75924284 | C | T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0129 others(1): Show |
4 | HG00741.hp2 HG01071.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.969-643G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75924284 | |||||||
| chr17:75924346 | A | G | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.969-705T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75924346 | |||||||
| chr17:75924475 | T | C | 1 | a0004c0004t0001g0052 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.969-834A>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75924475 | |||||||
| chr17:75924667 | G | A | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.968+680C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75924667 | |||||||
| chr17:75924831 | C | G | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.968+516G>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75924831 | |||||||
| chr17:75924882 | T | G | 14 | a0004c0004t0001g0010 a0004c0004t0001g0043 a0004c0004t0001g0044 others(11): Show |
15 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.968+465A>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75924882 | |||||||
| chr17:75925178 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.968+169G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75925178 | |||||||
| chr17:75925202 | C | T | 4 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0125 others(1): Show |
4 | HG02027.hp2 HG02055.hp2 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.968+145G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75925202 | |||||||
| chr17:75925237 | G | A | 1 | a0001c0007t0001g0066 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.968+110C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 13/29 | chr17 | 75925237 | |||||||
| chr17:75925495 | C | T | 6 | a0004c0004t0001g0148 a0004c0004t0001g0149 a0004c0004t0001g0150 others(3): Show |
6 | HG02280.hp1 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-49G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 12/29 | chr17 | 75925495 | |||||||
| chr17:75925572 | G | A | 1 | a0002c0002t0001g0183 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.869-126C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 12/29 | chr17 | 75925572 | |||||||
| chr17:75925664 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.869-218C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 12/29 | chr17 | 75925664 | |||||||
| chr17:75925851 | C | T | 1 | a0013c0032t0004g0209 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.868+179G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 12/29 | chr17 | 75925851 | |||||||
| chr17:75926008 | C | T | 1 | a0002c0002t0001g0202 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.868+22G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 12/29 | chr17 | 75926008 | |||||||
| chr17:75926269 | C | A | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.734+19G>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 11/29 | chr17 | 75926269 | |||||||
| chr17:75926957 | C | T | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.476-80G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 9/29 | chr17 | 75926957 | |||||||
| chr17:75927014 | TG | T | 3 | a0004c0010t0004g0163 a0004c0010t0004g0164 a0004c0010t0004g0199 |
3 | HG01074.hp2 HG03669.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.476-138delC | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 9/29 | chr17 | 75927014 | |||||||
| chr17:75927054 | G | A | 7 | a0004c0004t0001g0148 a0004c0004t0001g0149 a0004c0004t0001g0150 others(4): Show |
7 | HG02280.hp1 HG02572.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.476-177C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 9/29 | chr17 | 75927054 | |||||||
| chr17:75927116 | G | A | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.476-239C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 9/29 | chr17 | 75927116 | |||||||
| chr17:75927120 | G | A | 3 | a0003c0009t0002g0009 a0003c0009t0002g0237 a0003c0009t0002g0240 |
5 | HG02886.hp1 HG02970.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.476-243C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 9/29 | chr17 | 75927120 | |||||||
| chr17:75927135 | C | T | 2 | a0009c0018t0001g0056 a0009c0018t0001g0119 |
2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.476-258G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 9/29 | chr17 | 75927135 | |||||||
| chr17:75927155 | A | G | 10 | a0004c0004t0001g0007 a0004c0004t0001g0030 a0004c0004t0001g0037 others(7): Show |
12 | HG00639.hp1 HG01069.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.476-278T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 9/29 | chr17 | 75927155 | |||||||
| chr17:75927170 | A | G | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.475+285T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 9/29 | chr17 | 75927170 | |||||||
| chr17:75927753 | C | T | 1 | a0004c0028t0008g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.398-221G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 8/29 | chr17 | 75927753 | |||||||
| chr17:75927787 | G | A | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.398-255C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 8/29 | chr17 | 75927787 | |||||||
| chr17:75927984 | C | T | 16 | a0004c0004t0001g0010 a0004c0004t0001g0043 a0004c0004t0001g0044 others(13): Show |
18 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.397+92G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 8/29 | chr17 | 75927984 | |||||||
| chr17:75928005 | G | A | 14 | a0004c0004t0001g0010 a0004c0004t0001g0043 a0004c0004t0001g0044 others(11): Show |
15 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.397+71C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 8/29 | chr17 | 75928005 | |||||||
| chr17:75928268 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.280-75G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 7/29 | chr17 | 75928268 | |||||||
| chr17:75928418 | C | CA | 8 | a0003c0003t0002g0006 a0003c0003t0002g0217 a0003c0003t0002g0218 others(5): Show |
11 | HG02523.hp2 NA18939.hp1 NA18952.hp2 others(8): Show |
intron_variant | MODIFIER | c.280-226dupT | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 7/29 | chr17 | 75928418 | |||||||
| chr17:75928511 | C | A | 6 | a0002c0002t0001g0166 a0002c0002t0001g0184 a0002c0002t0001g0191 others(3): Show |
6 | HG00544.hp1 HG01168.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-318G>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 7/29 | chr17 | 75928511 | |||||||
| chr17:75928615 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.280-422G>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 7/29 | chr17 | 75928615 | |||||||
| chr17:75928721 | T | A | 1 | a0020c0020t0001g0031 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.280-528A>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 7/29 | chr17 | 75928721 | |||||||
| chr17:75928723 | G | A | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.280-530C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 7/29 | chr17 | 75928723 | |||||||
| chr17:75929005 | G | T | 2 | a0010c0014t0001g0121 a0010c0014t0001g0144 |
2 | HG02735.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.280-812C>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 7/29 | chr17 | 75929005 | |||||||
| chr17:75929069 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.280-876G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 7/29 | chr17 | 75929069 | |||||||
| chr17:75929081 | C | A | 1 | a0002c0002t0001g0186 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.280-888G>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 7/29 | chr17 | 75929081 | |||||||
| chr17:75929127 | A | G | 1 | a0018c0033t0001g0201 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.279+870T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 7/29 | chr17 | 75929127 | |||||||
| chr17:75929144 | T | A | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.279+853A>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 7/29 | chr17 | 75929144 | |||||||
| chr17:75929251 | G | A | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.279+746C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 7/29 | chr17 | 75929251 | |||||||
| chr17:75929297 | C | T | 8 | a0003c0003t0002g0006 a0003c0003t0002g0217 a0003c0003t0002g0218 others(5): Show |
11 | HG02523.hp2 NA18939.hp1 NA18952.hp2 others(8): Show |
intron_variant | MODIFIER | c.279+700G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 7/29 | chr17 | 75929297 | |||||||
| chr17:75929331 | T | TA | 5 | a0001c0001t0001g0142 a0001c0001t0001g0146 a0002c0002t0001g0194 others(2): Show |
5 | HG00544.hp2 HG03669.hp1 NA19083.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+665dupT | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 7/29 | chr17 | 75929331 | |||||||
| chr17:75929542 | A | T | 2 | a0003c0005t0002g0028 a0003c0008t0002g0239 |
3 | HG01069.hp1 HG01071.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.279+455T>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 7/29 | chr17 | 75929542 | |||||||
| chr17:75930104 | A | G | 3 | a0003c0005t0002g0232 a0003c0005t0002g0233 a0003c0005t0002g0238 |
3 | HG02630.hp2 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.229-57T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 6/29 | chr17 | 75930104 | |||||||
| chr17:75930150 | G | A | 40 | a0003c0003t0002g0006 a0003c0003t0002g0008 a0003c0003t0002g0023 others(37): Show |
53 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.229-103C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 6/29 | chr17 | 75930150 | |||||||
| chr17:75930151 | C | T | 4 | a0001c0001t0001g0114 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | NA18971.hp2 NA19005.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.229-104G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 6/29 | chr17 | 75930151 | |||||||
| chr17:75930185 | C | A | 40 | a0003c0003t0002g0006 a0003c0003t0002g0008 a0003c0003t0002g0023 others(37): Show |
53 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.229-138G>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 6/29 | chr17 | 75930185 | |||||||
| chr17:75930193 | T | G | 1 | a0002c0002t0001g0210 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.229-146A>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 6/29 | chr17 | 75930193 | |||||||
| chr17:75930194 | G | T | 1 | a0002c0002t0001g0210 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.229-147C>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 6/29 | chr17 | 75930194 | |||||||
| chr17:75930337 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0122 others(2): Show |
7 | HG00642.hp2 HG00741.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.229-290G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 6/29 | chr17 | 75930337 | |||||||
| chr17:75930514 | C | T | 1 | a0013c0032t0004g0209 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.229-467G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 6/29 | chr17 | 75930514 | |||||||
| chr17:75930526 | G | A | 1 | a0002c0002t0001g0166 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.229-479C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 6/29 | chr17 | 75930526 | |||||||
| chr17:75930589 | G | A | 1 | a0004c0004t0001g0030 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.229-542C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 6/29 | chr17 | 75930589 | |||||||
| chr17:75930778 | C | G | 1 | a0003c0005t0002g0232 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.228+451G>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 6/29 | chr17 | 75930778 | |||||||
| chr17:75930783 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.228+446C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 6/29 | chr17 | 75930783 | |||||||
| chr17:75930826 | G | A | 1 | a0001c0001t0004g0165 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.228+403C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 6/29 | chr17 | 75930826 | |||||||
| chr17:75930855 | A | G | 6 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(3): Show |
6 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.228+374T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 6/29 | chr17 | 75930855 | |||||||
| chr17:75930958 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.228+271C>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 6/29 | chr17 | 75930958 | |||||||
| chr17:75931176 | T | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0110 |
2 | NA18959.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.228+53A>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 6/29 | chr17 | 75931176 | |||||||
| chr17:75931197 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.228+32C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 6/29 | chr17 | 75931197 | |||||||
| chr17:75931319 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0122 others(2): Show |
7 | HG00642.hp2 HG00741.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.168-30C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75931319 | |||||||
| chr17:75931376 | G | A | 2 | a0009c0018t0001g0056 a0009c0018t0001g0119 |
2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.168-87C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75931376 | |||||||
| chr17:75931443 | T | C | 2 | a0002c0002t0001g0187 a0002c0002t0001g0207 |
2 | HG00609.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.168-154A>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75931443 | |||||||
| chr17:75931499 | T | C | 1 | a0003c0005t0002g0028 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.168-210A>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75931499 | |||||||
| chr17:75931503 | G | T | 7 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-214C>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75931503 | |||||||
| chr17:75931580 | T | C | 1 | a0001c0021t0001g0111 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.168-291A>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75931580 | |||||||
| chr17:75931687 | G | C | 2 | a0002c0002t0001g0188 a0002c0002t0001g0189 |
2 | HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.168-398C>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75931687 | |||||||
| chr17:75931739 | C | T | 40 | a0003c0003t0002g0006 a0003c0003t0002g0008 a0003c0003t0002g0023 others(37): Show |
53 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.168-450G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75931739 | |||||||
| chr17:75931795 | A | G | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168-506T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75931795 | |||||||
| chr17:75931877 | G | C | 24 | a0004c0004t0001g0007 a0004c0004t0001g0030 a0004c0004t0001g0032 others(21): Show |
26 | HG00639.hp1 HG01069.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.168-588C>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75931877 | |||||||
| chr17:75931931 | C | T | 3 | a0004c0004t0001g0148 a0004c0004t0001g0149 a0004c0004t0001g0150 |
3 | HG02970.hp2 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.168-642G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75931931 | |||||||
| chr17:75932019 | A | G | 1 | a0004c0004t0001g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.168-730T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75932019 | |||||||
| chr17:75932044 | C | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0084 a0001c0001t0001g0088 |
3 | HG02976.hp2 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.168-755G>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75932044 | |||||||
| chr17:75932114 | C | T | 6 | a0004c0004t0001g0148 a0004c0004t0001g0149 a0004c0004t0001g0150 others(3): Show |
6 | HG02280.hp1 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-825G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75932114 | |||||||
| chr17:75932454 | A | T | 6 | a0001c0001t0001g0061 a0001c0001t0001g0071 a0001c0001t0001g0072 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.167+541T>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75932454 | |||||||
| chr17:75932572 | T | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0140 |
2 | HG00423.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.167+423A>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75932572 | |||||||
| chr17:75932602 | G | A | 1 | a0004c0028t0008g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.167+393C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75932602 | |||||||
| chr17:75932861 | C | T | 1 | a0004c0004t0001g0030 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.167+134G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75932861 | |||||||
| chr17:75932878 | T | TA | 20 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0001g0128 others(17): Show |
22 | HG00544.hp1 HG01952.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.167+116dupT | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75932878 | |||||||
| chr17:75932878 | TA | T | 9 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(6): Show |
9 | HG01168.hp1 HG02976.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.167+116delT | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 5/29 | chr17 | 75932878 | |||||||
| chr17:75933113 | G | A | 3 | a0006c0012t0001g0040 a0006c0012t0001g0042 a0006c0012t0001g0057 |
3 | HG02109.hp2 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.74-25C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75933113 | |||||||
| chr17:75933277 | G | T | 1 | a0001c0001t0001g0129 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.74-189C>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75933277 | |||||||
| chr17:75933279 | A | T | 1 | a0001c0001t0001g0129 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.74-191T>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75933279 | |||||||
| chr17:75933329 | C | G | 4 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(1): Show |
4 | HG00323.hp2 HG02486.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.74-241G>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75933329 | |||||||
| chr17:75933486 | C | T | 56 | a0003c0003t0002g0006 a0003c0003t0002g0008 a0003c0003t0002g0023 others(53): Show |
71 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(68): Show |
intron_variant | MODIFIER | c.74-398G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75933486 | |||||||
| chr17:75933506 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.74-418C>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75933506 | |||||||
| chr17:75933803 | GA | G | 5 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0125 others(2): Show |
5 | HG02027.hp1 HG02027.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.74-716delT | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75933803 | |||||||
| chr17:75934276 | GCTACGTG others(3): Show |
G | 1 | a0001c0001t0001g0114 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.74-1198_74-1189del others(10): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934276 | |||||||
| chr17:75934294 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.74-1206C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934294 | |||||||
| chr17:75934296 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.74-1208A>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934296 | |||||||
| chr17:75934297 | A | T | 1 | a0001c0001t0001g0114 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.74-1209T>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934297 | |||||||
| chr17:75934301 | C | A | 1 | a0001c0001t0001g0114 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.74-1213G>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934301 | |||||||
| chr17:75934302 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.74-1214T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934302 | |||||||
| chr17:75934313 | C | G | 1 | a0001c0001t0001g0114 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.74-1225G>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934313 | |||||||
| chr17:75934314 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.74-1226G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934314 | |||||||
| chr17:75934316 | A | G | 1 | a0003c0030t0002g0219 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.74-1228T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934316 | |||||||
| chr17:75934317 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.74-1229T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934317 | |||||||
| chr17:75934326 | G | T | 1 | a0001c0001t0001g0114 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.74-1238C>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934326 | |||||||
| chr17:75934334 | G | GGCCATGG others(4): Show |
1 | a0001c0001t0001g0114 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.74-1247_74-1246ins others(11): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934334 | |||||||
| chr17:75934338 | G | C | 1 | a0001c0001t0001g0114 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.74-1250C>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934338 | |||||||
| chr17:75934350 | C | G | 1 | a0016c0025t0011g0244 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.74-1262G>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934350 | |||||||
| chr17:75934352 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.74-1264C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934352 | |||||||
| chr17:75934475 | C | T | 1 | a0005c0006t0001g0060 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.73+1157G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934475 | |||||||
| chr17:75934555 | C | CA | 59 | a0001c0001t0001g0115 a0002c0002t0001g0002 a0002c0002t0001g0021 others(56): Show |
81 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.73+1076dupT | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934555 | |||||||
| chr17:75934600 | G | A | 1 | a0004c0004t0001g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.73+1032C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934600 | |||||||
| chr17:75934827 | C | T | 1 | a0004c0004t0001g0030 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.73+805G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934827 | |||||||
| chr17:75934863 | G | A | 1 | a0013c0032t0004g0209 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.73+769C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934863 | |||||||
| chr17:75934879 | C | CA | 17 | a0001c0001t0001g0077 a0001c0001t0001g0116 a0001c0001t0001g0117 others(14): Show |
20 | HG01361.hp1 HG02523.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.73+752dupT | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75934879 | |||||||
| chr17:75935075 | A | G | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.73+557T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75935075 | |||||||
| chr17:75935166 | A | AT | 45 | a0001c0001t0001g0077 a0002c0002t0001g0167 a0002c0002t0001g0172 others(42): Show |
58 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.73+465dupA | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75935166 | |||||||
| chr17:75935166 | A | T | 1 | a0003c0008t0002g0239 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.73+466T>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75935166 | |||||||
| chr17:75935171 | T | A | 2 | a0007c0011t0005g0011 a0007c0011t0005g0054 |
3 | HG02965.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.73+461A>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75935171 | |||||||
| chr17:75935310 | G | A | 6 | a0001c0001t0004g0165 a0004c0010t0004g0162 a0004c0010t0004g0163 others(3): Show |
6 | HG01074.hp2 HG01261.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.73+322C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75935310 | |||||||
| chr17:75935349 | A | T | 1 | a0012c0022t0001g0076 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.73+283T>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75935349 | |||||||
| chr17:75935510 | T | C | 1 | a0002c0002t0003g0160 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.73+122A>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75935510 | |||||||
| chr17:75935523 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.73+109C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 4/29 | chr17 | 75935523 | |||||||
| chr17:75935706 | G | A | 60 | a0002c0002t0001g0002 a0002c0002t0001g0021 a0002c0002t0001g0022 others(57): Show |
82 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.32-33C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75935706 | |||||||
| chr17:75935766 | C | G | 147 | a0001c0001t0004g0165 a0002c0002t0001g0002 a0002c0002t0001g0021 others(144): Show |
186 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.32-93G>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75935766 | |||||||
| chr17:75935992 | A | T | 10 | a0004c0004t0001g0007 a0004c0004t0001g0030 a0004c0004t0001g0037 others(7): Show |
12 | HG00639.hp1 HG01069.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.32-319T>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75935992 | |||||||
| chr17:75936040 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.32-367G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75936040 | |||||||
| chr17:75936119 | C | T | 1 | a0005c0006t0001g0059 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.32-446G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75936119 | |||||||
| chr17:75936242 | TG | T | 24 | a0004c0004t0001g0007 a0004c0004t0001g0030 a0004c0004t0001g0032 others(21): Show |
26 | HG00639.hp1 HG01069.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.32-570delC | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75936242 | |||||||
| chr17:75936269 | G | A | 3 | a0006c0012t0001g0040 a0006c0012t0001g0042 a0006c0012t0001g0057 |
3 | HG02109.hp2 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.32-596C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75936269 | |||||||
| chr17:75936301 | G | A | 7 | a0004c0004t0001g0148 a0004c0004t0001g0149 a0004c0004t0001g0150 others(4): Show |
7 | HG02280.hp1 HG02572.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.32-628C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75936301 | |||||||
| chr17:75936330 | AC | A | 24 | a0004c0004t0001g0007 a0004c0004t0001g0030 a0004c0004t0001g0032 others(21): Show |
26 | HG00639.hp1 HG01069.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.32-658delG | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75936330 | |||||||
| chr17:75936350 | G | A | 3 | a0006c0012t0001g0040 a0006c0012t0001g0042 a0006c0012t0001g0057 |
3 | HG02109.hp2 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.32-677C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75936350 | |||||||
| chr17:75936399 | G | A | 40 | a0004c0004t0001g0007 a0004c0004t0001g0010 a0004c0004t0001g0030 others(37): Show |
44 | HG00639.hp1 HG01069.hp2 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.32-726C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75936399 | |||||||
| chr17:75936441 | G | A | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.32-768C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75936441 | |||||||
| chr17:75936476 | A | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0120 |
2 | NA18943.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.32-803T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75936476 | |||||||
| chr17:75936525 | A | G | 9 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(6): Show |
9 | HG01074.hp2 HG01261.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.32-852T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75936525 | |||||||
| chr17:75936569 | G | A | 40 | a0003c0003t0002g0006 a0003c0003t0002g0008 a0003c0003t0002g0023 others(37): Show |
53 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.32-896C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75936569 | |||||||
| chr17:75936610 | G | A | 1 | a0004c0004t0001g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.32-937C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75936610 | |||||||
| chr17:75936670 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.31+896C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75936670 | |||||||
| chr17:75936767 | G | C | 1 | a0002c0002t0001g0193 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.31+799C>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75936767 | |||||||
| chr17:75937069 | A | G | 2 | a0007c0011t0005g0011 a0007c0011t0005g0054 |
3 | HG02965.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.31+497T>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75937069 | |||||||
| chr17:75937081 | C | T | 4 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(1): Show |
4 | NA18943.hp2 NA18945.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.31+485G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75937081 | |||||||
| chr17:75937092 | C | T | 1 | a0003c0003t0002g0216 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.31+474G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75937092 | |||||||
| chr17:75937101 | C | G | 16 | a0004c0004t0001g0010 a0004c0004t0001g0043 a0004c0004t0001g0044 others(13): Show |
18 | HG01175.hp2 HG01952.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.31+465G>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75937101 | |||||||
| chr17:75937174 | A | AT | 8 | a0001c0007t0001g0147 a0002c0002t0001g0167 a0002c0002t0001g0194 others(5): Show |
9 | HG02559.hp2 HG02622.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.31+391dupA | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75937174 | |||||||
| chr17:75937209 | T | C | 147 | a0001c0001t0004g0165 a0002c0002t0001g0002 a0002c0002t0001g0021 others(144): Show |
186 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.31+357A>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75937209 | |||||||
| chr17:75937320 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.31+246C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75937320 | |||||||
| chr17:75937360 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0123 |
2 | HG00735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.31+206G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75937360 | |||||||
| chr17:75937392 | G | A | 3 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 |
3 | HG01884.hp1 HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.31+174C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75937392 | |||||||
| chr17:75937434 | C | T | 1 | a0004c0010t0004g0162 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.31+132G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75937434 | |||||||
| chr17:75937565 | C | T | 1 | a0002c0002t0001g0171 | 1 | NA18945.hp2 | splice_donor_variant&intron_variant | HIGH | c.31+1G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 3/29 | chr17 | 75937565 | |||||||
| chr17:75937775 | C | T | 1 | a0004c0004t0001g0153 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4-182G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 2/29 | chr17 | 75937775 | |||||||
| chr17:75937778 | G | C | 1 | a0004c0004t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4-185C>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 2/29 | chr17 | 75937778 | |||||||
| chr17:75937843 | G | A | 6 | a0004c0004t0001g0148 a0004c0004t0001g0149 a0004c0004t0001g0150 others(3): Show |
6 | HG02280.hp1 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-250C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 2/29 | chr17 | 75937843 | |||||||
| chr17:75937977 | T | G | 10 | a0004c0004t0001g0007 a0004c0004t0001g0030 a0004c0004t0001g0037 others(7): Show |
12 | HG00639.hp1 HG01069.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.3+170A>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 2/29 | chr17 | 75937977 | |||||||
| chr17:75938016 | C | T | 8 | a0001c0001t0007g0055 a0004c0004t0001g0032 a0004c0004t0001g0033 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.3+131G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 2/29 | chr17 | 75938016 | |||||||
| chr17:75938049 | G | A | 60 | a0002c0002t0001g0002 a0002c0002t0001g0021 a0002c0002t0001g0022 others(57): Show |
82 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.3+98C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 2/29 | chr17 | 75938049 | |||||||
| chr17:75938555 | C | CA | 112 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0145 others(109): Show |
146 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.-83-324dupT | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75938555 | |||||||
| chr17:75938555 | C | CAA | 29 | a0002c0002t0001g0194 a0002c0002t0001g0208 a0002c0002t0003g0161 others(26): Show |
34 | HG01175.hp2 HG01361.hp1 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.-83-325_-83-324dup others(2): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75938555 | |||||||
| chr17:75938555 | CA | C | 7 | a0001c0001t0001g0012 a0001c0001t0001g0061 a0001c0001t0001g0063 others(4): Show |
8 | HG01168.hp2 HG01255.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-83-324delT | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75938555 | |||||||
| chr17:75938584 | G | A | 1 | a0017c0026t0012g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-83-352C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75938584 | |||||||
| chr17:75938588 | G | A | 1 | a0006c0012t0001g0042 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-83-356C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75938588 | |||||||
| chr17:75938617 | T | C | 1 | a0002c0002t0010g0243 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-83-385A>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75938617 | |||||||
| chr17:75938618 | C | T | 1 | a0002c0002t0010g0243 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-83-386G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75938618 | |||||||
| chr17:75938790 | C | T | 1 | a0004c0004t0001g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-83-558G>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75938790 | |||||||
| chr17:75938793 | T | C | 1 | a0014c0031t0002g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-83-561A>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75938793 | |||||||
| chr17:75938864 | C | CA | 71 | a0002c0002t0001g0002 a0002c0002t0001g0021 a0002c0002t0001g0022 others(68): Show |
94 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.-83-633dupT | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75938864 | |||||||
| chr17:75938864 | C | CAA | 6 | a0001c0001t0004g0165 a0002c0002t0001g0210 a0004c0010t0004g0162 others(3): Show |
6 | HG01074.hp2 HG01261.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-83-634_-83-633dup others(2): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75938864 | |||||||
| chr17:75938875 | A | AG | 4 | a0003c0005t0002g0212 a0003c0005t0002g0213 a0003c0005t0002g0214 others(1): Show |
4 | HG01109.hp1 HG01361.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.-83-644_-83-643ins others(1): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75938875 | |||||||
| chr17:75939025 | G | T | 1 | a0002c0002t0010g0243 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-83-793C>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75939025 | |||||||
| chr17:75939026 | T | G | 1 | a0002c0002t0010g0243 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-83-794A>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75939026 | |||||||
| chr17:75939027 | G | T | 1 | a0002c0002t0010g0243 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-83-795C>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75939027 | |||||||
| chr17:75939152 | T | G | 45 | a0002c0002t0001g0002 a0002c0002t0001g0021 a0002c0002t0001g0022 others(42): Show |
57 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.-83-920A>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75939152 | |||||||
| chr17:75939199 | G | C | 2 | a0007c0011t0005g0011 a0007c0011t0005g0054 |
3 | HG02965.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-83-967C>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75939199 | |||||||
| chr17:75939295 | C | CA | 27 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0123 others(24): Show |
33 | HG00423.hp1 HG00544.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.-83-1064dupT | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75939295 | |||||||
| chr17:75939295 | CAAA | C | 27 | a0001c0001t0007g0055 a0002c0002t0001g0021 a0002c0002t0001g0022 others(24): Show |
32 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.-83-1066_-83-1064d others(5): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75939295 | |||||||
| chr17:75939295 | CAAAA | C | 75 | a0001c0001t0004g0165 a0002c0002t0001g0002 a0002c0002t0001g0158 others(72): Show |
96 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-83-1067_-83-1064d others(6): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75939295 | |||||||
| chr17:75939309 | A | AAC | 21 | a0003c0003t0002g0006 a0003c0003t0002g0008 a0003c0003t0002g0023 others(18): Show |
30 | HG00735.hp1 HG01243.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.-83-1078_-83-1077i others(4): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75939309 | |||||||
| chr17:75939317 | A | AAC | 7 | a0003c0005t0002g0028 a0003c0005t0002g0238 a0003c0008t0002g0234 others(4): Show |
10 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.-83-1086_-83-1085i others(4): Show |
FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75939317 | |||||||
| chr17:75939317 | A | AC | 3 | a0003c0005t0002g0232 a0003c0005t0002g0233 a0003c0008t0002g0027 |
4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-83-1086dupG | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75939317 | |||||||
| chr17:75939317 | A | C | 27 | a0003c0003t0002g0006 a0003c0003t0002g0008 a0003c0003t0002g0023 others(24): Show |
36 | HG00735.hp1 HG01123.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.-83-1085T>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75939317 | |||||||
| chr17:75939733 | C | A | 1 | a0003c0003t0002g0241 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-84+1115G>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75939733 | |||||||
| chr17:75939858 | T | A | 1 | a0002c0002t0010g0243 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-84+990A>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75939858 | |||||||
| chr17:75939957 | C | G | 4 | a0003c0005t0002g0212 a0003c0005t0002g0213 a0003c0005t0002g0214 others(1): Show |
4 | HG01109.hp1 HG01361.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.-84+891G>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75939957 | |||||||
| chr17:75939969 | G | A | 1 | a0001c0007t0001g0147 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-84+879C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75939969 | |||||||
| chr17:75939981 | T | A | 6 | a0004c0004t0001g0148 a0004c0004t0001g0149 a0004c0004t0001g0150 others(3): Show |
6 | HG02280.hp1 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-84+867A>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75939981 | |||||||
| chr17:75940251 | T | A | 41 | a0003c0003t0002g0006 a0003c0003t0002g0008 a0003c0003t0002g0023 others(38): Show |
54 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.-84+597A>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75940251 | |||||||
| chr17:75940311 | C | G | 1 | a0020c0020t0001g0031 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-84+537G>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75940311 | |||||||
| chr17:75940402 | G | A | 1 | a0016c0025t0011g0244 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-84+446C>T | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75940402 | |||||||
| chr17:75940409 | T | C | 1 | a0003c0003t0002g0242 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-84+439A>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75940409 | |||||||
| chr17:75940427 | A | T | 1 | a0003c0003t0002g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-84+421T>A | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75940427 | |||||||
| chr17:75940572 | G | C | 65 | a0001c0001t0004g0165 a0002c0002t0001g0002 a0002c0002t0001g0021 others(62): Show |
87 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.-84+276C>G | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75940572 | |||||||
| chr17:75940610 | C | G | 1 | a0004c0004t0001g0030 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-84+238G>C | FBF1 | ENSG00000188878.20 | transcript | ENST00000636174.2 | protein_coding | 1/29 | chr17 | 75940610 |