Item | Value |
---|---|
geneid | 401024 |
ensemblid | ENSG00000188738.16 |
hgncid | 21675 |
symbol | FSIP2 |
name | fibrous sheath interacting protein 2 |
refseq_nuc | NM_173651.4 |
refseq_prot | NP_775922.3 |
ensembl_nuc | ENST00000424728.6 |
ensembl_prot | ENSP00000401306.1 |
mane_status | MANE Select |
chr | chr2 |
start | 185738804 |
end | 185833290 |
strand | + |
ver | v1.2 |
region | chr2:185738804-185833290 |
region5000 | chr2:185733804-185838290 |
regionname0 | FSIP2_chr2_185738804_185833290 |
regionname5000 | FSIP2_chr2_185733804_185838290 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 6907 | 72 | 6 | 8 | 57 | 1 | 0 | 46 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0002 | 0/0 | 6907 | 49 | 4 | 6 | 37 | 0 | 2 | 28 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0003 | 0/0 | 6907 | 44 | 16 | 11 | 9 | 0 | 8 | 5 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0004 | 0/0 | 6907 | 29 | 6 | 6 | 15 | 0 | 2 | 10 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0005 | 0/0 | 6907 | 26 | 2 | 11 | 4 | 1 | 8 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0006 | 0/0 | 6907 | 14 | 13 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0007 | 0/0 | 6907 | 10 | 0 | 4 | 6 | 0 | 0 | 4 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0008 | 0/1 | 6907 | 10 | 0 | 4 | 1 | 1 | 3 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0009 | 0/0 | 6907 | 8 | 0 | 7 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0010 | 0/0 | 6907 | 7 | 0 | 2 | 0 | 1 | 4 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0011 | 1/0 | 6907 | 5 | 4 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0012 | 0/0 | 6907 | 5 | 0 | 0 | 0 | 3 | 2 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0013 | 0/0 | 6907 | 5 | 0 | 4 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0014 | 0/0 | 6907 | 5 | 0 | 1 | 4 | 0 | 0 | 4 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0015 | 0/0 | 6907 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0016 | 0/0 | 6907 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0017 | 0/0 | 6907 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0018 | 0/0 | 6907 | 4 | 0 | 1 | 3 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0019 | 0/0 | 6907 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0020 | 0/0 | 6907 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0021 | 0/0 | 6907 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0022 | 0/0 | 6907 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0023 | 0/0 | 6907 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0024 | 0/0 | 6907 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0025 | 0/0 | 6907 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0026 | 0/0 | 6907 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0027 | 0/0 | 6907 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0028 | 0/0 | 6907 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0029 | 0/0 | 6907 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0030 | 0/0 | 6907 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0031 | 0/0 | 6907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0032 | 0/0 | 6907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0033 | 0/0 | 6907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0034 | 0/0 | 6907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0035 | 0/0 | 6907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0036 | 0/0 | 6907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0037 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0038 | 0/0 | 4105 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(4100): Show |
chr2 | 185733804 | 185838290 |
a0039 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0040 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0041 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0042 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0043 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0044 | 0/0 | 6907 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0045 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0046 | 0/0 | 6907 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0047 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0048 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0049 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0050 | 0/0 | 6907 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0051 | 0/0 | 6907 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0052 | 0/0 | 6907 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0053 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0054 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0055 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0056 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0057 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0058 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0059 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0060 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0061 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
a0062 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | MELYL others(6902): Show |
chr2 | 185733804 | 185838290 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 20721 | 58 | 5 | 8 | 44 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0001c0008 | 0/0 | 20721 | 8 | 0 | 0 | 8 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0001c0023 | 0/0 | 20721 | 4 | 0 | 0 | 4 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0001c0043 | 0/0 | 20721 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0001c0051 | 0/0 | 20721 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0002c0002 | 0/0 | 20721 | 42 | 3 | 6 | 31 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0002c0018 | 0/0 | 20721 | 5 | 0 | 0 | 5 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0002c0057 | 0/0 | 20721 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0002c0062 | 0/0 | 20721 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0003c0003 | 0/0 | 20721 | 33 | 7 | 10 | 9 | 0 | 7 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0003c0012 | 0/0 | 20721 | 6 | 6 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0003c0066 | 0/0 | 20721 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0003c0072 | 0/0 | 20721 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0003c0075 | 0/0 | 20721 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0003c0076 | 0/0 | 20721 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0003c0081 | 0/0 | 20721 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0004c0004 | 0/0 | 20721 | 26 | 6 | 6 | 12 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0004c0031 | 0/0 | 20721 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0004c0041 | 0/0 | 20721 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0005c0005 | 0/0 | 20721 | 26 | 2 | 11 | 4 | 1 | 8 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0006c0006 | 0/0 | 20721 | 13 | 12 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0006c0069 | 0/0 | 20721 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0007c0007 | 0/0 | 20721 | 10 | 0 | 4 | 6 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0008c0010 | 0/0 | 20721 | 7 | 0 | 4 | 1 | 1 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0008c0027 | 0/1 | 20721 | 3 | 0 | 0 | 0 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0009c0009 | 0/0 | 20721 | 8 | 0 | 7 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0010c0011 | 0/0 | 20721 | 6 | 0 | 2 | 0 | 1 | 3 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0010c0047 | 0/0 | 20721 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0011c0015 | 1/0 | 20721 | 5 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0012c0019 | 0/0 | 20721 | 5 | 0 | 0 | 0 | 3 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0013c0013 | 0/0 | 20721 | 5 | 0 | 4 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0014c0016 | 0/0 | 20721 | 5 | 0 | 1 | 4 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0015c0014 | 0/0 | 20721 | 5 | 5 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0016c0022 | 0/0 | 20721 | 4 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0016c0038 | 0/0 | 20721 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0017c0017 | 0/0 | 20721 | 5 | 0 | 0 | 5 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0018c0024 | 0/0 | 20721 | 4 | 0 | 1 | 3 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0019c0020 | 0/0 | 20721 | 4 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0020c0021 | 0/0 | 20721 | 4 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0021c0028 | 0/0 | 20721 | 3 | 3 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0022c0026 | 0/0 | 20721 | 3 | 0 | 0 | 0 | 0 | 3 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0023c0025 | 0/0 | 20721 | 3 | 3 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0024c0034 | 0/0 | 20721 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0024c0082 | 0/0 | 20721 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0025c0033 | 0/0 | 20721 | 2 | 0 | 2 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0026c0029 | 0/0 | 20721 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0027c0030 | 0/0 | 20721 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0028c0032 | 0/0 | 20721 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0029c0068 | 0/0 | 20721 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0030c0067 | 0/0 | 20721 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0031c0056 | 0/0 | 20721 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0032c0065 | 0/0 | 20721 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0033c0058 | 0/0 | 20721 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0034c0046 | 0/0 | 20721 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0035c0055 | 0/0 | 20721 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0036c0054 | 0/0 | 20721 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0037c0077 | 0/0 | 20721 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0038c0070 | 0/0 | 20721 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0039c0078 | 0/0 | 20721 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0040c0045 | 0/0 | 20721 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0041c0036 | 0/0 | 20721 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0042c0080 | 0/0 | 20721 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0043c0079 | 0/0 | 20721 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0044c0049 | 0/0 | 20721 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0045c0050 | 0/0 | 20721 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0046c0061 | 0/0 | 20721 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0047c0073 | 0/0 | 20721 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0048c0035 | 0/0 | 20721 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0049c0048 | 0/0 | 20721 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0050c0071 | 0/0 | 20721 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0051c0037 | 0/0 | 20721 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0052c0044 | 0/0 | 20721 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0053c0063 | 0/0 | 20721 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0054c0059 | 0/0 | 20721 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0055c0042 | 0/0 | 20721 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0056c0064 | 0/0 | 20721 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0057c0074 | 0/0 | 20721 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0058c0060 | 0/0 | 20721 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0059c0053 | 0/0 | 20721 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0060c0040 | 0/0 | 20721 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0061c0052 | 0/0 | 20721 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 | ||
a0062c0039 | 0/0 | 20721 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATGGA others(20716): Show |
chr2 | 185733804 | 185838290 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 20880 | 58 | 5 | 8 | 44 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0001c0008t0002 | 0/0 | 20880 | 8 | 0 | 0 | 8 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0001c0023t0002 | 0/0 | 20880 | 4 | 0 | 0 | 4 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0001c0043t0002 | 0/0 | 20880 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0001c0051t0002 | 0/0 | 20880 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0002c0002t0001 | 0/0 | 20879 | 42 | 3 | 6 | 31 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0002c0018t0001 | 0/0 | 20879 | 5 | 0 | 0 | 5 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0002c0057t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0002c0062t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0003c0003t0001 | 0/0 | 20879 | 33 | 7 | 10 | 9 | 0 | 7 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0003c0012t0001 | 0/0 | 20879 | 4 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0003c0012t0003 | 0/0 | 20879 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0003c0066t0001 | 0/0 | 20879 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0003c0072t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0003c0075t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0003c0076t0001 | 0/0 | 20879 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0003c0081t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0004c0004t0001 | 0/0 | 20879 | 19 | 3 | 6 | 8 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0004c0004t0002 | 0/0 | 20880 | 6 | 2 | 0 | 4 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0004c0004t0004 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0004c0031t0002 | 0/0 | 20880 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0004c0041t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0005c0005t0001 | 0/0 | 20879 | 26 | 2 | 11 | 4 | 1 | 8 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0006c0006t0001 | 0/0 | 20879 | 12 | 11 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0006c0006t0002 | 0/0 | 20880 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0006c0069t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0007c0007t0001 | 0/0 | 20879 | 10 | 0 | 4 | 6 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0008c0010t0002 | 0/0 | 20880 | 7 | 0 | 4 | 1 | 1 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0008c0027t0002 | 0/1 | 20880 | 3 | 0 | 0 | 0 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0009c0009t0001 | 0/0 | 20879 | 8 | 0 | 7 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0010c0011t0002 | 0/0 | 20880 | 6 | 0 | 2 | 0 | 1 | 3 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0010c0047t0002 | 0/0 | 20880 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0011c0015t0001 | 1/0 | 20879 | 5 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0012c0019t0001 | 0/0 | 20879 | 5 | 0 | 0 | 0 | 3 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0013c0013t0002 | 0/0 | 20880 | 5 | 0 | 4 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0014c0016t0001 | 0/0 | 20879 | 5 | 0 | 1 | 4 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0015c0014t0002 | 0/0 | 20880 | 5 | 5 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0016c0022t0002 | 0/0 | 20880 | 4 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0016c0038t0002 | 0/0 | 20880 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0017c0017t0001 | 0/0 | 20879 | 5 | 0 | 0 | 5 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0018c0024t0001 | 0/0 | 20879 | 4 | 0 | 1 | 3 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0019c0020t0003 | 0/0 | 20879 | 4 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0020c0021t0001 | 0/0 | 20879 | 4 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0021c0028t0001 | 0/0 | 20879 | 3 | 3 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0022c0026t0002 | 0/0 | 20880 | 3 | 0 | 0 | 0 | 0 | 3 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0023c0025t0001 | 0/0 | 20879 | 3 | 3 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0024c0034t0001 | 0/0 | 20879 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0024c0082t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0025c0033t0001 | 0/0 | 20879 | 2 | 0 | 2 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0026c0029t0002 | 0/0 | 20880 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0027c0030t0002 | 0/0 | 20880 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0028c0032t0001 | 0/0 | 20879 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0029c0068t0001 | 0/0 | 20879 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0030c0067t0001 | 0/0 | 20879 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0031c0056t0001 | 0/0 | 20879 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0032c0065t0001 | 0/0 | 20879 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0033c0058t0001 | 0/0 | 20879 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0034c0046t0002 | 0/0 | 20880 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0035c0055t0001 | 0/0 | 20879 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0036c0054t0002 | 0/0 | 20880 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0037c0077t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0038c0070t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0039c0078t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0040c0045t0002 | 0/0 | 20880 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0041c0036t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0042c0080t0003 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0043c0079t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0044c0049t0002 | 0/0 | 20880 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0045c0050t0002 | 0/0 | 20880 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0046c0061t0001 | 0/0 | 20879 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0047c0073t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0048c0035t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0049c0048t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0050c0071t0001 | 0/0 | 20879 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0051c0037t0001 | 0/0 | 20879 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0052c0044t0002 | 0/0 | 20880 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0053c0063t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0054c0059t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0055c0042t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0056c0064t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0057c0074t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0058c0060t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0059c0053t0002 | 0/0 | 20880 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20875): Show |
chr2 | 185733804 | 185838290 |
a0060c0040t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0061c0052t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
a0062c0039t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | ATTCC others(20874): Show |
chr2 | 185733804 | 185838290 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0003 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0008t0002g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0008t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0008t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0008t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0023t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0023t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0023t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0043t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0001c0051t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0018t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0018t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0018t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0018t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0057t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0002c0062t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0012t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0012t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0012t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0012t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0012t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0012t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0066t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0072t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0075t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0076t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0003c0081t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0004t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0031t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0031t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0004c0041t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0011 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0005c0005t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0006c0006t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0006c0006t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0006c0006t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0006c0006t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0006c0006t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0006c0006t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0006c0006t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0006c0006t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0006c0006t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0006c0006t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0006c0006t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0006c0069t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0007c0007t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0007c0007t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0007c0007t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0007c0007t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0007c0007t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0007c0007t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0007c0007t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0007c0007t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0007c0007t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0007c0007t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0008c0010t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0008c0010t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0008c0010t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0008c0010t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0008c0010t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0008c0010t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0008c0010t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0008c0027t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0008c0027t0002g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0008c0027t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0009c0009t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0009c0009t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0009c0009t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0009c0009t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0009c0009t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0009c0009t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0010c0011t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0010c0011t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0010c0011t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0010c0011t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0010c0011t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0010c0011t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0010c0047t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0011c0015t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0011c0015t0001g0045 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0011c0015t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0011c0015t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0011c0015t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0012c0019t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0012c0019t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0012c0019t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0012c0019t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0013c0013t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0013c0013t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0013c0013t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0013c0013t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0013c0013t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0014c0016t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0014c0016t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0014c0016t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0014c0016t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0014c0016t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0015c0014t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0015c0014t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0015c0014t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0015c0014t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0015c0014t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0016c0022t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0016c0022t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0016c0022t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0016c0022t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0016c0038t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0017c0017t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0017c0017t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0017c0017t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0017c0017t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0018c0024t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0018c0024t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0018c0024t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0018c0024t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0019c0020t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0019c0020t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0019c0020t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0020c0021t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0020c0021t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0020c0021t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0021c0028t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0021c0028t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0022c0026t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0022c0026t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0023c0025t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0023c0025t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0024c0034t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0024c0034t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0024c0082t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0025c0033t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0025c0033t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0026c0029t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0026c0029t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0027c0030t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0027c0030t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0028c0032t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0029c0068t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0030c0067t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0031c0056t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0032c0065t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0033c0058t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0034c0046t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0035c0055t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0036c0054t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0037c0077t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0038c0070t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0039c0078t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0040c0045t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0041c0036t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0042c0080t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0043c0079t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0044c0049t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0045c0050t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0046c0061t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0047c0073t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0048c0035t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0049c0048t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0050c0071t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0051c0037t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0052c0044t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0053c0063t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0054c0059t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0055c0042t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0056c0064t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0057c0074t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0058c0060t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0059c0053t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0060c0040t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0061c0052t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
a0062c0039t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0029 | c0068 | t0001 | g0285 | EUR | GBR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00099 | hp2 | a0010 | c0011 | t0002 | g0108 | EUR | GBR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00280 | hp1 | a0012 | c0019 | t0001 | g0204 | EUR | FIN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00280 | hp2 | a0030 | c0067 | t0001 | g0283 | EUR | FIN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0163 | EUR | FIN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00323 | hp2 | a0012 | c0019 | t0001 | g0202 | EUR | FIN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00423 | hp2 | a0007 | c0007 | t0001 | g0048 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00544 | hp1 | a0004 | c0004 | t0001 | g0071 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00544 | hp2 | a0018 | c0024 | t0001 | g0238 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00558 | hp1 | a0004 | c0004 | t0001 | g0005 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00597 | hp2 | a0018 | c0024 | t0001 | g0236 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0246 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00639 | hp2 | a0025 | c0033 | t0001 | g0311 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00642 | hp1 | a0005 | c0005 | t0001 | g0290 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00642 | hp2 | a0003 | c0003 | t0001 | g0229 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00733 | hp1 | a0003 | c0066 | t0001 | g0288 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00733 | hp2 | a0031 | c0056 | t0001 | g0041 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00735 | hp1 | a0008 | c0010 | t0002 | g0097 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00735 | hp2 | a0003 | c0003 | t0001 | g0220 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00738 | hp1 | a0004 | c0004 | t0001 | g0067 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00738 | hp2 | a0005 | c0005 | t0001 | g0281 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00741 | hp1 | a0010 | c0011 | t0002 | g0111 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0245 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01070 | hp1 | a0008 | c0010 | t0002 | g0096 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01070 | hp2 | a0005 | c0005 | t0001 | g0292 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01071 | hp1 | a0005 | c0005 | t0001 | g0291 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01071 | hp2 | a0008 | c0010 | t0002 | g0088 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01081 | hp2 | a0003 | c0003 | t0001 | g0014 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01099 | hp1 | a0006 | c0006 | t0001 | g0274 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01099 | hp2 | a0005 | c0005 | t0001 | g0301 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01106 | hp1 | a0003 | c0003 | t0001 | g0227 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01106 | hp2 | a0010 | c0011 | t0002 | g0107 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01109 | hp1 | a0003 | c0003 | t0001 | g0228 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01109 | hp2 | a0013 | c0013 | t0002 | g0123 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01167 | hp1 | a0025 | c0033 | t0001 | g0224 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01167 | hp2 | a0009 | c0009 | t0001 | g0012 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01168 | hp1 | a0004 | c0004 | t0001 | g0074 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01168 | hp2 | a0013 | c0013 | t0002 | g0149 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01169 | hp1 | a0004 | c0004 | t0001 | g0073 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01169 | hp2 | a0009 | c0009 | t0001 | g0293 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01175 | hp1 | a0005 | c0005 | t0001 | g0032 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01175 | hp2 | a0013 | c0013 | t0002 | g0151 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0263 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01192 | hp2 | a0032 | c0065 | t0001 | g0287 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01243 | hp1 | a0003 | c0003 | t0001 | g0208 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01243 | hp2 | a0004 | c0004 | t0001 | g0078 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01255 | hp2 | a0033 | c0058 | t0001 | g0261 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01256 | hp1 | a0003 | c0003 | t0001 | g0025 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01256 | hp2 | a0004 | c0004 | t0001 | g0082 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01258 | hp1 | a0003 | c0003 | t0001 | g0025 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01258 | hp2 | a0034 | c0046 | t0002 | g0176 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01261 | hp1 | a0014 | c0016 | t0001 | g0061 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01261 | hp2 | a0005 | c0005 | t0001 | g0303 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01346 | hp2 | a0007 | c0007 | t0001 | g0053 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0084 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01361 | hp2 | a0005 | c0005 | t0001 | g0282 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01496 | hp1 | a0035 | c0055 | t0001 | g0280 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01516 | hp1 | a0005 | c0005 | t0001 | g0032 | EUR | IBS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01516 | hp2 | a0008 | c0010 | t0002 | g0095 | EUR | IBS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01884 | hp2 | a0004 | c0004 | t0001 | g0066 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01891 | hp1 | a0019 | c0020 | t0003 | g0044 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01891 | hp2 | a0011 | c0015 | t0001 | g0002 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01928 | hp1 | a0009 | c0009 | t0001 | g0299 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01943 | hp1 | a0007 | c0007 | t0001 | g0056 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01952 | hp1 | a0007 | c0007 | t0001 | g0054 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01952 | hp2 | a0005 | c0005 | t0001 | g0300 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01975 | hp1 | a0007 | c0007 | t0001 | g0055 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01975 | hp2 | a0004 | c0004 | t0001 | g0077 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01978 | hp1 | a0005 | c0005 | t0001 | g0011 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01978 | hp2 | a0013 | c0013 | t0002 | g0132 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01981 | hp1 | a0036 | c0054 | t0002 | g0171 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01981 | hp2 | a0009 | c0009 | t0001 | g0012 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02004 | hp2 | a0009 | c0009 | t0001 | g0298 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02015 | hp1 | a0037 | c0077 | t0001 | g0218 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02015 | hp2 | a0005 | c0005 | t0001 | g0296 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02055 | hp1 | a0005 | c0005 | t0001 | g0011 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02055 | hp2 | a0038 | c0070 | t0001 | g0271 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02056 | hp2 | a0004 | c0004 | t0001 | g0005 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02071 | hp2 | a0018 | c0024 | t0001 | g0258 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02074 | hp1 | a0005 | c0005 | t0001 | g0304 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02080 | hp2 | a0001 | c0008 | t0002 | g0004 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02083 | hp1 | a0039 | c0078 | t0001 | g0289 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02083 | hp2 | a0001 | c0008 | t0002 | g0148 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02132 | hp1 | a0003 | c0003 | t0001 | g0216 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02135 | hp2 | a0003 | c0003 | t0001 | g0230 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02145 | hp1 | a0021 | c0028 | t0001 | g0302 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02145 | hp2 | a0040 | c0045 | t0002 | g0122 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02148 | hp1 | a0009 | c0009 | t0001 | g0294 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02148 | hp2 | a0018 | c0024 | t0001 | g0239 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | CDX | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | CDX | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02165 | hp1 | a0004 | c0041 | t0001 | g0083 | EAS | CDX | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | CDX | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02257 | hp2 | a0015 | c0014 | t0002 | g0113 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02258 | hp1 | a0003 | c0081 | t0001 | g0206 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02258 | hp2 | a0011 | c0015 | t0001 | g0064 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02273 | hp2 | a0005 | c0005 | t0001 | g0286 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02280 | hp1 | a0006 | c0006 | t0001 | g0279 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02280 | hp2 | a0041 | c0036 | t0001 | g0194 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02293 | hp1 | a0009 | c0009 | t0001 | g0012 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0036 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02300 | hp2 | a0003 | c0003 | t0001 | g0014 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02523 | hp1 | a0004 | c0004 | t0001 | g0069 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02523 | hp2 | a0001 | c0008 | t0002 | g0004 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02572 | hp1 | a0006 | c0006 | t0001 | g0273 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02572 | hp2 | a0003 | c0003 | t0001 | g0207 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02602 | hp1 | a0010 | c0011 | t0002 | g0109 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02602 | hp2 | a0003 | c0003 | t0001 | g0209 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02615 | hp1 | a0006 | c0006 | t0001 | g0276 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02615 | hp2 | a0015 | c0014 | t0002 | g0105 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02630 | hp1 | a0016 | c0022 | t0002 | g0182 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02630 | hp2 | a0015 | c0014 | t0002 | g0112 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02647 | hp1 | a0042 | c0080 | t0003 | g0038 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02647 | hp2 | a0003 | c0072 | t0001 | g0184 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02698 | hp1 | a0005 | c0005 | t0001 | g0035 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02698 | hp2 | a0022 | c0026 | t0002 | g0087 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02717 | hp1 | a0023 | c0025 | t0001 | g0188 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02717 | hp2 | a0020 | c0021 | t0001 | g0198 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02723 | hp1 | a0043 | c0079 | t0001 | g0191 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02723 | hp2 | a0006 | c0006 | t0001 | g0030 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02735 | hp1 | a0005 | c0005 | t0001 | g0035 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02735 | hp2 | a0044 | c0049 | t0002 | g0124 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02738 | hp1 | a0010 | c0011 | t0002 | g0099 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02738 | hp2 | a0003 | c0076 | t0001 | g0265 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02809 | hp2 | a0019 | c0020 | t0003 | g0043 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02818 | hp1 | a0016 | c0022 | t0002 | g0180 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02818 | hp2 | a0003 | c0012 | t0001 | g0192 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02886 | hp1 | a0006 | c0006 | t0001 | g0031 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02886 | hp2 | a0045 | c0050 | t0002 | g0019 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02895 | hp1 | a0023 | c0025 | t0001 | g0022 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02895 | hp2 | a0003 | c0012 | t0001 | g0193 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02896 | hp1 | a0011 | c0015 | t0001 | g0052 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02896 | hp2 | a0004 | c0004 | t0001 | g0081 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02897 | hp1 | a0023 | c0025 | t0001 | g0022 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02897 | hp2 | a0011 | c0015 | t0001 | g0050 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02922 | hp1 | a0003 | c0003 | t0001 | g0269 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02922 | hp2 | a0020 | c0021 | t0001 | g0197 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02965 | hp1 | a0020 | c0021 | t0001 | g0023 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02965 | hp2 | a0019 | c0020 | t0003 | g0013 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02970 | hp1 | a0006 | c0006 | t0001 | g0031 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02970 | hp2 | a0003 | c0012 | t0001 | g0190 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02976 | hp1 | a0006 | c0006 | t0001 | g0270 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02976 | hp2 | a0021 | c0028 | t0001 | g0034 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03017 | hp1 | a0003 | c0003 | t0001 | g0205 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03017 | hp2 | a0046 | c0061 | t0001 | g0247 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03041 | hp1 | a0016 | c0038 | t0002 | g0181 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03041 | hp2 | a0026 | c0029 | t0002 | g0172 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03098 | hp1 | a0003 | c0012 | t0003 | g0039 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03098 | hp2 | a0047 | c0073 | t0001 | g0275 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03130 | hp1 | a0027 | c0030 | t0002 | g0118 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03130 | hp2 | a0003 | c0003 | t0001 | g0267 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03139 | hp1 | a0048 | c0035 | t0001 | g0042 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03139 | hp2 | a0027 | c0030 | t0002 | g0183 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03195 | hp1 | a0016 | c0022 | t0002 | g0179 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03195 | hp2 | a0021 | c0028 | t0001 | g0034 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03209 | hp2 | a0003 | c0075 | t0001 | g0189 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03225 | hp1 | a0016 | c0022 | t0002 | g0178 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03239 | hp1 | a0003 | c0003 | t0001 | g0199 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03239 | hp2 | a0022 | c0026 | t0002 | g0015 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03453 | hp1 | a0049 | c0048 | t0001 | g0186 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03453 | hp2 | a0006 | c0006 | t0001 | g0030 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03486 | hp1 | a0003 | c0012 | t0001 | g0195 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03486 | hp2 | a0004 | c0004 | t0004 | g0075 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03490 | hp1 | a0050 | c0071 | t0001 | g0221 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03490 | hp2 | a0008 | c0027 | t0002 | g0090 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03491 | hp1 | a0051 | c0037 | t0001 | g0001 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03491 | hp2 | a0012 | c0019 | t0001 | g0024 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03492 | hp1 | a0012 | c0019 | t0001 | g0024 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03492 | hp2 | a0008 | c0027 | t0002 | g0093 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03540 | hp1 | a0004 | c0004 | t0001 | g0072 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03540 | hp2 | a0006 | c0006 | t0002 | g0177 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03579 | hp1 | a0006 | c0006 | t0001 | g0277 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03579 | hp2 | a0004 | c0004 | t0002 | g0021 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03654 | hp1 | a0013 | c0013 | t0002 | g0142 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03654 | hp2 | a0004 | c0004 | t0001 | g0076 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03688 | hp1 | a0005 | c0005 | t0001 | g0033 | SAS | STU | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03688 | hp2 | a0010 | c0011 | t0002 | g0119 | SAS | STU | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03710 | hp1 | a0005 | c0005 | t0001 | g0295 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03710 | hp2 | a0022 | c0026 | t0002 | g0015 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03831 | hp1 | a0005 | c0005 | t0001 | g0033 | SAS | BEB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0233 | SAS | BEB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03942 | hp1 | a0010 | c0047 | t0002 | g0117 | SAS | BEB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG03942 | hp2 | a0003 | c0003 | t0001 | g0310 | SAS | BEB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG04115 | hp1 | a0005 | c0005 | t0001 | g0284 | SAS | STU | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG04115 | hp2 | a0004 | c0004 | t0001 | g0065 | SAS | STU | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG04184 | hp1 | a0003 | c0003 | t0001 | g0211 | SAS | BEB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG04184 | hp2 | a0052 | c0044 | t0002 | g0155 | SAS | BEB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG04199 | hp1 | a0003 | c0003 | t0001 | g0210 | SAS | STU | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG04199 | hp2 | a0008 | c0010 | t0002 | g0091 | SAS | STU | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG04204 | hp1 | a0005 | c0005 | t0001 | g0307 | SAS | STU | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0232 | SAS | STU | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18522 | hp1 | a0001 | c0051 | t0002 | g0106 | AFR | YRI | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18522 | hp2 | a0019 | c0020 | t0003 | g0013 | AFR | YRI | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18612 | hp1 | a0003 | c0003 | t0001 | g0226 | EAS | CHB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | CHB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18747 | hp1 | a0003 | c0003 | t0001 | g0222 | EAS | CHB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18747 | hp2 | a0007 | c0007 | t0001 | g0062 | EAS | CHB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18906 | hp1 | a0006 | c0069 | t0001 | g0272 | AFR | YRI | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | YRI | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18940 | hp1 | a0004 | c0004 | t0001 | g0070 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18944 | hp1 | a0017 | c0017 | t0001 | g0057 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18946 | hp1 | a0007 | c0007 | t0001 | g0047 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18948 | hp1 | a0014 | c0016 | t0001 | g0002 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18949 | hp1 | a0004 | c0031 | t0002 | g0170 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18951 | hp2 | a0007 | c0007 | t0001 | g0051 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18952 | hp1 | a0005 | c0005 | t0001 | g0297 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18953 | hp2 | a0004 | c0004 | t0002 | g0101 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18959 | hp1 | a0001 | c0043 | t0002 | g0129 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18959 | hp2 | a0024 | c0034 | t0001 | g0237 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18961 | hp2 | a0028 | c0032 | t0001 | g0029 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18964 | hp2 | a0007 | c0007 | t0001 | g0063 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18965 | hp2 | a0054 | c0059 | t0001 | g0001 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18967 | hp1 | a0004 | c0004 | t0002 | g0016 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18970 | hp2 | a0004 | c0004 | t0001 | g0068 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18972 | hp2 | a0017 | c0017 | t0001 | g0002 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18979 | hp2 | a0003 | c0003 | t0001 | g0215 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18980 | hp1 | a0003 | c0003 | t0001 | g0223 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18981 | hp1 | a0002 | c0018 | t0001 | g0241 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18981 | hp2 | a0001 | c0023 | t0002 | g0138 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18984 | hp2 | a0002 | c0018 | t0001 | g0260 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18986 | hp1 | a0001 | c0008 | t0002 | g0004 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18986 | hp2 | a0014 | c0016 | t0001 | g0059 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18989 | hp1 | a0017 | c0017 | t0001 | g0049 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18989 | hp2 | a0055 | c0042 | t0001 | g0079 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18990 | hp1 | a0017 | c0017 | t0001 | g0046 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18990 | hp2 | a0001 | c0008 | t0002 | g0162 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18991 | hp2 | a0001 | c0008 | t0002 | g0146 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18992 | hp1 | a0004 | c0031 | t0002 | g0169 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18993 | hp1 | a0007 | c0007 | t0001 | g0002 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18993 | hp2 | a0056 | c0064 | t0001 | g0243 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18998 | hp1 | a0001 | c0023 | t0002 | g0018 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18998 | hp2 | a0003 | c0003 | t0001 | g0213 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18999 | hp2 | a0002 | c0018 | t0001 | g0027 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19001 | hp1 | a0008 | c0010 | t0002 | g0130 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19002 | hp1 | a0005 | c0005 | t0001 | g0201 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19002 | hp2 | a0057 | c0074 | t0001 | g0212 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19003 | hp1 | a0001 | c0023 | t0002 | g0140 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19003 | hp2 | a0002 | c0057 | t0001 | g0250 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19004 | hp2 | a0024 | c0082 | t0001 | g0240 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19007 | hp2 | a0058 | c0060 | t0001 | g0006 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19009 | hp2 | a0001 | c0008 | t0002 | g0004 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19030 | hp1 | a0006 | c0006 | t0001 | g0268 | AFR | LWK | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19030 | hp2 | a0003 | c0003 | t0001 | g0266 | AFR | LWK | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19043 | hp1 | a0003 | c0003 | t0001 | g0203 | AFR | LWK | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | LWK | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19054 | hp2 | a0001 | c0023 | t0002 | g0018 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19056 | hp1 | a0059 | c0053 | t0002 | g0007 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19056 | hp2 | a0002 | c0018 | t0001 | g0027 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19060 | hp1 | a0003 | c0003 | t0001 | g0214 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19065 | hp1 | a0017 | c0017 | t0001 | g0002 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19065 | hp2 | a0060 | c0040 | t0001 | g0005 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19070 | hp1 | a0004 | c0004 | t0001 | g0080 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19070 | hp2 | a0028 | c0032 | t0001 | g0029 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19075 | hp1 | a0004 | c0004 | t0002 | g0100 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19075 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19077 | hp2 | a0014 | c0016 | t0001 | g0058 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19079 | hp2 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19080 | hp2 | a0004 | c0004 | t0002 | g0016 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19084 | hp2 | a0002 | c0018 | t0001 | g0242 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19085 | hp2 | a0014 | c0016 | t0001 | g0060 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19088 | hp2 | a0001 | c0008 | t0002 | g0004 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19089 | hp2 | a0024 | c0034 | t0001 | g0037 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19091 | hp2 | a0003 | c0003 | t0001 | g0254 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19240 | hp1 | a0006 | c0006 | t0001 | g0278 | AFR | YRI | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA19240 | hp2 | a0015 | c0014 | t0002 | g0104 | AFR | YRI | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA20129 | hp1 | a0003 | c0012 | t0003 | g0040 | AFR | ASW | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA20129 | hp2 | a0015 | c0014 | t0002 | g0103 | AFR | ASW | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA20752 | hp1 | a0012 | c0019 | t0001 | g0217 | EUR | TSI | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA20752 | hp2 | a0009 | c0009 | t0001 | g0306 | EUR | TSI | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA20905 | hp1 | a0005 | c0005 | t0001 | g0011 | SAS | GIH | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA20905 | hp2 | a0003 | c0003 | t0001 | g0308 | SAS | GIH | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01123 | hp1 | a0003 | c0003 | t0001 | g0309 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG01123 | hp2 | a0008 | c0010 | t0002 | g0094 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02109 | hp1 | a0026 | c0029 | t0002 | g0102 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0085 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02486 | hp1 | a0005 | c0005 | t0001 | g0305 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02486 | hp2 | a0004 | c0004 | t0002 | g0021 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02559 | hp1 | a0002 | c0062 | t0001 | g0231 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
HG02559 | hp2 | a0003 | c0003 | t0001 | g0264 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18955 | hp1 | a0053 | c0063 | t0001 | g0006 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA20300 | hp1 | a0061 | c0052 | t0001 | g0187 | AFR | USA | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA20300 | hp2 | a0020 | c0021 | t0001 | g0023 | AFR | USA | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA21309 | hp1 | a0003 | c0003 | t0001 | g0225 | AFR | LWK | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
NA21309 | hp2 | a0062 | c0039 | t0001 | g0196 | AFR | LWK | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
homoSapiens | chm13v2 | a0008 | c0027 | t0002 | g0092 | REF | REF | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
homoSapiens | grch38p0 | a0011 | c0015 | t0001 | g0045 | REF | REF | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:185745439 | C | G | 1 | a0024 | 3 | NA18959.hp2 NA19004.hp2 NA19089.hp2 |
missense_variant | MODERATE | c.488C>G | p.Ala163Gly | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/23 | 579/20879 | 488/20724 | 163/6907 | chr2 | 185745439 | |||
chr2:185746763 | C | T | 1 | a0021 | 3 | HG02145.hp1 HG02976.hp2 HG03195.hp2 |
missense_variant | MODERATE | c.712C>T | p.Arg238Trp | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 6/23 | 803/20879 | 712/20724 | 238/6907 | chr2 | 185746763 | |||
chr2:185753767 | A | G | 2 | a0019 a0042 |
5 | HG01891.hp1 HG02647.hp1 HG02809.hp2 others(2): Show |
missense_variant | MODERATE | c.916A>G | p.Met306Val | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/23 | 1007/20879 | 916/20724 | 306/6907 | chr2 | 185753767 | |||
chr2:185753824 | G | A | 1 | a0051 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.973G>A | p.Gly325Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/23 | 1064/20879 | 973/20724 | 325/6907 | chr2 | 185753824 | |||
chr2:185761994 | A | C | 1 | a0043 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.1217A>C | p.Asn406Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/23 | 1308/20879 | 1217/20724 | 406/6907 | chr2 | 185761994 | |||
chr2:185761994 | A | T | 1 | a0062 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1217A>T | p.Asn406Ile | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/23 | 1308/20879 | 1217/20724 | 406/6907 | chr2 | 185761994 | |||
chr2:185763216 | T | C | 34 | a0002 a0003 a0005 others(31): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.1274T>C | p.Ile425Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/23 | 1365/20879 | 1274/20724 | 425/6907 | chr2 | 185763216 | |||
chr2:185789591 | A | T | 3 | a0007 a0014 a0017 |
20 | HG00423.hp2 HG01261.hp1 HG01346.hp2 others(17): Show |
missense_variant | MODERATE | c.2455A>T | p.Ile819Phe | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 2546/20879 | 2455/20724 | 819/6907 | chr2 | 185789591 | |||
chr2:185789748 | A | G | 1 | a0039 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.2612A>G | p.Asn871Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 2703/20879 | 2612/20724 | 871/6907 | chr2 | 185789748 | |||
chr2:185789789 | A | G | 1 | a0037 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.2653A>G | p.Asn885Asp | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 2744/20879 | 2653/20724 | 885/6907 | chr2 | 185789789 | |||
chr2:185789865 | A | G | 34 | a0002 a0003 a0005 others(31): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.2729A>G | p.Asn910Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 2820/20879 | 2729/20724 | 910/6907 | chr2 | 185789865 | |||
chr2:185790140 | G | C | 13 | a0002 a0018 a0024 others(10): Show |
67 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(64): Show |
missense_variant | MODERATE | c.3004G>C | p.Asp1002His | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 3095/20879 | 3004/20724 | 1002/6907 | chr2 | 185790140 | |||
chr2:185790396 | C | T | 1 | a0056 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.3260C>T | p.Ser1087Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 3351/20879 | 3260/20724 | 1087/6907 | chr2 | 185790396 | |||
chr2:185790509 | C | T | 1 | a0053 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.3373C>T | p.Pro1125Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 3464/20879 | 3373/20724 | 1125/6907 | chr2 | 185790509 | |||
chr2:185790849 | T | C | 1 | a0052 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.3713T>C | p.Val1238Ala | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 3804/20879 | 3713/20724 | 1238/6907 | chr2 | 185790849 | |||
chr2:185790930 | G | A | 1 | a0022 | 3 | HG02698.hp2 HG03239.hp2 HG03710.hp2 |
missense_variant | MODERATE | c.3794G>A | p.Arg1265His | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 3885/20879 | 3794/20724 | 1265/6907 | chr2 | 185790930 | |||
chr2:185790999 | G | A | 57 | a0001 a0002 a0003 others(54): Show |
343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
missense_variant | MODERATE | c.3863G>A | p.Arg1288Gln | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 3954/20879 | 3863/20724 | 1288/6907 | chr2 | 185790999 | |||
chr2:185791173 | C | T | 1 | a0016 | 5 | HG02630.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
missense_variant | MODERATE | c.4037C>T | p.Thr1346Met | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 4128/20879 | 4037/20724 | 1346/6907 | chr2 | 185791173 | |||
chr2:185791278 | G | A | 1 | a0060 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.4142G>A | p.Arg1381His | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 4233/20879 | 4142/20724 | 1381/6907 | chr2 | 185791278 | |||
chr2:185792126 | G | A | 1 | a0035 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.4990G>A | p.Asp1664Asn | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5081/20879 | 4990/20724 | 1664/6907 | chr2 | 185792126 | |||
chr2:185792162 | A | T | 3 | a0016 a0020 a0062 |
10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
missense_variant | MODERATE | c.5026A>T | p.Thr1676Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5117/20879 | 5026/20724 | 1676/6907 | chr2 | 185792162 | |||
chr2:185792229 | T | C | 34 | a0002 a0003 a0005 others(31): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.5093T>C | p.Met1698Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5184/20879 | 5093/20724 | 1698/6907 | chr2 | 185792229 | |||
chr2:185792230 | G | A | 1 | a0024 | 1 | NA19004.hp2 | missense_variant | MODERATE | c.5094G>A | p.Met1698Ile | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5185/20879 | 5094/20724 | 1698/6907 | chr2 | 185792230 | |||
chr2:185792307 | A | G | 1 | a0059 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.5171A>G | p.Asp1724Gly | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5262/20879 | 5171/20724 | 1724/6907 | chr2 | 185792307 | |||
chr2:185792384 | A | T | 1 | a0041 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.5248A>T | p.Thr1750Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5339/20879 | 5248/20724 | 1750/6907 | chr2 | 185792384 | |||
chr2:185792658 | T | C | 1 | a0026 | 2 | HG02109.hp1 HG03041.hp2 |
missense_variant | MODERATE | c.5522T>C | p.Ile1841Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5613/20879 | 5522/20724 | 1841/6907 | chr2 | 185792658 | |||
chr2:185792966 | G | C | 1 | a0040 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.5830G>C | p.Val1944Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5921/20879 | 5830/20724 | 1944/6907 | chr2 | 185792966 | |||
chr2:185793026 | G | A | 1 | a0028 | 2 | NA18961.hp2 NA19070.hp2 |
missense_variant | MODERATE | c.5890G>A | p.Ala1964Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5981/20879 | 5890/20724 | 1964/6907 | chr2 | 185793026 | |||
chr2:185793329 | G | A | 33 | a0002 a0003 a0005 others(30): Show |
189 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(186): Show |
missense_variant | MODERATE | c.6193G>A | p.Asp2065Asn | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 6284/20879 | 6193/20724 | 2065/6907 | chr2 | 185793329 | |||
chr2:185793330 | A | G | 1 | a0043 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.6194A>G | p.Asp2065Gly | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 6285/20879 | 6194/20724 | 2065/6907 | chr2 | 185793330 | |||
chr2:185793362 | C | A | 1 | a0032 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.6226C>A | p.Leu2076Met | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 6317/20879 | 6226/20724 | 2076/6907 | chr2 | 185793362 | |||
chr2:185793711 | C | T | 34 | a0002 a0003 a0005 others(31): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.6575C>T | p.Thr2192Met | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 6666/20879 | 6575/20724 | 2192/6907 | chr2 | 185793711 | |||
chr2:185793838 | G | T | 34 | a0002 a0003 a0005 others(31): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.6702G>T | p.Glu2234Asp | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 6793/20879 | 6702/20724 | 2234/6907 | chr2 | 185793838 | |||
chr2:185794059 | A | T | 3 | a0016 a0020 a0062 |
10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
missense_variant | MODERATE | c.6923A>T | p.Asp2308Val | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 7014/20879 | 6923/20724 | 2308/6907 | chr2 | 185794059 | |||
chr2:185794125 | T | C | 1 | a0034 | 1 | HG01258.hp2 | missense_variant | MODERATE | c.6989T>C | p.Phe2330Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 7080/20879 | 6989/20724 | 2330/6907 | chr2 | 185794125 | |||
chr2:185794457 | C | A | 1 | a0010 | 7 | HG00099.hp2 HG00741.hp1 HG01106.hp2 others(4): Show |
missense_variant | MODERATE | c.7321C>A | p.Gln2441Lys | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 7412/20879 | 7321/20724 | 2441/6907 | chr2 | 185794457 | |||
chr2:185794632 | G | T | 34 | a0002 a0003 a0005 others(31): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.7496G>T | p.Arg2499Met | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 7587/20879 | 7496/20724 | 2499/6907 | chr2 | 185794632 | |||
chr2:185795244 | A | G | 1 | a0061 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.8108A>G | p.Lys2703Arg | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 8199/20879 | 8108/20724 | 2703/6907 | chr2 | 185795244 | |||
chr2:185795285 | A | G | 1 | a0015 | 5 | HG02257.hp2 HG02615.hp2 HG02630.hp2 others(2): Show |
missense_variant | MODERATE | c.8149A>G | p.Met2717Val | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 8240/20879 | 8149/20724 | 2717/6907 | chr2 | 185795285 | |||
chr2:185795834 | A | G | 1 | a0030 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.8698A>G | p.Lys2900Glu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 8789/20879 | 8698/20724 | 2900/6907 | chr2 | 185795834 | |||
chr2:185796014 | T | C | 3 | a0016 a0020 a0062 |
10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
missense_variant | MODERATE | c.8878T>C | p.Phe2960Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 8969/20879 | 8878/20724 | 2960/6907 | chr2 | 185796014 | |||
chr2:185796038 | A | G | 1 | a0017 | 5 | NA18944.hp1 NA18972.hp2 NA18989.hp1 others(2): Show |
missense_variant | MODERATE | c.8902A>G | p.Ser2968Gly | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 8993/20879 | 8902/20724 | 2968/6907 | chr2 | 185796038 | |||
chr2:185796296 | G | A | 1 | a0049 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.9160G>A | p.Glu3054Lys | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 9251/20879 | 9160/20724 | 3054/6907 | chr2 | 185796296 | |||
chr2:185796449 | G | C | 2 | a0006 a0038 |
15 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
missense_variant | MODERATE | c.9313G>C | p.Glu3105Gln | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 9404/20879 | 9313/20724 | 3105/6907 | chr2 | 185796449 | |||
chr2:185796672 | A | G | 1 | a0032 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.9536A>G | p.Asn3179Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 9627/20879 | 9536/20724 | 3179/6907 | chr2 | 185796672 | |||
chr2:185796840 | G | A | 2 | a0013 a0044 |
6 | HG01109.hp2 HG01168.hp2 HG01175.hp2 others(3): Show |
missense_variant | MODERATE | c.9704G>A | p.Cys3235Tyr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 9795/20879 | 9704/20724 | 3235/6907 | chr2 | 185796840 | |||
chr2:185800098 | G | A | 1 | a0009 | 8 | HG01167.hp2 HG01169.hp2 HG01928.hp1 others(5): Show |
missense_variant | MODERATE | c.10792G>A | p.Gly3598Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 10883/20879 | 10792/20724 | 3598/6907 | chr2 | 185800098 | |||
chr2:185800171 | A | G | 1 | a0049 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.10865A>G | p.Asp3622Gly | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 10956/20879 | 10865/20724 | 3622/6907 | chr2 | 185800171 | |||
chr2:185800236 | C | A | 34 | a0002 a0003 a0005 others(31): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.10930C>A | p.Leu3644Ile | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 11021/20879 | 10930/20724 | 3644/6907 | chr2 | 185800236 | |||
chr2:185800371 | A | G | 2 | a0023 a0048 |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
missense_variant | MODERATE | c.11065A>G | p.Thr3689Ala | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 11156/20879 | 11065/20724 | 3689/6907 | chr2 | 185800371 | |||
chr2:185800464 | G | C | 3 | a0016 a0020 a0062 |
10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
missense_variant | MODERATE | c.11158G>C | p.Gly3720Arg | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 11249/20879 | 11158/20724 | 3720/6907 | chr2 | 185800464 | |||
chr2:185800525 | C | A | 1 | a0050 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.11219C>A | p.Thr3740Asn | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 11310/20879 | 11219/20724 | 3740/6907 | chr2 | 185800525 | |||
chr2:185800705 | G | A | 34 | a0002 a0003 a0005 others(31): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.11399G>A | p.Gly3800Glu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 11490/20879 | 11399/20724 | 3800/6907 | chr2 | 185800705 | |||
chr2:185800903 | T | C | 1 | a0055 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.11597T>C | p.Leu3866Pro | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 11688/20879 | 11597/20724 | 3866/6907 | chr2 | 185800903 | |||
chr2:185801097 | A | G | 34 | a0002 a0003 a0005 others(31): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.11791A>G | p.Asn3931Asp | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 11882/20879 | 11791/20724 | 3931/6907 | chr2 | 185801097 | |||
chr2:185801616 | T | A | 1 | a0027 | 2 | HG03130.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.12310T>A | p.Ser4104Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 12401/20879 | 12310/20724 | 4104/6907 | chr2 | 185801616 | |||
chr2:185801624 | C | G | 1 | a0038 | 1 | HG02055.hp2 | stop_gained | HIGH | c.12318C>G | p.Tyr4106* | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 12409/20879 | 12318/20724 | 4106/6907 | chr2 | 185801624 | |||
chr2:185802394 | T | C | 34 | a0002 a0003 a0005 others(31): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.13088T>C | p.Phe4363Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 13179/20879 | 13088/20724 | 4363/6907 | chr2 | 185802394 | |||
chr2:185802633 | A | C | 7 | a0004 a0019 a0023 others(4): Show |
40 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(37): Show |
missense_variant | MODERATE | c.13327A>C | p.Ile4443Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 13418/20879 | 13327/20724 | 4443/6907 | chr2 | 185802633 | |||
chr2:185802924 | A | G | 1 | a0047 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.13618A>G | p.Ile4540Val | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 13709/20879 | 13618/20724 | 4540/6907 | chr2 | 185802924 | |||
chr2:185803293 | C | T | 1 | a0020 | 4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
missense_variant | MODERATE | c.13987C>T | p.His4663Tyr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 14078/20879 | 13987/20724 | 4663/6907 | chr2 | 185803293 | |||
chr2:185803357 | T | C | 1 | a0055 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.14051T>C | p.Leu4684Pro | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 14142/20879 | 14051/20724 | 4684/6907 | chr2 | 185803357 | |||
chr2:185803399 | T | C | 1 | a0035 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.14093T>C | p.Val4698Ala | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 14184/20879 | 14093/20724 | 4698/6907 | chr2 | 185803399 | |||
chr2:185803494 | A | C | 2 | a0016 a0020 |
9 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(6): Show |
missense_variant | MODERATE | c.14188A>C | p.Ile4730Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 14279/20879 | 14188/20724 | 4730/6907 | chr2 | 185803494 | |||
chr2:185803987 | A | T | 1 | a0012 | 5 | HG00280.hp1 HG00323.hp2 HG03491.hp2 others(2): Show |
missense_variant | MODERATE | c.14681A>T | p.Lys4894Ile | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 14772/20879 | 14681/20724 | 4894/6907 | chr2 | 185803987 | |||
chr2:185804208 | A | G | 17 | a0001 a0008 a0010 others(14): Show |
114 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
missense_variant | MODERATE | c.14902A>G | p.Met4968Val | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 14993/20879 | 14902/20724 | 4968/6907 | chr2 | 185804208 | |||
chr2:185804321 | T | A | 1 | a0023 | 3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.15015T>A | p.Asp5005Glu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 15106/20879 | 15015/20724 | 5005/6907 | chr2 | 185804321 | |||
chr2:185804469 | A | G | 1 | a0057 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.15163A>G | p.Arg5055Gly | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 15254/20879 | 15163/20724 | 5055/6907 | chr2 | 185804469 | |||
chr2:185804545 | C | A | 1 | a0044 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.15239C>A | p.Ser5080Tyr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 15330/20879 | 15239/20724 | 5080/6907 | chr2 | 185804545 | |||
chr2:185804598 | A | G | 1 | a0046 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.15292A>G | p.Ile5098Val | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 15383/20879 | 15292/20724 | 5098/6907 | chr2 | 185804598 | |||
chr2:185804813 | G | T | 2 | a0053 a0058 |
2 | NA18955.hp1 NA19007.hp2 |
missense_variant | MODERATE | c.15507G>T | p.Glu5169Asp | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 15598/20879 | 15507/20724 | 5169/6907 | chr2 | 185804813 | |||
chr2:185805177 | C | T | 1 | a0054 | 1 | NA18965.hp2 | missense_variant | MODERATE | c.15871C>T | p.Leu5291Phe | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 15962/20879 | 15871/20724 | 5291/6907 | chr2 | 185805177 | |||
chr2:185805377 | A | C | 58 | a0001 a0002 a0003 others(55): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
missense_variant | MODERATE | c.16071A>C | p.Glu5357Asp | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 16162/20879 | 16071/20724 | 5357/6907 | chr2 | 185805377 | |||
chr2:185805652 | C | T | 1 | a0014 | 5 | HG01261.hp1 NA18948.hp1 NA18986.hp2 others(2): Show |
missense_variant | MODERATE | c.16346C>T | p.Thr5449Ile | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 16437/20879 | 16346/20724 | 5449/6907 | chr2 | 185805652 | |||
chr2:185806053 | T | A | 30 | a0002 a0003 a0005 others(27): Show |
179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
missense_variant | MODERATE | c.16747T>A | p.Tyr5583Asn | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 16838/20879 | 16747/20724 | 5583/6907 | chr2 | 185806053 | |||
chr2:185806252 | T | C | 51 | a0001 a0002 a0003 others(48): Show |
304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
missense_variant | MODERATE | c.16946T>C | p.Ile5649Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 17037/20879 | 16946/20724 | 5649/6907 | chr2 | 185806252 | |||
chr2:185806387 | C | T | 4 | a0016 a0020 a0043 others(1): Show |
11 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(8): Show |
missense_variant | MODERATE | c.17081C>T | p.Ser5694Phe | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 17172/20879 | 17081/20724 | 5694/6907 | chr2 | 185806387 | |||
chr2:185806504 | A | T | 1 | a0062 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.17198A>T | p.Lys5733Ile | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 17289/20879 | 17198/20724 | 5733/6907 | chr2 | 185806504 | |||
chr2:185806630 | G | A | 34 | a0002 a0003 a0005 others(31): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.17324G>A | p.Arg5775Gln | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 17415/20879 | 17324/20724 | 5775/6907 | chr2 | 185806630 | |||
chr2:185807004 | C | A | 1 | a0055 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.17698C>A | p.Pro5900Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 17789/20879 | 17698/20724 | 5900/6907 | chr2 | 185807004 | |||
chr2:185807185 | G | A | 34 | a0002 a0003 a0005 others(31): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.17879G>A | p.Arg5960His | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 17970/20879 | 17879/20724 | 5960/6907 | chr2 | 185807185 | |||
chr2:185807596 | G | T | 1 | a0045 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.18290G>T | p.Gly6097Val | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 18381/20879 | 18290/20724 | 6097/6907 | chr2 | 185807596 | |||
chr2:185807800 | T | A | 8 | a0005 a0009 a0021 others(5): Show |
42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
missense_variant | MODERATE | c.18494T>A | p.Leu6165Gln | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 18585/20879 | 18494/20724 | 6165/6907 | chr2 | 185807800 | |||
chr2:185808588 | A | C | 1 | a0025 | 2 | HG00639.hp2 HG01167.hp1 |
missense_variant | MODERATE | c.19282A>C | p.Asn6428His | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 19373/20879 | 19282/20724 | 6428/6907 | chr2 | 185808588 | |||
chr2:185808891 | C | A | 2 | a0018 a0024 |
7 | HG00544.hp2 HG00597.hp2 HG02071.hp2 others(4): Show |
missense_variant | MODERATE | c.19585C>A | p.Pro6529Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 19676/20879 | 19585/20724 | 6529/6907 | chr2 | 185808891 | |||
chr2:185808901 | T | C | 1 | a0019 | 4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
missense_variant | MODERATE | c.19595T>C | p.Ile6532Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 19686/20879 | 19595/20724 | 6532/6907 | chr2 | 185808901 | |||
chr2:185809103 | G | C | 1 | a0033 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.19797G>C | p.Lys6599Asn | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 19888/20879 | 19797/20724 | 6599/6907 | chr2 | 185809103 | |||
chr2:185813906 | C | T | 2 | a0008 a0022 |
12 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(9): Show |
missense_variant | MODERATE | c.20189C>T | p.Thr6730Ile | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/23 | 20280/20879 | 20189/20724 | 6730/6907 | chr2 | 185813906 | |||
chr2:185833149 | A | G | 58 | a0001 a0002 a0003 others(55): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
missense_variant | MODERATE | c.20647A>G | p.Thr6883Ala | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 23/23 | 20738/20879 | 20647/20724 | 6883/6907 | chr2 | 185833149 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:185739456 | G | C | 1 | a0048c0035 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.210G>C | p.Thr70Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/23 | 301/20879 | 210/20724 | 70/6907 | chr2 | 185739456 | |||
chr2:185743162 | G | C | 1 | a0041c0036 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.255G>C | p.Leu85Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 3/23 | 346/20879 | 255/20724 | 85/6907 | chr2 | 185743162 | |||
chr2:185743184 | T | C | 1 | a0019c0020 | 4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
synonymous_variant | LOW | c.277T>C | p.Leu93Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 3/23 | 368/20879 | 277/20724 | 93/6907 | chr2 | 185743184 | |||
chr2:185746768 | A | G | 1 | a0003c0081 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.717A>G | p.Glu239Glu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 6/23 | 808/20879 | 717/20724 | 239/6907 | chr2 | 185746768 | |||
chr2:185761040 | G | A | 4 | a0016c0022 a0016c0038 a0020c0021 others(1): Show |
10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
synonymous_variant | LOW | c.1131G>A | p.Thr377Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 10/23 | 1222/20879 | 1131/20724 | 377/6907 | chr2 | 185761040 | |||
chr2:185761043 | A | G | 46 | a0002c0002 a0002c0018 a0002c0057 others(43): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
synonymous_variant | LOW | c.1134A>G | p.Lys378Lys | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 10/23 | 1225/20879 | 1134/20724 | 378/6907 | chr2 | 185761043 | |||
chr2:185788819 | G | A | 8 | a0004c0004 a0004c0041 a0019c0020 others(5): Show |
38 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(35): Show |
synonymous_variant | LOW | c.1683G>A | p.Thr561Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 1774/20879 | 1683/20724 | 561/6907 | chr2 | 185788819 | |||
chr2:185789227 | A | G | 1 | a0051c0037 | 1 | HG03491.hp1 | synonymous_variant | LOW | c.2091A>G | p.Lys697Lys | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 2182/20879 | 2091/20724 | 697/6907 | chr2 | 185789227 | |||
chr2:185789273 | C | A | 1 | a0001c0043 | 1 | NA18959.hp1 | synonymous_variant | LOW | c.2137C>A | p.Arg713Arg | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 2228/20879 | 2137/20724 | 713/6907 | chr2 | 185789273 | |||
chr2:185791930 | C | T | 55 | a0002c0002 a0002c0018 a0002c0057 others(52): Show |
230 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(227): Show |
synonymous_variant | LOW | c.4794C>T | p.Asn1598Asn | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 4885/20879 | 4794/20724 | 1598/6907 | chr2 | 185791930 | |||
chr2:185792113 | T | C | 8 | a0003c0066 a0005c0005 a0009c0009 others(5): Show |
42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
synonymous_variant | LOW | c.4977T>C | p.Asn1659Asn | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5068/20879 | 4977/20724 | 1659/6907 | chr2 | 185792113 | |||
chr2:185792362 | C | A | 46 | a0002c0002 a0002c0018 a0002c0057 others(43): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
synonymous_variant | LOW | c.5226C>A | p.Ser1742Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5317/20879 | 5226/20724 | 1742/6907 | chr2 | 185792362 | |||
chr2:185794186 | A | G | 1 | a0003c0076 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.7050A>G | p.Thr2350Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 7141/20879 | 7050/20724 | 2350/6907 | chr2 | 185794186 | |||
chr2:185794387 | T | A | 1 | a0016c0038 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.7251T>A | p.Ser2417Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 7342/20879 | 7251/20724 | 2417/6907 | chr2 | 185794387 | |||
chr2:185794502 | T | C | 1 | a0001c0008 | 8 | HG02080.hp2 HG02083.hp2 HG02523.hp2 others(5): Show |
synonymous_variant | LOW | c.7366T>C | p.Leu2456Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 7457/20879 | 7366/20724 | 2456/6907 | chr2 | 185794502 | |||
chr2:185794675 | C | T | 1 | a0002c0062 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.7539C>T | p.Asn2513Asn | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 7630/20879 | 7539/20724 | 2513/6907 | chr2 | 185794675 | |||
chr2:185796152 | T | C | 1 | a0004c0041 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.9016T>C | p.Leu3006Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 9107/20879 | 9016/20724 | 3006/6907 | chr2 | 185796152 | |||
chr2:185796346 | G | C | 1 | a0055c0042 | 1 | NA18989.hp2 | synonymous_variant | LOW | c.9210G>C | p.Arg3070Arg | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 9301/20879 | 9210/20724 | 3070/6907 | chr2 | 185796346 | |||
chr2:185796946 | A | G | 46 | a0002c0002 a0002c0018 a0002c0057 others(43): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
synonymous_variant | LOW | c.9810A>G | p.Leu3270Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 9901/20879 | 9810/20724 | 3270/6907 | chr2 | 185796946 | |||
chr2:185797189 | G | A | 1 | a0043c0079 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.10053G>A | p.Glu3351Glu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 10144/20879 | 10053/20724 | 3351/6907 | chr2 | 185797189 | |||
chr2:185797348 | G | A | 2 | a0019c0020 a0042c0080 |
5 | HG01891.hp1 HG02647.hp1 HG02809.hp2 others(2): Show |
synonymous_variant | LOW | c.10212G>A | p.Arg3404Arg | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 10303/20879 | 10212/20724 | 3404/6907 | chr2 | 185797348 | |||
chr2:185797369 | A | G | 2 | a0003c0012 a0003c0075 |
7 | HG02818.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
synonymous_variant | LOW | c.10233A>G | p.Gln3411Gln | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 10324/20879 | 10233/20724 | 3411/6907 | chr2 | 185797369 | |||
chr2:185799746 | T | C | 46 | a0002c0002 a0002c0018 a0002c0057 others(43): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
synonymous_variant | LOW | c.10440T>C | p.Tyr3480Tyr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 10531/20879 | 10440/20724 | 3480/6907 | chr2 | 185799746 | |||
chr2:185801525 | C | T | 1 | a0001c0023 | 4 | NA18981.hp2 NA18998.hp1 NA19003.hp1 others(1): Show |
synonymous_variant | LOW | c.12219C>T | p.Ala4073Ala | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 12310/20879 | 12219/20724 | 4073/6907 | chr2 | 185801525 | |||
chr2:185801687 | A | C | 1 | a0021c0028 | 3 | HG02145.hp1 HG02976.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.12381A>C | p.Leu4127Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 12472/20879 | 12381/20724 | 4127/6907 | chr2 | 185801687 | |||
chr2:185801708 | T | C | 2 | a0003c0072 a0047c0073 |
2 | HG02647.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.12402T>C | p.Tyr4134Tyr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 12493/20879 | 12402/20724 | 4134/6907 | chr2 | 185801708 | |||
chr2:185801786 | A | G | 1 | a0006c0069 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.12480A>G | p.Thr4160Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 12571/20879 | 12480/20724 | 4160/6907 | chr2 | 185801786 | |||
chr2:185803196 | T | G | 1 | a0003c0075 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.13890T>G | p.Val4630Val | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 13981/20879 | 13890/20724 | 4630/6907 | chr2 | 185803196 | |||
chr2:185804189 | T | G | 1 | a0010c0047 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.14883T>G | p.Leu4961Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 14974/20879 | 14883/20724 | 4961/6907 | chr2 | 185804189 | |||
chr2:185804585 | A | G | 1 | a0001c0051 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.15279A>G | p.Arg5093Arg | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 15370/20879 | 15279/20724 | 5093/6907 | chr2 | 185804585 | |||
chr2:185804999 | C | A | 1 | a0020c0021 | 4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
synonymous_variant | LOW | c.15693C>A | p.Ile5231Ile | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 15784/20879 | 15693/20724 | 5231/6907 | chr2 | 185804999 | |||
chr2:185806529 | T | C | 1 | a0008c0027 | 2 | HG03490.hp2 HG03492.hp2 |
synonymous_variant | LOW | c.17223T>C | p.Asn5741Asn | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 17314/20879 | 17223/20724 | 5741/6907 | chr2 | 185806529 | |||
chr2:185808170 | A | G | 23 | a0001c0001 a0001c0008 a0001c0023 others(20): Show |
114 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
synonymous_variant | LOW | c.18864A>G | p.Leu6288Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 18955/20879 | 18864/20724 | 6288/6907 | chr2 | 185808170 | |||
chr2:185808479 | T | G | 1 | a0002c0057 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.19173T>G | p.Ala6391Ala | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 19264/20879 | 19173/20724 | 6391/6907 | chr2 | 185808479 | |||
chr2:185808758 | C | T | 1 | a0062c0039 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.19452C>T | p.Asp6484Asp | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 19543/20879 | 19452/20724 | 6484/6907 | chr2 | 185808758 | |||
chr2:185814030 | G | A | 1 | a0002c0018 | 5 | NA18981.hp1 NA18984.hp2 NA18999.hp2 others(2): Show |
synonymous_variant | LOW | c.20313G>A | p.Lys6771Lys | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/23 | 20404/20879 | 20313/20724 | 6771/6907 | chr2 | 185814030 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:185738855 | C | A | 1 | a0004c0004t0004 | 1 | HG03486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-40C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 1/23 | 40 | chr2 | 185738855 | ||||||
chr2:185738878 | A | AG | 26 | a0001c0001t0002 a0001c0008t0002 a0001c0023t0002 others(23): Show |
126 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(123): Show |
5_prime_UTR_variant | MODIFIER | c.-12dupG | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 1/23 | 11 | INFO_REALIGN_3_PRIME | chr2 | 185738878 | |||||
chr2:185738891 | G | A | 3 | a0003c0012t0003 a0019c0020t0003 a0042c0080t0003 |
7 | HG01891.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-4G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 1/23 | 4 | chr2 | 185738891 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:185739096 | C | T | 1 | a0025c0033t0001g0311 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.99+103C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 1/22 | chr2 | 185739096 | |||||||
chr2:185739132 | G | A | 1 | a0024c0034t0001g0037 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.99+139G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 1/22 | chr2 | 185739132 | |||||||
chr2:185739232 | G | C | 3 | a0003c0012t0003g0039 a0003c0012t0003g0040 a0042c0080t0003g0038 |
3 | HG02647.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.100-114G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 1/22 | chr2 | 185739232 | |||||||
chr2:185739537 | G | A | 1 | a0031c0056t0001g0041 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.225+66G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185739537 | |||||||
chr2:185739644 | C | T | 2 | a0003c0012t0003g0039 a0003c0012t0003g0040 |
2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.225+173C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185739644 | |||||||
chr2:185739764 | A | T | 261 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(258): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.225+293A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185739764 | |||||||
chr2:185740123 | T | C | 109 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(106): Show |
126 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.225+652T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185740123 | |||||||
chr2:185740230 | G | A | 11 | a0001c0001t0002g0089 a0008c0010t0002g0088 a0008c0010t0002g0091 others(8): Show |
12 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.225+759G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185740230 | |||||||
chr2:185740237 | C | A | 1 | a0003c0072t0001g0184 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.225+766C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185740237 | |||||||
chr2:185740372 | C | A | 1 | a0002c0002t0001g0185 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.225+901C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185740372 | |||||||
chr2:185740380 | C | T | 137 | a0002c0002t0001g0001 a0002c0002t0001g0009 a0002c0002t0001g0010 others(134): Show |
162 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.225+909C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185740380 | |||||||
chr2:185740406 | G | A | 109 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(106): Show |
125 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.225+935G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185740406 | |||||||
chr2:185740680 | C | T | 1 | a0027c0030t0002g0183 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.225+1209C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185740680 | |||||||
chr2:185740803 | A | C | 3 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0001g0310 |
3 | HG01123.hp1 HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.225+1332A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185740803 | |||||||
chr2:185740953 | G | GA | 104 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(101): Show |
120 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.225+1489dupA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr2 | 185740953 | ||||||
chr2:185740983 | A | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.225+1512A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185740983 | |||||||
chr2:185741157 | C | G | 2 | a0002c0002t0001g0036 a0031c0056t0001g0041 |
3 | HG00733.hp2 HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.225+1686C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741157 | |||||||
chr2:185741198 | G | A | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.225+1727G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741198 | |||||||
chr2:185741284 | A | AT | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.225+1813_225+1814i others(3): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741284 | |||||||
chr2:185741291 | T | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.225+1820T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741291 | |||||||
chr2:185741299 | T | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.225+1828T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741299 | |||||||
chr2:185741399 | G | T | 1 | a0034c0046t0002g0176 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.226-1734G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741399 | |||||||
chr2:185741688 | T | C | 1 | a0003c0003t0001g0199 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.226-1445T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741688 | |||||||
chr2:185741700 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.226-1433G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741700 | |||||||
chr2:185741707 | G | A | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.226-1426G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741707 | |||||||
chr2:185741762 | A | G | 1 | a0001c0001t0002g0020 | 2 | NA19004.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.226-1371A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741762 | |||||||
chr2:185742063 | C | G | 1 | a0001c0001t0002g0175 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.226-1070C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185742063 | |||||||
chr2:185742153 | C | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.226-980C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185742153 | |||||||
chr2:185742474 | A | G | 9 | a0016c0022t0002g0178 a0016c0022t0002g0179 a0016c0022t0002g0180 others(6): Show |
10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.226-659A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185742474 | |||||||
chr2:185742768 | T | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.226-365T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185742768 | |||||||
chr2:185742791 | ATG | A | 9 | a0016c0022t0002g0178 a0016c0022t0002g0179 a0016c0022t0002g0180 others(6): Show |
10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.226-341_226-340del others(2): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185742791 | |||||||
chr2:185742792 | T | A | 154 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(151): Show |
180 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.226-341T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185742792 | |||||||
chr2:185743053 | A | G | 1 | a0003c0012t0001g0195 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.226-80A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185743053 | |||||||
chr2:185743612 | G | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.387+318G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 3/22 | chr2 | 185743612 | |||||||
chr2:185743654 | T | C | 1 | a0002c0002t0001g0200 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.387+360T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 3/22 | chr2 | 185743654 | |||||||
chr2:185743796 | C | T | 22 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(19): Show |
25 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.387+502C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 3/22 | chr2 | 185743796 | |||||||
chr2:185743811 | G | A | 1 | a0004c0004t0001g0065 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.388-511G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 3/22 | chr2 | 185743811 | |||||||
chr2:185743818 | G | T | 2 | a0005c0005t0001g0035 a0005c0005t0001g0307 |
3 | HG02698.hp1 HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.388-504G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 3/22 | chr2 | 185743818 | |||||||
chr2:185743987 | T | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.388-335T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 3/22 | chr2 | 185743987 | |||||||
chr2:185744022 | G | A | 1 | a0005c0005t0001g0201 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.388-300G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 3/22 | chr2 | 185744022 | |||||||
chr2:185744528 | A | G | 1 | a0004c0041t0001g0083 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.477+117A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185744528 | |||||||
chr2:185744705 | C | A | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.477+294C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185744705 | |||||||
chr2:185744773 | C | A | 1 | a0010c0011t0002g0099 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.477+362C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185744773 | |||||||
chr2:185744868 | T | C | 3 | a0023c0025t0001g0022 a0023c0025t0001g0188 a0048c0035t0001g0042 |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+457T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185744868 | |||||||
chr2:185744900 | A | T | 1 | a0011c0015t0001g0064 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.477+489A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185744900 | |||||||
chr2:185744963 | GGTGTGTG others(10): Show |
G | 34 | a0003c0066t0001g0288 a0005c0005t0001g0011 a0005c0005t0001g0032 others(31): Show |
42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.478-452_478-436del others(17): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 185744963 | ||||||
chr2:185744978 | GGT | G | 161 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(158): Show |
186 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.478-432_478-431del others(2): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 185744978 | ||||||
chr2:185745052 | A | G | 1 | a0035c0055t0001g0280 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.478-377A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185745052 | |||||||
chr2:185745139 | T | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.478-290T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185745139 | |||||||
chr2:185745263 | A | G | 1 | a0004c0004t0001g0065 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.478-166A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185745263 | |||||||
chr2:185745306 | A | C | 19 | a0003c0003t0001g0266 a0003c0003t0001g0267 a0003c0003t0001g0269 others(16): Show |
21 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.478-123A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185745306 | |||||||
chr2:185745350 | A | G | 2 | a0001c0001t0002g0019 a0045c0050t0002g0019 |
2 | HG01081.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.478-79A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185745350 | |||||||
chr2:185745617 | T | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.617+49T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | chr2 | 185745617 | |||||||
chr2:185745661 | G | A | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.617+93G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | chr2 | 185745661 | |||||||
chr2:185745785 | A | G | 1 | a0001c0001t0002g0174 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.617+217A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | chr2 | 185745785 | |||||||
chr2:185745848 | T | C | 3 | a0003c0012t0001g0190 a0003c0012t0001g0195 a0003c0075t0001g0189 |
3 | HG02970.hp2 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.617+280T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | chr2 | 185745848 | |||||||
chr2:185745858 | G | A | 195 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(192): Show |
228 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.617+290G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | chr2 | 185745858 | |||||||
chr2:185745985 | A | G | 1 | a0001c0001t0002g0173 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.617+417A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | chr2 | 185745985 | |||||||
chr2:185746100 | A | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.617+532A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | chr2 | 185746100 | |||||||
chr2:185746284 | G | T | 4 | a0006c0006t0001g0276 a0006c0006t0001g0277 a0006c0006t0001g0278 others(1): Show |
4 | HG02280.hp1 HG02615.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-385G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | chr2 | 185746284 | |||||||
chr2:185746288 | GT | G | 162 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(159): Show |
189 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.618-370delT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 185746288 | ||||||
chr2:185746539 | A | C | 1 | a0009c0009t0001g0306 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.618-130A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | chr2 | 185746539 | |||||||
chr2:185746839 | C | A | 296 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(293): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.759+29C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 6/22 | chr2 | 185746839 | |||||||
chr2:185747001 | C | T | 9 | a0016c0022t0002g0178 a0016c0022t0002g0179 a0016c0022t0002g0180 others(6): Show |
10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.759+191C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 6/22 | chr2 | 185747001 | |||||||
chr2:185747107 | A | G | 101 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(98): Show |
116 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.760-206A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 6/22 | chr2 | 185747107 | |||||||
chr2:185747211 | G | A | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.760-102G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 6/22 | chr2 | 185747211 | |||||||
chr2:185747434 | C | G | 55 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(52): Show |
68 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.870+11C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185747434 | |||||||
chr2:185747467 | G | T | 1 | a0005c0005t0001g0305 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.870+44G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185747467 | |||||||
chr2:185747668 | T | C | 1 | a0004c0004t0001g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.870+245T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185747668 | |||||||
chr2:185747707 | T | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.870+284T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185747707 | |||||||
chr2:185747731 | A | C | 1 | a0005c0005t0001g0304 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.870+308A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185747731 | |||||||
chr2:185747785 | T | C | 19 | a0003c0003t0001g0266 a0003c0003t0001g0267 a0003c0003t0001g0269 others(16): Show |
21 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.870+362T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185747785 | |||||||
chr2:185747875 | A | G | 1 | a0026c0029t0002g0172 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.870+452A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185747875 | |||||||
chr2:185748210 | G | A | 3 | a0003c0012t0001g0190 a0003c0012t0001g0195 a0003c0075t0001g0189 |
3 | HG02970.hp2 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.870+787G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185748210 | |||||||
chr2:185748729 | G | A | 1 | a0026c0029t0002g0102 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.870+1306G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185748729 | |||||||
chr2:185748824 | T | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.870+1401T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185748824 | |||||||
chr2:185748844 | T | C | 5 | a0016c0022t0002g0178 a0016c0022t0002g0179 a0016c0022t0002g0180 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.870+1421T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185748844 | |||||||
chr2:185748862 | A | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.870+1439A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185748862 | |||||||
chr2:185748905 | T | C | 1 | a0043c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.870+1482T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185748905 | |||||||
chr2:185749020 | C | T | 1 | a0003c0003t0001g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.870+1597C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185749020 | |||||||
chr2:185749156 | G | A | 98 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(95): Show |
113 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.870+1733G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185749156 | |||||||
chr2:185749205 | TG | T | 10 | a0016c0022t0002g0178 a0016c0022t0002g0179 a0016c0022t0002g0180 others(7): Show |
11 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.870+1784delG | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185749205 | ||||||
chr2:185749335 | T | C | 34 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(31): Show |
40 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.870+1912T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185749335 | |||||||
chr2:185749356 | C | T | 62 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(59): Show |
76 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.870+1933C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185749356 | |||||||
chr2:185749734 | G | T | 1 | a0043c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.870+2311G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185749734 | |||||||
chr2:185749793 | G | A | 3 | a0019c0020t0003g0013 a0019c0020t0003g0043 a0019c0020t0003g0044 |
4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2370G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185749793 | |||||||
chr2:185750155 | G | T | 7 | a0003c0012t0001g0190 a0003c0012t0001g0192 a0003c0012t0001g0193 others(4): Show |
7 | HG02818.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.870+2732G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185750155 | |||||||
chr2:185750227 | G | A | 93 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(90): Show |
109 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.870+2804G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185750227 | |||||||
chr2:185750519 | C | A | 1 | a0012c0019t0001g0202 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.870+3096C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185750519 | |||||||
chr2:185750603 | G | GT | 269 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(266): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.871-3107dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185750603 | ||||||
chr2:185750646 | T | C | 1 | a0003c0003t0001g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.871-3076T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185750646 | |||||||
chr2:185750936 | A | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.871-2786A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185750936 | |||||||
chr2:185751194 | G | C | 30 | a0003c0066t0001g0288 a0005c0005t0001g0011 a0005c0005t0001g0032 others(27): Show |
37 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.871-2528G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751194 | |||||||
chr2:185751217 | G | A | 1 | a0002c0062t0001g0231 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.871-2505G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751217 | |||||||
chr2:185751423 | T | C | 2 | a0002c0002t0001g0036 a0031c0056t0001g0041 |
3 | HG00733.hp2 HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.871-2299T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751423 | |||||||
chr2:185751439 | C | T | 3 | a0020c0021t0001g0023 a0020c0021t0001g0197 a0020c0021t0001g0198 |
4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.871-2283C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751439 | |||||||
chr2:185751461 | C | CTCTG | 5 | a0003c0012t0001g0190 a0003c0012t0001g0192 a0003c0012t0003g0039 others(2): Show |
5 | HG02818.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-2260_871-2259i others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | ||||||
chr2:185751461 | C | CTCTGTGT others(3): Show |
1 | a0001c0001t0002g0121 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.871-2260_871-2259i others(12): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | ||||||
chr2:185751461 | C | CTG | 34 | a0001c0001t0002g0017 a0002c0002t0001g0026 a0003c0003t0001g0205 others(31): Show |
38 | HG00423.hp2 HG01346.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.871-2224_871-2223d others(4): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | ||||||
chr2:185751461 | C | CTGTG | 81 | a0002c0002t0001g0001 a0002c0002t0001g0009 a0002c0002t0001g0010 others(78): Show |
97 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.871-2226_871-2223d others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | ||||||
chr2:185751461 | C | CTGTGTG | 42 | a0001c0001t0002g0007 a0001c0001t0002g0019 a0001c0001t0002g0120 others(39): Show |
47 | HG00423.hp1 HG01071.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.871-2228_871-2223d others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | ||||||
chr2:185751461 | C | CTGTGTGT others(1): Show |
41 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0020 others(38): Show |
49 | HG00099.hp2 HG00597.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.871-2230_871-2223d others(10): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | ||||||
chr2:185751461 | C | CTGTGTGT others(3): Show |
39 | a0001c0001t0002g0098 a0001c0001t0002g0114 a0001c0001t0002g0115 others(36): Show |
43 | HG00323.hp1 HG00438.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.871-2232_871-2223d others(12): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | ||||||
chr2:185751461 | C | CTGTGTGT others(5): Show |
7 | a0001c0001t0002g0167 a0003c0003t0001g0264 a0003c0072t0001g0184 others(4): Show |
7 | HG02559.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.871-2234_871-2223d others(14): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | ||||||
chr2:185751461 | C | CTGTGTGT others(9): Show |
1 | a0001c0001t0002g0168 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.871-2238_871-2223d others(18): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | ||||||
chr2:185751461 | CTG | C | 24 | a0003c0003t0001g0203 a0004c0004t0001g0005 a0004c0004t0001g0065 others(21): Show |
28 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.871-2224_871-2223d others(4): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | ||||||
chr2:185751486 | T | TGTGTGCG others(1): Show |
29 | a0003c0066t0001g0288 a0005c0005t0001g0011 a0005c0005t0001g0032 others(26): Show |
36 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.871-2231_871-2230i others(10): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751486 | ||||||
chr2:185751486 | T | TGTGTGTG others(3): Show |
3 | a0005c0005t0001g0300 a0021c0028t0001g0034 a0021c0028t0001g0302 |
4 | HG01952.hp2 HG02145.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-2229_871-2228i others(12): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751486 | ||||||
chr2:185751524 | T | C | 2 | a0010c0011t0002g0107 a0010c0011t0002g0108 |
2 | HG00099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.871-2198T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751524 | |||||||
chr2:185751644 | A | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.871-2078A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751644 | |||||||
chr2:185751712 | G | A | 1 | a0004c0004t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.871-2010G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751712 | |||||||
chr2:185751768 | CTTTAA | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.871-1949_871-1945d others(7): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751768 | ||||||
chr2:185751849 | T | C | 3 | a0020c0021t0001g0023 a0020c0021t0001g0197 a0020c0021t0001g0198 |
4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.871-1873T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751849 | |||||||
chr2:185751858 | A | AT | 93 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(90): Show |
109 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.871-1857dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751858 | ||||||
chr2:185751937 | A | T | 13 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0137 others(10): Show |
17 | HG02273.hp1 NA18939.hp2 NA18949.hp1 others(14): Show |
intron_variant | MODIFIER | c.871-1785A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751937 | |||||||
chr2:185751979 | TGTA | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.871-1742_871-1740d others(5): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751979 | |||||||
chr2:185752067 | A | AT | 66 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(63): Show |
80 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.871-1646dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185752067 | ||||||
chr2:185752166 | T | C | 5 | a0003c0003t0001g0025 a0003c0003t0001g0199 a0003c0003t0001g0205 others(2): Show |
6 | HG01243.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.871-1556T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185752166 | |||||||
chr2:185752200 | G | A | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.871-1522G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185752200 | |||||||
chr2:185752399 | T | G | 1 | a0014c0016t0001g0061 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.871-1323T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185752399 | |||||||
chr2:185752639 | T | C | 1 | a0003c0003t0001g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.871-1083T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185752639 | |||||||
chr2:185753072 | C | T | 1 | a0002c0002t0001g0259 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.871-650C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185753072 | |||||||
chr2:185753108 | C | A | 32 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(29): Show |
38 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.871-614C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185753108 | |||||||
chr2:185753280 | T | G | 153 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(150): Show |
179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.871-442T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185753280 | |||||||
chr2:185753346 | A | T | 1 | a0001c0001t0002g0163 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.871-376A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185753346 | |||||||
chr2:185753360 | G | C | 1 | a0017c0017t0001g0046 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.871-362G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185753360 | |||||||
chr2:185753497 | C | A | 1 | a0004c0004t0001g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.871-225C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185753497 | |||||||
chr2:185753526 | A | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.871-196A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185753526 | |||||||
chr2:185753599 | C | A | 1 | a0062c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871-123C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185753599 | |||||||
chr2:185753643 | T | TGTCACA | 3 | a0015c0014t0002g0103 a0015c0014t0002g0104 a0015c0014t0002g0105 |
3 | HG02615.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.871-78_871-73dupGT others(4): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185753643 | ||||||
chr2:185753929 | A | G | 1 | a0002c0002t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.991+87A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185753929 | |||||||
chr2:185753980 | T | C | 1 | a0001c0001t0002g0017 | 2 | NA18953.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.991+138T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185753980 | |||||||
chr2:185754163 | G | A | 1 | a0005c0005t0001g0282 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.991+321G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185754163 | |||||||
chr2:185754166 | C | A | 1 | a0005c0005t0001g0282 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.991+324C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185754166 | |||||||
chr2:185754632 | T | C | 1 | a0004c0004t0001g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.991+790T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185754632 | |||||||
chr2:185755061 | C | T | 9 | a0016c0022t0002g0178 a0016c0022t0002g0179 a0016c0022t0002g0180 others(6): Show |
10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.992-1131C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185755061 | |||||||
chr2:185755152 | C | G | 1 | a0003c0003t0001g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.992-1040C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185755152 | |||||||
chr2:185755486 | G | T | 1 | a0022c0026t0002g0087 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.992-706G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185755486 | |||||||
chr2:185755524 | A | G | 2 | a0004c0004t0001g0081 a0004c0004t0002g0021 |
3 | HG02486.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.992-668A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185755524 | |||||||
chr2:185755765 | A | G | 2 | a0026c0029t0002g0102 a0026c0029t0002g0172 |
2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.992-427A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185755765 | |||||||
chr2:185755890 | A | G | 1 | a0004c0004t0001g0080 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.992-302A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185755890 | |||||||
chr2:185755967 | A | T | 1 | a0004c0004t0002g0021 | 2 | HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.992-225A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185755967 | |||||||
chr2:185756062 | T | C | 296 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(293): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.992-130T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185756062 | |||||||
chr2:185756340 | T | A | 10 | a0016c0022t0002g0178 a0016c0022t0002g0179 a0016c0022t0002g0180 others(7): Show |
11 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1078+62T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185756340 | |||||||
chr2:185756366 | G | T | 1 | a0055c0042t0001g0079 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1078+88G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185756366 | |||||||
chr2:185756559 | T | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1078+281T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185756559 | |||||||
chr2:185756585 | T | G | 101 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(98): Show |
116 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1078+307T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185756585 | |||||||
chr2:185756684 | A | G | 1 | a0001c0008t0002g0162 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1078+406A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185756684 | |||||||
chr2:185756732 | T | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1078+454T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185756732 | |||||||
chr2:185756837 | G | A | 65 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(62): Show |
79 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1078+559G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185756837 | |||||||
chr2:185756911 | T | C | 2 | a0021c0028t0001g0034 a0021c0028t0001g0302 |
3 | HG02145.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1078+633T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185756911 | |||||||
chr2:185756995 | T | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1078+717T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185756995 | |||||||
chr2:185757172 | C | A | 3 | a0020c0021t0001g0023 a0020c0021t0001g0197 a0020c0021t0001g0198 |
4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078+894C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185757172 | |||||||
chr2:185757256 | C | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1078+978C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185757256 | |||||||
chr2:185757366 | TA | T | 3 | a0020c0021t0001g0023 a0020c0021t0001g0197 a0020c0021t0001g0198 |
4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078+1091delA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 185757366 | ||||||
chr2:185757526 | A | G | 1 | a0041c0036t0001g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1078+1248A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185757526 | |||||||
chr2:185757616 | A | T | 3 | a0023c0025t0001g0022 a0023c0025t0001g0188 a0048c0035t0001g0042 |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078+1338A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185757616 | |||||||
chr2:185757673 | G | T | 1 | a0001c0001t0002g0098 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1078+1395G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185757673 | |||||||
chr2:185757676 | CCATA | C | 153 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(150): Show |
179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1078+1401_1078+140 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 185757676 | ||||||
chr2:185757746 | T | C | 1 | a0001c0008t0002g0162 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1078+1468T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185757746 | |||||||
chr2:185758066 | T | G | 1 | a0010c0011t0002g0109 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1078+1788T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185758066 | |||||||
chr2:185758092 | T | C | 10 | a0001c0001t0002g0110 a0001c0001t0002g0114 a0001c0001t0002g0115 others(7): Show |
10 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1078+1814T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185758092 | |||||||
chr2:185758156 | C | T | 1 | a0005c0005t0001g0303 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1078+1878C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185758156 | |||||||
chr2:185758159 | G | A | 2 | a0013c0013t0002g0123 a0044c0049t0002g0124 |
2 | HG01109.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1078+1881G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185758159 | |||||||
chr2:185758603 | T | C | 153 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(150): Show |
181 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.1078+2325T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185758603 | |||||||
chr2:185758661 | T | C | 112 | a0002c0002t0001g0219 a0002c0002t0001g0234 a0002c0002t0001g0263 others(109): Show |
126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1079-2327T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185758661 | |||||||
chr2:185758682 | T | G | 296 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(293): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1079-2306T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185758682 | |||||||
chr2:185758798 | T | A | 45 | a0002c0002t0001g0001 a0002c0002t0001g0009 a0002c0002t0001g0010 others(42): Show |
57 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.1079-2190T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185758798 | |||||||
chr2:185758893 | G | A | 65 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(62): Show |
79 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1079-2095G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185758893 | |||||||
chr2:185759016 | G | T | 1 | a0004c0004t0002g0100 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1079-1972G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185759016 | |||||||
chr2:185759416 | ATAT | A | 14 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0137 others(11): Show |
18 | HG02273.hp1 HG03486.hp1 NA18939.hp2 others(15): Show |
intron_variant | MODIFIER | c.1079-1566_1079-156 others(7): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 185759416 | ||||||
chr2:185759497 | T | C | 34 | a0003c0066t0001g0288 a0005c0005t0001g0011 a0005c0005t0001g0032 others(31): Show |
42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1079-1491T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185759497 | |||||||
chr2:185759600 | ATAT | A | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1079-1382_1079-138 others(7): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 185759600 | ||||||
chr2:185759801 | G | C | 1 | a0004c0004t0001g0068 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1079-1187G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185759801 | |||||||
chr2:185760011 | CA | C | 146 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(143): Show |
172 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1079-976delA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185760011 | |||||||
chr2:185760100 | A | G | 1 | a0009c0009t0001g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1079-888A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185760100 | |||||||
chr2:185760101 | A | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1079-887A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185760101 | |||||||
chr2:185760188 | TTCTC | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1079-794_1079-791d others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 185760188 | ||||||
chr2:185760329 | T | A | 1 | a0043c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1079-659T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185760329 | |||||||
chr2:185760408 | G | GA | 100 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(97): Show |
115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1079-571dupA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 185760408 | ||||||
chr2:185760591 | T | C | 1 | a0001c0001t0002g0141 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1079-397T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185760591 | |||||||
chr2:185760715 | C | T | 1 | a0024c0034t0001g0037 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1079-273C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185760715 | |||||||
chr2:185760770 | T | C | 32 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(29): Show |
38 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1079-218T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185760770 | |||||||
chr2:185760918 | TTTGA | T | 100 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(97): Show |
115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1079-66_1079-63del others(4): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 185760918 | ||||||
chr2:185760943 | TA | T | 126 | a0001c0023t0002g0140 a0002c0002t0001g0001 a0002c0002t0001g0006 others(123): Show |
145 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.1079-31delA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 185760943 | ||||||
chr2:185760943 | TAA | T | 35 | a0003c0066t0001g0288 a0005c0005t0001g0011 a0005c0005t0001g0032 others(32): Show |
43 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1079-32_1079-31del others(2): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 185760943 | ||||||
chr2:185761153 | C | G | 32 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(29): Show |
38 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1194+50C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 10/22 | chr2 | 185761153 | |||||||
chr2:185761298 | A | G | 3 | a0003c0003t0001g0227 a0003c0003t0001g0228 a0003c0003t0001g0229 |
3 | HG00642.hp2 HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1194+195A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 10/22 | chr2 | 185761298 | |||||||
chr2:185761425 | T | C | 1 | a0042c0080t0003g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1194+322T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 10/22 | chr2 | 185761425 | |||||||
chr2:185761562 | T | A | 34 | a0003c0066t0001g0288 a0005c0005t0001g0011 a0005c0005t0001g0032 others(31): Show |
42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1195-410T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 10/22 | chr2 | 185761562 | |||||||
chr2:185761827 | T | C | 2 | a0003c0012t0003g0039 a0003c0012t0003g0040 |
2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1195-145T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 10/22 | chr2 | 185761827 | |||||||
chr2:185762024 | A | T | 1 | a0062c0039t0001g0196 | 1 | NA21309.hp2 | splice_region_variant&intron_variant | LOW | c.1240+7A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762024 | |||||||
chr2:185762206 | G | T | 1 | a0062c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1240+189G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762206 | |||||||
chr2:185762289 | G | C | 296 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(293): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1240+272G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762289 | |||||||
chr2:185762313 | A | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1240+296A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762313 | |||||||
chr2:185762371 | A | T | 1 | a0008c0010t0002g0095 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1240+354A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762371 | |||||||
chr2:185762372 | C | A | 1 | a0008c0010t0002g0095 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1240+355C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762372 | |||||||
chr2:185762469 | T | C | 32 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(29): Show |
38 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1240+452T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762469 | |||||||
chr2:185762514 | T | G | 296 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(293): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1240+497T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762514 | |||||||
chr2:185762597 | T | G | 1 | a0061c0052t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1240+580T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762597 | |||||||
chr2:185762643 | A | G | 296 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(293): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1241-540A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762643 | |||||||
chr2:185762809 | C | A | 93 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(90): Show |
109 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1241-374C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762809 | |||||||
chr2:185762884 | T | C | 10 | a0004c0004t0001g0005 a0004c0004t0001g0068 a0004c0004t0001g0069 others(7): Show |
12 | HG00544.hp1 HG00558.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.1241-299T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762884 | |||||||
chr2:185763163 | G | A | 1 | a0013c0013t0002g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1241-20G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185763163 | |||||||
chr2:185763310 | C | T | 1 | a0001c0001t0002g0160 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1347+21C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | chr2 | 185763310 | |||||||
chr2:185763476 | G | A | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1347+187G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | chr2 | 185763476 | |||||||
chr2:185763745 | G | A | 1 | a0003c0081t0001g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1347+456G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | chr2 | 185763745 | |||||||
chr2:185763778 | G | T | 295 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(292): Show |
343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.1347+489G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | chr2 | 185763778 | |||||||
chr2:185763974 | T | C | 1 | a0005c0005t0001g0201 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1348-528T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | chr2 | 185763974 | |||||||
chr2:185764024 | T | A | 3 | a0001c0051t0002g0106 a0018c0024t0001g0236 a0026c0029t0002g0172 |
3 | HG00597.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1348-478T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | chr2 | 185764024 | |||||||
chr2:185764090 | TA | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1348-404delA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr2 | 185764090 | ||||||
chr2:185764104 | T | C | 3 | a0020c0021t0001g0023 a0020c0021t0001g0197 a0020c0021t0001g0198 |
4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348-398T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | chr2 | 185764104 | |||||||
chr2:185764112 | A | T | 1 | a0002c0002t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1348-390A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | chr2 | 185764112 | |||||||
chr2:185764464 | T | G | 100 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(97): Show |
115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1348-38T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | chr2 | 185764464 | |||||||
chr2:185764595 | T | A | 1 | a0013c0013t0002g0132 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1411+30T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185764595 | |||||||
chr2:185764604 | C | A | 1 | a0062c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1411+39C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185764604 | |||||||
chr2:185764622 | G | A | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1411+57G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185764622 | |||||||
chr2:185764655 | T | C | 7 | a0018c0024t0001g0236 a0018c0024t0001g0238 a0018c0024t0001g0239 others(4): Show |
7 | HG00544.hp2 HG00597.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411+90T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185764655 | |||||||
chr2:185764701 | T | A | 4 | a0002c0018t0001g0027 a0002c0018t0001g0241 a0002c0018t0001g0242 others(1): Show |
5 | NA18981.hp1 NA18984.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.1411+136T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185764701 | |||||||
chr2:185764822 | A | G | 2 | a0003c0012t0003g0039 a0003c0012t0003g0040 |
2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1411+257A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185764822 | |||||||
chr2:185764846 | A | G | 1 | a0002c0002t0001g0257 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1411+281A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185764846 | |||||||
chr2:185764948 | C | A | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1411+383C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185764948 | |||||||
chr2:185765074 | G | A | 1 | a0003c0003t0001g0199 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1411+509G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765074 | |||||||
chr2:185765130 | C | T | 2 | a0008c0010t0002g0096 a0008c0010t0002g0097 |
2 | HG00735.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.1411+565C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765130 | |||||||
chr2:185765142 | G | A | 4 | a0003c0012t0001g0192 a0003c0012t0001g0193 a0003c0012t0003g0039 others(1): Show |
4 | HG02818.hp2 HG02895.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411+577G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765142 | |||||||
chr2:185765195 | A | T | 3 | a0001c0001t0002g0007 a0001c0001t0002g0131 a0059c0053t0002g0007 |
4 | HG02071.hp1 NA18967.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411+630A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765195 | |||||||
chr2:185765501 | A | G | 1 | a0003c0003t0001g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1411+936A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765501 | |||||||
chr2:185765647 | G | A | 10 | a0016c0022t0002g0178 a0016c0022t0002g0179 a0016c0022t0002g0180 others(7): Show |
11 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1411+1082G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765647 | |||||||
chr2:185765660 | G | A | 1 | a0004c0004t0001g0068 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1411+1095G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765660 | |||||||
chr2:185765676 | T | C | 34 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(31): Show |
40 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1411+1111T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765676 | |||||||
chr2:185765711 | T | C | 1 | a0049c0048t0001g0186 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1411+1146T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765711 | |||||||
chr2:185765734 | C | A | 1 | a0003c0003t0001g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1411+1169C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765734 | |||||||
chr2:185765741 | G | A | 1 | a0006c0006t0002g0177 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1411+1176G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765741 | |||||||
chr2:185765752 | G | A | 98 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(95): Show |
113 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1411+1187G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765752 | |||||||
chr2:185765798 | T | A | 3 | a0019c0020t0003g0013 a0019c0020t0003g0043 a0019c0020t0003g0044 |
4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411+1233T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765798 | |||||||
chr2:185765827 | C | T | 3 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0001g0310 |
3 | HG01123.hp1 HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1411+1262C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765827 | |||||||
chr2:185765928 | T | C | 1 | a0030c0067t0001g0283 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1411+1363T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765928 | |||||||
chr2:185766391 | T | C | 7 | a0003c0012t0001g0190 a0003c0012t0001g0192 a0003c0012t0001g0193 others(4): Show |
7 | HG02818.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411+1826T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766391 | |||||||
chr2:185766399 | A | G | 1 | a0014c0016t0001g0060 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1411+1834A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766399 | |||||||
chr2:185766406 | G | T | 132 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(129): Show |
153 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.1411+1841G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766406 | |||||||
chr2:185766436 | A | T | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(51): Show |
67 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1411+1871A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766436 | |||||||
chr2:185766498 | G | T | 3 | a0023c0025t0001g0022 a0023c0025t0001g0188 a0048c0035t0001g0042 |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411+1933G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766498 | |||||||
chr2:185766503 | T | C | 1 | a0004c0004t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1411+1938T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766503 | |||||||
chr2:185766519 | A | T | 1 | a0003c0003t0001g0222 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1411+1954A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766519 | |||||||
chr2:185766587 | T | G | 1 | a0003c0003t0001g0210 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1411+2022T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766587 | |||||||
chr2:185766630 | A | C | 34 | a0003c0066t0001g0288 a0005c0005t0001g0011 a0005c0005t0001g0032 others(31): Show |
42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1411+2065A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766630 | |||||||
chr2:185766700 | A | G | 3 | a0010c0011t0002g0099 a0010c0011t0002g0119 a0010c0047t0002g0117 |
3 | HG02738.hp1 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1411+2135A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766700 | |||||||
chr2:185766734 | T | C | 1 | a0001c0001t0002g0114 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1411+2169T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766734 | |||||||
chr2:185766760 | C | T | 146 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(143): Show |
172 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1411+2195C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766760 | |||||||
chr2:185766832 | G | A | 1 | a0003c0076t0001g0265 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1411+2267G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766832 | |||||||
chr2:185766834 | C | T | 1 | a0042c0080t0003g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1411+2269C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766834 | |||||||
chr2:185766851 | A | G | 3 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0001g0310 |
3 | HG01123.hp1 HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1411+2286A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766851 | |||||||
chr2:185766862 | C | T | 164 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(161): Show |
191 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1411+2297C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766862 | |||||||
chr2:185766864 | C | T | 1 | a0042c0080t0003g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1411+2299C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766864 | |||||||
chr2:185766881 | T | C | 1 | a0042c0080t0003g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1411+2316T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766881 | |||||||
chr2:185767044 | C | G | 1 | a0027c0030t0002g0118 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1411+2479C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767044 | |||||||
chr2:185767062 | G | A | 1 | a0043c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1411+2497G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767062 | |||||||
chr2:185767099 | A | G | 3 | a0003c0012t0001g0190 a0003c0012t0001g0195 a0003c0075t0001g0189 |
3 | HG02970.hp2 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1411+2534A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767099 | |||||||
chr2:185767110 | T | C | 3 | a0023c0025t0001g0022 a0023c0025t0001g0188 a0048c0035t0001g0042 |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411+2545T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767110 | |||||||
chr2:185767130 | G | A | 5 | a0016c0022t0002g0178 a0016c0022t0002g0179 a0016c0022t0002g0180 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1411+2565G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767130 | |||||||
chr2:185767198 | C | T | 4 | a0020c0021t0001g0023 a0020c0021t0001g0197 a0020c0021t0001g0198 others(1): Show |
6 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1411+2633C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767198 | |||||||
chr2:185767201 | G | C | 3 | a0019c0020t0003g0013 a0019c0020t0003g0043 a0019c0020t0003g0044 |
4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411+2636G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767201 | |||||||
chr2:185767218 | A | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1411+2653A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767218 | |||||||
chr2:185767331 | T | A | 3 | a0019c0020t0003g0013 a0019c0020t0003g0043 a0019c0020t0003g0044 |
4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411+2766T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767331 | |||||||
chr2:185767369 | A | C | 1 | a0003c0012t0001g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1411+2804A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767369 | |||||||
chr2:185767430 | C | T | 9 | a0016c0022t0002g0178 a0016c0022t0002g0179 a0016c0022t0002g0180 others(6): Show |
10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1411+2865C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767430 | |||||||
chr2:185767513 | T | C | 3 | a0003c0012t0001g0190 a0003c0012t0001g0195 a0003c0075t0001g0189 |
3 | HG02970.hp2 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1411+2948T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767513 | |||||||
chr2:185767528 | T | A | 19 | a0003c0003t0001g0266 a0003c0003t0001g0267 a0003c0003t0001g0269 others(16): Show |
21 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1411+2963T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767528 | |||||||
chr2:185767540 | T | C | 1 | a0003c0003t0001g0222 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1411+2975T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767540 | |||||||
chr2:185767647 | T | A | 2 | a0001c0001t0002g0121 a0040c0045t0002g0122 |
2 | HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1411+3082T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767647 | |||||||
chr2:185767793 | T | G | 1 | a0004c0004t0001g0081 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1411+3228T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767793 | |||||||
chr2:185767914 | G | A | 1 | a0005c0005t0001g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1411+3349G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767914 | |||||||
chr2:185768121 | T | A | 1 | a0056c0064t0001g0243 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1411+3556T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185768121 | |||||||
chr2:185768349 | A | G | 2 | a0001c0043t0002g0129 a0008c0010t0002g0130 |
2 | NA18959.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1411+3784A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185768349 | |||||||
chr2:185768528 | A | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1411+3963A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185768528 | |||||||
chr2:185768665 | C | T | 1 | a0009c0009t0001g0298 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1411+4100C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185768665 | |||||||
chr2:185768798 | A | G | 162 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(159): Show |
189 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1411+4233A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185768798 | |||||||
chr2:185768892 | T | C | 1 | a0003c0012t0001g0195 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1411+4327T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185768892 | |||||||
chr2:185768941 | T | C | 27 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(24): Show |
31 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1411+4376T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185768941 | |||||||
chr2:185768990 | T | C | 197 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(194): Show |
230 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1411+4425T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185768990 | |||||||
chr2:185769102 | C | T | 4 | a0001c0001t0002g0159 a0020c0021t0001g0023 a0020c0021t0001g0197 others(1): Show |
5 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1411+4537C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185769102 | |||||||
chr2:185769292 | C | T | 1 | a0019c0020t0003g0044 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1411+4727C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185769292 | |||||||
chr2:185769824 | G | A | 1 | a0004c0004t0001g0069 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1411+5259G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185769824 | |||||||
chr2:185769844 | T | G | 1 | a0001c0001t0002g0143 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1411+5279T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185769844 | |||||||
chr2:185769970 | T | G | 1 | a0001c0001t0002g0137 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1411+5405T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185769970 | |||||||
chr2:185770122 | G | C | 100 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(97): Show |
115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1411+5557G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185770122 | |||||||
chr2:185770122 | G | T | 1 | a0050c0071t0001g0221 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1411+5557G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185770122 | |||||||
chr2:185770126 | G | A | 1 | a0050c0071t0001g0221 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1411+5561G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185770126 | |||||||
chr2:185770200 | A | G | 19 | a0003c0003t0001g0266 a0003c0003t0001g0267 a0003c0003t0001g0269 others(16): Show |
21 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1411+5635A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185770200 | |||||||
chr2:185770241 | G | C | 1 | a0003c0003t0001g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1411+5676G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185770241 | |||||||
chr2:185770360 | T | C | 1 | a0003c0003t0001g0308 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1411+5795T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185770360 | |||||||
chr2:185770388 | G | A | 1 | a0048c0035t0001g0042 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1411+5823G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185770388 | |||||||
chr2:185770821 | T | C | 1 | a0016c0022t0002g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1411+6256T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185770821 | |||||||
chr2:185771002 | C | T | 9 | a0006c0006t0001g0031 a0006c0006t0001g0273 a0006c0006t0001g0274 others(6): Show |
10 | HG01099.hp1 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1411+6437C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771002 | |||||||
chr2:185771033 | C | G | 1 | a0005c0005t0001g0297 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1411+6468C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771033 | |||||||
chr2:185771142 | T | A | 1 | a0003c0075t0001g0189 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1411+6577T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771142 | |||||||
chr2:185771184 | G | A | 7 | a0003c0012t0001g0190 a0003c0012t0001g0192 a0003c0012t0001g0193 others(4): Show |
7 | HG02818.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411+6619G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771184 | |||||||
chr2:185771324 | G | A | 7 | a0003c0012t0001g0190 a0003c0012t0001g0192 a0003c0012t0001g0193 others(4): Show |
7 | HG02818.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411+6759G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771324 | |||||||
chr2:185771350 | G | T | 34 | a0003c0066t0001g0288 a0005c0005t0001g0011 a0005c0005t0001g0032 others(31): Show |
42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1411+6785G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771350 | |||||||
chr2:185771356 | A | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1411+6791A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771356 | |||||||
chr2:185771606 | A | G | 1 | a0016c0022t0002g0182 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1411+7041A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771606 | |||||||
chr2:185771607 | A | G | 1 | a0062c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1411+7042A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771607 | |||||||
chr2:185771615 | C | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1411+7050C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771615 | |||||||
chr2:185772124 | C | T | 4 | a0019c0020t0003g0013 a0019c0020t0003g0043 a0019c0020t0003g0044 others(1): Show |
5 | HG01891.hp1 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1411+7559C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772124 | |||||||
chr2:185772145 | T | A | 1 | a0003c0003t0001g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1411+7580T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772145 | |||||||
chr2:185772431 | G | A | 2 | a0003c0003t0001g0014 a0057c0074t0001g0212 |
3 | HG01081.hp2 HG02300.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1411+7866G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772431 | |||||||
chr2:185772568 | A | G | 296 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(293): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1411+8003A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772568 | |||||||
chr2:185772584 | C | T | 1 | a0001c0001t0002g0158 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1411+8019C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772584 | |||||||
chr2:185772589 | C | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1411+8024C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772589 | |||||||
chr2:185772757 | T | C | 101 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(98): Show |
116 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1411+8192T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772757 | |||||||
chr2:185772759 | A | G | 101 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(98): Show |
116 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1411+8194A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772759 | |||||||
chr2:185772775 | G | A | 3 | a0023c0025t0001g0022 a0023c0025t0001g0188 a0048c0035t0001g0042 |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411+8210G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772775 | |||||||
chr2:185772788 | T | A | 1 | a0049c0048t0001g0186 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1411+8223T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772788 | |||||||
chr2:185772804 | T | TCCTCC | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1411+8250_1411+825 others(9): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185772804 | ||||||
chr2:185772843 | C | T | 1 | a0002c0002t0001g0256 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1411+8278C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772843 | |||||||
chr2:185772983 | C | T | 3 | a0019c0020t0003g0013 a0019c0020t0003g0043 a0019c0020t0003g0044 |
4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411+8418C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772983 | |||||||
chr2:185773106 | T | C | 1 | a0002c0002t0001g0036 | 2 | HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1411+8541T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773106 | |||||||
chr2:185773153 | C | T | 2 | a0027c0030t0002g0118 a0027c0030t0002g0183 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1411+8588C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773153 | |||||||
chr2:185773207 | G | A | 1 | a0025c0033t0001g0311 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1411+8642G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773207 | |||||||
chr2:185773283 | T | C | 296 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(293): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1411+8718T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773283 | |||||||
chr2:185773324 | A | G | 2 | a0003c0072t0001g0184 a0047c0073t0001g0275 |
2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1411+8759A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773324 | |||||||
chr2:185773327 | C | G | 1 | a0003c0003t0001g0220 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1411+8762C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773327 | |||||||
chr2:185773333 | T | C | 2 | a0003c0072t0001g0184 a0047c0073t0001g0275 |
2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1411+8768T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773333 | |||||||
chr2:185773712 | C | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-8993C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773712 | |||||||
chr2:185773747 | T | C | 2 | a0023c0025t0001g0022 a0023c0025t0001g0188 |
3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1412-8958T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773747 | |||||||
chr2:185773835 | G | A | 9 | a0016c0022t0002g0178 a0016c0022t0002g0179 a0016c0022t0002g0180 others(6): Show |
10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1412-8870G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773835 | |||||||
chr2:185773939 | A | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-8766A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773939 | |||||||
chr2:185774434 | C | T | 7 | a0003c0012t0001g0190 a0003c0012t0001g0192 a0003c0012t0001g0193 others(4): Show |
7 | HG02818.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412-8271C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774434 | |||||||
chr2:185774503 | C | CTAAT | 101 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(98): Show |
116 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1412-8200_1412-819 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185774503 | ||||||
chr2:185774512 | T | C | 101 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(98): Show |
116 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1412-8193T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774512 | |||||||
chr2:185774581 | ATT | A | 160 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(157): Show |
186 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1412-8113_1412-811 others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185774581 | ||||||
chr2:185774648 | G | A | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-8057G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774648 | |||||||
chr2:185774690 | C | A | 1 | a0003c0003t0001g0222 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1412-8015C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774690 | |||||||
chr2:185774730 | C | G | 2 | a0005c0005t0001g0201 a0005c0005t0001g0296 |
2 | HG02015.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1412-7975C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774730 | |||||||
chr2:185774768 | T | C | 2 | a0001c0001t0002g0164 a0001c0001t0002g0165 |
2 | NA18961.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1412-7937T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774768 | |||||||
chr2:185774822 | A | T | 3 | a0004c0004t0002g0016 a0004c0004t0002g0100 a0004c0004t0002g0101 |
4 | NA18953.hp2 NA18967.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.1412-7883A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774822 | |||||||
chr2:185774828 | A | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-7877A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774828 | |||||||
chr2:185774847 | C | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-7858C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774847 | |||||||
chr2:185774872 | A | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-7833A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774872 | |||||||
chr2:185774879 | A | G | 32 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(29): Show |
38 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1412-7826A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774879 | |||||||
chr2:185774916 | A | C | 101 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(98): Show |
116 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1412-7789A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774916 | |||||||
chr2:185774955 | T | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-7750T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774955 | |||||||
chr2:185775008 | T | A | 1 | a0016c0022t0002g0182 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1412-7697T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775008 | |||||||
chr2:185775026 | A | G | 32 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(29): Show |
38 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1412-7679A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775026 | |||||||
chr2:185775031 | G | A | 1 | a0002c0002t0001g0257 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1412-7674G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775031 | |||||||
chr2:185775040 | A | C | 101 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(98): Show |
116 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1412-7665A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775040 | |||||||
chr2:185775080 | C | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-7625C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775080 | |||||||
chr2:185775210 | C | T | 2 | a0001c0001t0002g0157 a0043c0079t0001g0191 |
2 | HG02300.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1412-7495C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775210 | |||||||
chr2:185775211 | G | A | 7 | a0003c0012t0001g0190 a0003c0012t0001g0192 a0003c0012t0001g0193 others(4): Show |
7 | HG02818.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412-7494G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775211 | |||||||
chr2:185775232 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1412-7473C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775232 | |||||||
chr2:185775327 | T | G | 296 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(293): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1412-7378T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775327 | |||||||
chr2:185775503 | G | A | 162 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(159): Show |
189 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1412-7202G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775503 | |||||||
chr2:185775548 | A | G | 1 | a0003c0012t0001g0195 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1412-7157A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775548 | |||||||
chr2:185775647 | G | C | 3 | a0001c0001t0002g0137 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | NA19082.hp2 NA19085.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1412-7058G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775647 | |||||||
chr2:185775656 | TTTTG | T | 3 | a0019c0020t0003g0013 a0019c0020t0003g0043 a0019c0020t0003g0044 |
4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-7037_1412-703 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185775656 | ||||||
chr2:185775682 | T | G | 1 | a0061c0052t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1412-7023T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775682 | |||||||
chr2:185775813 | A | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-6892A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775813 | |||||||
chr2:185775873 | A | C | 2 | a0001c0001t0002g0120 a0001c0001t0002g0128 |
2 | HG00423.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1412-6832A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775873 | |||||||
chr2:185775883 | T | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-6822T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775883 | |||||||
chr2:185775943 | G | A | 1 | a0029c0068t0001g0285 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1412-6762G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775943 | |||||||
chr2:185775984 | A | G | 3 | a0020c0021t0001g0023 a0020c0021t0001g0197 a0020c0021t0001g0198 |
4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1412-6721A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775984 | |||||||
chr2:185776008 | G | A | 2 | a0001c0001t0002g0144 a0001c0001t0002g0158 |
2 | NA18945.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1412-6697G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776008 | |||||||
chr2:185776024 | C | T | 1 | a0062c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1412-6681C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776024 | |||||||
chr2:185776041 | G | A | 1 | a0035c0055t0001g0280 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1412-6664G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776041 | |||||||
chr2:185776050 | G | A | 19 | a0003c0003t0001g0266 a0003c0003t0001g0267 a0003c0003t0001g0269 others(16): Show |
21 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1412-6655G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776050 | |||||||
chr2:185776109 | A | G | 1 | a0005c0005t0001g0282 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1412-6596A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776109 | |||||||
chr2:185776203 | A | G | 296 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(293): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1412-6502A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776203 | |||||||
chr2:185776212 | G | T | 1 | a0061c0052t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1412-6493G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776212 | |||||||
chr2:185776269 | C | G | 1 | a0005c0005t0001g0282 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1412-6436C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776269 | |||||||
chr2:185776298 | AAATTAT | A | 3 | a0003c0012t0001g0190 a0003c0012t0001g0195 a0003c0075t0001g0189 |
3 | HG02970.hp2 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1412-6403_1412-639 others(10): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185776298 | ||||||
chr2:185776309 | A | T | 19 | a0003c0003t0001g0266 a0003c0003t0001g0267 a0003c0003t0001g0269 others(16): Show |
21 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1412-6396A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776309 | |||||||
chr2:185776401 | C | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-6304C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776401 | |||||||
chr2:185776449 | C | T | 1 | a0005c0005t0001g0282 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1412-6256C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776449 | |||||||
chr2:185776467 | C | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-6238C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776467 | |||||||
chr2:185776485 | A | T | 25 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(22): Show |
29 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1412-6220A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776485 | |||||||
chr2:185776542 | A | G | 1 | a0003c0003t0001g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1412-6163A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776542 | |||||||
chr2:185776694 | A | G | 1 | a0001c0001t0002g0165 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1412-6011A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776694 | |||||||
chr2:185776746 | T | C | 7 | a0003c0012t0001g0190 a0003c0012t0001g0192 a0003c0012t0001g0193 others(4): Show |
7 | HG02818.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412-5959T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776746 | |||||||
chr2:185776801 | C | T | 1 | a0002c0002t0001g0257 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1412-5904C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776801 | |||||||
chr2:185776805 | G | C | 2 | a0007c0007t0001g0047 a0007c0007t0001g0048 |
2 | HG00423.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1412-5900G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776805 | |||||||
chr2:185777009 | C | G | 1 | a0003c0003t0001g0220 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1412-5696C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777009 | |||||||
chr2:185777393 | G | GT | 11 | a0003c0012t0001g0192 a0003c0012t0001g0193 a0003c0012t0003g0040 others(8): Show |
11 | HG00544.hp1 HG01261.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412-5294dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185777393 | ||||||
chr2:185777393 | GT | G | 143 | a0001c0001t0002g0019 a0001c0001t0002g0131 a0001c0001t0002g0136 others(140): Show |
168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1412-5294delT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185777393 | ||||||
chr2:185777393 | GTT | G | 78 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(75): Show |
86 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1412-5295_1412-529 others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185777393 | ||||||
chr2:185777393 | GTTT | G | 22 | a0001c0001t0002g0003 a0001c0001t0002g0089 a0001c0001t0002g0110 others(19): Show |
30 | HG00323.hp1 HG01255.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.1412-5296_1412-529 others(7): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185777393 | ||||||
chr2:185777420 | C | A | 2 | a0003c0012t0001g0190 a0003c0075t0001g0189 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1412-5285C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777420 | |||||||
chr2:185777439 | G | A | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-5266G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777439 | |||||||
chr2:185777625 | T | G | 2 | a0001c0001t0002g0125 a0001c0001t0002g0145 |
2 | NA18941.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1412-5080T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777625 | |||||||
chr2:185777637 | A | G | 1 | a0062c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1412-5068A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777637 | |||||||
chr2:185777711 | C | T | 1 | a0003c0003t0001g0209 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1412-4994C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777711 | |||||||
chr2:185777826 | T | C | 3 | a0023c0025t0001g0022 a0023c0025t0001g0188 a0048c0035t0001g0042 |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1412-4879T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777826 | |||||||
chr2:185777837 | A | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-4868A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777837 | |||||||
chr2:185777848 | C | A | 1 | a0003c0003t0001g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1412-4857C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777848 | |||||||
chr2:185777862 | C | A | 1 | a0002c0002t0001g0244 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1412-4843C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777862 | |||||||
chr2:185778089 | G | T | 195 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(192): Show |
228 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1412-4616G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185778089 | |||||||
chr2:185778546 | T | G | 1 | a0005c0005t0001g0032 | 2 | HG01175.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1412-4159T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185778546 | |||||||
chr2:185778912 | G | C | 34 | a0003c0066t0001g0288 a0005c0005t0001g0011 a0005c0005t0001g0032 others(31): Show |
42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1412-3793G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185778912 | |||||||
chr2:185778950 | A | G | 1 | a0001c0008t0002g0148 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1412-3755A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185778950 | |||||||
chr2:185779061 | T | C | 1 | a0001c0001t0002g0089 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1412-3644T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185779061 | |||||||
chr2:185779075 | G | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-3630G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185779075 | |||||||
chr2:185779077 | T | G | 1 | a0003c0012t0001g0195 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1412-3628T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185779077 | |||||||
chr2:185779300 | G | GT | 159 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(156): Show |
186 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1412-3395dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185779300 | ||||||
chr2:185779541 | T | C | 109 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(106): Show |
125 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1412-3164T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185779541 | |||||||
chr2:185779549 | T | C | 112 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(109): Show |
130 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1412-3156T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185779549 | |||||||
chr2:185779666 | G | T | 32 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(29): Show |
38 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1412-3039G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185779666 | |||||||
chr2:185779668 | TTTC | T | 3 | a0010c0011t0002g0099 a0010c0011t0002g0119 a0010c0047t0002g0117 |
3 | HG02738.hp1 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1412-3034_1412-303 others(7): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185779668 | ||||||
chr2:185779677 | ATT | A | 3 | a0016c0022t0002g0180 a0016c0022t0002g0182 a0016c0038t0002g0181 |
3 | HG02630.hp1 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1412-3027_1412-302 others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185779677 | |||||||
chr2:185779824 | C | T | 1 | a0002c0002t0001g0256 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1412-2881C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185779824 | |||||||
chr2:185780039 | C | T | 1 | a0005c0005t0001g0307 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1412-2666C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185780039 | |||||||
chr2:185780072 | C | CA | 16 | a0002c0002t0001g0006 a0002c0002t0001g0026 a0002c0002t0001g0084 others(13): Show |
18 | HG01192.hp1 HG01361.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1412-2619dupA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185780072 | ||||||
chr2:185780072 | C | CAA | 7 | a0010c0011t0002g0099 a0010c0011t0002g0107 a0010c0011t0002g0108 others(4): Show |
7 | HG00099.hp2 HG00741.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412-2620_1412-261 others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185780072 | ||||||
chr2:185780082 | A | T | 2 | a0001c0001t0002g0147 a0001c0001t0002g0160 |
2 | NA18966.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1412-2623A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185780082 | |||||||
chr2:185780164 | C | T | 1 | a0006c0006t0001g0274 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1412-2541C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185780164 | |||||||
chr2:185780253 | A | T | 1 | a0033c0058t0001g0261 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1412-2452A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185780253 | |||||||
chr2:185780256 | T | C | 6 | a0003c0003t0001g0213 a0003c0003t0001g0214 a0003c0003t0001g0215 others(3): Show |
6 | HG02135.hp2 NA18747.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.1412-2449T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185780256 | |||||||
chr2:185780407 | T | C | 2 | a0005c0005t0001g0286 a0005c0005t0001g0300 |
2 | HG01952.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1412-2298T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185780407 | |||||||
chr2:185780567 | C | CT | 27 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(24): Show |
31 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1412-2136dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185780567 | ||||||
chr2:185780570 | C | T | 27 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(24): Show |
31 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1412-2135C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185780570 | |||||||
chr2:185780574 | A | T | 27 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(24): Show |
31 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1412-2131A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185780574 | |||||||
chr2:185780723 | A | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-1982A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185780723 | |||||||
chr2:185780987 | T | TATC | 4 | a0005c0005t0001g0303 a0005c0005t0001g0305 a0021c0028t0001g0034 others(1): Show |
5 | HG01261.hp2 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1412-1717_1412-171 others(7): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185780987 | ||||||
chr2:185781044 | T | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-1661T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781044 | |||||||
chr2:185781058 | G | T | 25 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(22): Show |
29 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1412-1647G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781058 | |||||||
chr2:185781059 | A | AT | 150 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(147): Show |
176 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1412-1633dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185781059 | ||||||
chr2:185781126 | GACTT | G | 195 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(192): Show |
228 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1412-1572_1412-156 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185781126 | ||||||
chr2:185781434 | T | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-1271T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781434 | |||||||
chr2:185781441 | G | A | 1 | a0062c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1412-1264G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781441 | |||||||
chr2:185781443 | G | T | 2 | a0002c0002t0001g0252 a0002c0002t0001g0253 |
2 | NA19054.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1412-1262G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781443 | |||||||
chr2:185781465 | C | T | 195 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(192): Show |
228 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1412-1240C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781465 | |||||||
chr2:185781527 | G | A | 1 | a0004c0004t0002g0100 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1412-1178G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781527 | |||||||
chr2:185781843 | C | CT | 159 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(156): Show |
185 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1412-850dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185781843 | ||||||
chr2:185781900 | C | T | 1 | a0001c0001t0002g0126 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1412-805C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781900 | |||||||
chr2:185781912 | A | G | 1 | a0043c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1412-793A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781912 | |||||||
chr2:185781959 | T | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-746T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781959 | |||||||
chr2:185781963 | C | G | 8 | a0016c0022t0002g0178 a0016c0022t0002g0179 a0016c0022t0002g0180 others(5): Show |
9 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-742C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781963 | |||||||
chr2:185782004 | C | A | 1 | a0004c0004t0001g0072 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1412-701C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185782004 | |||||||
chr2:185782076 | T | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-629T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185782076 | |||||||
chr2:185782202 | A | G | 9 | a0016c0022t0002g0178 a0016c0022t0002g0179 a0016c0022t0002g0180 others(6): Show |
10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1412-503A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185782202 | |||||||
chr2:185782218 | A | T | 2 | a0005c0005t0001g0033 a0005c0005t0001g0295 |
3 | HG03688.hp1 HG03710.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1412-487A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185782218 | |||||||
chr2:185782294 | TTCAGGTA | T | 153 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(150): Show |
179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1412-410_1412-404d others(9): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185782294 | |||||||
chr2:185782431 | C | T | 1 | a0062c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1412-274C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185782431 | |||||||
chr2:185782543 | T | TA | 34 | a0003c0066t0001g0288 a0005c0005t0001g0011 a0005c0005t0001g0032 others(31): Show |
42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1412-161dupA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185782543 | ||||||
chr2:185782845 | G | A | 1 | a0062c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1469+83G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185782845 | |||||||
chr2:185782941 | T | C | 2 | a0001c0001t0002g0125 a0001c0001t0002g0145 |
2 | NA18941.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1469+179T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185782941 | |||||||
chr2:185783174 | C | A | 1 | a0043c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1469+412C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185783174 | |||||||
chr2:185783742 | G | C | 5 | a0016c0022t0002g0178 a0016c0022t0002g0179 a0016c0022t0002g0180 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1469+980G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185783742 | |||||||
chr2:185783913 | A | G | 1 | a0004c0004t0001g0065 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1469+1151A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185783913 | |||||||
chr2:185783942 | C | G | 3 | a0019c0020t0003g0013 a0019c0020t0003g0043 a0019c0020t0003g0044 |
4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1469+1180C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185783942 | |||||||
chr2:185784069 | T | C | 1 | a0032c0065t0001g0287 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1469+1307T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185784069 | |||||||
chr2:185784125 | T | A | 1 | a0013c0013t0002g0149 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1469+1363T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185784125 | |||||||
chr2:185784168 | T | C | 1 | a0013c0013t0002g0149 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1469+1406T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185784168 | |||||||
chr2:185784191 | G | C | 1 | a0013c0013t0002g0149 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1469+1429G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185784191 | |||||||
chr2:185784247 | G | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1469+1485G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185784247 | |||||||
chr2:185784606 | A | C | 1 | a0003c0003t0001g0308 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1470-1646A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185784606 | |||||||
chr2:185785210 | T | C | 296 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(293): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1470-1042T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185785210 | |||||||
chr2:185785261 | T | G | 1 | a0006c0069t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1470-991T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185785261 | |||||||
chr2:185785569 | A | ATATT | 102 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(99): Show |
117 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1470-677_1470-674d others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr2 | 185785569 | ||||||
chr2:185785653 | C | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1470-599C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185785653 | |||||||
chr2:185785685 | T | C | 162 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(159): Show |
189 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1470-567T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185785685 | |||||||
chr2:185785736 | C | CTT | 3 | a0023c0025t0001g0022 a0023c0025t0001g0188 a0048c0035t0001g0042 |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1470-515_1470-514d others(4): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr2 | 185785736 | ||||||
chr2:185785938 | T | C | 1 | a0042c0080t0003g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1470-314T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185785938 | |||||||
chr2:185786171 | T | A | 3 | a0020c0021t0001g0023 a0020c0021t0001g0197 a0020c0021t0001g0198 |
4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1470-81T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185786171 | |||||||
chr2:185786425 | C | T | 3 | a0023c0025t0001g0022 a0023c0025t0001g0188 a0048c0035t0001g0042 |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506+137C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786425 | |||||||
chr2:185786510 | C | T | 54 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(51): Show |
67 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1506+222C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786510 | |||||||
chr2:185786543 | A | G | 9 | a0016c0022t0002g0178 a0016c0022t0002g0179 a0016c0022t0002g0180 others(6): Show |
10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1506+255A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786543 | |||||||
chr2:185786654 | G | A | 101 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(98): Show |
116 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1506+366G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786654 | |||||||
chr2:185786660 | T | C | 25 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(22): Show |
29 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1506+372T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786660 | |||||||
chr2:185786784 | C | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1506+496C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786784 | |||||||
chr2:185786834 | C | T | 1 | a0006c0006t0001g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1506+546C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786834 | |||||||
chr2:185786891 | T | C | 1 | a0018c0024t0001g0238 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1506+603T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786891 | |||||||
chr2:185786915 | C | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1506+627C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786915 | |||||||
chr2:185786926 | A | C | 1 | a0043c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1506+638A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786926 | |||||||
chr2:185786937 | A | G | 1 | a0003c0003t0001g0014 | 2 | HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1506+649A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786937 | |||||||
chr2:185786958 | T | A | 4 | a0003c0012t0001g0192 a0003c0012t0001g0193 a0003c0012t0003g0039 others(1): Show |
4 | HG02818.hp2 HG02895.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506+670T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786958 | |||||||
chr2:185786982 | C | T | 4 | a0003c0012t0001g0192 a0003c0012t0001g0193 a0003c0012t0003g0039 others(1): Show |
4 | HG02818.hp2 HG02895.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506+694C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786982 | |||||||
chr2:185787032 | G | A | 146 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(143): Show |
172 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1506+744G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185787032 | |||||||
chr2:185787173 | G | C | 1 | a0062c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1506+885G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185787173 | |||||||
chr2:185787183 | T | A | 2 | a0002c0002t0001g0245 a0002c0002t0001g0246 |
2 | HG00639.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1506+895T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185787183 | |||||||
chr2:185787199 | A | G | 1 | a0006c0069t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1506+911A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185787199 | |||||||
chr2:185787232 | T | TAAG | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1506+946_1506+948d others(5): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr2 | 185787232 | ||||||
chr2:185787242 | A | G | 1 | a0003c0003t0001g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1506+954A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185787242 | |||||||
chr2:185787644 | G | A | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1507-999G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185787644 | |||||||
chr2:185787849 | C | T | 19 | a0003c0003t0001g0266 a0003c0003t0001g0267 a0003c0003t0001g0269 others(16): Show |
21 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1507-794C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185787849 | |||||||
chr2:185787884 | T | G | 2 | a0007c0007t0001g0047 a0007c0007t0001g0048 |
2 | HG00423.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1507-759T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185787884 | |||||||
chr2:185787982 | T | C | 1 | a0003c0003t0001g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1507-661T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185787982 | |||||||
chr2:185788089 | A | G | 3 | a0001c0001t0002g0135 a0001c0001t0002g0157 a0001c0001t0002g0161 |
3 | HG01496.hp2 HG02300.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1507-554A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185788089 | |||||||
chr2:185788091 | A | G | 10 | a0004c0004t0001g0005 a0004c0004t0001g0068 a0004c0004t0001g0069 others(7): Show |
12 | HG00544.hp1 HG00558.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.1507-552A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185788091 | |||||||
chr2:185788119 | G | T | 1 | a0002c0002t0001g0251 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1507-524G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185788119 | |||||||
chr2:185788164 | C | G | 1 | a0002c0002t0001g0026 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1507-479C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185788164 | |||||||
chr2:185788220 | A | C | 1 | a0002c0057t0001g0250 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1507-423A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185788220 | |||||||
chr2:185788300 | T | C | 1 | a0001c0001t0002g0175 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1507-343T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185788300 | |||||||
chr2:185788631 | C | T | 4 | a0018c0024t0001g0238 a0024c0034t0001g0037 a0024c0034t0001g0237 others(1): Show |
4 | HG00544.hp2 NA18959.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1507-12C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185788631 | |||||||
chr2:185797735 | C | A | 1 | a0001c0001t0002g0175 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.10390+209C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185797735 | |||||||
chr2:185797759 | G | T | 1 | a0003c0003t0001g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.10390+233G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185797759 | |||||||
chr2:185797917 | C | G | 1 | a0002c0002t0001g0233 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.10390+391C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185797917 | |||||||
chr2:185798039 | A | G | 3 | a0023c0025t0001g0022 a0023c0025t0001g0188 a0048c0035t0001g0042 |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.10390+513A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798039 | |||||||
chr2:185798049 | G | A | 1 | a0005c0005t0001g0282 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.10390+523G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798049 | |||||||
chr2:185798068 | T | C | 1 | a0014c0016t0001g0058 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.10390+542T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798068 | |||||||
chr2:185798109 | G | C | 1 | a0043c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.10390+583G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798109 | |||||||
chr2:185798216 | C | G | 1 | a0005c0005t0001g0296 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.10390+690C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798216 | |||||||
chr2:185798228 | C | A | 1 | a0043c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.10390+702C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798228 | |||||||
chr2:185798271 | A | C | 99 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(96): Show |
114 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.10390+745A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798271 | |||||||
chr2:185798406 | CAT | C | 3 | a0006c0006t0001g0277 a0006c0006t0001g0278 a0006c0006t0001g0279 |
3 | HG02280.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.10390+881_10390+88 others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798406 | |||||||
chr2:185798428 | C | T | 1 | a0003c0003t0001g0215 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.10390+902C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798428 | |||||||
chr2:185798670 | G | A | 34 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(31): Show |
40 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.10391-1027G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798670 | |||||||
chr2:185798810 | T | A | 3 | a0023c0025t0001g0022 a0023c0025t0001g0188 a0048c0035t0001g0042 |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.10391-887T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798810 | |||||||
chr2:185798813 | A | G | 4 | a0006c0006t0001g0030 a0006c0006t0001g0268 a0006c0006t0001g0270 others(1): Show |
5 | HG02055.hp2 HG02723.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.10391-884A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798813 | |||||||
chr2:185799052 | C | A | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.10391-645C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185799052 | |||||||
chr2:185799563 | C | A | 14 | a0006c0006t0001g0030 a0006c0006t0001g0031 a0006c0006t0001g0268 others(11): Show |
16 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.10391-134C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185799563 | |||||||
chr2:185809178 | A | T | 1 | a0043c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.19827+45A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185809178 | |||||||
chr2:185809492 | C | T | 34 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(31): Show |
40 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.19827+359C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185809492 | |||||||
chr2:185809500 | A | G | 1 | a0008c0010t0002g0094 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19827+367A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185809500 | |||||||
chr2:185809696 | A | G | 1 | a0017c0017t0001g0057 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.19827+563A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185809696 | |||||||
chr2:185809705 | G | T | 1 | a0001c0001t0002g0134 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.19827+572G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185809705 | |||||||
chr2:185809759 | A | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.19827+626A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185809759 | |||||||
chr2:185810002 | C | A | 1 | a0003c0012t0001g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.19827+869C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810002 | |||||||
chr2:185810018 | G | A | 4 | a0003c0003t0001g0216 a0003c0003t0001g0223 a0003c0003t0001g0226 others(1): Show |
4 | HG02132.hp1 NA18612.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.19827+885G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810018 | |||||||
chr2:185810244 | A | G | 34 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(31): Show |
40 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.19827+1111A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810244 | |||||||
chr2:185810469 | G | T | 1 | a0002c0002t0001g0262 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.19827+1336G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810469 | |||||||
chr2:185810506 | A | C | 1 | a0003c0003t0001g0223 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.19827+1373A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810506 | |||||||
chr2:185810537 | CT | C | 123 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(120): Show |
144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.19827+1430delT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185810537 | ||||||
chr2:185810537 | CTT | C | 9 | a0001c0001t0002g0150 a0004c0004t0001g0073 a0004c0004t0001g0074 others(6): Show |
10 | HG01168.hp1 HG01169.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.19827+1429_19827+1 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185810537 | ||||||
chr2:185810537 | CTTTTTTT | C | 5 | a0002c0002t0001g0026 a0002c0062t0001g0231 a0006c0006t0001g0277 others(2): Show |
6 | HG02257.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.19827+1424_19827+1 others(13): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185810537 | ||||||
chr2:185810537 | CTTTTTTT others(1): Show |
C | 136 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(133): Show |
161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.19827+1423_19827+1 others(14): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185810537 | ||||||
chr2:185810537 | CTTTTTTT others(3): Show |
C | 1 | a0017c0017t0001g0049 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.19827+1421_19827+1 others(16): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185810537 | ||||||
chr2:185810563 | T | A | 1 | a0003c0003t0001g0220 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.19827+1430T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810563 | |||||||
chr2:185810578 | C | T | 100 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(97): Show |
115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.19827+1445C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810578 | |||||||
chr2:185810594 | C | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.19827+1461C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810594 | |||||||
chr2:185810623 | A | G | 1 | a0004c0004t0001g0070 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.19827+1490A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810623 | |||||||
chr2:185810723 | C | CCT | 34 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(31): Show |
40 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.19827+1593_19827+1 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185810723 | ||||||
chr2:185810774 | T | C | 1 | a0010c0047t0002g0117 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.19827+1641T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810774 | |||||||
chr2:185810847 | T | G | 1 | a0005c0005t0001g0304 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.19827+1714T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810847 | |||||||
chr2:185811100 | TATTCTCA others(5): Show |
T | 1 | a0062c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.19827+1969_19827+1 others(18): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185811100 | ||||||
chr2:185811144 | T | G | 1 | a0002c0002t0001g0244 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.19827+2011T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185811144 | |||||||
chr2:185811175 | T | C | 2 | a0015c0014t0002g0103 a0015c0014t0002g0104 |
2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.19827+2042T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185811175 | |||||||
chr2:185811351 | C | T | 6 | a0009c0009t0001g0012 a0009c0009t0001g0293 a0009c0009t0001g0294 others(3): Show |
8 | HG01167.hp2 HG01169.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.19828-2194C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185811351 | |||||||
chr2:185811468 | C | CA | 16 | a0001c0001t0002g0019 a0001c0001t0002g0157 a0002c0002t0001g0245 others(13): Show |
17 | HG00741.hp2 HG01081.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.19828-2060dupA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185811468 | ||||||
chr2:185811496 | C | T | 1 | a0009c0009t0001g0298 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.19828-2049C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185811496 | |||||||
chr2:185811519 | GTTGT | G | 4 | a0002c0002t0001g0028 a0002c0002t0001g0251 a0002c0002t0001g0259 others(1): Show |
6 | NA18951.hp1 NA18961.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.19828-2003_19828-2 others(10): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185811519 | ||||||
chr2:185811523 | T | G | 1 | a0003c0003t0001g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.19828-2022T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185811523 | |||||||
chr2:185811611 | G | A | 1 | a0009c0009t0001g0293 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.19828-1934G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185811611 | |||||||
chr2:185811679 | C | T | 13 | a0006c0006t0001g0030 a0006c0006t0001g0031 a0006c0006t0001g0268 others(10): Show |
15 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.19828-1866C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185811679 | |||||||
chr2:185811990 | G | A | 1 | a0043c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.19828-1555G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185811990 | |||||||
chr2:185811995 | A | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.19828-1550A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185811995 | |||||||
chr2:185812010 | G | A | 1 | a0009c0009t0001g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.19828-1535G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812010 | |||||||
chr2:185812054 | T | C | 1 | a0001c0001t0002g0175 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.19828-1491T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812054 | |||||||
chr2:185812118 | C | T | 5 | a0005c0005t0001g0035 a0005c0005t0001g0290 a0005c0005t0001g0291 others(2): Show |
6 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.19828-1427C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812118 | |||||||
chr2:185812286 | C | T | 1 | a0002c0002t0001g0263 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.19828-1259C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812286 | |||||||
chr2:185812297 | A | T | 1 | a0008c0010t0002g0091 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.19828-1248A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812297 | |||||||
chr2:185812339 | G | A | 2 | a0002c0002t0001g0245 a0002c0002t0001g0246 |
2 | HG00639.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.19828-1206G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812339 | |||||||
chr2:185812386 | C | T | 4 | a0003c0012t0001g0192 a0003c0012t0001g0193 a0003c0012t0003g0039 others(1): Show |
4 | HG02818.hp2 HG02895.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.19828-1159C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812386 | |||||||
chr2:185812564 | C | T | 1 | a0039c0078t0001g0289 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.19828-981C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812564 | |||||||
chr2:185812749 | T | A | 1 | a0006c0006t0001g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19828-796T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812749 | |||||||
chr2:185812849 | C | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.19828-696C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812849 | |||||||
chr2:185812928 | T | G | 1 | a0008c0010t0002g0091 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.19828-617T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812928 | |||||||
chr2:185813500 | G | T | 1 | a0001c0001t0002g0159 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.19828-45G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185813500 | |||||||
chr2:185813514 | A | AT | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.19828-27dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185813514 | ||||||
chr2:185814150 | A | G | 22 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0067 others(19): Show |
25 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.20325+108A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185814150 | |||||||
chr2:185814160 | T | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20325+118T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185814160 | |||||||
chr2:185814244 | C | T | 19 | a0003c0003t0001g0266 a0003c0003t0001g0267 a0003c0003t0001g0269 others(16): Show |
21 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.20325+202C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185814244 | |||||||
chr2:185814317 | A | G | 27 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(24): Show |
31 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.20325+275A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185814317 | |||||||
chr2:185814627 | T | C | 1 | a0001c0001t0002g0161 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.20325+585T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185814627 | |||||||
chr2:185814795 | A | C | 1 | a0007c0007t0001g0056 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.20326-576A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185814795 | |||||||
chr2:185814983 | G | A | 99 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(96): Show |
114 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.20326-388G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185814983 | |||||||
chr2:185815120 | T | C | 1 | a0005c0005t0001g0301 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.20326-251T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185815120 | |||||||
chr2:185815215 | C | G | 34 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(31): Show |
40 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.20326-156C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185815215 | |||||||
chr2:185815298 | C | CA | 4 | a0003c0012t0001g0192 a0003c0012t0001g0193 a0003c0012t0003g0039 others(1): Show |
4 | HG02818.hp2 HG02895.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.20326-67dupA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr2 | 185815298 | ||||||
chr2:185815314 | G | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20326-57G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185815314 | |||||||
chr2:185815702 | A | C | 162 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(159): Show |
189 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.20426+231A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185815702 | |||||||
chr2:185815702 | A | T | 1 | a0062c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.20426+231A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185815702 | |||||||
chr2:185815934 | A | G | 296 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(293): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.20426+463A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185815934 | |||||||
chr2:185816171 | A | G | 3 | a0023c0025t0001g0022 a0023c0025t0001g0188 a0048c0035t0001g0042 |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.20426+700A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185816171 | |||||||
chr2:185816200 | ATT | A | 162 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(159): Show |
189 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.20426+740_20426+74 others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185816200 | ||||||
chr2:185816234 | A | AT | 30 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(27): Show |
35 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.20426+773dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185816234 | ||||||
chr2:185816560 | G | T | 3 | a0006c0006t0001g0030 a0006c0006t0001g0270 a0038c0070t0001g0271 |
4 | HG02055.hp2 HG02723.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.20426+1089G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185816560 | |||||||
chr2:185816585 | C | T | 1 | a0043c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20426+1114C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185816585 | |||||||
chr2:185816596 | G | T | 1 | a0002c0002t0001g0263 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.20426+1125G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185816596 | |||||||
chr2:185816614 | G | T | 2 | a0003c0003t0001g0267 a0003c0003t0001g0269 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.20426+1143G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185816614 | |||||||
chr2:185816663 | C | A | 1 | a0002c0002t0001g0009 | 3 | NA18949.hp2 NA18964.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.20426+1192C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185816663 | |||||||
chr2:185816724 | C | T | 1 | a0043c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20426+1253C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185816724 | |||||||
chr2:185816855 | C | CAG | 7 | a0016c0022t0002g0179 a0016c0022t0002g0180 a0016c0022t0002g0182 others(4): Show |
8 | HG01891.hp1 HG02630.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.20426+1408_20426+1 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185816855 | ||||||
chr2:185816855 | CAG | C | 247 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(244): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.20426+1408_20426+1 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185816855 | ||||||
chr2:185816855 | CAGAGAG | C | 6 | a0013c0013t0002g0132 a0020c0021t0001g0023 a0020c0021t0001g0197 others(3): Show |
7 | HG01978.hp2 HG02717.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.20426+1404_20426+1 others(12): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185816855 | ||||||
chr2:185816902 | AAG | A | 3 | a0019c0020t0003g0013 a0019c0020t0003g0043 a0019c0020t0003g0044 |
4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.20426+1439_20426+1 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185816902 | ||||||
chr2:185816976 | AAAG | A | 153 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(150): Show |
179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.20426+1508_20426+1 others(9): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185816976 | ||||||
chr2:185817007 | GA | G | 92 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(89): Show |
108 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.20426+1537delA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185817007 | |||||||
chr2:185817209 | C | A | 1 | a0001c0023t0002g0138 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.20426+1738C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185817209 | |||||||
chr2:185817246 | G | A | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20426+1775G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185817246 | |||||||
chr2:185817563 | G | C | 146 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(143): Show |
172 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.20426+2092G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185817563 | |||||||
chr2:185817825 | A | G | 1 | a0012c0019t0001g0202 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.20426+2354A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185817825 | |||||||
chr2:185817851 | C | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20426+2380C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185817851 | |||||||
chr2:185817966 | C | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20426+2495C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185817966 | |||||||
chr2:185817975 | T | G | 1 | a0004c0004t0004g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.20426+2504T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185817975 | |||||||
chr2:185818049 | A | C | 1 | a0005c0005t0001g0304 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.20426+2578A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185818049 | |||||||
chr2:185818108 | T | A | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20426+2637T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185818108 | |||||||
chr2:185818143 | A | G | 2 | a0003c0003t0001g0267 a0003c0003t0001g0269 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.20426+2672A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185818143 | |||||||
chr2:185818268 | G | A | 1 | a0003c0003t0001g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.20426+2797G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185818268 | |||||||
chr2:185818315 | A | G | 3 | a0020c0021t0001g0023 a0020c0021t0001g0197 a0020c0021t0001g0198 |
4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.20426+2844A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185818315 | |||||||
chr2:185818702 | A | T | 1 | a0041c0036t0001g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.20426+3231A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185818702 | |||||||
chr2:185818744 | G | A | 55 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(52): Show |
68 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.20426+3273G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185818744 | |||||||
chr2:185818770 | A | G | 3 | a0020c0021t0001g0023 a0020c0021t0001g0197 a0020c0021t0001g0198 |
4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.20426+3299A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185818770 | |||||||
chr2:185818796 | G | C | 4 | a0003c0003t0001g0225 a0003c0003t0001g0227 a0003c0003t0001g0228 others(1): Show |
4 | HG00642.hp2 HG01106.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.20426+3325G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185818796 | |||||||
chr2:185819088 | A | T | 4 | a0007c0007t0001g0053 a0007c0007t0001g0054 a0007c0007t0001g0055 others(1): Show |
4 | HG01346.hp2 HG01943.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.20426+3617A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185819088 | |||||||
chr2:185819393 | T | C | 99 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(96): Show |
114 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.20426+3922T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185819393 | |||||||
chr2:185819466 | G | C | 1 | a0003c0003t0001g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.20426+3995G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185819466 | |||||||
chr2:185819481 | G | A | 27 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(24): Show |
31 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.20426+4010G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185819481 | |||||||
chr2:185819624 | TG | T | 99 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(96): Show |
114 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.20426+4154delG | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185819624 | |||||||
chr2:185819640 | A | C | 1 | a0001c0051t0002g0106 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.20426+4169A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185819640 | |||||||
chr2:185819641 | A | AT | 5 | a0006c0006t0001g0031 a0006c0006t0001g0273 a0006c0006t0001g0274 others(2): Show |
6 | HG01099.hp1 HG02572.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.20426+4177dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185819641 | ||||||
chr2:185819838 | GTATGA | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20426+4371_20426+4 others(11): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185819838 | ||||||
chr2:185820316 | G | T | 1 | a0003c0003t0001g0310 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.20427-4118G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185820316 | |||||||
chr2:185820345 | C | T | 1 | a0003c0003t0001g0264 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.20427-4089C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185820345 | |||||||
chr2:185820463 | CCTAT | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20427-3962_20427-3 others(10): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185820463 | ||||||
chr2:185820485 | A | G | 1 | a0061c0052t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.20427-3949A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185820485 | |||||||
chr2:185820599 | T | C | 3 | a0010c0011t0002g0099 a0010c0011t0002g0119 a0010c0047t0002g0117 |
3 | HG02738.hp1 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.20427-3835T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185820599 | |||||||
chr2:185820834 | A | C | 296 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(293): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.20427-3600A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185820834 | |||||||
chr2:185820939 | A | T | 1 | a0043c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20427-3495A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185820939 | |||||||
chr2:185820967 | A | G | 1 | a0004c0004t0001g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.20427-3467A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185820967 | |||||||
chr2:185821009 | TA | T | 41 | a0001c0001t0002g0110 a0001c0001t0002g0115 a0001c0001t0002g0116 others(38): Show |
47 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.20427-3396delA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | ||||||
chr2:185821009 | TAA | T | 15 | a0001c0001t0002g0089 a0001c0001t0002g0126 a0001c0001t0002g0137 others(12): Show |
15 | HG01106.hp2 HG01175.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.20427-3397_20427-3 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | ||||||
chr2:185821009 | TAAA | T | 71 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(68): Show |
85 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.20427-3398_20427-3 others(9): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | ||||||
chr2:185821009 | TAAAA | T | 8 | a0001c0001t0002g0156 a0001c0001t0002g0158 a0001c0001t0002g0161 others(5): Show |
9 | HG01070.hp1 HG02257.hp2 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.20427-3399_20427-3 others(10): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | ||||||
chr2:185821009 | TAAAAA | T | 8 | a0002c0002t0001g0006 a0002c0002t0001g0084 a0002c0002t0001g0085 others(5): Show |
8 | HG01361.hp1 HG02109.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.20427-3400_20427-3 others(11): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | ||||||
chr2:185821009 | TAAAAAA | T | 22 | a0002c0002t0001g0009 a0002c0002t0001g0026 a0002c0057t0001g0250 others(19): Show |
26 | HG00639.hp2 HG00735.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.20427-3401_20427-3 others(12): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | ||||||
chr2:185821009 | TAAAAAAA | T | 65 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0028 others(62): Show |
78 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.20427-3402_20427-3 others(13): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | ||||||
chr2:185821009 | TAAAAAAA others(1): Show |
T | 34 | a0002c0002t0001g0249 a0003c0012t0001g0190 a0003c0075t0001g0189 others(31): Show |
41 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.20427-3403_20427-3 others(14): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | ||||||
chr2:185821009 | TAAAAAAA others(2): Show |
T | 20 | a0003c0003t0001g0266 a0003c0003t0001g0267 a0003c0003t0001g0269 others(17): Show |
21 | HG01070.hp2 HG02083.hp1 HG02630.hp1 others(18): Show |
intron_variant | MODIFIER | c.20427-3404_20427-3 others(15): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | ||||||
chr2:185821009 | TAAAAAAA others(3): Show |
T | 13 | a0006c0006t0001g0030 a0006c0006t0001g0031 a0006c0006t0001g0268 others(10): Show |
15 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.20427-3405_20427-3 others(16): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | ||||||
chr2:185821009 | TAAAAAAA others(4): Show |
T | 1 | a0006c0006t0001g0270 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.20427-3406_20427-3 others(17): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | ||||||
chr2:185821023 | A | G | 25 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0067 others(22): Show |
29 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.20427-3411A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821023 | |||||||
chr2:185821024 | A | G | 2 | a0004c0004t0001g0066 a0004c0004t0001g0077 |
2 | HG01884.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.20427-3410A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821024 | |||||||
chr2:185821057 | C | T | 27 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(24): Show |
31 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.20427-3377C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821057 | |||||||
chr2:185821082 | A | AAAGAG | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20427-3348_20427-3 others(11): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821082 | ||||||
chr2:185821256 | C | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20427-3178C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821256 | |||||||
chr2:185821313 | C | T | 2 | a0008c0027t0002g0090 a0008c0027t0002g0093 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.20427-3121C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821313 | |||||||
chr2:185821380 | C | T | 1 | a0043c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20427-3054C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821380 | |||||||
chr2:185821408 | C | T | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20427-3026C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821408 | |||||||
chr2:185821500 | C | G | 2 | a0012c0019t0001g0024 a0012c0019t0001g0217 |
3 | HG03491.hp2 HG03492.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.20427-2934C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821500 | |||||||
chr2:185821522 | C | T | 296 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(293): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.20427-2912C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821522 | |||||||
chr2:185821601 | G | A | 1 | a0002c0018t0001g0241 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.20427-2833G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821601 | |||||||
chr2:185821925 | C | CA | 7 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0008t0002g0146 others(4): Show |
7 | HG03540.hp1 HG04199.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.20427-2491dupA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821925 | ||||||
chr2:185821925 | CA | C | 98 | a0001c0001t0002g0156 a0001c0001t0002g0158 a0003c0003t0001g0014 others(95): Show |
112 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.20427-2491delA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821925 | ||||||
chr2:185821925 | CAA | C | 63 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(60): Show |
76 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.20427-2492_20427-2 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821925 | ||||||
chr2:185821933 | A | C | 1 | a0043c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20427-2501A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821933 | |||||||
chr2:185821941 | A | C | 1 | a0002c0002t0001g0185 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.20427-2493A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821941 | |||||||
chr2:185821976 | T | C | 1 | a0004c0004t0001g0073 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.20427-2458T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821976 | |||||||
chr2:185821986 | G | T | 1 | a0043c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20427-2448G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821986 | |||||||
chr2:185822004 | G | C | 1 | a0005c0005t0001g0301 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.20427-2430G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822004 | |||||||
chr2:185822033 | A | G | 1 | a0005c0005t0001g0296 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.20427-2401A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822033 | |||||||
chr2:185822191 | C | T | 1 | a0002c0002t0001g0233 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.20427-2243C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822191 | |||||||
chr2:185822293 | A | C | 2 | a0001c0001t0002g0019 a0045c0050t0002g0019 |
2 | HG01081.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.20427-2141A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822293 | |||||||
chr2:185822313 | C | A | 1 | a0003c0003t0001g0264 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.20427-2121C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822313 | |||||||
chr2:185822605 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.20427-1829G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822605 | |||||||
chr2:185822663 | C | A | 17 | a0003c0003t0001g0266 a0003c0003t0001g0267 a0003c0003t0001g0269 others(14): Show |
19 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.20427-1771C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822663 | |||||||
chr2:185822753 | C | A | 1 | a0001c0001t0002g0114 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.20427-1681C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822753 | |||||||
chr2:185822885 | C | T | 1 | a0003c0003t0001g0199 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.20427-1549C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822885 | |||||||
chr2:185822989 | T | A | 1 | a0002c0002t0001g0252 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.20427-1445T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822989 | |||||||
chr2:185823120 | G | T | 3 | a0003c0012t0001g0193 a0003c0012t0003g0039 a0003c0012t0003g0040 |
3 | HG02895.hp2 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.20427-1314G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185823120 | |||||||
chr2:185823280 | T | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20427-1154T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185823280 | |||||||
chr2:185823500 | C | T | 1 | a0002c0002t0001g0086 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.20427-934C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185823500 | |||||||
chr2:185823989 | C | A | 1 | a0006c0006t0001g0276 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.20427-445C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185823989 | |||||||
chr2:185824158 | G | A | 1 | a0003c0003t0001g0264 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.20427-276G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185824158 | |||||||
chr2:185824217 | A | G | 34 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0066 others(31): Show |
40 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.20427-217A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185824217 | |||||||
chr2:185824240 | G | A | 99 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(96): Show |
114 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.20427-194G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185824240 | |||||||
chr2:185824255 | A | G | 1 | a0002c0002t0001g0248 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.20427-179A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185824255 | |||||||
chr2:185824416 | C | G | 1 | a0062c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.20427-18C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185824416 | |||||||
chr2:185824832 | T | C | 153 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(150): Show |
179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.20473+352T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185824832 | |||||||
chr2:185825016 | G | A | 19 | a0003c0003t0001g0266 a0003c0003t0001g0267 a0003c0003t0001g0269 others(16): Show |
21 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.20473+536G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185825016 | |||||||
chr2:185825260 | T | G | 93 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(90): Show |
109 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.20473+780T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185825260 | |||||||
chr2:185825467 | A | G | 1 | a0007c0007t0001g0062 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.20473+987A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185825467 | |||||||
chr2:185825468 | T | C | 38 | a0003c0003t0001g0014 a0003c0003t0001g0025 a0003c0003t0001g0199 others(35): Show |
41 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.20473+988T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185825468 | |||||||
chr2:185826007 | A | T | 1 | a0006c0006t0001g0273 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.20473+1527A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185826007 | |||||||
chr2:185826096 | T | C | 1 | a0001c0001t0002g0165 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.20473+1616T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185826096 | |||||||
chr2:185826110 | G | A | 1 | a0023c0025t0001g0022 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.20473+1630G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185826110 | |||||||
chr2:185826255 | A | G | 1 | a0003c0012t0001g0190 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.20473+1775A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185826255 | |||||||
chr2:185826293 | C | G | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20473+1813C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185826293 | |||||||
chr2:185826321 | T | C | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20474-1835T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185826321 | |||||||
chr2:185826540 | G | C | 4 | a0001c0001t0002g0089 a0001c0001t0002g0154 a0001c0001t0002g0173 others(1): Show |
4 | HG00438.hp1 NA18959.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.20474-1616G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185826540 | |||||||
chr2:185826624 | T | A | 163 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(160): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20474-1532T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185826624 | |||||||
chr2:185826967 | GGGCACCA others(3): Show |
G | 1 | a0001c0001t0002g0152 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.20474-1188_20474-1 others(16): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185826967 | |||||||
chr2:185827032 | G | A | 99 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(96): Show |
114 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.20474-1124G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185827032 | |||||||
chr2:185827275 | C | G | 1 | a0044c0049t0002g0124 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.20474-881C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185827275 | |||||||
chr2:185827316 | G | A | 99 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(96): Show |
114 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.20474-840G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185827316 | |||||||
chr2:185827354 | T | A | 1 | a0004c0004t0001g0077 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.20474-802T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185827354 | |||||||
chr2:185827922 | C | T | 14 | a0006c0006t0001g0030 a0006c0006t0001g0031 a0006c0006t0001g0268 others(11): Show |
16 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.20474-234C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185827922 | |||||||
chr2:185828144 | T | A | 1 | a0062c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.20474-12T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185828144 | |||||||
chr2:185828403 | T | C | 1 | a0001c0001t0002g0153 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.20517+204T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185828403 | |||||||
chr2:185828863 | A | G | 93 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(90): Show |
109 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.20517+664A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185828863 | |||||||
chr2:185828881 | G | A | 296 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(293): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.20517+682G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185828881 | |||||||
chr2:185828976 | G | T | 1 | a0003c0003t0001g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.20517+777G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185828976 | |||||||
chr2:185829125 | T | G | 1 | a0037c0077t0001g0218 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.20517+926T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185829125 | |||||||
chr2:185829317 | T | C | 94 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(91): Show |
110 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.20517+1118T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185829317 | |||||||
chr2:185829394 | A | G | 1 | a0001c0043t0002g0129 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.20517+1195A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185829394 | |||||||
chr2:185829480 | T | C | 2 | a0003c0003t0001g0205 a0003c0003t0001g0209 |
2 | HG02602.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.20517+1281T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185829480 | |||||||
chr2:185829531 | G | A | 35 | a0003c0003t0001g0014 a0003c0003t0001g0025 a0003c0003t0001g0199 others(32): Show |
38 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.20517+1332G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185829531 | |||||||
chr2:185829963 | A | C | 98 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(95): Show |
113 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.20517+1764A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185829963 | |||||||
chr2:185830095 | A | G | 165 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(162): Show |
192 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.20518-1718A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830095 | |||||||
chr2:185830154 | C | A | 1 | a0004c0004t0004g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.20518-1659C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830154 | |||||||
chr2:185830256 | A | G | 1 | a0002c0002t0001g0009 | 3 | NA18949.hp2 NA18964.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.20518-1557A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830256 | |||||||
chr2:185830276 | A | G | 24 | a0005c0005t0001g0011 a0005c0005t0001g0032 a0005c0005t0001g0033 others(21): Show |
29 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.20518-1537A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830276 | |||||||
chr2:185830323 | T | C | 1 | a0037c0077t0001g0218 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.20518-1490T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830323 | |||||||
chr2:185830408 | T | G | 1 | a0043c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20518-1405T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830408 | |||||||
chr2:185830508 | T | C | 20 | a0003c0003t0001g0014 a0003c0003t0001g0210 a0003c0003t0001g0213 others(17): Show |
21 | HG00639.hp2 HG00735.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.20518-1305T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830508 | |||||||
chr2:185830669 | A | G | 155 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(152): Show |
181 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.20518-1144A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830669 | |||||||
chr2:185830675 | G | A | 31 | a0003c0072t0001g0184 a0004c0004t0001g0005 a0004c0004t0001g0065 others(28): Show |
37 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.20518-1138G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830675 | |||||||
chr2:185830687 | A | G | 1 | a0001c0001t0002g0133 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.20518-1126A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830687 | |||||||
chr2:185831217 | C | A | 1 | a0002c0002t0001g0257 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.20518-596C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185831217 | |||||||
chr2:185831389 | A | C | 3 | a0006c0006t0001g0277 a0006c0006t0001g0278 a0006c0006t0001g0279 |
3 | HG02280.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.20518-424A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185831389 | |||||||
chr2:185831531 | C | G | 296 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(293): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.20518-282C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185831531 | |||||||
chr2:185831642 | C | G | 196 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(193): Show |
229 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.20518-171C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185831642 | |||||||
chr2:185831761 | A | G | 1 | a0009c0009t0001g0294 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.20518-52A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185831761 | |||||||
chr2:185831979 | C | G | 2 | a0005c0005t0001g0291 a0005c0005t0001g0292 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.20587+97C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185831979 | |||||||
chr2:185832032 | C | T | 196 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(193): Show |
229 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.20587+150C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832032 | |||||||
chr2:185832123 | C | T | 18 | a0004c0004t0001g0005 a0004c0004t0001g0065 a0004c0004t0001g0067 others(15): Show |
21 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.20587+241C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832123 | |||||||
chr2:185832132 | T | C | 1 | a0021c0028t0001g0302 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.20587+250T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832132 | |||||||
chr2:185832244 | G | A | 1 | a0013c0013t0002g0149 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.20587+362G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832244 | |||||||
chr2:185832370 | G | C | 2 | a0001c0001t0002g0120 a0001c0001t0002g0128 |
2 | HG00423.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.20587+488G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832370 | |||||||
chr2:185832656 | G | A | 3 | a0023c0025t0001g0022 a0023c0025t0001g0188 a0048c0035t0001g0042 |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.20588-434G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832656 | |||||||
chr2:185832667 | G | C | 196 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0009 others(193): Show |
229 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.20588-423G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832667 | |||||||
chr2:185832672 | T | A | 3 | a0006c0006t0001g0277 a0006c0006t0001g0278 a0006c0006t0001g0279 |
3 | HG02280.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.20588-418T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832672 | |||||||
chr2:185832768 | T | G | 23 | a0003c0003t0001g0266 a0003c0003t0001g0267 a0003c0003t0001g0269 others(20): Show |
25 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(22): Show |
intron_variant | MODIFIER | c.20588-322T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832768 | |||||||
chr2:185832961 | C | A | 6 | a0013c0013t0002g0123 a0013c0013t0002g0132 a0013c0013t0002g0142 others(3): Show |
6 | HG01109.hp2 HG01168.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.20588-129C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832961 | |||||||
chr2:185832983 | C | T | 9 | a0006c0006t0001g0031 a0006c0006t0001g0273 a0006c0006t0001g0274 others(6): Show |
10 | HG01099.hp1 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.20588-107C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832983 |