Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6624 |
| ensemblid | ENSG00000075618.18 |
| hgncid | 11148 |
| symbol | FSCN1 |
| name | fascin actin-bundling protein 1 |
| refseq_nuc | NM_003088.4 |
| refseq_prot | NP_003079.1 |
| ensembl_nuc | ENST00000382361.8 |
| ensembl_prot | ENSP00000371798.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 5592816 |
| end | 5606655 |
| strand | + |
| ver | v1.2 |
| region | chr7:5592816-5606655 |
| region5000 | chr7:5587816-5611655 |
| regionname0 | FSCN1_chr7_5592816_5606655 |
| regionname5000 | FSCN1_chr7_5587816_5611655 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 493 | 375 | 97 | 76 | 144 | 12 | 44 | 96 | FSCN1_chr7_5587816_5611655 | FSCN1 | MTANG others(488): Show |
chr7 | 5587816 | 5611655 |
| a0002 | 0/0 | 493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | MTANG others(488): Show |
chr7 | 5587816 | 5611655 |
| a0003 | 0/0 | 493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | MTANG others(488): Show |
chr7 | 5587816 | 5611655 |
| a0004 | 0/0 | 493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | MTANG others(488): Show |
chr7 | 5587816 | 5611655 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1479 | 267 | 58 | 57 | 111 | 9 | 30 | FSCN1_chr7_5587816_5611655 | FSCN1 | ATGAC others(1474): Show |
chr7 | 5587816 | 5611655 | ||
| a0001c0002 | 0/0 | 1479 | 98 | 31 | 18 | 32 | 3 | 14 | FSCN1_chr7_5587816_5611655 | FSCN1 | ATGAC others(1474): Show |
chr7 | 5587816 | 5611655 | ||
| a0001c0003 | 0/0 | 1479 | 3 | 2 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | ATGAC others(1474): Show |
chr7 | 5587816 | 5611655 | ||
| a0001c0004 | 0/0 | 1479 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | ATGAC others(1474): Show |
chr7 | 5587816 | 5611655 | ||
| a0001c0005 | 0/0 | 1479 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | ATGAC others(1474): Show |
chr7 | 5587816 | 5611655 | ||
| a0001c0006 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | ATGAC others(1474): Show |
chr7 | 5587816 | 5611655 | ||
| a0001c0010 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | ATGAC others(1474): Show |
chr7 | 5587816 | 5611655 | ||
| a0001c0011 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | ATGAC others(1474): Show |
chr7 | 5587816 | 5611655 | ||
| a0002c0009 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | ATGAC others(1474): Show |
chr7 | 5587816 | 5611655 | ||
| a0003c0008 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | ATGAC others(1474): Show |
chr7 | 5587816 | 5611655 | ||
| a0004c0007 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | ATGAC others(1474): Show |
chr7 | 5587816 | 5611655 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2784 | 214 | 25 | 50 | 102 | 8 | 27 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| a0001c0001t0002 | 0/0 | 2784 | 3 | 1 | 2 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| a0001c0001t0003 | 0/0 | 2784 | 14 | 1 | 5 | 7 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| a0001c0001t0004 | 0/0 | 2783 | 15 | 15 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2778): Show |
chr7 | 5587816 | 5611655 |
| a0001c0001t0005 | 0/0 | 2784 | 9 | 9 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| a0001c0001t0006 | 0/0 | 2783 | 6 | 6 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2778): Show |
chr7 | 5587816 | 5611655 |
| a0001c0001t0007 | 0/0 | 2784 | 3 | 0 | 0 | 0 | 1 | 2 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| a0001c0001t0011 | 0/0 | 2785 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2780): Show |
chr7 | 5587816 | 5611655 |
| a0001c0001t0012 | 0/0 | 2785 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2780): Show |
chr7 | 5587816 | 5611655 |
| a0001c0001t0013 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| a0001c0002t0001 | 0/0 | 2784 | 60 | 21 | 14 | 11 | 3 | 11 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| a0001c0002t0002 | 0/0 | 2784 | 32 | 7 | 4 | 18 | 0 | 3 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| a0001c0002t0003 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| a0001c0002t0004 | 0/0 | 2783 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2778): Show |
chr7 | 5587816 | 5611655 |
| a0001c0002t0008 | 0/0 | 2785 | 2 | 0 | 0 | 2 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2780): Show |
chr7 | 5587816 | 5611655 |
| a0001c0002t0010 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| a0001c0003t0001 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| a0001c0003t0009 | 0/0 | 2784 | 2 | 1 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| a0001c0004t0001 | 0/0 | 2784 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| a0001c0005t0001 | 0/0 | 2784 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| a0001c0006t0001 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| a0001c0010t0003 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| a0001c0011t0001 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| a0002c0009t0001 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| a0003c0008t0003 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| a0004c0007t0003 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | GTGGA others(2779): Show |
chr7 | 5587816 | 5611655 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 38 | 2 | 6 | 25 | 2 | 3 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0002 | 0/0 | 16 | 1 | 5 | 8 | 1 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0003 | 0/0 | 12 | 3 | 1 | 8 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0004 | 0/0 | 7 | 1 | 1 | 2 | 1 | 2 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0017 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0018 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0020 | 1/0 | 3 | 0 | 1 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0001g0229 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0003g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0003g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0005g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0006g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0007g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0007g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0011g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0001t0013g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0005 | 0/0 | 6 | 1 | 3 | 1 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0010 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0023 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0019 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0008g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0008g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0002t0010g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0003t0009g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0003t0009g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0004t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0005t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0005t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0006t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0010t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0001c0011t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0002c0009t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0003c0008t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| a0004c0007t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0013 | EUR | GBR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00140 | hp1 | a0001 | c0001 | t0007 | g0031 | EUR | GBR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0097 | EUR | GBR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | CHS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | CHS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | CHS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0044 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0146 | EAS | CHS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0217 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0077 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0074 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0076 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0134 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01243 | hp2 | a0001 | c0003 | t0009 | g0082 | AMR | PUR | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0073 | AMR | CLM | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | CLM | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01891 | hp2 | a0001 | c0005 | t0001 | g0002 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0151 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0150 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0213 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0182 | EAS | CDX | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CDX | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | CDX | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0061 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0047 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0063 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0166 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0198 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0196 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0067 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0089 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0149 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0143 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0211 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0216 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0046 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0136 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02886 | hp1 | a0001 | c0010 | t0003 | g0080 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0109 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0024 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0071 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0070 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | ESN | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02922 | hp2 | a0001 | c0011 | t0001 | g0033 | AFR | ESN | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | ESN | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0112 | AFR | ESN | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | ESN | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0069 | AFR | ESN | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | ESN | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03017 | hp1 | a0001 | c0001 | t0007 | g0153 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | MSL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | MSL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03130 | hp1 | a0001 | c0004 | t0001 | g0047 | AFR | ESN | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | ESN | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | ESN | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0060 | AFR | ESN | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | ESN | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | MSL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03209 | hp2 | a0003 | c0008 | t0003 | g0165 | AFR | MSL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0144 | AFR | MSL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0019 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0141 | AFR | MSL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0049 | AFR | MSL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0206 | AFR | MSL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0230 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | ESN | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03516 | hp2 | a0001 | c0002 | t0004 | g0029 | AFR | ESN | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03540 | hp1 | a0004 | c0007 | t0003 | g0104 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | GWD | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | MSL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0210 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0145 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0019 | SAS | STU | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0052 | SAS | PJL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0139 | SAS | BEB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03834 | hp2 | a0001 | c0001 | t0007 | g0031 | SAS | BEB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | STU | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0096 | SAS | STU | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | STU | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0050 | SAS | STU | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0023 | SAS | STU | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0056 | SAS | STU | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | YRI | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18522 | hp2 | a0001 | c0001 | t0013 | g0225 | AFR | YRI | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0137 | AFR | YRI | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0226 | AFR | YRI | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18963 | hp2 | a0001 | c0001 | t0011 | g0138 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18977 | hp2 | a0001 | c0002 | t0008 | g0045 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18993 | hp1 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0227 | AFR | LWK | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0164 | AFR | LWK | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19043 | hp1 | a0001 | c0002 | t0004 | g0007 | AFR | LWK | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19043 | hp2 | a0001 | c0003 | t0009 | g0083 | AFR | LWK | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19054 | hp2 | a0001 | c0002 | t0008 | g0148 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19066 | hp1 | a0001 | c0006 | t0001 | g0147 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19077 | hp2 | a0001 | c0002 | t0010 | g0041 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0100 | AFR | YRI | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | YRI | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ASW | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0046 | AFR | ASW | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0014 | EUR | TSI | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | TSI | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | GIH | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02109 | hp2 | a0002 | c0009 | t0001 | g0003 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG02559 | hp2 | a0001 | c0002 | t0003 | g0054 | AFR | ACB | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03471 | hp1 | a0001 | c0005 | t0001 | g0003 | AFR | MSL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | USA | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | USA | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | USA | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | USA | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0215 | AFR | LWK | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | LWK | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0229 | REF | REF | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0020 | REF | REF | FSCN1_chr7_5587816_5611655 | FSCN1 | chr7 | 5587816 | 5611655 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:5603356 | C | T | 1 | a0002 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.932C>T | p.Thr311Met | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 2/5 | 1053/2784 | 932/1482 | 311/493 | chr7 | 5603356 | |||
| chr7:5604007 | A | G | 1 | a0003 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1256A>G | p.Asn419Ser | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/5 | 1377/2784 | 1256/1482 | 419/493 | chr7 | 5604007 | |||
| chr7:5605328 | G | A | 1 | a0004 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.1336G>A | p.Asp446Asn | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 5/5 | 1457/2784 | 1336/1482 | 446/493 | chr7 | 5605328 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:5593191 | C | T | 1 | a0001c0011 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.255C>T | p.Pro85Pro | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/5 | 376/2784 | 255/1482 | 85/493 | chr7 | 5593191 | |||
| chr7:5593257 | G | T | 1 | a0001c0010 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.321G>T | p.Ala107Ala | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/5 | 442/2784 | 321/1482 | 107/493 | chr7 | 5593257 | |||
| chr7:5593398 | C | T | 1 | a0001c0005 | 2 | HG01891.hp2 HG03471.hp1 |
synonymous_variant | LOW | c.462C>T | p.His154His | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/5 | 583/2784 | 462/1482 | 154/493 | chr7 | 5593398 | |||
| chr7:5593611 | C | T | 1 | a0001c0004 | 2 | HG02258.hp1 HG03130.hp1 |
synonymous_variant | LOW | c.675C>T | p.Asp225Asp | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/5 | 796/2784 | 675/1482 | 225/493 | chr7 | 5593611 | |||
| chr7:5593725 | C | T | 1 | a0001c0004 | 2 | HG02258.hp1 HG03130.hp1 |
synonymous_variant | LOW | c.789C>T | p.Val263Val | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/5 | 910/2784 | 789/1482 | 263/493 | chr7 | 5593725 | |||
| chr7:5603514 | T | C | 2 | a0001c0002 a0001c0006 |
99 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(96): Show |
synonymous_variant | LOW | c.1008T>C | p.Phe336Phe | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 3/5 | 1129/2784 | 1008/1482 | 336/493 | chr7 | 5603514 | |||
| chr7:5604014 | C | T | 1 | a0001c0003 | 3 | HG01243.hp2 HG02895.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.1263C>T | p.Gly421Gly | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/5 | 1384/2784 | 1263/1482 | 421/493 | chr7 | 5604014 | |||
| chr7:5605408 | C | A | 1 | a0001c0006 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.1416C>A | p.Gly472Gly | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 5/5 | 1537/2784 | 1416/1482 | 472/493 | chr7 | 5605408 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:5605483 | C | T | 1 | a0001c0001t0007 | 3 | HG00140.hp1 HG03017.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 5/5 | 9 | chr7 | 5605483 | ||||||
| chr7:5605485 | T | C | 3 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0008 |
37 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*11T>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 5/5 | 11 | chr7 | 5605485 | ||||||
| chr7:5605567 | G | C | 1 | a0001c0003t0009 | 2 | HG01243.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*93G>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 5/5 | 93 | chr7 | 5605567 | ||||||
| chr7:5605699 | GC | G | 3 | a0001c0001t0004 a0001c0001t0006 a0001c0002t0004 |
23 | HG02257.hp2 HG02258.hp2 HG02451.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*228delC | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 5/5 | 228 | INFO_REALIGN_3_PRIME | chr7 | 5605699 | |||||
| chr7:5605722 | C | T | 1 | a0001c0001t0013 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*248C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 5/5 | 248 | chr7 | 5605722 | ||||||
| chr7:5605914 | T | A | 1 | a0001c0001t0005 | 9 | HG01884.hp1 HG02257.hp1 HG02723.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*440T>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 5/5 | 440 | chr7 | 5605914 | ||||||
| chr7:5606010 | G | GT | 3 | a0001c0001t0011 a0001c0001t0012 a0001c0002t0008 |
4 | NA18963.hp2 NA18977.hp2 NA18993.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*543dupT | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 5/5 | 544 | INFO_REALIGN_3_PRIME | chr7 | 5606010 | |||||
| chr7:5606051 | G | A | 1 | a0001c0002t0010 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*577G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 5/5 | 577 | chr7 | 5606051 | ||||||
| chr7:5606600 | T | C | 8 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(5): Show |
34 | HG01081.hp1 HG01081.hp2 HG01884.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1126T>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 5/5 | 1126 | chr7 | 5606600 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:5593899 | G | A | 17 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0006g0060 others(14): Show |
26 | HG00642.hp1 HG01358.hp1 HG01943.hp1 others(23): Show |
intron_variant | MODIFIER | c.832+131G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5593899 | |||||||
| chr7:5593984 | G | C | 2 | a0001c0001t0004g0063 a0001c0002t0001g0064 |
2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.832+216G>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5593984 | |||||||
| chr7:5593992 | A | G | 2 | a0001c0002t0001g0011 a0001c0002t0001g0062 |
4 | HG02055.hp2 HG02572.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.832+224A>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5593992 | |||||||
| chr7:5594014 | G | A | 2 | a0001c0002t0001g0065 a0001c0002t0001g0066 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.832+246G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594014 | |||||||
| chr7:5594045 | A | AC | 62 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0017 others(59): Show |
90 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.832+288dupC | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5594045 | ||||||
| chr7:5594045 | A | ACC | 31 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0079 others(28): Show |
38 | HG00140.hp2 HG00735.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.832+287_832+288dup others(2): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5594045 | ||||||
| chr7:5594045 | AC | A | 27 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0057 others(24): Show |
33 | HG01358.hp1 HG01943.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.832+288delC | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5594045 | ||||||
| chr7:5594047 | C | A | 1 | a0001c0001t0004g0067 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.832+279C>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594047 | |||||||
| chr7:5594048 | C | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0004g0012 others(9): Show |
13 | HG02258.hp2 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.832+280C>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594048 | |||||||
| chr7:5594049 | C | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0072 others(7): Show |
19 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.832+281C>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594049 | |||||||
| chr7:5594049 | C | G | 1 | a0001c0001t0003g0231 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.832+281C>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594049 | |||||||
| chr7:5594073 | C | T | 1 | a0001c0001t0004g0226 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.832+305C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594073 | |||||||
| chr7:5594220 | C | T | 1 | a0001c0001t0013g0225 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.832+452C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594220 | |||||||
| chr7:5594251 | T | A | 2 | a0001c0001t0007g0031 a0001c0001t0007g0153 |
3 | HG00140.hp1 HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.832+483T>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594251 | |||||||
| chr7:5594303 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.832+535C>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594303 | |||||||
| chr7:5594343 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.832+575G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594343 | |||||||
| chr7:5594360 | GT | G | 5 | a0001c0001t0001g0057 a0001c0002t0001g0005 a0001c0002t0001g0010 others(2): Show |
6 | HG00642.hp1 HG01981.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.832+593delT | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594360 | |||||||
| chr7:5594361 | T | TG | 28 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(25): Show |
32 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.832+602dupG | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5594361 | ||||||
| chr7:5594362 | G | A | 2 | a0001c0010t0003g0080 a0004c0007t0003g0104 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.832+594G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594362 | |||||||
| chr7:5594362 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.832+594G>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594362 | |||||||
| chr7:5594366 | G | C | 1 | a0001c0002t0001g0052 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.832+598G>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594366 | |||||||
| chr7:5594368 | G | A | 13 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0004g0012 others(10): Show |
14 | HG02258.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.832+600G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594368 | |||||||
| chr7:5594368 | G | C | 1 | a0001c0001t0001g0154 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.832+600G>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594368 | |||||||
| chr7:5594426 | A | T | 3 | a0001c0001t0001g0078 a0001c0001t0003g0151 a0001c0001t0003g0231 |
3 | HG01928.hp1 HG01952.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.832+658A>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594426 | |||||||
| chr7:5594572 | G | A | 16 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0081 others(13): Show |
25 | HG00642.hp1 HG01358.hp1 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+804G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594572 | |||||||
| chr7:5594580 | C | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0155 |
2 | NA18959.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.832+812C>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594580 | |||||||
| chr7:5594615 | G | T | 2 | a0001c0001t0007g0031 a0001c0001t0007g0153 |
3 | HG00140.hp1 HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.832+847G>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594615 | |||||||
| chr7:5594685 | C | A | 1 | a0001c0002t0001g0053 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.832+917C>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594685 | |||||||
| chr7:5594704 | C | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | NA18945.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.832+936C>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594704 | |||||||
| chr7:5594809 | C | T | 3 | a0001c0001t0001g0224 a0001c0002t0001g0065 a0001c0002t0001g0066 |
3 | HG02486.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.832+1041C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594809 | |||||||
| chr7:5594871 | T | G | 8 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0107 others(5): Show |
9 | HG01496.hp1 HG02055.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.832+1103T>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5594871 | |||||||
| chr7:5595150 | G | A | 1 | a0001c0001t0003g0108 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.832+1382G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5595150 | |||||||
| chr7:5595151 | C | T | 1 | a0001c0001t0003g0108 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.832+1383C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5595151 | |||||||
| chr7:5595281 | T | A | 3 | a0001c0002t0001g0011 a0001c0002t0001g0049 a0001c0002t0001g0062 |
5 | HG02055.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+1513T>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5595281 | |||||||
| chr7:5595424 | A | T | 1 | a0001c0001t0001g0027 | 2 | HG02602.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.832+1656A>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5595424 | |||||||
| chr7:5595490 | C | T | 1 | a0001c0001t0001g0048 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.832+1722C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5595490 | |||||||
| chr7:5595553 | C | G | 1 | a0001c0002t0001g0059 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.832+1785C>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5595553 | |||||||
| chr7:5595585 | G | A | 3 | a0001c0003t0001g0109 a0001c0003t0009g0082 a0001c0003t0009g0083 |
3 | HG01243.hp2 HG02895.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832+1817G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5595585 | |||||||
| chr7:5595609 | G | T | 13 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0004g0012 others(10): Show |
14 | HG02258.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.832+1841G>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5595609 | |||||||
| chr7:5595612 | G | A | 2 | a0001c0001t0007g0031 a0001c0001t0007g0153 |
3 | HG00140.hp1 HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.832+1844G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5595612 | |||||||
| chr7:5595767 | T | G | 2 | a0001c0001t0007g0031 a0001c0001t0007g0153 |
3 | HG00140.hp1 HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.832+1999T>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5595767 | |||||||
| chr7:5595773 | C | G | 32 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0223 others(29): Show |
42 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.832+2005C>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5595773 | |||||||
| chr7:5595986 | G | A | 2 | a0001c0001t0007g0031 a0001c0001t0007g0153 |
3 | HG00140.hp1 HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.832+2218G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5595986 | |||||||
| chr7:5596120 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.832+2352G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5596120 | |||||||
| chr7:5596216 | C | G | 1 | a0001c0001t0003g0108 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.832+2448C>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5596216 | |||||||
| chr7:5596255 | G | A | 3 | a0001c0003t0001g0109 a0001c0003t0009g0082 a0001c0003t0009g0083 |
3 | HG01243.hp2 HG02895.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832+2487G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5596255 | |||||||
| chr7:5596368 | TTCAGCCT others(10): Show |
T | 1 | a0001c0001t0004g0067 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.832+2601_832+2617d others(19): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5596368 | |||||||
| chr7:5596414 | T | C | 29 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0002t0001g0042 others(26): Show |
38 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.832+2646T>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5596414 | |||||||
| chr7:5596522 | C | T | 3 | a0001c0002t0001g0145 a0001c0002t0001g0211 a0001c0002t0001g0230 |
3 | HG02735.hp1 HG03491.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.832+2754C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5596522 | |||||||
| chr7:5596576 | C | G | 2 | a0001c0002t0002g0150 a0001c0002t0002g0222 |
2 | HG02056.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.832+2808C>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5596576 | |||||||
| chr7:5596590 | TTCTCTCA others(2): Show |
T | 13 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0004g0012 others(10): Show |
14 | HG02258.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.832+2835_832+2843d others(11): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5596590 | ||||||
| chr7:5596625 | C | T | 2 | a0001c0001t0005g0143 a0001c0001t0005g0144 |
2 | HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.832+2857C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5596625 | |||||||
| chr7:5596645 | T | A | 2 | a0001c0001t0007g0031 a0001c0001t0007g0153 |
3 | HG00140.hp1 HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.832+2877T>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5596645 | |||||||
| chr7:5596694 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.832+2926A>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5596694 | |||||||
| chr7:5596695 | T | A | 1 | a0001c0001t0001g0142 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.832+2927T>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5596695 | |||||||
| chr7:5596743 | C | G | 14 | a0001c0002t0002g0024 a0001c0002t0002g0030 a0001c0002t0002g0045 others(11): Show |
18 | HG00408.hp1 HG00609.hp2 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.832+2975C>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5596743 | |||||||
| chr7:5596781 | C | T | 12 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0107 others(9): Show |
15 | HG00140.hp1 HG01496.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+3013C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5596781 | |||||||
| chr7:5596807 | G | C | 2 | a0001c0001t0005g0143 a0001c0001t0005g0144 |
2 | HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.832+3039G>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5596807 | |||||||
| chr7:5596979 | G | T | 31 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0002t0001g0042 others(28): Show |
41 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.832+3211G>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5596979 | |||||||
| chr7:5596980 | G | T | 34 | a0001c0001t0001g0040 a0001c0001t0001g0101 a0001c0001t0001g0142 others(31): Show |
42 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.832+3212G>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5596980 | |||||||
| chr7:5596987 | G | A | 27 | a0001c0001t0001g0040 a0001c0001t0001g0142 a0001c0001t0001g0203 others(24): Show |
32 | HG01070.hp2 HG01071.hp1 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.832+3219G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5596987 | |||||||
| chr7:5597107 | AGGCCAAG others(16): Show |
A | 11 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0107 others(8): Show |
13 | HG00140.hp1 HG01496.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.832+3363_832+3385d others(25): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5597107 | ||||||
| chr7:5597150 | C | CTTCAGCC others(5): Show |
1 | a0001c0001t0001g0202 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.832+3383_832+3394d others(14): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5597150 | ||||||
| chr7:5597249 | G | A | 4 | a0001c0002t0001g0007 a0001c0002t0001g0029 a0001c0002t0004g0007 others(1): Show |
6 | HG01243.hp1 HG02809.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.832+3481G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597249 | |||||||
| chr7:5597310 | A | G | 3 | a0001c0002t0001g0145 a0001c0002t0001g0211 a0001c0002t0001g0230 |
3 | HG02735.hp1 HG03491.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.832+3542A>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597310 | |||||||
| chr7:5597323 | C | T | 2 | a0001c0001t0004g0070 a0001c0001t0004g0071 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.832+3555C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597323 | |||||||
| chr7:5597341 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.832+3573C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597341 | |||||||
| chr7:5597355 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.832+3587C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597355 | |||||||
| chr7:5597376 | T | A | 110 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0033 others(107): Show |
140 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.832+3608T>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597376 | |||||||
| chr7:5597392 | G | T | 1 | a0001c0002t0001g0066 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.832+3624G>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597392 | |||||||
| chr7:5597404 | G | A | 1 | a0001c0010t0003g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+3636G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597404 | |||||||
| chr7:5597405 | C | CCT | 4 | a0001c0002t0001g0051 a0001c0002t0001g0055 a0001c0002t0001g0059 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.832+3638_832+3639d others(4): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5597405 | ||||||
| chr7:5597436 | T | C | 150 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(147): Show |
193 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.832+3668T>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597436 | |||||||
| chr7:5597493 | C | A | 1 | a0001c0001t0001g0171 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.832+3725C>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597493 | |||||||
| chr7:5597523 | C | T | 2 | a0001c0001t0005g0143 a0001c0001t0005g0144 |
2 | HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.832+3755C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597523 | |||||||
| chr7:5597536 | G | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0081 a0001c0001t0001g0085 others(5): Show |
9 | HG01168.hp1 HG01433.hp1 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.832+3768G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597536 | |||||||
| chr7:5597666 | TCA | T | 9 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0107 others(6): Show |
10 | HG01496.hp1 HG02055.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.832+3899_832+3900d others(4): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597666 | |||||||
| chr7:5597683 | A | C | 14 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0161 others(11): Show |
21 | HG00642.hp1 HG01358.hp1 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.832+3915A>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597683 | |||||||
| chr7:5597684 | C | A | 38 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0058 others(35): Show |
50 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.832+3916C>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597684 | |||||||
| chr7:5597684 | C | CA | 11 | a0001c0001t0001g0101 a0001c0001t0001g0172 a0001c0001t0001g0173 others(8): Show |
14 | HG01243.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.832+3924dupA | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5597684 | ||||||
| chr7:5597710 | CAAAA | C | 2 | a0001c0001t0007g0031 a0001c0001t0007g0153 |
3 | HG00140.hp1 HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.832+3945_832+3948d others(6): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5597710 | ||||||
| chr7:5597747 | T | TA | 17 | a0001c0001t0007g0031 a0001c0002t0001g0064 a0001c0002t0002g0024 others(14): Show |
22 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.832+3993dupA | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5597747 | ||||||
| chr7:5597747 | T | TAA | 12 | a0001c0001t0001g0214 a0001c0002t0001g0042 a0001c0002t0001g0212 others(9): Show |
17 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.832+3992_832+3993d others(4): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5597747 | ||||||
| chr7:5597747 | TA | T | 20 | a0001c0001t0001g0022 a0001c0001t0001g0039 a0001c0001t0001g0098 others(17): Show |
23 | HG01069.hp2 HG01070.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.832+3993delA | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5597747 | ||||||
| chr7:5597762 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.832+3994G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597762 | |||||||
| chr7:5597791 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0162 a0001c0001t0001g0163 |
4 | HG02486.hp2 HG03239.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.832+4023G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597791 | |||||||
| chr7:5597857 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.832+4089G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597857 | |||||||
| chr7:5597895 | C | T | 4 | a0001c0001t0003g0038 a0001c0001t0003g0131 a0001c0001t0003g0151 others(1): Show |
5 | HG01081.hp2 HG01928.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.832+4127C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597895 | |||||||
| chr7:5597897 | G | C | 2 | a0001c0001t0007g0031 a0001c0001t0007g0153 |
3 | HG00140.hp1 HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.832+4129G>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597897 | |||||||
| chr7:5597982 | AAC | A | 30 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0014 others(27): Show |
42 | HG00099.hp1 HG00735.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.832+4218_832+4219d others(4): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5597982 | ||||||
| chr7:5597986 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.832+4218C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5597986 | |||||||
| chr7:5598016 | G | A | 12 | a0001c0002t0002g0030 a0001c0002t0002g0045 a0001c0002t0002g0102 others(9): Show |
13 | HG00408.hp1 HG00609.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.832+4248G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5598016 | |||||||
| chr7:5598019 | G | C | 1 | a0001c0002t0001g0052 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.832+4251G>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5598019 | |||||||
| chr7:5598094 | T | G | 112 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0028 others(109): Show |
143 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.832+4326T>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5598094 | |||||||
| chr7:5598114 | A | C | 1 | a0001c0002t0001g0066 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.832+4346A>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5598114 | |||||||
| chr7:5598150 | C | T | 3 | a0001c0002t0001g0013 a0001c0002t0001g0073 a0001c0002t0001g0074 |
5 | HG00099.hp2 HG00642.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.832+4382C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5598150 | |||||||
| chr7:5598591 | C | G | 23 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0058 others(20): Show |
35 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.833-4666C>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5598591 | |||||||
| chr7:5598810 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0117 |
2 | HG01106.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.833-4447G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5598810 | |||||||
| chr7:5598827 | C | G | 7 | a0001c0002t0001g0007 a0001c0002t0001g0029 a0001c0002t0001g0099 others(4): Show |
9 | HG01243.hp1 HG02280.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.833-4430C>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5598827 | |||||||
| chr7:5598828 | G | A | 1 | a0004c0007t0003g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.833-4429G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5598828 | |||||||
| chr7:5598865 | C | T | 19 | a0001c0001t0001g0040 a0001c0001t0001g0142 a0001c0001t0001g0203 others(16): Show |
22 | HG01070.hp2 HG01071.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.833-4392C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5598865 | |||||||
| chr7:5598977 | GGCTCCCT others(8): Show |
G | 3 | a0001c0001t0001g0118 a0001c0001t0001g0175 a0001c0001t0001g0202 |
3 | NA18997.hp1 NA18997.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.833-4277_833-4263d others(17): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5598977 | ||||||
| chr7:5599096 | G | T | 1 | a0001c0001t0001g0197 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.833-4161G>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5599096 | |||||||
| chr7:5599212 | C | T | 1 | a0001c0004t0001g0047 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.833-4045C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5599212 | |||||||
| chr7:5599495 | C | A | 53 | a0001c0001t0001g0040 a0001c0001t0001g0142 a0001c0001t0001g0160 others(50): Show |
67 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.833-3762C>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5599495 | |||||||
| chr7:5599602 | T | A | 50 | a0001c0001t0001g0040 a0001c0001t0001g0142 a0001c0001t0001g0203 others(47): Show |
64 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.833-3655T>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5599602 | |||||||
| chr7:5600015 | C | T | 19 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0058 others(16): Show |
29 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.833-3242C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5600015 | |||||||
| chr7:5600016 | G | A | 1 | a0001c0002t0001g0139 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.833-3241G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5600016 | |||||||
| chr7:5600038 | C | A | 1 | a0001c0001t0001g0176 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.833-3219C>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5600038 | |||||||
| chr7:5600215 | C | T | 11 | a0001c0002t0002g0030 a0001c0002t0002g0045 a0001c0002t0002g0102 others(8): Show |
12 | HG00408.hp1 HG00609.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.833-3042C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5600215 | |||||||
| chr7:5600232 | T | C | 1 | a0003c0008t0003g0165 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.833-3025T>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5600232 | |||||||
| chr7:5600290 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.833-2967T>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5600290 | |||||||
| chr7:5600346 | A | G | 3 | a0001c0001t0004g0158 a0001c0001t0004g0196 a0001c0001t0004g0198 |
3 | HG02451.hp1 HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.833-2911A>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5600346 | |||||||
| chr7:5600404 | A | T | 52 | a0001c0001t0001g0040 a0001c0001t0001g0116 a0001c0001t0001g0142 others(49): Show |
66 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.833-2853A>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5600404 | |||||||
| chr7:5600458 | C | T | 2 | a0001c0002t0002g0076 a0001c0002t0002g0077 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.833-2799C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5600458 | |||||||
| chr7:5600469 | C | A | 1 | a0001c0004t0001g0047 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.833-2788C>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5600469 | |||||||
| chr7:5600486 | A | T | 7 | a0001c0001t0001g0101 a0001c0001t0005g0009 a0001c0001t0005g0100 others(4): Show |
10 | HG01884.hp1 HG02257.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.833-2771A>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5600486 | |||||||
| chr7:5600658 | AT | A | 50 | a0001c0001t0001g0040 a0001c0001t0001g0142 a0001c0001t0001g0178 others(47): Show |
64 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.833-2586delT | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5600658 | ||||||
| chr7:5600732 | C | T | 2 | a0001c0002t0001g0049 a0001c0002t0001g0062 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.833-2525C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5600732 | |||||||
| chr7:5600809 | G | A | 2 | a0001c0001t0001g0087 a0001c0002t0001g0042 |
3 | HG01943.hp2 NA18970.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.833-2448G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5600809 | |||||||
| chr7:5600810 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.833-2447T>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5600810 | |||||||
| chr7:5600820 | AT | A | 47 | a0001c0001t0001g0040 a0001c0001t0001g0101 a0001c0001t0001g0142 others(44): Show |
59 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.833-2425delT | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5600820 | ||||||
| chr7:5600851 | G | T | 3 | a0001c0003t0001g0109 a0001c0003t0009g0082 a0001c0003t0009g0083 |
3 | HG01243.hp2 HG02895.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.833-2406G>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5600851 | |||||||
| chr7:5600859 | C | T | 27 | a0001c0002t0001g0042 a0001c0002t0001g0212 a0001c0002t0002g0019 others(24): Show |
36 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.833-2398C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5600859 | |||||||
| chr7:5600882 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.833-2375C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5600882 | |||||||
| chr7:5600900 | TGCCTCGG others(128): Show |
T | 52 | a0001c0001t0001g0040 a0001c0001t0001g0142 a0001c0001t0001g0203 others(49): Show |
66 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.833-2324_833-2190d others(2): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5600900 | ||||||
| chr7:5600906 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0003 |
2 | NA18990.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.833-2351G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5600906 | |||||||
| chr7:5600929 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.833-2328C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5600929 | |||||||
| chr7:5601039 | T | C | 2 | a0001c0002t0001g0099 a0001c0002t0001g0136 |
2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.833-2218T>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5601039 | |||||||
| chr7:5601109 | G | A | 3 | a0001c0003t0001g0109 a0001c0003t0009g0082 a0001c0003t0009g0083 |
3 | HG01243.hp2 HG02895.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.833-2148G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5601109 | |||||||
| chr7:5601115 | G | A | 1 | a0001c0001t0003g0108 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.833-2142G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5601115 | |||||||
| chr7:5601197 | C | CT | 16 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0037 others(13): Show |
19 | HG00140.hp1 HG00639.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.833-2037dupT | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5601197 | ||||||
| chr7:5601197 | CT | C | 16 | a0001c0001t0001g0079 a0001c0001t0001g0088 a0001c0001t0001g0098 others(13): Show |
19 | HG00099.hp2 HG00642.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.833-2037delT | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5601197 | ||||||
| chr7:5601197 | CTTTT | C | 50 | a0001c0001t0001g0040 a0001c0001t0001g0142 a0001c0001t0001g0203 others(47): Show |
64 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.833-2040_833-2037d others(6): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5601197 | ||||||
| chr7:5601229 | T | G | 1 | a0001c0001t0001g0119 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.833-2028T>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5601229 | |||||||
| chr7:5601241 | C | A | 1 | a0004c0007t0003g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.833-2016C>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5601241 | |||||||
| chr7:5601247 | G | C | 2 | a0001c0001t0004g0070 a0001c0001t0004g0071 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.833-2010G>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5601247 | |||||||
| chr7:5601348 | A | G | 62 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0058 others(59): Show |
83 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.833-1909A>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5601348 | |||||||
| chr7:5601472 | G | T | 2 | a0001c0001t0007g0031 a0001c0001t0007g0153 |
3 | HG00140.hp1 HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.833-1785G>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5601472 | |||||||
| chr7:5601499 | AC | A | 2 | a0001c0001t0007g0031 a0001c0001t0007g0153 |
3 | HG00140.hp1 HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.833-1755delC | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5601499 | ||||||
| chr7:5601671 | G | A | 61 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0058 others(58): Show |
82 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.833-1586G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5601671 | |||||||
| chr7:5601693 | A | T | 1 | a0001c0001t0001g0129 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.833-1564A>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5601693 | |||||||
| chr7:5601726 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.833-1531G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5601726 | |||||||
| chr7:5601849 | G | GAA | 62 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0058 others(59): Show |
83 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.833-1407_833-1406i others(4): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5601849 | ||||||
| chr7:5601920 | C | CT | 12 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0004g0012 others(9): Show |
13 | HG02258.hp2 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.833-1329dupT | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5601920 | ||||||
| chr7:5601943 | GC | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0157 a0001c0001t0001g0224 |
3 | HG03486.hp1 NA18998.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.833-1313delC | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5601943 | |||||||
| chr7:5601944 | C | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.833-1313C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5601944 | |||||||
| chr7:5601947 | A | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0157 a0001c0001t0001g0224 |
3 | HG03486.hp1 NA18998.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.833-1310A>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5601947 | |||||||
| chr7:5601955 | A | AT | 11 | a0001c0001t0001g0021 a0001c0001t0001g0078 a0001c0001t0001g0116 others(8): Show |
13 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.833-1286dupT | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5601955 | ||||||
| chr7:5601955 | A | T | 3 | a0001c0003t0001g0109 a0001c0003t0009g0082 a0001c0003t0009g0083 |
3 | HG01243.hp2 HG02895.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.833-1302A>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5601955 | |||||||
| chr7:5601955 | AT | A | 9 | a0001c0001t0001g0120 a0001c0001t0001g0181 a0001c0001t0001g0200 others(6): Show |
11 | HG00140.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.833-1286delT | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5601955 | ||||||
| chr7:5601955 | ATT | A | 61 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0058 others(58): Show |
82 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.833-1287_833-1286d others(4): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5601955 | ||||||
| chr7:5601956 | T | A | 2 | a0001c0001t0001g0018 a0001c0001t0004g0189 |
2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.833-1301T>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5601956 | |||||||
| chr7:5601976 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.833-1281C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5601976 | |||||||
| chr7:5601993 | T | C | 20 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0002t0001g0005 others(17): Show |
31 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.833-1264T>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5601993 | |||||||
| chr7:5601997 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0169 |
2 | HG00735.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.833-1260C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5601997 | |||||||
| chr7:5602031 | G | A | 28 | a0001c0002t0001g0042 a0001c0002t0001g0212 a0001c0002t0002g0019 others(25): Show |
37 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.833-1226G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602031 | |||||||
| chr7:5602038 | A | C | 63 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0058 others(60): Show |
84 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.833-1219A>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602038 | |||||||
| chr7:5602131 | C | G | 1 | a0001c0004t0001g0047 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.833-1126C>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602131 | |||||||
| chr7:5602133 | C | T | 60 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0058 others(57): Show |
81 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.833-1124C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602133 | |||||||
| chr7:5602139 | C | T | 7 | a0001c0001t0001g0101 a0001c0001t0005g0009 a0001c0001t0005g0100 others(4): Show |
10 | HG01884.hp1 HG02257.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.833-1118C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602139 | |||||||
| chr7:5602148 | T | C | 63 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0058 others(60): Show |
84 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.833-1109T>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602148 | |||||||
| chr7:5602201 | T | C | 63 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0058 others(60): Show |
84 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.833-1056T>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602201 | |||||||
| chr7:5602202 | G | A | 60 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0058 others(57): Show |
81 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.833-1055G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602202 | |||||||
| chr7:5602203 | G | C | 1 | a0001c0002t0002g0215 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.833-1054G>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602203 | |||||||
| chr7:5602207 | CT | C | 30 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0085 others(27): Show |
36 | HG00140.hp1 HG01069.hp2 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.833-1036delT | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5602207 | ||||||
| chr7:5602208 | T | C | 62 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0058 others(59): Show |
83 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.833-1049T>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602208 | |||||||
| chr7:5602221 | T | TTAAG | 21 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0058 others(18): Show |
31 | HG00642.hp1 HG01243.hp1 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.833-1036_833-1035i others(6): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602221 | |||||||
| chr7:5602221 | T | TTTAAG | 42 | a0001c0001t0003g0108 a0001c0002t0001g0023 a0001c0002t0001g0041 others(39): Show |
53 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.833-1036_833-1035i others(7): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602221 | |||||||
| chr7:5602264 | T | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0004g0012 others(9): Show |
13 | HG02258.hp2 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.833-993T>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602264 | |||||||
| chr7:5602301 | G | T | 63 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0058 others(60): Show |
84 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.833-956G>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602301 | |||||||
| chr7:5602378 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0115 |
2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.833-879C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602378 | |||||||
| chr7:5602450 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.833-807C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602450 | |||||||
| chr7:5602567 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.833-690A>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602567 | |||||||
| chr7:5602627 | C | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0205 |
3 | NA18960.hp2 NA18998.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.833-630C>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602627 | |||||||
| chr7:5602707 | GT | G | 88 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0033 others(85): Show |
107 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.833-542delT | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 5602707 | ||||||
| chr7:5602766 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.833-491C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602766 | |||||||
| chr7:5602798 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.833-459C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602798 | |||||||
| chr7:5602887 | G | A | 1 | a0001c0002t0001g0227 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.833-370G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602887 | |||||||
| chr7:5602979 | C | T | 1 | a0001c0002t0002g0103 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.833-278C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5602979 | |||||||
| chr7:5603000 | G | A | 91 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0033 others(88): Show |
111 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.833-257G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5603000 | |||||||
| chr7:5603115 | T | C | 11 | a0001c0001t0001g0110 a0001c0002t0001g0023 a0001c0002t0001g0041 others(8): Show |
13 | HG01070.hp2 HG01071.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.833-142T>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5603115 | |||||||
| chr7:5603149 | A | C | 1 | a0001c0001t0001g0129 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.833-108A>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5603149 | |||||||
| chr7:5603217 | C | T | 11 | a0001c0002t0001g0042 a0001c0002t0001g0212 a0001c0002t0002g0019 others(8): Show |
16 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.833-40C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 1/4 | chr7 | 5603217 | |||||||
| chr7:5603420 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02155.hp2 | splice_region_variant&intron_variant | LOW | c.989+7G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 2/4 | chr7 | 5603420 | |||||||
| chr7:5603425 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.989+12G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 2/4 | chr7 | 5603425 | |||||||
| chr7:5603647 | C | T | 44 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0033 others(41): Show |
51 | HG00140.hp1 HG01081.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.1111+30C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 3/4 | chr7 | 5603647 | |||||||
| chr7:5603664 | G | A | 1 | a0001c0002t0001g0227 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1111+47G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 3/4 | chr7 | 5603664 | |||||||
| chr7:5603712 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1111+95C>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 3/4 | chr7 | 5603712 | |||||||
| chr7:5603740 | C | T | 2 | a0001c0001t0001g0207 a0001c0004t0001g0047 |
3 | HG02258.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1111+123C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 3/4 | chr7 | 5603740 | |||||||
| chr7:5603759 | G | GGCT | 75 | a0001c0001t0001g0224 a0001c0002t0001g0005 a0001c0002t0001g0007 others(72): Show |
99 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1112-103_1112-102i others(5): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 5603759 | ||||||
| chr7:5603803 | C | T | 1 | a0001c0010t0003g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1112-60C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 3/4 | chr7 | 5603803 | |||||||
| chr7:5603848 | C | T | 66 | a0001c0002t0001g0005 a0001c0002t0001g0007 a0001c0002t0001g0010 others(63): Show |
90 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1112-15C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 3/4 | chr7 | 5603848 | |||||||
| chr7:5604186 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1279+156G>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604186 | |||||||
| chr7:5604210 | T | C | 14 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0004g0012 others(11): Show |
15 | HG02258.hp2 HG02280.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1279+180T>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604210 | |||||||
| chr7:5604212 | C | A | 1 | a0001c0002t0002g0219 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1279+182C>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604212 | |||||||
| chr7:5604215 | CTT | C | 5 | a0001c0001t0003g0108 a0001c0003t0001g0109 a0001c0003t0009g0082 others(2): Show |
5 | HG01081.hp1 HG01243.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+186_1279+187d others(4): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604215 | |||||||
| chr7:5604224 | G | A | 3 | a0001c0001t0004g0063 a0001c0001t0004g0070 a0001c0001t0004g0071 |
3 | HG02258.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1279+194G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604224 | |||||||
| chr7:5604250 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0188 |
2 | HG02027.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1279+220C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604250 | |||||||
| chr7:5604367 | T | G | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1279+337T>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604367 | |||||||
| chr7:5604369 | T | A | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1279+339T>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604369 | |||||||
| chr7:5604372 | A | G | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1279+342A>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604372 | |||||||
| chr7:5604374 | A | G | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1279+344A>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604374 | |||||||
| chr7:5604378 | T | G | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1279+348T>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604378 | |||||||
| chr7:5604382 | C | A | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1279+352C>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604382 | |||||||
| chr7:5604387 | G | T | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1279+357G>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604387 | |||||||
| chr7:5604388 | A | G | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1279+358A>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604388 | |||||||
| chr7:5604391 | A | C | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1279+361A>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604391 | |||||||
| chr7:5604392 | C | G | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1279+362C>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604392 | |||||||
| chr7:5604394 | C | G | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1279+364C>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604394 | |||||||
| chr7:5604405 | T | A | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1279+375T>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604405 | |||||||
| chr7:5604431 | A | T | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1279+401A>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604431 | |||||||
| chr7:5604432 | CCCCCAAC others(10): Show |
C | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1279+403_1279+419d others(19): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604432 | |||||||
| chr7:5604450 | T | A | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1279+420T>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604450 | |||||||
| chr7:5604511 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1279+481C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604511 | |||||||
| chr7:5604520 | C | CT | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
203 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1279+491dupT | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 5604520 | ||||||
| chr7:5604524 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1279+494A>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604524 | |||||||
| chr7:5604612 | G | A | 1 | a0001c0002t0002g0217 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1279+582G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604612 | |||||||
| chr7:5604626 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0004g0035 a0001c0001t0004g0112 |
3 | HG02965.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1279+596G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604626 | |||||||
| chr7:5604656 | ATTAT | A | 23 | a0001c0001t0001g0125 a0001c0001t0001g0187 a0001c0002t0001g0227 others(20): Show |
30 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1280-605_1280-602d others(6): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 5604656 | ||||||
| chr7:5604697 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0122 |
2 | HG02080.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1280-575G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604697 | |||||||
| chr7:5604866 | G | GCCTCAAG others(129): Show |
6 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0001c0001t0001g0132 others(3): Show |
6 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(3): Show |
intron_variant | MODIFIER | c.1280-374_1280-239d others(138): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 5604866 | ||||||
| chr7:5604866 | GCCTCAAG others(129): Show |
G | 1 | a0001c0001t0003g0089 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1280-374_1280-239d others(2): Show |
FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 5604866 | ||||||
| chr7:5604880 | G | A | 1 | a0001c0002t0001g0133 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1280-392G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604880 | |||||||
| chr7:5604906 | G | C | 1 | a0001c0001t0001g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1280-366G>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604906 | |||||||
| chr7:5604962 | C | G | 11 | a0001c0001t0001g0224 a0001c0001t0002g0124 a0001c0001t0006g0060 others(8): Show |
11 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1280-310C>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604962 | |||||||
| chr7:5604967 | C | T | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1280-305C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604967 | |||||||
| chr7:5604968 | T | A | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1280-304T>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604968 | |||||||
| chr7:5604969 | T | G | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1280-303T>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604969 | |||||||
| chr7:5604970 | C | G | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1280-302C>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604970 | |||||||
| chr7:5604989 | G | A | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1280-283G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5604989 | |||||||
| chr7:5605027 | C | G | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1280-245C>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5605027 | |||||||
| chr7:5605030 | C | G | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1280-242C>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5605030 | |||||||
| chr7:5605034 | A | T | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1280-238A>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5605034 | |||||||
| chr7:5605037 | T | G | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1280-235T>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5605037 | |||||||
| chr7:5605062 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(125): Show |
210 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.1280-210T>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5605062 | |||||||
| chr7:5605066 | G | A | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1280-206G>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5605066 | |||||||
| chr7:5605067 | C | T | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1280-205C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5605067 | |||||||
| chr7:5605069 | G | T | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1280-203G>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5605069 | |||||||
| chr7:5605079 | C | T | 2 | a0001c0002t0001g0013 a0001c0002t0001g0074 |
4 | HG00099.hp2 HG00642.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1280-193C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5605079 | |||||||
| chr7:5605082 | T | G | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1280-190T>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5605082 | |||||||
| chr7:5605083 | C | T | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1280-189C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5605083 | |||||||
| chr7:5605084 | T | A | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1280-188T>A | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5605084 | |||||||
| chr7:5605085 | A | G | 1 | a0001c0002t0002g0220 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1280-187A>G | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5605085 | |||||||
| chr7:5605122 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1280-150C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5605122 | |||||||
| chr7:5605178 | T | C | 1 | a0001c0001t0001g0036 | 2 | NA18948.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1280-94T>C | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5605178 | |||||||
| chr7:5605208 | C | T | 1 | a0001c0002t0001g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1280-64C>T | FSCN1 | ENSG00000075618.18 | transcript | ENST00000382361.8 | protein_coding | 4/4 | chr7 | 5605208 |